Works matching AU Wright, Alan F.

Results: 82

Identity-by-descent-based phasing and imputation in founder populations using graphical models.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 8, p. 853, doi. 10.1002/gepi.20635

By:

Palin, Kimmo;
Campbell, Harry;
Wright, Alan F.;
Wilson, James F.;
Durbin, Richard

Publication type:

Article

Genetic comparison of a Croatian isolate and CEPH European founders.

Published in:

Genetic Epidemiology, 2010, v. 34, n. 2, p. 140, doi. 10.1002/gepi.20443

By:

Navarro, Pau;
Vitart, Véronique;
Hayward, Caroline;
Tenesa, Albert;
Zgaga, Lina;
Juricic, Danica;
Polasek, Ozren;
Hastie, Nicholas D.;
Rudan, Igor;
Campbell, Harry;
Wright, Alan F.;
Haley, Chris S.;
Knott, Sara A.

Publication type:

Article

The human retinitis pigmentosa GTPase regulator gene variant database.

Published in:

2008

By:

Shu, Xinhua;
McDowall, Ewan;
Brown, Alastair F.;
Wright, Alan F.

Publication type:

Other

RPGR mutation analysis and disease: an update.

Published in:

Human Mutation, 2007, v. 28, n. 4, p. 322, doi. 10.1002/humu.20461

By:

Shu, Xinhua;
Black, Graeme C.;
Rice, Jacqueline M.;
Hart-Holden, Niki;
Jones, Alison;
O'Grady, Anna;
Ramsden, Simon;
Wright, Alan F.

Publication type:

Article

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome.

Published in:

Human Mutation, 2004, v. 24, n. 5, p. 439, doi. 10.1002/humu.9285

By:

Wright, Alan F.;
Reddick, Adam C.;
Schwartz, Sharon B.;
Ferguson, Julie S.;
Aleman, Tomas S.;
Kellner, Ulrich;
Jurklies, Bernhard;
Schuster, Andreas;
Zrenner, Eberhart;
Wissinger, Bernd;
Lennon, Alan;
Shu, Xinhua;
Cideciyan, Artur V.;
Stone, Edwin M.;
Jacobson, Samuel G.;
Swaroop, Anand

Publication type:

Article

Mutations of RPGR in X-linked retinitis pigmentosa (RP3).

Published in:

Human Mutation, 2002, v. 19, n. 5, p. 486, doi. 10.1002/humu.10057

By:

Vervoort, Raf;
Wright, Alan F.

Publication type:

Article

Genes predict village of origin in rural Europe.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1269, doi. 10.1038/ejhg.2010.92

By:

O'Dushlaine, Colm;
McQuillan, Ruth;
Weale, Michael E.;
Crouch, Daniel J. M.;
Johansson, Åsa;
Aulchenko, Yurii;
Franklin, Christopher S.;
Pola&;#x0161;ek, Ozren;
Fuchsberger, Christian;
Corvin, Aiden;
Hicks, Andrew A.;
Vitart, Veronique;
Hayward, Caroline;
Wild, Sarah H.;
Meitinger, Thomas;
van Duijn, Cornelia M.;
Gyllensten, Ulf;
Wright, Alan F.;
Campbell, Harry;
Pramstaller, Peter P.

Publication type:

Article

For want of a disc, the cell was lost….

Published in:

Nature Medicine, 2000, v. 6, n. 5, p. 508, doi. 10.1038/74985

By:

Wright, Alan F.

Publication type:

Article

Defining the role of common variation in the genomic and biological architecture of adult human height.

