| Year |
Citation |
Score |
| 2021 |
Halvorsen M, Samuels J, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Knowles JA, Zoghbi AW, Pottinger TD, Grados MA, Riddle MA, Bienvenu OJ, Nestadt PS, Krasnow J, et al. Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants. Nature Neuroscience. PMID 34183866 DOI: 10.1038/s41593-021-00876-8 |
0.303 |
|
| 2021 |
Mullins N, Forstner AJ, O'Connell KS, Coombes B, Coleman JRI, Qiao Z, Als TD, Bigdeli TB, Børte S, Bryois J, Charney AW, Drange OK, Gandal MJ, Hagenaars SP, Ikeda M, ... ... Knowles JA, et al. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature Genetics. PMID 34002096 DOI: 10.1038/s41588-021-00857-4 |
0.345 |
|
| 2020 |
Aldinger KA, Timms AE, MacDonald JW, McNamara HK, Herstein JS, Bammler TK, Evgrafov OV, Knowles JA, Levitt P. Transcriptome data of temporal and cingulate cortex in the Rett syndrome brain. Scientific Data. 7: 192. PMID 32561870 DOI: 10.1038/S41597-020-0527-2 |
0.303 |
|
| 2019 |
Glanville KP, Coleman JRI, Hanscombe KB, Euesden J, Choi SW, Purves KL, Breen G, Air TM, Andlauer TFM, Baune BT, Binder EB, Blackwood DHR, Boomsma DI, Buttenschøn HN, Colodro-Conde L, ... ... Knowles JA, et al. Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. Biological Psychiatry. PMID 31570195 DOI: 10.1016/J.Biopsych.2019.06.031 |
0.309 |
|
| 2019 |
Doostparast Torshizi A, Armoskus C, Zhang H, Forrest MP, Zhang S, Souaiaia T, Evgrafov OV, Knowles JA, Duan J, Wang K. Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia. Science Advances. 5: eaau4139. PMID 31535015 DOI: 10.1126/Sciadv.Aau4139 |
0.306 |
|
| 2019 |
Fox AS, Souaiaia T, Oler JA, Kovner R, Kim JMH, Nguyen J, French DA, Riedel MK, Fekete EM, Rabska MR, Olsen ME, Brodsky EK, Alexander AL, Block WF, Roseboom PH, ... Knowles JA, et al. Dorsal Amygdala Neurotrophin-3 Decreases Anxious Temperament in Primates. Biological Psychiatry. PMID 31422797 DOI: 10.1016/J.Biopsych.2019.06.022 |
0.307 |
|
| 2019 |
Stahl EA, Breen G, Forstner AJ, McQuillin A, Ripke S, Trubetskoy V, Mattheisen M, Wang Y, Coleman JRI, Gaspar HA, de Leeuw CA, Steinberg S, Pavlides JMW, Trzaskowski M, Byrne EM, ... ... Knowles JA, et al. Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics. PMID 31043756 DOI: 10.1038/S41588-019-0397-8 |
0.353 |
|
| 2019 |
Mufford M, Cheung J, Jahanshad N, van der Merwe C, Ding L, Groenewold N, Koen N, Chimusa ER, Dalvie S, Ramesar R, Knowles JA, Lochner C, Hibar DP, Paschou P, et al. Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational Psychiatry. 9: 120. PMID 30902966 DOI: 10.1038/S41398-019-0452-3 |
0.406 |
|
| 2019 |
van der Merwe C, Jahanshad N, Cheung JW, Mufford M, Groenewold NA, Koen N, Ramesar R, Dalvie S, Knowles JA, Hibar DP, Nievergelt CM, Koenen KC, Liberzon I, Ressler KJ, et al. Concordance of genetic variation that increases risk for anxiety disorders and posttraumatic stress disorders and that influences their underlying neurocircuitry. Journal of Affective Disorders. 245: 885-896. PMID 30699873 DOI: 10.1016/J.Jad.2018.11.082 |
0.303 |
|
| 2019 |
Bigdeli T, Bacanu S, Kelly B, Maher B, Knowles J, McCarroll S, Pato M, Pato C, Fanous A. WHOLE GENOME SEQUENCING OF MULTIPLY-AFFECTED SCHIZOPHRENIA AND BIPOLAR DISORDER FAMILIES FROM THE AZORES AND MADEIRA European Neuropsychopharmacology. 29: S1002-S1003. DOI: 10.1016/J.Euroneuro.2017.08.394 |
0.318 |
|
| 2019 |
Davis L, Beiter E, Khramtsova E, Van Der Merwe C, Chimusa E, Simonti C, Stein D, Capra J, Knowles J, Straub P, Hucks D, Stranger B. Polygenic Adaptation Underlies Evolution of Brain Structures and Behavioral Traits European Neuropsychopharmacology. 29: S755-S756. DOI: 10.1016/J.Euroneuro.2017.06.102 |
0.349 |
|
| 2018 |
Charney AW, Stahl EA, Green EK, Chen CY, Moran JL, Chambert K, Belliveau RA, Forty L, Gordon-Smith K, Lee PH, Bromet EJ, Buckley PF, Escamilla MA, Fanous AH, Fochtmann LJ, ... ... Knowles JA, et al. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases. Biological Psychiatry. PMID 30686506 DOI: 10.1016/J.Biopsych.2018.12.009 |
0.307 |
|
| 2018 |
Yilmaz Z, Halvorsen M, Bryois J, Yu D, Thornton LM, Zerwas S, Micali N, Moessner R, Burton CL, Zai G, Erdman L, Kas MJ, Arnold PD, Davis LK, Knowles JA, et al. Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. Molecular Psychiatry. PMID 30087453 DOI: 10.1038/S41380-018-0115-4 |
0.426 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Knowles JA, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.316 |
|
| 2018 |
Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, ... ... Knowles JA, et al. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics. PMID 29700475 DOI: 10.1038/S41588-018-0090-3 |
0.347 |
|
| 2018 |
Coba MP, Ramaker MJ, Ho EV, Thompson SL, Komiyama NH, Grant SGN, Knowles JA, Dulawa SC. Dlgap1 knockout mice exhibit alterations of the postsynaptic density and selective reductions in sociability. Scientific Reports. 8: 2281. PMID 29396406 DOI: 10.1038/S41598-018-20610-Y |
0.334 |
|
| 2017 |
Samuels J, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, McCracken JT, Piacentini J, et al. Self-reported executive function and hoarding in adults with obsessive-compulsive disorder. Comprehensive Psychiatry. 81: 53-59. PMID 29268152 DOI: 10.1016/J.Comppsych.2017.11.009 |
0.359 |
|
| 2017 |
Noh HJ, Tang R, Flannick J, O'Dushlaine C, Swofford R, Howrigan D, Genereux DP, Johnson J, van Grootheest G, Grünblatt E, Andersson E, Djurfeldt DR, Patel PD, Koltookian M, M Hultman C, ... ... Knowles JA, et al. Integrating evolutionary and regulatory information with a multispecies approach implicates genes and pathways in obsessive-compulsive disorder. Nature Communications. 8: 774. PMID 29042551 DOI: 10.1038/S41467-017-00831-X |
0.336 |
|
| 2017 |
Arpawong TE, Pendleton N, Mekli K, McArdle JJ, Gatz M, Armoskus C, Knowles JA, Prescott CA. Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Plos One. 12: e0182448. PMID 28800603 DOI: 10.1371/Journal.Pone.0182448 |
0.315 |
|
| 2017 |
Li J, Zhang W, Yang H, Howrigan DP, Wilkinson B, Souaiaia T, Evgrafov OV, Genovese G, Clementel VA, Tudor JC, Abel T, Knowles JA, Neale BM, Wang K, Sun F, et al. Spatiotemporal profile of postsynaptic interactomes integrates components of complex brain disorders. Nature Neuroscience. PMID 28671696 DOI: 10.1038/Nn.4594 |
0.31 |
|
| 2017 |
Guo W, Samuels JF, Wang Y, Cao H, Ritter M, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, et al. Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 27: 657-666. PMID 28641744 DOI: 10.1016/J.Euroneuro.2017.03.011 |
0.455 |
|
| 2017 |
Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, ... ... Knowles JA, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010 |
0.384 |
|
| 2017 |
Ritter ML, Guo W, Samuels JF, Wang Y, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, et al. Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Frontiers in Molecular Neuroscience. 10: 83. PMID 28386217 DOI: 10.3389/Fnmol.2017.00083 |
0.396 |
|
| 2017 |
Samuels J, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, Nestadt P, McCracken JT, et al. An investigation of doubt in obsessive-compulsive disorder. Comprehensive Psychiatry. 75: 117-124. PMID 28359017 DOI: 10.1016/J.Comppsych.2017.03.004 |
0.358 |
|
| 2017 |
Bigdeli TB, Ripke S, Peterson RE, Trzaskowski M, Bacanu SA, Abdellaoui A, Andlauer TF, Beekman AT, Berger K, Blackwood DH, Boomsma DI, Breen G, Buttenschøn HN, Byrne EM, Cichon S, ... ... Knowles JA, et al. Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry. 7: e1074. PMID 28350396 DOI: 10.1038/Tp.2016.292 |
0.432 |
|
| 2017 |
Charney AW, Ruderfer DM, Stahl EA, Moran JL, Chambert K, Belliveau RA, Forty L, Gordon-Smith K, Di Florio A, Lee PH, Bromet EJ, Buckley PF, Escamilla MA, Fanous AH, Fochtmann LJ, ... ... Knowles JA, et al. Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder. Translational Psychiatry. 7: e993. PMID 28072414 DOI: 10.1038/Tp.2016.242 |
0.445 |
|
| 2016 |
DeWitt JJ, Hecht PM, Grepo N, Wilkinson B, Evgrafov OV, Morris KV, Knowles JA, Campbell DB. Transcriptional Gene Silencing of the Autism-Associated Long Noncoding RNA MSNP1AS in Human Neural Progenitor Cells. Developmental Neuroscience. PMID 28030860 DOI: 10.1159/000453258 |
0.385 |
|
| 2016 |
Chen D, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, McCracken JT, Piacentini J, et al. Parental bonding and hoarding in obsessive-compulsive disorder. Comprehensive Psychiatry. 73: 43-52. PMID 27915218 DOI: 10.1016/J.Comppsych.2016.11.004 |
0.311 |
|
| 2016 |
DeWitt JJ, Grepo N, Wilkinson B, Evgrafov OV, Knowles JA, Campbell DB. Impact of the Autism-Associated Long Noncoding RNA MSNP1AS on Neuronal Architecture and Gene Expression in Human Neural Progenitor Cells. Genes. 7. PMID 27690106 DOI: 10.3390/Genes7100076 |
0.371 |
|
| 2016 |
Park JM, Samuels JF, Grados MA, Riddle MA, Bienvenu OJ, Goes FS, Cullen B, Wang Y, Krasnow J, Murphy DL, Rasmussen SA, McLaughlin NC, Piacentini J, Pauls DL, Stewart SE, ... ... Knowles JA, et al. ADHD and executive functioning deficits in OCD youths who hoard. Journal of Psychiatric Research. 82: 141-148. PMID 27501140 DOI: 10.1016/J.Jpsychires.2016.07.024 |
0.308 |
|
| 2015 |
Akbarian S, Liu C, Knowles JA, Vaccarino FM, Farnham PJ, Crawford GE, Jaffe AE, Pinto D, Dracheva S, Geschwind DH, Mill J, Nairn AC, Abyzov A, Pochareddy S, Prabhakar S, et al. The PsychENCODE project. Nature Neuroscience. 18: 1707-1712. PMID 26605881 DOI: 10.1038/Nn.4156 |
0.426 |
|
| 2015 |
Hecht PM, Ballesteros-Yanez I, Grepo N, Knowles JA, Campbell DB. Noncoding RNA in the transcriptional landscape of human neural progenitor cell differentiation. Frontiers in Neuroscience. 9: 392. PMID 26557050 DOI: 10.3389/Fnins.2015.00392 |
0.326 |
|
| 2015 |
Mroczkowski MM, Goes FS, Riddle MA, Grados MA, Bienvenu OJ, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Knowles JA, Piacentini J, Cullen B, Rasmussen SA, Pauls DL, et al. Dependent personality, separation anxiety disorder and other anxiety disorders in OCD. Personality and Mental Health. PMID 26542617 DOI: 10.1002/Pmh.1321 |
0.352 |
|
| 2015 |
Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes. Translational Psychiatry. 5: e568. PMID 25989142 DOI: 10.1038/Tp.2015.62 |
0.349 |
|
| 2015 |
Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Knowles JA, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306 |
0.422 |
|
| 2015 |
Mattheisen M, Samuels JF, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, McLaughlin NC, Nurmi EL, Askland KD, et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Molecular Psychiatry. 20: 337-44. PMID 24821223 DOI: 10.1038/mp.2014.43 |
0.32 |
|
| 2014 |
Samuels J, Grados MA, Riddle MA, Bienvenu OJ, Goes FS, Cullen B, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller D, Murphy DL, Knowles JA, Rasmussen SA, McLaughlin NC, et al. Hoarding in Children and Adolescents with Obsessive-Compulsive Disorder. Journal of Obsessive-Compulsive and Related Disorders. 3: 325-331. PMID 25309849 DOI: 10.1016/J.Jocrd.2014.08.001 |
