| Year |
Citation |
Score |
| 2023 |
Han S, DiBlasi E, Monson ET, Shabalin A, Ferris E, Chen D, Fraser A, Yu Z, Staley M, Callor WB, Christensen ED, Crockett DK, Li QS, Willour V, Bakian AV, ... ... Coon H, et al. Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genes. Molecular Psychiatry. PMID 37794117 DOI: 10.1038/s41380-023-02282-x |
0.77 |
|
| 2023 |
Docherty AR, Mullins N, Ashley-Koch AE, Qin X, Coleman JRI, Shabalin A, Kang J, Murnyak B, Wendt F, Adams M, Campos AI, DiBlasi E, Fullerton JM, Kranzler HR, Bakian AV, ... ... Coon H, et al. GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. The American Journal of Psychiatry. 180: 723-738. PMID 37777856 DOI: 10.1176/appi.ajp.21121266 |
0.736 |
|
| 2023 |
Yang G, Ullah HMA, Parker E, Gorsi B, Libowitz M, Maguire C, King JB, Coon H, Lopez-Larson M, Anderson JS, Yandell M, Shcheglovitov A. Neurite outgrowth deficits caused by rare PLXNB1 mutation in pediatric bipolar disorder. Molecular Psychiatry. PMID 37032361 DOI: 10.1038/s41380-023-02035-w |
0.309 |
|
| 2023 |
Ashley-Koch AE, Kimbrel NA, Qin XJ, Lindquist JH, Garrett ME, Dennis MF, Hair LP, Huffman JE, Jacobson DA, Madduri RK, Coon H, Docherty AR, Kang J, Mullins N, Ruderfer DM, et al. Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veterans Program. Plos Genetics. 19: e1010623. PMID 36940203 DOI: 10.1371/journal.pgen.1010623 |
0.735 |
|
| 2023 |
Mirza S, Docherty AR, Monson ET, Coon H, Keeshin B, Fries GR. Understanding heterogeneity in suicidal thoughts and behaviours and the implications for genetic studies - a commentary on Lannoy et al. (2022). Journal of Child Psychology and Psychiatry, and Allied Disciplines. PMID 36892557 DOI: 10.1111/jcpp.13778 |
0.725 |
|
| 2023 |
Das SC, Schulmann A, Callor WB, Jerominski L, Panicker MM, Christensen ED, Bunney WE, Williams ME, Coon H, Vawter MP. Altered transcriptomes, cell type proportions, and dendritic spine morphology in hippocampus of suicide deaths. Medrxiv : the Preprint Server For Health Sciences. PMID 36778310 DOI: 10.1101/2023.01.28.23285121 |
0.484 |
|
| 2022 |
Kimbrel NA, Ashley-Koch AE, Qin XJ, Lindquist JH, Garrett ME, Dennis MF, Hair LP, Huffman JE, Jacobson DA, Madduri RK, Trafton JA, Coon H, Docherty AR, Mullins N, Ruderfer DM, et al. Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans. Jama Psychiatry. PMID 36515925 DOI: 10.1001/jamapsychiatry.2022.3896 |
0.772 |
|
| 2022 |
Li QS, Shabalin AA, DiBlasi E, Gopal S, Canuso CM, Palotie A, Drevets WC, Docherty AR, Coon H. Genome-wide association study meta-analysis of suicide death and suicidal behavior. Molecular Psychiatry. PMID 36253440 DOI: 10.1038/s41380-022-01828-9 |
0.787 |
|
| 2022 |
Mirza S, Docherty AR, Bakian A, Coon H, Soares JC, Walss-Bass C, Fries GR. Genetics and epigenetics of self-injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 35975759 DOI: 10.1002/ajmg.b.32917 |
0.704 |
|
| 2022 |
Kimbrel NA, Ashley-Koch AE, Qin XJ, Lindquist JH, Garrett ME, Dennis MF, Hair LP, Huffman JE, Jacobson DA, Madduri RK, Trafton JA, Coon H, Docherty AR, Kang J, Mullins N, et al. A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Molecular Psychiatry. PMID 35347246 DOI: 10.1038/s41380-022-01472-3 |
0.742 |
|
| 2022 |
Coon H, Shabalin A, Bakian AV, DiBlasi E, Monson ET, Kirby A, Chen D, Fraser A, Yu Z, Staley M, Callor WB, Christensen ED, Crowell SE, Gray D, Crockett DK, et al. Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 35212135 DOI: 10.1002/ajmg.b.32890 |
0.774 |
|
| 2021 |
Bakian AV, Chen D, Zhang C, Hanson HA, Docherty AR, Keeshin B, Gray D, Smith KR, VanDerslice JA, Yu DZ, Zhang Y, Coon H. A population-wide analysis of the familial risk of suicide in Utah, USA. Psychological Medicine. 53: 1448-1457. PMID 37010215 DOI: 10.1017/S0033291721003020 |
0.711 |
|
| 2021 |
Mullins N, Kang J, Campos AI, Coleman JRI, Edwards AC, Galfalvy H, Levey DF, Lori A, Shabalin A, Starnawska A, Su MH, Watson HJ, Adams M, Awasthi S, Gandal M, ... ... Coon H, et al. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Biological Psychiatry. PMID 34861974 DOI: 10.1016/j.biopsych.2021.05.029 |
0.746 |
|
| 2021 |
Colbert SMC, Hatoum AS, Shabalin A, Li QS, Coon H, Nelson EC, Agrawal A, Docherty AR, Johnson EC. Exploring the genetic overlap of suicide-related behaviors and substance use disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34821019 DOI: 10.1002/ajmg.b.32880 |
0.76 |
|
| 2021 |
Docherty AR, Bakian AV, DiBlasi E, Shabalin AA, Chen D, Keeshin B, Monson E, Christensen ED, Li Q, Gray D, Coon H. Suicide and Psychosis: Results From a Population-Based Cohort of Suicide Death (N = 4380). Schizophrenia Bulletin. PMID 34559220 DOI: 10.1093/schbul/sbab113 |