Published in:

Nature Genetics, 2014, v. 46, n. 11, p. 1173, doi. 10.1038/ng.3097

By:

Wood, Andrew R;
Pasko, Dorota;
Weedon, Michael N;
Frayling, Timothy M;
Kutalik, Zoltán;
Hassinen, Maija;
Hayward, Caroline;
Wright, Alan F;
Heard-Costa, Nancy L;
Helmer, Quinta;
Hillege, Hans L;
Hlatky, Mark A;
Assimes, Themistocles L;
Quertermous, Thomas;
Hoffmann, Wolfgang;
Völzke, Henry;
Hoffmann, Per;
Holmen, Oddgeir;
Hveem, Kristian;
Houwing-Duistermaat, Jeanine J

Publication type:

Article

A rare variant in CFH directly links age-related macular degeneration with rare glomerular nephropathies.

Published in:

Nature Genetics, 2011, v. 43, n. 12, p. 1176, doi. 10.1038/ng.1012

By:

Wright, Alan F.

Publication type:

Article

Contribution of consanguinuity to polygenic and multifactorial diseases.

Published in:

2006

By:

Rudan, Igor;
Campbell, Harry;
Carothers, Andrew D.;
Hastie, Nicholas D.;
Wright, Alan F.

Publication type:

Letter

Lifespan and mitochondrial control of neurodegeneration.

Published in:

Nature Genetics, 2004, v. 36, n. 11, p. 1153, doi. 10.1038/ng1448

By:

Wright, Alan F.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Roman, Alejandro J;
Shu, Xinhua;
Vlachantoni, Dafni;
McInnes, Roderick R.;
Riemersma, Rudolph A.

Publication type:

Article

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

Published in:

Nature Genetics, 2001, v. 28, n. 2, p. 188, doi. 10.1038/88925

By:

Mykytyn, Kirk;
Braun, Terry;
Carmi, Rivka;
Haider, Neena B.;
Searby, Charles C.;
Shastri, Mythreyi;
Beck, Gretel;
Wright, Alan F.;
Iannaccone, Alessandro;
Elbedour, Khalil;
Riise, Ruth;
Baldi, Alfonso;
Raas-Rothschild, Annick;
Gorman, Susan W.;
Duhl, David M.;
Jacobson, Samuel G.;
Casavant, Thomas;
Stone, Edwin M.;
Sheffield, Val C.

Publication type:

Article

Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa.

Published in:

Nature Genetics, 2000, v. 25, n. 4, p. 462, doi. 10.1038/78182

By:

Vervoort, Raf;
Lennon, Alan;
Bird, Alan C.;
Tulloch, Brian;
Axton, Richard;
Miano, Maria G.;
Meindl, Alfons;
Meitinger, Thomas;
Ciccodicola, Alfredo;
Wright, Alan F.

Publication type:

Article

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 127, doi. 10.1038/72777

By:

Haider, Neena B.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Swiderski, Ruth;
Streb, Luan M.;
Searby, Charles;
Beck, Gretel;
Hockey, Robin;
Hanna, David B.;
Gorman, Susan;
Duhl, David;
Carmi, Rivka;
Bennett, Jean;
Weleber, Richard G.;
Fishman, Gerald A.;
Wright, Alan F.;
Stone, Edwin M.;
Sheffield, Val C.

Publication type:

Article

Population choice in mapping genes for complex diseases.

Published in:

Nature Genetics, 1999, v. 23, n. 4, p. 397, doi. 10.1038/70501

By:

Wright, Alan F;
Carothers, Andrew D;
Pirastu, Mario

Publication type:

Article

Mortality in women with turner syndrome in Great Britain: a national cohort study.

Published in:

2008

By:

Schoemaker, Minouk J;
Swerdlow, Anthony J;
Higgins, Craig D;
Wright, Alan F;
Jacobs, Patricia A;
United Kingdom Clinical Cytogenetics Group

Publication type:

journal article

Mortality in Patients with Klinefelter Syndrome in Britain: A Cohort Study.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 12, p. 6516, doi. 10.1210/jc.2005-1077

By:

Swerdlow, Anthony J.;
Higgins, Craig D.;
Schoemaker, Minouk J.;
Wright, Alan F.;
Jacobs, Patricia A.

