نتائج البحث - "Christopher Grace"

1

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

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

المصدر: Genetic epidemiology. 46(1)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6241b11e89c8372fd6c513e9789bb76cTest
https://pubmed.ncbi.nlm.nih.gov/34672391Test

2

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

المؤلفون: Helgadottir A, Giannakopoulou O, Costanzo Mc, Heribert Schunkert, Giardoglou P, Markus M. Nöthen, Zhou W, Thomas Meitinger, Deepak Atri, Murgia F, Amit Khera, Tao Jiang, Munz M, Jeanette Erdmann, Patrick T. Ellinor, Marju Orho-Melander, Rajat M. Gupta, Kazuyoshi Ishigaki, Satoshi Koyama, Güldener U, Dongkeun Jang, Hilary K. Finucane, George Hindy, George Dedoussis, Cristen J. Willer, Johan L.M. Björkegren, Aris Baras, Marc S. Sabatine, Flannick J, Arno Ruusalepp, Alanna C. Morrison, Danesh J, Christopher P. Nelson, Nicholas A Marston, Thorgeirsson G, Ida Surakka, Sherliker P, Kastrati A, Ibrahim M, Ito K, Robert Clarke, Christopher Grace, Minxian Wang, Boerwinkle E, Haider Smi, Anuj Goel, Ben Michael Brumpton, Lijiang Ma, Sekar Kathiresan, Li L, Pang S, Carolina Roselli, Issei Komuro, de Vries Ps, Kristian Hveem, Hilma Holm, Adam S. Butterworth, Lotta La, Panagiotis Deloukas, Unnur Thorsteinsdottir, Thorsten Kessler, Kamanu Fk, Roberts R, Arnar Do, Tom R. Webb, Ulirsch Jk, Jonas B. Nielsen, Reinberger T, Martin Farrall, Daniel F. Gudbjartsson, Elle M. Weeks, Kari Stefansson, Brooke N. Wolford, Krishna G. Aragam, Hugh Watkins, von Scheidt M, Yoichiro Kamatani, Pierre Zalloua, Christian T. Ruff, Muñoz Venegas L, Iftikhar J. Kullo, Gudmar Thorleifsson, Stavroula Kanoni, Olle Melander, Nilesh J. Samani, Michael R. Brown, Loukianos S. Rallidis, Jemma C. Hopewell, Mucha S

مصطلحات موضوعية: Coronary artery disease, Pathogenesis, medicine, CAD, Genome-wide association study, Vascular proliferation, Computational biology, Biology, Disease pathogenesis, medicine.disease, Gene

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::47d11a72d970014198bb51e68669a88bTest
https://doi.org/10.1101/2021.05.24.21257377Test

