Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Natalie R van Zuydam"'
Autor:
Makiko Taira, Minako Imamura, Atsushi Takahashi, Yoichiro Kamatani, Toshimasa Yamauchi, Shin-Ichi Araki, Nobue Tanaka, Natalie R van Zuydam, Emma Ahlqvist, Masao Toyoda, Tomoya Umezono, Koichi Kawai, Masahito Imanishi, Hirotaka Watada, Daisuke Suzuki, Hiroshi Maegawa, Tetsuya Babazono, Kohei Kaku, Ryuzo Kawamori, SUMMIT Consortium, Leif C Groop, Mark I McCarthy, Takashi Kadowaki, Shiro Maeda
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0208654 (2018)
To explore novel genetic loci for diabetic nephropathy, we performed genome-wide association studies (GWAS) for diabetic nephropathy in Japanese patients with type 2 diabetes. We analyzed the association of 5,768,242 single nucleotide polymorphisms (
Externí odkaz:
https://doaj.org/article/b7d9dc02c33e497781b39a7048146b3e
Autor:
Tove Fall, Sara Hägg, Reedik Mägi, Alexander Ploner, Krista Fischer, Momoko Horikoshi, Antti-Pekka Sarin, Gudmar Thorleifsson, Claes Ladenvall, Mart Kals, Maris Kuningas, Harmen H M Draisma, Janina S Ried, Natalie R van Zuydam, Ville Huikari, Massimo Mangino, Emily Sonestedt, Beben Benyamin, Christopher P Nelson, Natalia V Rivera, Kati Kristiansson, Huei-Yi Shen, Aki S Havulinna, Abbas Dehghan, Louise A Donnelly, Marika Kaakinen, Marja-Liisa Nuotio, Neil Robertson, Renée F A G de Bruijn, M Arfan Ikram, Najaf Amin, Anthony J Balmforth, Peter S Braund, Alexander S F Doney, Angela Döring, Paul Elliott, Tõnu Esko, Oscar H Franco, Solveig Gretarsdottir, Anna-Liisa Hartikainen, Kauko Heikkilä, Karl-Heinz Herzig, Hilma Holm, Jouke Jan Hottenga, Elina Hyppönen, Thomas Illig, Aaron Isaacs, Bo Isomaa, Lennart C Karssen, Johannes Kettunen, Wolfgang Koenig, Kari Kuulasmaa, Tiina Laatikainen, Jaana Laitinen, Cecilia Lindgren, Valeriya Lyssenko, Esa Läärä, Nigel W Rayner, Satu Männistö, Anneli Pouta, Wolfgang Rathmann, Fernando Rivadeneira, Aimo Ruokonen, Markku J Savolainen, Eric J G Sijbrands, Kerrin S Small, Jan H Smit, Valgerdur Steinthorsdottir, Ann-Christine Syvänen, Anja Taanila, Martin D Tobin, Andre G Uitterlinden, Sara M Willems, Gonneke Willemsen, Jacqueline Witteman, Markus Perola, Alun Evans, Jean Ferrières, Jarmo Virtamo, Frank Kee, David-Alexandre Tregouet, Dominique Arveiler, Philippe Amouyel, Marco M Ferrario, Paolo Brambilla, Alistair S Hall, Andrew C Heath, Pamela A F Madden, Nicholas G Martin, Grant W Montgomery, John B Whitfield, Antti Jula, Paul Knekt, Ben Oostra, Cornelia M van Duijn, Brenda W J H Penninx, George Davey Smith, Jaakko Kaprio, Nilesh J Samani, Christian Gieger, Annette Peters, H Erich Wichmann, Dorret I Boomsma, Eco J C de Geus, TiinaMaija Tuomi, Chris Power, Christopher J Hammond, Tim D Spector, Lars Lind, Marju Orho-Melander, Colin Neil Alexander Palmer, Andrew D Morris, Leif Groop, Marjo-Riitta Järvelin, Veikko Salomaa, Erkki Vartiainen, Albert Hofman, Samuli Ripatti, Andres Metspalu, Unnur Thorsteinsdottir, Kari Stefansson, Nancy L Pedersen, Mark I McCarthy, Erik Ingelsson, Inga Prokopenko, European Network for Genetic and Genomic Epidemiology (ENGAGE) consortium
Publikováno v:
PLoS Medicine, Vol 10, Iss 6, p e1001474 (2013)
BackgroundThe association between adiposity and cardiometabolic traits is well known from epidemiological studies. Whilst the causal relationship is clear for some of these traits, for others it is not. We aimed to determine whether adiposity is caus
Externí odkaz:
https://doaj.org/article/b5132a1a19434786853b884448f17682
Autor:
Xueling Sim, Richard A Jensen, M Kamran Ikram, Mary Frances Cotch, Xiaohui Li, Stuart MacGregor, Jing Xie, Albert Vernon Smith, Eric Boerwinkle, Paul Mitchell, Ronald Klein, Barbara E K Klein, Nicole L Glazer, Thomas Lumley, Barbara McKnight, Bruce M Psaty, Paulus T V M de Jong, Albert Hofman, Fernando Rivadeneira, Andre G Uitterlinden, Cornelia M van Duijn, Thor Aspelund, Gudny Eiriksdottir, Tamara B Harris, Fridbert Jonasson, Lenore J Launer, Wellcome Trust Case Control Consortium, John Attia, Paul N Baird, Stephen Harrap, Elizabeth G Holliday, Michael Inouye, Elena Rochtchina, Rodney J Scott, Ananth Viswanathan, Global BPGen Consortium, Guo Li, Nicholas L Smith, Kerri L Wiggins, Jane Z Kuo, Kent D Taylor, Alex W Hewitt, Nicholas G Martin, Grant W Montgomery, Cong Sun, Terri L Young, David A Mackey, Natalie R van Zuydam, Alex S F Doney, Colin N A Palmer, Andrew D Morris, Jerome I Rotter, E Shyong Tai, Vilmundur Gudnason, Johannes R Vingerling, David S Siscovick, Jie Jin Wang, Tien Y Wong
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65804 (2013)
