Works matching AU Farrall, Martin

Results: 65

Robust estimates of heritable coronary disease risk in individuals with type 2 diabetes.

Published in:

Genetic Epidemiology, 2022, v. 46, n. 1, p. 51, doi. 10.1002/gepi.22434

By:

Grace, Christopher;
Hopewell, Jemma C.;
Watkins, Hugh;
Farrall, Martin;
Goel, Anuj

Publication type:

Article

Affected sibpair linkage tests for multiple linked susceptibility genes.

Published in:

Genetic Epidemiology, 1997, v. 14, n. 2, p. 103, doi. 10.1002/(SICI)1098-2272(1997)14:2<103::AID-GEPI1>3.0.CO;2-8

By:

Farrall, Martin

Publication type:

Article

European rational approach for the genetics of diabetic complications EURAGEDIC: patient populations and strategy.

Published in:

Nephrology Dialysis Transplantation, 2008, v. 23, n. 1, p. 161

By:

Lise Tarnow;
Per-Henrik Groop;
Samy Hadjadj;
Gbenga Kazeem;
Francois Cambien;
Michel Marre;
Carol Forsblom;
Hans-Henrik Parving;
David TrÃ©gouÃ«t;
Alexandre ThÃ©vard;
Martin Farrall;
Ivo Gut;
Dominique Gauguier;
Roger Cox;
Fumihiko Matsuda;
Mark Lathrop;
Nathalie Vionnet;
for the EURAGEDIC Consortium

Publication type:

Article

Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 2, p. 221, doi. 10.1038/sj.ejhg.5201732

By:

Barlera, Simona;
Specchia, Claudia;
Farrall, Martin;
Chiodini, Benedetta D.;
Franzosi, Maria Grazia;
Rust, Stephan;
Green, Fiona;
Nicolis, Enrico B.;
Peden, John;
Assmann, Gerd;
Collins, Rory;
Hamsten, Anders;
Tognoni, Gianni;
Watkins, Hugh

Publication type:

Article

Measured haplotype analysis of the aldosterone synthase gene and heart size.

Published in:

2005

By:

Mayosi, Bongani M.;
Keavney, Bernard;
Watkins, Hugh;
Farrall, Martin

Publication type:

Correction Notice

Angiotensin I-converting enzyme polymorphisms, ACE level and blood pressure among Nigerians, Jamaicans and African-Americans.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 6, p. 460, doi. 10.1038/sj.ejhg.5201166

By:

Bouzekri, Nourdine;
Xiaofeng Zhu;
Yanming Jiang;
McKenzie, Colin A.;
Luke, Amy;
Forrester, Terrence;
Adeyemo, Adebowale;
Donghui Kan;
Farrall, Martin;
Anderson, Simon;
Cooper, Richard S.;
Ward, Ryk

Publication type:

Article

Measured haplotype analysis of the aldosterone synthase gene and heart size.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 5, p. 395, doi. 10.1038/sj.ejhg.5200967

By:

Mayosi, Bongani M;
Keavney, Bernard;
Watkins, Hugh;
Farrall, Martin

Publication type:

Article

High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 9, p. 553, doi. 10.1038/sj.ejhg.5200847

By:

Soubrier, Florent;
Martin, Sabrina;
Alonso, Amalia;
Visvikis, Sophie;
Tiret, Laurence;
Matsuda, Fumihiko;
Lathrop, G. Mark;
Farrall, Martin

Publication type:

Article

Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2.

Published in:

Annals of Human Genetics, 2014, v. 78, n. 6, p. 434, doi. 10.1111/ahg.12077

By:

Menzel, Stephan;
Rooks, Helen;
Zelenika, Diana;
Mtatiro, Siana N.;
Gnanakulasekaran, Akshala;
Drasar, Emma;
Cox, Sharon;
Liu, Li;
Masood, Mariam;
Silver, Nicholas;
Garner, Chad;
Vasavda, Nisha;
Howard, Jo;
Makani, Julie;
Adekile, Adekunle;
Pace, Betty;
Spector, Tim;
Farrall, Martin;
Lathrop, Mark;
Thein, Swee Lay

Publication type:

Article

Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus.

