Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Vasiliki Mamakou"'
Autor:
George Dedoussis, M. Arfan Ikram, Marit E. Jørgensen, Christian Herder, Gudmar Thorleifsson, Oscar H. Franco, Xueling Sim, Philippe Froguel, Symen Ligthart, Ellen M. Schmidt, Jason M. Torres, Karen L. Mohlke, Markku Laakso, Barbara Thorand, Erwin P. Bottinger, Matthias Thurner, Torben Hansen, Jerome I. Rotter, Weihua Zhang, Ching-Ti Liu, Michael Boehnke, Kristi Läll, Konstantin Strauch, Kent D. Taylor, Andrew D. Morris, Daniel R. Witte, Anna L. Gloyn, Jonathan Marchini, Andres Metspalu, Florian Kronenberg, Anubha Mahajan, Claudia Schurmann, Jennifer Kriebel, James S. Pankow, Matthias Wuttke, Valeriya Lyssenko, Jose C. Florez, Josée Dupuis, Patricia A. Peyser, Leif Groop, John C. Chambers, Torben Jørgensen, Timothy M. Frayling, Lawrence F. Bielak, Nicholas J. Wareham, Thomas Meitinger, Alena Stančáková, Vasiliki Mamakou, Cramer Christensen, Michael Preuss, Bram P. Prins, Niels Grarup, Amanda J. Bennett, Vilmantas Giedraitis, Jian'an Luan, Young-Jin Kim, Mickaël Canouil, Robert A. Scott, Kari Stefansson, Jana Nano, Donald W. Bowden, Oluf Pedersen, Cécile Lecoeur, Anna Köttgen, Jette Bork-Jensen, Francis S. Collins, Unnur Thorsteinsdottir, Naveed Sattar, Stella Trompet, Martin Ingelsson, Maggie C.Y. Ng, Jaakko Tuomilehto, Reedik Mägi, James B. Meigs, Lauren E. Petty, J. Wouter Jukema, Andrew T. Hattersley, Claudia Langenberg, Harald Grallert, Christian Gieger, Chad M. Brummett, Ian Ford, Andrew P. Morris, James P. Cook, Vibe Nylander, Sebastian Schönherr, Daniel Taliun, Xiuqing Guo, Valgerdur Steinthorsdottir, Cecilia M. Lindgren, Jennifer E. Below, Eleftheria Zeggini, Anthony Payne, Loic Yengo, Sharon L.R. Kardia, Neil R. Robertson, Abbas Dehghan, Ivan Brandslund, Erik Ingelsson, Colin N. A. Palmer, Ruth J. F. Loos, Girish N. Nadkarni, Gonçalo R. Abecasis, Adam E. Locke, Johanna Kuusisto, Lars Lind, Krista Fischer, Annette Peters, Kai-Uwe Ec Kardt, Ioanna Ntalla, Chloé Sarnowski, Mark I. McCarthy, N. William Rayner, Allan Linneberg, Sophie Hackinger
Publikováno v:
Mahajan, A, Taliun, D, Thurner, M, Robertson, N R, Torres, J M, Rayner, N W, Payne, A J, Steinthorsdottir, V, Scott, R A, Grarup, N, Cook, J P, Schmidt, E M, Wuttke, M, Sarnowski, C, Mägi, R, Nano, J, Gieger, C, Trompet, S, Lecoeur, C, Preuss, M H, Prins, B P, Guo, X, Bielak, L F, Below, J E, Bowden, D W, Chambers, J C, Kim, Y J, Ng, M C Y, Petty, L E, Sim, X, Zhang, W, Bennett, A J, Bork-Jensen, J, Brummett, C M, Canouil, M, Ec Kardt, K-U, Fischer, K, Kardia, S L R, Kronenberg, F, Läll, K, Liu, C-T, Locke, A E, Luan, J, Ntalla, I, Nylander, V, Schönherr, S, Schurmann, C, Yengo, L, Bottinger, E P, Brandslund, I, Christensen, C, Dedoussis, G, Florez, J C, Ford, I, Franco, O H, Frayling, T M, Giedraitis, V, Hackinger, S, Hattersley, A T, Herder, C, Ikram, M A, Ingelsson, M, Jørgensen, M