Narrow arterioles in the retina have been shown to predict hypertension as well as other vascular diseases, likely through an increase in the peripheral resistance of the microcirculatory flow. In this study, we performed a genome-wide association st
Externí odkaz:
https://doaj.org/article/6ccad1da877741939787723ca8571867
Autor:
Emma Ahlqvist, Catherine Godson, Rany M. Salem, Katalin Susztak, Alexander P. Maxwell, Colin N. A. Palmer, Eoin P. Brennan, Matthias Kretzler, Xin Sheng, Jose C. Florez, Robert G. Nelson, Leif Groop, Laura Smyth, Ross Doyle, Natalie R. van Zuydam, Viji Nair, Carol Forsblom, Valma Harjutsalo, Per-Henrik Groop, Gareth J. McKay, Erkka Valo, Darrell Andrews, Helen C. Looker, Mark I. McCarthy, Joel N. Hirschhorn, Niina Sandholm, Hongbo Liu, Damian Fermin, Amy Jayne McKnight, Joanne B. Cole, Emma H. Dahlström
BackgroundDiabetes is the leading cause of kidney disease, and heritability studies demonstrate a substantial, yet poorly understood, contribution of genetics to kidney complications in people with diabetes.MethodsWe performed genome-wide association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b7ffaf330078e25c026fe7cb4822f02
https://doi.org/10.1101/2021.08.27.21262264
https://doi.org/10.1101/2021.08.27.21262264
Autor:
Urmo Võsa, Alexander Kurilshikov, Marije Oosting, Leo A. B. Joosten, Natalie R. van Zuydam, Daisy Jonkers, Jingyuan Fu, Serena Sanna, Zlatan Mujagic, Mark I. McCarthy, Ad A.M. Masclee, Lude Franke, Alexandra Zhernakova, Mihai G. Netea, Cisca Wijmenga, Anubha Mahajan, Arnau Vich Vila
Publikováno v:
Nature Genetics, 51(4), 600-605. Nature Publishing Group
Nature Genetics, 51, 600-605
Nature Genetics, 51, 4, pp. 600-605
Nature Genetics
Nature Genetics, 51, 600-605
Nature Genetics, 51, 4, pp. 600-605
Nature Genetics
Contains fulltext : 202884.pdf (Publisher’s version ) (Closed access) Microbiome-wide association studies on large population cohorts have highlighted associations between the gut microbiome and complex traits, including type 2 diabetes (T2D) and o
Autor:
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
Publikováno v:
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⟩
Journal of the American College of Cardiology, Elsevier, 2019, 73 (1), pp.58-66. ⟨10.1016/j.jacc.2018.09.085⟩
Background: \ud Spontaneous coronary artery dissection (SCAD) is an increasingly recognized cause of acute coronary syndromes (ACS) afflicting predominantly younger to middle-aged women. Observational studies have reported a high prevalence of extrac
Autor:
Natalie R. van Zuydam, Alexander Stiby, Moustafa Abdalla, Erin Austin, Emma H. Dahlström, Stela McLachlan, Efthymia Vlachopoulou, Emma Ahlqvist, Chen Di Liao, Niina Sandholm, Carol Forsblom, Anubha Mahajan, Neil R. Robertson, N. William Rayner, Eero Lindholm, Juha Sinisalo, Markus Perola, Milla Kallio, Emily Weiss, Jackie Price, Andrew Paterson, Barbara Klein, Veikko Salomaa, Colin N.A. Palmer, Per-Henrik Groop, Leif Groop, Mark I. McCarthy, Mariza de Andrade, Andrew P. Morris, Jemma C. Hopewell, Helen M. Colhoun, Iftikhar J. Kullo, Sólveig Grétarsdóttir, Guðmar Þorleifsson, Unnur þorsteinsdóttir, Kari Stefansson, Michael Mark, Timo Kanninen, Barbara Thorand, Giuseppe Remuzzi, David Dunger, Angela Shore, Ulf Smith, Seppo Ylä-Herttuala, Claudio Cobelli, Riccardo Bellazzi, Ele Ferrannini, Carlo Patrono, Pirjo Nuutila, Paul McKeague, Birgit Steckel-Hamann, Li-ming Gan, Everson Nogoceke, Piero Tortoli, Bernd Jablonka, Mary-Julia Brosnan
Publikováno v:
Circulation. Genomic and Precision Medicine
Van Zuydam, N R, Stiby, A, Abdalla, M, Dahlstrom, EH, McLachlan, S, Vlachopoulou, E, Price, J F, Ahlqvist, E, Di Liao, C, Sandholm, N, Forsblom, C, Mahajan, A, Robertson, N R, Rayner, N W, Lindholm, E, Sinisalo, J, Perola, M, Kallio, M, Weiss, E, Paterson, A, Klein, B, Salomaa, V, McCarthy, M, de Andrade, M, Morris, AP, Hopewell, JC, Colhoun, H M & Kullo, IJ 2021, ' A genome-wide association study of peripheral artery disease ', Circulation: Genomic and Precision Medicine . https://doi.org/10.1161/CIRCGEN.119.002862
Circ. Genom. Precis. Med. 14:e002862 (2021)
Circulation: Genomic and Precision Medicine
Van Zuydam, N R, Stiby, A, Abdalla, M, Dahlstrom, EH, McLachlan, S, Vlachopoulou, E, Price, J F, Ahlqvist, E, Di Liao, C, Sandholm, N, Forsblom, C, Mahajan, A, Robertson, N R, Rayner, N W, Lindholm, E, Sinisalo, J, Perola, M, Kallio, M, Weiss, E, Paterson, A, Klein, B, Salomaa, V, McCarthy, M, de Andrade, M, Morris, AP, Hopewell, JC, Colhoun, H M & Kullo, IJ 2021, ' A genome-wide association study of peripheral artery disease ', Circulation: Genomic and Precision Medicine . https://doi.org/10.1161/CIRCGEN.119.002862
Circ. Genom. Precis. Med. 14:e002862 (2021)
Circulation: Genomic and Precision Medicine
Supplemental Digital Content is available in the text.