Published in:

Annals of Human Genetics, 2013, v. 77, n. 6, p. 465, doi. 10.1111/ahg.12034

By:

Terao, Chikashi;
Bayoumi, Nervana;
McKenzie, Colin A.;
Zelenika, Diana;
Muro, Shigeo;
Mishima, Michiaki;
Connell, John M C;
Vickers, Mark A.;
Lathrop, G. Mark;
Farrall, Martin;
Matsuda, Fumihiko;
Keavney, Bernard D.

Publication type:

Article

Bayesian refinement of association signals for 14 loci in 3 common diseases.

Published in:

Nature Genetics, 2012, v. 44, n. 12, p. 1294, doi. 10.1038/ng.2435

By:

Maller, Julian B;
McVean, Gilean;
Byrnes, Jake;
Vukcevic, Damjan;
Palin, Kimmo;
Su, Zhan;
Howson, Joanna M M;
Auton, Adam;
Myers, Simon;
Morris, Andrew;
Pirinen, Matti;
Brown, Matthew A;
Burton, Paul R;
Caulfield, Mark J;
Compston, Alastair;
Farrall, Martin;
Hall, Alistair S;
Hattersley, Andrew T;
Hill, Adrian V S;
Mathew, Christopher G

Publication type:

Article

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.

Published in:

Nature Genetics, 2011, v. 43, n. 4, p. 339, doi. 10.1038/ng.782

By:

Peden, John F;
Hopewell, Jemma C;
Saleheen, Danish;
Chambers, John C;
Hager, Jorg;
Soranzo, Nicole;
Collins, Rory;
Danesh, John;
Elliott, Paul;
Farrall, Martin;
Stirrups, Kathy;
Zhang, Weihua;
Hamsten, Anders;
Parish, Sarah;
Lathrop, Mark;
Watkins, Hugh;
Clarke, Robert;
Deloukas, Panos;
Kooner, Jaspal S;
Goel, Anuj

Publication type:

Article

Genome-wide association study identifies eight loci associated with blood pressure.

Published in:

Nature Genetics, 2009, v. 41, n. 6, p. 666, doi. 10.1038/ng.361

By:

Newton-Cheh, Christopher;
Johnson, Toby;
Gateva, Vesela;
Tobin, Martin D.;
Bochud, Murielle;
Coin, Lachlan;
Najjar, Samer S.;
Jing Hua Zhao;
Heath, Simon C.;
Eyheramendy, Susana;
Papadakis, Konstantinos;
Voight, Benjamin F.;
Scott, Laura J.;
Feng Zhang;
Farrall, Martin;
Tanaka, Toshiko;
Wallace, Chris;
Chambers, John C.;
Kay-Tee Khaw;
Nilsson, Peter

Publication type:

Article

Genome-wide association analysis identifies 20 loci that influence adult height.

Published in:

Nature Genetics, 2008, v. 40, n. 5, p. 575, doi. 10.1038/ng.121

By:

Weedon, Michael N.;
Lango, Hana;
Lindgren, Cecilia M.;
Wallace, Chris;
Evans, David M.;
Mangino, Massimo;
Freathy, Rachel M.;
Perry, John R. B.;
Stevens, Suzanne;
Hall, Alistair S.;
Samani, Nilesh J.;
Shields, Beverly;
Prokopenko, Inga;
Farrall, Martin;
Dominiczak, Anna;
Johnson, Toby;
Bergmann, Sven;
Beckmann, Jacques S.;
Vollenweider, Peter;
Waterworth, Dawn M.

Publication type:

Article

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

Published in:

Nature Genetics, 2007, v. 39, n. 10, p. 1197, doi. 10.1038/ng2108

By:

Menzel, Stephan;
Garner, Chad;
Gut, Ivo;
Matsuda, Fumihiko;
Yamaguchi, Masao;
Heath, Simon;
Foglio, Mario;
Zelenika, Diana;
Boland, Anne;
Rooks, Helen;
Best, Steve;
Spector, Tim D.;
Farrall, Martin;
Lathrop, Mark;
Thein, Swee Lay

Publication type:

Article

A genome-wide association study of global gene expression.

