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Genetic Epidemiology|September 10, 2016
When do myopia genes have their effect? Comparison of genetic risks between children and adultsJ Willem L Tideman, Qiao Fan, Jan Roelof Polling, et al.
Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.
Human Molecular Genetics|September 13, 2011
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adultsJennifer E Huffman, Ana Knezevic, Veronique Vitart, et al.
Human Molecular Genetics|July 16, 2015
Homozygous loss-of-function variants in European cosmopolitan and isolate populationsVera B Kaiser, Victoria Svinti, James G Prendergast, et al.
Obesity (Silver Spring, Md.)|October 24, 2009
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 geneAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Nature Genetics|April 2, 2020
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopiaPirro G Hysi, Hélène Choquet, Anthony P Khawaja, et al.
Investigative Ophthalmology & Visual Science|April 28, 2021
IMI 2021 Yearly DigestMonica Jong, Jost B Jonas, James S Wolffsohn, et al.
Human Molecular Genetics|July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degenerationMorad Ansari, Paul M McKeigue, Christine Skerka, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
Communications Biology|December 5, 2019
Multi-trait genome-wide association study identifies new loci associated with optic disc parametersPieter W M Bonnemaijer, Elisabeth M van Leeuwen, Adriana I Iglesias, et al.
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