| Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22 LA Cannon-Albright, DE Goldgar, LJ Meyer, CM Lewis, DE Anderson, ... Science 258 (5085), 1148-1152, 1992 | 704 | 1992 |
| PRAD1, a candidate BCL1 oncogene: mapping and expression in centrocytic lymphoma. CL Rosenberg, E Wong, EM Petty, AE Bale, Y Tsujimoto, NL Harris, ... Proceedings of the National Academy of Sciences 88 (21), 9638-9642, 1991 | 578 | 1991 |
| White Americans' genetic lay theories of race differences and sexual orientation: Their relationship with prejudice toward Blacks, and gay men and lesbians TE Jayaratne, O Ybarra, JP Sheldon, TN Brown, M Feldbaum, CA Pfeffer, ... Group Processes & Intergroup Relations 9 (1), 77-94, 2006 | 443 | 2006 |
| Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene A Colige, AL Sieron, SW Li, U Schwarze, E Petty, W Wertelecki, W Wilcox, ... The American Journal of Human Genetics 65 (2), 308-317, 1999 | 443 | 1999 |
| Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia CF Boerkoel, H Takashima, J John, J Yan, P Stankiewicz, L Rosenbarker, ... Nature genetics 30 (2), 215-220, 2002 | 386 | 2002 |
| Exploring the public understanding of basic genetic concepts AD Lanie, TE Jayaratne, JP Sheldon, SLR Kardia, ES Anderson, ... Journal of genetic counseling 13 (4), 305-320, 2004 | 363 | 2004 |
| MicroRNAs in development and disease AE Erson, EM Petty Clinical genetics 74 (4), 296-306, 2008 | 333 | 2008 |
| Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1) C Meredith, R Herrmann, C Parry, K Liyanage, DE Dye, HJ Durling, ... The American Journal of Human Genetics 75 (4), 703-708, 2004 | 241 | 2004 |
| Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV U Schwarze, WI Schievink, E Petty, MR Jaff, D Babovic-Vuksanovic, ... The American Journal of Human Genetics 69 (5), 989-1001, 2001 | 207 | 2001 |
| Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections DM Milewicz, H Chen, ES Park, EM Petty, H Zaghi, GS Pai, M Willing, ... The American journal of cardiology 82 (4), 474-479, 1998 | 199 | 1998 |
| Mutant deoxynucleotide carrier is associated with congenital microcephaly MJ Rosenberg, R Agarwala, G Bouffard, J Davis, G Fiermonte, MS Hilliard, ... Nature genetics 32 (1), 175-179, 2002 | 180 | 2002 |
| Mammalian septins nomenclature IG Macara, R Baldarelli, CM Field, M Glotzer, Y Hayashi, SC Hsu, ... Molecular biology of the cell 13 (12), 4111-4113, 2002 | 162 | 2002 |
| Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors SEH Russell, MA McIlhatton, JF Burrows, PG Donaghy, S Chanduloy, ... Cancer research 60 (17), 4729-4734, 2000 | 144 | 2000 |
| Conquering the complex world of human septins: implications for health and disease EA Peterson, EM Petty Clinical genetics 77 (6), 511-524, 2010 | 140 | 2010 |
| Beliefs about the etiology of homosexuality and about the ramifications of discovering its possible genetic origin JP Sheldon, CA Pfeffer, TE Jayaratne, M Feldbaum, EM Petty Journal of homosexuality 52 (3-4), 111-150, 2007 | 131 | 2007 |
| Genomic and Expression Analyses of Alternatively Spliced Transcripts of the MLL Septin-like Fusion Gene (MSF) That Map to a 17q25 Region of Loss in Breast … LM Kalikin, HL Sims, EM Petty Genomics 63 (2), 165-172, 2000 | 129 | 2000 |
| Understandings of basic genetics in the United States: results from a national survey of black and white men and women KD Christensen, TE Jayaratne, JS Roberts, SLR Kardia, EM Petty Public health genomics 13 (7-8), 467-476, 2010 | 128 | 2010 |
| Expression and mutational analyses of the human MAD2L1 gene in breast cancer cells MJ Percy, KA Myrie, CK Neeley, JN Azim, SP Ethier, EM Petty Genes, Chromosomes and Cancer 29 (4), 356-362, 2000 | 126 | 2000 |
| Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen. LT Smith, W Wertelecki, LM Milstone, EM Petty, MR Seashore, ... American journal of human genetics 51 (2), 235, 1992 | 124 | 1992 |
| The perennial debate: Nature, nurture, or choice? Black and White Americans’ explanations for individual differences TE Jayaratne, SA Gelman, M Feldbaum, JP Sheldon, EM Petty, ... Review of General Psychology 13 (1), 24-33, 2009 | 123 | 2009 |
Toby Epstein JayaratneHealth Behavior and Health Education, School of Public Health, University of MichiganVerified email at umich.edu
