1.
Common variants conferring risk of schizophrenia
by Stefansson, Hreinn
Nature (London), 2009, Vol.460 (7256), p.744-747
2.
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
3.
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
by Cardon, Lon R
Nature, 2007, Vol.447 (7145), p.661-678
4.
CRISPR/Cas9-mediated gene editing in human zygotes using Cas9 protein
by Tang, Lichun
Molecular genetics and genomics : MGG, 2017-03-01, Vol.292 (3), p.525-533
5.
Large recurrent microdeletions associated with schizophrenia
by Stefansson, Hreinn
Nature, 2008, Vol.455 (7210), p.232-236
6.
Parental origin of sequence variants associated with complex diseases
by Gudjonsson, Sigurjon A
Nature (London), 2009-12-17, Vol.462 (7275), p.868-874
7.
A genome-wide association study identifies novel risk loci for type 2 diabetes
by Meyre, David
Nature, 2007-02-22, Vol.445 (7130), p.881-885
8.
Rare chromosomal deletions and duplications increase risk of schizophrenia
by Stone, JL
Nature, 2008-09-11, Vol.455 (7210), p.237-241
9.
Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis
by Lafaille, Fabien G
Nature Medicine, 2019-12, Vol.25 (12), p.1873-1884
10.
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome
by Joshi, Ricky S
American journal of human genetics, 2016-09-01, Vol.99 (3), p.555-566
11.
Human Genome Sequencing in Health and Disease
by Gonzaga-Jauregui, Claudia
Annual review of medicine, 2012-02-18, Vol.63 (1), p.35-61
12.
Reconstructing Indian population history
by Reich, David
Nature, 2009-09-24, Vol.461 (7263), p.489-494
13.
Genome Partitioning of Genetic Variation for Height from 11,214 Sibling Pairs
by Visscher, Peter M
American journal of human genetics, 2007, Vol.81 (5), p.1104-1110
14.
Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements
by Zepeda-Mendoza, Cinthya J
American journal of human genetics, 2017-08-03, Vol.101 (2), p.206-217
15.
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
by Sanders, Stephan J
Neuron (Cambridge, Mass.), 2011-06-09, Vol.70 (5), p.863-885
16.
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study
by Dehghan, Abbas, MD
The Lancet (British edition), 2008, Vol.372 (9654), p.1953-1961
17.
Mendelian Inheritance in Man and Its Online Version, OMIM
by McKusick, Victor A
American journal of human genetics, 2007, Vol.80 (4), p.588-604
18.
HLA-C Level Is Regulated by a Polymorphic Oct1 Binding Site in the HLA-C Promoter Region
by Vince, Nicolas
American journal of human genetics, 2016-12-01, Vol.99 (6), p.1353-1358
19.
Genomic Patterns of Homozygosity in Worldwide Human Populations
by Pemberton, Trevor J
American journal of human genetics, 2012-08-10, Vol.91 (2), p.275-292
20.
Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24
by Jones, Angela M
Journal of medical genetics, 2012-03, Vol.49 (3), p.158-163