Published in:

Nature Genetics, 2007, v. 39, n. 10, p. 1202, doi. 10.1038/ng2109

By:

Dixon, Anna L.;
Liming Liang;
Moffatt, Miriam F.;
Wei Chen;
Heath, Simon;
Wong, Kenny C. C.;
Taylor, Jenny;
Burnett, Edward;
Gut, Ivo;
Farrall, Martin;
Lathrop, G. Mark;
Abecasis, Gonçalo R.;
Cookson, William O. C.

Publication type:

Article

Fine-mapping of an ancestral recombination breakpoint in DCP1.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 270, doi. 10.1038/15449

By:

Farrall, Martin;
Keavney, Bernard;
McKenzie, Colin;
Delépine, Marc;
Matsuda, Fumihiko;
Lathrop, G. Mark

Publication type:

Article

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations.

Published in:

PLoS Genetics, 2009, v. 5, n. 6, p. 1, doi. 10.1371/journal.pgen.1000504

By:

Kolz, Melanie;
Johnson, Toby;
Sanna, Serena;
Teumer, Alexander;
Vitart, Veronique;
Perola, Markus;
Mangino, Massimo;
Albrecht, Eva;
Wallace, Chris;
Farrall, Martin;
Johansson, Åsa;
Nyholt, Dale R.;
Aulchenko, Yurii;
Beckmann, Jacques S.;
Bergmann, Sven;
Bochud, Murielle;
Brown, Morris;
Campbell, Harry;
Connell, John;
Dominiczak, Anna

Publication type:

Article

Genome-Wide Mapping of Susceptibility to Coronary Artery Disease Identifies a Novel Replicated Locus on Chromosome 17.

Published in:

PLoS Genetics, 2006, v. 2, n. 5, p. e72, doi. 10.1371/journal.pgen.0020072

By:

Farrall, Martin;
Green, Fiona R.;
Peden, John F.;
Olsson, Per G.;
Clarke, Robert;
Hellenius, Mai-Lis;
Rust, Stephan;
Lagercrantz, Jacob;
Franzosi, Maria Grazia;
Schulte, Helmut;
Carey, Alisoun;
Olsson, Gunnar;
Assmann, Gerd;
Tognoni, Gianni;
Collins, Rory;
Hamsten, Anders;
Watkins, Hugh

Publication type:

Article

Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.

Published in:

2017

By:

Manousaki, Despoina;
Paternoster, Lavinia;
Standl, Marie;
Moffatt, Miriam F.;
Farrall, Martin;
Bouzigon, Emmanuelle;
Strachan, David P.;
Demenais, Florence;
Lathrop, Mark;
Cookson, William O. C. M.;
Richards, J. Brent

Publication type:

journal article

SLC2A9 Is a High-Capacity Urate Transporter in Humans.

Published in:

PLoS Medicine, 2008, v. 5, n. 10, p. 1509, doi. 10.1371/journal.pmed.0050197

By:

Caulfield, Mark J.;
Munroe, Patricia B.;
O'Neill, Deb;
Witkowska, Kate;
Charchar, Fadi J.;
Doblado, Manuel;
Evans, Sarah;
Eyheramendy, Susana;
Onipinla, Abiodun;
Howard, Philip;
Shaw-Hawkins, Sue;
Dobson, Richard J.;
Wallace, Chris;
Newhouse, Stephen J.;
Brown, Morris;
Connell, John M.;
Dominiczak, Anna;
Farrall, Martin;
Lathrop, G. Mark;
Samani, Nilesh J.

Publication type:

Article

Quantitative Trait Genetic Linkage Analysis of Body Mass Index in Familial Coronary Artery Disease.

Published in:

Human Heredity, 2008, v. 66, n. 1, p. 19, doi. 10.1159/000114162

By:

Specchia, Claudia;
Barlera, Simona;
Chiodini, Benedetta D.;
Nicolis, Enrico B.;
Farrall, Martin;
Peden, John;
Collins, Rory;
Watkins, Hugh;
Tognoni, Gianni;
Franzosi, Maria Grazia

Publication type:

Article

Finding Associations in Dense Genetic Maps: A Genetic Algorithm Approach.

