| Year |
Citation |
Score |
| 2020 |
Ferraro NM, Strober BJ, Einson J, Abell NS, Aguet F, Barbeira AN, Brandt M, Bucan M, Castel SE, Davis JR, Greenwald E, Hess GT, Hilliard AT, Kember RL, Kotis B, et al. Transcriptomic signatures across human tissues identify functional rare genetic variation. Science (New York, N.Y.). 369. PMID 32913073 DOI: 10.1126/Science.Aaz5900 |
0.392 |
|
| 2020 |
Cacheiro P, Muñoz-Fuentes V, Murray SA, Dickinson ME, Bucan M, Nutter LMJ, Peterson KA, Haselimashhadi H, Flenniken AM, Morgan H, Westerberg H, Konopka T, Hsu CW, Christiansen A, Lanza DG, et al. Human and mouse essentiality screens as a resource for disease gene discovery. Nature Communications. 11: 655. PMID 32005800 DOI: 10.1038/S41467-020-14284-2 |
0.403 |
|
| 2019 |
Myers L, Blyth M, Moradkhani K, Hranilović D, Polesie S, Isaksson J, Nordgren A, Bucan M, Vincent M, Bölte S, Anderlid BM, Tammimies K. Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications. Molecular Genetics & Genomic Medicine. e1013. PMID 31730283 DOI: 10.1002/Mgg3.1013 |
0.362 |
|
| 2019 |
Gehrman PR, Ghorai A, Goodman M, McCluskey R, Barilla H, Almasy L, Roenneberg T, Bucan M. Twin-based Heritability of Actimetry Traits. Genes, Brain, and Behavior. e12569. PMID 30916437 DOI: 10.1111/Gbb.12569 |
0.323 |
|
| 2019 |
Kember R, Ji X, Zhang J, Brown C, Rader D, Almasy L, Bucan M. Spectrum Of Common And Rare Mutations Contributing To Autism Risk In Families European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.322 |
0.349 |
|
| 2018 |
Kember RL, Hou L, Ji X, Andersen LH, Ghorai A, Estrella LN, Almasy L, McMahon FJ, Brown C, Bućan M. Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree. Translational Psychiatry. 8: 218. PMID 30315151 DOI: 10.1038/S41398-018-0226-3 |
0.339 |
|
| 2018 |
Pizzo L, Jensen M, Polyak A, Rosenfeld JA, Mannik K, Krishnan A, McCready E, Pichon O, Le Caignec C, Van Dijck A, Pope K, Voorhoeve E, Yoon J, Stankiewicz P, Cheung SW, ... ... Bucan M, et al. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30190612 DOI: 10.1038/S41436-018-0266-3 |
0.348 |
|
| 2018 |
Glahn DC, Nimgaonkar VL, Raventós H, Contreras J, McIntosh AM, Thomson PA, Jablensky A, McCarthy NS, Charlesworth JC, Blackburn NB, Peralta JM, Knowles EEM, Mathias SR, Ament SA, McMahon FJ, ... ... Bucan M, et al. Rediscovering the value of families for psychiatric genetics research. Molecular Psychiatry. PMID 29955165 DOI: 10.1038/S41380-018-0073-X |
0.363 |
|
| 2017 |
Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bućan M, Takumi T. Functional significance of rare neuroligin 1 variants found in autism. Plos Genetics. 13: e1006940. PMID 28841651 DOI: 10.1371/Journal.Pgen.1006940 |
0.333 |
|
| 2017 |
Hou L, Kember RL, Roach JC, O'Connell JR, Craig DW, Bucan M, Scott WK, Pericak-Vance M, Haines JL, Crawford MH, Shuldiner AR, McMahon FJ. A population-specific reference panel empowers genetic studies of Anabaptist populations. Scientific Reports. 7: 6079. PMID 28729679 DOI: 10.1038/S41598-017-05445-3 |
0.325 |
|
| 2016 |
Ji X, Kember RL, Brown CD, Bućan M. Increased burden of deleterious variants in essential genes in autism spectrum disorder. Proceedings of the National Academy of Sciences of the United States of America. PMID 27956632 DOI: 10.1073/Pnas.1613195113 |
0.402 |
|
| 2016 |
Dickinson ME, Flenniken AM, Ji X, Teboul L, Wong MD, White JK, Meehan TF, Weninger WJ, Westerberg H, Adissu H, Baker CN, Bower L, Brown JM, Caddle LB, Chiani F, et al. High-throughput discovery of novel developmental phenotypes. Nature. PMID 27626380 DOI: 10.1038/Nature19356 |
0.455 |
|
| 2016 |
