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Kidney International|October 22, 2015
Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUTNayia Nicolaou, Sara L Pulit, Isaac J Nijman, et al.Pediatrics|March 20, 2013
Cultural bias in the AAP's 2012 Technical Report and Policy Statement on male circumcisionMorten Frisch, Yves Aigrain, Vidmantas Barauskas, et al.Human Molecular Genetics|March 24, 2011
Common genetic variants associated with open-angle glaucomaWishal D Ramdas, Leonieke M E van Koolwijk, Hans G Lemij, et al.Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.Nature Genetics|September 14, 2010
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14Abbas M Solouki, Virginie J M Verhoeven, Cornelia M van Duijn, et al.Clinical Psychology in Europe|February 15, 2024
Harbingers of Hope: Scientists and the Pursuit of World PeaceSeithikurippu R Pandi-Perumal, Willem A C M van de Put, Andreas Maercker, et al.Human Mutation|September 2, 2011
Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studiesGareth J McKay, Chris C Patterson, Usha Chakravarthy, et al.Plos One|February 9, 2013
Genome-wide association study of retinopathy in individuals without diabetesRichard A Jensen, Xueling Sim, Xiaohui Li, et al.International Journal of Epidemiology|January 19, 2012
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtypeReecha Sofat, Juan P Casas, Andrew R Webster, et al.Plos Genetics|May 10, 2012
Common genetic determinants of intraocular pressure and primary open-angle glaucomaLeonieke M E van Koolwijk, Wishal D Ramdas, M Kamran Ikram, et al.Pageof 34