Søgeresultater - Ralph McGinnis
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Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease af Samani Nj, Panos Deloukas, J. Erdmann, Christian Hengstenberg, Kari Kuulasmaa, Ralph McGinnis, Heribert Schunkert, Nicole Soranzo, John R. Thompson, Laurence Tiret, Andreas Ziegler
Udgivet 2009Artigo -
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Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia af Isabel Benzel, Aruna T. Bansal, Brian L. Browning, N. W. Galwey, Peter R. Maycox, Ralph McGinnis, Devi H. Smart, David St Clair, Phillip A. Yates, Ian J. Purvis
Udgivet 2007Artigo -
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A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose af Fumihiko Takeuchi, Ralph McGinnis, Stéphane Bourgeois, C. Barnes, Niclas Eriksson, Nicole Soranzo, Pamela Whittaker, Venkatesh Ranganath, Vasudev Kumanduri, William McLaren, Lennart Holm, Jonatan D. Lindh, Anders Rane, Mia Wadelius, Panos Deloukas
Udgivet 2009Artigo -
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Vitamin D and risk of pregnancy related hypertensive disorders: mendelian randomisation study af Maria C. Magnus, Kozeta Miliku, Anna E. Bauer, Stephanie M. Engel, Janine F. Felix, Vincent W. V. Jaddoe, Debbie A. Lawlor, Stephanie J. London, Per Magnus, Ralph McGinnis, Wenche Nystad, Christian M. Page, Fernando Rivadeneira, Lars C. Stene, German Tapia, Nicholas Williams, Carolina Bonilla, Abigail Fraser
Udgivet 2018Artigo -
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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 af David A. van Heel, Lude Franke, Karen A. Hunt, Rhian Gwilliam, Alexandra Zhernakova, Michael Inouye, Martin C. Wapenaar, Martin Barnardo, Graeme Bethel, Geoffrey Holmes, C. Feighery, Derek P. Jewell, Dermot Kelleher, Parveen Kumar, Simon Travis, Julian R.F. Walters, David S. Sanders, P D Howdle, Jill Swift, Raymond J. Playford, William McLaren, M. Luisa Mearin, Chris J. Mulder, Ross McManus, Ralph McGinnis, Lon R. Cardon, Panos Deloukas, Cisca Wijmenga
Udgivet 2007Artigo -
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Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease af Heribert Schunkert, Anika Götz, Peter S. Braund, Ralph McGinnis, David‐Alexandre Trégouët, Massimo Mangino, Patrick Linsel‐Nitschke, François Cambien, Christian Hengstenberg, Klaus Stark, Stefan Blankenberg, Laurence Tiret, Pierre Ducimetière, Andrew Keniry, Mohammed J. R. Ghori, Stefan Schreiber, Nour Eddine El Mokhtari, Alistair S. Hall, Richard J. Dixon, Alison H. Goodall, Henrike Liptau, Helen Perlstein Pollard, Dániel Schwarz, Ludwig A. Hothorn, H.‐Erich Wichmann, Inke R. König, Marcus Fischer, Christa Meisinger, Willem H. Ouwehand, Panos Deloukas, John R. Thompson, Jeanette Erdmann, Andreas Ziegler, Nilesh J. Samani
Udgivet 2008Revisão -
