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.
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

3.
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

4.
Assessing the Privacy Risks of Data Sharing in Genomics
by Heeney, C
Community genetics, 2011-01-01, Vol.14 (1), p.17-25

5.
Recasting Asilomar's lessons for human germline editing
by Miller, Henry I
Nature biotechnology, 2015-11, Vol.33 (11), p.1132-1134

6.
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

7.
The Impact of Commercialisation and Genetic Data Sharing Arrangements on Public Trust and the Intention to Participate in Biobank Research
by Critchley, Christine
Community genetics, 2015-01-01, Vol.18 (3), p.160-172

8.
"Trust is not something you can reclaim easily": patenting in the field of direct-to-consumer genetic testing
by Sterckx, S
Genetics in medicine, 2013, Vol.15 (5), p.382-387

9.
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

10.
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

11.
Bandwagons I, too, have known
by Bernardo, Rex
Theoretical and applied genetics, 2016-09-28, Vol.129 (12), p.2323-2332

12.
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

13.
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

14.
Processes and factors involved in decisions regarding return of incidental genomic findings in research
by Klitzman, Robert
Genetics in medicine, 2014-04, Vol.16 (4), p.311-317

15.
Clinical assessment incorporating a personal genome
by Ashley, Euan A, Dr
The Lancet (British edition), 2010, Vol.375 (9725), p.1525-1535

16.
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

17.
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

18.
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

19.
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

20.
Multiscale Analysis of Independent Alzheimer’s Cohorts Finds Disruption of Molecular, Genetic, and Clinical Networks by Human Herpesvirus
by Readhead, Ben
Neuron (Cambridge, Mass.), 2018-07-11, Vol.99 (1), p.64-82.e7
