Works by Wright, Alan F.

Results: 82

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

Late-Onset Retinal Degeneration Caused by C1QTNF5 Mutation: Sub-Retinal Pigment Epithelium Deposits and Visual Consequences.

Published in:

JAMA Ophthalmology, 2014, v. 132, n. 10, p. 1252, doi. 10.1001/jamaophthalmol.2014.2059

By:

Jacobson, Samuel G.;
Cideciyan, Artur V.;
Sumaroka, Alexander;
Roman, Alejandro J.;
Wright, Alan F.

Publication type:

Article

The TCF7L2 Diabetes Risk Variant is Associated with HbA<sub>1C</sub> Levels: a Genome-Wide Association Meta-Analysis.

Published in:

Annals of Human Genetics, 2010, v. 74, n. 6, p. 471, doi. 10.1111/j.1469-1809.2010.00607.x

By:

Franklin, Christopher S.;
Aulchenko, Yurii S.;
Huffman, Jennifer E.;
Vitart, Veronique;
Hayward, Caroline;
Polašek, Ozren;
Knott, Sara;
Zgaga, Lina;
Zemunik, Tatijana;
Rudan, Igor;
Campbell, Harry;
Wright, Alan F.;
Wild, Sarah H.;
Wilson, James F.

Publication type:

Article

Mortality and Cancer Incidence in Carriers of Balanced Robertsonian Translocations: A National Cohort Study.

Published in:

American Journal of Epidemiology, 2019, v. 188, n. 3, p. 500, doi. 10.1093/aje/kwy266

By:

Schoemaker, Minouk J;
Jones, Michael E;
Higgins, Craig D;
Wright, Alan F;
Swerdlow, Anthony J

Publication type:

Article

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2.

Published in:

Nephrology Dialysis Transplantation, 2012, v. 27, n. 3, p. 1035, doi. 10.1093/ndt/gfr419

By:

Dinour, Dganit;
Gray, Nicola K.;
Ganon, Liat;
Knox, Andrew J.S.;
Shalev, Hanna;
Sela, Ben-Ami;
Campbell, Susan;
Sawyer, Lindsay;
Shu, Xinhua;
Valsamidou, Evgenia;
Landau, Daniel;
Wright, Alan F.;
Holtzman, Eliezer J.

Publication type:

Article

Gelsolin dysfunction causes photoreceptor loss in induced pluripotent cell and animal retinitis pigmentosa models.

Published in:

Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00111-8

By:

Megaw, Roly;
Abu-Arafeh, Hashem;
Jungnickel, Melissa;
Mellough, Carla;
Gurniak, Christine;
Witke, Walter;
Wei Zhang;
Khanna, Hemant;
MillA, Pleasantine;
Dhillon, Baljean;
Wright, Alan F.;
Lako, Majlinda;
ffrench-Constant, Charles

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

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

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

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

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

Common aberrations from the normal human plasma N-glycan profile.

Published in:

Glycobiology, 2010, v. 20, n. 8, p. 970, doi. 10.1093/glycob/cwq052

By:

Pučić, Maja;
Pinto, Sofia;
Novokmet, Mislav;
Knežević, Ana;
Gornik, Olga;
Polašek, Ozren;
Vlahoviček, Kristian;
Wei Wang;
Rudd, Pauline M.;
Wright, Alan F.;
Campbell, Harry;
Rudan, Igor;
Lauc, Gordan

Publication type:

Article

Effects of aging, body mass index, plasma lipid profiles, and smoking on human plasma N-glycans.

Published in:

Glycobiology, 2010, v. 20, n. 8, p. 959, doi. 10.1093/glycob/cwq051

By:

Knežević, Ana;
Gornik, Olga;
Polašek, Ozren;
Pučić, Maja;
Redčić, Irma;
Novokmet, Mislav;
Rudd, Pauline M.;
Wright, Alan F.;
Campbell, Harry;
Rudan, Igor;
Lauc, Gordan

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

Effects of angiotensin converting enzyme inhibition in adult polycystic kidney disease.

Published in:

Kidney International, 1992, v. 41, n. 1, p. 206, doi. 10.1038/ki.1992.28

By:

Watson, Michael L.;
Macnicol, Anne M.;
Allan, Paul L.;
Wright, Alan F.

Publication type:

Article

Renal, cardiovascular and hormonal characteristics of young adults with autosomal dominant polycystic kidney disease.

Published in:

Kidney International, 1991, v. 40, n. 3, p. 501, doi. 10.1038/ki.1991.238

By:

Harrap, Stephen B.;
Davies, David L.;
Macnicol, Ann M.;
Dominiczak, Anna F.;
Fraser, Robert;
Wright, Alan F.;
Watson, Michael L.;
Briggs, I. Douglas

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

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

Identification of a 5′ splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3).

Published in:

Human Mutation, 1999, v. 13, n. 2, p. 141, doi. 10.1002/(SICI)1098-1004(1999)13:2<141::AID-HUMU6>3.0.CO;2-Q

By:

Dry, Katherine L.;
Manson, Forbes D.C.;
Lennon, Alan;
Bergen, Arthur A.B.;
Van Dorp, Dieuwke B.;
Wright, Alan F.

