Daniel E. Weeks
Daniel E. Weeks
Professor of Human Genetics and Biostatistics, University of Pittsburgh
Verified email at pitt.edu - Homepage
Cited by
Cited by
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
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
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
Programs for pedigree analysis: MENDEL, FISHER, and dGENE
K Lange, D Weeks, M Boehnke, JW MacCluer, JW MacCluer
Genetic epidemiology 5 (6), 471-472, 1988
The affected-pedigree-member method of linkage analysis.
DE Weeks, K Lange
American journal of human genetics 42 (2), 315, 1988
Seven new loci associated with age-related macular degeneration
LG Fritsche, W Chen, M Schu, BL Yaspan, Y Yu, G Thorleifsson, DJ Zack, ...
Nature genetics 45 (4), 433, 2013
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
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
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
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
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
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
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
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
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
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
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), 2009
A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
E Maestrini, AP Monaco, JA McGrath, A Ishida-Yamamoto, C Camisa, ...
Nature genetics 13 (1), 70-77, 1996
Polygenic disease: methods for mapping complex disease traits
DE Weeks, GM Lathrop
Trends in Genetics 11 (12), 513-519, 1995
Similarity of DNA fingerprints due to chance and relatedness
CC Li, DE Weeks, A Chakravarti
Human heredity 43 (1), 45-52, 1993
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