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Exploring the unknown: assumptions about allelic architecture and strategies for susceptibility variant discovery
Mark I McCarthy
Genome Med. 2009; 1(7): 66. Published online 2009 July 3. doi: 10.1186/gm66
PMCID:
PMC2717392
Abstract Full Text PDF–61K
 Is Cited by the Following 7 Articles in this Archive:
A Systems Genetics Approach Provides a Bridge from Discovered Genetic Variants to Biological Pathways in Rheumatoid Arthritis
Hirofumi Nakaoka, Tailin Cui, Atsushi Tajima, Akira Oka, Shigeki Mitsunaga, Koichi Kashiwase, Yasuhiko Homma, Shinji Sato, Yasuo Suzuki, Hidetoshi Inoko, Ituro Inoue
PLoS One. 2011; 6(9): e25389. Published online 2011 September 28. doi: 10.1371/journal.pone.0025389
PMCID:
PMC3182219
Abstract Full Text PDF–948K Supplementary Material
Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe
Emmanuelle Génin, Martin Schumacher, Jean-Claude Roujeau, Luigi Naldi, Yvonne Liss, Rémi Kazma, Peggy Sekula, Alain Hovnanian, Maja Mockenhaupt
Orphanet J Rare Dis. 2011; 6: 52. Published online 2011 July 29. doi: 10.1186/1750-1172-6-52
PMCID:
PMC3173287
Abstract Full Text PDF–455K Supplementary Material
Progress and Promise of Genome-Wide Association Studies for Human Complex Trait Genetics
Barbara E. Stranger, Eli A. Stahl, Towfique Raj
Genetics. 2011 February; 187(2): 367–383. doi: 10.1534/genetics.110.120907
PMCID:
PMC3030483
Abstract Full Text PDF–1.0M
Three Ways of Combining Genotyping and Resequencing in Case-Control Association Studies
Jeffrey A. Longmate, Garrett P. Larson, Theodore G. Krontiris, Steve S. Sommer
PLoS One. 2010; 5(12): e14318. Published online 2010 December 20. doi: 10.1371/journal.pone.0014318
PMCID:
PMC3004857
Abstract Full Text PDF–133K
Identification of Novel Loci for Alzheimer Disease and Replication of CLU, PICALM, and BIN1 in Caribbean Hispanic Individuals
Joseph H. Lee, Rong Cheng, Sandra Barral, Christiane Reitz, Martin Medrano, Rafael Lantigua, Ivonne Z. Jiménez-Velazquez, Ekaterina Rogaeva, Peter H. St. George-Hyslop, Richard Mayeux
Arch Neurol. Author manuscript; available in PMC 2012 January 30.
Published in final edited form as: Arch Neurol. 2011 March; 68(3): 320–328. Published online 2010 November 8. doi: 10.1001/archneurol.2010.292
PMCID:
PMC3268783
Abstract Full Text PDF–1.2M
A Data-Adaptive Sum Test for Disease Association with Multiple Common or Rare Variants
Fang Han, Wei Pan
Hum Hered. 2010 June; 70(1): 42–54. Published online 2010 April 23. doi: 10.1159/000288704
PMCID:
PMC2912645
Abstract Full Text PDF–264K
Refined QTLs of osteoporosis-related traits by linkage analysis with genome-wide SNPs: Framingham SHARe
David Karasik, Josée Dupuis, Kelly Cho, L. Adrienne Cupples, Yanhua Zhou, Douglas P. Kiel, Serkalem Demissie
Bone. Author manuscript; available in PMC 2011 April 1.
Published in final edited form as: Bone. 2010 April; 46(4): 1114–1121. Published online 2010 January 11. doi: 10.1016/j.bone.2010.01.001
PMCID:
PMC2842472
Abstract Full Text PDF–707K
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