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
22361998
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
14582007
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
7921988
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
7362016
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics 45 (4), 433, 2013
6852013
Programs for pedigree analysis: MENDEL, FISHER, and dGENE
K Lange, D Weeks, M Boehnke, J MacCluer
Wiley Subscription Services, Inc., A Wiley Company, 1988
6821988
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
6272005
The affected-pedigree-member method of linkage analysis.
DE Weeks, K Lange
American journal of human genetics 42 (2), 315, 1988
6241988
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
5731995
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
5092010
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
4591994
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
4431998
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
3901999
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
3352001
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
3242001
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 genet 5 (2), e1000337, 2009
2962009
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
2902005
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
2851996
Polygenic disease: methods for mapping complex disease traits
DE Weeks, GM Lathrop
Trends in Genetics 11 (12), 513-519, 1995
2771995
Similarity of DNA fingerprints due to chance and relatedness
CC Li, DE Weeks, A Chakravarti
Human heredity 43 (1), 45-52, 1993
2661993
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