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Common variants near TERC are associated with mean telomere length.
Published in:
Nature Genetics, 2010, v. 42, n. 3, p. 197, doi. 10.1038/ng.532
By:
- Codd, Veryan;
- Mangino, Massimo;
- van der Harst, Pim;
- Braund, Peter S.;
- Kaiser, Michael;
- Beveridge, Alan J.;
- Rafelt, Suzanne;
- Moore, Jasbir;
- Nelson, Chris;
- Soranzo, Nicole;
- Guangju Zhai;
- Valdes, Ana M.;
- Blackburn, Hannah;
- Leach, Irene Mateo;
- de Boer, Rudolf A.;
- Goodall, Alison H.;
- Ouwehand, Willem;
- van Veldhuisen, Dirk J.;
- van Gilst, Wiek H.;
- Navis, Gerjan
Publication type:
Article
New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Published in:
Nature Genetics, 2009, v. 41, n. 3, p. 280, doi. 10.1038/ng.307
By:
- Erdmann, Jeanette;
- Groβhennig, Anika;
- Braund, Peter S.;
- König, Inke R.;
- Hengstenberg, Christian;
- Hall, Alistair S.;
- Linsel-Nitschke, Patrick;
- Kathiresan, Sekar;
- Wright, Ben;
- Trögouët, David-Alexandre;
- Cambien, Francois;
- Bruse, Petra;
- Aherrahrou, Zouhair;
- Wagner, Arnika K.;
- Stark, Klaus;
- Schwartz, Stephen M.;
- Salomaa, Veikko;
- Elosua, Roberto;
- Melander, Olle;
- Voight, Benjamin F.
Publication type:
Article
Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.
Published in:
Nature Genetics, 2009, v. 41, n. 3, p. 283, doi. 10.1038/ng.314
By:
- Trégoueët, David-Alexandre;
- König, Inke R.;
- Erdmann, Jeanette;
- Munteanu, Alexandru;
- Braund, Peter S.;
- Hall, Alistair S.;
- Groβhennig, Anika;
- Linsel-Nitschke, Patrick;
- Perret, Claire;
- DeSuremain, Maylis;
- Meitinger, Thomas;
- Wright, Ben J.;
- Preuss, Michael;
- Balmforth, Anthony J.;
- Ball, Stephen G.;
- Meisinger, Christa;
- Germain, Cécile;
- Evans, Alun;
- Arveiler, Dominique;
- Luc, Gérald
Publication type:
Article
Novel Loci Associated with Increased Risk of Sudden Cardiac Death in the Context of Coronary Artery Disease.
Published in:
PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0059905
By:
- Huertas-Vazquez, Adriana;
- Nelson, Christopher P.;
- Guo, Xiuqing;
- Reinier, Kyndaron;
- Uy-Evanado, Audrey;
- Teodorescu, Carmen;
- Ayala, Jo;
- Jerger, Katherine;
- Chugh, Harpriya;
- WTCCC+;
- Braund, Peter S.;
- Deloukas, Panos;
- Hall, Alistair S.;
- Balmforth, Anthony J.;
- Jones, Michelle;
- Taylor, Kent D.;
- Pulit, Sara L.;
- Newton-Cheh, Christopher;
- Gunson, Karen;
- Jui, Jonathan
Publication type:
Article
Large-Scale Candidate Gene Analysis of HDL Particle Features.
Published in:
PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0014529
By:
- Kaess, Bernhard M.;
- Tomaszewski, Maciej;
- Braund, Peter S.;
- Stark, Klaus;
- Rafelt, Suzanne;
- Fischer, Marcus;
- Hardwick, Robert;
- Nelson, Christopher P.;
- Debiec, Radoslaw;
- Huber, Fritz;
- Kremer, Werner;
- Kalbitzer, Hans Robert;
- Rose, Lynda M.;
- Chasman, Daniel I.;
- Hopewell, Jemma;
- Clarke, Robert;
- Burton, Paul R.;
- Tobin, Martin D.;
- Hengstenberg, Christian;
- Samani, Nilesh J.
Publication type:
Article
Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease--A Mendelian Randomisation Study.