Publication type:

Article

Comparative assessment of methods for estimatingindividual genome-wide homozygosity-by-descentfrom human genomic data.

Published in:

BMC Genomics, 2010, v. 11, p. 139, doi. 10.1186/1471-2164-11-139

By:

Polašek, Ozren;
Hayward, Caroline;
Bellenguez, Celine;
Vitart, Veronique;
Kolčić, Ivana;
McQuillan, Ruth;
Saftić, Vanja;
Gyllensten, Ulf;
Wilson, James F.;
Rudan, Igor;
Wright, Alan F.;
Campbell, Harry;
Leutenegger, Anne-Louise

Publication type:

Article

Exome Sequencing to Detect Rare Variants Associated With General Cognitive Ability: A Pilot Study.

Published in:

Twin Research & Human Genetics, 2015, v. 18, n. 2, p. 117, doi. 10.1017/thg.2015.10

By:

Luciano, Michelle;
Svinti, Victoria;
Campbell, Archie;
Marioni, Riccardo E.;
Hayward, Caroline;
Wright, Alan F.;
Taylor, Martin S.;
Porteous, David J.;
Thomson, Pippa;
Prendergast, James G.D.;
Hastie, Nicholas D.;
Farrington, Susan M.;
Scotland, Generation;
Dunlop, Malcolm G.;
Deary, Ian J.

Publication type:

Article

Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies.

Published in:

PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068604

By:

Joshi, Peter K.;
Prendergast, James;
Fraser, Ross M.;
Huffman, Jennifer E.;
Vitart, Veronique;
Hayward, Caroline;
McQuillan, Ruth;
Glodzik, Dominik;
Polašek, Ozren;
Hastie, Nicholas D.;
Rudan, Igor;
Campbell, Harry;
Wright, Alan F.;
Haley, Chris S.;
Wilson, James F.;
Navarro, Pau

Publication type:

Article

Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping.

Published in:

PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046501

By:

Nagamine, Yoshitaka;
Pong-Wong, Ricardo;
Navarro, Pau;
Vitart, Veronique;
Hayward, Caroline;
Rudan, Igor;
Campbell, Harry;
Wilson, James;
Wild, Sarah;
Hicks, Andrew A.;
Pramstaller, Peter P.;
Hastie, Nicholas;
Wright, Alan F.;
Haley, Chris S.

Publication type:

Article

The Association of Dietary Intake of Purine-Rich Vegetables, Sugar-Sweetened Beverages and Dairy with Plasma Urate, in a Cross-Sectional Study.

Published in:

PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038123

By:

Zgaga, Lina;
Theodoratou, Evropi;
Kyle, Janet;
Farrington, Susan M.;
Agakov, Felix;
Tenesa, Albert;
Walker, Marion;
McNeill, Geraldine;
Wright, Alan F.;
Rudan, Igor;
Dunlop, Malcolm G.;
Campbell, Harry

Publication type:

Article

Characterisation of a C1qtnf5 Ser163Arg Knock-In Mouse Model of Late-Onset Retinal Macular Degeneration.

Published in:

PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027433

By:

Xinhua Shu;
Luhmann, Ulrich F. O.;
Aleman, Tomas S.;
Barker, Susan E.;
Lennon, Alan;
Tulloch, Brian;
Mei Chen;
Heping Xu;
Jacobson, Samuel G.;
Ali, Robin;
Wright, Alan F.

Publication type:

Article

Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates.

Published in:

PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023836

By:

Wei, Wenhua;
Hemani, Gibran;
Hicks, Andrew A.;
Vitart, Veronique;
Cabrera-Cardenas, Claudia;
Navarro, Pau;
Huffman, Jennifer;
Hayward, Caroline;
Knott, Sara A.;
Rudan, Igor;
Pramstaller, Peter P.;
Wild, Sarah H.;
Wilson, James F.;
Campbell, Harry;
Dunlop, Malcolm G.;
Hastie, Nicholas;
Wright, Alan F.;
Haley, Chris S.