Background: Peripheral artery disease (PAD) affects >200 million people worldwide and is associated with high mortality and morbidity. We sought to identify genomic variants associated with
Background: Peripheral artery disease (PAD) affects >200 million people worldwide and is associated with high mortality and morbidity. We sought to identify genomic variants associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1331a7c40e7d9286577d43c5d5fbb16a
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-458405
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-458405
Autor:
Natalie R. van Zuydam, Claes Ladenvall, Benjamin F. Voight, Rona J. Strawbridge, Juan Fernandez-Tajes, N. William Rayner, Neil R. Robertson, Anubha Mahajan, Efthymia Vlachopoulou, Anuj Goel, Marcus E. Kleber, Christopher P. Nelson, Lydia Coulter Kwee, Tõnu Esko, Evelin Mihailov, Reedik Mägi, Lili Milani, Krista Fischer, Stavroula Kanoni, Jitender Kumar, Ci Song, Jaana A. Hartiala, Nancy L. Pedersen, Markus Perola, Christian Gieger, Annette Peters, Liming Qu, Sara M. Willems, Alex S.F. Doney, Andrew D. Morris, Yan Zheng, Giorgio Sesti, Frank B. Hu, Lu Qi, Markku Laakso, Unnur Thorsteinsdottir, Harald Grallert, Cornelia van Duijn, Muredach P. Reilly, Erik Ingelsson, Panos Deloukas, Sek Kathiresan, Andres Metspalu, Svati H. Shah, Juha Sinisalo, Veikko Salomaa, Anders Hamsten, Nilesh J. Samani, Winfried März, Stanley L. Hazen, Hugh Watkins, Danish Saleheen, Andrew P. Morris, Helen M. Colhoun, Leif Groop, Mark I. McCarthy, Colin N.A. Palmer, John Danesh, Jeanette Erdmann, Dongfeng Gu, Jaspal S. Kooner, Robert Roberts, Heribert Schunkert, Themistocles L. Assimes, Stefan Blankenberg, Bernhard O. Boehm, John C. Chambers, Robert Clarke, Rory Collins, George Dedoussis, Paul W. Franks, G. Kees Hovingh, Bong-Jo Kim, Terho Lehtimäki, Ruth McPherson, Markku S Nieminen, Christopher O’Donnell, Samuli Ripatti, Manjinder S Sandhu, Stefan Schreiber, Agneta Siegbahn, Cristen J. Willer, Pierre A. Zalloua, Michael Mark, Timo Kanninen, Barbara Thorand, Giuseppe Remuzzi, David Dunger, Angela Shore, Ulf Smith, Per-Henrik Groop, Seppo Ylä-Herttuala, Claudio Cobelli, Riccardo Bellazzi, Ele Ferrannini, Carlo Patrono, Pirjo Nuutila, Paul McKeague, Birgit Steckel-Hamann, Li-ming Gan, Everson Nogoceke, Piero Tortoli, Bernd Jablonka, Mary-Julia Brosnan
Publikováno v:
Circ. Genom. Precis. Med. 13, 640-648 (2020)
Van Zuydam, N R, Ladenvall, C, Voight, B F, Strawbridge, R J, Fernandez-tajes, J, Rayner, N W, Robertson, N R, Mahajan, A, Vlachopoulou, E, Goel, A, Kleber, M E, Nelson, C P, Kwee, L C, Esko, T, Mihailov, E, Mägi, R, Milani, L, Fischer, K, Kanoni, S, Kumar, J, Song, C, Hartiala, J A, Pedersen, N L, Perola, M, Gieger, C, Peters, A, Qu, L, Willems, S M, Doney, A S F, Morris, A P, Zheng, Y, Sesti, G, Hu, F B, Qi, L, Laakso, M, Thorsteinsdottir, U, Grallert, H, Van Duijn, C, Reilly, M P, Ingelsson, E, Deloukas, P, Kathiresan, S, Metspalu, A, Shah, S H, Sinisalo, J, Salomaa, V, Hamsten, A, Samani, N J, März, W, Hazen, S L, Watkins, H, Saleheen, D, Morris, A P, Colhoun, H M, Groop, L, Mccarthy, M I, Palmer, C N A, Danesh, J, Erdmann, J, Gu, D, Kooner, J S, Roberts, R, Schunkert, H, Assimes, T L, Blankenberg, S, Boehm, B O, Chambers, J C, Clarke, R, Collins, R, Dedoussis, G, Franks, P W, Hovingh, G K, Kim, B, Lehtimäki, T, Mcpherson, R, Nieminen, M S, O’donnell, C, Ripatti, S, Sandhu, M S, Schreiber, S, Siegbahn, A, Willer, C J, Zalloua, P A, Mark, M, Kanninen, T, Thorand, B, Remuzzi, G, Dunger, D, Shore, A, Smith, U, Groop, P, Ylä-herttuala, S, Cobelli, C, Bellazzi, R, Ferrannini, E, Patrono, C, Nuutila, P, Mckeague, P, Steckel-hamann, B, Gan, L, Nogoceke, E, Tortoli, P, Jablonka, B & Brosnan, M 2020, ' Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ', Circulation: Genomic and precision medicine, vol. 13, no. 6 . https://doi.org/10.1161/CIRCGEN.119.002769
2020, ' Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ', Circulation: Genomic and Precision Medicine, vol. 13, no. 6, pp. e002769 . https://doi.org/10.1161/CIRCGEN.119.002769
Circulation. Genomic and Precision Medicine
Circulation-Genomic and Precision Medicine, 13(6), 640-648. Lippincott Williams & Wilkins
