1.
Five Years of GWAS Discovery
by VISSCHER, Peter M
American journal of human genetics, 2012, Vol.90 (1), p.7-24
2.
Estimating Missing Heritability for Disease from Genome-wide Association Studies
by Lee, Sang Hong
American journal of human genetics, 2011, Vol.88 (3), p.294-305
3.
GCTA: A Tool for Genome-wide Complex Trait Analysis
by Yang, Jian
American journal of human genetics, 2011, Vol.88 (1), p.76-82
4.
10 Years of GWAS Discovery: Biology, Function, and Translation
by Visscher, Peter M
American journal of human genetics, 2017, Vol.101 (1), p.5-22
5.
Large Sample Size, Wide Variant Spectrum, and Advanced Machine-Learning Technique Boost Risk Prediction for Inflammatory Bowel Disease
by Wei, Zhi
American journal of human genetics, 2013, Vol.92 (6), p.1008-1012
6.
A Versatile Gene-Based Test for Genome-wide Association Studies
by Liu, Jimmy Z
American journal of human genetics, 2010, Vol.87 (1), p.139-145
7.
Mixed model with correction for case-control ascertainment increases association power
by Hayeck, Tristan J
American journal of human genetics, 2015, Vol.96 (5), p.720-730
8.
Estimation of SNP Heritability from Dense Genotype Data
by Lee, S. Hong
American journal of human genetics, 2013, Vol.93 (6), p.1151-1155
9.
The Genetic Architecture of Gene Expression in Peripheral Blood
by Lloyd-Jones, Luke R
American journal of human genetics, 2017, Vol.100 (2), p.228-237
10.
Estimation and Partition of Heritability in Human Populations Using Whole-Genome Analysis Methods
by Vinkhuyzen, Anna A.E
Annual review of genetics, 2013, Vol.47 (1), p.75-95
11.
The Genetic Architecture of Gene Expression in Peripheral Blood
by Lloyd-Jones, Luke R
American journal of human genetics, 2017, Vol.100 (2), p.228-237
12.
Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent
by de Candia, Teresa R
American journal of human genetics, 2013, Vol.93 (3), p.463-470
13.
Variants in TF and HFE Explain ∼40% of Genetic Variation in Serum-Transferrin Levels
by Benyamin, Beben
American journal of human genetics, 2009, Vol.84 (1), p.60-65
14.
Concepts and Misconceptions about the Polygenic Additive Model Applied to Disease
by Visscher, Peter M
Human heredity, 2015, Vol.80 (4), p.165-170
15.
The Genetic Architecture of Gene Expression in Peripheral Blood
by Lloyd-Jones, Luke R
American journal of human genetics, 2017, Vol.100 (2), p.371-371
16.
Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time
by Houlihan, Lorna M
American journal of human genetics, 2010, Vol.86 (4), p.626-631
17.
Whole-Genome Genetic Diversity in a Sample of Australians with Deep Aboriginal Ancestry
by McEvoy, Brian P
American journal of human genetics, 2010, Vol.87 (2), p.297-305
18.
Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese
by Davidson, Stuart I
Annals of the Rheumatic Diseases, 2011, Vol.70 (2), p.289-292
19.
Response to Browning and Browning
by Goddard, Michael E.
American journal of human genetics, 2011, Vol.89 (1), p.193-195
20.
Genome Partitioning of Genetic Variation for Height from 11,214 Sibling Pairs
by Visscher, Peter M
American journal of human genetics, 2007, Vol.81 (5), p.1104-1110