Published in:

Human Heredity, 2005, v. 60, n. 2, p. 97, doi. 10.1159/000088845

By:

Clark, Taane G.;
De Iorio, Maria;
Griffiths, Robert C.;
Farrall, Martin

Publication type:

Article

Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.

Published in:

Human Molecular Genetics, 2021, v. 30, n. 6, p. 500, doi. 10.1093/hmg/ddab002

By:

McGurk, Kathryn A;
Williams, Simon G;
Guo, Hui;
Watkins, Hugh;
Farrall, Martin;
Cordell, Heather J;
Nicolaou, Anna;
Keavney, Bernard D

Publication type:

Article

Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease.

Published in:

JAMA: Journal of the American Medical Association, 2009, v. 302, n. 1, p. 37, doi. 10.1001/jama.2009.954

By:

Elliott, Paul;
Chambers, John C.;
Weihua Zhang;
Clarke, Robert;
Hopewell, Jemma C.;
Peden, John F.;
Erdmann, Jeanette;
Braund, Peter;
Engert, James C.;
Bennett, Derrick;
Coin, Lachlan;
Ashby, Deborah;
Tzoulaki, Ioanna;
Brown, Ian J.;
Mt-Isa, Shahrul;
McCarthy, Mark I.;
Peltonen, Leena;
Freimer, Nelson B.;
Farrall, Martin;
Ruokonen, Aimo

Publication type:

Article

Meta-analysis of gene-level tests for rare variant association.

Published in:

Nature Genetics, 2014, v. 46, n. 2, p. 200, doi. 10.1038/ng.2852

By:

Liu, Dajiang J;
Peloso, Gina M;
Zhan, Xiaowei;
Holmen, Oddgeir L;
Zawistowski, Matthew;
Feng, Shuang;
Nikpay, Majid;
Auer, Paul L;
Goel, Anuj;
Zhang, He;
Peters, Ulrike;
Farrall, Martin;
Orho-Melander, Marju;
Kooperberg, Charles;
McPherson, Ruth;
Watkins, Hugh;
Willer, Cristen J;
Hveem, Kristian;
Melander, Olle;
Kathiresan, Sekar

Publication type:

Article

Large-scale association analysis identifies new risk loci for coronary artery disease.

Published in:

Nature Genetics, 2013, v. 45, n. 1, p. 25, doi. 10.1038/ng.2480

By:

Deloukas, Panos;
Kanoni, Stavroula;
Willenborg, Christina;
Farrall, Martin;
Assimes, Themistocles L;
Thompson, John R;
Ingelsson, Erik;
Saleheen, Danish;
Erdmann, Jeanette;
Goldstein, Benjamin A;
Stirrups, Kathleen;
König, Inke R;
Cazier, Jean-Baptiste;
Johansson, Åsa;
Hall, Alistair S;
Lee, Jong-Young;
Willer, Cristen J;
Chambers, John C;
Esko, Tõnu;
Folkersen, Lasse

Publication type:

Article

Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers.

Published in:

BMC Bioinformatics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12859-019-3201-y

By:

Grace, Christopher;
Farrall, Martin;
Watkins, Hugh;
Goel, Anuj

Publication type:

Article

Mapping of mutation causing Friedreich's ataxia to human chromosome 9.

Published in:

Nature, 1988, v. 334, n. 6179, p. 248, doi. 10.1038/334248a0

By:

Chamberlain, Susan;
Shaw, Jacqui;
Rowland, Alison;
Wallis, Julie;
South, Sally;
Nakamura, Yusuke;
von Gabain, Alexander;
Farrall, Martin;
Williamson, Robert

Publication type:

Article

The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension.