Van Zuydam, N R, Ladenvall, C, Voight, B F, Strawbridge, R J, Fernandez-tajes, J, Rayner, N W, Robertson, N R, Mahajan, A, Vlachopoulou, E, Goel, A, Kleber, M E, Nelson, C P, Kwee, L C, Esko, T, Mihailov, E, Mägi, R, Milani, L, Fischer, K, Kanoni, S, Kumar, J, Song, C, Hartiala, J A, Pedersen, N L, Perola, M, Gieger, C, Peters, A, Qu, L, Willems, S M, Doney, A S F, Morris, A P, Zheng, Y, Sesti, G, Hu, F B, Qi, L, Laakso, M, Thorsteinsdottir, U, Grallert, H, Van Duijn, C, Reilly, M P, Ingelsson, E, Deloukas, P, Kathiresan, S, Metspalu, A, Shah, S H, Sinisalo, J, Salomaa, V, Hamsten, A, Samani, N J, März, W, Hazen, S L, Watkins, H, Saleheen, D, Morris, A P, Colhoun, H M, Groop, L, Mccarthy, M I, Palmer, C N A, Danesh, J, Erdmann, J, Gu, D, Kooner, J S, Roberts, R, Schunkert, H, Assimes, T L, Blankenberg, S, Boehm, B O, Chambers, J C, Clarke, R, Collins, R, Dedoussis, G, Franks, P W, Hovingh, G K, Kim, B, Lehtimäki, T, Mcpherson, R, Nieminen, M S, O’donnell, C, Ripatti, S, Sandhu, M S, Schreiber, S, Siegbahn, A, Willer, C J, Zalloua, P A, Mark, M, Kanninen, T, Thorand, B, Remuzzi, G, Dunger, D, Shore, A, Smith, U, Groop, P, Ylä-herttuala, S, Cobelli, C, Bellazzi, R, Ferrannini, E, Patrono, C, Nuutila, P, Mckeague, P, Steckel-hamann, B, Gan, L, Nogoceke, E, Tortoli, P, Jablonka, B & Brosnan, M 2020, ' Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ', Circulation: Genomic and precision medicine, vol. 13, no. 6 . https://doi.org/10.1161/CIRCGEN.119.002769
2020, ' Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ', Circulation: Genomic and Precision Medicine, vol. 13, no. 6, pp. e002769 . https://doi.org/10.1161/CIRCGEN.119.002769
Circulation. Genomic and Precision Medicine
Circulation-Genomic and Precision Medicine, 13(6), 640-648. Lippincott Williams & Wilkins
Supplemental Digital Content is available in the text.
Background: Coronary artery disease (CAD) is accelerated in subjects with type 2 diabetes mellitus (T2D). Methods: To test whether this reflects differential genetic influences on CAD risk i
Background: Coronary artery disease (CAD) is accelerated in subjects with type 2 diabetes mellitus (T2D). Methods: To test whether this reflects differential genetic influences on CAD risk i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c110178bdcbf867d2320b1757655095
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60858
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60858
Autor:
David Torrents, Thorkild I. A. Sørensen, André G. Uitterlinden, Dorret I. Boomsma, Harry Campbell, Vasiliki Lagou, Joachim Heinrich, Anna Murray, Nicholas J. Timpson, George Dedoussis, Beverley M. Shields, Timo A. Lakka, Lawrence J. Beilin, Carmen J. Marsit, Katharina E. Schraut, Marie Standl, Torben Hansen, James F. Wilson, Jonas Bacelis, Allan Vaag, Louis J. Muglia, Wei Ang, Josep M. Mercader, Ruifang Li-Gao, Ying Wu, Jessica Tyrrell, Pål R. Njølstad, Mohammad Hadi Zafarmand, Marie-France Hivert, Ioanna Ntalla, Debbie A Lawlor, Martina Müller-Nurasyid, Alana Cavadino, Natalia Vilor-Tejedor, Andrew R. Wood, Zoltán Kutalik, Jodie N. Painter, Tanja G. M. Vrijkotte, Kyle J. Gaulton, Xavier Estivill, George Davey Smith, Christine Power, Andrew T. Hattersley, Berthold Hocher, Gibran Hemani, Sheila J. Barton, Aino-Maija Eloranta, Kathryn L. Lunetta, Kim F. Michaelsen, Frank Geller, Bjarke Feenstra, Carol A. Wang, Peter Vollenweider, Wieland Kiess, Anubha Mahajan, Elina Hyppönen, Elisabeth M. van Leeuwen, Felix R. Day, Natalie R. van Zuydam, Leda Chatzi, Bo L. Chawes, Antje Körner, Dennis O. Mook-Kanamori, Ken K. Ong, Joanne M. Murabito, David M. Hougaard, Jian'an Luan, Letizia Marullo, Catharina E. M. van Beijsterveldt, Yik Ying Teo, Andrew P. Morris, Sarah E. Medland, Juan Fernández-Tajes, Jouke-Jan Hottenga, Frits R. Rosendaal, Inga Prokopenko, Katja Pahkala, Struan F.A. Grant, Sylvain Sebert, Judith B. Borja, Camilla Schmidt Morgen, Charlotta Pisinger, Jia Chen, Øyvind Helgeland, Christian Theil Have, Vincent W. V. Jaddoe, Marjolein N. Kooijman, Mika Kähönen, Timothy M. Frayling, Diana L. Cousminer, Bo Jacobsson, Antoine H. C. van Kampen, Eco J. C. de Geus, Manolis Kogevinas, Rico Rueedi, Grant W. Montgomery, Raimo Joro, Craig E. Pennell, Jonathan P. Bradfield, Janine F. Felix, Ge Zhang, Loreto Santa-Marina, Kalliope Panoutsopoulou, John R. B. Perry, Jeff Murray, Albert Hofman, Terho Lehtimäki, John W. Holloway, Barbera D. C. van Schaik, Pedro