Hakutulokset - Hugoline G. de Haan
- Näytetään 1 - 14 yhteensä 14 tuloksesta
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1
Multiple SNP testing improves risk prediction of first venous thrombosis Tekijä Hugoline G. de Haan, Irene D. Bezemer, Carine J.M. Doggen, Saskia le Cessie, Pieter H. Reitsma, André R. Arellano, Carmen H. Tong, James J. Devlin, Lance A. Bare, Frits R. Rosendaal, Carla Y. Vossen
Julkaistu 2012Artigo -
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Assessing the causal relationship between obesity and venous thromboembolism through a Mendelian Randomization study Tekijä Sara Lindström, Marine Germain, Marta Crous‐Bou, Erin N. Smith, Pierre‐Emmanuel Morange, Astrid van Hylckama Vlieg, Hugoline G. de Haan, Daniel I. Chasman, Paul M. Ridker, Jennifer A. Brody, Mariza de Andrade, John A Heit, Weihong Tang, Immaculata De Vivo, Francine Grodstein, Nicholas L. Smith, David‐Alexandre Trégouët, Christopher Kabrhel
Julkaistu 2017Artigo -
3
Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels Tekijä Bengt Sennblad, Saonli Basu, Johanna Mazur, Pierre Suchon, Ángel Martínez-Pérez, Astrid van Hylckama Vlieg, Vinh Trương, Yuhuang Li, Jesper R. Gådin, Weihong Tang, Vera Grossman, Hugoline G. de Haan, Niklas Handin, Angela Silveira, Juan Carlos Souto, Anders Franco‐Cereceda, Pierre‐Emmanuel Morange, France Gagnon, José Manuel Soria, Per Eriksson, Anders Hamsten, Lars Mäegdefessel, Frits R. Rosendaal, Philipp S. Wild, Aaron R. Folsom, David‐Alexandre Trégouët, Maria Sabater‐Lleal
Julkaistu 2016Artigo -
4
A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology Tekijä Paul S. de Vries, Maria Sabater‐Lleal, Jennifer E. Huffman, Jonathan Marten, Ci Song, Nathan Pankratz, Traci M. Bartz, Hugoline G. de Haan, Graciela E. Delgado, John D. Eicher, Ángel Martínez-Pérez, Cavin Ward‐Caviness, Jennifer A. Brody, Ming‐Huei Chen, Moniek P.M. de Maat, Mattias Frånberg, Dipender Gill, Marcus E. Kleber, Fernando Rivadeneira, José Manuel Soria, Weihong Tang, Geoffrey H. Tofler, André G. Uitterlinden, Astrid van Hylckama Vlieg, Sudha Seshadri, Eric Boerwinkle, Neil M Davies, Anne‐Katrin Giese, M. Kamran Ikram, Steven J. Kittner, Barbara McKnight, Bruce M. Psaty, Alex P. Reiner, Muralidharan Sargurupremraj, Kent D. Taylor, Myriam Fornage, Anders Hamsten, Winfried März, Frits R. Rosendaal, Juan Carlos Souto, Abbas Dehghan, Andrew D. Johnson, Alanna C. Morrison, Christopher J. O’Donnell, Nicholas L. Smith
Julkaistu 2019Artigo -