0.316 |
|
| 2014 |
McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Knowles JA, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/J.Jaac.2014.04.022 |
0.421 |
|
| 2014 |
Samuels J, Shugart YY, Wang Y, Grados MA, Bienvenu OJ, Pinto A, Rauch SL, Greenberg BD, Knowles JA, Fyer AJ, Piacentini J, Pauls DL, Cullen B, Rasmussen SA, Stewart SE, et al. Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive-compulsive disorder: Results from the OCD Collaborative Genetics Study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 326-36. PMID 24798771 DOI: 10.1002/Ajmg.B.32235 |
0.359 |
|
| 2014 |
Hodges LM, Fyer AJ, Weissman MM, Logue MW, Haghighi F, Evgrafov O, Rotondo A, Knowles JA, Hamilton SP. Evidence for linkage and association of GABRB3 and GABRA5 to panic disorder. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 39: 2423-31. PMID 24755890 DOI: 10.1038/Npp.2014.92 |
0.359 |
|
| 2013 |
Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... Knowles JA, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864 |
0.448 |
|
| 2013 |
Bigdeli TB, Maher BS, Zhao Z, Sun J, Medeiros H, Akula N, McMahon FJ, Carvalho C, Ferreira SR, Azevedo MH, Knowles JA, Pato MT, Pato CN, Fanous AH. Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence-based prioritization algorithm. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 898-906. PMID 24123842 DOI: 10.1002/Ajmg.B.32200 |
0.377 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Knowles JA, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.411 |
|
| 2013 |
Pato MT, Sobell JL, Medeiros H, Abbott C, Sklar BM, Buckley PF, Bromet EJ, Escamilla MA, Fanous AH, Lehrer DS, Macciardi F, Malaspina D, McCarroll SA, Marder SR, Moran J, ... ... Knowles JA, et al. The genomic psychiatry cohort: partners in discovery. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 306-12. PMID 23650244 DOI: 10.1002/Ajmg.B.32160 |
0.322 |
|
| 2013 |
Stewart SE, Mayerfeld C, Arnold PD, Crane JR, O'Dushlaine C, Fagerness JA, Yu D, Scharf JM, Chan E, Kassam F, Moya PR, Wendland JR, Delorme R, Richter MA, Kennedy JL, ... ... Knowles JA, et al. Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 367-79. PMID 23606572 DOI: 10.1002/Ajmg.B.32137 |
0.415 |
|
| 2013 |
Guffanti G, Torri F, Rasmussen J, Clark AP, Lakatos A, Turner JA, Fallon JH, Saykin AJ, Weiner M, Vawter MP, Knowles JA, Potkin SG, Macciardi F. Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sample. Genomics. 102: 112-22. PMID 23583670 DOI: 10.1016/J.Ygeno.2013.04.004 |
0.301 |
|
| 2013 |
Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Knowles JA, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69 |
0.416 |
|
| 2013 |
Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Davis LK, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, ... ... Knowles JA, et al. Genome-wide association study of obsessive-compulsive disorder. Molecular Psychiatry. 18: 788-98. PMID 22889921 DOI: 10.1038/Mp.2012.85 |
0.415 |
|
| 2013 |
Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM, Breen G, Byrne EM, Blackwood DH, Boomsma DI, Cichon S, Heath AC, Holsboer F, Lucae S, Madden PA, ... ... Knowles JA, et al. A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry. 18: 497-511. PMID 22472876 DOI: 10.1038/Mp.2012.21 |
0.425 |
|
| 2013 |
Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, Illman C, ... ... Knowles JA, et al. Erratum: Genome-wide association study of obsessive-compulsive disorder Molecular Psychiatry. 18: 843-843. DOI: 10.1038/Mp.2013.15 |
0.309 |
|
| 2012 |
Torri F, Dinov ID, Zamanyan A, Hobel S, Genco A, Petrosyan P, Clark AP, Liu Z, Eggert P, Pierce J, Knowles JA, Ames J, Kesselman C, Toga AW, Potkin SG, et al. Next generation sequence analysis and computational genomics using graphical pipeline workflows. Genes. 3: 545-75. PMID 23139896 DOI: 10.3390/Genes3030545 |
0.371 |
|
| 2012 |
Webb BT, Guo AY, Maher BS, Zhao Z, van den Oord EJ, Kendler KS, Riley BP, Gillespie NA, Prescott CA, Middeldorp CM, Willemsen G, de Geus EJ, Hottenga JJ, Boomsma DI, Slagboom EP, ... ... Knowles JA, et al. Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics : Ejhg. 20: 1078-84. PMID 22473089 DOI: 10.1038/Ejhg.2012.47 |
0.434 |
|
| 2012 |
Fanous AH, Middleton FA, Gentile K, Amdur RL, Maher BS, Zhao Z, Sun J, Medeiros H, Carvalho C, Ferreira SR, Macedo A, Knowles JA, Azevedo MH, Pato MT, Pato CN. Genetic overlap of schizophrenia and bipolar disorder in a high-density linkage survey in the Portuguese Island population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 383-91. PMID 22461138 DOI: 10.1002/Ajmg.B.32041 |
0.403 |
|
| 2012 |
Logue MW, Bauver SR, Knowles JA, Gameroff MJ, Weissman MM, Crowe RR, Fyer AJ, Hamilton SP. Multivariate analysis of anxiety disorders yields further evidence of linkage to chromosomes 4q21 and 7p in panic disorder families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 274-80. PMID 22253211 DOI: 10.1002/Ajmg.B.32024 |
0.343 |
|
| 2012 |
Nestadt G, Wang Y, Grados MA, Riddle MA, Greenberg BD, Knowles JA, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Piacentini J, Geller D, Pauls D, et al. Homeobox genes in obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 53-60. PMID 22095678 DOI: 10.1002/Ajmg.B.32001 |
0.427 |
|
| 2012 |
Bienvenu OJ, Samuels JF, Wuyek LA, Liang KY, Wang Y, Grados MA, Cullen BA, Riddle MA, Greenberg BD, Rasmussen SA, Fyer AJ, Pinto A, Rauch SL, Pauls DL, McCracken JT, ... ... Knowles JA, et al. Is obsessive-compulsive disorder an anxiety disorder, and what, if any, are spectrum conditions? A family study perspective. Psychological Medicine. 42: 1-13. PMID 21733222 DOI: 10.1017/S0033291711000742 |
0.383 |
|
| 2011 |
Wang Y, Mehta G, Mayani R, Lu J, Souaiaia T, Chen Y, Clark A, Yoon HJ, Wan L, Evgrafov OV, Knowles JA, Deelman E, Chen T. RseqFlow: workflows for RNA-Seq data analysis. Bioinformatics (Oxford, England). 27: 2598-600. PMID 21795323 DOI: 10.1093/Bioinformatics/Btr441 |
0.304 |
|
| 2011 |
Samuels J, Wang Y, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Knowles JA, Piacentini J, Cullen B, Bienvenu OJ, Rasmussen SA, Geller D, et al. Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 472-7. PMID 21445956 DOI: 10.1002/Ajmg.B.31184 |
0.373 |
|
| 2011 |
Shi J, Potash JB, Knowles JA, Weissman MM, Coryell W, Scheftner WA, Lawson WB, DePaulo JR, Gejman PV, Sanders AR, Johnson JK, Adams P, Chaudhury S, Jancic D, Evgrafov O, et al. Genome-wide association study of recurrent early-onset major depressive disorder. Molecular Psychiatry. 16: 193-201. PMID 20125088 DOI: 10.1038/Mp.2009.124 |
0.414 |
|
| 2011 |
Shyn SI, Shi J, Kraft JB, Potash JB, Knowles JA, Weissman MM, Garriock HA, Yokoyama JS, McGrath PJ, Peters EJ, Scheftner WA, Coryell W, Lawson WB, Jancic D, Gejman PV, et al. Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. Molecular Psychiatry. 16: 202-15. PMID 20038947 DOI: 10.1038/Mp.2009.125 |
0.378 |
|
| 2011 |
Voyiaziakis E, Evgrafov O, Li D, Yoon HJ, Tabares P, Samuels J, Wang Y, Riddle MA, Grados MA, Bienvenu OJ, Shugart YY, Liang KY, Greenberg BD, Rasmussen SA, Murphy DL, ... ... Knowles JA, et al. Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study. Molecular Psychiatry. 16: 108-20. PMID 19806148 DOI: 10.1038/Mp.2009.100 |
0.408 |
|
| 2010 |
Brisbin A, Weissman MM, Fyer AJ, Hamilton SP, Knowles JA, Bustamante CD, Mezey JG. Bayesian linkage analysis of categorical traits for arbitrary pedigree designs. Plos One. 5: e12307. PMID 20865038 DOI: 10.1371/Journal.Pone.0012307 |
0.337 |
|
| 2010 |
Dao DT, Mahon PB, Cai X, Kovacsics CE, Blackwell RA, Arad M, Shi J, Zandi PP, O'Donnell P, Knowles JA, Weissman MM, Coryell W, Scheftner WA, Lawson WB, et al. Mood disorder susceptibility gene CACNA1C modifies mood-related behaviors in mice and interacts with sex to influence behavior in mice and diagnosis in humans. Biological Psychiatry. 68: 801-10. PMID 20723887 DOI: 10.1016/J.Biopsych.2010.06.019 |
0.379 |
|
| 2010 |
Wang Y, Adamczyk A, Shugart YY, Samuels JF, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Pinto A, Fyer AJ, Piacentini J, et al. A screen of SLC1A1 for OCD-related alleles. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 675-9. PMID 19569082 DOI: 10.1002/Ajmg.B.31001 |
0.337 |
|
| 2009 |
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Ruderfer DM, McQuillin A, Morris DW, Oĝdushlaine CT, Corvin A, Holmans PA, Oĝdonovan MC, MacGregor S, Gurling H, ... ... Knowles JA, et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Nature. 460: 748-752. PMID 19571811 DOI: 10.1038/Nature08185 |
0.358 |
|
| 2009 |
Logue MW, Durner M, Heiman GA, Hodge SE, Hamilton SP, Knowles JA, Fyer AJ, Weissman MM. A linkage search for joint panic disorder/bipolar genes. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 1139-46. PMID 19308964 DOI: 10.1002/Ajmg.B.30939 |
0.316 |
|
| 2009 |
Roberts KE, Fallon MB, Krowka MJ, Benza RL, Knowles JA, Badesch DB, Brown RS, Taichman DB, Trotter J, Zacks S, Horn EM, Kawut SM. Serotonin transporter polymorphisms in patients with portopulmonary hypertension. Chest. 135: 1470-5. PMID 19141529 DOI: 10.1378/Chest.08-1909 |
0.306 |
|
| 2009 |
Bienvenu OJ, Wang Y, Shugart YY, Welch JM, Grados MA, Fyer AJ, Rauch SL, McCracken JT, Rasmussen SA, Murphy DL, Cullen B, Valle D, Hoehn-Saric R, Greenberg BD, Pinto A, ... Knowles JA, et al. Sapap3 and pathological grooming in humans: Results from the OCD collaborative genetics study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 710-20. PMID 19051237 DOI: 10.1002/Ajmg.B.30897 |
0.305 |
|
| 2009 |
Nestadt G, Di CZ, Riddle MA, Grados MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Pinto A, Knowles JA, Piacentini J, Pauls DL, et al. Obsessive-compulsive disorder: subclassification based on co-morbidity. Psychological Medicine. 39: 1491-501. PMID 19046474 DOI: 10.1017/S0033291708004753 |
0.366 |
|
| 2009 |
Hodges LM, Weissman MM, Haghighi F, Costa R, Bravo O, Evgrafov O, Knowles JA, Fyer AJ, Hamilton SP. Association and linkage analysis of candidate genes GRP, GRPR, CRHR1, and TACR1 in panic disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 65-73. PMID 18452185 DOI: 10.1002/Ajmg.B.30773 |
0.363 |
|
| 2009 |
Wang Y, Samuels JF, Chang YC, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Hoehn-Saric R, Pinto A, Fyer AJ, Piacentini J, et al. Gender differences in genetic linkage and association on 11p15 in obsessive-compulsive disorder families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 33-40. PMID 18425788 DOI: 10.1002/Ajmg.B.30760 |
0.359 |
|
| 2008 |