0.766 |
|
| 2021 |
Docherty A, Kious B, Brown T, Francis L, Stark L, Keeshin B, Botkin J, DiBlasi E, Gray D, Coon H. Ethical concerns relating to genetic risk scores for suicide. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34472199 DOI: 10.1002/ajmg.b.32871 |
0.775 |
|
| 2021 |
Monson ET, Shabalin AA, Docherty AR, DiBlasi E, Bakian AV, Li QS, Gray D, Keeshin B, Crowell SE, Mullins N, Willour VL, Coon H. Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach. Translational Psychiatry. 11: 379. PMID 34234108 DOI: 10.1038/s41398-021-01500-w |
0.779 |
|
| 2021 |
William N, Reissner C, Sargent R, Darlington TM, DiBlasi E, Li QS, Keeshin B, Callor WB, Ferris E, Jerominski L, Smith KR, Christensen ED, Gray DM, Camp NJ, Missler M, ... ... Coon H, et al. Neurexin 1 variants as risk factors for suicide death. Molecular Psychiatry. PMID 34168285 DOI: 10.1038/s41380-021-01190-2 |
0.603 |
|
| 2021 |
DiBlasi E, Shabalin AA, Monson ET, Keeshin BR, Bakian AV, Kirby AV, Ferris E, Chen D, William N, Gaj E, Klein M, Jerominski L, Callor WB, Christensen E, Smith KR, ... ... Coon H, et al. Rare protein-coding variants implicate genes involved in risk of suicide death. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 34042246 DOI: 10.1002/ajmg.b.32861 |
0.767 |
|
| 2020 |
Kious BM, Docherty AR, Botkin JR, Brown TR, Francis LP, Gray DD, Keeshin BR, Stark LA, Witte B, Coon H. Correction: Ethical and public health implications of genetic testing for suicide risk: family and survivor perspectives. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33353974 DOI: 10.1038/s41436-020-01059-9 |
0.697 |
|
| 2020 |
Kious BM, Docherty AR, Botkin JR, Brown TR, Francis LP, Gray DD, Keeshin BR, Stark LA, Witte B, Coon H. Ethical and public health implications of genetic testing for suicide risk: family and survivor perspectives. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33020592 DOI: 10.1038/s41436-020-00982-1 |
0.748 |
|
| 2020 |
Docherty AR, Shabalin AA, DiBlasi E, Monson E, Mullins N, Adkins DE, Bacanu SA, Bakian AV, Crowell S, Chen D, Darlington TM, Callor WB, Christensen ED, Gray D, Keeshin B, ... ... Coon H, et al. Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents. The American Journal of Psychiatry. 177: 917-927. PMID 32998551 DOI: 10.1176/appi.ajp.2020.19101025 |
0.733 |
|
| 2020 |
DiBlasi E, Kirby AV, Gaj E, Docherty AR, Keeshin BR, Bakian AV, Coon H. Brief Report: Genetic Links Between Autism and Suicidal Behavior-A Preliminary Investigation. Journal of Autism and Developmental Disorders. PMID 32096122 DOI: 10.1007/S10803-020-04419-1 |
0.698 |
|
| 2019 |
Shade J, Coon H, Docherty AR. Ethical implications of using biobanks and population databases for genetic suicide research. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 30779308 DOI: 10.1002/Ajmg.B.32718 |
0.653 |
|
| 2019 |
Kirby AV, Bakian AV, Zhang Y, Bilder DA, Keeshin BR, Coon H. A 20-year study of suicide death in a statewide autism population. Autism Research : Official Journal of the International Society For Autism Research. PMID 30663277 DOI: 10.1002/aur.2076 |
0.554 |
|
| 2018 |
Coon H, Darlington TM, DiBlasi E, Callor WB, Ferris E, Fraser A, Yu Z, William N, Das SC, Crowell SE, Chen D, Anderson JS, Klein M, Jerominski L, Cannon D, et al. Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide. Molecular Psychiatry. PMID 30353169 DOI: 10.1038/S41380-018-0282-3 |
0.746 |
|
| 2018 |
Waller RG, Darlington TM, Wei X, Madsen MJ, Thomas A, Curtin K, Coon H, Rajamanickam V, Musinsky J, Jayabalan D, Atanackovic D, Rajkumar SV, Kumar S, Slager S, Middha M, et al. Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. Plos Genetics. 14: e1007111. PMID 29389935 DOI: 10.1371/Journal.Pgen.1007111 |
0.322 |
|
| 2017 |
Keeshin BR, Gray D, Zhang C, Presson AP, Coon H. Youth Suicide Deaths: Investigation of Clinical Predictors in a Statewide Sample. Suicide & Life-Threatening Behavior. PMID 28833472 DOI: 10.1111/Sltb.12386 |
0.439 |
|
| 2016 |
McGlade E, Bakian A, Coon H, Yurgelun-Todd D, Callor WB, Byrd J, Gray D. Male suspected suicide decedents in Utah: A comparison of Veterans and nonveterans. Comprehensive Psychiatry. 69: 1-10. PMID 27423339 DOI: 10.1016/J.Comppsych.2016.04.014 |
0.547 |
|
| 2016 |
Hollingshaus MS, Coon H, Crowell SE, Gray DD, Hanson HA, Pimentel R, Smith KR. Differential Vulnerability to Early-Life Parental Death: The Moderating Effects of Family Suicide History on Risks for Major Depression and Substance Abuse in Later Life. Biodemography and Social Biology. 62: 105-25. PMID 27050036 DOI: 10.1080/19485565.2016.1138395 |