Marques-Vidal, Ronny Myhre, Haja N. Kadarmideen, Robert A. Scott, Frank D. Mentch, Katherine S. Ruth, Hans Bisgaard, Marjo-Riitta Järvelin, Catherine Allard, Rachel M. Freathy, Julie A. Marsh, Mariona Bustamante, Elisabeth Thiering, Cæcilie Trier, Marcus A. Tuke, William L. Lowe, Elisabeth Widen, Caroline L Relton, Christoph Reichetzeder, Penelope A. Lind, M. Geoffrey Hayes, Charles Laurin, Tarunveer S. Ahluwalia, Meike Bartels, Mads Melbye, Claudia Langenberg, Ke Hao, Shouneng Peng, Nicholas J. Wareham, Susan M. Ring, Hamdi Mbarek, Mario Murcia, Jing Hua Zhao, Michael Nodzenski, Cornelia M. van Duijn, Hakon Hakonarson, Hanieh Yaghootkar, Po-Ru Loh, Linda S. Adair, Sílvia Bonàs-Guarch, Eleftheria Zeggini, Sarah Metrustry, Shikta Das, Gonneke Willemsen, Ana Espinosa, Lavinia Paternoster, Marc Vaudel, Theresia M. Schnurr, Michael Stumvoll, David M. Evans, Bridget A. Knight, Luigi Bouchard, Robin N Beaumont, Mustafa Atalay, Zhen Qiao, Denise M. Scholtens, Klaus Bønnelykke, Samuel E. Jones, Peter K. Joshi, Oluf Pedersen, Jin-Fang Chai, Fernando Rivadeneira, Leo-Pekka Lyytikäinen, Rebecca K. Vinding, Hazel Inskip, Sara M. Willems, Cilius Esmann Fonvig, Momoko Horikoshi, Ellen A. Nohr, Jani Heikkinen, Emil V. R. Appel, Niels Grarup, Michael N. Weedon, Rebecca C Richmond, Peter Kovacs, Jorma Viikari, Amanda J. Bennett, Jens-Christian Holm, Carolina Medina-Gomez, Nicole M. Warrington, Anke Tönjes, Jakob Stokholm, Hugoline G. de Haan, Seang-Mei Saw, Ville Huikari, N. William Rayner, Johan G. Eriksson, Niina Pitkänen, Allan Linneberg, Gunn-Helen Moen, Olli T. Raitakari, Martine Vrijheid, Neil Robertson, Stefan Johansson, Tim D. Spector, Friman Sánchez, Mark I. McCarthy, Harri Niinikoski, Karen L. Mohlke
Publikováno v:
Warrington, N M, Beaumont, R N, Horikoshi, M, Day, F R, Helgeland, Ø, Laurin, C, Bacelis, J, Peng, S, Hao, K, Feenstra, B, Wood, A R, Mahajan, A, Tyrrell, J, Robertson, N R, Rayner, N W, Qiao, Z, Moen, G-H, Vaudel, M, Marsit, C J, Chen, J, Nodzenski, M, Schnurr, T M, Zafarmand, M H, Bradfield, J P, Grarup, N, Kooijman, M N, Li-Gao, R, Geller, F, Ahluwalia, T S, Paternoster, L, Rueedi, R, Huikari, V, Hottenga, J-J, Lyytikäinen, L-P, Cavadino, A, Metrustry, S, Cousminer, D L, Wu, Y, Thiering, E, Wang, C A, Have, C T, Vilor-Tejedor, N, Joshi, P K, Painter, J N, Ntalla, I, Myhre, R, Pitkänen, N, van Leeuwen, E M, Joro, R, Lagou, V, Richmond, R C, Espinosa, A, Barton, S J, Inskip, H M, Holloway, J W, Marina, L S, Estivill, X, Ang, W, Marsh, J A, Reichetzeder, C, Marullo, L, Hocher, B, Lunetta, K L, Murabito, J M, Relton, C L, Kogevinas, M, Chatzi, L, Allard, C, Bouchard, L, Hivert, M-F, Zhang, G, Muglia, L J, Heikkinen, J, Morgen, C S, van Kampen, A H C, van Schaik, B D C, Mentch, F D, Langenberg, C, Luan, J, Scott, R A, Zhao, J H, Hemani, G, Ring, S M, Bennett, A J, Gaulton, K J, Fernandez-Tajes, J, van Zuydam, N R, Medina-Gomez, C, de Haan, H G, Rosendaal, F R, Kutalik, Z, Marques-Vidal, P, Das, S, Willemsen, G, Mbarek, H, Müller-Nurasyid, M, Standl, M, Appel, E V R, Fonvig, C E, Trier, C, van Beijsterveldt, C E M, Murcia, M, Bustamante, M, Bonas-Guarch, S, Hougaard, D M, Mercader, J M, Linneberg, A, Schraut, K, Lind, P A, Medland, S E, Shields, B M, Knight, B A, Chai, J-F, Panoutsopoulou, K, Bartels, M, Sánchez, F, Stokholm, J, Torrents, D, Vinding, R K, Willems, S M, Atalay, M, Chawes, B L, Kovacs, P, Prokopenko, I, Tuke, M A, Yaghootkar, H, Ruth, K S, Jones, S E, Loh, P-R, Murray, A, Weedon, M N, Tönjes, A, Stumvoll, M, Michaelsen, K F, Eloranta, A-M, Lakka, T A, van Duijn, C M, Kiess, W, Körner, A, Niinikoski, H, Pahkala, K, Raitakari, O T, Jacobsson, B, Zeggini, E, Dedoussis, G V, Teo, Y Y, Saw, S M, Montgomery, G W, Campbell, H, Wilson, J F, Vrijkotte, T G M, Vrijheid, M, de Geus, E J C N, Hayes, M G, Kadarmideen, H N, Holm, J-C, Beilin, L J, Pennell, C E, Heinrich, J, Adair, L S, Borja, J B, Mohlke, K L, Eriksson, J G, Widén, E, Hattersley, A T, Spector, T D, Kähönen, M, Viikari, J S, Lehtimäki, T, Boomsma, D I, Sebert, S, Vollenweider, P, Sørensen, T I A, Bisgaard, H, Bønnelykke, K, Murray, J C, Melbye, M, Nohr, E A, Mook-Kanamori, D O, Rivadeneira, F, Hofman, A, Felix, J F, Jaddoe, V W V, Hansen, T, Pisinger, C, Vaag, A A, Pedersen, O, Uitterlinden, A G, Järvelin, M-R, Power, C, Hyppönen, E, Scholtens, D M, Lowe Jr, W L, Smith, G D, Timpson, N J, Morris, A P, Wareham, N J, Hakonarson, H, Grant, S F A, Frayling, T M, Lawlor, D A, Njølstad, P R, Johansson, S, Ong, K K, McCarthy, M I, Perry, J R B & Evans, D M & Freathy, R M 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804–814 . https://doi.org/10.1038/s41588-019-0403-1