Samuels JF, Bienvenu OJ, Pinto A, Murphy DL, Piacentini J, Rauch SL, Fyer AJ, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Cullen B, Riddle MA, Rasmussen SA, Pauls DL, et al. Sex-specific clinical correlates of hoarding in obsessive-compulsive disorder. Behaviour Research and Therapy. 46: 1040-6. PMID 18692168 DOI: 10.1016/J.Brat.2008.06.005 |
0.33 |
|
| 2008 |
Stone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DHR, Corvin A, Craddock NJ, Gill M, Hultman CM, Lichtenstein P, McQuillin A, Pato CN, Ruderfer DM, Owen MJ, St Clair D, ... ... Knowles JA, et al. Rare chromosomal deletions and duplications increase risk of schizophrenia Nature. 455: 237-241. PMID 18668038 DOI: 10.1038/Nature07239 |
0.355 |
|
| 2008 |
Verma R, Holmans P, Knowles JA, Grover D, Evgrafov OV, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR, Potash JB, Levinson DF. Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3. Biological Psychiatry. 63: 1185-9. PMID 18367154 DOI: 10.1016/J.Biopsych.2008.02.005 |
0.336 |
|
| 2008 |
Liang KY, Wang Y, Shugart YY, Grados M, Fyer AJ, Rauch S, Murphy D, McCracken J, Rasmussen S, Cullen B, Hoehn-Saric R, Greenberg B, Pinto A, Knowles J, Piacentini J, et al. Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive-compulsive disorder with compulsive hoarding. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1000-2. PMID 18286588 DOI: 10.1002/Ajmg.B.30713 |
0.371 |
|
| 2007 |
Verma R, Cutler DJ, Holmans P, Knowles JA, Crowe RR, Scheftner WA, Weissman MM, DePaulo JR, Levinson DF, Potash JB. Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 1079-82. PMID 17510952 DOI: 10.1002/Ajmg.B.30514 |
0.364 |
|
| 2006 |
Samuels JF, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Pinto A, Knowles JA, Piacentini J, Cannistraro PA, Cullen B, Bienvenu OJ, Rasmussen SA, et al. The OCD collaborative genetics study: methods and sample description. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 201-7. PMID 16511842 DOI: 10.1002/Ajmg.B.30224 |
0.3 |
|
| 2004 |
Hemmings SM, Kinnear CJ, Lochner C, Niehaus DJ, Knowles JA, Moolman-Smook JC, Corfield VA, Stein DJ. Early- versus late-onset obsessive-compulsive disorder: investigating genetic and clinical correlates. Psychiatry Research. 128: 175-82. PMID 15488960 DOI: 10.1016/J.Psychres.2004.05.007 |
0.302 |
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| 2004 |
Hamilton SP, Slager SL, Mayo D, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA. Investigation of polymorphisms in the CREM gene in panic disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 126: 111-5. PMID 15048659 DOI: 10.1002/Ajmg.B.20121 |
0.361 |
|
| 2004 |
Hamilton SP, Slager SL, De Leon AB, Heiman GA, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 29: 558-65. PMID 14666117 DOI: 10.1038/Sj.Npp.1300311 |
0.335 |
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| 2002 |
Hamilton SP, Slager SL, Heiman GA, Deng Z, Haghighi F, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. Evidence for a susceptibility locus for panic disorder near the catechol-O-methyltransferase gene on chromosome 22. Biological Psychiatry. 51: 591-601. PMID 11950461 DOI: 10.1016/S0006-3223(01)01322-1 |
0.308 |
|
| 2001 |
Hamilton SP, Slager SL, Helleby L, Heiman GA, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder. Molecular Psychiatry. 6: 59-65. PMID 11244486 DOI: 10.1038/Sj.Mp.4000788 |
0.327 |
|
| 2000 |
Hamilton SP, Slager SL, Heiman GA, Haghighi F, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder. Molecular Psychiatry. 5: 465-6. PMID 11032378 DOI: 10.1038/Sj.Mp.4000772 |
0.307 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2016 |
Shi L, Guo Y, Dong C, Huddleston J, Yang H, Han X, Fu A, Li Q, Li N, Gong S, Lintner KE, Ding Q, Wang Z, Hu J, Wang D, ... ... Knowles JA, et al. Long-read sequencing and de novo assembly of a Chinese genome. Nature Communications. 7: 12065. PMID 27356984 DOI: 10.1038/Ncomms12065 |
0.3 |
|
| 2018 |
Wang D, Liu S, Warrell J, Won H, Shi X, Navarro FCP, Clarke D, Gu M, Emani P, Yang YT, Xu M, Gandal MJ, Lou S, Zhang J, Park JJ, ... ... Knowles JA, et al. Comprehensive functional genomic resource and integrative model for the human brain. Science (New York, N.Y.). 362. PMID 30545857 DOI: 10.1126/Science.Aat8464 |
0.298 |
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| 2008 |
Pinto A, Greenberg BD, Grados MA, Bienvenu OJ, Samuels JF, Murphy DL, Hasler G, Stout RL, Rauch SL, Shugart YY, Pauls DL, Knowles JA, Fyer AJ, McCracken JT, Piacentini J, et al. Further development of YBOCS dimensions in the OCD Collaborative Genetics study: symptoms vs. categories. Psychiatry Research. 160: 83-93. PMID 18514325 DOI: 10.1016/J.Psychres.2007.07.010 |
0.297 |
|
| 2016 |
Lin M, Dominguez R, Kim JM, Souaiaia T, Walker C, Adrian C, Nguyen J, Herstein J, Christi Francois M, Mack WJ, Liu C, Evgrafov OV, Knowles JA, Chow RH. Single-Cell RNA-Seq of Neurons in the Human Nervous System Biophysical Journal. 110: 321a. DOI: 10.1016/J.Bpj.2015.11.1724 |
0.294 |
|
| 2017 |
Sousa AMM, Zhu Y, Raghanti MA, Kitchen RR, Onorati M, Tebbenkamp ATN, Stutz B, Meyer KA, Li M, Kawasawa YI, Liu F, Perez RG, Mele M, Carvalho T, Skarica M, ... ... Knowles JA, et al. Molecular and cellular reorganization of neural circuits in the human lineage. Science (New York, N.Y.). 358: 1027-1032. PMID 29170230 DOI: 10.1126/Science.Aan3456 |
0.294 |
|
| 1996 |
Knowles J, Vieland V, Weissman M, Heiman G, de Jesus G, Judenberg A, Cunjak J, Mick S, Adams P, Hodge S, Klein D, Fyer A, Gilliam T. Panic disorder is unlikely to be a homogeneous autosomal dominant disorder: Results of a genome-wide genetic screen Biological Psychiatry. 39: 567. DOI: 10.1016/0006-3223(96)84178-3 |
0.293 |
|
| 2021 |
Blokland GAM, Grove J, Chen CY, Cotsapas C, Tobet S, Handa R, St Clair D, Lencz T, Mowry BJ, Periyasamy S, Cairns MJ, Tooney PA, Wu JQ, Kelly B, ... ... Knowles JA, et al. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biological Psychiatry. PMID 34099189 DOI: 10.1016/j.biopsych.2021.02.972 |
0.292 |
|
| 2016 |
Wong EH, Khrunin A, Nichols L, Pushkarev D, Khokhrin D, Verbenko D, Evgrafov O, Knowles J, Novembre J, Limborska S, Valouev A. Reconstructing genetic history of Siberian and Northeastern European populations. Genome Research. PMID 27965293 DOI: 10.1101/Gr.202945.115 |
0.292 |
|
| 1999 |
Hamilton SP, Heiman GA, Haghighi F, Mick S, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA. Lack of genetic linkage or association between a functional serotonin transporter polymorphism and panic disorder. Psychiatric Genetics. 9: 1-6. PMID 10335545 DOI: 10.1097/00041444-199903000-00001 |
0.291 |
|
| 2014 |
Hartz SM, Pato CN, Medeiros H, Cavazos-Rehg P, Sobell JL, Knowles JA, Bierut LJ, Pato MT. Comorbidity of severe psychotic disorders with measures of substance use. Jama Psychiatry. 71: 248-54. PMID 24382686 DOI: 10.1001/Jamapsychiatry.2013.3726 |
0.291 |
|
| 2013 |
Wrobel BB, Mazza JM, Evgrafov OV, Knowles JA. Assessing the efficacy of endoscopic office olfactory biopsy sites to produce neural progenitor cell cultures for the study of neuropsychiatric disorders. International Forum of Allergy & Rhinology. 3: 133-8. PMID 23192985 DOI: 10.1002/Alr.21080 |
0.29 |
|
| 2018 |
Knowles JA, Chow RH, Evgrafov OV, Mack W, Walker CP, Russin JJ, Gao F, Kim JM, Kim J, Lin MY, Liu CY, Wang K. Evaluation of biological and technical variations in low-input RNA-Seq and single-cell RNA-Seq International Journal of Computational Biology and Drug Design. 11: 5. DOI: 10.1504/Ijcbdd.2018.10011905 |
0.29 |
|
| 2012 |
Fyer AJ, Costa R, Haghighi F, Logue MW, Knowles JA, Weissman MM, Hodge SE, Hamilton SP. Linkage analysis of alternative anxiety phenotypes in multiply affected panic disorder families. Psychiatric Genetics. 22: 123-9. PMID 22525237 DOI: 10.1097/Ypg.0B013E328353956A |
0.286 |
|
| 2019 |
Zhang X, Abdellaoui A, Rucker J, de Jong S, Potash JB, Weissman MM, Shi J, Knowles JA, Pato C, Pato M, Sobell J, Smit JH, Hottenga JJ, de Geus EJC, Lewis CM, et al. Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts. Biological Psychiatry. PMID 31003785 DOI: 10.1016/J.Biopsych.2019.02.022 |
0.285 |
|
| 2014 |
Miller JA, Ding SL, Sunkin SM, Smith KA, Ng L, Szafer A, Ebbert A, Riley ZL, Royall JJ, Aiona K, Arnold JM, Bennet C, Bertagnolli D, Brouner K, Butler S, ... ... Knowles JA, et al. Transcriptional landscape of the prenatal human brain. Nature. 508: 199-206. PMID 24695229 DOI: 10.1038/Nature13185 |
0.285 |
|
| 2007 |
Holmans P, Weissman MM, Zubenko GS, Scheftner WA, Crowe RR, Depaulo JR, Knowles JA, Zubenko WN, Murphy-Eberenz K, Marta DH, Boutelle S, McInnis MG, Adams P, Gladis M, Steele J, et al. Genetics of recurrent early-onset major depression (GenRED): final genome scan report. The American Journal of Psychiatry. 164: 248-58. PMID 17267787 DOI: 10.1176/Appi.Ajp.164.2.248 |
0.285 |
|
| 2007 |
Samuels JF, Bienvenu OJ, Pinto A, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Greenberg BD, Knowles JA, Piacentini J, Cannistraro PA, Cullen B, Riddle MA, Rasmussen SA, et al. Hoarding in obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. Behaviour Research and Therapy. 45: 673-86. PMID 16824483 DOI: 10.1016/J.Brat.2006.05.008 |
0.284 |
|
| 2000 |
Hamilton SP, Haghighi F, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA. Investigation of dopamine receptor (DRD4) and dopamine transporter (DAT) polymorphisms for genetic linkage or association to panic disorder. American Journal of Medical Genetics. 96: 324-30. PMID 10898909 DOI: 10.1002/1096-8628(20000612)96:3<324::Aid-Ajmg18>3.0.Co;2-W |
0.282 |
|
| 2012 |
Qiu S, Luo S, Evgrafov O, Li R, Schroth GP, Levitt P, Knowles JA, Wang K. Single-neuron RNA-Seq: technical feasibility and reproducibility. Frontiers in Genetics. 3: 124. PMID 22934102 DOI: 10.3389/Fgene.2012.00124 |
0.28 |
|
| 2000 |
Weissman MM, Fyer AJ, Haghighi F, Heiman G, Deng Z, Hen R, Hodge SE, Knowles JA. Potential panic disorder syndrome: clinical and genetic linkage evidence. American Journal of Medical Genetics. 96: 24-35. PMID 10686548 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<24::Aid-Ajmg7>3.0.Co;2-E |
0.279 |
|
| 2018 |
Hibar DP, Cheung JW, Medland SE, Mufford MS, Jahanshad N, Dalvie S, Ramesar R, Stewart E, van den Heuvel OA, Pauls DL, Knowles JA, Stein DJ, Thompson PM. Significant concordance of genetic variation that increases both the risk for obsessive-compulsive disorder and the volumes of the nucleus accumbens and putamen. The British Journal of Psychiatry : the Journal of Mental Science. 213: 430-436. PMID 29947313 DOI: 10.1192/Bjp.2018.62 |
0.278 |
|
| 2019 |
Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, ... ... Knowles JA, et al. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227. PMID 30818990 DOI: 10.1176/Appi.Ajp.2018.18070857 |
0.277 |
|
| 2015 |
Ho EV, Thompson SL, Katzka WR, Sharifi MF, Knowles JA, Dulawa SC. Clinically effective OCD treatment prevents 5-HT1B receptor-induced repetitive behavior and striatal activation. Psychopharmacology. PMID 26423528 DOI: 10.1007/S00213-015-4086-8 |