3

Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

المؤلفون: David Adlam, Timothy M. Olson, Nicolas Combaret, Jason C. Kovacic, Siiri E. Iismaa, Abtehale Al-Hussaini, Megan M. O'Byrne, Sara Bouajila, Adrien Georges, Ketan Mishra, Peter S. Braund, Valentina d’Escamard, Siying Huang, Marios Margaritis, Christopher P. Nelson, Mariza de Andrade, Daniella Kadian-Dodov, Catherine A. Welch, Stephani Mazurkiewicz, Xavier Jeunemaitre, Claire Mei Yi Wong, Eleni Giannoulatou, Michael Sweeting, David Muller, Alice Wood, Lucy McGrath-Cadell, Diane Fatkin, Sally L. Dunwoodie, Richard Harvey, Cameron Holloway, Jean-Philippe Empana, Xavier Jouven, Jeffrey W. Olin, Rajiv Gulati, Marysia S. Tweet, Sharonne N. Hayes, Nilesh J. Samani, Robert M. Graham, Pascal Motreff, Nabila Bouatia-Naji, Loïc Belle, Patrick Dupouy, Pierre Barnay, Nicolas Meneveau, Martine Gilard, Gilles Rioufol, Grégoire Range, Philippe Brunel, Nicolas Delarche, Emmanuelle Filippi, Louis Le Bivic, Brahim Harbaoui, Hakim Benamer, Guillaume Cayla, Olivier Varenne, Stephane Peggy Manzo-Silberman, Johanne Silvain, Christian Spaulding, Christophe Caussin, Edouard Gerbaud, Yann Valy, René Koning, Thibault Lhermusier, Stanislas Champin, Emmanuel Salengro, Arnaud Fluttaz, Amer Zabalawi, Yves Cottin, Emmanuel Teiger, Christophe Saint-Etienne, Grégory Ducrocq, Stéphanie Marliere, Emmanuel Boiffard, Pierre Aubry, Jean Louis Georges, Didier Bresson, Fabien De Poli, Gaëtan Karrillon, Vincent Roule, Laurent Bali, Mathieu Valla, Antoine Gerbay, David Houpe, Olivier Dubreuil, Arsène Monnier, Norbert Mayaud, Aurélie Manchuelle, Philippe Commeau, Marc Bedossa, Majid Nikpay, Anuj Goel, Hong-Hee Won, Leanne M. Hall, Christina Willenborg, Stavroula Kanoni, Danish Saleheen, Theodosios Kyriakou, Jemma C. Hopewell, Thomas R. Webb, Lingyao Zeng, Abbas Dehghan, Maris Alver, Sebastian M. Armasu, Kirsi Auro, Andrew Bjonnes, Daniel I. Chasman, Shufeng Chen, Ian Ford, Nora Franceschini, Christian Gieger, Christopher Grace, Stefan Gustafsson, Jie Huang, Shih-Jen Hwang, Yun Kyoung Kim, Marcus E. Kleber, King Wai Lau, Xiangfeng Lu, Yingchang Lu, Leo P. Lyytikäinen, Evelin Mihailov, Alanna Morrison, Natalia Pervjakova, Liming Qu, Lynda M. Rose, Elias Salfati, Richa Saxena, Markus Scholz, Albert V. Smith, Emmi Tikkanen, Andre Uitterlinden, Xueli Yang, Weihua Zhang, Wei Zhao, Paul S. de Vries, Natalie R. van Zuydam, Sonia S. Anand, Lars Bertram, Frank Beutner, George Dedoussis, Philippe Frossard, Dominique Gauguier, Alison H. Goodall, Omri Gottesman, Marc Haber, Bok-Ghee Han, Jianfeng Huang, Shapour Jalilzadeh, Thorsten Kessler, Inke R. König, Lars Lannfelt, Wolfgang Lieb, Lars Lind, Cecilia M. Lindgren, Maisa Lokki, Patrik K. Magnusson, Nadeem H. Mallick, Narinder Mehra, Thomas Meitinger, Fazal-ur-Rehman Memon, Andrew P. Morris, Markku S. Nieminen, Nancy L. Pedersen, Annette Peters, Loukianos S. Rallidis, Asif Rasheed, Maria Samuel, Svati H. Shah, Juha Sinisalo, Kathleen E. Stirrups, Stella Trompet, Laiyuan Wang, Khan S. Zaman, Diego Ardissino, Eric Boerwinkle, Ingrid B. Borecki, Erwin P. Bottinger, Julie E. Buring, John C. Chambers, Rory Collins, L Adrienne Cupples, John Danesh, Ilja Demuth, Roberto Elosua, Stephen E. Epstein, Tõnu Esko, Mary F. Feitosa, Oscar H. Franco, Maria Grazia Franzosi, Christopher B. Granger, Dongfeng Gu, Vilmundur Gudnason, Alistair S. Hall, Anders Hamsten, Tamara B. Harris, Stanley L. Hazen, Christian Hengstenberg, Albert Hofman, Erik Ingelsson, Carlos Iribarren, J Wouter Jukema, Pekka J. Karhunen, Bong-Jo Kim, Jaspal S. Kooner, Iftikhar J. Kullo, Terho Lehtimäki, Ruth J. Loos, Olle Melander, Andres Metspalu, Winfried März, Colin N. Palmer, Markus Perola, Thomas Quertermous, Daniel J. Rader, Paul M. Ridker, Samuli Ripatti, Robert Roberts, Veikko Salomaa, Dharambir K. Sanghera, Stephen M. Schwartz, Udo Seedorf, Alexandre F. Stewart, David J. Stott, Joachim Thiery, Pierre A. Zalloua, Christopher J. O'Donnell, Muredach P. Reilly, Themistocles L. Assimes, John R. Thompson, Jeanette Erdmann, Robert Clarke, Hugh Watkins, Sekar Kathiresan, Ruth McPherson, Panos Deloukas, Heribert Schunkert, Martin Farrall

المساهمون: Department of Cardiovascular Sciences, University of Leicester and NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, Mayo Clinic [Rochester], Service de Cardiologie Maladies Vasculaires [CHU Clermont-Ferrand], CHU Gabriel Montpied [Clermont-Ferrand], CHU Clermont-Ferrand-CHU Clermont-Ferrand, Icahn School of Medicine at Mount Sinai [New York] (MSSM), Victor Chang Cardiac Research Institute, University of New South Wales [Sydney] (UNSW), St. Vincent’s Clinical School [Sydney, Australia], UNSW Faculty of Medicine [Sydney], University of New South Wales [Sydney] (UNSW)-University of New South Wales [Sydney] (UNSW), Department of Health Sciences Research [Mayo Clinic] (HSR), Mayo Clinic, Paris-Centre de Recherche Cardiovasculaire (PARCC (UMR_S 970/ U970)), Hôpital Européen Georges Pompidou [APHP] (HEGP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), Université Paris Descartes - Faculté de Médecine (UPD5 Médecine), Université Paris Descartes - Paris 5 (UPD5), Sorbonne Université - Faculté de Médecine (SU FM), Sorbonne Université (SU), Service de génétique [CHU HEGP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Européen Georges Pompidou [APHP] (HEGP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO), Department of Cardiovascular Medicine, Mayo Clinic, Hôpital Universitaire Carémeau [Nîmes] (CHU Nîmes), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)

