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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
2.
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
3.
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
4.
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
5.
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
6.
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
7.
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
8.
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
9.
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
10.
A comprehensive transcriptional portrait of human cancer cell lines
by Klijn, Christiaan
Nature biotechnology, 2015-03, Vol.33 (3), p.306-312
11.
Identification and development of a functional marker of TaGW2 associated with grain weight in bread wheat (Triticum aestivum L.)
by Su, Zhenqi
Theoretical and applied genetics, 2010-09-14, Vol.122 (1), p.211-223
12.
The diploid genome sequence of an Asian individual
by Wang, Jun
Nature, 2008-11-06, Vol.456 (7218), p.60-65
13.
Common genetic variants on 5p14.1 associate with autism spectrum disorders
by Hakonarson, Hakon
Nature, 2009-05-28, Vol.459 (7246), p.528-533
14.
Efficient generation of targeted large insertions by microinjection into two-cell-stage mouse embryos
by Gu, Bin
Nature biotechnology, 2018-08, Vol.36 (7), p.632-637
15.
Resequencing 302 wild and cultivated accessions identifies genes related to domestication and improvement in soybean
by Zhou, Zhengkui
Nature biotechnology, 2015-04, Vol.33 (4), p.408-414
16.
Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing
by Tsai, Shengdar Q
Nature biotechnology, 2014-06, Vol.32 (6), p.569-576
17.
Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
by Jordan, Catherine T
American journal of human genetics, 2012-05-04, Vol.90 (5), p.796-808
18.
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
by Pinto, Dalila
American journal of human genetics, 2014-05-01, Vol.94 (5), p.677-694
19.
Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia
by Ntziachristos, Panagiotis
Nature medicine, 2012-02-06, Vol.18 (2), p.298-302
20.
Single-cell multiomic analysis identifies regulatory programs in mixed-phenotype acute leukemia
by Granja, JM
Nature biotechnology, 2019, Vol.37 (12), p.1458
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