Rare Variants Create Synthetic Genome-Wide Associations

Common Genetic Variation and Human Traits

(2009) David B. Goldstein   NEW ENGLAND JOURNAL OF MEDICINE

Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

(2009) S. Nejentsev et al.   SCIENCE

Lack of association between the CALM1 core promoter polymorphism (-16C/T) and susceptibility to knee osteoarthritis in a Chinese Han population

(2008) Dongquan Shi et al.   BMC Medical Genetics

Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTOvariants confer a significant risk

(2008) Dharambir K Sanghera et al.   BMC Medical Genetics

Worldwide population differentiation at disease-associated SNPs

(2008) Sean Myles et al.   BMC Medical Genomics

Hormone-dependent effects of FGFR2 and MAP3K1 in breast cancer susceptibility in a population-based sample of post-menopausal African-American and European-American women

(2008) T. R. Rebbeck et al.   CARCINOGENESIS

Association Analysis in African Americans of European-Derived Type 2 Diabetes Single Nucleotide Polymorphisms From Whole-Genome Association Studies

(2008) J. P. Lewis et al.   DIABETES

Evaluation of coverage variation of SNP chips for genome-wide association studies

(2008) Mingyao Li et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

CD226 Gly307Ser association with multiple autoimmune diseases

(2008) J P Hafler et al.   GENES AND IMMUNITY

Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci

(2008) Shu-Feng Lei et al.   HUMAN GENETICS

Genome-wide association studies: potential next steps on a genetic journey

(2008) M. I. McCarthy et al.   HUMAN MOLECULAR GENETICS

Replication of Genome-Wide Association Studies of Type 2 Diabetes Susceptibility in Japan

(2008) Yukio Horikawa et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population

(2008) Yong-Ho Lee et al.   JOURNAL OF HUMAN GENETICS

Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?

(2008) Nele Hilgert et al.   MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH

Personal genomes: The case of the missing heritability

(2008) Brendan Maher   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

(2008) W H Linda Kao et al.   NATURE GENETICS

Genetic analysis of reelin gene (RELN) SNPs: No association with autism spectrum disorder in the Indian population

(2008) Shruti Dutta et al.   NEUROSCIENCE LETTERS

Pulmonary Complications of Sickle Cell Disease

(2008) Mark T. Gladwin et al.   NEW ENGLAND JOURNAL OF MEDICINE