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

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.

Published in:

Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0414-4

By:

Nagy, Reka;
Boutin, Thibaud S.;
Marten, Jonathan;
Huffman, Jennifer E.;
Kerr, Shona M.;
Campbell, Archie;
Evenden, Louise;
Gibson, Jude;
Amador, Carmen;
Howard, David M.;
Navarro, Pau;
Morris, Andrew;
Deary, Ian J.;
Hocking, Lynne J.;
Padmanabhan, Sandosh;
Smith, Blair H.;
Joshi, Peter;
Wilson, James F.;
Hastie, Nicholas D.;
Wright, Alan F.

Publication type:

Article

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.

Published in:

BMC Genetics, 2007, v. 8, p. 43, doi. 10.1186/1471-2156-8-43

By:

Harris, Sarah E;
Fox, Helen;
Wright, Alan F;
Hayward, Caroline;
Starr, John M;
Whalley, Lawrence J;
Deary, Ian J

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

Organic carbon, total carbon, and total nitrogen determinations in soils of variable calcium carbonate contents using a Leco CN-2000 dry combustion analyzer.

Published in:

Communications in Soil Science & Plant Analysis, 2001, v. 32, n. 19/20, p. 3243, doi. 10.1081/CSS-120001118

By:

Wright, Alan F.;
Bailey, John S.

Publication type:

Article

Cognitive change and the APOE ε4 allele.

Published in:

Nature, 2002, v. 418, n. 6901, p. 932, doi. 10.1038/418932a

By:

Deary, Ian J.;
Whiteman, Martha C.;
Pattie, Alison;
Starr, John M.;
Hayward, Caroline;
Wright, Alan F.;
Carothers, Andrew;
Whalley, Lawrence J.

Publication type:

Article

Short cut to disease genes.

Published in:

Nature, 2001, v. 414, n. 6865, p. 705, doi. 10.1038/414705a

By:

Wright, Alan F.;
Van Heyningen, Veronica

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 myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.

Published in:

Nature Communications, 2015, v. 6, n. 3, p. 6689, doi. 10.1038/ncomms7689

By:

Miyake, Masahiro;
Yamashiro, Kenji;
Tabara, Yasuharu;
Suda, Kenji;
Morooka, Satoshi;
Nakanishi, Hideo;
Khor, Chiea-Chuen;
Chen, Peng;
Qiao, Fan;
Nakata, Isao;
Akagi-Kurashige, Yumiko;
Gotoh, Norimoto;
Tsujikawa, Akitaka;
Meguro, Akira;
Kusuhara, Sentaro;
Polasek, Ozen;
Hayward, Caroline;
Wright, Alan F.;
Campbell, Harry;
Richardson, Andrea J.

Publication type:

Article

Inference of identity by descent in population isolates and optimal sequencing studies.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1140, doi. 10.1038/ejhg.2012.307

By:

Glodzik, Dominik;
Navarro, Pau;
Vitart, Veronique;
Hayward, Caroline;
McQuillan, Ruth;
Wild, Sarah H;
Dunlop, Malcolm G;
Rudan, Igor;
Campbell, Harry;
Haley, Chris;
Wright, Alan F;
Wilson, James F;
McKeigue, Paul

Publication type:

Article

Genome-wide analysis of epistasis in body mass index using multiple human populations.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 8, p. 857, doi. 10.1038/ejhg.2012.17

By:

Wei, Wen-Hua;
Hemani, Gib;
Gyenesei, Attila;
Vitart, Veronique;
Navarro, Pau;
Hayward, Caroline;
Cabrera, Claudia P;
Huffman, Jennifer E;
Knott, Sara A;
Hicks, Andrew A;
Rudan, Igor;
Pramstaller, Peter P;
Wild, Sarah H;
Wilson, James F;
Campbell, Harry;
Hastie, Nicholas D;
Wright, Alan F;
Haley, Chris S

Publication type:

Article

No evidence of association between complement factor I genetic variant rs10033900 and age-related macular degeneration.

Published in:

2012

By:

Cipriani, Valentina;
Matharu, Baljinder K;
Khan, Jane C;
Shahid, Humma;
Hayward, Caroline;
Wright, Alan F;
Armbrecht, Ana Maria;
Dhillon, Baljean;
Harding, Simon P;
Bishop, Paul N;
Bunce, Catey;
Clayton, David G;
Moore, Anthony T;
Yates, John RW

Publication type:

Letter

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

Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycome.

Published in:

Epigenetics, 2012, v. 7, n. 2, p. 164, doi. 10.4161/epi.7.2.18918

By:

Zoldoš, Vlatka;
Horvat, Tomislav;
Novokmet, Mislav;
Cuenin, Cyrille;
Mužinić, Ana;
Pučić, Maja;
Huffman, Jennifer E.;
Gornik, Olga;
Polašek, Ozren;
Campbell, Harry;
Hayward, Caroline;
Wright, Alan F.;
Rudan, Igor;
Owen, Katharine;
McCarthy, Mark I.;
Herceg, Zdenko;
Lauc, Gordan

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

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