1.
Inferring Genetic Ancestry: Opportunities, Challenges, and Implications
by Royal, Charmaine D
American journal of human genetics, 2010-05-14, Vol.86 (5), p.661-673
2.
Genomic sovereignty and the African promise: mining the African genome for the benefit of Africa
by de Vries, Jantina
Journal of Medical Ethics, 2012-08, Vol.38 (8), p.474-478
3.
The return of individual research findings in paediatric genetic research
by Hens, Kristien
Journal of medical ethics, 2011-03, Vol.37 (3), p.179-183
4.
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
by Smoller, J.W
The Lancet (British edition), 2013, Vol.381 (9875), p.1371-1379
5.
Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity
by Lopez-Herrera, Gabriela
American journal of human genetics, 2012-06-08, Vol.90 (6), p.986-1001
6.
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
by Trynka, Gosia
American journal of human genetics, 2014-11-06, Vol.95 (5), p.535-552
7.
The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States
by Bryc, Katarzyna
American journal of human genetics, 2015-01-08, Vol.96 (1), p.37-53
8.
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
by Ripke, Stephan
American journal of human genetics, 2015-10-01, Vol.97 (4), p.576-592
9.
BOOST: A Fast Approach to Detecting Gene-Gene Interactions in Genome-wide Case-Control Studies
by Wan, Xiang
American journal of human genetics, 2010-09-10, Vol.87 (3), p.325-340
10.
Clinical assessment incorporating a personal genome
by Ashley, Euan A, Dr
The Lancet (British edition), 2010, Vol.375 (9725), p.1525-1535
11.
Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks
by Peloso, Gina M
American journal of human genetics, 2014-02-06, Vol.94 (2), p.223-232
12.
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study
by Cleynen, Isabelle, PhD
The Lancet (British edition), 2016, Vol.387 (10014), p.156-167
13.
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
by Purcell, Shaun
American journal of human genetics, 2007, Vol.81 (3), p.559-575
14.
Five Years of GWAS Discovery
by VISSCHER, Peter M
American journal of human genetics, 2012, Vol.90 (1), p.7-24
15.
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
by Miraoui, Hichem
American journal of human genetics, 2013-05-02, Vol.92 (5), p.725-743
16.
Combined Analysis of Genome-wide Association Studies for Crohn Disease and Psoriasis Identifies Seven Shared Susceptibility Loci
by Ellinghaus, David
American journal of human genetics, 2012-04-06, Vol.90 (4), p.636-647
17.
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia
by Bogliolo, Massimo
American journal of human genetics, 2013-05-02, Vol.92 (5), p.800-806
18.
A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
by Rutsch, Frank
American journal of human genetics, 2015-02-05, Vol.96 (2), p.275-282
19.
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
by Chong, Jessica X
American journal of human genetics, 2015-08-06, Vol.97 (2), p.199-215
20.
Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia
by Galinsky, Kevin J
American journal of human genetics, 2016-03-03, Vol.98 (3), p.456-472
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