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Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism Tekijä Marine Germain, Daniel I. Chasman, Hugoline G. de Haan, Weihong Tang, Sara Lindström, Lu‐Chen Weng, Mariza de Andrade, Marieke C. Visser, Kerri L. Wiggins, Pierre Suchon, Noémie Saut, David M. Smadja, Grégoire Le Gal, Astrid van Hylckama Vlieg, Antonio Di Narzo, Ke Hao, Christopher P. Nelson, Ares Rocañín-Arjó, Lasse Folkersen, Ramin Monajemi, Lynda M. Rose, Jennifer A. Brody, P. Eline Slagboom, Dylan Aïssi, France Gagnon, Jean‐François Deleuze, Panos Deloukas, Christophe Tzourio, Jean‐François Dartigues, Claudine Berr, Kent D. Taylor, Mete Civelek, Per Eriksson, Bruce M. Psaty, Jeanine Houwing-Duitermaat, Alison H. Goodall, François Cambien, Peter Kraft, Philippe Amouyel, Nilesh J. Samani, Saonli Basu, Paul M. Ridker, Frits R. Rosendaal, Christopher Kabrhel, Aaron R. Folsom, John A. Heit, Pieter H. Reitsma, David‐Alexandre Trégouët, Nicholas L. Smith, Pierre‐Emmanuel Morange
Julkaistu 2015Revisão -
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Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels Tekijä Maria Sabater‐Lleal, Jennifer E. Huffman, Paul S. de Vries, Jonathan Marten, Michael A. Mastrangelo, Ci Song, Nathan Pankratz, Cavin Ward‐Caviness, Lisa R. Yanek, Stella Trompet, Graciela E. Delgado, Xiuqing Guo, Traci M. Bartz, Ángel Martínez-Pérez, Marine Germain, Hugoline G. de Haan, Ayse Bilge Ozel, Ozren Polašek, Albert V. Smith, John D. Eicher, Alex P. Reiner, Weihong Tang, Neil M Davies, David J. Stott, Jerome I. Rotter, Geoffrey H. Tofler, Eric Boerwinkle, Moniek P.M. de Maat, Marcus E. Kleber, Paul Welsh, Jennifer A. Brody, Ming‐Huei Chen, Dhananjay Vaidya, José Manuel Soria, Pierre Suchon, Astrid van Hylckama Vlieg, Karl C. Desch, Ivana Kolčić, Peter K. Joshi, Lenore J. Launer, Tamara B. Harris, Harry Campbell, Igor Rudan, Diane M. Becker, Jun Z. Li, Fernando Rivadeneira, André G. Uitterlinden, Albert Hofman, Oscar H. Franco, Mary Cushman, Bruce M. Psaty, Pierre‐Emmanuel Morange, Barbara McKnight, Michael Chong, Israel Fernández‐Cadenas, Jonathan Rosand, Cecilia M. Lindgren, Vilmundur Guðnason, James F. Wilson, Caroline Hayward, David Ginsburg, Myriam Fornage, Frits R. Rosendaal, Juan Carlos Souto, Lewis C. Becker, Nancy S. Jenny, Winfried März, J. Wouter Jukema, Abbas Dehghan, David‐Alexandre Trégouët, Alanna C. Morrison, Andrew D. Johnson, Christopher J. O’Donnell, David P. Strachan, Charles J. Lowenstein, Nicholas L. Smith
Julkaistu 2019Revisão -
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Directional dominance on stature and cognition in diverse human populations Tekijä Peter K. Joshi, Tõnu Esko, Hannele Mattsson, Niina Eklund, Ilaria Gandin, Teresa Nutile, Anne Jackson, Claudia Schurmann, Albert V. Smith, Weihua Zhang, Yukinori Okada, Alena Stančáková, Jessica D. Faul, Wei Zhao, Traci M. Bartz, Maria Pina Concas, Nora Franceschini, Stefan Enroth, Véronique Vitart, Stella Trompet, Xiuqing Guo, Daniel I. Chasman, Jeffrey R. O’Connel, Tanguy Corre, Suraj S. Nongmaithem, Yuning Chen, Massimo Mangino, Daniela Ruggiero, Michela Traglia, Aliki‐Eleni Farmaki, Tim Kacprowski, Andrew Bjonnes, Ashley van der Spek, Ying Wu, Anil K. Giri, Lisa