المؤلفون: Speliotes, Elizabeth K, Yerges-Armstrong, Laura M, Wu, Jun, Hernaez, Ruben, Kim, Lauren J, Palmer, Cameron D, Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E, Launer, Lenore J, Nalls, Michael A, Clark, Jeanne M, Mitchell, Braxton D, Shuldiner, Alan R, Butler, Johannah L, Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M, O'Donnell, Christopher J, Sahani, Dushyant V, Salomaa, Veikko, Schadt, Eric E, Schwartz, Stephen M, Siscovick, David S, NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F, Carr, J Jeffrey, Feitosa, Mary F, Harris, Tamara B, Fox, Caroline S, Smith, Albert V, Kao, WH Linda, Hirschhorn, Joel N, Borecki, Ingrid B, GOLD Consortium

المصدر: PLoS genetics. 7(3)

مصطلحات موضوعية: NASH CRN, GIANT Consortium, MAGIC Investigators, GOLD Consortium, Humans, Fatty Liver, Insulin, Lipase, Blood Glucose, Adaptor Proteins, Signal Transducing, Lectins, C-Type, Membrane Proteins, Nerve Tissue Proteins, Tomography, X-Ray Computed, Case-Control Studies, Cohort Studies, Mutation, Missense, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Adult, Aged, Aged, 80 and over, Middle Aged, Male, Genome-Wide Association Study, Chondroitin Sulfate Proteoglycans, Non-alcoholic Fatty Liver Disease, Prevention, Human Genome, Digestive Diseases, Liver Disease, Hepatitis, Chronic Liver Disease and Cirrhosis, Genetics, Clinical Research, 2.1 Biological and endogenous factors, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/5766v2gw

المؤلفون: Asif Rasheed, Mary F. Feitosa, Ian J. Deary, Melissa E. Garcia, Danish Saleheen, Christian Gieger, Andrea Maschio, Lia E. Bang, Cliona Molony, Ivan Brandslund, Dan M. Roden, Ian Ford, Paul M. Ridker, Alisa K. Manning, Giorgio Pistis, Anette Varbo, Alexander P. Reiner, Kathleen Stirrups, David C. Liewald, Tim D. Spector, Paul W. Franks, Cristen J. Willer, Daniel I. Chasman, Jean Ferrières, Vilmundur Gudnason, Tapani Ebeling, Neil Poulter, Magdalena Zoledziewska, Elizabeth K. Speliotes, Eleftheria Zeggini, Megan L. Grove, Hua Tang, Stavroula Kanoni, Peter Weeke, Panos Deloukas, Daniel J. Rader, Amit Khera, Serena Sanna, Dorota Pasko, Gina M. Peloso, Charles Kooperberg, Suthesh Sivapalaratnam, Natalie R. van Zuydam, Christian M. Shaffer, Fredrik Karpe, Naveed Sattar, Pieter Muntendam, Ruth J. F. Loos, Eric Boerwinkle, Wei Gao, Mark J. Caulfield, Matt Neville, Sangeetha Somayajula, Olle Melander, Hayato Tada, Jose M. Ordovas, He Zhang, John D. Rioux, Michael Boehnke, Erwin P. Bottinger, Franco Giulianini, Martina Müller-Nurasyid, Stella Trompet, Connor A. Emdin, Andrew P. Morris, Johanne Marie Justesen, Alan R. Tall, Kari Kuulasmaa, Adam S. Butterworth, Marie-Pierre Dubé, Dajiang J. Liu, Paul L. Auer, Jennifer E. Huffman, Usman Baber, John Danesh, Xiao Wang, Anna F. Dominiczak, Jarmo Virtamo, John M. Starr, Ozren Polasek, Gonçalo R. Abecasis, Timo A. Lakka, Stephen S. Rich, Marco M Ferrario, Marju Orho-Melander, Xueling Sim, Dominique Arveiler, Dermot F. Reilly, Torsten Lauritzen, Gudny Eiriksdottir, Marit E. Jørgensen, Anubha Mahajan, Colin N. A. Palmer, Veikko