E, Jørgensen, T, Kriebel, J, Kuusisto, J, Ligthart, S, Lindgren, C M, Linneberg, A, Lyssenko, V, Mamakou, V, Meitinger, T, Mohlke, K L, Morris, A D, Nadkarni, G, Pankow, J S, Peters, A, Sattar, N, Stančáková, A, Strauch, K, Taylor, K D, Thorand, B, Thorleifsson, G, Thorsteinsdottir, U, Tuomilehto, J, Witte, D R, Dupuis, J, Peyser, P A, Zeggini, E, Loos, R J F, Froguel, P, Ingelsson, E, Lind, L, Groop, L, Laakso, M, Collins, F S, Jukema, J W, Palmer, C N A, Grallert, H, Metspalu, A, Dehghan, A, Köttgen, A, Abecasis, G R, Meigs, J B, Rotter, J I, Marchini, J, Pedersen, O, Hansen, T, Langenberg, C, Wareham, N J, Stefansson, K, Gloyn, A L, Morris, A P, Boehnke, M & McCarthy, M I 2018, ' Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps ', Nature Genetics, vol. 50, no. 11, pp. 1505-1513 . https://doi.org/10.1038/s41588-018-0241-6
Nat. Genet. 50, 1505-1513 (2018)
Nature Genetics
Nature Genetics, 50(11), 1505
Mahajan, A, Taliun, D, Thurner, M, Robertson, N R, Torres, J M, Rayner, N W, Payne, A J, Steinthorsdottir, V, Scott, R A, Grarup, N, Cook, J P, Schmidt, E M, Wuttke, M, Sarnowski, C, Mägi, R, Nano, J, Gieger, C, Trompet, S, Lecoeur, C, Preuss, M H, Prins, B P, Guo, X, Bielak, L F, Below, J E, Bowden, D W, Chambers, J C, Kim, Y J, Ng, M C Y, Petty, L E, Sim, X, Zhang, W, Bennett, A J, Bork-Jensen, J, Brummett, C M, Canouil, M, Ec Kardt, K-U, Fischer, K, Kardia, S L R, Kronenberg, F, Läll, K, Liu, C-T, Locke, A E, Luan, J, Ntalla, I, Nylander, V, Schönherr, S, Schurmann, C, Yengo, L, Bottinger, E P, Brandslund, I, Christensen, C, Dedoussis, G, Florez, J C, Ford, I, Franco, O H, Frayling, T M, Giedraitis, V, Hackinger, S, Hattersley, A T, Herder, C, Ikram, M A, Ingelsson, M, Jørgensen, M E, Jørgensen, T, Kriebel, J, Kuusisto, J, Ligthart, S, Lindgren, C M, Linneberg, A, Lyssenko, V, Mamakou, V, Meitinger, T, Mohlke, K L, Morris, A D, Nadkarni, G, Pankow, J S, Peters, A, Sattar, N, Stančáková, A, Strauch, K, Taylor, K D, Thorand, B, Thorleifsson, G, Thorsteinsdottir, U, Tuomilehto, J, Witte, D R, Dupuis, J, Peyser, P A, Zeggini, E, Loos, R J F, Froguel, P, Ingelsson, E, Lind, L, Groop, L, Laakso, M, Collins, F S, Jukema, J W, Palmer, C N A, Grallert, H, Metspalu, A, Dehghan, A, Köttgen, A, Abecasis, G R, Meigs, J B, Rotter, J I, Marchini, J, Pedersen, O, Hansen, T, Langenberg, C, Wareham, N J, Stefansson, K, Gloyn, A L, Morris, A P, Boehnke, M & McCarthy, M I 2018, ' Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps ', Nature Genetics, vol. 50, no. 11, pp. 1505–1513 . https://doi.org/10.1038/s41588-018-0241-6
Nature Genetics, 50(11), 1505-+. Nature Publishing Group
NATURE GENETICS
Nat. Genet. 50, 1505-1513 (2018)
Nature Genetics
Nature Genetics, 50(11), 1505