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Newly identified genetic risk variants for celiac disease related to the immune response af Karen A. Hunt, Alexandra Zhernakova, Graham Turner, Graham Heap, Lude Franke, Marcel Bruinenberg, Jihane Romanos, Lotte C. Dinesen, Anthony W. Ryan, Davinder Panesar, Rhian Gwilliam, Fumihiko Takeuchi, William McLaren, Geoffrey Holmes, P D Howdle, Julian R.F. Walters, David S. Sanders, Raymond J. Playford, Gosia Trynka, Chris J. Mulder, M. Luisa Mearin, Wieke H.M. Verbeek, Valerie Trimble, Fiona Stevens, Colm O’Morain, Nicholas Kennedy, Dermot Kelleher, Daniel J. Pennington, David P. Strachan, Wendy L. McArdle, Charles A. Mein, Martin C. Wapenaar, Panos Deloukas, Ralph McGinnis, Ross McManus, Cisca Wijmenga, David A. van Heel
Udgivet 2008Artigo -
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Integrating common and rare genetic variation in diverse human populations af David Altshuler, Richard A Gibbs, Leena Peltonen, David Altshuler, Richard A Gibbs, Leena Peltonen, Emmanouil T. Dermitzakis, S. F. Schaffner, Fuli Yu, Leena Peltonen, Emmanouil T. Dermitzakis, Penelope E. Bonnen, David Altshuler, Richard A Gibbs, Paul I. W. de Bakker, Panos Deloukas, Stacey B. Gabriel, Rhian Gwilliam, Sarah Hunt, Michael Inouye, Xiaoming Jia, Aarno Palotie, Melissa Parkin, Pamela Whittaker, Fuli Yu, Kyle Chang, Alicia Hawes, Lora Lewis, Yanru Ren, David A. Wheeler, Richard A. Gibbs, Donna M. Muzny, C. Barnes, Katayoon Darvishi, Matthew E. Hurles, Joshua M. Korn, Kati Kristiansson, Charles Lee, Steven A. McCarrol, James Nemesh, Emmanouil T. Dermitzakis, Alon Keinan, Stephen B. Montgomery, Samuela Pollack, Alkes L. Price, Nicole Soranzo, Penelope E. Bonnen, Richard A Gibbs, Claudia Gonzaga‐Jauregui, Alon Keinan, Alkes L. Price, Fuli Yu, Verneri Anttila, Wendy Brodeur, Mark J. Daly, Stephen Leslie, Gil McVean, Loukas Moutsianas, Huy Nguyen, S. F. Schaffner, Qingrun Zhang, Mohammed J. R. Ghori, Ralph McGinnis, William McLaren, Samuela Pollack, Alkes L. Price, S. F. Schaffner, Fumihiko Takeuchi, Sharon R. Grossman, Ilya Shlyakhter, Elizabeth Hostetter, Pardis C. Sabeti, Clement Adebamowo, Morris W. Foster, Deborah R Gordon, Júlio Licinio, María Cristina Manca, Patricia A. Marshall, Ichiro Matsuda, Duncan Ngare, Vivian Ota Wang, Deepa Reddy, Charles N. Rotimi, Charmaine Royal, Richard R. Sharp, Changqing Zeng, Lisa Brooks, Jean E. McEwen
Udgivet 2010Artigo -
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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women af Valgerður Steinthórsdóttir, Ralph McGinnis, Nicholas Williams, Lilja Stefánsdóttir, Guðmar Þorleifsson, Scott Shooter, João Fadista, Jon K. Sigurdsson, Kirsi Auro, Galina Berezina, Maria Carolina Borges, Suzannah Bumpstead, Jonas Bybjerg‐Grauholm, Irina Colgiu, Vivien A. Dolby, Frank Dudbridge, Stephanie M. Engel, Christopher Franklin, Michael L. Frigge, Yr Frisbæk, Reynir Tómas Geirsson, Frank Geller, Sólveig Grétarsdóttir, Daníel F. Guðbjartsson, Quaker E. Harmon, David M. Hougaard, Tatyana Hegay, Anna Helgadóttir, Sigrun Hjartardottir, Tiina Jääskeläinen, Hrefna Johannsdottir, Ingileif Jónsdóttir, Thorhildur Juliusdottir, Noor Kalsheker, A. K. Kasimov, John P. Kemp, Katja Kivinen, Kari Klungsøyr, Wai Lee, Mads Melbye, Zosia Miedzybrodska, Ashley Moffett, Dilbar Najmutdinova, F Nishanova, Thorunn A. Olafsdottir, Markus Perola, Fiona Broughton Pipkin, Lucilla Poston, Gordon Prescott, Saedís