Salomaa, Nicholas J. Wareham, Dewan S. Alam, Anne Tybjærg-Hansen, Ellen M. Schmidt, Y. Eugene Chen, Heather M. Stringham, Bruce M. Psaty, Christie M. Ballantyne, Nan Wang, Joshua C. Bis, Myriam Fornage, Neil S Zheng, Kristian Hveem, Praveen Surendran, Yingchang Lu, Peter S. Sever, James B. Meigs, Heikki A. Koistinen, Charlotta Pisinger, Tibor V. Varga, Yii-Der Ida Chen, Konstantin Strauch, Timothy M. Frayling, Patricia B. Munroe, Albert V. Smith, Ruth Frikke-Schmidt, Lorraine Southam, Frida Renström, Philippe Amouyel, Nicholas G. D. Masca, Alexessander Couto Alves, Xiangfeng Lu, Andres Metspalu, Anne Langsted, Joanna M. M. Howson, Tamara B. Harris, Leif Groop, Chad A. Cowan, Cramer Christensen, Audrey Y. Chu, Markku Laakso, Torben Hansen, Li-An Lin, John C. Chambers, Jonas B. Nielsen, Niels Grarup, Neil R. Robertson, Kiran Musunuru, Joshua S. Weinstock, Morris J. Brown, Jean-Claude Tardif, Gorm B. Jensen, Jerome I. Rotter, Harald Grallert, Yan Zhang, Kerrin S. Small, Nathan O. Stitziel, Fabio Busonero, Jennifer Wessel, Themistocles L. Assimes, Lenore J. Launer, Lars G. Fritsche, Mark O. Goodarzi, Peter W.F. Wilson, Sekar Kathiresan, Philippe M. Frossard, Emanuele Di Angelantonio, Yanhua Zhou, James G. Wilson, Frank Kee, Scott M. Damrauer, Weihua Zhang, Gail Davies, Oluf Pedersen, Sune F. Nielsen, Alanna C. Morrison, Raquel S. Sevilla, Helen R. Warren, Johanna Kuusisto, Hanieh Yaghootkar, Sandosh Padmanabhan, Philip S. Tsao, Caroline Hayward, Tõnu Esko, Ming Xu, Anders Mälarstig, Anne U. Jackson, Eirini Marouli, Jette Bork-Jensen, Robin Young, C.J. O'Donnell, Yong Huo, Melanie Waldenberger, Jaspal S. Kooner, Pekka Mäntyselkä, Marjo-Riitta Järvelin, Santhi K. Ganesh, Annette Peters, L. Adrienne Cupples, Wei Zhou, Derek Klarin, Markus Perola, Francesco Cucca, Allan Linneberg, Mark I. McCarthy, Joel N. Hirschhorn, Pia R. Kamstrup, Nilesh J. Samani, J. Wouter Jukema, Valentin Fuster, Claudia Langenberg, Roxana Mehran, Børge G. Nordestgaard, Jaakko Tuomilehto, Reedik Mägi, Blair H. Smith, Johanna Jakobsdottir, Marianne Benn, Kent D. Taylor, Ani Manichaikul, Igor Rudan, Aniruddh P. Patel, Joshua C. Denny, Oddgeir L. Holmen, John M. C. Connell, Robert A. Scott, Haojie Yu, Rajiv Chowdhury, Sehrish Jabeen, Antonella Mulas, Aliki-Eleni Farmaki, Rainer Rauramaa, George Dedoussis

المساهمون: Vascular Medicine, Nielsen, Jonas B [0000-0002-6654-2852], Kathiresan, Sekar [0000-0002-6724-032X], Apollo - University of Cambridge Repository, Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)

المصدر: Nature genetics, 49(12), 1758-1766. Nature Publishing Group
NATURE GENETICS
Liu, D J, Peloso, G M, Yu, H, Butterworth, A S, Wang, X, Mahajan, A, Saleheen, D, Emdin, C, Alam, D, Alves, A C, Amouyel, P, Di Angelantonio, E, Arveiler, D, Assimes, T L, Auer, P L, Baber, U, Ballantyne, C M, Bang, L E, Benn, M, Bis, J C, Boehnke, M, Boerwinkle, E, Bork-Jensen, J, Bottinger, E P, Brandslund, I, Brown, M, Busonero, F, Caulfield, M J, Chambers, J C, Chasman, D I, Chen, Y E, Chen, Y-D I, Chowdhury, R, Christensen, C, Chu, A Y, Connell, J M, Cucca, F, Cupples, L A, Damrauer, S M, Davies, G, Deary, I J, Dedoussis, G, Denny, J C, Dominiczak, A, Dubé, M-P, Ebeling, T, Eiriksdottir, G, Hansen, T, Jensen, G B, Jørgensen, M E & Charge Diabetes Working Group 2017, ' Exome-wide association study of plasma lipids in >300,000 individuals ', Nature Genetics, vol. 49, no. 12, pp. 1758–1766 . https://doi.org/10.1038/ng.3977