0.276 |
|
| 2017 |
Thompson S, Ho E, Morais M, Klinger M, Welch A, Ramaker M, Knowles J, Bessa J, Young J, Sousa N, Dulawa S. 799. Behavioral and Molecular Effects of Putative OCD Risk Gene BTBD3 Biological Psychiatry. 81: S325. DOI: 10.1016/J.Biopsych.2017.02.866 |
0.275 |
|
| 2015 |
Qin H, Samuels JF, Wang Y, Zhu Y, Grados MA, Riddle MA, Greenberg BD, Knowles JA, Fyer AJ, McCracken JT, Murphy DL, Rasmussen SA, Cullen BA, Piacentini J, Geller D, et al. Whole-genome association analysis of treatment response in obsessive-compulsive disorder. Molecular Psychiatry. PMID 25824302 DOI: 10.1038/mp.2015.32 |
0.274 |
|
| 2010 |
Roberts KE, Kawut SM, Krowka MJ, Brown RS, Trotter JF, Shah V, Peter I, Tighiouart H, Mitra N, Handorf E, Knowles JA, Zacks S, Fallon MB. Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease. Gastroenterology. 139: 130-9.e24. PMID 20346360 DOI: 10.1053/J.Gastro.2010.03.044 |
0.274 |
|
| 2000 |
Kinnear CJ, Niehaus DJ, Moolman-Smook JC, du Toit PL, van Kradenberg J, Weyers JB, Potgieter A, Marais V, Emsley RA, Knowles JA, Corfield VA, Brink PA, Stein DJ. Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population. The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (Cinp). 3: 327-331. PMID 11343612 DOI: 10.1017/S1461145700002054 |
0.273 |
|
| 2022 |
Trubetskoy V, Pardiñas AF, Qi T, Panagiotaropoulou G, Awasthi S, Bigdeli TB, Bryois J, Chen CY, Dennison CA, Hall LS, Lam M, Watanabe K, Frei O, Ge T, Harwood JC, ... ... Knowles JA, et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. PMID 35396580 DOI: 10.1038/s41586-022-04434-5 |
0.273 |
|
| 2014 |
Chen EA, Souaiaia T, Herstein JS, Evgrafov OV, Spitsyna VN, Rebolini DF, Knowles JA. Effect of RNA integrity on uniquely mapped reads in RNA-Seq. Bmc Research Notes. 7: 753. PMID 25339126 DOI: 10.1186/1756-0500-7-753 |
0.271 |
|
| 2011 |
Mroczkowski MM, Goes FS, Riddle MA, Grados MA, Bienvenu OJ, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Knowles JA, Piacentini J, Cullen B, Rasmussen SA, Geller DA, et al. Separation anxiety disorder in OCD. Depression and Anxiety. 28: 256-62. PMID 21308883 DOI: 10.1002/Da.20773 |
0.269 |
|
| 2003 |
Levinson DF, Zubenko GS, Crowe RR, DePaulo RJ, Scheftner WS, Weissman MM, Holmans P, Zubenko WN, Boutelle S, Murphy-Eberenz K, MacKinnon D, McInnis MG, Marta DH, Adams P, Sassoon S, ... Knowles JA, et al. Genetics of recurrent early-onset depression (GenRED): design and preliminary clinical characteristics of a repository sample for genetic linkage studies. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 119: 118-30. PMID 12707949 DOI: 10.1002/Ajmg.B.20009 |
0.267 |
|
| 2015 |
Sook Lee N, Evgrafov OV, Souaiaia T, Bonyad A, Herstein J, Yeun Lee J, Kim J, Ning Y, Sixto M, Weitz AC, Lenz HJ, Wang K, Knowles JA, Press MF, Salvaterra PM, et al. Non-coding RNAs derived from an alternatively spliced REST transcript (REST-003) regulate breast cancer invasiveness. Scientific Reports. 5: 11207. PMID 26053433 DOI: 10.1038/Srep11207 |
0.266 |
|
| 2011 |
Lo SM, Liu J, Chen F, Pastores GM, Knowles J, Boxer M, Aleck K, Mistry PK. Pulmonary vascular disease in Gaucher disease: clinical spectrum, determinants of phenotype and long-term outcomes of therapy. Journal of Inherited Metabolic Disease. 34: 643-50. PMID 21445609 DOI: 10.1007/S10545-011-9313-9 |
0.265 |
|
| 2009 |
Mahon PB, Payne JL, MacKinnon DF, Mondimore FM, Goes FS, Schweizer B, Jancic D, Coryell WH, Holmans PA, Shi J, Knowles JA, Scheftner WA, Weissman MM, et al. Genome-wide linkage and follow-up association study of postpartum mood symptoms. The American Journal of Psychiatry. 166: 1229-37. PMID 19755578 DOI: 10.1176/Appi.Ajp.2009.09030417 |
0.264 |
|
| 2006 |
Fyer AJ, Hamilton SP, Durner M, Haghighi F, Heiman GA, Costa R, Evgrafov O, Adams P, de Leon AB, Taveras N, Klein DF, Hodge SE, Weissman MM, Knowles JA. A third-pass genome scan in panic disorder: evidence for multiple susceptibility loci. Biological Psychiatry. 60: 388-401. PMID 16919526 DOI: 10.1016/J.Biopsych.2006.04.018 |
0.263 |
|
| 2015 |
Riddle MA, Maher BS, Wang Y, Grados M, Bienvenu OJ, Goes FS, Cullen B, Murphy DL, Rauch SL, Greenberg BD, Knowles JA, McCracken JT, Pinto A, Piacentini J, Pauls DL, et al. OBSESSIVE-COMPULSIVE PERSONALITY DISORDER: EVIDENCE FOR TWO DIMENSIONS. Depression and Anxiety. PMID 26594839 DOI: 10.1002/Da.22452 |
0.262 |
|
| 1999 |
Aita VM, Liu J, Knowles JA, Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z, Penchaszadeh G, Gilliam TC, Baron M. A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. American Journal of Human Genetics. 64: 210-7. PMID 9915960 DOI: 10.1086/302185 |
0.261 |
|
| 2004 |
Lochner C, Hemmings SM, Kinnear CJ, Moolman-Smook JC, Corfield VA, Knowles JA, Niehaus DJ, Stein DJ. Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113]. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 14: 437-45. PMID 15468463 DOI: 10.1016/J.Euroneuro.2004.05.002 |
0.261 |
|
| 2004 |
Lochner C, Hemmings SM, Kinnear CJ, Moolman-Smook JC, Corfield VA, Knowles JA, Niehaus DJ, Stein DJ. Gender in obsessive-compulsive disorder: clinical and genetic findings. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 14: 105-13. PMID 15013025 DOI: 10.1016/S0924-977X(03)00063-4 |
0.26 |
|
| 2020 |
Kim JMH, Camarena A, Walker C, Lin MY, Wolseley V, Souaiaia T, Thornton M, Grubbs B, Chow RH, Evgrafov OV, Knowles JA. Robust RNA-Seq of aRNA-amplified single cell material collected by patch clamp. Scientific Reports. 10: 1979. PMID 32029778 DOI: 10.1038/S41598-020-58715-Y |
0.26 |
|
| 2017 |
Kovner R, Fox A, Souaiaia T, Roseboom P, French D, Oler J, Fudge J, Knowles J, Kalin N. 848. Characterizing Extended Amygdala Neuron Populations in Primates as a Basis for Exploring Altered Ce and BST Function in Anxiety Biological Psychiatry. 81: S343-S344. DOI: 10.1016/J.Biopsych.2017.02.573 |
0.26 |
|
| 1998 |
Knowles JA, Rao PA, Cox-Matise T, Loth JE, de Jesus GM, Levine L, Das K, Penchaszadeh GK, Alexander JR, Lerer B, Endicott J, Ott J, Gilliam TC, Baron M. No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees. American Journal of Human Genetics. 62: 916-24. PMID 9529343 DOI: 10.1086/301785 |
0.26 |
|
| 2014 |
Staab TA, Evgrafov O, Egrafov O, Knowles JA, Sieburth D. Regulation of synaptic nlg-1/neuroligin abundance by the skn-1/Nrf stress response pathway protects against oxidative stress. Plos Genetics. 10: e1004100. PMID 24453991 DOI: 10.1371/Journal.Pgen.1004100 |
0.258 |
|
| 2009 |
Shugart YY, Wang Y, Samuels JF, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Hoehn-Saric R, Pinto A, Fyer AJ, Piacentini J, et al. A family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder in 378 families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 886-92. PMID 19152386 DOI: 10.1002/Ajmg.B.30914 |
0.258 |
|
| 2016 |
Dueck HR, Ai R, Camarena A, Ding B, Dominguez R, Evgrafov OV, Fan JB, Fisher SA, Herstein JS, Kim TK, Kim JM, Lin MY, Liu R, Mack WJ, McGroty S, ... ... Knowles JA, et al. Assessing characteristics of RNA amplification methods for single cell RNA sequencing. Bmc Genomics. 17: 966. PMID 27881084 DOI: 10.1186/S12864-016-3300-3 |
0.258 |
|
| 2018 |
Li M, Santpere G, Imamura Kawasawa Y, Evgrafov OV, Gulden FO, Pochareddy S, Sunkin SM, Li Z, Shin Y, Zhu Y, Sousa AMM, Werling DM, Kitchen RR, Kang HJ, Pletikos M, ... ... Knowles JA, et al. Integrative functional genomic analysis of human brain development and neuropsychiatric risks. Science (New York, N.Y.). 362. PMID 30545854 DOI: 10.1126/Science.Aat7615 |
0.257 |
|
| 2011 |
Dinov ID, Torri F, Macciardi F, Petrosyan P, Liu Z, Zamanyan A, Eggert P, Pierce J, Genco A, Knowles JA, Clark AP, Van Horn JD, Ames J, Kesselman C, Toga AW. Applications of the pipeline environment for visual informatics and genomics computations. Bmc Bioinformatics. 12: 304. PMID 21791102 DOI: 10.1186/1471-2105-12-304 |
0.254 |
|
| 2004 |
Abdalla SA, Gallione CJ, Barst RJ, Horn EM, Knowles JA, Marchuk DA, Letarte M, Morse JH. Primary pulmonary hypertension in families with hereditary haemorrhagic telangiectasia. The European Respiratory Journal. 23: 373-7. PMID 15065824 DOI: 10.1183/09031936.04.00085504 |
0.254 |
|
| 2021 |
Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA, Aschauer H, Stamenkovic M, ... ... Knowles JA, et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational Psychiatry. 11: 56. PMID 33462189 DOI: 10.1038/s41398-020-01082-z |
0.254 |
|
| 2013 |
Staab TA, Griffen TC, Corcoran C, Evgrafov O, Knowles JA, Sieburth D. The conserved SKN-1/Nrf2 stress response pathway regulates synaptic function in Caenorhabditis elegans. Plos Genetics. 9: e1003354. PMID 23555279 DOI: 10.1371/Journal.Pgen.1003354 |
0.251 |
|
| 2015 |
Sobell JL, Pato MT, Pato CN, Knowles JA. Obsessive-Compulsive Disorder Genetics: Current and Future Directions Focus. 13: 142-147. DOI: 10.1176/APPI.FOCUS.130208 |
0.251 |
|
| 2007 |
Levinson DF, Evgrafov OV, Knowles JA, Potash JB, Weissman MM, Scheftner WA, Depaulo JR, Crowe RR, Murphy-Eberenz K, Marta DH, McInnis MG, Adams P, Gladis M, Miller EB, Thomas J, et al. Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers. The American Journal of Psychiatry. 164: 259-64. PMID 17267788 DOI: 10.1176/Ajp.2007.164.2.259 |
0.251 |
|
| 2016 |
Ding SL, Royall JJ, Sunkin SM, Ng L, Facer BA, Lesnar P, Guillozet-Bongaarts A, McMurray B, Szafer A, Dolbeare TA, Stevens A, Tirrell L, Benner T, Caldejon S, Dalley RA, ... ... Knowles JA, et al. Comprehensive cellular-resolution atlas of the adult human brain. The Journal of Comparative Neurology. PMID 27418273 DOI: 10.1002/Cne.24080 |
0.25 |
|
| 2005 |
Lochner C, Kinnear CJ, Hemmings SM, Seller C, Niehaus DJ, Knowles JA, Daniels W, Moolman-Smook JC, Seedat S, Stein DJ. Hoarding in obsessive-compulsive disorder: clinical and genetic correlates. The Journal of Clinical Psychiatry. 66: 1155-60. PMID 16187774 DOI: 10.4088/Jcp.V66N0911 |
0.248 |
|
| 2006 |
Shugart YY, Samuels J, Willour VL, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Wang Y, Pinto A, Fyer AJ, Piacentini J, Pauls DL, Cullen B, et al. Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Molecular Psychiatry. 11: 763-70. PMID 16755275 DOI: 10.1038/Sj.Mp.4001847 |
0.246 |
|
| 2007 |
Hasler G, Pinto A, Greenberg BD, Samuels J, Fyer AJ, Pauls D, Knowles JA, McCracken JT, Piacentini J, Riddle MA, Rauch SL, Rasmussen SA, Willour VL, Grados MA, Cullen B, et al. Familiality of factor analysis-derived YBOCS dimensions in OCD-affected sibling pairs from the OCD Collaborative Genetics Study. Biological Psychiatry. 61: 617-25. PMID 17027929 DOI: 10.1016/J.Biopsych.2006.05.040 |
0.246 |
|
| 2020 |
Moon S, Lee S, Caesar JA, Pruchenko S, Leask A, Knowles JA, Sinon J, Chaqour B. A CTGF-YAP Regulatory Pathway Is Essential for Angiogenesis and Barriergenesis in the Retina. Iscience. 23: 101184. PMID 32502964 DOI: 10.1016/J.Isci.2020.101184 |