0.45 |
|
| 2015 |
Bakian AV, Huber RS, Coon H, Gray D, Wilson P, McMahon WM, Renshaw PF. Acute air pollution exposure and risk of suicide completion. American Journal of Epidemiology. 181: 295-303. PMID 25673816 DOI: 10.1093/aje/kwu341 |
0.463 |
|
| 2015 |
Bakian AV, Huber RS, Coon H, Gray D, Wilson P, McMahon WM, Renshaw PF. Bakian et al. respond to "Assessing air pollution and suicide risk". American Journal of Epidemiology. 181: 309-10. PMID 25673815 DOI: 10.1093/aje/kwu343 |
0.335 |
|
| 2014 |
Gray D, Coon H, McGlade E, Callor WB, Byrd J, Viskochil J, Bakian A, Yurgelun-Todd D, Grey T, McMahon WM. Comparative analysis of suicide, accidental, and undetermined cause of death classification. Suicide & Life-Threatening Behavior. 44: 304-16. PMID 25057525 DOI: 10.1111/Sltb.12079 |
0.463 |
|
| 2014 |
Huber RS, Coon H, Kim N, Renshaw PF, Kondo DG. Altitude is a risk factor for completed suicide in bipolar disorder. Medical Hypotheses. 82: 377-81. PMID 24495565 DOI: 10.1016/j.mehy.2014.01.006 |
0.545 |
|
| 2010 |
Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon H. Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders. Molecular Autism. 1: 3. PMID 20678246 DOI: 10.1186/2040-2392-1-3 |
0.326 |
|
| 2010 |
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Coon H, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/Hmg/Ddq307 |
0.305 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2012 |
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Coon H, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/Hmg/Dds301 |
0.292 |
|
| 2012 |
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, ... ... Coon H, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. 131: 565-79. PMID 21996756 DOI: 10.1007/S00439-011-1094-6 |
0.292 |
|
| 2010 |
Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H. A unified theory of autism revisited: Linkage evidence points to chromosome X using a high-risk subset of AGRE families Autism Research. 3: 47-52. PMID 20437600 DOI: 10.1002/Aur.119 |
0.284 |
|
| 2013 |
Bilder D, Botts EL, Smith KR, Pimentel R, Farley M, Viskochil J, McMahon WM, Block H, Ritvo E, Ritvo RA, Coon H. Excess mortality and causes of death in autism spectrum disorders: a follow up of the 1980s Utah/UCLA autism epidemiologic study. Journal of Autism and Developmental Disorders. 43: 1196-204. PMID 23008058 DOI: 10.1007/S10803-012-1664-Z |
0.273 |
|
| 2006 |
Coon H. Current perspectives on the genetic analysis of autism. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 24-32. PMID 16419097 DOI: 10.1002/ajmg.c.30079 |
0.27 |
|
| 2007 |
Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Coon H, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.269 |
|
| 2015 |
Chapman NH, Nato AQ, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. Human Genetics. 134: 1055-68. PMID 26204995 DOI: 10.1007/S00439-015-1585-Y |
0.268 |
|
| 2009 |
Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, ... ... Coon H, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 459: 569-73. PMID 19404257 DOI: 10.1038/Nature07953 |
0.264 |
|
| 2014 |
Hu H, Roach JC, Coon H, Guthery SL, Voelkerding KV, Margraf RL, Durtschi JD, Tavtigian SV, Shankaracharya, Wu W, Scheet P, Wang S, Xing J, Glusman G, Hubley R, et al. A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. Nature Biotechnology. 32: 663-9. PMID 24837662 DOI: 10.1038/Nbt.2895 |
0.247 |
|
| 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, ... ... Coon H, 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 |
0.246 |
|
| 2009 |
Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, ... ... Coon H, et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. Plos Genetics. 5: e1000536. PMID 19557195 DOI: 10.1371/Journal.Pgen.1000536 |
0.243 |
|
| 2008 |
Brune CW, Korvatska E, Allen-Brady K, Cook EH, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H. Heterogeneous association between engrailed-2 and autism in the CPEA network. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 187-93. PMID 17948868 DOI: 10.1002/Ajmg.B.30585 |
0.235 |
|
| 2009 |
Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, ... ... Coon H, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.233 |
|
| 2015 |
Schwantes-An TH, Zhang J, Chen LS, Hartz SM, Culverhouse RC, Chen X, Coon H, Frank J, Kamens HM, Konte B, Kovanen L, Latvala A, Legrand LN, Maher BS, Melroy WE, et al. Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics. PMID 26392368 DOI: 10.1007/S10519-015-9737-3 |
