PedCheck: a program for identification of genotype incompatibilities in linkage analysis JR O'Connell, DE Weeks The American Journal of Human Genetics 63 (1), 259-266, 1998 | 2299 | 1998 |
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1654 | 2007 |
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ... Nature genetics 48 (2), 134-143, 2016 | 1456 | 2016 |
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1411 | 2021 |
Localization of an ataxia-telangiectasia gene to chromosome 11q22–23 RA Gatti, I Berkel, E Boder, G Braedt, P Charmley, P Concannon, F Ersoy, ... Nature 336 (6199), 577-580, 1988 | 885 | 1988 |
Seven new loci associated with age-related macular degeneration Nature genetics 45 (4), 433-439, 2013 | 862 | 2013 |
Programs for pedigree analysis: MENDEL, FISHER, and dGENE K Lange, D Weeks, M Boehnke, J MacCluer Wiley Subscription Services, Inc., A Wiley Company, 1988 | 775 | 1988 |
Susceptibility genes for age-related maculopathy on chromosome 10q26 J Jakobsdottir, YP Conley, DE Weeks, TS Mah, RE Ferrell, MB Gorin The American Journal of Human Genetics 77 (3), 389-407, 2005 | 695 | 2005 |
The affected-pedigree-member method of linkage analysis. DE Weeks, K Lange American journal of human genetics 42 (2), 315, 1988 | 664 | 1988 |
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritance JR O'Connell, DE Weeks Nature genetics 11 (4), 402-408, 1995 | 615 | 1995 |
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration W Chen, D Stambolian, AO Edwards, KE Branham, M Othman, ... Proceedings of the National Academy of Sciences 107 (16), 7401-7406, 2010 | 609 | 2010 |
A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium Human Molecular Genetics 7 (3), 571-578, 1998 | 503 | 1998 |
Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility gene. WH Berrettini, TN Ferraro, LR Goldin, DE Weeks, S Detera-Wadleigh, ... Proceedings of the National Academy of Sciences 91 (13), 5918-5921, 1994 | 477 | 1994 |
Inherited causes of clonal haematopoiesis in 97,691 whole genomes AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ... Nature 586 (7831), 763-768, 2020 | 465 | 2020 |
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia SE Fisher, AJ Marlow, J Lamb, E Maestrini, DF Williams, AJ Richardson, ... The American journal of human genetics 64 (1), 146-156, 1999 | 415 | 1999 |
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p International Molecular Genetic Study of Autism Consortium The American Journal of Human Genetics 69 (3), 570-581, 2001 | 411 | 2001 |
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci SH Laval, A Timms, S Edwards, L Bradbury, S Brophy, A Milicic, L Rubin, ... The American Journal of Human Genetics 68 (4), 918-926, 2001 | 359 | 2001 |
Similarity of DNA fingerprints due to chance and relatedness CC Li, DE Weeks, A Chakravarti Human heredity 43 (1), 45-52, 1993 | 339 | 1993 |
Meta-analysis of genome scans of age-related macular degeneration SA Fisher, GR Abecasis, BM Yashar, S Zareparsi, A Swaroop, SK Iyengar, ... Human molecular genetics 14 (15), 2257-2264, 2005 | 328 | 2005 |
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers J Jakobsdottir, MB Gorin, YP Conley, RE Ferrell, DE Weeks PLoS genetics 5 (2), e1000337, 2009 | 324 | 2009 |