Bućan M. Expanding the phenotype half of the genotype-phenotype space. Proceedings of the National Academy of Sciences of the United States of America. 113: 1477-9. PMID 26825113 DOI: 10.1073/Pnas.1525363113 |
0.318 |
|
| 2013 |
Georgi B, Voight BF, Bućan M. From mouse to human: evolutionary genomics analysis of human orthologs of essential genes. Plos Genetics. 9: e1003484. PMID 23675308 DOI: 10.1371/Journal.Pgen.1003484 |
0.43 |
|
| 2010 |
Wang K, Bucan M, Grant SF, Schellenberg G, Hakonarson H. Strategies for genetic studies of complex diseases. Cell. 142: 351-3; author reply . PMID 20691891 DOI: 10.1016/J.Cell.2010.07.025 |
0.353 |
|
| 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, 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 |
0.447 |
|
| 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, ... ... Bucan M, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 459: 569-73. PMID 19404257 DOI: 10.1038/Nature07953 |
0.401 |
|
| 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, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 459: 528-33. PMID 19404256 DOI: 10.1038/Nature07999 |
0.321 |
|
| 2009 |
Yang S, Wang K, Gregory B, Berrettini W, Wang LS, Hakonarson H, Bucan M. Genomic landscape of a three-generation pedigree segregating affective disorder. Plos One. 4: e4474. PMID 19214233 DOI: 10.1371/Journal.Pone.0004474 |
0.423 |
|
| 2008 |
Wang K, Chen Z, Tadesse MG, Glessner J, Grant SF, Hakonarson H, Bucan M, Li M. Modeling genetic inheritance of copy number variations. Nucleic Acids Research. 36: e138. PMID 18832372 DOI: 10.1093/Nar/Gkn641 |
0.312 |
|
| 2008 |
Girirajan S, Patel N, Slager RE, Tokarz ME, Bucan M, Wiley JL, Elsea SH. How much is too much? Phenotypic consequences of Rai1 overexpression in mice. European Journal of Human Genetics : Ejhg. 16: 941-54. PMID 18285828 DOI: 10.1038/Ejhg.2008.21 |
0.365 |
|
| 2007 |
Yang S, Wang K, Valladares O, Hannenhalli S, Bucan M. Genome-wide expression profiling and bioinformatics analysis of diurnally regulated genes in the mouse prefrontal cortex. Genome Biology. 8: R247. PMID 18028544 DOI: 10.1186/Gb-2007-8-11-R247 |
0.303 |
|
| 2007 |
Wang K, Li M, Bucan M. Pathway-based approaches for analysis of genomewide association studies. American Journal of Human Genetics. 81: 1278-83. PMID 17966091 DOI: 10.1086/522374 |
0.306 |
|
| 2007 |
Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SFA, Hakonarson H, Bucan M. PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome Research. 17: 1665-1674. PMID 17921354 DOI: 10.1101/Gr.6861907 |
0.326 |
|
| 2007 |
Chatterjee B, Richards K, Bucan M, Lo C. Nt mutation causing laterality defects associated with deletion of rotatin. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 310-5. PMID 17551791 DOI: 10.1007/S00335-007-9023-7 |
0.506 |
|
| 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, ... ... Bucan M, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985 |
0.435 |
|
| 2006 |
Hadley D, Murphy T, Valladares O, Hannenhalli S, Ungar L, Kim J, Bućan M. Patterns of sequence conservation in presynaptic neural genes. Genome Biology. 7: R105. PMID 17096848 DOI: 10.1186/Gb-2006-7-11-R105 |
0.376 |
|
| 2005 |
Wilson L, Ching YH, Farias M, Hartford SA, Howell G, Shao H, Bucan M, Schimenti JC. Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutations. Genome Research. 15: 1095-105. PMID 16024820 DOI: 10.1101/Gr.3826505 |
0.462 |
|
| 2004 |
Austin CP, Battey JF, Bradley A, Bucan M, Capecchi M, Collins FS, Dove WF, Duyk G, Dymecki S, Eppig JT, Grieder FB, Heintz N, Hicks G, Insel TR, Joyner A, et al. The knockout mouse project. Nature Genetics. 36: 921-4. PMID 15340423 DOI: 10.1038/Ng0904-921 |
0.384 |
|
| 2002 |