R. Yanek, Lihua Wang, Edith Hofer, Cornelius A. Rietveld, Olga McLeod, Marilyn C. Cornelis, Cristian Pattaro, Niek Verweij, Clemens Baumbach, Abdel Abdellaoui, Helen R. Warren, Dragana Vuckovic, Hao Mei, Claude Bouchard, John R. B. Perry, Stefania Cappellani, Saira Saeed Mirza, Miles C. Benton, Ulrich Broeckel, Sarah E. Medland, Penelope A. Lind, Giovanni Malerba, Alexander Drong, Loïc Yengo, Lawrence F. Bielak, Degui Zhi, Peter J. van der Most, Daniel Shriner, Reedik Mägi, Gibran Hemani, Tugce Karaderi, Thomas J. Wang, Tian Liu, Ilja Demuth, Jing Hua Zhao, Weihua Meng, Lazaros Lataniotis, Sander W. van der Laan, Jonathan P. Bradfield, Andrew R. Wood, Amélie Bonnefond, Tarunveer S. Ahluwalia, Leanne M. Hall, Erika Salvi, Seyhan Yazar, Lisbeth Carstensen, Hugoline G. de Haan, Mark Abney, Uzma Afzal, Matthew Allison, Najaf Amin, Folkert W. Asselbergs, Stephan J. L. Bakker, R. Graham Barr, Sebastian E. Baumeister, Daniel J. Benjamin, Sven Bergmann, Eric Boerwinkle, Erwin P. Böttinger, Archie Campbell, Aravinda Chakravarti, Yingleong Chan, Stephen J. Chanock, Constance Chen, Y.-D. Ida Chen
Julkaistu 2015Revisão -
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The trans-ancestral genomic architecture of glycemic traits Tekijä Jihua Chen, Cassandra N. Spracklen, Gaëlle Marenne, Arushi Varshney, Laura J. Corbin, Jian’an Luan, Sara M. Willems, Ying Wu, Xiaoshuai Zhang, Momoko Horikoshi, Thibaud Boutin, Reedik Mägi, Johannes Waage, Ruifang Li‐Gao, Kei Hang Katie Chan, Jie Yao, Mila Desi Anasanti, Audrey Y. Chu, Annique Claringbould, Jani Heikkinen, Jaeyoung Hong, Jouke‐Jan Hottenga, Shaofeng Huo, Marika Kaakinen, Tin Louie, Winfried März, Hortensia Moreno-Macías, Anne Ndungu, Sarah C. Nelson, Ilja M. Nolte, Kari E. North, Chelsea K. Raulerson, Debashree Ray, Rebecca Rohde, Denis Rybin, Claudia Schurmann, Xueling Sim, Lorraine Southam, Isobel D. Stewart, Carol A. Wang, Yujie Wang, Peitao Wu, Weihua Zhang, Tarunveer S. Ahluwalia, Emil V. R. Appel, Lawrence F. Bielak, Jennifer A. Brody, Noël P. Burtt, Claudia Cabrera, Brian E. Cade, Jin Fang Chai, Xiaoran Chai, Li-Ching Chang, Chien-Hsiun Chen, Brian H. Chen, Kumaraswamy Naidu Chitrala, Yen‐Feng Chiu, Hugoline G. de Haan, Graciela E. Delgado, Ayşe Demirkan, Qing Duan, Jorgen Engmann, Segun Fatumo, Javier Gayán, Franco Giulianini, Jung Ho Gong, Stefan Gustafsson, Yang Hai, Fernando Pires Hartwig, Jing He, Yoriko Heianza, Tao Huang, Alicia Huerta-Chagoya, Mi Yeong Hwang, Richard A. Jensen, Takahisa Kawaguchi, Katherine A. Kentistou, Young Jin Kim, Marcus E. Kleber, Ishminder K. Kooner, Shuiqing Lai, Leslie A. Lange, Carl D. Langefeld, Marie Lauzon, Man Li, Symen Ligthart, Jun Liu, Marie Loh, Jirong Long, Valeriya Lyssenko, Massimo Mangino, Carola Marzi, May E. Montasser, Abhishek Nag, Masahiro Nakatochi, Damia Noce, Raymond Noordam, Giorgio Pistis, Michael Preuß, Laura M. Raffield