Published in:

International Journal of Epidemiology, 2007, v. 36, n. 6, p. 1356, doi. 10.1093/ije/dym213

By:

Michelle Baker;
Thahira Rahman;
Darroch Hall;
Peter J Avery;
Bongani M Mayosi;
John M C Connell;
Martin Farrall;
Hugh Watkins;
Bernard Keavney

Publication type:

Article

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 806, doi. 10.1093/hmg/ddm352

By:

Broadbent, Helen M.;
Peden, John F.;
Lorkowski, Stefan;
Goel, Anuj;
Ongen, Halit;
Green, Fiona;
Clarke, Robert;
Collins, Rory;
Franzosi, Maria Grazia;
Tognoni, Gianni;
Seedorf, Udo;
Rust, Stephan;
Eriksson, Per;
Hamsten, Anders;
Farrall, Martin;
Watkins, Hugh

Publication type:

Article

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 8, p. 1365, doi. 10.1093/hmg/ddl058

By:

Bell, Jordana Tzenova;
Wallace, Chris;
Dobson, Richard;
Wiltshire, Steven;
Mein, Charles;
Pembroke, Janine;
Brown, Morris;
Clayton, David;
Samani, Nilesh;
Dominiczak, Anna;
Webster, John;
Lathrop, G. Mark;
Connell, John;
Munroe, Patricia;
Caulfield, Mark;
Farrall, Martin

Publication type:

Article

Interpreting gene-association studies.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 17, p. 2489, doi. 10.1093/hmg/ddi253

By:

Farrall, Martin

Publication type:

Article

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 13, p. 1805, doi. 10.1093/hmg/ddi187

By:

Newhouse, Stephen J.;
Wallace, Chris;
Dobson, Richard;
Mein, Charles;
Pembroke, Janine;
Farrall, Martin;
Clayton, David;
Brown, Morris;
Samani, Nilesh;
Dominiczak, Anna;
Connell, John M.;
Webster, John;
Lathrop, G. Mark;
Caulfield, Mark;
Munroe, Patricia B.

Publication type:

Article

Gearing up for genome-wide gene-association studies.

Published in:

Human Molecular Genetics, 2005, v. 14, n. 2, p. r157, doi. 10.1093/hmg/ddi273

By:

Farrall, Martin;
Morris, Andrew P.

Publication type:

Article

Gearing up for genome-wide gene-association studies.

Published in:

Human Molecular Genetics, 2005, v. 14, n. suppl_2, p. R157, doi. 10.1093/hmg/ddi273

By:

Farrall, Martin;
Morris, Andrew P.

Publication type:

Article

Quantitative genetic variation: a post-modern view.

Published in:

Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R1

By:

Farrall, Martin

Publication type:

Article

Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 23, p. 2969, doi. 10.1093/hmg/11.23.2969

By:

Cox, Roger;
Bouzekri, Nourdine;
Martin, Sabrina;
Southam, Lorraine;
Hugill, Alison;
Golamaully, Mahamadee;
Cooper, Richard;
Adeyemo, Adebowale;
Soubrier, Florent;
Ward, Ryk;
Lathrop, G. Mark;
Matsuda, Fumihiko;
Farrall, Martin

Publication type:

Article

Measured haplotype analysis of the angiotensin-I converting enzyme gene.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 11, p. 1745, doi. 10.1093/hmg/7.11.1745

By:

Keavney, Bernard;
McKenzie, Colin A.;
Connell, John M. C.;
Julier, Cécile;
Ratcliffe, Peter J.;
Sobel, Eric;
Lathrop, Mark;
Farrall, Martin

Publication type:

Article

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.

Published in:

2006

By:

Imrie, Helen;
Freel, Marie;
Mayosi, Bongani M;
Davies, Eleanor;
Fraser, Robert;
Ingram, Mary;
Cordell, Heather J;
Farrall, Martin;
Avery, Peter J;
Watkins, Hugh;
Keavney, Bernard;
Connell, John M C

Publication type:

journal article

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.

Published in:

2005

By:

Keavney, Bernard;
Mayosi, Bongani;
Gaukrodger, Nicole;
Imrie, Helen;
Baker, Michelle;
Fraser, Robert;
Ingram, Mary;
Watkins, Hugh;
Farrall, Martin;
Davies, Eleanor;
Connell, John

Publication type:

journal article

Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease.

Published in:

Bioinformatics, 2020, v. 36, n. 2, p. 552, doi. 10.1093/bioinformatics/btz590

By:

Magosi, Lerato E;
Goel, Anuj;
Hopewell, Jemma C;
Farrall, Martin

Publication type:

Article

Genetic susceptibility to coronary artery disease: from promise to progress.