Zhang Z, Sapiro R, Kapfhamer D, Bucan M, Bray J, Chennathukuzhi V, McNamara P, Curtis A, Zhang M, Blanchette-Mackie EJ, Strauss JF. A sperm-associated WD repeat protein orthologous to Chlamydomonas PF20 associates with Spag6, the mammalian orthologue of Chlamydomonas PF16. Molecular and Cellular Biology. 22: 7993-8004. PMID 12391165 DOI: 10.1128/Mcb.22.22.7993-8004.2002 |
0.745 |
|
| 2001 |
Hurle B, Lane K, Kenney J, Tarantino LM, Bucan M, Brownstein BH, Ornitz DM. Physical mapping of the mouse tilted locus identifies an association between human deafness loci DFNA6/14 and vestibular system development. Genomics. 77: 189-99. PMID 11597144 DOI: 10.1006/Geno.2001.6632 |
0.495 |
|
| 2001 |
Crabtree J, Wiltshire T, Brunk B, Zhao S, Schug J, Stoeckert CJ, Bucan M. High-resolution BAC-based map of the central portion of mouse chromosome 5 Genome Research. 11: 1746-1757. PMID 11591652 DOI: 10.1101/Gr.195101 |
0.447 |
|
| 2001 |
Alavizadeh A, Kiernan AE, Nolan P, Lo C, Steel KP, Bucan M. The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects Developmental Biology. 234: 244-260. PMID 11356033 DOI: 10.1006/Dbio.2001.0241 |
0.69 |
|
| 2000 |
Schimenti JC, Libby BJ, Bergstrom RA, Wilson LA, Naf D, Tarantino LM, Alavizadeh A, Lengeling A, Bucan M. Interdigitated deletion complexes on mouse chromosome 5 induced by irradiation of embryonic stem cells. Genome Research. 10: 1043-50. PMID 10899153 DOI: 10.1101/Gr.10.7.1043 |
0.716 |
|
| 2000 |
Tarantino LM, Gould TJ, Druhan JP, Bucan M. Behavior and mutagenesis screens: the importance of baseline analysis of inbred strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 555-64. PMID 10886023 DOI: 10.1007/S003350010107 |
0.394 |
|
| 2000 |
Tarantino LM, Feiner L, Alavizadeh A, Wiltshire T, Hurle B, Ornitz DM, Webber AL, Raper J, Lengeling A, Rowe LB, Bucan M. A high-resolution radiation hybrid map of the proximal portion of mouse chromosome 5. Genomics. 66: 55-64. PMID 10843805 DOI: 10.1006/Geno.2000.6183 |
0.702 |
|
| 2000 |
Tarantino LM, Bucan M. Dissection of behavior and psychiatric disorders using the mouse as a model. Human Molecular Genetics. 9: 953-65. PMID 10767319 DOI: 10.1093/Hmg/9.6.953 |
0.442 |
|
| 2000 |
Sapiro R, Tarantino LM, Velazquez F, Kiriakidou M, Hecht NB, Bucan M, Strauss JF. Sperm antigen 6 is the murine homologue of the Chlamydomonas reinhardtii central apparatus protein encoded by the PF16 locus. Biology of Reproduction. 62: 511-8. PMID 10684790 DOI: 10.1095/Biolreprod62.3.511 |
0.419 |
|
| 2000 |
Veasey SC, Valladares O, Fenik P, Kapfhamer D, Sanford L, Benington J, Bucan M. An Automated System for Recording and Analysis of Sleep in Mice Sleep. 23: 1-16. DOI: 10.1093/Sleep/23.8.1C |
0.688 |
|
| 1999 |
Schimenti J, Bucan M. Functional genomics in the mouse: phenotype-based mutagenesis screens. Genome Research. 8: 698-710. PMID 9685317 DOI: 10.1101/Gr.8.7.698 |
0.455 |
|
| 1999 |
Lengeling A, Wiltshire T, Otmani C, Bućan M. A Sequence-Ready BAC Contig of the GABAA Receptor Gene Cluster Gabrg1–Gabra2–Gabrb1 on Mouse Chromosome 5 Genome Research. 9: 732-738. DOI: 10.1101/Gr.9.8.732 |
0.445 |
|
| 1998 |
Hough RB, Lengeling A, Bedian V, Lo C, Bućan M. Rump white inversion in the mouse disrupts dipeptidyl aminopeptidase-like protein 6 and causes dysregulation of Kit expression. Proceedings of the National Academy of Sciences of the United States of America. 95: 13800-5. PMID 9811881 DOI: 10.1073/Pnas.95.23.13800 |
0.471 |
|
| 1997 |
Zimmerman JE, Bui QT, SteingrÃmsson E, Nagle DL, Fu W, Genin A, Spinner NB, Copeland NG, Jenkins NA, Bucan M, Bonini NM. Cloning and characterization of two vertebrate homologs of the Drosophila eyes absent gene. Genome Research. 7: 128-41. PMID 9049631 DOI: 10.1101/Gr.7.2.128 |
0.462 |
|
| 1996 |