Nature Genetics
Liu, D J, Peloso, G M, Yu, H, Butterworth, A S, Wang, X, Mahajan, A, Saleheen, D, Emdin, C, Alam, D, Alves, A C, Amouyel, P, Angelantonio, E DI, Arveiler, D, Assimes, T L, Auer, P L, Baber, U, Ballantyne, C M, Bang, L E, Benn, M, Bis, J C, Boehnke, M, Boerwinkle, E, Bork-Jensen, J, Bottinger, E P, Brandslund, I, Brown, M, Busonero, F, Caulfield, M J, Chambers, J C, Chasman, D I, Chen, Y E, Chen, Y D I, Chowdhury, R, Christensen, C, Chu, A Y, Connell, J M, Cucca, F, Cupples, L A, Damrauer, S M, Davies, G, Deary, I J, Dedoussis, G, Denny, J C, Dominiczak, A, Dubé, M P, Ebeling, T, Eiriksdottir, G, Esko, T, Farmaki, A E, Feitosa, M F, Ferrario, M, Ferrieres, J, Ford, I, Fornage, M, Franks, P W, Frayling, T M, Frikke-Schmidt, R, Fritsche, L G, Frossard, P, Fuster, V, Ganesh, S K, Gao, W, Garcia, M E, Gieger, C, Giulianini, F, Goodarzi, M O, Grallert, H, Grarup, N, Groop, L, Grove, M L, Gudnason, V, Hansen, T, Harris, T B, Hayward, C, Hirschhorn, J N, Holmen, O L, Huffman, J, Huo, Y, Hveem, K, Jabeen, S, Jackson, A U, Jakobsdottir, J, Jarvelin, M R, Jensen, G B, Jørgensen, M E, Jukema, J W, Justesen, J M, Kamstrup, P R, Kanoni, S, Karpe, F, Kee, F, Khera, A V, Klarin, D, Koistinen, H A, Kooner, J S, Kooperberg, C, Kuulasmaa, K, Kuusisto, J, Laakso, M, Lakka, T, Langenberg, C, Langsted, A, Launer, L J, Lauritzen, T, MLiewald, D C, Lin, L A, Linneberg, A, Loos, R J F, Lu, Y, Lu, X, Mägi, R, Malarstig, A, Manichaikul, A, Manning, A K, Mäntyselkä, P, Marouli, E, Masca, N G D, Maschio, A, Meigs, J B, Melander, O, Metspalu, A, Morris, A P, Morrison, A C, Mulas, A, Müller-Nurasyid, M, Munroe, P B, Neville, M J, Nielsen, S F, Nielsen, J B, Nordestgaard, B G, Ordovas, J M, Mehran, R, O'Donnell, C J, Orho-Melander, M, Molony, C M, Muntendam, P, Padmanabhan, S, Palmer, C N A, Pasko, D, Patel, A P, Pedersen, O, Perola, M, Peters, A, Pisinger, C, Pistis, G, Polasek, O, Poulter, N, Psaty, B M, Rader, D J, Rasheed, A, Rauramaa, R, Reilly, D F, Reiner, A P, Renström, F, Rich, S S, Ridker, P M, Rioux, J D, Robertson, N R, Roden, D M, Rotter, J I, Rudan, I, Salomaa, V, Samani, N J, Sanna, S, Sattar, N, Schmidt, E M, Scott, R A, Sever, P, Sevilla, R S, Shaffer, C M, Sim, X, Sivapalaratnam, S, Small, K S, Smith, A V, Smith, B H, Somayajula, S, Southam, L, Spector, T D, Speliotes, E K, Starr, J M, Stirrups, K E, Stitziel, N, Strauch, K, Stringham, H M, Surendran, P, Tada, H, Tall, A R, Tang, H, Tardif, J C, Taylor, K D, Trompet, S, Tsao, P S, Tuomilehto, J, Tybjaerg-Hansen, A, Zuydam, N R V, Varbo, A, Varga, T V, Virtamo, J, Waldenberger, M, Wang, N, Wareham, N J, Warren, H R, Weeke, P E, Weinstock, J, Wessel, J, Wilson, J G, Wilson, P W F, Xu, M, Yaghootkar, H, Young, R, Zeggini, E, Zhang, H, Zheng, N S, Zhang, W, Zhang, Y, Zhou, W, Zhou, Y, Zoledziewska, M, Howson, J M M, Danesh, J, McCarthy, M I, Cowan, C A, Abecasis, G, Deloukas, P, Musunuru, K, Willer, C J, Kathiresan, S & V Varga, T 2017, ' Exome-wide association study of plasma lipids in >300,000 individuals ', Nature Genetics, vol. 49, no. 12, pp. 1758-1766 . https://doi.org/10.1038/ng.3977
