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Daniel E. Weeks
Daniel E. Weeks
Professor of Human Genetics and Biostatistics, University of Pittsburgh
Verified email at pitt.edu - Homepage
Title
Cited by
Cited by
Year
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
22931998
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
16512007
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
14152016
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
13422021
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
8851988
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
8572013
Programs for pedigree analysis: MENDEL, FISHER, and dGENE
K Lange, D Weeks, M Boehnke, J MacCluer
Wiley Subscription Services, Inc., A Wiley Company, 1988
7761988
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
6932005
The affected-pedigree-member method of linkage analysis.
DE Weeks, K Lange
American journal of human genetics 42 (2), 315, 1988
6671988
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
6181995
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
6052010
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
5021998
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
4761994
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
4442020
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
4201999
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
4092001
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
3592001
Similarity of DNA fingerprints due to chance and relatedness
CC Li, DE Weeks, A Chakravarti
Human heredity 43 (1), 45-52, 1993
3391993
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
3332005
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
3222009
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