Julkaistu 2021Artigo -
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Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome Tekijä Sarah Stephenson, Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong, Dana E. Alhuzaimi, James J. Dowling, Susan Walker, Kimberly Amburgey, Robin Z. Hayeems, Lance H. Rodan, Marc A. Schwartz, Jonathan Picker, Sally Ann Lynch, Aditi Gupta, Kristen Rasmussen, Lisa A. Schimmenti, Eric W. Klee, Zhiyv Niu, Katherine Agre, Ilana Chilton, Wendy K. Chung, Anya Revah‐Politi, Ping Yee Billie Au, Christopher Griffith, Melissa Racobaldo, Annick Raas‐Rothschild, Bruria Ben Zeev, Ortal Barel, Sébastien Moutton, Fanny Morice‐Picard, Virginie Carmignac, Jenny Cornaton, Nathalie Marle, Orrin Devinsky, Chandler L. Stimach, Stephanie Burns Wechsler, Bryan E. Hainline, Katie Sapp, Marjolaine Willems, Ange‐Line Bruel, Kerith‐Rae Dias, Carey‐Anne Evans, Tony Roscioli, Rani Sachdev, Suzanna E.L. Temple, Ying Zhu, Joshua Baker, Ingrid E. Scheffer, Fiona Gardiner, Amy L. Schneider, Alison M. Muir, Heather C Mefford, Amy Crunk, Elizabeth M. Heise, Francisca Millan, Kristin G. Monaghan, Richard Person, Lindsay Rhodes, Sarah Richards, Ingrid M. Wentzensen, Benjamin Cogné, Bertrand Isidor, Mathilde Nizon, Marie Vincent, Thomas Besnard, Amélie Piton, Carlo Marcelis, Kohji Kato, Norihisa Koyama, Tomoo Ogi, Elaine Goh, Christopher M. Richmond, David J. Amor, Jessica O. Boyce, Angela Morgan, Michael S. Hildebrand, Antony Kaspi, Melanie Bahlo, Rún Friðriksdóttir, Hildigunnur Katrínardóttir, Patrick Sulem, Kāri Stefánsson, Hans T. Björnsson, Simone Mandelstam, Manuela Morleo, Milena Mariani, Marcello Scala, Andrea Accogli, Annalaura Torella, Valeria Capra, Mathew Wallis, Sandra Jansen, Quinten Waisfisz, Hugoline G. de Haan, Simon Sadedin, Sze Chern Lim, Susan M. White, David B. Ascher
Julkaistu 2022Artigo -
10
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors Tekijä Nicole M. Warrington, Robin N. Beaumont, Momoko Horikoshi, Felix R. Day, Øyvind Helgeland, Charles Laurin, Jonas Bacelis, Shouneng Peng, Ke Hao, Bjarke Feenstra, Andrew R. Wood, Anubha Mahajan, Jessica Tyrrell, Neil R. Robertson, Nigel W. Rayner, Zhen Qiao, Gunn-Helen Moen, Marc Vaudel, Carmen J. Marsit, Jia Chen, Michael Nodzenski, Theresia M. Schnurr, Mohammad Hadi Zafarmand, Jonathan P. Bradfield, Niels Grarup, Marjolein N. Kooijman, Ruifang Li‐Gao, Frank Geller, Tarunveer S. Ahluwalia, Lavinia Paternoster, Rico Rueedi, Ville Huikari, Jouke‐Jan Hottenga, Leo‐Pekka Lyytikäinen, Alana Cavadino, Sarah Metrustry, Diana L. Cousminer, Ying Wu, Elisabeth Thiering, Carol A. Wang, Henri Theil, Natàlia Vilor‐Tejedor, Peter K. Joshi, Jodie N. Painter, Ιωάννα Ντάλλα, Ronny Myhre, Niina Pitkänen, Jin‐Moo Lee, Raimo Joro, Vasiliki Lagou, Rebecca C. Richmond, Ana Espinosa, Sheila J. Barton, Hazel Inskip, John W. Holloway, Loreto