0.229 |
|
| 2011 |
Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum JD. No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set. Autism Research : Official Journal of the International Society For Autism Research. 4: 293-6. PMID 21491612 DOI: 10.1002/Aur.195 |
0.227 |
|
| 2003 |
Kim UK, Jorgenson E, Coon H, Leppert M, Risch N, Drayna D. Positional cloning of the human quantitative trait locus underlying taste sensitivity to phenylthiocarbamide. Science (New York, N.Y.). 299: 1221-5. PMID 12595690 DOI: 10.1126/Science.1080190 |
0.227 |
|
| 2018 |
Werling DM, Brand H, An JY, Stone MR, Zhu L, Glessner JT, Collins RL, Dong S, Layer RM, Markenscoff-Papadimitriou E, Farrell A, Schwartz GB, Wang HZ, Currall BB, Zhao X, ... ... Coon H, et al. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics. PMID 29700473 DOI: 10.1038/S41588-018-0107-Y |
0.225 |
|
| 2010 |
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Coon H, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/Nature09146 |
0.215 |
|
| 2021 |
den Hoed J, de Boer E, Voisin N, Dingemans AJM, Guex N, Wiel L, Nellaker C, Amudhavalli SM, Banka S, Bena FS, Ben-Zeev B, Bonagura VR, Bruel AL, Brunet T, Brunner HG, ... ... Coon H, et al. Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction. American Journal of Human Genetics. PMID 33513338 DOI: 10.1016/j.ajhg.2021.01.007 |
0.214 |
|
| 2019 |
Bilder DA, Esplin MS, Coon H, Burghardt P, Clark EAS, Fraser A, Smith KR, Worsham W, Chappelle K, Rayner T, Bakian AV. Early Second Trimester Maternal Serum Steroid-Related Biomarkers Associated with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 31410696 DOI: 10.1007/s10803-019-04162-2 |
0.212 |
|
| 2016 |
Christensen ED, Berger J, Alashari MM, Coon H, Robison C, Ho HT, Adams DR, Gahl WA, Smith KR, Opitz JM, Johnson DR. Sudden infant death "syndrome"-Insights and future directions from a Utah population database analysis. American Journal of Medical Genetics. Part A. PMID 27792857 DOI: 10.1002/Ajmg.A.37994 |
0.211 |
|
| 2018 |
An JY, Lin K, Zhu L, Werling DM, Dong S, Brand H, Wang HZ, Zhao X, Schwartz GB, Collins RL, Currall BB, Dastmalchi C, Dea J, Duhn C, Gilson MC, ... ... Coon H, et al. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362. PMID 30545852 DOI: 10.1126/Science.Aat6576 |
0.21 |
|
| 2014 |
Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, et al. The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. Molecular Autism. 5: 34. PMID 25392729 DOI: 10.1186/2040-2392-5-34 |
0.209 |
|
| 2005 |
Coon H, Dunn D, Lainhart J, Miller J, Hamil C, Battaglia A, Tancredi R, Leppert MF, Weiss R, McMahon W. Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 42-6. PMID 15768392 DOI: 10.1002/Ajmg.B.30168 |
0.209 |
|
| 2010 |
Knight S, Coon H, Johnson M, Leppert MF, Camp NJ, McMahon WM, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Santangelo S, Stewart SE, Scharf J, et al. Linkage analysis of Tourette syndrome in a large Utah pedigree American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 656-662. PMID 19777563 DOI: 10.1002/Ajmg.B.31035 |
0.208 |
|
| 2023 |
Workalemahu T, Avery C, Lopez S, Blue NR, Wallace A, Quinlan AR, Coon H, Warner D, Varner MW, Branch DW, Jorde LB, Silver RM. Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study. Plos One. 18: e0281934. PMID 36800380 DOI: 10.1371/journal.pone.0281934 |
0.203 |
|
| 2013 |
Bilder DA, Bakian AV, Viskochil J, Clark EA, Botts EL, Smith KR, Pimentel R, McMahon WM, Coon H. Maternal prenatal weight gain and autism spectrum disorders. Pediatrics. 132: e1276-83. PMID 24167172 DOI: 10.1542/peds.2013-1188 |
0.202 |
|
| 2003 |
Drayna D, Coon H, Kim UK, Elsner T, Cromer K, Otterud B, Baird L, Peiffer AP, Leppert M. Genetic analysis of a complex trait in the Utah Genetic Reference Project: A major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p Human Genetics. 112: 567-572. PMID 12624758 |
0.195 |
|
| 2015 |
Addis L, Ahn JW, Dobson R, Dixit A, Ogilvie CM, Pinto D, Vaags AK, Coon H, Chaste P, Wilson S, Parr JR, Andrieux J, Lenne B, Tumer Z, Leuzzi V, et al. Microdeletions of ELP4 are Associated with Language Impairment, Autism Spectrum Disorder and Mental Retardation. Human Mutation. PMID 26010655 DOI: 10.1002/Humu.22816 |
0.194 |
|
| 2020 |
Lin BD, Colas F, Nijman IJ, Medic J, Brands W, Parr JR, van Eijk KR, Klauck SM, Chiocchetti AG, Freitag CM, Maestrini E, Bacchelli E, Coon H, Vicente A, Oliveira G, et al. The role of rare compound heterozygous events in autism spectrum disorder. Translational Psychiatry. 10: 204. PMID 32572023 DOI: 10.1038/S41398-020-00866-7 |