Published in:
PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002986
By:
- Linsel-Nitschke, Patrick;
- Götz, Anika;
- Erdmann, Jeanette;
- Braenne, Ingrid;
- Braund, Peter;
- Hengstenberg, Christian;
- Stark, Klaus;
- Fischer, Marcus;
- Schreiber, Stefan;
- El Mokhtari, Nour Eddine;
- Schaefer, Arne;
- Schrezenmeier, Jürgen;
- Rubin, Diana;
- Hinney, Anke;
- Reinehr, Thomas;
- Roth, Christian;
- Ortlepp, Jan;
- Hanrath, Peter;
- Hall, Alistair S.;
- Mangino, Massimo
Publication type:
Article
Polygenic risk score adds to a clinical risk score in the prediction of cardiovascular disease in a clinical setting.
Published in:
European Heart Journal, 2024, v. 45, n. 34, p. 3152, doi. 10.1093/eurheartj/ehae342
By:
- Samani, Nilesh J;
- Beeston, Emma;
- Greengrass, Chris;
- Riveros-McKay, Fernando;
- Debiec, Radoslaw;
- Lawday, Daniel;
- Wang, Qingning;
- Budgeon, Charley A;
- Braund, Peter S;
- Bramley, Richard;
- Kharodia, Shireen;
- Newton, Michelle;
- Marshall, Andrea;
- Krzeminski, Andre;
- Zafar, Azhar;
- Chahal, Anuj;
- Heer, Amadeeep;
- Khunti, Kamlesh;
- Joshi, Nitin;
- Lakhani, Mayur
Publication type:
Article
The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol.
Published in:
Journal of Molecular Medicine, 2008, v. 86, n. 11, p. 1233, doi. 10.1007/s00109-008-0387-2
By:
- Samani, Nilesh;
- Braund, Peter;
- Erdmann, Jeanette;
- Götz, Anika;
- Tomaszewski, Maciej;
- Linsel-Nitschke, Patrick;
- Hajat, Cother;
- Mangino, Massimo;
- Hengstenberg, Christian;
- Stark, Klaus;
- Ziegler, Andreas;
- Caulfield, Mark;
- Burton, Paul;
- Schunkert, Heribert;
- Tobin, Martin
Publication type:
Article
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
Published in:
Journal of Molecular Medicine, 2008, v. 86, n. 10, p. 1163, doi. 10.1007/s00109-008-0376-5
By:
- Wolfgang Lieb;
- Zeller, Tanja;
- Mangino, Massimo;
- Götz, Anika;
- Braund, Peter;
- Wenzel, Juergen;
- Horn, Christian;
- Proust, Carole;
- Linsel-Nitschke, Patrick;
- Amouyel, Philippe;
- Bruse, Petra;
- Arveiler, Dominique;
- König, Inke;
- Ferrières, Jean;
- Ziegler, Andreas;
- Balmforth, Anthony;
- Evans, Alun;
- Ducimetière, Pierre;
- Cambien, Francois;
- Hengstenberg, Christian
Publication type:
Article
Association analysis of IL-12B and IL-23R polymorphisms in myocardial infarction.
Published in:
Journal of Molecular Medicine, 2008, v. 86, n. 1, p. 99, doi. 10.1007/s00109-007-0264-4
By:
- Mangino, Massimo;
- Braund, Peter;
- Singh, Ravi;
- Steeds, Richard;
- Stevens, Suzanne;
- Channer, Kevin S.;
- Samani, Nilesh J.
Publication type:
Article
Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia.
Published in:
European Journal of Human Genetics, 2007, v. 15, n. 3, p. 313, doi. 10.1038/sj.ejhg.5201752
By:
- Nsengimana, Jérémie;
- Samani, Nilesh J.;
- Hall, Alistair S.;
- Balmforth, Anthony J.;
- Mangino, Massimo;
- Yuldasheva, Nadira;
- Maqbool, Azhar;
- Braund, Peter;
- Burton, Paul;
- Bishop, D. Timothy;
- Ball, Stephen G.;
- Barrett, Jennifer H.
Publication type:
Article
Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study.
Published in:
European Heart Journal, 2004, v. 25, n. 6, p. 459, doi. 10.1016/j.ehj.2003.11.014
By:
- Tobin, Martin D;
- Braund, Peter S;
- Burton, Paul R;
- Thompson, John R;
- Steeds, Richard;
- Channer, Kevin;
- Cheng, Suzanne;
- Lindpaintner, Klaus;
- Samani, Nilesh J
Publication type:
Article
A polymorphism of the cholesteryl ester transfer protein gene predicts cardiovascular events in non-smokers in the West of Scotland Coronary Prevention Study.