Warrington, N M, Li-Gao, R, Hottenga, J J, Willemsen, G, Mbarek, H, van Beijsterveldt, C E M, Bartels, M, de Geus, E J C N, Boomsma, D I, Freathy, R M & EGG Consortium 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. MAY, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Nature Genetics, 51(MAY), 804-814. Nature Publishing Group
Warrington, N M, Beaumont, R N, Horikoshi, M, Day, F R, Helgeland, Ø, Laurin, C, Bacelis, J, Peng, S, Hao, K, Feenstra, B, Wood, A R, Mahajan, A, Tyrrell, J, Robertson, N R, Rayner, N W, Qiao, Z, Moen, G H, Vaudel, M, Marsit, C J, Chen, J, Nodzenski, M, Schnurr, T M, Zafarmand, M H, Bradfield, J P, Grarup, N, Kooijman, M N, Li-Gao, R, Geller, F, Ahluwalia, T S, Paternoster, L, Rueedi, R, Huikari, V, Hottenga, J J, Lyytikäinen, L P, Cavadino, A, Metrustry, S, Cousminer, D L, Wu, Y, Thiering, E, Wang, C A, Have, C T, Vilor-Tejedor, N, Joshi, P K, Painter, J N, Ntalla, I, Myhre, R, Morgen, C S, Fonvig, C E, Nohr, E A, Hansen, T & EGG Consortium 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Nature Genetics, 51(5), 804
Warrington, N M, Beaumont, R N, Horikoshi, M, Day, F R, Helgeland, Ø, Laurin, C, Bacelis, J, Peng, S, Hao, K, Feenstra, B, Wood, A R, Mahajan, A, Tyrrell, J, Robertson, N R, Rayner, N W, Qiao, Z, Moen, G-H, Vaudel, M, Marsit, C J, Chen, J J J, Nodzenski, M, Schnurr, T M, Zafarmand, M H, Bradfield, J P, Grarup, N, Kooijman, M N, Li-Gao, R, Geller, F, Ahluwalia, T S, Paternoster, L, Rueedi, R, Huikari, V, Hottenga, J-J, Lyytikäinen, L-P, Cavadino, A, Metrustry, S, Cousminer, D L, Wu, Y, Thiering, E, Wang, C A, Have, C T, Vilor-Tejedor, N, Joshi, P K, Painter, J N, Ntalla, I, Myhre, R, Pitkänen, N, van Leeuwen, E M, Joro, R, Lagou, V, Richmond, R C, Espinosa, A, Barton, S J, Inskip, H M, Holloway, J W, Santa-Marina, L, Estivill, X, Ang, W, Marsh, J A, Reichetzeder, C, Marullo, L, Hocher, B, Lunetta, K L, Murabito, J M, Relton, C L, Kogevinas, M, Chatzi, L, Allard, C, Bouchard, L, Hivert, M-F, Zhang, G, Muglia, L J, Heikkinen, J, Consortium, EGG, Morgen, C S, van Kampen, A H C, van Schaik, B D C, Mentch, F D, Langenberg, C, Luan, J, Scott, R A, Zhao, J H, Hemani, G, Ring, S M, Bennett, A J, Gaulton, K J, Fernandez-Tajes, J, van Zuydam, N R, Medina-Gomez, C, de Haan, H G, Rosendaal, F R, Kutalik, Z, Marques-Vidal, P, Das, S, Willemsen, G, Mbarek, H, Müller-Nurasyid, M, Standl, M, Appel, E V R, Fonvig, C E, Trier, C, van Beijsterveldt, C E M, Murcia, M, Bustamante, M, Bonas-Guarch, S, Hougaard, D M, Mercader, J M, Linneberg, A, Schraut, K E, Lind, P A, Medland, S E, Shields, B M, Knight, B A, Chai, J-F, Panoutsopoulou, K, Bartels, M, Sánchez, F, Stokholm, J, Torrents, D, Vinding, R K, Willems, S M, Atalay, M, Chawes, B L, Kovacs, P, Prokopenko, I, Tuke, M A, Yaghootkar, H, Ruth, K S, Jones, S E, Loh, P-R, Murray, A, Weedon, M N, Tönjes, A, Stumvoll, M, Michaelsen, K F, Eloranta, A-M, Lakka, T A, van Duijn, C M, Kiess, W, Körner, A, Niinikoski, H, Pahkala, K, Raitakari, O T, Jacobsson, B, Zeggini, E, Dedoussis, G V, Teo, Y-Y, Saw, S-M, Montgomery, G W, Campbell, H, Wilson, J F, Vrijkotte, T G M, Vrijheid, M, de Geus, E J C N, Hayes, M G, Kadarmideen, H N, Holm, J-C, Beilin, L J, Pennell, C E, Heinrich, J, Adair, L S, Borja, J B, Mohlke, K L, Eriksson, J G, Widén, E E, Hattersley, A T, Spector, T D, Kähönen, M, Viikari, J S, Lehtimäki, T, Boomsma, D I, Sebert, S, Vollenweider, P, Sørensen, T I A, Bisgaard, H F, Bønnelykke, K, Murray, J C, Melbye, M, Nohr, E A, Mook-Kanamori, D O, Rivadeneira, F, Hofman, A, Felix, J F, Jaddoe, V W V, Hansen, T, Pisinger, C, Vaag, A A, Pedersen, O, Uitterlinden, A G, Järvelin, M-R, Power, C, Hyppönen, E, Scholtens, D M, Lowe, W L, Davey Smith, G, Timpson, N J, Morris, A P, Wareham, N J, Hakonarson, H, Grant, S F A, Frayling, T M, Lawlor, D A, Njølstad, P R, Johansson, S, Ong, K K, McCarthy, M I, Perry, J R B, Evans, D M & Freathy, R M 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Nature Genetics, 51(5), 804-814. Nature Publishing Group