Liu, D J, Peloso, G M, Yu, H, Butterworth, A S, Wang, X, Mahajan, A, Saleheen, D, Emdin, C, Alam, D, Alves, A C, Amouyel, P, Di Angelantonio, E, Arveiler, D, Assimes, T L, Auer, P L, Baber, U, Ballantyne, C M, Bang, L E, Benn, M, Bis, J C, Boehnke, M, Boerwinkle, E, Bork-jensen, J, Bottinger, E P, Brandslund, I, Brown, M, Busonero, F, Caulfield, M J, Chambers, J C, Chasman, D I, Chen, Y E, Chen, Y I, Chowdhury, R, Christensen, C, Chu, A Y, Connell, J M, Cucca, F, Cupples, L A, Damrauer, S M, Davies, G, Deary, I J, Dedoussis, G, Denny, J C, Dominiczak, A, Dubé, M, Ebeling, T, Eiriksdottir, G, Esko, T, Farmaki, A, Feitosa, M F, Ferrario, M, Ferrieres, J, Ford, I, Fornage, M, Franks, P W, Frayling, T M, Frikke-schmidt, R, Fritsche, L G, Frossard, P, Fuster, V, Ganesh, S K, Gao, W, Garcia, M E, Gieger, C, Giulianini, F, Goodarzi, M O, Grallert, H, Grarup, N, Groop, L, Grove, M L, Gudnason, V, Hansen, T, Harris, T B, Hayward, C, Hirschhorn, J N, Holmen, O L, Huffman, J, Huo, Y, Hveem, K, Jabeen, S, Jackson, A U, Jakobsdottir, J, Jarvelin, M, Jensen, G B, Jørgensen, M E, Jukema, J W, Justesen, J M, Kamstrup, P R, Kanoni, S, Karpe, F, Kee, F, Khera, A V, Klarin, D, Koistinen, H A, Kooner, J S, Kooperberg, C, Kuulasmaa, K, Kuusisto, J, Laakso, M, Lakka, T, Langenberg, C, Langsted, A, Launer, L J, Lauritzen, T, Liewald, D C M, Lin, L A, Linneberg, A, Loos, R J F, Lu, Y, Lu, X, Mägi, R, Malarstig, A, Manichaikul, A, Manning, A K, Mäntyselkä, P, Marouli, E, Masca, N G D, Maschio, A, Meigs, J B, Melander, O, Metspalu, A, Morris, A P, Morrison, A C, Mulas, A, Müller-nurasyid, M, Munroe, P B, Neville, M J, Nielsen, J B, Nielsen, S F, Nordestgaard, B G, Ordovas, J M, Mehran, R, O'donnell, C J, Orho-melander, M, Molony, C M, Muntendam, P, Padmanabhan, S, Palmer, C N A, Pasko, D, Patel, A P, Pedersen, O, Perola, M, Peters, A, Pisinger, C, Pistis, G, Polasek, O, Poulter, N, Psaty, B M, Rader, D J, Rasheed, A, Rauramaa, R, Reilly, D F, Reiner, A P, Renström, F, Rich, S S, Ridker, P M, Rioux, J D, Robertson, N R, Roden, D M, Rotter, J I, Rudan, I, Salomaa, V, Samani, N J, Sanna, S, Sattar, N, Schmidt, E M, Scott, R A, Sever, P, Sevilla, R S, Shaffer, C M, Sim, X, Sivapalaratnam, S, Small, K S, Smith, A V, Smith, B H, Somayajula, S, Southam, L, Spector, T D, Speliotes, E K, Starr, J M, Stirrups, K E, Stitziel, N, Strauch, K, Stringham, H M, Surendran, P, Tada, H, Tall, A R, Tang, H, Tardif, J, Taylor, K D, Trompet, S, Tsao, P S, Tuomilehto, J, Tybjaerg-hansen, A, Van Zuydam, N R, Varbo, A, Varga, T V, Virtamo, J, Waldenberger, M, Wang, N, Wareham, N J, Warren, H R, Weeke, P E, Weinstock, J, Wessel, J, Wilson, J G, Wilson, P W F, Xu, M, Yaghootkar, H, Young, R, Zeggini, E, Zhang, H, Zheng, N S, Zhang, W, Zhang, Y, Zhou, W, Zhou, Y, Zoledziewska, M, Howson, J M M, Danesh, J, Mccarthy, M I, Cowan, C A, Abecasis, G, Deloukas, P, Musunuru, K, Willer, C J & Kathiresan, S 2017, ' Exome-wide association study of plasma lipids in >300,000 individuals ', Nature Genetics, vol. 49, no. 12, pp. 1758–1766 . https://doi.org/10.1038/ng.3977