Bucan M, Gatalica B, Baba T, Gerton GL. Mapping of Grn, the gene encoding the granulin/epithelin precursor (acrogranin), to mouse Chromosome 11 Mammalian Genome. 7: 704-705. PMID 8703129 DOI: 10.1007/S003359900212 |
0.505 |
|
| 1995 |
Pickard GE, Sollars PJ, Rinchik EM, Nolan PM, Bucan M. Mutagenesis and behavioral screening for altered circadian activity identifies the mouse mutant, Wheels. Brain Research. 705: 255-66. PMID 8821757 DOI: 10.1016/0006-8993(95)01171-4 |
0.389 |
|
| 1995 |
Brunkow ME, Nagle DL, Bernstein A, Bucan M. A 1.8-Mb YAC contig spanning three members of the receptor tyrosine kinase gene family (Pdgfra, Kit, and Flk1) on mouse chromosome 5 Genomics. 25: 421-432. PMID 7540588 DOI: 10.1016/0888-7543(95)80042-K |
0.495 |
|
| 1994 |
Robin NH, Adewale OO, McDonald-McGinn D, Nadeau JH, Zackai EH, Bućan M. Human malformations similar to those in the mouse mutation disorganization (Ds). Human Genetics. 92: 461-4. PMID 8244336 DOI: 10.1007/Bf00216451 |
0.4 |
|
| 1994 |
Pauken CM, Nagle DL, Bucan M, Lo CW. Molecular cloning, expression analysis, and chromosomal localization of mouse Hmg1-containing sequences Mammalian Genome. 5: 91-99. PMID 8180479 DOI: 10.1007/Bf00292334 |
0.46 |
|
| 1994 |
Nagle DL, Martin-DeLeon P, Hough RB, Bućan M. Structural analysis of chromosomal rearrangements associated with the developmental mutations Ph, W19H, and Rw on mouse chromosome 5. Proceedings of the National Academy of Sciences of the United States of America. 91: 7237-41. PMID 8041773 DOI: 10.1073/Pnas.91.15.7237 |
0.504 |
|
| 1994 |
Gåfvels ME, Paavola LG, Boyd CO, Nolan PM, Wittmaack F, Chawla A, Lazar MA, Bucan M, Angelin BO, Strauss JF. Cloning of a complementary deoxyribonucleic acid encoding the murine homolog of the very low density lipoprotein/apolipoprotein-E receptor: expression pattern and assignment of the gene to mouse chromosome 19. Endocrinology. 135: 387-94. PMID 8013374 DOI: 10.1210/Endo.135.1.8013374 |
0.382 |
|
| 1994 |
Nasir J, Lin B, Bucan M, Koizumi T, Nadeau JH, Hayden MR. The murine homologues of the Huntington disease gene (Hdh) and the alpha-adducin gene (Add1) map to mouse chromosome 5 within a region of conserved synteny with human chromosome 4p16.3. Genomics. 22: 198-201. PMID 7959767 DOI: 10.1006/Geno.1994.1361 |
0.519 |
|
| 1994 |
Lee J, Greenbaum L, Haber BA, Nagle D, Lee V, Miles V, Mohn KL, Bucan M, Taub R. Structure and localization of the IGFBP-1 gene and its expression during liver regeneration. Hepatology (Baltimore, Md.). 19: 656-65. PMID 7509771 DOI: 10.1002/Hep.1840190317 |
0.358 |
|
| 1993 |
Malek TR, Vincek V, Gatalica B, Bucan M. The IL-2 receptor beta chain gene (Il-2rb) is closely linked to the Pdgfb locus on mouse chromosome 15. Immunogenetics. 38: 154-6. PMID 8482578 DOI: 10.1007/Bf00190904 |
0.309 |
|
| 1993 |
Bućan M, Gatalica B, Nolan P, Chung A, Leroux A, Grossman MH, Nadeau JH, Emanuel BS, Budarf M. Comparative mapping of 9 human chromosome 22q loci in the laboratory mouse Human Molecular Genetics. 2: 1245-1252. PMID 8401507 DOI: 10.1093/Hmg/2.8.1245 |
0.487 |
|
| 1989 |
Youngman S, Sarfarazi M, Bucan M, MacDonald M, Smith B, Zimmer M, Gilliam C, Frischauf AM, Wasmuth JJ, Gusella JF, Lehrach H, Harper PS, Shaw DJ. A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene Genomics. 5: 802-809. PMID 2574148 DOI: 10.1016/0888-7543(89)90122-5 |
0.481 |
|
| 1987 |
Avner P, Bućan M, Arnaud D, Lehrach H, Rapp U. A-raf oncogene localizes on mouse X chromosome to region some 10-17 centimorgans proximal to hypoxanthine phosphoribosyltransferase gene. Somatic Cell and Molecular Genetics. 13: 267-272. PMID 3299748 DOI: 10.1007/Bf01535208 |
0.428 |
|
| Show low-probability matches. |