Mahajan, A, Taliun, D, Thurner, M, Robertson, N R, Torres, J M, Rayner, N W, Payne, A J, Steinthorsdottir, V, Scott, R A, Grarup, N, Cook, J P, Schmidt, E M, Wuttke, M, Sarnowski, C, Mägi, R, Nano, J, Gieger, C, Trompet, S, Lecoeur, C, Preuss, M H, Prins, B P, Guo, X, Bielak, L F, Below, J E, Bowden, D W, Chambers, J C, Kim, Y J, Ng, M C Y, Petty, L E, Sim, X, Zhang, W, Bennett, A J, Bork-Jensen, J, Brummett, C M, Canouil, M, Ec Kardt, K-U, Fischer, K, Kardia, S L R, Kronenberg, F, Läll, K, Liu, C-T, Locke, A E, Luan, J, Ntalla, I, Nylander, V, Schönherr, S, Schurmann, C, Yengo, L, Bottinger, E P, Brandslund, I, Christensen, C, Dedoussis, G, Florez, J C, Ford, I, Franco, O H, Frayling, T M, Giedraitis, V, Hackinger, S, Hattersley, A T, Herder, C, Ikram, M A, Ingelsson, M, Jørgensen, M E, Jørgensen, T, Kriebel, J, Kuusisto, J, Ligthart, S, Lindgren, C M, Linneberg, A, Lyssenko, V, Mamakou, V, Meitinger, T, Mohlke, K L, Morris, A D, Nadkarni, G, Pankow, J S, Peters, A, Sattar, N, Stančáková, A, Strauch, K, Taylor, K D, Thorand, B, Thorleifsson, G, Thorsteinsdottir, U, Tuomilehto, J, Witte, D R, Dupuis, J, Peyser, P A, Zeggini, E, Loos, R J F, Froguel, P, Ingelsson, E, Lind, L, Groop, L, Laakso, M, Collins, F S, Jukema, J W, Palmer, C N A, Grallert, H, Metspalu, A, Dehghan, A, Köttgen, A, Abecasis, G R, Meigs, J B, Rotter, J I, Marchini, J, Pedersen, O, Hansen, T, Langenberg, C, Wareham, N J, Stefansson, K, Gloyn, A L, Morris, A P, Boehnke, M & McCarthy, M I 2018, ' Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps ', Nature Genetics, vol. 50, no. 11, pp. 1505–1513 . https://doi.org/10.1038/s41588-018-0241-6
Nature Genetics, 50(11), 1505-+. Nature Publishing Group
NATURE GENETICS
We aggregated genome-wide genotyping data from 32 European-descent GWAS (74,124 T2D cases, 824,006 controls) imputed to high-density reference panels of >30,000 sequenced haplotypes. Analysis of ˜27M variants (˜21M with minor allele frequency [MAF]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbae95dc861b6b5097449d0559849042
https://vbn.aau.dk/da/publications/988454e1-d6c9-49b9-aad9-99c686756cc3
https://vbn.aau.dk/da/publications/988454e1-d6c9-49b9-aad9-99c686756cc3
Autor:
Ching-Ti Liu, Michael Boehnke, George Dedoussis, Sophie V. Eastwood, Ruth J. F. Loos, Keng-Hung Lin, Denis Rybin, Fredrik Karpe, Martina Müller-Nurasyid, Michael A. Province, Alison D. Murray, Bo Isomaa, Eirini Marouli, Konstantin Strauch, Michael Preuss, Paul M. Ridker, Jette Bork-Jensen, Albert V. Smith, Hugoline G. de Haan, Wayne Huey-Herng Sheu, Barbara Thorand, Wolfgang Rathmann, Lawrence F. Bielak, Peter Kovacs, Marit E. Jørgensen, Jennifer Wessel, Danish Saleheen, Jung-Jin Lee, James B. Meigs, Veikko Salomaa, Alena Stančáková, Tibor V. Varga, Hidetoshi Kitajima, Inês Barroso, Kent D. Taylor, Claudia Langenberg, Yoon Shin Cho, Joanna M. M. Howson, Andrew T. Hattersley, Marie-France Hivert, Markku Laakso, Kai-Uwe Eckardt, Bram P. Prins, Matthias B. Schulze, Andrew D. Morris, Susanne Jäger, Francis S. Collins, Kristi Läll, Xu Lin, Anette Varbo, Benjamin Lehne, Girish N. Nadkarni, Jonathan