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BMC Genomics|February 27, 2010
Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic dataOzren Polasek, Caroline Hayward, Celine Bellenguez, et al.
European Journal of Human Genetics : EJHG|January 31, 2013
Inference of identity by descent in population isolates and optimal sequencing studiesDominik Glodzik, Pau Navarro, Veronique Vitart, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|September 10, 2013
The association between galactosylation of immunoglobulin G and body mass indexMatea Nikolac Perkovic, Maja Pucic Bakovic, Jasminka Kristic, et al.
Journal of Molecular Neuroscience : MN|July 1, 2010
Variation in the uric acid transporter gene SLC2A9 and its association with AAO of Parkinson's diseaseMaurizio F Facheris, Andrew A Hicks, Cosetta Minelli, et al.
Plos One|October 19, 2012
Localising loci underlying complex trait variation using Regional Genomic Relationship MappingYoshitaka Nagamine, Ricardo Pong-Wong, Pau Navarro, et al.
Annals of Human Genetics|September 21, 2010
The TCF7L2 diabetes risk variant is associated with HbA₁(C) levels: a genome-wide association meta-analysisChristopher S Franklin, Yurii S Aulchenko, Jennifer E Huffman, et al.
European Journal of Human Genetics : EJHG|March 7, 2008
Quantifying the increase in average human heterozygosity due to urbanisationIgor Rudan, Andrew D Carothers, Ozren Polasek, et al.
Human Molecular Genetics|April 29, 2015
Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-modelsAthina Spiliopoulou, Reka Nagy, Mairead L Bermingham, et al.
Human Molecular Genetics|June 5, 2014
Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconusJudith Lechner, Louise F Porter, Aine Rice, et al.
Scientific Reports|September 24, 2017
Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degenerationChloe M Stanton, Shyamanga Borooah, Camilla Drake, et al.
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