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.
Informed consent in genomics and genetic research
by McGuire, Amy L
Annual review of genomics and human genetics, 2010, Vol.11 (1), p.361-381
3.
Subjects matter: a survey of public opinions about a large genetic cohort study
by Kaufman, David
Genetics in medicine, 2008-11, Vol.10 (11), p.831-839
4.
Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents
by Munung, Nchangwi Syntia
Journal of medical ethics, 2016-02, Vol.42 (2), p.132-137
5.
Assessing the Privacy Risks of Data Sharing in Genomics
by Heeney, C
Community genetics, 2011-01-01, Vol.14 (1), p.17-25
6.
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
7.
Recasting Asilomar's lessons for human germline editing
by Miller, Henry I
Nature biotechnology, 2015-11, Vol.33 (11), p.1132-1134
8.
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
9.
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
10.
IRB perspectives on the return of individual results from genomic research
by Dressler, Lynn G
Genetics in medicine, 2012-02, Vol.14 (2), p.215-222
11.
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
12.
Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases
by Kleiderman, Erika
Journal of Medical Ethics, 2014-10, Vol.40 (10), p.691-696
13.
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
14.
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
15.
Bandwagons I, too, have known
by Bernardo, Rex
Theoretical and applied genetics, 2016-09-28, Vol.129 (12), p.2323-2332
16.
Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers
by Hilton, Isaac B
Nature biotechnology, 2015-05, Vol.33 (5), p.510-517
17.
Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells
by Chu, Van Trung
Nature biotechnology, 2015-05, Vol.33 (5), p.543-548
18.
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
19.
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
20.
Mutation effects predicted from sequence co-variation
by Hopf, Thomas A
Nature biotechnology, 2017-02, Vol.35 (2), p.128-135
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