Marchini, Daniel I. Chasman, Michael Stumvoll, Mark O. Goodarzi, Cécile Lecoeur, Philippe M. Frossard, Noël P. Burtt, Frank Kee, Jasmina Kravic, Alain G. Bertoni, Ivan Brandslund, Najaf Amin, Lenore J. Launer, Oluf Pedersen, Johanna Kuusisto, Line Rode, Eleftheria Zeggini, Yingchang Lu, Markus Perola, Helen R. Warren, André G. Uitterlinden, Hanieh Yaghootkar, Torben Hansen, Harald Grallert, Annemari Käräjämäki, Abbas Dehghan, Gina M. Peloso, Yii-Der Ida Chen, Man Li, Shaofeng Huo, Lars Lind, Karen L. Mohlke, Adrienne Tin, Yang Hai, Renée de Mutsert, Gudmar Thorleifsson, Marie Moitry, Sune F. Nielsen, Sara M. Willems, Matthias Wuttke, Weihua Zhang, Young-Jin Kim, Giovanni Malerba, Richard A. Jensen, Loic Yengo, Mickaël Canouil, Kurt Lohman, Robert A. Scott, Tamara B. Harris, Ruifang Li-Gao, Florian Kronenberg, Anke Tönjes, Bok-Ghee Han, Krista Fischer, Thomas Meitinger, James S. Pankow, Jaakko Tuomilehto, Adam S. Butterworth, Jerome I. Rotter, Olov Rolandsson, Xiuqing Guo, Cramer Christensen, Marie Loh, Elizabeth Selvin, Bong-Jo Kim, Audrey Y. Chu, Reedik Mägi, Josée Dupuis, Anna Köttgen, Jean Ferrières, Jin Li, Robert Sladek, Leslie A. Lange, Niels Grarup, Roberta McKean-Cowdin, Cristen J. Willer, Jose C. Florez, Valgerdur Steinthorsdottir, Karina Meidtner, Annette Peters, Børge G. Nordestgaard, Rajiv Chowdhury, Ioanna Ntalla, Emma Ahlqvist, Leif Groop, Nicholas J. Wareham, Kerrin S. Small, Tiinamaija Tuomi, Cecilia M. Lindgren, Katharine R. Owen, Giovanni Gambaro, Cornelia M. van Duijn, Dennis O. Mook-Kanamori, Kenneth Rice, Erik Ingelsson, Colin N. A. Palmer, Sharon L.R. Kardia, Neil R. Robertson, Dajiang J. Liu, Sebastian Schönherr, Daniel Taliun, Sekar Kathiresan, James G. Wilson, Ping An, Patricia A. Peyser, Matthias Blüher, Frits R. Rosendaal, John C. Chambers, Caroline Hayward, Shoaib Afzal, Fernando Rivadineira, Marielisa Graff, Pranav Yajnik, Vasiliki Mamakou, Juan Fernandez Tajes, Stefan Gustafsson, Heather M. Highland, Vilmantas Giedraitis, Andrew R. Wood, Saima Afaq, Jaspal S. Kooner, Megan L. Grove, Jennifer A. Brody, Andrew P. Morris, James P. Cook, Praveen Surendran, Jennifer Kriebel, Heikki A. Koistinen, Kari Stefansson, Anders Rosengren, Rainer Rauramaa, Satu Männistö, Oscar H. Franco, Yongmei Liu, N. William Rayner, Blair H. Smith, Erwin P. Bottinger, Ayse Demirkan, Allan Linneberg, Jonathan Marten, Huaixing Li, Sung Soo Kim, Sophie Hackinger, Cristina Bombieri, Lia B. Bang, Jun Liu, Asif Rasheed, Tim D. Spector, Paul W. Franks, Mark I. McCarthy, Heiner Boeing, Anne E. Justice, Vilmundur Gudnason, Sohee Han, Unnur Thorsteinsdottir, Panos Deloukas, Naveed Sattar, Eric Boerwinkle, Martin Ingelsson, John Danesh, Vassily Trubetskoy, Marco M Ferrario, Marju Orho-Melander, Wei Gan, Philippe Froguel, Symen Ligthart, Susan R. Heckbert, Jie Yao, Anne Tybjærg-Hansen, Robin Young, Daniel R. Witte, Anubha Mahajan, Peter Almgren, Timothy M. Frayling, Tanya M. Teslovich, Matt Neville, Philippe Amouyel, Wei Zhao, Andres Metspalu, Yao Hu, Olle Melander, Kari Kuulasmaa, Jason Flannick, Torben Jørgensen, Stephen S. Rich, Nicole Soranzo, Bruce M. Psaty, Rohit Varma