Nature Genetics
EGG Consortium & Morris, A P 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
NATURE GENETICS
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Nat. Genet. 51, 804-814 (2019)
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Nature Genetics, 51(5), 804-+. Nature Publishing Group
Nature genetics, 51(5), 804-814. Nature Publishing Group
2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Warrington, N M, Li-Gao, R, Hottenga, J J, Willemsen, G, Mbarek, H, van Beijsterveldt, C E M, Bartels, M, de Geus, E J C N, Boomsma, D I, Freathy, R M & EGG Consortium 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. MAY, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Nature Genetics, 51(MAY), 804-814. Nature Publishing Group
Warrington, N M, Beaumont, R N, Horikoshi, M, Day, F R, Helgeland, Ø, Laurin, C, Bacelis, J, Peng, S, Hao, K, Feenstra, B, Wood, A R, Mahajan, A, Tyrrell, J, Robertson, N R, Rayner, N W, Qiao, Z, Moen, G H, Vaudel, M, Marsit, C J, Chen, J, Nodzenski, M, Schnurr, T M, Zafarmand, M H, Bradfield, J P, Grarup, N, Kooijman, M N, Li-Gao, R, Geller, F, Ahluwalia, T S, Paternoster, L, Rueedi, R, Huikari, V, Hottenga, J J, Lyytikäinen, L P, Cavadino, A, Metrustry, S, Cousminer, D L, Wu, Y, Thiering, E, Wang, C A, Have, C T, Vilor-Tejedor, N, Joshi, P K, Painter, J N, Ntalla, I, Myhre, R, Morgen, C S, Fonvig, C E, Nohr, E A, Hansen, T & EGG Consortium 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Nature Genetics, 51(5), 804
Warrington, N M, Beaumont, R N, Horikoshi, M, Day, F R, Helgeland, Ø, Laurin, C, Bacelis, J, Peng, S, Hao, K, Feenstra, B, Wood, A R, Mahajan, A, Tyrrell, J, Robertson, N R, Rayner, N W, Qiao, Z, Moen, G-H, Vaudel, M, Marsit, C J, Chen, J J J, Nodzenski, M, Schnurr, T M, Zafarmand, M H, Bradfield, J P, Grarup, N, Kooijman, M N, Li-Gao, R, Geller, F, Ahluwalia, T S, Paternoster, L, Rueedi, R, Huikari, V, Hottenga, J-J, Lyytikäinen, L-P, Cavadino, A, Metrustry, S, Cousminer, D L, Wu, Y, Thiering, E, Wang, C A, Have, C T, Vilor-Tejedor, N, Joshi, P K, Painter, J N, Ntalla, I, Myhre, R, Pitkänen, N, van Leeuwen, E M, Joro, R, Lagou, V, Richmond, R C, Espinosa, A, Barton, S J, Inskip, H M, Holloway, J W, Santa-Marina, L, Estivill, X, Ang, W, Marsh, J A, Reichetzeder, C, Marullo, L, Hocher, B, Lunetta, K L, Murabito, J M, Relton, C L, Kogevinas, M, Chatzi, L, Allard, C, Bouchard, L, Hivert, M-F, Zhang, G, Muglia, L J, Heikkinen, J, Consortium, EGG, Morgen, C S, van Kampen, A H C, van Schaik, B D C, Mentch, F D, Langenberg, C, Luan, J, Scott, R A, Zhao, J H, Hemani, G, Ring, S M, Bennett, A J, Gaulton, K J, Fernandez-Tajes, J, van Zuydam, N R, Medina-Gomez, C, de Haan, H G, Rosendaal, F R, Kutalik, Z, Marques-Vidal, P, Das, S, Willemsen, G, Mbarek, H, Müller-Nurasyid, M, Standl, M, Appel, E V R, Fonvig, C E, Trier, C, van Beijsterveldt, C E M, Murcia, M, Bustamante, M, Bonas-Guarch, S, Hougaard, D M, Mercader, J M, Linneberg, A, Schraut, K E, Lind, P A, Medland, S E, Shields, B M, Knight, B A, Chai, J-F, Panoutsopoulou, K, Bartels, M, Sánchez, F, Stokholm, J, Torrents, D, Vinding, R K, Willems, S M, Atalay, M, Chawes, B L, Kovacs, P, Prokopenko, I, Tuke, M A, Yaghootkar, H, Ruth, K S, Jones, S E, Loh, P-R, Murray, A, Weedon, M N, Tönjes, A, Stumvoll, M, Michaelsen, K F, Eloranta, A-M, Lakka, T A, van Duijn, C M, Kiess, W, Körner, A, Niinikoski, H, Pahkala, K, Raitakari, O T, Jacobsson, B, Zeggini, E, Dedoussis, G V, Teo, Y-Y, Saw, S-M, Montgomery, G W, Campbell, H, Wilson, J F, Vrijkotte, T G M, Vrijheid, M, de Geus, E J C N, Hayes, M G, Kadarmideen, H N, Holm, J-C, Beilin, L J, Pennell, C E, Heinrich, J, Adair, L S, Borja, J B, Mohlke, K L, Eriksson, J G, Widén, E E, Hattersley, A T, Spector, T D, Kähönen, M, Viikari, J S, Lehtimäki, T, Boomsma, D I, Sebert, S, Vollenweider, P, Sørensen, T I A, Bisgaard, H F, Bønnelykke, K, Murray, J C, Melbye, M, Nohr, E A, Mook-Kanamori, D O, Rivadeneira, F, Hofman, A, Felix, J F, Jaddoe, V W V, Hansen, T, Pisinger, C, Vaag, A A, Pedersen, O, Uitterlinden, A G, Järvelin, M-R, Power, C, Hyppönen, E, Scholtens, D M, Lowe, W L, Davey Smith, G, Timpson, N J, Morris, A P, Wareham, N J, Hakonarson, H, Grant, S F A, Frayling, T M, Lawlor, D A, Njølstad, P R, Johansson, S, Ong, K K, McCarthy, M I, Perry, J R B, Evans, D M & Freathy, R M 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Nature Genetics, 51(5), 804-814. Nature Publishing Group
