1.
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, Vol.40 (10), p.691-696
2.
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
3.
Clinical assessment incorporating a personal genome
by Ashley, Euan A, Dr
The Lancet (British edition), 2010, Vol.375 (9725), p.1525-1535
4.
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
5.
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, Vol.94 (2), p.223-232
6.
The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository
by Harris, Erin D
Genetics in medicine, 2012, Vol.14 (3), p.330-337
7.
Playing a Part in Research? University Students’ Attitudes to Direct-To-Consumer Genomics
by Vayena, Effy
Community genetics, 2014, Vol.17 (3), p.158-168
8.
Mutations in DDX58, which Encodes RIG-I, Cause Atypical Singleton-Merten Syndrome
by Jang, Mi-Ae
American journal of human genetics, 2015, Vol.96 (2), p.266-274
9.
Population genetic screening efficiently identifies carriers of autosomal dominant diseases
by Grzymski, J J
Nature medicine, 2020, Vol.26 (8), p.1235-1239
10.
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
by Davies, R.W
Nature Medicine, 2020, Vol.26 (12), p.1912-1918
11.
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing
by Jiang, Yong-hui
American journal of human genetics, 2013, Vol.93 (2), p.249-263
12.
Whole-genome sequencing of quartet families with autism spectrum disorder
by Yuen, Ryan K C
Nature medicine, 2015, Vol.21 (2), p.185-191
13.
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort
by Waszak, Sebastian M
The lancet oncology, 2018, Vol.19 (6), p.785-798
14.
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
by Schmidt, Ellen M
American journal of human genetics, 2014, Vol.94 (2), p.233-245
15.
Increased l1 retrotransposition in the neuronal genome in schizophrenia
by Bundo, Miki
Neuron (Cambridge, Mass.), 2014, Vol.81 (2), p.306-313
16.
Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood
by Moser, Gerhard
American journal of human genetics, 2018, Vol.102 (6), p.1185-1194
17.
DNA Methylation Signatures in Development and Aging of the Human Prefrontal Cortex
by Numata, Shusuke
American journal of human genetics, 2012, Vol.90 (2), p.260-272
18.
Mutations in EZH2 Cause Weaver Syndrome
by Gibson, William T
American journal of human genetics, 2012, Vol.90 (1), p.110-118
19.
High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants
by Razavi, Pedram
Nature medicine, 2019, Vol.25 (12), p.1928-1937
20.
Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease
by Guo, Dong-Chuan
American journal of human genetics, 2009, Vol.84 (5), p.617-627
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