Saevarsdóttir, Damilya Salimbayeva, Paula J. Scaife, Line Skotte, Eleonora Staines-Urias, Ólafur Andri Stefánsson, Karina Meden Sørensen, Liv Cecilie Vestrheim Thomsen, Vinicius Tragante, Lill Trogstad, Nigel Simpson, Hannele Laivuori, Seppo Heinonen, Eero Kajantie, Juha Kere, Katja Kivinen, Anneli Pouta, Linda Morgan, Fiona Broughton Pipkin, Noor Kalsheker, James J. Walker, Sheila Macphail, Mark D. Kilby, Marwan Habiba, Catherine Williamson, Kevin M. O’Shaughnessy, Shaughn O’Brien, Alan C. Cameron, Christopher W.G. Redman, Martin Farrall, Mark J. Caulfield, Anna F. Dominiczak, Tamara Aripova, Juan P. Casas, Anna F. Dominiczak, James J. Walker, Unnur Þorsteinsdóttir, Ann‐Charlotte Iversen, Bjarke Feenstra, Debbie A. Lawlor, Heather A. Boyd, Per Magnus, Hannele Laivuori, Nodira Zakhidova, Gulnara Svyatova, Kāri Stefánsson, Linda Morgan
Udgivet 2020Revisão -
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Common variants near MC4R are associated with fat mass, weight and risk of obesity af Ruth J. F. Loos, Cecilia M. Lindgren, Shengxu Li, Eleanor Wheeler, Jing Hua Zhao, Inga Prokopenko, Michael Inouye, Rachel M. Freathy, Antony Attwood, J. Beckmann, Sonja I Berndt, Sven Bergmann, Amanda J. Bennett, Sheila Bingham, Murielle Bochud, Matthew A. Brown, Stéphane Cauchi, John Connell, Cyrus Cooper, George Davey Smith, Ian N.M. Day, Christian Dina, Subhajyoti De, Emmanouil T. Dermitzakis, Alex S. F. Doney, Katherine S. Elliott, Paul Elliott, David M. Evans, I. Sadaf Farooqi, Philippe Froguel, Jilur Ghori, Christopher J. Groves, Rhian Gwilliam, David Hadley, Alistair S. Hall, Andrew T. Hattersley, Johannes Hebebrand, Iris M. Heid, Blanca Herrera, Anke Hinney, Sarah Hunt, Marjo‐Riitta Järvelin, Toby Johnson, Jennifer D M Jolley, Fredrik Karpe, Andrew Keniry, Kay-Tee Khaw, Robert Luben, Massimo Mangino, Jonathan Marchini, Wendy L. McArdle, Ralph McGinnis, Stephen Eyre, Patricia B. Munroe, Andrew D Morris, Andy Ness, Matthew Neville, Alexandra C. Nica, Ken K. Ong, Stephen O’Rahilly, Katharine R. Owen, Colin N. A. Palmer, Konstantinos A. Papadakis, Simon Potter, Anneli Pouta, Lu Qi, Joshua C. Randall, Nigel W. Rayner, Susan M. Ring, Manjinder S. Sandhu, André Scherag, Matthew Sims, Kijoung Song, Nicole Soranzo, Elizabeth K. Speliotes, Holly Syddall, Sarah A. Teichmann, Nicholas J. Timpson, Jonathan H. Tobias, Manuela Uda, Carla Ivane Ganz Vogel, Chris Wallace, Dawn Waterworth, Michael N. Weedon, Cristen J. Willer, Vicki Wraight, Xin Yuan, Eleftheria Zeggini, Joel N. Hirschhorn, David P. Strachan, Willem H. Ouwehand, Mark J. Caulfield, Nilesh J. Samani, Timothy M. Frayling, Péter Vollenweider, Gérard Waeber, Vincent Mooser, Panos Deloukas, Mark I. McCarthy, Nicholas J. Wareham
Udgivet 2008Artigo
Søgeredskaber:
Relaterede emner
Biology
Gene
Genetics
Genotype
Medicine
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Allele
Genetic association
Haplotype
Odds ratio
Atrial fibrillation
CYP2C9
Confidence interval
Disease
Linkage disequilibrium
VKORC1
Warfarin
Body mass index
Case-control study
Coronary artery disease
Gestational hypertension
Locus (genetics)
Obstetrics
Pharmacogenetics
Preeclampsia
Pregnancy
Receptor
SNP