Publication type:

Article

Copy Number Variation across European Populations.

Published in:

PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023087

By:

Wanting Chen;
Hayward, Caroline;
Wright, Alan F.;
Hicks, Andrew A.;
Vitart, Veronique;
Knott, Sara;
Wild, Sarah H.;
Pramstaller, Peter P.;
Wilson, James F.;
Rudan, Igor;
Porteous, David J.

Publication type:

Article

Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits.

Published in:

PLoS Genetics, 2020, v. 16, n. 7, p. 1, doi. 10.1371/journal.pgen.1008785

By:

Bretherick, Andrew D.;
Canela-Xandri, Oriol;
Joshi, Peter K.;
Clark, David W.;
Rawlik, Konrad;
Boutin, Thibaud S.;
Zeng, Yanni;
Amador, Carmen;
Navarro, Pau;
Rudan, Igor;
Wright, Alan F.;
Campbell, Harry;
Vitart, Veronique;
Hayward, Caroline;
Wilson, James F.;
Tenesa, Albert;
Ponting, Chris P.;
Baillie, J. Kenneth;
Haley, Chris

Publication type:

Article

Strategy for Mapping Quantitative Trait Loci (QTL) by Using Human Metapopulations.

Published in:

Croatian Medical Journal, 2006, v. 47, n. 4, p. 532

By:

Rudan, Igor;
Biloglav, Zrinka;
Carothers, Andrew D.;
Wright, Alan F.;
Campbell, Harry

Publication type:

Article

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 1, p. 175, doi. 10.1093/hmg/ddy342

By:

Charng, Jason;
Cideciyan, Artur V;
Jacobson, Samuel G;
Sumaroka, Alexander;
Schwartz, Sharon B;
Swider, Malgorzata;
Roman, Alejandro J;
Sheplock, Rebecca;
Anand, Manisha;
Peden, Marc C;
Khanna, Hemant;
Heon, Elise;
Wright, Alan F;
Swaroop, Anand

Publication type:

Article

Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 24, p. 5444, doi. 10.1093/hmg/ddw361

By:

Charng, Jason;
Cideciyan, Artur V.;
Jacobson, Samuel G.;
Sumaroka, Alexander;
Schwartz, Sharon B.;
Swider, Malgorzata;
Roman, Alejandro J.;
Sheplock, Rebecca;
Anand, Manisha;
Peden, Marc C.;
Khanna, Hemant;
Heon, Elise;
Wright, Alan F.;
Swaroop, Anand

Publication type:

Article

Homozygous loss-of-function variants in European cosmopolitan and isolate populations.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 19, p. 5464, doi. 10.1093/hmg/ddv272

By:

Kaiser, Vera B.;
Svinti, Victoria;
Prendergast, James G.;
You-Ying Chau;
Campbell, Archie;
Patarcic, Inga;
Barroso, Inês;
Joshi, Peter K.;
Hastie, Nicholas D.;
Miljkovic, Ana;
Taylor, Martin S.;
Scotland, Generation;
Enroth, Stefan;
Memari, Yasin;
Kolb-Kokocinski, Anja;
Wright, Alan F.;
Gyllensten, Ulf;
Durbin, Richard;
Rudan, Igor;
Campbell, Harry

Publication type:

Article

Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 14, p. 4167, doi. 10.1093/hmg/ddv145

By:

Spiliopoulou, Athina;
Nagy, Reka;
Bermingham, Mairead L.;
Huffman, Jennifer E.;
Hayward, Caroline;
Vitart, Veronique;
Rudan, Igor;
Campbell, Harry;
Wright, Alan F.;
Wilson, James F.;
Pong-Wong, Ricardo;
Agakov, Felix;
Navarro, Pau;
Haley, Chris S.