0.194 |
|
| 2014 |
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, ... ... Coon H, et al. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics. 94: 677-94. PMID 24768552 DOI: 10.1016/J.Ajhg.2014.03.018 |
0.192 |
|
| 2005 |
Odell D, Maciulis A, Cutler A, Warren L, McMahon WM, Coon H, Stubbs G, Henley K, Torres A. Confirmation of the association of the C4B null allelle in autism. Human Immunology. 66: 140-5. PMID 15694999 DOI: 10.1016/J.Humimm.2004.11.002 |
0.192 |
|
| 2021 |
Gustavson DE, Friedman NP, Stallings MC, Reynolds CA, Coon H, Corley RP, Hewitt JK, Gordon RL. Musical instrument engagement in adolescence predicts verbal ability 4 years later: A twin and adoption study. Developmental Psychology. 57: 1943-1957. PMID 34914455 DOI: 10.1037/dev0001245 |
0.189 |
|
| 2015 |
Bakian AV, Bilder DA, Coon H, McMahon WM. Spatial relative risk patterns of autism spectrum disorders in Utah. Journal of Autism and Developmental Disorders. 45: 988-1000. PMID 25241009 DOI: 10.1007/s10803-014-2253-0 |
0.189 |
|
| 2003 |
Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, ... ... Coon H, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics. 73: 49-62. PMID 12802785 DOI: 10.1086/376547 |
0.187 |
|
| 2003 |
Lewis CM, Levinson DF, Wise LH, DeLisi LE, Straub RE, Hovatta I, Williams NM, Schwab SG, Pulver AE, Faraone SV, Brzustowicz LM, Kaufmann CA, Garver DL, Gurling HM, Lindholm E, ... Coon H, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. American Journal of Human Genetics. 73: 34-48. PMID 12802786 DOI: 10.1086/376549 |
0.186 |
|
| 2013 |
Burton BK, Leviton L, Vespa H, Coon H, Longo N, Lundy BD, Johnson M, Angelino A, Hamosh A, Bilder D. A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics. Molecular Genetics and Metabolism. 108: 8-12. PMID 23266195 DOI: 10.1016/j.ymgme.2012.11.003 |
0.185 |
|
| 2002 |
Kronenberg F, Coon H, Ellison RC, Borecki I, Arnett DK, Province MA, Eckfeldt JH, Hopkins PN, Hunt SC. Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees. European Journal of Human Genetics : Ejhg. 10: 367-74. PMID 12080388 DOI: 10.1038/Sj.Ejhg.5200818 |
0.181 |
|
| 2014 |
Coon H, Piasecki TM, Cook EH, Dunn D, Mermelstein RJ, Weiss RB, Cannon DS. Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. Alcoholism, Clinical and Experimental Research. 38: 930-7. PMID 24428733 DOI: 10.1111/Acer.12319 |
0.18 |
|
| 2016 |
Hu H, Coon H, Li M, Yandell M, Huff CD. VARPRISM: incorporating variant prioritization in tests of de novo mutation association. Genome Medicine. 8: 91. PMID 27562213 DOI: 10.1186/S13073-016-0341-9 |
0.17 |
|
| 2022 |
Workalemahu T, Page JM, Meeks H, Yu Z, Guinto E, Fraser A, Varner MW, Theilen LH, Quinlan A, Coon H, Enquobahrie DA, Ananth CV, Tekola-Ayele F, Jorde LB, Silver RM. Familial aggregation of stillbirth: a pedigree analysis of a matched case control study. Bjog : An International Journal of Obstetrics and Gynaecology. PMID 36161750 DOI: 10.1111/1471-0528.17301 |
0.169 |
|
| 2005 |
Coon H, Matsunami N, Stevens J, Miller J, Pingree C, Camp NJ, Thomas A, Krasny L, Lainhart J, Leppert MF, McMahon W. Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree. Human Heredity. 60: 220-6. PMID 16391490 DOI: 10.1159/000090546 |
0.169 |
|
| 2004 |
Coon H, Singh N, Dunn D, Eckfeldt JH, Province MA, Hopkins PN, Weiss R, Hunt SC, Leppert MF. TXNIP gene not associated with familial combined hyperlipidemia in the NHLBI Family Heart Study Atherosclerosis. 174: 357-362. PMID 15136067 DOI: 10.1016/J.Atherosclerosis.2004.02.004 |
0.164 |
|
| 2013 |
Miller JS, Bilder D, Farley M, Coon H, Pinborough-Zimmerman J, Jenson W, Rice CE, Fombonne E, Pingree CB, Ritvo E, Ritvo RA, McMahon WM. Autism spectrum disorder reclassified: a second look at the 1980s Utah/UCLA Autism Epidemiologic Study. Journal of Autism and Developmental Disorders. 43: 200-10. PMID 22696195 DOI: 10.1007/S10803-012-1566-0 |
0.164 |
|
| 2014 |
Buck TR, Viskochil J, Farley M, Coon H, McMahon WM, Morgan J, Bilder DA. Psychiatric comorbidity and medication use in adults with autism spectrum disorder. Journal of Autism and Developmental Disorders. 44: 3063-71. PMID 24958436 DOI: 10.1007/s10803-014-2170-2 |
0.163 |
|
| 2005 |
Coon H, Xin Y, Hopkins PN, Cawthon RM, Hasstedt SJ, Hunt SC. Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides Human Genetics. 117: 444-451. PMID 15959806 DOI: 10.1007/s00439-005-1340-x |
0.162 |
|
| 2005 |
Lin JP, Myers RH, Almasy L, Coon HH, Arnett DK, Hong Y, Hunt SC. Linkage of the cholesterol 7alpha-hydroxylase gene and low-density lipoprotein cholesterol conditional on apolipoprotein E association: the National Heart, Lung, and Blood Institute Family Heart Study. Chinese Medical Journal. 118: 362-9. PMID 15780204 |