0.244 |
|
| 2018 |
Aydogan DB, Jacobs R, Dulawa S, Thompson SL, Francois MC, Toga AW, Dong H, Knowles JA, Shi Y. When tractography meets tracer injections: a systematic study of trends and variation sources of diffusion-based connectivity. Brain Structure & Function. PMID 29663135 DOI: 10.1007/S00429-018-1663-8 |
0.243 |
|
| 2015 |
Kim YJ, Ibrahim LA, Wang SZ, Yuan W, Evgrafov OV, Knowles JA, Wang K, Tao HW, Zhang LI. EphA7 regulates spiral ganglion innervation of cochlear hair cells. Developmental Neurobiology. PMID 26178595 DOI: 10.1002/Dneu.22326 |
0.243 |
|
| 2007 |
Samuels J, Shugart YY, Grados MA, Willour VL, Bienvenu OJ, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Wang Y, Pinto A, Fyer AJ, Piacentini J, Pauls DL, et al. Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. The American Journal of Psychiatry. 164: 493-9. PMID 17329475 DOI: 10.1176/Ajp.2007.164.3.493 |
0.241 |
|
| 2022 |
Valkovskaya M, Hassan A, Zartaloudi E, Hussain F, Umar M, Khizar B, Khattak I, Gill SA, Khan SA, Dogar IA, Mustafa AB, Ansari MA, Qalb I Hyder S, Ali M, Ilyas N, ... ... Knowles JA, et al. Study protocol of DIVERGE, the first genetic epidemiological study of major depressive disorder in Pakistan. Psychiatric Genetics. PMID 36538573 DOI: 10.1097/YPG.0000000000000333 |
0.24 |
|
| 2009 |
Roberts KE, Fallon MB, Krowka MJ, Brown RS, Trotter JF, Peter I, Tighiouart H, Knowles JA, Rabinowitz D, Benza RL, Badesch DB, Taichman DB, Horn EM, Zacks S, Kaplowitz N, et al. Genetic risk factors for portopulmonary hypertension in patients with advanced liver disease. American Journal of Respiratory and Critical Care Medicine. 179: 835-42. PMID 19218192 DOI: 10.1164/Rccm.200809-1472Oc |
0.237 |
|
| 2001 |
Niehaus DJ, Kinnear CJ, Corfield VA, du Toit PL, van Kradenburg J, Moolman-Smook JC, Weyers JB, Potgieter A, Seedat S, Emsley RA, Knowles JA, Brink PA, Stein DJ. Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population. Journal of Affective Disorders. 65: 61-5. PMID 11426511 DOI: 10.1016/S0165-0327(00)00246-9 |
0.237 |
|
| 1999 |
Baron M, Knowles JA. Chromosome 18p11 and linkage to bipolar disorder revisited. Psychiatric Genetics. 9: 201-3, 205-6. PMID 10697828 |
0.235 |
|
| 1998 |
Knowles JA, Fyer AJ, Vieland VJ, Weissman MM, Hodge SE, Heiman GA, Haghighi F, de Jesus GM, Rassnick H, Preud'homme-Rivelli X, Austin T, Cunjak J, Mick S, Fine LD, Woodley KA, et al. Results of a genome-wide genetic screen for panic disorder. American Journal of Medical Genetics. 81: 139-47. PMID 9613853 DOI: 10.1002/(Sici)1096-8628(19980328)81:2<139::Aid-Ajmg4>3.0.Co;2-R |
0.233 |
|
| 2003 |
Hemmings SM, Kinnear CJ, Niehaus DJ, Moolman-Smook JC, Lochner C, Knowles JA, Corfield VA, Stein DJ. Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 13: 93-8. PMID 12650952 DOI: 10.1016/S0924-977X(02)00129-3 |
0.233 |
|
| 2014 |
Macciardi F, Guffanti G, Fallon J, Erp TGMv, Pato M, Potkin SG, Knowles JA, McCarroll SA, Pato CN, Gaudi S. Poster #T149 LINE1 POLYMORPHIC RETROTRANSPOSITIONS IN SCHIZOPHRENIA Schizophrenia Research. 153. DOI: 10.1016/S0920-9964(14)70966-1 |
0.232 |
|
| 2013 |
Qiu S, Luo S, Evgrafov O, Li R, Schroth GP, Levitt P, Knowles JA, Wang K. Erratum: Single-neuron RNA-Seq: technical feasibility and reproducibility Frontiers in Genetics. 4. DOI: 10.3389/Fgene.2013.00023 |
0.232 |
|
| 2004 |
Holmans P, Zubenko GS, Crowe RR, DePaulo JR, Scheftner WA, Weissman MM, Zubenko WN, Boutelle S, Murphy-Eberenz K, MacKinnon D, McInnis MG, Marta DH, Adams P, Knowles JA, Gladis M, et al. Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. American Journal of Human Genetics. 74: 1154-67. PMID 15108123 DOI: 10.1086/421333 |
0.229 |
|
| 2019 |
Gerstenblith TA, Jaramillo-Huff A, Ruutiainen T, Nestadt PS, Samuels JF, Grados MA, Cullen BA, Riddle MA, Liang KY, Greenberg BD, Rasmussen SA, Rauch SL, McCracken JT, Piacentini J, Knowles JA, et al. Trichotillomania comorbidity in a sample enriched for familial obsessive-compulsive disorder. Comprehensive Psychiatry. 94: 152123. PMID 31518848 DOI: 10.1016/J.Comppsych.2019.152123 |
0.227 |
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| 2022 |
Singh T, Poterba T, Curtis D, Akil H, Al Eissa M, Barchas JD, Bass N, Bigdeli TB, Breen G, Bromet EJ, Buckley PF, Bunney WE, Bybjerg-Grauholm J, Byerley WF, Chapman SB, ... ... Knowles JA, et al. Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature. PMID 35396579 DOI: 10.1038/s41586-022-04556-w |
0.226 |
|
| 2019 |
Bigdeli TB, Genovese G, Georgakopoulos P, Meyers JL, Peterson RE, Iyegbe CO, Medeiros H, Valderrama J, Achtyes ED, Kotov R, Stahl EA, Abbott C, Azevedo MH, Belliveau RA, Bevilacqua E, ... ... Knowles JA, et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Molecular Psychiatry. PMID 31591465 DOI: 10.1038/S41380-019-0517-Y |
0.225 |
|
| 2024 |
Panagiotaropoulou G, Hellberg KG, Coleman JRI, Seok D, Kalman J, Mitchell PB, Schofield PR, Forstner AJ, Bauer M, Scott LJ, Pato CN, Pato MT, Li QS, Kirov G, Landén M, ... ... Knowles JA, et al. Identifying genetic differences between bipolar disorder and major depression through multiple GWAS. Medrxiv : the Preprint Server For Health Sciences. PMID 38410442 DOI: 10.1101/2024.01.29.24301816 |
0.224 |
|
| 2000 |
Baron M, Knowles JA. Bipolar disorder and chromosome 18p11: uncertainties redux. Psychiatric Genetics. 10: 55-8. PMID 10909130 |
0.224 |
|
| 2021 |
Kalman JL, Olde Loohuis LM, Vreeker A, McQuillin A, Stahl EA, Ruderfer D, Grigoroiu-Serbanescu M, Panagiotaropoulou G, Ripke S, Bigdeli TB, Stein F, Meller T, Meinert S, Pelin H, Streit F, ... ... Knowles JA, et al. Characterisation of age and polarity at onset in bipolar disorder. The British Journal of Psychiatry : the Journal of Mental Science. 219: 659-669. PMID 35048876 DOI: 10.1192/bjp.2021.102 |
0.223 |
|
| 2019 |
Westwell-Roper C, Williams KA, Samuels J, Bienvenu OJ, Cullen B, Goes FS, Grados MA, Geller D, Greenberg BD, Knowles JA, Krasnow J, McLaughlin NC, Nestadt P, Shugart YY, Nestadt G, et al. Immune-Related Comorbidities in Childhood-Onset Obsessive Compulsive Disorder: Lifetime Prevalence in the Obsessive Compulsive Disorder Collaborative Genetics Association Study. Journal of Child and Adolescent Psychopharmacology. PMID 31170001 DOI: 10.1089/cap.2018.0140 |
0.223 |
|
| 2013 |
Wang H, Girskis K, Janssen T, Chan JP, Dasgupta K, Knowles JA, Schoofs L, Sieburth D. Neuropeptide secreted from a pacemaker activates neurons to control a rhythmic behavior. Current Biology : Cb. 23: 746-54. PMID 23583549 DOI: 10.1016/J.Cub.2013.03.049 |
0.222 |
|
| 2011 |
Lo S, Liu J, Pastores G, Knowles J, Boxer M, Korson M, Alec K, Mistry P. Pulmonary vascular disease in Gaucher disease: Genotype/Phenotype characteristics and long-term outcomes Molecular Genetics and Metabolism. 102. DOI: 10.1016/J.Ymgme.2010.11.086 |
0.219 |
|
| 2007 |
Lachman HM, Fann CS, Bartzis M, Evgrafov OV, Rosenthal RN, Nunes EV, Miner C, Santana M, Gaffney J, Riddick A, Hsu CL, Knowles JA. Genomewide suggestive linkage of opioid dependence to chromosome 14q. Human Molecular Genetics. 16: 1327-34. PMID 17409192 DOI: 10.1093/hmg/ddm081 |
0.218 |
|
| 2019 |
Samuels J, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, Mclaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, Mccracken JT, Piacentini J, et al. General personality dimensions, impairment and treatment response in obsessive-compulsive disorder. Personality and Mental Health. PMID 31859455 DOI: 10.1002/Pmh.1472 |
0.217 |
|
| 2003 |
Hamilton SP, Fyer AJ, Durner M, Heiman GA, Baisre de Leon A, Hodge SE, Knowles JA, Weissman MM. Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q. Proceedings of the National Academy of Sciences of the United States of America. 100: 2550-5. PMID 12604791 DOI: 10.1073/Pnas.0335669100 |
0.215 |
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| 2000 |
Goedken R, Ludington E, Crowe R, Fyer AJ, Hodge SE, Knowles JA, Vieland VJ, Weissman MM. Drawbacks of GENEHUNTER for larger pedigrees: application to panic disorder. American Journal of Medical Genetics. 96: 781-3. PMID 11121181 DOI: 10.1002/1096-8628(20001204)96:6<781::Aid-Ajmg17>3.0.Co;2-J |
0.213 |
|
| 2021 |
Mattheisen M, Pato MT, Pato CN, Knowles JA. What Have We Learned About the Genetics of Obsessive-Compulsive and Related Disorders in Recent Years? Focus (American Psychiatric Publishing). 19: 384-391. PMID 35747302 DOI: 10.1176/appi.focus.20210017 |
0.21 |
|
| 2021 |
Mattheisen M, Pato MT, Pato CN, Knowles JA. What Have We Learned About the Genetics of Obsessive-Compulsive and Related Disorders in Recent Years? Focus (American Psychiatric Publishing). 19: 384-391. PMID 35747302 DOI: 10.1176/appi.focus.20210017 |
0.21 |
|
| 1994 |
Knowles JA, Shugart Y, Banerjee P, Gilliam TC, Lewis CA, Jacobson SG, Ott J. Identification of a locus, distinct from RDS-peripherin, for autosomal recessive retinitis pigmentosa on chromosome 6p. Human Molecular Genetics. 3: 1401-3. PMID 7987322 DOI: 10.1093/Hmg/3.8.1401 |
0.21 |
|
| 2017 |
Fox A, Souaiaia T, Roseboom P, Oler J, Kovner R, Riedel M, Fekete E, Mun Kim J, Nguyen J, Knowles J, Kalin N. 22. Neurotrophin-3 Signaling in the Dorsal Amygdala Decreases Early-Life Anxious Temperament in Non-Human Primates Biological Psychiatry. 81: S10. DOI: 10.1016/J.Biopsych.2017.02.033 |
0.208 |
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| 2023 |
Samuels J, Bienvenu OJ, Krasnow J, Grados MA, Cullen BA, Goes FS, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, McCracken JT, Geller D, Riddle MA, Piacentini J, Stewart SE, et al. Prevalence and correlates of lifetime suicide attempt in obsessive-compulsive disorder with major depression. Journal of Psychiatric Research. 161: 228-236. PMID 36940628 DOI: 10.1016/j.jpsychires.2023.02.027 |
0.207 |
|
| 1997 |
Ranta S, Lehesjoki AE, de Fatima Bonaldo M, Knowles JA, Hirvasniemi A, Ross B, de Jong PJ, Soares MB, de la Chapelle A, Gilliam TC. High-resolution mapping and transcript identification at the progressive epilepsy with mental retardation locus on chromosome 8p. Genome Research. 7: 887-96. PMID 9314494 DOI: 10.1101/Gr.7.9.887 |
0.206 |
|
| 2023 |
Ho EV, Welch A, Thompson SL, Knowles JA, Dulawa SC. Mice lacking Ptprd exhibit deficits in goal-directed behavior and female-specific impairments in sensorimotor gating. Plos One. 18: e0277446. PMID 37205689 DOI: 10.1371/journal.pone.0277446 |
0.203 |
|
| 1998 |
Banerjee P, Lewis CA, Kleyn PW, Shugart YY, Ross BM, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC, Knowles JA. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. Genomics. 48: 171-7. PMID 9521870 DOI: 10.1006/Geno.1997.5174 |
0.199 |
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| 2008 |
