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.
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
3.
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
4.
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
5.
Clinical assessment incorporating a personal genome
by Ashley, Euan A, Dr
The Lancet (British edition), 2010, Vol.375 (9725), p.1525-1535
6.
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
7.
Five Years of GWAS Discovery
by VISSCHER, Peter M
American journal of human genetics, 2012, Vol.90 (1), p.7-24
8.
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
9.
Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome
by Lederer, Damien
American journal of human genetics, 2012-01-13, Vol.90 (1), p.119-124
10.
Common genetic variants on 5p14.1 associate with autism spectrum disorders
by Hakonarson, Hakon
Nature, 2009-05-28, Vol.459 (7246), p.528-533
11.
DNA methylation and body-mass index: a genome-wide analysis
by Dick, Katherine J, PhD
The Lancet (British edition), 2014, Vol.383 (9933), p.1990-1998
12.
Genetic associations in diabetic nephropathy: a meta-analysis
by Mooyaart, A. L
Diabetologia, 2010-12-03, Vol.54 (3), p.544-553
13.
A “Copernican” Reassessment of the Human Mitochondrial DNA Tree from its Root
by Behar, Doron M
American journal of human genetics, 2012-04-06, Vol.90 (4), p.675-684
14.
Allelic Skewing of DNA Methylation Is Widespread across the Genome
by Schalkwyk, Leonard C
American journal of human genetics, 2010-02-12, Vol.86 (2), p.196-212
15.
Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly
by Lines, Matthew A
American journal of human genetics, 2012-02-10, Vol.90 (2), p.369-377
16.
DNA Methylation Signatures in Development and Aging of the Human Prefrontal Cortex
by Numata, Shusuke
American journal of human genetics, 2012-02-10, Vol.90 (2), p.260-272
17.
Mutations in EZH2 Cause Weaver Syndrome
by Gibson, William T
American journal of human genetics, 2012-01-13, Vol.90 (1), p.110-118
18.
Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
by Itsara, Andy
American journal of human genetics, 2009-02-13, Vol.84 (2), p.148-161
19.
Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering
by Browning, Sharon R
American journal of human genetics, 2007, Vol.81 (5), p.1084-1097
20.
Most Rare Missense Alleles Are Deleterious in Humans: Implications for Complex Disease and Association Studies
by Kryukov, Gregory V
American journal of human genetics, 2007, Vol.80 (4), p.727-739
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