Nature Genetics
EGG Consortium & Morris, A P 2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
NATURE GENETICS
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Nat. Genet. 51, 804-814 (2019)
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Nature Genetics, 51(5), 804-+. Nature Publishing Group
Nature genetics, 51(5), 804-814. Nature Publishing Group
2019, ' Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors ', Nature Genetics, vol. 51, no. 5, pp. 804-814 . https://doi.org/10.1038/s41588-019-0403-1
Birth weight (BW) variation is influenced by fetal and maternal genetic and non-genetic factors, and has been reproducibly associated with future cardio-metabolic health outcomes. These associations have been proposed to reflect the lifelong conseque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8d827b8c5a784827a5a5b94b330c98d
https://eprints.soton.ac.uk/430656/
https://eprints.soton.ac.uk/430656/
Autor:
Emma Ahlqvist, Catherine Godson, Darrell Andrews, Per-Henrik Groop, Raimund Weitgasser, Andrzej S. Krolewski, Kristine E. Lee, Lina Radzeviciene, Stuart J. McGurnaghan, Colin N. A. Palmer, Joanne B. Cole, Shelley B. Bull, Andrew P. Boright, Lars Stechemesser, Katalin Susztak, Barbara E.K. Klein, Wei-Min Chen, Kerstin Brismar, Carol Forsblom, Jani K. Haukka, Beata Gyorgy, Adam M. Smiles, Jose C. Florez, Harvest F. Gu, Niina Sandholm, Leif Groop, Gareth J. McKay, Maria Hughes, Mark I. McCarthy, Joel N. Hirschhorn, Athina Spiliopoulou, Michael Mauer, Samy Hadjadj, Nicolae Mircea Panduru, Helen M. Colhoun, Jingchuan Guo, Robert G. Nelson, Matthias Kretzler, Valdis Pīrāgs, Marcus G. Pezzolesi, Tarunveer S. Ahluwalia, Rasa Verkauskiene, Michel Marre, Linda T. Hiraki, Janet K. Snell-Bergeon, Bernhard Paulweber, Stephen S. Rich, Erkka Valo, Chen Di Liao, David M. Maahs, Vita Rovīte, Rachel G. Miller, Eoin P. Brennan, Peter Rossing, Natalie R. van Zuydam, Maria Luiza Caramori, Jan Skupien, Rany M. Salem, A. Peter Maxwell, Paul M. McKeigue, Maria Lajer, Gianpaolo Zerbini, Chengxiang Qiu, David-Alexandre Trégouët, Henrik Falhammar, Jennifer Todd, Rajasree Menon, Jelizaveta Sokolovska, Valma Harjutsalo, Anna Möllsten, Ronald Klein, Xiaoyu Gao, Viji Nair, Jihwan Park, Amy Jayne McKnight, Jing Jing Cao, Silvia Maestroni, Edita Prakapiene, Ian H. de Boer, Finian Martin, Andrew D. Paterson, Suna Onengut-Gumuscu, Ross Doyle, Hyun Min Kang, Angelo J. Canty, Andrew C. Liu, Tina Costacou, Carine M. Boustany-Kari
Publikováno v:
Salem, R M, Todd, J N, Sandholm, N, Rossing, P, Rich, S S, Hirschhorn, J N, Florez, J C & SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium 2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology, vol. 30, no. 10, pp. 2000-2016 . https://doi.org/10.1681/ASN.2019030218
2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology . https://doi.org/10.1681/ASN.2019030218
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium, Kretzler, M, Susztak, K, Colhoun, H M, Krolewski, A S, Paterson, A D, Groop, P-H, Rich, S S, Hirschhorn, J N & Florez, J C 2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology, vol. 30, no. 10, pp. 2000-2016 . https://doi.org/10.1681/ASN.2019030218
J Am Soc Nephrol
2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology . https://doi.org/10.1681/ASN.2019030218
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium, Kretzler, M, Susztak, K, Colhoun, H M, Krolewski, A S, Paterson, A D, Groop, P-H, Rich, S S, Hirschhorn, J N & Florez, J C 2019, ' Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen ', Journal of the American Society of Nephrology, vol. 30, no. 10, pp. 2000-2016 . https://doi.org/10.1681/ASN.2019030218
J Am Soc Nephrol
BACKGROUND: Although diabetic kidney disease demonstrates both familial clustering and single nucleotide polymorphism heritability, the specific genetic factors influencing risk remain largely unknown.METHODS: To identify genetic variants predisposin
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https://curis.ku.dk/portal/da/publications/genomewide-association-study-of-diabetic-kidney-disease-highlights-biology-involved-in-glomerular-basement-membrane-collagen(b30453e6-4f70-4b36-83fd-2afa1bcee756).html