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Nature Genetics|August 17, 2010
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsyHyun Hor, Zoltán Kutalik, Yves Dauvilliers, et al.
Journal of Medical Genetics|October 12, 2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersFlore Zufferey, Elliott H Sherr, Noam D Beckmann, et al.
Nature Genetics|April 5, 2020
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancerAlex H Wagner, Brian Walsh, Georgia Mayfield, et al.
Plos Genetics|December 31, 2009
Common genetic variation and the control of HIV-1 in humansJacques Fellay, Dongliang Ge, Kevin V Shianna, et al.
Plos Genetics|October 8, 2011
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRDCarsten A Böger, Mathias Gorski, Man Li, et al.
Nature Genetics|April 9, 2008
Genome-wide association analysis identifies 20 loci that influence adult heightMichael N Weedon, Hana Lango, Cecilia M Lindgren, et al.
Plos Genetics|June 9, 2009
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrationsMelanie Kolz, Toby Johnson, Serena Sanna, et al.
Hypertension (Dallas, Tex. : 1979)|December 21, 2011
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthaseErika Salvi, Zoltán Kutalik, Nicola Glorioso, et al.
JAMA Psychiatry|December 3, 2015
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical ComorbiditiesDebra D'Angelo, Sébastien Lebon, Qixuan Chen, et al.
Human Mutation|September 28, 2011
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeatsPaweł Stankiewicz, Shashikant Kulkarni, Avinash V Dharmadhikari, et al.
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