Publikováno v:
Grarup, N, Jørgensen, M E, Witte, D R, Hansen, T, Pedersen, O, ExomeBP Consortium, MAGIC Consortium & GIANT Consortium 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Mahajan, A, Wessel, J, Willems, S M, Zhao, W, Robertson, N R, Chu, A Y, Gan, W, Kitajima, H, Taliun, D, Rayner, N W, Guo, X, Lu, Y, Li, M, Jensen, R A, Hu, Y, Huo, S, Lohman, K K, Zhang, W, Cook, J P, Prins, B P, Flannick, J, Grarup, N, Trubetskoy, V V, Kravic, J, Kim, Y J, Rybin, D V, Yaghootkar, H, Müller-Nurasyid, M, Meidtner, K, Li-Gao, R, Varga, T V, Marten, J, Li, J, Smith, A V, An, P, Ligthart, S, Gustafsson, S, Malerba, G, Demirkan, A, Tajes, J F, Steinthorsdottir, V, Wuttke, M, Lecoeur, C, Preuss, M, Bielak, L F, Graff, M, Highland, H M, Morris, A & Hayward, C & Morris, A P 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Mahajan, A, Wessel, J, Willems, S M, Zhao, W, Robertson, N R, Chu, A Y, Gan, W, Kitajima, H, Taliun, D, Rayner, N W, Guo, X, Lu, Y, Li, M, Jensen, R A, Hu, Y, Huo, S, Lohman, K K, Zhang, W, Cook, J P, Prins, B P, Flannick, J, Grarup, N, Trubetskoy, V V, Kravic, J, Kim, Y J, Rybin, D V, Yaghootkar, H, Müller-Nurasyid, M, Meidtner, K, Li-Gao, R, Varga, T V, Marten, J, Li, J, Smith, A V, An, P, Ligthart, S, Gustafsson, S, Malerba, G, Demirkan, A, Tajes, J F, Steinthorsdottir, V, Wuttke, M, Lecoeur, C, Preuss, M, Bielak, L F, Graff, M, Highland, H M, Justice, A E, Liu, D J, Marouli, E, Peloso, G M, Warren, H R, ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Afaq, S, Afzal, S, Ahlqvist, E, Almgren, P, Amin, N, Bang, L B, Bertoni, A G, Bombieri, C, Bork-Jensen, J, Brandslund, I, Brody, J A, Burtt, N P, Canouil, M, Chen, Y-D I, Cho, Y S, Christensen, C, Eastwood, S V, Eckardt, K-U, Fischer, K, Gambaro, G, Giedraitis, V, Grove, M L, de Haan, H G, Hackinger, S, Hai, Y, Han, S, Tybjærg-Hansen, A, Hivert, M-F, Isomaa, B, Jäger, S, Jørgensen, M E, Jørgensen, T, Käräjämäki, A, Kim, B-J, Kim, S S, Koistinen, H A, Kovacs, P, Kriebel, J, Kronenberg, F, Läll, K, Lange, L A, Lee, J-J, Lehne, B, Li, H, Lin, K-H, Linneberg, A, Liu, C-T, Liu, J, Loh, M, Mägi, R, Mamakou, V, McKean-Cowdin, R, Nadkarni, G, Neville, M, Nielsen, S F, Ntalla, I, Peyser, P A, Rathmann, W, Rice, K, Rich, S S, Rode, L, Rolandsson, O, Schönherr, S, Selvin, E, Small, K S, Stančáková, A, Surendran, P, Taylor, K D, Teslovich, T M, Thorand, B, Thorleifsson, G, Tin, A, Tönjes, A, Varbo, A, Witte, D R, Wood, A R, Yajnik, P, Yao, J, Yengo, L, Young, R, Amouyel, P, Boeing, H, Boerwinkle, E, Bottinger, E P, Chowdhury, R, Collins, F S, Dedoussis, G, Dehghan, A, Deloukas, P, Ferrario, M M, Ferrieres, J, Florez, J C, Frossard, P, Gudnason, V, Harris, T B, Heckbert, S