Nature Genetics, 49(12), 1758
Liu, D J, Peloso, G M, Yu, H, Butterworth, A S, Wang, X, Mahajan, A, Saleheen, D, Emdin, C, Alam, D, Alves, A C, Amouyel, P, Di Angelantonio, E, Arveiler, D, Assimes, T L, Auer, P L, Baber, U, Ballantyne, C M, Bang, L E, Benn, M, Bis, J C, Boehnke, M, Boerwinkle, E, Bork-Jensen, J, Bottinger, E P, Brandslund, I, Brown, M, Busonero, F, Caulfield, M J, Chambers, J C, Chasman, D I, Chen, Y E, Chen, Y-D I, Chowdhury, R, Christensen, C, Chu, A Y, Connell, J M, Cucca, F, Cupples, L A, Damrauer, S M, Davies, G, Grarup, N, Hansen, T, Jørgensen, M E, Lauritzen, T, Lin, L A, Nielsen, J B, Nielsen, S F, Pedersen, O, Pisinger, C, Zhang, Y & Charge Diabetes Working Group 2017, ' Exome-wide association study of plasma lipids in >300,000 individuals ', Nature Genetics, vol. 49, no. 12, pp. 1758-1766 . https://doi.org/10.1038/ng.3977
Nature Genetics, 49(12), 1758-1766. Nature Publishing Group
Nat. Genet. 49, 1758-1766 (2017)
Nature genetics

مصطلحات موضوعية: 0301 basic medicine, Exome/genetics, Genome-wide association study, Type 2 diabetes, Coronary Artery Disease, 030204 cardiovascular system & hematology, Bioinformatics, Charge Diabetes Working Group, Macular Degeneration, chemistry.chemical_compound, 0302 clinical medicine, Risk Factors, Exome, Macular Degeneration/blood, Genetics & Heredity, Genetic Predisposition to Disease/genetics, CLONAL HEMATOPOIESIS, 11 Medical And Health Sciences, CODING-SEQUENCE VARIANTS, Lipids, Phenotype, CARDIOVASCULAR-DISEASE, VA Million Veteran Program, lipids (amino acids, peptides, and proteins), GOLD Consortium, LOW-FREQUENCY, EPIC-InterAct Consortium, Diabetes Mellitus, Type 2/blood, Life Sciences & Biomedicine, Type 2, medicine.medical_specialty, Genotype, APOBEC-1 COMPLEMENTATION FACTOR, Biology, Lower risk, Article, EPIC-CVD Consortium, GENETIC ARCHITECTURE, 03 medical and health sciences, Coronary Artery Disease/blood, Diabetes mellitus, Internal medicine, Genetics, medicine, Diabetes Mellitus, Journal Article, Lipolysis, Humans, Genetic Predisposition to Disease, Allele, TYROSINE KINASE JAK2, Genetic Association Studies, B MESSENGER-RNA, Science & Technology, MACULAR DEGENERATION, MYELOPROLIFERATIVE DISORDERS, Cholesterol, Lipids/blood, Genetic Variation, 06 Biological Sciences, medicine.disease, cardiovascular diseases, genome wide association studies, Genetic Association Studies/methods, 030104 developmental biology, Endocrinology, chemistry, Diabetes Mellitus, Type 2, TM6SF2, Developmental Biology

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http://hdl.handle.net/11383/2098126