Publication type:

Article

Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 20, p. 5527, doi. 10.1093/hmg/ddu253

By:

Lechner, Judith;
Porter, Louise F.;
Rice, Aine;
Vitart, Veronique;
Armstrong, David J.;
Schorderet, Daniel F.;
Munier, Francis L.;
Wright, Alan F.;
Inglehearn, Chris F.;
Black, Graeme C.;
Simpson, David A.;
Manson, Forbes;
Willoughby, Colin E.

Publication type:

Article

Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 15, p. 3174, doi. 10.1093/hmg/ddt169

By:

Kirin, Mirna;
Chandra, Aman;
Charteris, David G.;
Hayward, Caroline;
Campbell, Susan;
Celap, Ivana;
Bencic, Goran;
Vatavuk, Zoran;
Kirac, Iva;
Richards, Allan J.;
Tenesa, Albert;
Snead, Martin P.;
Fleck, Brian W.;
Singh, Jaswinder;
Harsum, Steven;
MacLaren, Robert E.;
den Hollander, Anneke I.;
Dunlop, Malcolm G.;
Hoyng, Carel B.;
Wright, Alan F.

Publication type:

Article

ATR localizes to the photoreceptor connecting cilium and deficiency leads to severe photoreceptor degeneration in mice.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 8, p. 1507

By:

Valdés-Sánchez, Lourdes;
De la Cerda, Berta;
Diaz-Corrales, Francisco J.;
Massalini, Simone;
Chakarova, Christina F.;
Wright, Alan F.;
Bhattacharya, Shomi S.

Publication type:

Article

Individual multi-locus heterozygosity is associated with lower morning plasma cortisol concentrations.

Published in:

European Journal of Endocrinology, 2013, v. 169, n. 1, p. 59, doi. 10.1530/EJE-12-0916

By:

Zgaga, Lina;
Vitart, Veronique;
Hayward, Caroline;
Kastelan, Darko;
Polašek, Ozren;
Jakovljevic, Miro;
Kolcic, Ivana;
Biloglav, Zrinka;
Wright, Alan F.;
Campbell, Harry;
Walker, Brian R.;
Rudan, Igor

Publication type:

Article

Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort study.

Published in:

Human Genetics, 2008, v. 123, n. 2, p. 215, doi. 10.1007/s00439-008-0465-0

By:

Swerdlow, Anthony J.;
Schoemaker, Minouk J.;
Higgins, Craig D.;
Wright, Alan F.;
Jacobs, Patricia A.

Publication type:

Article

Mortality and cancer incidence in women with extra X chromosomes: a cohort study in Britain.

Published in:

Human Genetics, 2005, v. 118, n. 2, p. 255, doi. 10.1007/s00439-005-0043-7

By:

Swerdlow, Anthony J.;
Schoemaker, Minouk J.;
Higgins, Craig D.;
Wright, Alan F.;
Jacobs, Patricia A.

Publication type:

Article

Cancer Incidence and Mortality in Men with Klinefelter Syndrome: A Cohort Study.

Published in:

JNCI: Journal of the National Cancer Institute, 2005, v. 97, n. 16, p. 1204, doi. 10.1093/jnci/dji240

By:

Swerdlow, Anthony J.;
Schoemaker, Minouk J.;
Higgins, Craig D.;
Wright, Alan F.;
Jacobs, Patricia A.

Publication type:

Article

Choroidal neovascularisation in a predicted female choroideraemia carrier treated with intravitreal anti-vascular endothelial growth factor.

Published in:

European Journal of Ophthalmology, 2021, v. 31, p. 4, doi. 10.1177/1120672120965495

By:

Ang, Juan Lyn;
Wright, Alan F.;
Dhillon, Baljean;
Cackett, Peter

Publication type:

Article

Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3).