0.161 |
|
| 2004 |
Hasstedt SJ, Camp NJ, Hopkins PN, Coon H, McKinney JT, Cawthon RM, Hunt SC. Model-fitting and linkage analysis of sodium-lithium countertransport. European Journal of Human Genetics : Ejhg. 12: 1055-61. PMID 15383825 DOI: 10.1038/Sj.Ejhg.5201262 |
0.159 |
|
| 2004 |
Pankow JS, Heiss G, Evans GW, Sholinsky P, Province MA, Coon H, Ellison RC, Miller MB, Qaqish B. Familial aggregation and genome-wide linkage analysis of carotid artery plaque: the NHLBI family heart study. Human Heredity. 57: 80-9. PMID 15192280 DOI: 10.1159/000077545 |
0.158 |
|
| 2018 |
Nobre C, Gehlenborg N, Coon H, Lex A. Lineage: Visualizing Multivariate Clinical Data in Genealogy Graphs. Ieee Transactions On Visualization and Computer Graphics. 25: 1543-1558. PMID 29993603 DOI: 10.1109/TVCG.2018.2811488 |
0.157 |
|
| 2005 |
Malhotra A, Coon H, Feitosa MF, Li WD, North KE, Price RA, Bouchard C, Hunt SC, Wolford JK, Boerwinkle E, Buse J, DeFronzo R, Ehrmann D, Elbein SC, Fujimoto W, et al. Meta-analysis of genome-wide linkage studies for quantitative lipid traits in African Americans Human Molecular Genetics. 14: 3955-3962. PMID 16301214 DOI: 10.1093/Hmg/Ddi419 |
0.154 |
|
| 2018 |
Lin CY, Chang KW, Lin CY, Wu JY, Coon H, Huang PH, Ho HN, Akbarian S, Gau SS, Huang HS. Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes. Scientific Reports. 8: 4277. PMID 29523860 DOI: 10.1038/s41598-018-22753-4 |
0.153 |
|
| 2004 |
Arnett DK, Miller MB, Coon H, Ellison RC, North KE, Province M, Leppert M, Eckfeldt JH. Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Human Genetics. 115: 468-74. PMID 15375693 DOI: 10.1007/S00439-004-1182-Y |
0.153 |
|
| 2004 |
Hunt SC, Coon H, Hasstedt SJ, Cawthon RM, Camp NJ, Wu LL, Hopkins PN. Linkage of serum creatinine and glomerular filtration rate to chromosome 2 in Utah pedigrees. American Journal of Hypertension. 17: 511-5. PMID 15177524 DOI: 10.1016/J.Amjhyper.2004.02.019 |
0.152 |
|
| 2002 |
Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC. A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Human Genetics. 111: 263-9. PMID 12215839 DOI: 10.1007/S00439-002-0773-8 |
0.151 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Coon H, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.15 |
|
| 2017 |
Figueroa KP, Coon H, Santos N, Velazquez L, Mederos LA, Pulst SM. Genetic analysis of age at onset variation in spinocerebellar ataxia type 2. Neurology. Genetics. 3: e155. PMID 28534046 DOI: 10.1212/Nxg.0000000000000155 |
0.148 |
|
| 2013 |
Scholand MB, Coon H, Wolff R, Cannon-Albright L. Use of a genealogical database demonstrates heritability of pulmonary fibrosis. Lung. 191: 475-81. PMID 23867963 DOI: 10.1007/s00408-013-9484-2 |
0.145 |
|
| 2003 |
Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC. Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees. Hypertension. 42: 322-8. PMID 12874090 DOI: 10.1161/01.Hyp.0000084874.85653.46 |
0.144 |
|
| 2002 |
Lainhart JE, Ozonoff S, Coon H, Krasny L, Dinh E, Nice J, McMahon W. Autism, regression, and the broader autism phenotype. American Journal of Medical Genetics. 113: 231-7. PMID 12439889 DOI: 10.1002/Ajmg.10615 |
0.144 |
|
| 2008 |
Rainier S, Bui M, Mark E, Thomas D, Tokarz D, Ming L, Delaney C, Richardson RJ, Albers JW, Matsunami N, Stevens J, Coon H, Leppert M, Fink JK. Neuropathy target esterase gene mutations cause motor neuron disease. American Journal of Human Genetics. 82: 780-5. PMID 18313024 DOI: 10.1016/J.Ajhg.2007.12.018 |
0.139 |
|
| 2006 |
Lainhart JE, Bigler ED, Bocian M, Coon H, Dinh E, Dawson G, Deutsch CK, Dunn M, Estes A, Tager-Flusberg H, Folstein S, Hepburn S, Hyman S, McMahon W, Minshew N, et al. Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism. American Journal of Medical Genetics. Part A. 140: 2257-74. PMID 17022081 DOI: 10.1002/Ajmg.A.31465 |
0.136 |
|
| 2014 |
Cannon DS, Mermelstein RJ, Hedeker D, Coon H, Cook EH, McMahon WM, Hamil C, Dunn D, Weiss RB. Effect of neuronal nicotinic acetylcholine receptor genes (CHRN) on longitudinal cigarettes per day in adolescents and young adults. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. 16: 137-44. PMID 23943838 DOI: 10.1093/Ntr/Ntt125 |
0.135 |
|
| 2007 |
Wu J, Province MA, Coon H, Hunt SC, Eckfeldt JH, Arnett DK, Heiss G, Lewis CE, Ellison RC, Rao DC, Rice T, Kraja AT. An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study. Bmc Genetics. 8: 60. PMID 17845730 DOI: 10.1186/1471-2156-8-60 |