المؤلفون: Benjamin Voight, Amelie Bonnefond, Mark Caulfield, Guillaume Pare, Manal Abdelmalek, Eleftheria Zeggini, Jeffrey Schwimmer, Anna Gloyn, Michael Preuss, Åsa Johansson, LAURA CRISPONI, Eco De Geus, Michael Weedon, Jeanne Clark, Joyce Van Meurs, Torben Jørgensen, Kirsi Pietiläinen, Nicole Glazer, Jaakko Kaprio, Alan Shuldiner, Braxton Mitchell, Patricia Munroe, Ozren Polasek, Elisabeth Thiering, Carla Vogel, Jennie Hui, ROBERTO ELOSUA, Amanda Bennett, Yurii Aulchenko, Michael Stumvoll, Andrew Hattersley, Alexander Doney, Peter P Pramstaller, Christian Dina, Lambertus Kiemeney, Sophie Visvikis-Siest, ANGELO SCUTERI, Udo Seedorf, Vilmundur Gudnason, Peter Kraft, Aroon Hingorani, Michael Marmot, Dale Nyholt, Mika Kivimaki, Mary Feitosa, Danielle Posthuma, Claudia Langenberg, Stavroula Kanoni, Mika Kähönen, David Hillman, Lachlan Coin, Eric Brunner, Terho Lehtimäki, Man Li, John Beilby, Peter Visscher, Anette P Gjesing, James Pankow, Ruben Hernaez, Taina Lajunen, Katja Aben, Daniel Witte, Willem Ouwehand, Eleanor Wheeler, Peter Kovacs, Debbie A Lawlor, Kevin Jacobs, Jianjun Liu, Joseph Massaro, Hana Lango Allen, Inga Prokopenko, Rafn Benediktsson, Philippe Froguel, Soumya Raychaudhuri, Cornelia Van Duijn, Annette Peters, Nita Forouhi, Chiara Lanzani, Tonu Esko, Ko Willems van Dijk, Sadaf Farooqi, John Carr, Reedik Mägi, David Melzer, Gerard Waeber, Sutapa Mukherjee, Lyle John Palmer, Francois Pattou, Claes Ohlsson, Perry Elliott, André Scherag, Inke König, Stephen O'rahilly, Thomas Meitinger, Michael Goddard, Lina Zgaga, Robert Weyant, Paul Elliott, Robert Luben, Albert Vernon Smith, MANUELA UDA, Avan Aihie Sayer, Richard Bergman, Gonneke Willemsen, Cecilia Lindgren, Olle Melander, Igor Rudan, Maris Teder-Laving, Hugh Watkins, Ulrich John

المساهمون: Epidemiology, Scherag, Andre (Beitragende*r), Hinney, Anke (Beitragende*r), Scherag, S. (Beitragende*r), Vogel, C. I. (Beitragende*r), Hebebrand, Johannes (Beitragende*r), Functional Genomics, Biological Psychology, Neuroscience Campus Amsterdam - integrative Analysis & Modeling, Neuroscience Campus Amsterdam - Attention & Cognition, EMGO+ - Mental Health, McCarthy, Mark I, Apollo - University of Cambridge Repository, Medical Research Council (MRC), Speliotes, Ek, YERGES ARMSTRONG, Lm, Wu, J, Hernaez, R, Kim, Lj, Palmer, Cd, Gudnason, V, Eiriksdottir, G, Garcia, Me, Launer, Lj, Nalls, Ma, Clark, Jm, Mitchell, Bd, Shuldiner, Ar, Butler, Jl, Tomas, M, Hoffmann, U, Hwang, Sj, Massaro, Jm, O'Donnell, Cj, Sahani, Dv, Salomaa, V, Schadt, Ee, Schwartz, Sm, Siscovick, D, Nash, Crn, Manunta, Paolo, Giant, Consortium, Magic, Investigator, Voight, Bf, Carr, Jj, Feitosa, Mf, Harris, Tb, Fox, C, Smith, Av, Kao, Wh, Hirschhorn, Jn, Borecki, Ib, Gold, Consortium, Hjelt Institute (-2014), Department of Public Health, Institute for Molecular Medicine Finland, Haartman Institute (-2014), Transplantation Laboratory, Genetic Epidemiology, O', Donnell, Cj, Giant, Paolisso, Giuseppe

المصدر: PLoS Genetics (print), 7(3). Public Library of Science
PLoS Genetics, 7(3):e1001324. Public Library of Science
