1.
Simulation of Finnish Population History, Guided by Empirical Genetic Data, to Assess Power of Rare-Variant Tests in Finland
by Wang, Sophie R
American journal of human genetics, 2014, Vol.94 (5), p.710-720
2.
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects
by Lill, Christina M
Journal of medical genetics, 2012, Vol.49 (9), p.558-562
3.
RFMix: A Discriminative Modeling Approach for Rapid and Robust Local-Ancestry Inference
by Maples, Brian K
American journal of human genetics, 2013, Vol.93 (2), p.278-288
4.
The Arabian Cradle: Mitochondrial Relicts of the First Steps along the Southern Route out of Africa
by Fernandes, Verónica
American journal of human genetics, 2012, Vol.90 (2), p.347-355
5.
Fast Principal-Component Analysis Reveals Convergent Evolution of ADH1B in Europe and East Asia
by Galinsky, Kevin J
American journal of human genetics, 2016, Vol.98 (3), p.456-472
6.
The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States
by Bryc, Katarzyna
American journal of human genetics, 2015, Vol.96 (1), p.37-53
7.
Genome-wide Association Study Identifies TNFSF15 and POU2AF1 as Susceptibility Loci for Primary Biliary Cirrhosis in the Japanese Population
by NAKAMURA, Minoru
American journal of human genetics, 2012, Vol.91 (4), p.721-728
8.
Prevalence of BRCA Mutations Among Women with Triple-Negative Breast Cancer (TNBC) in a Genetic Counseling Cohort
by Greenup, Rachel
Annals of surgical oncology, 2013, Vol.20 (10), p.3254-3258
9.
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as Susceptibility Loci for Systemic Lupus Erythematosus in a Large-Scale Multiracial Replication Study
by Lessard, Christopher J
American journal of human genetics, 2012, Vol.90 (4), p.648-660
10.
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
by Halbritter, Jan
American journal of human genetics, 2013, Vol.93 (5), p.915-925
11.
Complex History of Admixture between Modern Humans and Neandertals
by Vernot, Benjamin
American journal of human genetics, 2015, Vol.96 (3), p.448-453
12.
Variants conferring risk of atrial fibrillation on chromosome 4q25
by Helgason, Agnar
Nature, 2007, Vol.448 (7151), p.353-357
13.
The Genetic Diversity of the Americas
by Adhikari, Kaustubh
Annual review of genomics and human genetics, 2017, Vol.18 (1), p.277-296
14.
Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci
by Leslie, Elizabeth J
American journal of human genetics, 2015, Vol.96 (3), p.397-411
15.
Haemochromatosis
by Powell, Lawrie W, Prof
The Lancet (British edition), 2016, Vol.388 (10045), p.706-716
16.
Genetic Evidence for Recent Population Mixture in India
by Moorjani, Priya
American journal of human genetics, 2013, Vol.93 (3), p.422-438
17.
Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid Arthritis
by Okada, Yukinori
American journal of human genetics, 2016, Vol.99 (2), p.366-374
18.
Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome Sequences
by Haber, Marc
American journal of human genetics, 2017, Vol.101 (2), p.274-282
19.
Variants in DENND1A Are Associated with Polycystic Ovary Syndrome in Women of European Ancestry
by Welt, Corrine K
The journal of clinical endocrinology and metabolism, 2012, Vol.97 (7), p.E1342-E1347
20.
Alternative Splicing QTLs in European and African Populations
by Ongen, Halit
American journal of human genetics, 2015, Vol.97 (4), p.567-575