Cullen B, Samuels JF, Pinto A, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Greenberg BD, Knowles JA, Piacentini J, Bienvenu OJ, Grados MA, Riddle MA, Rasmussen SA, Pauls DL, et al. Demographic and clinical characteristics associated with treatment status in family members with obsessive-compulsive disorder. Depression and Anxiety. 25: 218-24. PMID 17345603 DOI: 10.1002/Da.20293 |
0.196 |
|
| 2020 |
Evgrafov OV, Armoskus C, Wrobel BB, Spitsyna VN, Souaiaia T, Herstein JS, Walker CP, Nguyen JD, Camarena A, Weitz JR, Kim JMH, Lopez Duarte E, Wang K, Simpson GM, Sobell JL, ... ... Knowles JA, et al. Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia. Biological Psychiatry. PMID 32143829 DOI: 10.1016/J.Biopsych.2020.01.005 |
0.195 |
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| 2020 |
Valderrama J, Hansen SK, Pato C, Phillips K, Knowles J, Pato MT. Greater history of traumatic event exposure and PTSD associated with comorbid body dysmorphic disorder in a large OCD cohort. Psychiatry Research. 289: 112962. PMID 32446006 DOI: 10.1016/J.Psychres.2020.112962 |
0.194 |
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| 2021 |
Ayub M, Arsalan A, Khan SA, Bajwa S, Hussain F, Umar M, Khizar B, Sibtain M, Butt A, Mukhtar-Ul-Haq M, Dogar IA, Ansari MA, Shafiq S, Tariq M, Hussain MI, ... ... Knowles JA, et al. Self-reported health and smoking status, and body mass index: a case-control comparison based on GEN SCRIP (GENetics of SChizophRenia In Pakistan) data Bmj Open. 11: e042331. DOI: 10.1136/bmjopen-2020-042331 |
0.188 |
|
| 1999 |
Niehaus DJ, Knowles JA, van Kradenberg J, du Toit W, Kaminer D, Seedat S, Daniels W, Cotton M, Brink P, Beyers AD, Bouic P, Chapman F, Zabriskie JB, Stein DJ. D8/17 in obsessive-compulsive disorder and trichotillomania. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde. 89: 755-6. PMID 10470312 |
0.188 |
|
| 2011 |
Evgrafov OV, Wrobel BB, Kang X, Simpson G, Malaspina D, Knowles JA. Olfactory neuroepithelium-derived neural progenitor cells as a model system for investigating the molecular mechanisms of neuropsychiatric disorders. Psychiatric Genetics. 21: 217-28. PMID 21451437 DOI: 10.1097/YPG.0b013e328341a2f0 |
0.188 |
|
| 2000 |
Deng Z, Morse JH, Slager SL, Cuervo N, Moore KJ, Venetos G, Kalachikov S, Cayanis E, Fischer SG, Barst RJ, Hodge SE, Knowles JA. Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene. American Journal of Human Genetics. 67: 737-44. PMID 10903931 DOI: 10.1086/303059 |
0.182 |
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| 2018 |
Rhie SK, Schreiner S, Witt H, Armoskus C, Lay FD, Camarena A, Spitsyna VN, Guo Y, Berman BP, Evgrafov OV, Knowles JA, Farnham PJ. Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation. Science Advances. 4: eaav8550. PMID 30555922 DOI: 10.1126/Sciadv.Aav8550 |
0.181 |
|
| 2019 |
Bigdeli T, Genovese G, Medeiros H, Sobell J, Knowles J, Pato M, Fanous A, McCarroll S, Pato C. F118Contributions Of Common Genetic Variants To Schizophrenia Risk In Individuals With African And Latino Ancestry European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.198 |
0.175 |
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| 2018 |
Wilkinson B, Evgrafov OV, Zheng D, Hartel N, Knowles JA, Graham NA, Ichida JK, Coba MP. Endogenous Cell Type-Specific Disrupted in Schizophrenia 1 Interactomes Reveal Protein Networks Associated With Neurodevelopmental Disorders. Biological Psychiatry. PMID 29961565 DOI: 10.1016/J.Biopsych.2018.05.009 |
0.173 |
|
| 1997 |
Surguchov A, Bronson JD, Banerjee P, Knowles JA, Ruiz C, Subbaraya I, Palczewski K, Baehr W. The human GCAP1 and GCAP2 genes are arranged in a tail-to-tail array on the short arm of chromosome 6 (p21.1). Genomics. 39: 312-22. PMID 9119368 DOI: 10.1006/Geno.1996.4513 |
0.171 |
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| 2003 |
Liu J, Juo SH, Dewan A, Grunn A, Tong X, Brito M, Park N, Loth JE, Kanyas K, Lerer B, Endicott J, Penchaszadeh G, Knowles JA, Ott J, Gilliam TC, et al. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12. Molecular Psychiatry. 8: 333-42. PMID 12660806 DOI: 10.1038/Sj.Mp.4001254 |
0.169 |
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| 2009 |
Dursun A, Ozgul RK, Soydas A, Tugrul T, Gurgey A, Celiker A, Barst RJ, Knowles JA, Mahesh M, Morse JH. Familial pulmonary arterial hypertension, leucopenia, and atrial septal defect: a probable new familial syndrome with multisystem involvement. Clinical Dysmorphology. 18: 19-23. PMID 19011569 DOI: 10.1097/MCD.0b013e32831841f7 |
0.168 |
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| 2000 |
Deng Z, Haghighi F, Helleby L, Vanterpool K, Horn EM, Barst RJ, Hodge SE, Morse JH, Knowles JA. Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33. American Journal of Respiratory and Critical Care Medicine. 161: 1055-9. PMID 10712363 DOI: 10.1164/Ajrccm.161.3.9906051 |
0.167 |
|
| 2018 |
Roseboom P, Kovner R, Souaiaia T, Lu J, Dong Y, Fathi A, Tao Y, French D, Fox A, Oler J, Bhattacharyya A, Zhang S, Knowles J, Kalin N. F14. Characterizing Neurotrophic Systems in the Primate Amygdala That are Relevant to Mediating and Treating Anxiety Disorders Biological Psychiatry. 83: S242. DOI: 10.1016/J.Biopsych.2018.02.627 |
0.165 |
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| 2023 |
Tung VSK, Mathews F, Boruk M, Suppa G, Foronjy R, Pato M, Pato C, Knowles JA, Evgrafov OV. Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology. Biorxiv : the Preprint Server For Biology. PMID 37034711 DOI: 10.1101/2023.03.28.534295 |
0.165 |
|
| 2023 |
Tung VSK, Mathews F, Boruk M, Suppa G, Foronjy R, Pato MT, Pato CN, Knowles JA, Evgrafov OV. Cultured Mesenchymal Cells from Nasal Turbinate as a Cellular Model of the Neurodevelopmental Component of Schizophrenia Etiology. International Journal of Molecular Sciences. 24. PMID 37895019 DOI: 10.3390/ijms242015339 |
0.164 |
|
| 1999 |
Haghighi F, Fyer AJ, Weissman MM, Knowles JA, Hodge SE. Parent-of-origin effect in panic disorder. American Journal of Medical Genetics. 88: 131-5. PMID 10206231 DOI: 10.1002/(Sici)1096-8628(19990416)88:2<131::Aid-Ajmg7>3.0.Co;2-L |
0.164 |
|
| 1993 |
Soares VM, Brzustowicz LM, Kleyn PW, Knowles JA, Palmer DA, Asokan S, Penchaszadeh GK, Munsat TL, Gilliam TC. Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B. Genomics. 15: 365-71. PMID 8449502 DOI: 10.1006/Geno.1993.1069 |
0.164 |
|
| 1995 |
Shugart YY, Banerjee P, Knowles JA, Lewis CA, Jacobson SG, Matise TC, Penchaszadeh G, Gilliam TC, Ott J. Fine genetic mapping of a gene for autosomal recessive retinitis pigmentosa on chromosome 6p21. American Journal of Human Genetics. 57: 499-502. PMID 7668276 |
0.162 |
|
| 2023 |
Xu J, Liu D, Hassan A, Genovese G, Cote AC, Fennessy B, Cheng E, Charney AW, Knowles JA, Ayub M, Peterson RE, Bigdeli TB, Huckins LM. Evaluation of imputation performance of multiple reference panels in a Pakistani population. Medrxiv : the Preprint Server For Health Sciences. PMID 38234809 DOI: 10.1101/2023.12.22.23300448 |
0.159 |
|
| 2019 |
Thompson SL, Welch AC, Ho EV, Bessa JM, Portugal-Nunes C, Morais M, Young JW, Knowles JA, Dulawa SC. Btbd3 expression regulates compulsive-like and exploratory behaviors in mice. Translational Psychiatry. 9: 222. PMID 31501410 DOI: 10.1038/S41398-019-0558-7 |
0.154 |
|
| 2005 |
Crawford MH, Banerjee P, Demarchi DA, Zlojutro M, McComb J, Livshits G, Henneberg M, Mosher MJ, Schanfield MS, Knowles JA. Applications of pooled DNA samples to the assessment of population affinities: short tandem repeats. Human Biology. 77: 723-33. PMID 16715834 DOI: 10.1353/Hub.2006.0012 |
0.152 |
|
| 2004 |
Lee JH, Mayeux R, Mayo D, Mo J, Santana V, Williamson J, Flaquer A, Ciappa A, Rondon H, Estevez P, Lantigua R, Kawarai T, Toulina A, Medrano M, Torres M, ... ... Knowles JA, et al. Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics. Molecular Psychiatry. 9: 1042-51. PMID 15241431 DOI: 10.1038/Sj.Mp.4001538 |
0.15 |
|
| 2000 |
Goldman D, Tsuang MT, Knowles JA, Friedman TB. 186. Molecular genetics of substance abuse: analyzing complex traits Biological Psychiatry. 47. DOI: 10.1016/S0006-3223(00)00449-2 |
0.148 |
|
| 2002 |
Leimig T, Mann L, Martin Mdel P, Bonten E, Persons D, Knowles J, Allay JA, Cunningham J, Nienhuis AW, Smeyne R, d'Azzo A. Functional amelioration of murine galactosialidosis by genetically modified bone marrow hematopoietic progenitor cells. Blood. 99: 3169-78. PMID 11964280 DOI: 10.1182/Blood.V99.9.3169 |
0.145 |
|
| 2015 |
Davis LK, Lee SH, Gamazon ER, Im H, Yu D, Williams S, Sullivan PF, Mathews C, Knowles J, Scharf J, Wray N, Cox NJ. Characterizing an inverse axis between orthogonal sources of genetic risk Genetic Epidemiology. 39: 542-543. DOI: 10.1002/Gepi.21916 |
0.141 |
|
| 2000 |
Romas SN, Mayeux R, Tang MX, Lantigua R, Medrano M, Tycko B, Knowles J. No association between a presenilin 1 polymorphism and Alzheimer disease. Archives of Neurology. 57: 699-702. PMID 10815136 DOI: 10.1001/Archneur.57.5.699 |
0.139 |
|
| 2002 |
Mayeux R, Lee JH, Romas SN, Mayo D, Santana V, Williamson J, Ciappa A, Rondon HZ, Estevez P, Lantigua R, Medrano M, Torres M, Stern Y, Tycko B, Knowles JA. Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics. American Journal of Human Genetics. 70: 237-43. PMID 11715112 DOI: 10.1086/324773 |
0.137 |
|
| 2000 |
Romas SN, Mayeux R, Rabinowitz D, Tang MX, Zadroga HR, Lantigua R, Medrano M, Tycko B, Knowles JA. The deletion polymorphism and Val1000Ile in alpha-2-macroglobulin and Alzheimer disease in Caribbean Hispanics. Neuroscience Letters. 279: 133-6. PMID 10688047 DOI: 10.1016/S0304-3940(99)00972-6 |
0.137 |
|
| 2021 |
Claudio-Campos K, Stevens D, Koo SW, Valko A, Bienvenu OJ, Budman CB, Cath DC, Darrow S, Geller D, Goes FS, Grados MA, Greenberg BD, Greenberg E, Hirschtritt ME, Illmann C, ... ... Knowles JA, et al. Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome? Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33942911 DOI: 10.1002/mds.28593 |
0.136 |
|
| 2004 |
Newman JH, Fanburg BL, Archer SL, Badesch DB, Barst RJ, Garcia JG, Kao PN, Knowles JA, Loyd JE, McGoon MD, Morse JH, Nichols WC, Rabinovitch M, Rodman DM, Stevens T, et al. Pulmonary arterial hypertension: future directions: report of a National Heart, Lung and Blood Institute/Office of Rare Diseases workshop. Circulation. 109: 2947-52. PMID 15210611 DOI: 10.1161/01.Cir.0000132476.87231.6F |
0.135 |
|
| 2020 |
Whitman MC, Di Gioia SA, Chan WM, Gelber A, Pratt BM, Bell JL, Collins TE, Knowles JA, Armoskus C, Pato M, Pato C, Shaaban S, Staffieri S, MacKinnon S, Maconachie GDE, et al. Recurrent Rare Copy Number Variants Increase Risk for Esotropia. Investigative Ophthalmology & Visual Science. 61: 22. PMID 32780866 DOI: 10.1167/Iovs.61.10.22 |
0.134 |
|
| 1997 |
Lawton LN, Bonaldo MF, Jelenc PC, Qiu L, Baumes SA, Marcelino RA, de Jesus GM, Wellington S, Knowles JA, Warburton D, Brown S, Soares MB. Identification of a novel member of the TGF-beta superfamily highly expressed in human placenta. Gene. 203: 17-26. PMID 9426002 DOI: 10.1016/S0378-1119(97)00485-X |