0.128 |
|
| 2012 |
Hartz SM, Short SE, Saccone NL, Culverhouse R, Chen L, Schwantes-An TH, Coon H, Han Y, Stephens SH, Sun J, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, et al. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry. 69: 854-60. PMID 22868939 DOI: 10.1001/Archgenpsychiatry.2012.124 |
0.126 |
|
| 2008 |
Weiss RB, Baker TB, Cannon DS, von Niederhausern A, Dunn DM, Matsunami N, Singh NA, Baird L, Coon H, McMahon WM, Piper ME, Fiore MC, Scholand MB, Connett JE, Kanner RE, et al. A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction. Plos Genetics. 4: e1000125. PMID 18618000 DOI: 10.1371/Journal.Pgen.1000125 |
0.126 |
|
| 2010 |
Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM. Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees. Molecular Autism. 1: 8. PMID 20678250 DOI: 10.1186/2040-2392-1-8 |
0.126 |
|
| 2005 |
North KE, Miller MB, Coon H, Martin LJ, Peacock JM, Arnett D, Zhang B, Province M, Oberman A, Blangero J, Almasy L, Ellison RC, Heiss G. Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q. Atherosclerosis. 179: 119-25. PMID 15721017 DOI: 10.1016/J.Atherosclerosis.2004.09.009 |
0.125 |
|
| 2024 |
Brown DG, Murphy M, Cadeddu R, Bell R, Weis A, Chiaro T, Klag K, Morgan J, Coon H, Stephens WZ, Bortolato M, Round JL. Colitis reduces active social engagement in mice and is ameliorated by supplementation with human microbiota members. Nature Communications. 15: 2769. PMID 38553486 DOI: 10.1038/s41467-024-46733-7 |
0.123 |
|
| 2004 |
Djoussé L, Arnett DK, Coon H, Province MA, Moore LL, Ellison RC. Fruit and vegetable consumption and LDL cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study. The American Journal of Clinical Nutrition. 79: 213-7. PMID 14749225 DOI: 10.1093/Ajcn/79.2.213 |
0.12 |
|
| 2002 |
Kronenberg F, Coon H, Gutin A, Abkevich V, Samuels ME, Ballinger DG, Hopkins PN, Hunt SC. A genome scan for loci influencing anti-atherogenic serum bilirubin levels. European Journal of Human Genetics : Ejhg. 10: 539-46. PMID 12173031 DOI: 10.1038/sj.ejhg.5200842 |
0.12 |
|
| 2015 |
Hasstedt SJ, Coon H, Xin Y, Adams TD, Hunt SC. APOH interacts with FTO to predispose to healthy thinness. Human Genetics. PMID 26711810 DOI: 10.1007/s00439-015-1629-3 |
0.12 |
|
| 2007 |
Cannon DS, Tiffany ST, Coon H, Scholand MB, McMahon WM, Leppert MF. The PHQ-9 as a brief assessment of lifetime major depression. Psychological Assessment. 19: 247-51. PMID 17563207 DOI: 10.1037/1040-3590.19.2.247 |
0.118 |
|
| 2006 |
Hunt SC, Xin Y, Wu LL, Cawthon RM, Coon H, Hasstedt SJ, Hopkins PN. Sodium bicarbonate cotransporter polymorphisms are associated with baseline and 10-year follow-up blood pressures. Hypertension. 47: 532-6. PMID 16365189 DOI: 10.1161/01.HYP.0000196949.26088.3c |
0.115 |
|
| 2015 |
Jones KB, Cottle K, Bakian A, Farley M, Bilder D, Coon H, McMahon WM. A description of medical conditions in adults with autism spectrum disorder: A follow-up of the 1980s Utah/UCLA Autism Epidemiologic Study. Autism : the International Journal of Research and Practice. PMID 26162628 DOI: 10.1177/1362361315594798 |
0.114 |
|
| 2013 |
Stephens SH, Hartz SM, Hoft NR, Saccone NL, Corley RC, Hewitt JK, Hopfer CJ, Breslau N, Coon H, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Han Y, et al. Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology. 37: 846-59. PMID 24186853 DOI: 10.1002/Gepi.21760 |
0.114 |
|
| 2013 |
Bilder DA, Burton BK, Coon H, Leviton L, Ashworth J, Lundy BD, Vespa H, Bakian AV, Longo N. Psychiatric symptoms in adults with phenylketonuria. Molecular Genetics and Metabolism. 108: 155-60. PMID 23339767 DOI: 10.1016/j.ymgme.2012.12.006 |
0.113 |
|
| 2004 |
Ozonoff S, Cook I, Coon H, Dawson G, Joseph RM, Klin A, McMahon WM, Minshew N, Munson JA, Pennington BF, Rogers SJ, Spence MA, Tager-Flusberg H, Volkmar FR, Wrathall D. Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network. Journal of Autism and Developmental Disorders. 34: 139-50. PMID 15162933 DOI: 10.1023/B:Jadd.0000022605.81989.Cc |
0.112 |
|
| 2010 |
Hersh CP, Pillai SG, Zhu G, Lomas DA, Bakke P, Gulsvik A, DeMeo DL, Klanderman BJ, Lazarus R, Litonjua AA, Sparrow D, Reilly JJ, Agusti A, Calverley PM, Donner CF, ... ... Coon H, et al. Multistudy fine mapping of chromosome 2q identifies XRCC5 as a chronic obstructive pulmonary disease susceptibility gene. American Journal of Respiratory and Critical Care Medicine. 182: 605-13. PMID 20463177 DOI: 10.1164/Rccm.200910-1586Oc |
0.108 |
|
| 2008 |