Published in:

Human Molecular Genetics, 1995, v. 4, n. 12, p. 2347

By:

Dry, Katherine L.;
Aldred, Micheala A.;
Edgar, Alexander J.;
Brown, John;
Manson, Forbes D.C.;
Ho, Meng-Fatt;
Prosser, Jane;
Hardwick, Lee J.;
Lennon, Alan A.;
Thomson, Kate;
Van Keuren, Margaret;
Kurnit, David M.;
Bird, Alan C.;
Jay, Marcelle;
Monaco, Anthony P.;
Wright, Alan F.

Publication type:

Article

Choosing genes.

Published in:

Nature, 1996, v. 383, n. 6598, p. 312, doi. 10.1038/383312a0

By:

Wright, Alan F.;
Boyd, A. Christopher

Publication type:

Article

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait.

Published in:

2010

By:

Wright, Alan F.;
Chakarova, Christina F.;
Abd El-Aziz, Mai M.;
Bhattacharya, Shomi S.

Publication type:

journal article

Bayesian methods for instrumental variable analysis with genetic instruments ('Mendelian randomization'): example with urate transporter SLC2A9 as an instrumental variable for effect of urate levels on metabolic syndrome.

Published in:

2010

By:

McKeigue, Paul M.;
Campbell, Harry;
Wild, Sarah;
Vitart, Veronique;
Hayward, Caroline;
Rudan, Igor;
Wright, Alan F;
Wilson, James F.

Publication type:

journal article

The role of RPGR in cilia formation and actin stability.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 24, p. 4840, doi. 10.1093/hmg/ddr423

By:

Gakovic, Milica;
Shu, Xinhua;
Kasioulis, Ioannis;
Carpanini, Sarah;
Moraga, Ignacio;
Wright, Alan F.

Publication type:

Article

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 5, p. 1042, doi. 10.1093/hmg/ddq538

By:

Oexle, Konrad;
Ried, Janina S.;
Hicks, Andrew A.;
Tanaka, Toshiko;
Hayward, Caroline;
Bruegel, Mathias;
Gögele, Martin;
Lichtner, Peter;
Müller-Myhsok, Bertram;
Döring, Angela;
Illig, Thomas;
Schwienbacher, Christine;
Minelli, Cosetta;
Pichler, Irene;
Fiedler, G. Martin;
Thiery, Joachim;
Rudan, Igor;
Wright, Alan F.;
Campbell, Harry;
Ferrucci, Luigi

Publication type:

Article

Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration.

Published in:

Human Molecular Genetics, 2011, v. 20, n. 2, p. 322, doi. 10.1093/hmg/ddq467

By:

Vlachantoni, Dafni;
Bramall, Alexa N.;
Murphy, Michael P.;
Taylor, Robert W.;
Shu, Xinhua;
Tulloch, Brian;
Van Veen, Theo;
Turnbull, Douglass M.;
McInnes, Roderick R.;
Wright, Alan F.

Publication type:

Article

Variation in the uric acid transporter gene (SLC2A9) and memory performance.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 11, p. 2321, doi. 10.1093/hmg/ddq097

By:

Houlihan, Lorna M.;
Wyatt, Niki D.;
Harris, Sarah E.;
Hayward, Caroline;
Gow, Alan J.;
Marioni, Riccardo E.;
Strachan, Mark W.J.;
Price, Jackie F.;
Starr, John M.;
Wright, Alan F.;
Deary, Ian J.

Publication type:

Article

Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processes.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 4, p. 657, doi. 10.1093/hmg/ddp533

By:

Shu, Xinhua;
Zeng, Zhiqiang;
Gautier, Philippe;
Lennon, Alan;
Gakovic, Milica;
Patton, E. Elizabeth;
Wright, Alan F.

Publication type:

Article

Recent insights into the pathogenesis of hyperuricaemia and gout.

Published in:

Human Molecular Genetics, 2009, v. 18, n. R2, p. R177, doi. 10.1093/hmg/ddp369

By:

Riches, Philip L.;
Wright, Alan F.;
Ralston, Stuart H.

Publication type:

Article