Santa‐Marina, Xavier Estivill, Wei Ang, Julie Marsh, Christoph Reichetzeder, Letizia Marullo, Berthold Hocher, Kathryn L. Lunetta, Joanne M. Murabito, Caroline L. Relton, Manolis Kogevinas, Leda Chatzi, Catherine Allard, Luigi Bouchard, Marie‐France Hivert, Ge Zhang, Louis J. Muglia, Jani Heikkinen, Camilla S. Morgen, Antoine H. C. van Kampen, Barbera D. C. van Schaik, Frank Mentch, Claudia Langenberg, Jian'an Luan, Robert A. Scott, Wei Zhao, Gibran Hemani, Susan M. Ring, Amanda J. Bennett, Kyle J. Gaulton, Juan Fernández‐Tajes, Natalie R. van Zuydam, Carolina Medina‐Gómez, Hugoline G. de Haan, Frits R. Rosendaal, Zoltán Kutalik, Pedro Marques‐Vidal, Shikta Das, Gonneke Willemsen, Hamdi Mbarek, Martina Müller‐Nurasyid, Marie Standl, Emil V. R. Appel, Cilius Esmann Fonvig, Cæcilie Trier
Julkaistu 2019Revisão -
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Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits Tekijä Aldi T. Kraja, Chunyu Liu, Jessica L. Fetterman, Mariaelisa Graff, Henri Theil, C. Charles Gu, Lisa R. Yanek, Mary F. Feitosa, Dan E. Arking, Daniel I. Chasman, Kristin L. Young, Symen Ligthart, W. David Hill, Stefan Weiß, Jian’an Luan, Franco Giulianini, Ruifang Li‐Gao, Fernando Pires Hartwig, Shiow J. Lin, Lihua Wang, Tom G. Richardson, Jie Yao, Eliana Portilla-Fernández, Mohsen Ghanbari, Mary K. Wojczynski, Wen‐Jane Lee, Maria Argos, Sebastian M. Armasu, Ruteja A. Barve, Kathleen A. Ryan, Ping An, Thomas Baranski, Suzette J. Bielinski, Donald W. Bowden, Ulrich Broeckel, Kaare Christensen, Audrey Y. Chu, Janie Corley, Simon R. Cox, André G. Uitterlinden, Fernando Rivadeneira, Cheryl D. Cropp, E. Warwick Daw, Alan B. Zonderman, Lisa de las Fuentes, He Gao, Ioanna Tzoulaki, Tarunveer S. Ahluwalia, Renée de Mutsert, Leslie Emery, A. Mesut Erzurumluoglu, James A. Perry, Mao Fu, Nita G. Forouhi, Zhenglong Gu, Yang Hai, Sarah E. Harris, Gibran Hemani, Steven C. Hunt, Marguerite R. Irvin, Anna Jonsson, Anne E. Justice, Nicola D. Kerrison, Nicholas B. Larson, Keng-Hung Lin, Latisha Love‐Gregory, Rasika A. Mathias, Joseph H. Lee, Matthias Nauck, Raymond Noordam, Ken K. Ong, James S. Pankow, Amit Patki, Alison Pattie, Astrid Petersmann, Qibin Qi, Rasmus Ribel‐Madsen, Rebecca Rohde, Kevin Sandow, Theresia M. Schnurr, Tamar Sofer, John M. Starr, Adele M. Taylor, Alexander Teumer, Nicholas J. Timpson, Hugoline G. de Haan, Yujie Wang, Peter Weeke, Christine A. Williams, Hongsheng Wu, Wei Yang, Donglin Zeng, Daniel R. Witte, Bruce S. Weir, Nicholas J. Wareham, Henrik Vestergaard, Stephen T. Turner, Christian Torp‐Pedersen, Evie Stergiakouli, Wayne Huey‐Herng Sheu
Julkaistu 2018Artigo -
12