Published in:
European Heart Journal, 2003, v. 24, n. 20, p. 1833, doi. 10.1016/j.ehj.2003.07.001
By:
- Freeman, Dilys J;
- Samani, Nilesh J;
- Wilson, Valerie;
- McMahon, Alex D;
- Braund, Peter S;
- Cheng, Suzanne;
- Caslake, Muriel J;
- Packard, Chris J;
- Gaffney, Dairena
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
Elucidation of the genetic causes of bicuspid aortic valve disease.
Published in:
Cardiovascular Research, 2023, v. 119, n. 3, p. 857, doi. 10.1093/cvr/cvac099
By:
- Gehlen, Jan;
- Stundl, Anja;
- Debiec, Radoslaw;
- Fontana, Federica;
- Krane, Markus;
- Sharipova, Dinara;
- Nelson, Christopher P;
- Al-Kassou, Baravan;
- Giel, Ann-Sophie;
- Sinning, Jan-Malte;
- Bruenger, Christopher M H;
- Zelck, Carolin F;
- Koebbe, Laura L;
- Braund, Peter S;
- Webb, Thomas R;
- Hetherington, Simon;
- Ensminger, Stephan;
- Fujita, Buntaro;
- Mohamed, Salah A;
- Shrestha, Malakh
Publication type:
Article
Analysis with the exome array identifies multiple new independent variants in lipid loci.
Published in:
Human Molecular Genetics, 2016, v. 25, n. 18, p. 4094, doi. 10.1093/hmg/ddw227
By:
- Kanoni, Stavroula;
- Masca, Nicholas G. D.;
- Stirrups, Kathleen E.;
- Varga, Tibor V.;
- Warren, Helen R.;
- Scott, Robert A.;
- Southam, Lorraine;
- Zhang, Weihua;
- Yaghootkar, Hanieh;
- Müller-Nurasyid, Martina;
- Couto Alves, Alexessander;
- Strawbridge, Rona J.;
- Lataniotis, Lazaros;
- Hashim, Nikman An;
- Besse, Céline;
- Boland, Anne;
- Braund, Peter S.;
- Connell, John M.;
- Dominiczak, Anna;
- Farmaki, Aliki-Eleni
Publication type:
Article
Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.
Published in:
2017
By:
- Khera, Amit V.;
- Hong-Hee Won;
- Peloso, Gina M.;
- O’Dushlaine, Colm;
- Dajiang Liu;
- Stitziel, Nathan O.;
- Natarajan, Pradeep;
- Akihiro Nomura;
- Emdin, Connor A.;
- Gupta, Namrata;
- Borecki, Ingrid B.;
- Asselta, Rosanna;
- Duga, Stefano;
- Merlini, Piera Angelica;
- Correa, Adolfo;
- Kessler, Thorsten;
- Wilson, James G.;
- Bown, Matthew J.;
- Hall, Alistair S.;
- Braund, Peter S.
Publication type:
journal article
Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations.
Published in:
International Journal of Epidemiology, 2008, v. 37, n. 5, p. 1132, doi. 10.1093/ije/dyn091
By:
- Martin D Tobin;
- Mika Kähönen;
- Peter Braund;
- Tuomo Nieminen;
- Cother Hajat;
- Maciej Tomaszewski;
- Jari Viik;
- Rami Lehtinen;
- G Andre Ng;
- Peter W Macfarlane;
- Paul R Burton;
- Terho Lehtimäki;
- Nilesh J Samani
Publication type:
Article
A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 16, p. 2518, doi. 10.1093/hmg/ddn152
By:
- Mangino, Massimo;
- Brouilette, Scott;
- Braund, Peter;
- Tirmizi, Nighat;
- Vasa-Nicotera, Mariuca;
- Thompson, John R.;
- Samani, Nilesh J.
Publication type:
Article
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
Published in:
PLoS Genetics, 2022, v. 18, n. 4, p. 1, doi. 10.1371/journal.pgen.1010068
By:
- Calabrese, Claudia;
- Pyle, Angela;
- Griffin, Helen;
- Coxhead, Jonathan;
- Hussain, Rafiqul;
- Braund, Peter S;
- Li, Linxin;
- Burgess, Annette;
- Munroe, Patricia B;
- Little, Louis;
- Warren, Helen R;
- Cabrera, Claudia;
- Hall, Alistair;
- Caulfield, Mark J;
- Rothwell, Peter M;
- Samani, Nilesh J;
- Hudson, Gavin;
- Chinnery, Patrick F.
Publication type:
Article

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