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Digital quantification of human eye color highlights genetic association of three new loci

author

Fernando Rivadeneira

2000 -

André Uitterlinden

2000 -

David L. Duffy

Fan Liu

2000 -

Oscar Lao

Christopher J. Hammond

Grant W. Montgomery

David A. Mackey

Nick Martin

1950 -

Susan Walsh

Albert Hofman

1951 -

Manfred Kayser

Tim Spector

1958 -

published in: PLOS Genetics

date of publication: 2010-05-06

Cites articles 42

Date

Title

Authors

2010-03-27

IrisPlex: a sensitive DNA tool for accurate prediction of blue and brown eye colour in the absence of ancestry information

Fan Liu, Mannis van Oven, Oscar Lao, Susan Walsh, Kaye N. Ballantyne
2009

The Rotterdam Study: 2010 objectives and design update

Cornelia M. van Duijn, André Uitterlinden, Henning Tiemeier, Albert Hofman, Ernst Kuipers, Jacqueline C M Witteman, Monique Breteler, Bruno H Stricker
2009-01-01

Genotype imputation

Cristen J. Willer, Serena Sanna, Gonçalo Abecasis
2009-07-08

Genetics of human iris colour and patterns

Richard A Sturm
2009-09-15

A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation

Fernando Rivadeneira, Cornelia M. van Duijn, Gonneke Willemsen, Karol Estrada, Jouke-Jan Hottenga, André Uitterlinden, Albert Hofman, Yurii S. Aulchenko, Fan Liu, Claes Ohlsson, Michael Krawczak, Mattias Lorentzon, Dorret Boomsma, Eco de Geus, Manfred Kayser, Brenda Penninx, Joyce B J van Meurs, Paul Lips, Stefan Schreiber, Nicole Vogelzangs, Ben A Oostra, Kate van Duijn, Lisette Stolk
2009-06-13

Molecular genetic analysis of Down syndrome
2009-06-08

A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortium

Nicole Soranzo, Frances M. Williams, Panos Deloukas, Ingrid Meulenbelt, Ana M. Valdes, Eline Slagboom, Tim Spector
2009-02-25

DNA-based prediction of human externally visible characteristics in forensics: motivations, scientific challenges, and ethical considerations
2009-03-22

Common variants at ten loci influence QT interval duration in the QTGEN Study

Fernando Rivadeneira, André Uitterlinden, Christopher Newton-Cheh, Jan A Kors, Martin G Larson, Jerome I Rotter, Albert Hofman, Bruce M. Psaty, Susan R Heckbert, Joshua C Bis, Thomas Lumley, Jacqueline C M Witteman
2009-03-01

Eye color and the prediction of complex phenotypes from genotypes.

Fan Liu, Cecile Janssens, Albert Hofman, André Uitterlinden
2008-11-21

Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome

Michael Anderson, John H. Fingert
2008-11-06

Personal genomes: The case of the missing heritability
2008-09-04

Characterization of a canine model of autosomal recessive retinitis pigmentosa due to a PDE6A mutation
2008-06-01

Pharmacogenetics of Gilbert's syndrome
2008-05-18

Two newly identified genetic determinants of pigmentation in Europeans

Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Gudmar Thorleifsson, Thorunn Rafnar, Arnar Palsson, Lambertus Kiemeney, Augustine Kong, Patrick Sulem, Jeffrey Gulcher, Kári Stefánsson, Kristrun R Benediktsdottir, Katja K H Aben
2008-05-16

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

David L. Duffy, Grant W. Montgomery, Nick Martin, Hongmei Nan, Frank Hu, Stephen Chanock, David J. Hunter, Susan E. Hankinson, Abrar A Qureshi, Yuan Yi Constance Chen, Peter Kraft, Robert N. Hoover
2008-02

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color

David L. Duffy, Mitchell S. Stark, Richard A Sturm, Grant W. Montgomery, Nick Martin
2008-02

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene

Fernando Rivadeneira, Cornelia M. van Duijn, André Uitterlinden, Diana Zelenika, Albert Hofman, Oscar Lao, Wilfred F J van IJcken, Yurii S. Aulchenko, Cecile Janssens, Manfred Kayser, Ben A Oostra, Caroline C Klaver, Kate van Duijn, Pascal Arp, P Mila Jhamai, Simon Heath, Dominiek D.G. Despriet, Johannes R. Vingerling, Paulus T V M de Jong
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Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression

Jesper Thorvald Troelsen, Jonas Mengel-From
2008-01

Chediak-Higashi syndrome
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2007-10-23

The Rotterdam Study: objectives and design update

Henning Tiemeier, Cornelia M. van Duijn, André Uitterlinden, Albert Hofman, Jacqueline C M Witteman, Monique Breteler
2007-12

Genetic determinants of hair, eye and skin pigmentation in Europeans

Unnur Þorsteinsdóttir, Patrick Sulem, Gudmar Thorleifsson, Kári Stefánsson, Thorunn Rafnar, Arnar Palsson, Daníel F. Guðbjartsson, Lambertus Kiemeney, Jeffrey Gulcher, Kristrun R Benediktsdottir, Katja K H Aben
2007-08-16

Genetic effects on coat colour in cattle: dilution of eumelanin and phaeomelanin pigments in an F2-Backcross Charolais x Holstein population

John L. Williams
2007-09

PLINK: a tool set for whole-genome association and population-based linkage analyses

Shaun Purcell, Julian Maller, Mark Joseph Daly, Pamela Sklar, Benjamin M. Neale
2007-03-23

GenABEL: an R library for genome-wide association analysis

Yurii S. Aulchenko, Aaron Isaacs, Cornelia M. van Duijn, Stephan Ripke
2007-02

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

David L. Duffy, Grant W. Montgomery, Nick Martin
2007-05-01

Human skin-color sexual dimorphism: a test of the sexual selection hypothesis

Peter Frost
2006-09-14

KRAS variation and risk of endometriosis

Nick Martin, Grant W. Montgomery, Dale R Nyholt, Susan A Treloar
2006-08-15

UGT1A polymorphisms in a Swedish cohort and a human diversity panel, and the relation to bilirubin plasma levels in males and females

Jorge Andrade, Peter Höglund, Jacob Odeberg
2006-06-06

A scan for signatures of positive selection in candidate loci for skin pigmentation in humans.
2006-10-25

A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions

David L. Duffy, Grant W. Montgomery, Nick Martin

Article - wd:Q33576746

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