0.133 |
|
| 1998 |
Banerjee P, Kleyn PW, Knowles JA, Lewis CA, Ross BM, Parano E, Kovats SG, Lee JJ, Penchaszadeh GK, Ott J, Jacobson SG, Gilliam TC. TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa. Nature Genetics. 18: 177-9. PMID 9462751 DOI: 10.1038/ng0298-177 |
0.131 |
|
| 2020 |
Kovner R, Souaiaia T, Fox AS, French DA, Goss CE, Roseboom PH, Oler JA, Riedel MK, Fekete EM, Fudge JL, Knowles JA, Kalin NH. Transcriptional Profiling of Primate Central Nucleus of the Amygdala Neurons to Understand the Molecular Underpinnings of Early-Life Anxious Temperament. Biological Psychiatry. PMID 32709417 DOI: 10.1016/J.Biopsych.2020.05.009 |
0.129 |
|
| 2001 |
Morse JH, Deng Z, Knowles JA. Genetic aspects of pulmonary arterial hypertension. Annals of Medicine. 33: 596-603. PMID 11817654 |
0.129 |
|
| 2018 |
Schrauwen I, Kari E, Mattox J, Llaci L, Smeeton J, Naymik M, Raible DW, Knowles JA, Crump JG, Huentelman MJ, Friedman RA. De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness. Human Genetics. PMID 29955957 DOI: 10.1007/S00439-018-1898-8 |
0.128 |
|
| 2019 |
Evgrafov O, Armoskus C, Spitsyna V, Wrobel B, Sobell J, Souaiaia T, Medeiros H, Wang K, Walker C, Camarena A, Simpson G, Pato M, Pato C, Knowles J. 48 Gene Expression Of Patient-Derived Neural Progenitor Cell Lines Developed From Olfactory Neuroepithelium Implicates Wnt Signaling In The Etiology Of Schizophrenia European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.189 |
0.122 |
|
| 1986 |
Knowles JA, Childs GJ. Comparison of the late H1 histone genes of the sea urchins Lytechinus pictus and Strongelocentrotus purpuratus. Nucleic Acids Research. 14: 8121-33. PMID 3022245 DOI: 10.1093/nar/14.20.8121 |
0.121 |
|
| 2003 |
Nunes H, Humbert M, Sitbon O, Morse JH, Deng Z, Knowles JA, Le Gall C, Parent F, Garcia G, Hervé P, Barst RJ, Simonneau G. Prognostic factors for survival in human immunodeficiency virus-associated pulmonary arterial hypertension. American Journal of Respiratory and Critical Care Medicine. 167: 1433-9. PMID 12615632 DOI: 10.1164/rccm.200204-330OC |
0.113 |
|
| 2006 |
Wong WK, Morse JH, Knowles JA. Evolutionary conservation and mutational spectrum of BMPR2 gene. Gene. 368: 84-93. PMID 16361068 DOI: 10.1016/j.gene.2005.10.025 |
0.11 |
|
| 2023 |
Mathews F, Tung VSK, Foronjy R, Boruk M, Knowles JA, Evgrafov OV. Cell Type Catalog of Middle Turbinate Epithelium (). Oto Open. 7: e91. PMID 38093720 DOI: 10.1002/oto2.91 |
0.109 |
|
| 2001 |
Morse JH, Knowles JA. Genetics of primary pulmonary hypertension Progress in Pediatric Cardiology. 12: 271-278. DOI: 10.1016/S1058-9813(01)00073-X |
0.107 |
|
| 1999 |
Lewis CA, Batlle IR, Batlle KG, Banerjee P, Cideciyan AV, Huang J, Alemán TS, Huang Y, Ott J, Gilliam TC, Knowles JA, Jacobson SG. Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration. Investigative Ophthalmology & Visual Science. 40: 2106-14. PMID 10440267 |
0.106 |
|
| 1984 |
Knowles JA, Childs GJ. Temporal expression of late histone messenger RNA in the sea urchin Lytechinus pictus. Proceedings of the National Academy of Sciences of the United States of America. 81: 2411-5. PMID 6585806 |
0.104 |
|
| 1992 |
Knowles JA, Vieland VJ, Gilliam TC. Perils of gene mapping with microsatellite markers. American Journal of Human Genetics. 51: 905-9. PMID 1415237 |
0.102 |
|
| 2004 |
Peters EJ, Slager SL, McGrath PJ, Knowles JA, Hamilton SP. Investigation of serotonin-related genes in antidepressant response. Molecular Psychiatry. 9: 879-89. PMID 15052272 DOI: 10.1038/sj.mp.4001502 |
0.099 |
|
| 2004 |
Newman JH, Trembath RC, Morse JA, Grunig E, Loyd JE, Adnot S, Coccolo F, Ventura C, Phillips JA, Knowles JA, Janssen B, Eickelberg O, Eddahibi S, Herve P, Nichols WC, et al. Genetic basis of pulmonary arterial hypertension: current understanding and future directions. Journal of the American College of Cardiology. 43: 33S-39S. PMID 15194176 DOI: 10.1016/j.jacc.2004.02.028 |
0.091 |
|
| 1997 |
Hirano M, Shtilbans A, Mayeux R, Davidson MM, DiMauro S, Knowles JA, Schon EA. Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes. Proceedings of the National Academy of Sciences of the United States of America. 94: 14894-9. PMID 9405710 DOI: 10.1073/Pnas.94.26.14894 |
0.09 |
|
| 2003 |
Morse J, Barst R, Horn E, Cuervo N, Deng Z, Knowles J. Pulmonary hypertension in scleroderma spectrum of disease: lack of bone morphogenetic protein receptor 2 mutations. The Journal of Rheumatology. 29: 2379-81. PMID 12415595 |
0.088 |
|
| 2021 |
Gray NS, John A, McKinnon A, Raybould S, Knowles J, Snowden RJ. Structured Professional Judgment to Assist the Evaluation and Safety Planning of Suicide Risk: The Risk of Suicide Protocol (RoSP). Frontiers in Psychiatry. 12: 607120. PMID 34079476 DOI: 10.3389/fpsyt.2021.607120 |
0.087 |
|
| 2002 |
Humbert M, Deng Z, Simonneau G, Barst RJ, Sitbon O, Wolf M, Cuervo N, Moore KJ, Hodge SE, Knowles JA, Morse JH. BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives. The European Respiratory Journal. 20: 518-23. PMID 12358323 DOI: 10.1183/09031936.02.01762002 |
0.086 |
|
| 2006 |
Willers ED, Newman JH, Loyd JE, Robbins IM, Wheeler LA, Prince MA, Stanton KC, Cogan JA, Runo JR, Byrne D, Humbert M, Simonneau G, Sztrymf B, Morse JA, Knowles JA, et al. Serotonin transporter polymorphisms in familial and idiopathic pulmonary arterial hypertension. American Journal of Respiratory and Critical Care Medicine. 173: 798-802. PMID 16339917 DOI: 10.1164/rccm.200509-1361OC |
0.085 |
|
| 2020 |
Kari E, Llaci L, Go JL, Naymik M, Knowles JA, Leal SM, Rangasamy S, Huentelman MJ, Liang W, Friedman RA, Schrauwen I. Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve Malformations. Ear and Hearing. PMID 31985533 DOI: 10.1097/Aud.0000000000000819 |
0.084 |
|
| 2007 |
Chen X, Hale GA, Neale GA, Knowles J, Barfield RC, Wang YD, Kaushal D, Naeve DC, Srivastava DK, Tong X, Turner V, Naeve CW, Handgretinger R. A novel approach for the analysis of T-cell reconstitution by using a T-cell receptor beta-based oligonucleotide microarray in hematopoietic stem cell transplantation. Experimental Hematology. 35: 831-41. PMID 17577931 DOI: 10.1016/J.Exphem.2007.02.003 |
0.081 |
|
| 2019 |
Arsalan A, Bajwa S, Hussain F, Umar M, Khizar B, Khan M, Jawad A, Sibtain M, Naeem F, Knowles J, Ayub M. S77SELF REPORTED PARENTAL AND GRANDPARENTAL RELATEDNESS IN A CASE CONTROL SAMPLE OF SCHIZOPHRENIA FROM PAKISTAN European Neuropsychopharmacology. 29: S153. DOI: 10.1016/j.euroneuro.2019.08.078 |
0.081 |
|
| 2019 |
Kovner R, Souaiaia T, Fox A, Roseboom P, French D, Oler J, Knowles J, Fudge J, Kalin N. 208. Transcriptional Profiling of Primate Central Nucleus of the Amygdala Neurons: A Role for PKCd Neurons in Early Life Anxious Temperament Biological Psychiatry. 85: S86. DOI: 10.1016/J.Biopsych.2019.03.222 |
0.078 |
|
| 2004 |
Lee JH, Mayo D, Mo J, Santana V, Williamson J, Flaquer A, Estevez P, Lantigua R, Kawarai T, Toulina A, Medrano M, Stern Y, Tycko B, Rogaeva E, George-Hyslop PS, ... Knowles JA, et al. O3-02-08 Fine mapping of chromosome 10 using memory and related neuropsychological phenotypes in the Caribbean hispanics Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80190-8 |
0.077 |
|
| 2005 |
Wong WP, Knowles JA, Morse JH. Comparative analysis of BMPR2 gene and its mutations in idiopathic pulmonary arterial hypertension. Chest. 128: 615S. PMID 16373869 DOI: 10.1378/chest.128.6_suppl.615S |
0.075 |
|
| 2004 |
Roberts KE, McElroy JJ, Wong WP, Yen E, Widlitz A, Barst RJ, Knowles JA, Morse JH. BMPR2 mutations in pulmonary arterial hypertension with congenital heart disease. The European Respiratory Journal. 24: 371-4. PMID 15358693 DOI: 10.1183/09031936.04.00018604 |
0.072 |
|
| 2008 |
Rosenzweig EB, Morse JH, Knowles JA, Chada KK, Khan AM, Roberts KE, McElroy JJ, Juskiw NK, Mallory NC, Rich S, Diamond B, Barst RJ. Clinical implications of determining BMPR2 mutation status in a large cohort of children and adults with pulmonary arterial hypertension. The Journal of Heart and Lung Transplantation : the Official Publication of the International Society For Heart Transplantation. 27: 668-74. PMID 18503968 DOI: 10.1016/j.healun.2008.02.009 |
0.068 |
|
| 2010 |
Deng Z, Sobell JL, Knowles JA. Epigenetic Alterations in Schizophrenia Focus. 8: 358-365. DOI: 10.1176/FOC.8.3.FOC358 |
0.067 |
|
| 1982 |
Childs G, Nocente-McGrath C, Lieber T, Holt C, Knowles JA. Sea urchin (lytechinus pictus) late-stage histone H3 and H4 genes: characterization and mapping of a clustered but nontandemly linked multigene family. Cell. 31: 383-93. PMID 6297764 DOI: 10.1016/0092-8674(82)90132-5 |
0.066 |
|
| 2020 |
Gray NS, O'Connor C, Knowles J, Pink J, Simkiss NJ, Williams SD, Snowden RJ. The Influence of the COVID-19 Pandemic on Mental Well-Being and Psychological Distress: Impact Upon a Single Country. Frontiers in Psychiatry. 11: 594115. PMID 33262714 DOI: 10.3389/fpsyt.2020.594115 |
0.065 |
|
| 2017 |
Ding SL, Royall JJ, Sunkin SM, Ng L, Facer BA, Lesnar P, Guillozet-Bongaarts A, McMurray B, Szafer A, Dolbeare TA, Stevens A, Tirrell L, Benner T, Caldejon S, Dalley RA, ... ... Knowles JA, et al. Comprehensive cellular-resolution atlas of the adult human brain. The Journal of Comparative Neurology. 525: 407. PMID 27917481 DOI: 10.1002/cne.24130 |
0.063 |
|
| 1987 |
Knowles JA, Lai ZC, Childs GJ. Isolation, characterization, and expression of the gene encoding the late histone subtype H1-gamma of the sea urchin Strongylocentrotus purpuratus. Molecular and Cellular Biology. 7: 478-85. PMID 3031476 |
0.062 |
|
| 2010 |
Dean NR, Knowles JA, Helman EE, Aldridge JC, Carroll WR, Magnuson JS, Clemons L, Ziober B, Rosenthal EL. Anti-EMMPRIN antibody treatment of head and neck squamous cell carcinoma in an ex-vivo model. Anti-Cancer Drugs. 21: 861-7. PMID 20700044 DOI: 10.1097/CAD.0b013e32833d1a11 |
0.062 |
|
| 2019 |
Kari E, Llaci L, Go JL, Naymik M, Knowles JA, Leal SM, Rangasamy S, Huentelman MJ, Friedman RA, Schrauwen I. A de novo SIX1 variant in a patient with a rare nonsyndromic cochleovestibular nerve abnormality, cochlear hypoplasia, and bilateral sensorineural hearing loss. Molecular Genetics & Genomic Medicine. e995. PMID 31595699 DOI: 10.1002/Mgg3.995 |
0.06 |
|
| 2005 |
Wong WK, Knowles JA, Morse JH. Bone morphogenetic protein receptor type II C-terminus interacts with c-Src: implication for a role in pulmonary arterial hypertension. American Journal of Respiratory Cell and Molecular Biology. 33: 438-46. PMID 16002577 DOI: 10.1165/rcmb.2005-0103OC |
0.06 |
|
| 2005 |
Roberts KE, Barst RJ, McElroy JJ, Widlitz A, Chada K, Knowles JA, Morse JH. Bone morphogenetic protein receptor 2 mutations in adults and children with idiopathic pulmonary arterial hypertension: association with thyroid disease. Chest. 128: 618S. PMID 16373874 DOI: 10.1378/Chest.128.6_Suppl.618S |
