1.
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
2.
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
3.
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
4.
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
by Purcell, Shaun
American journal of human genetics, 2007, Vol.81 (3), p.559-575
5.
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
6.
Engineered CRISPR-Cas12a variants with increased activities and improved targeting ranges for gene, epigenetic and base editing
by Kleinstiver, Benjamin P
Nature biotechnology, 2019-03, Vol.37 (3), p.276-282
7.
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities
by Chong, Jessica X
American journal of human genetics, 2015-08-06, Vol.97 (2), p.199-215
8.
DNA methylation-based classification and grading system for meningioma: a multicentre, retrospective analysis
by Sahm, Felix, MD
The lancet oncology, 2017, Vol.18 (5), p.682-694
9.
Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
by Ling, Shuo-Chien
Neuron (Cambridge, Mass.), 2013-08-07, Vol.79 (3), p.416-438
10.
Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder
by Girirajan, Santhosh
American journal of human genetics, 2013-02-07, Vol.92 (2), p.221-237
11.
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
12.
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
by Davies, R.W
Nature Medicine, 2020-12-01, Vol.26 (12), p.1912-1918
13.
Clonal seeds from hybrid rice by simultaneous genome engineering of meiosis and fertilization genes
by Wang, Chun
Nature biotechnology, 2019-03, Vol.37 (3), p.283-286
14.
Genetic Removal of p70 S6 Kinase 1 Corrects Molecular, Synaptic, and Behavioral Phenotypes in Fragile X Syndrome Mice
by Bhattacharya, Aditi
Neuron (Cambridge, Mass.), 2012-10-18, Vol.76 (2), p.325-337
15.
A genomic perspective on HLA evolution
by Meyer, Diogo
Immunogenetics (New York), 2017-07-07, Vol.70 (1), p.5-27
16.
Genetic associations in diabetic nephropathy: a meta-analysis
by Mooyaart, A. L
Diabetologia, 2010-12-03, Vol.54 (3), p.544-553
17.
Increased l1 retrotransposition in the neuronal genome in schizophrenia
by Bundo, Miki
Neuron (Cambridge, Mass.), 2014-01-22, Vol.81 (2), p.306-313
18.
Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood
by Moser, Gerhard
American journal of human genetics, 2018-06-07, Vol.102 (6), p.1185-1194
19.
Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies
by Wu, Michael C
American journal of human genetics, 2010, Vol.86 (6), p.929-942
20.
The Arabian Cradle: Mitochondrial Relicts of the First Steps along the Southern Route out of Africa
by Fernandes, Verónica
American journal of human genetics, 2012-02-10, Vol.90 (2), p.347-355
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