Published in:

Nature Reviews Genetics, 2006, v. 7, n. 3, p. 163, doi. 10.1038/nrg1805

By:

Watkins, Hugh;
Farrall, Martin

Publication type:

Article

Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49961-w

By:

Nethononda, Richard M.;
McGurk, Kathryn A.;
Whitworth, Polly;
Francis, Jane;
Mamasoula, Chysovalanto;
Cordell, Heather J.;
Neubauer, Stefan;
Keavney, Bernard D.;
Mayosi, Bongani M.;
Farrall, Martin;
Watkins, Hugh

Publication type:

Article

Autosomal dominant cerebellar ataxia with dementla: evidence for a fourth disease locus.

Published in:

Human Molecular Genetics, 1994, v. 3, n. 1, p. 177

By:

Twells, Rebecca;
Yenchitsomanus, Pa-Thai;
Sirinavin, Chintanta;
Allotey, Rebecca;
Roungvarin, Niphon;
Viriyavejakul, Adulya;
Cemal, Cemal;
Weber, James;
Farrall, Martin;
Rodprasert, Praklt;
Prayoonwiwat, Naraporn;
Williamson, Robert;
Chamberlain, Susan

Publication type:

Article

Gene targeting for somatic cell manipulation: rapid analysis of reduced chromosome hybrids by Alu-PCR fingerprinting and chromosome painting.

Published in:

Human Molecular Genetics, 1992, v. 1, n. 1, p. 53

By:

Dorin, Julia R.;
Emslie, Elizabeth;
Hanratty, Diane;
Farrall, Martin;
Gosden, John;
J.Porteous, David

Publication type:

Article

Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.

Published in:

Human Mutation, 2009, v. 30, n. 10, p. 1378, doi. 10.1002/humu.21079

By:

Iseri, Sibel Ugur;
Osborne, Robert J.;
Farrall, Martin;
Wyatt, Alexander William;
Mirza, Ghazala;
Nürnberg, Gudrun;
Kluck, Christian;
Herbert, Helen;
Martin, Angela;
Hussain, Muhammad Sajid;
Collin, J. Richard O.;
Lathrop, Mark;
Nürnberg, Peter;
Ragoussis, Jiannis;
Ragge, Nicola K.

Publication type:

Article

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes.

Published in:

Diabetes, 2008, v. 57, n. 10, p. 2843, doi. 10.2337/db08-0073

By:

Trégouet, David-Alexandre;
Groop, Per-Henrik;
McGinn, Steven;
Forsblom, Carol;
Hadjadj, Samy;
Marre, Michel;
Parving, Hans-Henrik;
Tarnow, Lise;
Telgmann, Ralph;
Godefroy, Tiphaine;
Nicaud, Viviane;
Rousseau, Rachel;
Parkkonen, Maikki;
Hoverfält, Anna;
Gut, Ivo;
Heath, Simon;
Matsuda, Fumihiko;
Cox, Roger;
Kazeem, Gbenga;
Farrall, Martin

Publication type:

Article

Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations.

Published in:

Diabetes, 2006, v. 55, n. 11, p. 3166, doi. 10.2337/db06-0271

By:

Vionnet, Nathalie;
Tregouët, David;
Kazeem, Gbenga;
Gut, Ivo;
Groop, Per-Henrik;
Tarnow, Lise;
Parving, Hans-Henrik;
Hadjadj, Samy;
Forsblom, Carol;
Farrall, Martin;
Gauguier, Dominique;
Cox, Roger;
Matsuda, Fumihiko;
Heath, Simon;
Thévard, Alexandre;
Rousseau, Rachel;
Cambien, François;
Marre, Michel;
Lathrop, Mark

Publication type:

Article

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.

Published in:

2005

By:

Baker M;
Gaukrodger N;
Mayosi BM;
Imrie H;
Farrall M;
Watkins H;
Connell JMC;
Avery PJ;
Keavney B;
Baker, Michelle;
Gaukrodger, Nicole;
Mayosi, Bongani M;
Imrie, Helen;
Farrall, Martin;
Watkins, Hugh;
Connell, John M C;
Avery, Peter J;
Keavney, Bernard

Publication type:

journal article