المصدر: Journal of the American College of Cardiology
Journal of the American College of Cardiology, Elsevier, 2019, 73 (1), pp.58-66. ⟨10.1016/j.jacc.2018.09.085⟩

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Myocardial infarction, Coronary Vessel Anomalies, Fibromuscular dysplasia, 030204 cardiovascular system & hematology, 03 medical and health sciences, 0302 clinical medicine, [SDV.MHEP.CSC]Life Sciences [q-bio]/Human health and pathology/Cardiology and cardiovascular system, Internal medicine, medicine, Prevalence, Fibromuscular Dysplasia, Humans, 030212 general & internal medicine, Vascular Diseases, Artery dissection, MESH: Australia, United Kingdom, USA, Coronary Vessel Anomalies / epidemiology, Endothelin-1 / genetics, Microfilament proteins / genetics, Genetic association, Aged, Endothelin-1, business.industry, Microfilament Proteins, Australia, Cardiovascular disease in women, Middle Aged, medicine.disease, R1, United States, 3. Good health, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Genetic Loci, Case-Control Studies, Cardiology, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Female, France, Cardiology and Cardiovascular Medicine, Scad, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dadef6515e5a6f0d5cee60ad6cf2846Test
https://pure.eur.nl/en/publications/e68967ea-374a-444c-bd31-5a9e71f42f30Test

4

Association analyses based on false discovery rate implicate new loci for coronary artery disease

المؤلفون: Martin Farrall, Themistocles L. Assimes, Florence Lai, Theodosios Kyriakou, Evangelos Evangelou, Winfried März, Emanuele Di Angelantonio, Aroon D. Hingorani, Ruth J. F. Loos, Erik Ingelsson, Colin N. A. Palmer, Tao Jiang, George Dedoussis, Panos Deloukas, Stavroula Kanoni, Pierre Zalloua, Ruth McPherson, Patrick T. Ellinor, Tom R. Webb, Heribert Schunkert, Mar Pujades-Rodriguez, Adnan Kastrati, Eleftheria Zeggini, Riyaz S. Patel, CARDIoGRAMplusC D, Eric E. Schadt, Christopher P. Nelson, Michael J. Sweeting, John Danesh, Bernard Keavney, Paul W. Franks, Jaspal S. Kooner, Robert Clarke, Richard M Cubbon, Yingchang Lu, Raili Ermel, Nilesh J. Samani, Adam S. Butterworth, Anuj Goel, Martin K. Rutter, Dongfeng Gu, Lingyao Zeng, Christopher Grace, Xiangfeng Lu, Ioanna Tzoulaki, Andres Metspalu, John C. Chambers, Amand F. Schmidt, Johan L.M. Björkegren, Hugh Watkins, Erwin P. Bottinger, Olga Giannakopoulou, Maciej Tomaszewski, Arno Ruusalepp, Stephen E. Hamby, Jemma C. Hopewell, Ioanna Ntalla, Kamal Alghalayini, Joanna M. M. Howson, Eirini Marouli, Thorsten Kessler, Terho Lehtimäki, Jeanette Erdmann

المساهمون: Butterworth, Adam [0000-0002-6915-9015], Di Angelantonio, Emanuele [0000-0001-8776-6719], Howson, Joanna [0000-0001-7618-0050], Sweeting, Michael [0000-0003-0980-8965], Danesh, John [0000-0003-1158-6791], Apollo - University of Cambridge Repository

المصدر: Keavney, B, Rutter, M, Tomaszewski, M, EPIC-CVD Consortium, CARDIoGRAMplusC4D & The UK Biobank CardioMetabolic Consortium CHD working group 2017, ' Association analyses based on false discovery rate implicate many new loci for coronary artery disease ', Nature Genetics, vol. 49, pp. 1385–1391 . https://doi.org/10.1038/ng.3913Test

مصطلحات موضوعية: 0301 basic medicine, False discovery rate, UK Biobank CardioMetabolic Consortium CHD working group, Genome-wide association study, Blood vessel morphogenesis, Coronary Artery Disease, 030204 cardiovascular system & hematology, ANNOTATION, Angina, Coronary artery disease, Health Information Systems, 0302 clinical medicine, RARE, Risk Factors, Polymorphism (computer science), GENETIC-VARIANTS, genetics, Genetics & Heredity, Genetics, sequence annotation, 11 Medical And Health Sciences, Phenotype, Medical genetics, LOW-FREQUENCY, Life Sciences & Biomedicine, medicine.medical_specialty, Genotype, DATABASE, Biology, Polymorphism, Single Nucleotide, EPIC-CVD Consortium, 03 medical and health sciences, Meta-Analysis as Topic, medicine, Humans, Genetic Predisposition to Disease, GENOME-WIDE ASSOCIATION, METAANALYSIS, Genetic Association Studies, Genetic association, Science & Technology, Reproducibility of Results, PROFILES, 06 Biological Sciences, medicine.disease, RISK LOCI, United Kingdom, cardiovascular diseases, 030104 developmental biology, ATHEROSCLEROSIS, Genetic Loci, genome-wide association studies, CARDIoGRAMplusC4D, Developmental Biology, Genome-Wide Association Study