Libbey JE, Coon HH, Kirkman NJ, Sweeten TL, Miller JN, Stevenson EK, Lainhart JE, McMahon WM, Fujinami RS. Are there enhanced MBP autoantibodies in autism? Journal of Autism and Developmental Disorders. 38: 324-32. PMID 17588145 DOI: 10.1007/S10803-007-0400-6 |
0.097 |
|
| 2019 |
Bilder DA, Esplin MS, Coon H, Burghardt P, Clark EAS, Fraser A, Smith KR, Worsham W, Chappelle K, Rayner T, Bakian AV. Correction to: Early Second Trimester Maternal Serum Steroid‑Related Biomarkers Associated with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 31482371 DOI: 10.1007/s10803-019-04206-7 |
0.097 |
|
| 2017 |
Farley M, Cottle KJ, Bilder D, Viskochil J, Coon H, McMahon W. Mid-life social outcomes for a population-based sample of adults with ASD. Autism Research : Official Journal of the International Society For Autism Research. 11: 142-152. PMID 29266823 DOI: 10.1002/aur.1897 |
0.086 |
|
| 2005 |
Cannon DS, Baker TB, Piper ME, Scholand MB, Lawrence DL, Drayna DT, McMahon WM, Villegas GM, Caton TC, Coon H, Leppert MF. Associations between phenylthiocarbamide gene polymorphisms and cigarette smoking Nicotine and Tobacco Research. 7: 853-858. PMID 16298720 DOI: 10.1080/14622200500330209 |
0.083 |
|
| 2002 |
Hunt SC, Hasstedt SJ, Coon H, Camp NJ, Cawthon RM, Wu LL, Hopkins PN. Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat. Kidney International. 62: 1143-8. PMID 12234284 DOI: 10.1111/J.1523-1755.2002.Kid557.X |
0.076 |
|
| 2002 |
Hobbs MR, Udhayakumar V, Levesque MC, Booth J, Roberts JM, Tkachuk AN, Pole A, Coon H, Kariuki S, Nahlen BL, Mwaikambo ED, Lal AL, Granger DL, Anstey NM, Weinberg JB. A new NOS2 promoter polymorphism associated with increased nitric oxide production and protection from severe malaria in Tanzanian and Kenyan children. Lancet. 360: 1468-75. PMID 12433515 DOI: 10.1016/S0140-6736(02)11474-7 |
0.073 |
|
| 2019 |
Das SC, Chen D, Callor WB, Christensen E, Coon H, Williams ME. DiI-mediated analysis of pre- and postsynaptic structures in human postmortem brain tissue. The Journal of Comparative Neurology. PMID 31152449 DOI: 10.1002/cne.24722 |
0.07 |
|
| 2009 |
Farley MA, McMahon WM, Fombonne E, Jenson WR, Miller J, Gardner M, Block H, Pingree CB, Ritvo ER, Ritvo RA, Coon H. Twenty-year outcome for individuals with autism and average or near-average cognitive abilities. Autism Research : Official Journal of the International Society For Autism Research. 2: 109-18. PMID 19455645 DOI: 10.1002/Aur.69 |
0.068 |
|
| 2009 |
Baker TB, Weiss RB, Bolt D, von Niederhausern A, Fiore MC, Dunn DM, Piper ME, Matsunami N, Smith SS, Coon H, McMahon WM, Scholand MB, Singh N, Hoidal JR, Kim SY, et al. Human neuronal acetylcholine receptor A5-A3-B4 haplotypes are associated with multiple nicotine dependence phenotypes. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. 11: 785-96. PMID 19436041 DOI: 10.1093/Ntr/Ntp064 |
0.066 |
|
| 2007 |
Libbey JE, Coon HH, Kirkman NJ, Sweeten TL, Miller JN, Lainhart JE, McMahon WM, Fujinami RS. Are there altered antibody responses to measles, mumps, or rubella viruses in autism? Journal of Neurovirology. 13: 252-9. PMID 17613715 DOI: 10.1080/13550280701278462 |
0.063 |
|
| 2008 |
Kirkman NJ, Libbey JE, Sweeten TL, Coon HH, Miller JN, Stevenson EK, Lainhart JE, McMahon WM, Fujinami RS. How relevant are GFAP autoantibodies in autism and Tourette Syndrome? Journal of Autism and Developmental Disorders. 38: 333-41. PMID 17578659 DOI: 10.1007/S10803-007-0398-9 |
0.056 |
|
| 2003 |
Bigler ED, Tate DF, Neeley ES, Wolfson LJ, Miller MJ, Rice SA, Cleavinger H, Anderson C, Coon H, Ozonoff S, Johnson M, Dinh E, Lu J, Mc Mahon W, Lainhart JE. Temporal lobe, autism, and macrocephaly. Ajnr. American Journal of Neuroradiology. 24: 2066-76. PMID 14625235 |
0.054 |
|
| 2014 |
Scholand MB, Wolff R, Crossno PF, Sundar K, Winegar M, Whipple S, Carey P, Sunchild N, Coon H. Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype. Cough (London, England). 10: 3. PMID 24667072 DOI: 10.1186/1745-9974-10-3 |
0.044 |
|
| 2010 |
Whitehouse AJ, Coon H, Miller J, Salisbury B, Bishop DV. Narrowing the broader autism phenotype: a study using the Communication Checklist-Adult Version (CC-A). Autism : the International Journal of Research and Practice. 14: 559-74. PMID 20923891 DOI: 10.1177/1362361310382107 |
0.04 |
|
| 2016 |
Cannon DS, Medina TR, Mermelstein RJ, Hedeker D, Bakian AV, Coon H, Cook EH, Hamil C, Weiss RB. CYP2A6 Longitudinal Effects in Young Smokers. Nicotine & Tobacco Research : Official Journal of the Society For Research On Nicotine and Tobacco. 18: 196-203. PMID 25744963 DOI: 10.1093/Ntr/Ntv049 |
0.013 |
|
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