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors Tekijä Nicole M. Warrington, Robin N. Beaumont, Momoko Horikoshi, Felix R. Day, Øyvind Helgeland, Charles Laurin, Jonas Bacelis, Shouneng Peng, Ke Hao, Bjarke Feenstra, Andrew R. Wood, Anubha Mahajan, Jessica Tyrrell, Neil R. Robertson, N. William Rayner, Zhen Qiao, Gunn-Helen Moen, Marc Vaudel, Carmen J. Marsit, Jia Chen, Michael Nodzenski, Theresia M. Schnurr, Mohammad Hadi Zafarmand, Jonathan P. Bradfield, Niels Grarup, Marjolein N. Kooijman, Ruifang Li‐Gao, Frank Geller, Tarunveer S. Ahluwalia, Lavinia Paternoster, Rico Rueedi, Ville Huikari, Jouke‐Jan Hottenga, Leo‐Pekka Lyytikäinen, Alana Cavadino, Sarah Metrustry, Diana L. Cousminer, Ying Wu, Elisabeth Thiering, Carol A. Wang, Henri Theil, Natàlia Vilor‐Tejedor, Peter K. Joshi, Jodie N. Painter, Ιωάννα Ντάλλα, Ronny Myhre, Niina Pitkänen, Jin‐Moo Lee, Raimo Joro, Vasiliki Lagou, Rebecca C. Richmond, Ana Espinosa, Sheila J. Barton, Hazel Inskip, John W. Holloway, Loreto Santa‐Marina, Xavier Estivill, Wei Ang, Julie Marsh, Christoph Reichetzeder, Letizia Marullo, Berthold Hocher, Kathryn L. Lunetta, Joanne M. Murabito, Caroline L. Relton, Manolis Kogevinas, Leda Chatzi, Catherine Allard, Luigi Bouchard, Marie‐France Hivert, Ge Zhang, Louis J. Muglia, Jani Heikkinen, Camilla S. Morgen, Antoine H. C. van Kampen, Barbera D. C. van Schaik, Frank Mentch, Claudia Langenberg, Jian’an Luan, Robert A. Scott, Wei Zhao, Gibran Hemani, Susan M. Ring, Amanda J. Bennett, Kyle J. Gaulton, Juan Fernández‐Tajes, Natalie R. van Zuydam, Carolina Medina‐Gómez, Hugoline G. de Haan, Frits R. Rosendaal, Zoltán Kutalik, Pedro Marques‐Vidal, Shikta Das, Gonneke Willemsen, Hamdi Mbarek, Martina Müller‐Nurasyid, Marie Standl, Emil V. R. Appel, Cilius Esmann Fonvig, Cæcilie Trier
Julkaistu 2018Pré-impressão -
13
Associations of autozygosity with a broad range of human phenotypes Tekijä David W. Clark, Yukinori Okada, Kristjan H. S. Moore, Dan Mason, Nicola Pirastu, Ilaria Gandin, Hannele Mattsson, Catriona L. K. Barnes, Kuang Lin, Jing Hua Zhao, Patrick Deelen, Rebecca Rohde, Claudia Schurmann, Xiuqing Guo, Franco Giulianini, Weihua Zhang, Carolina Medina‐Gómez, Robert Karlsson, Yanchun Bao, Traci M. Bartz, Clemens Baumbach, Ginevra Biino, Matthew J. Bixley, Marco Brumat, Jin Fang Chai, Tanguy Corre, Diana L. Cousminer, Annelot M. Dekker, David Eccles, Kristel R. van Eijk, Christian Fuchsberger, He Gao, Marine Germain, Scott D. Gordon, Hugoline G. de Haan, Sarah E. Harris, Edith Hofer, Alicia Huerta-Chagoya, Catherine Igartua, Iris E. Jansen, Yucheng Jia, Tim Kacprowski, Torgny Karlsson, Marcus E. Kleber, Shengchao Alfred Li, Ruifang Li‐Gao, Anubha Mahajan, Koichi Matsuda, Karina Meidtner, Weihua Meng, May E. Montasser, Peter J. van der Most, Matthias Munz, Teresa Nutile, Teemu Palviainen, Gauri Prasad, Rashmi B. Prasad, Tallapragada Divya Sri Priyanka, Federica Rizzi, Erika Salvi, Bishwa R. Sapkota, Daniel Shriner, Line Skotte, Melissa Smart, Albert V. Smith, Ashley van der Spek, Cassandra N. Spracklen, Rona J. Strawbridge, Salman M. Tajuddin, Stella