Speliotes, E K, Yerges-Armstrong, L M, Wu, J, Hernaez, R, Kim, L J, Palmer, C D, Gudnason, V, Eiriksdottir, G, Garcia, M E, Launer, L J, Nalls, M A, Clark, J M, Mitchell, B D, Shuldiner, A R, Butler, J L, Tomas, M, Hoffmann, U, Hwang, S J, Massaro, J M, O'Donnell, C J, Sahani, D V, Salomaa, V, Schadt, E E, Schwartz, S M, Siscovick, D S, Posthuma, D, Voight, B F, Carr, J J, Feitosa, M F, Harris, T B, Fox, C S, Smith, A V, Kao, W H L, Hottenga, J J, Willemsen, G, de Geus, E J C, Boomsma, D I, Hirschhorn, J N & Borecki, I B 2011, ' Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits ', PLoS Genetics, vol. 7, no. 3, e1001324 . https://doi.org/10.1371/journal.pgen.1001324
PLoS genetics, vol 7, iss 3
PLoS Genetics, Vol 7, Iss 3, p e1001324 (2011)
PLoS Genetics
PLoS Genetics, 7(3)

مصطلحات موضوعية: Blood Glucose, Male, Netherlands Twin Register (NTR), Cancer Research, Medizin, Genome-wide association study, Hepatitis, Diabetes and Endocrinology/Obesity, Cohort Studies, 0302 clinical medicine, Non-alcoholic Fatty Liver Disease, Lectins, Nonalcoholic fatty liver disease, 80 and over, Insulin, 2.1 Biological and endogenous factors, Aetiology, Tomography, Adaptor Proteins, Signal Transducing/genetics Adult Aged Aged, 80 and over Blood Glucose/analysis Case-Control Studies Chondroitin Sulfate Proteoglycans/genetics Cohort Studies Fatty Liver/*genetics/metabolism/radiography Genome-Wide Association Study Humans Insulin/blood Lectins, C-Type/genetics Lipase/genetics Male Membrane Proteins/genetics Middle Aged Mutation, Missense Nerve Tissue Proteins/genetics Polymorphism, Single Nucleotide Quantitative Trait Loci Tomography, X-Ray Computed, Genetics (clinical), Aged, 80 and over, Genetics, 0303 health sciences, education.field_of_study, Framingham Risk Score, C-Type, Liver Disease, Fatty liver, Adaptor Proteins, Single Nucleotide, Middle Aged, X-Ray Computed, 3. Good health, GOLD Consortium, 030211 gastroenterology & hepatology, Research Article, Adult, lcsh:QH426-470, Quantitative Trait Loci, Chronic Liver Disease and Cirrhosis, Mutation, Missense, genome-wide, fatty liver, metabolic, Nerve Tissue Proteins, Genetics and Genomics/Complex Traits, Biology, Polymorphism, Single Nucleotide, Gastroenterology and Hepatology/Hepatology, MAGIC Investigators, 03 medical and health sciences, Clinical Research, GIANT Consortium, medicine, Humans, Lectins, C-Type, Adiponutrin, NASH CRN, ddc:610, Polymorphism, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Adaptor Proteins, Signal Transducing, Aged, 030304 developmental biology, 0604 Genetics, Genetic heterogeneity, Prevention, Human Genome, Signal Transducing, Membrane Proteins, Lipase, medicine.disease, 3141 Health care science, Fatty Liver, lcsh:Genetics, Chondroitin Sulfate Proteoglycans, Case-Control Studies, Mutation, Missense, Steatosis, Steatohepatitis, Tomography, X-Ray Computed, Digestive Diseases, Neurocan, Genome-Wide Association Study, Developmental Biology

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da6a087b46b57b1d80a3ac0f6f2a0890
https://pure.eur.nl/en/publications/2db8f511-49f4-4120-8115-915411e3636a