0.055 |
|
| 1967 |
Knowles JA, Ezekiel SG. Pinworms--Incidence, predictability and treatment with thiabendazole. California Medicine. 107: 315-8. PMID 6062278 |
0.05 |
|
| 2013 |
Hudis C, Swanton C, Janjigian YY, Lee R, Sutherland S, Lehman R, Chandarlapaty S, Hamilton N, Gajria D, Knowles J, Shah J, Shannon K, Tetteh E, Sullivan DM, Moreno C, et al. A phase 1 study evaluating the combination of an allosteric AKT inhibitor (MK-2206) and trastuzumab in patients with HER2-positive solid tumors. Breast Cancer Research : Bcr. 15: R110. PMID 24252402 DOI: 10.1186/Bcr3577 |
0.05 |
|
| 2011 |
Liu Z, Hartman YE, Warram JM, Knowles JA, Sweeny L, Zhou T, Rosenthal EL. Fibroblast growth factor receptor mediates fibroblast-dependent growth in EMMPRIN-depleted head and neck cancer tumor cells. Molecular Cancer Research : McR. 9: 1008-17. PMID 21665938 DOI: 10.1158/1541-7786.Mcr-11-0043 |
0.048 |
|
| 2005 |
Chen X, Barfield R, Benaim E, Leung W, Knowles J, Lawrence D, Otto M, Shurtleff SA, Neale GA, Behm FG, Turner V, Handgretinger R. Prediction of T-cell reconstitution by assessment of T-cell receptor excision circle before allogeneic hematopoietic stem cell transplantation in pediatric patients. Blood. 105: 886-93. PMID 15358630 DOI: 10.1182/blood-2004-04-1405 |
0.047 |
|
| 1980 |
McHugh SL, Kirkman SK, Knowles JA. Macro- and micromethods for high-performance liquid chromatographic analysis of oxaprozin in plasma. Journal of Pharmaceutical Sciences. 69: 794-6. PMID 7391941 |
0.046 |
|
| 2006 |
Chen X, Hale GA, Barfield R, Benaim E, Leung WH, Knowles J, Horwitz EM, Woodard P, Kasow K, Yusuf U, Behm FG, Hayden RT, Shurtleff SA, Turner V, Srivastava DK, et al. Rapid immune reconstitution after a reduced-intensity conditioning regimen and a CD3-depleted haploidentical stem cell graft for paediatric refractory haematological malignancies. British Journal of Haematology. 135: 524-32. PMID 17010105 DOI: 10.1111/j.1365-2141.2006.06330.x |
0.043 |
|
| 2011 |
Kim H, Zhai G, Liu Z, Samuel S, Shah N, Helman EE, Knowles JA, Stockard CR, Fineberg NS, Grizzle WE, Zhou T, Zinn KR, Rosenthal EL. Extracelluar matrix metalloproteinase as a novel target for pancreatic cancer therapy. Anti-Cancer Drugs. 22: 864-74. PMID 21730821 DOI: 10.1097/Cad.0B013E328349311E |
0.041 |
|
| 1971 |
Elliott HW, Nomof N, Navarro G, Ruelius HW, Knowles JA, Comer WH. Central nervous system and cardiovascular effects of lorazepam in man. Clinical Pharmacology and Therapeutics. 12: 468-81. PMID 4936036 |
0.037 |
|
| 2011 |
Knowles JA, Golden B, Yan L, Carroll WR, Helman EE, Rosenthal EL. Disruption of the AKT pathway inhibits metastasis in an orthotopic model of head and neck squamous cell carcinoma. The Laryngoscope. 121: 2359-65. PMID 22020886 DOI: 10.1002/lary.22180 |
0.035 |
|
| 2007 |
Otto M, Chen X, Martin WJ, Leung W, Knowles J, Holladay M, Houston J, Handgretinger R, Barfield RC. Selection of stem cells by using antibodies that target different CD34 epitopes yields different patterns of T-cell differentiation. Stem Cells (Dayton, Ohio). 25: 537-42. PMID 17023516 DOI: 10.1634/stemcells.2006-0319 |
0.035 |
|
| 2017 |
Jones A, Reller L, Knowles J, Lin FC, Lohr J. Decisions Regarding Newborn Feeding by Latina Mothers. Clinical Pediatrics. 9922817692317. PMID 28952343 DOI: 10.1177/0009922817692317 |
0.033 |
|
| 1977 |
Greenblatt DJ, Comer WH, Elliott HW, Shader RI, Knowles JA, Ruelius HW. Clinical pharmacokinetics of lorazepam. III. Intravenous injection. Preliminary results. Journal of Clinical Pharmacology. 17: 490-4. PMID 19508 |
0.033 |
|
| 2010 |
Nguyen H, Knowles J. Demand for voluntary health insurance in developing countries: the case of Vietnam's school-age children and adolescent student health insurance program. Social Science & Medicine (1982). 71: 2074-82. PMID 20974514 DOI: 10.1016/j.socscimed.2010.09.033 |
0.033 |
|
| 1977 |
Greenblatt DJ, Joyce TH, Comer WH, Knowles JA, Shader RI, Kyriakopoulos AA, MacLaughlin DS, Ruelius HW. Clinical pharmacokinetics of lorazepam. II. Intramuscular injection. Clinical Pharmacology and Therapeutics. 21: 222-30. PMID 13960 |
0.032 |
|
| 2012 |
Carre AL, Larson BJ, Knowles JA, Kawai K, Longaker MT, Lorenz HP. Fetal mouse skin heals scarlessly in a chick chorioallantoic membrane model system. Annals of Plastic Surgery. 69: 85-90. PMID 21712703 DOI: 10.1097/Sap.0B013E31822128A9 |
0.032 |
|
| 2014 |
Knowles JA, Lowenberg MH, Neild SA, Krauskopf B. A bifurcation study to guide the design of a landing gear with a combined uplock/downlock mechanism. Proceedings. Mathematical, Physical, and Engineering Sciences / the Royal Society. 470: 20140332. PMID 25484601 DOI: 10.1098/rspa.2014.0332 |
0.031 |
|
| 1977 |
Greenblatt DJ, Knowles JA, Comer WH, Shader RI, Harmatz JS, Ruelius HW. Clinical pharmacokinetics of lorazepam. IV. Long-term oral administration. Journal of Clinical Pharmacology. 17: 495-500. PMID 19509 |
0.031 |
|
| 2004 |
Kasow KA, Chen X, Knowles J, Wichlan D, Handgretinger R, Riberdy JM. Human CD4+CD25+ regulatory T cells share equally complex and comparable repertoires with CD4+CD25- counterparts. Journal of Immunology (Baltimore, Md. : 1950). 172: 6123-8. PMID 15128798 DOI: 10.4049/jimmunol.172.10.6123 |
0.023 |
|
| 1985 |
Leelavathi DE, Dressler DE, Soffer EF, Yachetti SD, Knowles JA. Determination of promethazine in human plasma by automated high-performance liquid chromatography with electrochemical detection and by gas chromatography-mass spectrometry. Journal of Chromatography. 339: 105-15. PMID 4019661 |
0.022 |
|
| 1968 |
Knowles JA. Venereal disease in adolescence. Medical Arts and Sciences. 22: 45-8. PMID 5756521 |
0.022 |
|
| 2002 |
Knowles JA. Emergency air evacuation of critically ill patients from cruise ships. Journal of Travel Medicine. 9: 335; author reply 33. PMID 12962593 |
0.022 |
|
| 2012 |
Knowles JA, Heath CH, Saini R, Umphrey H, Warram J, Hoyt K, Rosenthal EL. Molecular targeting of ultrasonographic contrast agent for detection of head and neck squamous cell carcinoma. Archives of Otolaryngology--Head & Neck Surgery. 138: 662-8. PMID 22801891 DOI: 10.1001/Archoto.2012.1081 |
0.021 |
|
| 1976 |
Greenblatt DJ, Schillings RT, Kyriakopoulos AA, Shader RI, Sisenwine SF, Knowles JA, Ruelius HW. Clinical pharmacokinetics of lorazepam. I. Absorption and disposition of oral 14C-lorazepam. Clinical Pharmacology and Therapeutics. 20: 329-41. PMID 8232 |
0.019 |
|
| 1971 |
Knowles JA, Comer WH, Ruelius HW. Disposition of 7-chloro-5-(o-chlorophenyl)-1,3-dihydro-3-hydroxy-2H-1,4-benzodiazepin-2-one (lorazepam) in humans. Determination of the drug by electron capture gas chromatography. Arzneimittel-Forschung. 21: 1055-9. PMID 5109347 |
0.019 |
|
| 1972 |
Knowles JA, Ruelius HW. Absorption and excretion of 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one (oxazepam) in humans. Determination of the drug by gas-liquid chromatography with electron capture detection. Arzneimittel-Forschung. 22: 687-92. PMID 5068248 |
0.019 |
|
| 2017 |
Kari E, Schrauwen I, Llaci L, Fisher LM, Go JL, Naymik M, Knowles JA, Huentelman MJ, Friedman RA. Compound heterozygous mutations in MASP1 in a deaf child with absent cochlear nerves. Neurology. Genetics. 3: e153. PMID 28534045 DOI: 10.1212/Nxg.0000000000000153 |
0.018 |
|
| 1982 |
Chiang ST, Morrison G, Knowles JA, Ruelius HW, Walker BR. Oxaprozin disposition in renal disease. Clinical Pharmacology and Therapeutics. 31: 509-15. PMID 7060332 |
0.018 |
|
| 2021 |
Gray NS, Knowles J, George D, Harvey A, Powell R, Zadeh MV, Wansing C, Snowden RJ. Explicit and Implicit Hopelessness and Self-injury. Suicide & Life-Threatening Behavior. PMID 33634908 DOI: 10.1111/sltb.12743 |
0.017 |
|
| 2012 |
Shah N, Zhai G, Knowles JA, Stockard CR, Grizzle WE, Fineberg N, Zhou T, Zinn KR, Rosenthal EL, Kim H. (18)F-FDG PET/CT imaging detects therapy efficacy of anti-EMMPRIN antibody and gemcitabine in orthotopic pancreatic tumor xenografts. Molecular Imaging and Biology : Mib : the Official Publication of the Academy of Molecular Imaging. 14: 237-44. PMID 21494920 DOI: 10.1007/S11307-011-0491-5 |
0.016 |
|
| 1974 |
Knowles JA. Breast milk: a source of more than nutrition for the neonate. Clinical Toxicology. 7: 69-82. PMID 4135128 DOI: 10.3109/15563657408987978 |
0.015 |
|
| 2008 |
Hantash BM, Zhao L, Knowles JA, Lorenz HP. Adult and fetal wound healing. Frontiers in Bioscience : a Journal and Virtual Library. 13: 51-61. PMID 17981527 |
0.015 |
|
| 1969 |
Janssen FW, Knowles JA, Kirkman SK, Ruelius HW. Determination of cycloleucine in biological fluids. Analytical Biochemistry. 30: 217-21. PMID 5809664 |
0.013 |
|
| 1988 |
Audet PR, Knowles JA, Troy SM, Walker BR, Morrison G. Effect of chronic renal failure on oxaprozin multiple-dose pharmacokinetics. Clinical Pharmacology and Therapeutics. 44: 303-9. PMID 3416552 |
0.013 |
|
| 1982 |
Knowles JA, White GR, Kick CJ, Spangler TB, Ruelius HW. Gas chromatographic determination of guanabenz in biological fluids by electron-capture detection. Journal of Pharmaceutical Sciences. 71: 710-1. PMID 7097542 |
0.013 |
|
| 1981 |
Lucas SB, Knowles JA, Calder J. Pulmonary alveolar proteinosis in an infant. East African Medical Journal. 58: 539-42. PMID 7308112 |
0.01 |
|
| 2009 |
Knowles JA. National solid waste management plan for Iraq. Waste Management & Research : the Journal of the International Solid Wastes and Public Cleansing Association, Iswa. 27: 322-7. PMID 19470543 DOI: 10.1177/0734242X09104129 |
0.01 |
|
| 1988 |
Colatsky TJ, Bird LB, Knowles JA. Cardiac electrophysiology of the antiarrhythmic agent recainam (Wy-42,362) in anesthetized dogs: relation to plasma and myocardial concentrations. Journal of Cardiovascular Pharmacology. 11: 308-16. PMID 2452923 |
0.01 |
|
| 1984 |
Chiang ST, Knowles JA, Hubsher JA, Ruelius HW, Walker BR. Effects of food on oxaprozin bioavailability. Journal of Clinical Pharmacology. 24: 381-5. PMID 6480879 |
0.01 |
|
| 1979 |
Ruelius HW, Tio CO, Knowles JA, McHugh SL, Schillings RT, Sisenwine SF. Diastereoisomeric glucuronides of oxazepam. Isolation and stereoselective enzymic hydrolysis. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 7: 40-3. PMID 35325 |
0.01 |
|
| 1978 |
Janssen FW, Kirkman SK, Knowles JA, Ruelius HW. Disposition of 4,5-diphenyl-2-oxazolepropionic acid (oxaprozin) in beagle dogs and rhesus monkeys. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 6: 465-75. PMID 28928 |
0.01 |
|
| 1973 |
Knowles JA. Effects on the infant of drug therapy in nursing mothers. Drug Therapy. 3: 57-9, 65. PMID 12262536 |
0.01 |
|
| 1965 |
KNOWLES JA. EXCRETION OF DRUGS IN MILK--A REVIEW. The Journal of Pediatrics. 66: 1068-82. PMID 14288461 |
0.01 |
|
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