Trompet, Constance Turman, Niek Verweij, Clara Viberti, Lihua Wang, Helen R. Warren, Robyn E. Wootton, Lisa R. Yanek, Jie Yao, Noha A. Yousri, Wei Zhao, Adebowale Adeyemo, Saima Afaq, Carlos A. Aguilar‐Salinas, Masato Akiyama, Matthew L. Albert, Matthew Allison, Maris Alver, Tin Aung, Fereidoun Azizi, Amy R. Bentley, Heiner Boeing, Eric Boerwinkle, Judith B. Borja, Gert J. de Borst, Erwin P. Böttinger, Linda Broer, Harry Campbell, Stephen J. Chanock, Miao-Li Chee, Guanjie Chen
Julkaistu 2019Revisão -
14
Genome-wide associations for birth weight and correlations with adult disease Tekijä Momoko Horikoshi, Robin N. Beaumont, Felix R. Day, Nicole M. Warrington, Marjolein N. Kooijman, Juan Fernández‐Tajes, Bjarke Feenstra, Natalie R. van Zuydam, Kyle J. Gaulton, Niels Grarup, Jonathan P. Bradfield, David P. Strachan, Ruifang Li‐Gao, Tarunveer S. Ahluwalia, Eskil Kreiner, Rico Rueedi, Leo‐Pekka Lyytikäinen, Diana L. Cousminer, Ying Wu, Elisabeth Thiering, Carol A. Wang, Henri Theil, Jouke‐Jan Hottenga, Natàlia Vilor‐Tejedor, Peter K. Joshi, Eileen Tai Hui Boh, Ιωάννα Ντάλλα, Niina Pitkänen, Anubha Mahajan, Jin‐Moo Lee, Raimo Joro, Vasiliki Lagou, Michael Nodzenski, Louise A Diver, Krina T. Zondervan, Mariona Bustamante, Pedro Marques‐Vidal, Josep M. Mercader, Amanda J. Bennett, Nilüfer Rahmioğlu, Dale R. Nyholt, Ronald C.W., Claudia H.T. Tam, Wing Hung Tam, Santhi K. Ganesh, Frank J.A. van Rooij, Samuel E. Jones, Po‐Ru Loh, Katherine S. Ruth, Marcus A. Tuke, Jessica Tyrrell, Andrew R. Wood, Hanieh Yaghootkar, Denise Scholtens, Lavinia Paternoster, Inga Prokopenko, Péter Kovács, Mustafa Atalay, Sara M. Willems, Kalliope Panoutsopoulou, Xu Wang, Lisbeth Carstensen, Frank Geller, Katharina E. Schraut, Mario Murcia, C.E.M. van Beijsterveldt, Gonneke Willemsen, Emil V. R. Appel, Cilius Esmann Fonvig, Cæcilie Trier, Carla M. T. Tiesler, Marie Standl, Zoltán Kutalik, Sílvia Bonàs‐Guarch, David M. Hougaard, Friman Sánchez, David Torrents, Johannes Waage, Mads V. Hollegaard, Hugoline G. de Haan, Frits R. Rosendaal, Carolina Medina‐Gómez, Susan M. Ring, Gibran Hemani, George McMahon, Neil R. Robertson, Christopher J. Groves, Claudia Langenberg, Jian’an Luan, Robert A. Scott, Wei Zhao, Frank Mentch, Scott M. MacKenzie, Rebecca M. Reynolds, William L. Lowe, Anke Tönjes, Michael Stümvoll, Virpi Lindi, Timo A. Lakka, Cornelia M. van Duijn
Julkaistu 2016Revisão
Työkalut:
Liittyvät aiheet
Biology
Gene
Genetics
Genotype
Medicine
Internal medicine
Single-nucleotide polymorphism
Genome-wide association study
Endocrinology
Genetic association
Genetic variants
Mendelian randomization
Bioinformatics
Computer science
Offspring
Pregnancy
Birth weight
Confounding
Demography
Diabetes mellitus
Fetus
Inbreeding
Inbreeding depression
Maternal effect
Odds ratio
Phenotype
Physiology
Population
Programming language
Runs of Homozygosity