R, Howson, J M M, Ingelsson, M, Kathiresan, S, Kee, F, Kuusisto, J, Langenberg, C, Launer, L J, Lindgren, C M, Männistö, S, Meitinger, T, Melander, O, Mohlke, K L, Moitry, M, Morris, A P, Murray, A D, de Mutsert, R, Orho-Melander, M, Owen, K R, Perola, M, Peters, A, Province, M A, Rasheed, A, Ridker, P M, Rivadineira, F, Rosendaal, F R, Rosengren, A H, Salomaa, V, Sheu, W H-H, Sladek, R, Willer, C J, Blüher, M, Butterworth, A S, Chambers, J C, Chasman, D I, Danesh, J, van Duijn, C M, Dupuis, J, Franco, O H, Franks, P W, Froguel, P, Grallert, H, Groop, L, Kardia, S L R, Karpe, F, Kooner, J S, Köttgen, A, Kuulasmaa, K, Laakso, M, Lin, X, Lind, L, Liu, Y, Loos, R J F, Marchini, J, Metspalu, A, Mook-Kanamori, D O, Nordestgaard, B G, Palmer, C N A, Pankow, J S, Pedersen, O, Psaty, B M, Rauramaa, R, Sattar, N, Schulze, M B, Soranzo, N, Spector, T D, Stefansson, K, Stumvoll, M, Thorsteinsdottir, U, Tuomi, T, Tuomilehto, J, Wareham, N J, Wilson, J G, Zeggini, E, Scott, R A, Barroso, I, Frayling, T M, Goodarzi, M O, Meigs, J B, Boehnke, M, Saleheen, D, Morris, A P, Rotter, J I & McCarthy, M I 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
ExomeBP Consortium 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Nature Genetics
Nat. Genet. 50, 559-571 (2018)
NATURE GENETICS
ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Witte, D R & Hansen, T 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Nature genetics
Nature Genetics, 50(4), 559-+. Nature Publishing Group
Nature Genetics, 50(4), 559
Mahajan, A, Wessel, J, Willems, S M, Zhao, W, Robertson, N R, Chu, A Y, Gan, W, Kitajima, H, Taliun, D, Rayner, N W, Guo, X, Lu, Y, Li, M, Jensen, R A, Hu, Y, Huo, S, Lohman, K K, Zhang, W, Cook, J P, Prins, B P, Flannick, J, Grarup, N, Trubetskoy, V V, Kravic, J, Kim, Y J, Rybin, D V, Yaghootkar, H, Müller-Nurasyid, M, Meidtner, K, Li-Gao, R, Varga, T V, Marten, J, Li, J, Smith, A V, An, P, Ligthart, S, Gustafsson, S, Malerba, G, Demirkan, A, Tajes, J F, Steinthorsdottir, V, Wuttke, M, Lecoeur, C, Preuss, M, Bielak, L F, Graff, M, Highland, H M, Morris, A & Hayward, C & Morris, A P 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Mahajan, A, Wessel, J, Willems, S M, Zhao, W, Robertson, N R, Chu, A Y, Gan, W, Kitajima, H, Taliun, D, Rayner, N W, Guo, X, Lu, Y, Li, M, Jensen, R A, Hu, Y, Huo, S, Lohman, K K, Zhang, W, Cook, J P, Prins, B P, Flannick, J, Grarup, N, Trubetskoy, V V, Kravic, J, Kim, Y J, Rybin, D V, Yaghootkar, H, Müller-Nurasyid, M, Meidtner, K, Li-Gao, R, Varga, T V, Marten, J, Li, J, Smith, A V, An, P, Ligthart, S, Gustafsson, S, Malerba, G, Demirkan, A, Tajes, J F, Steinthorsdottir, V, Wuttke, M, Lecoeur, C, Preuss, M, Bielak, L F, Graff, M, Highland, H M, Justice, A E, Liu, D J, Marouli, E, Peloso, G M, Warren, H R, ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Afaq, S, Afzal, S, Ahlqvist, E, Almgren, P, Amin, N, Bang, L B, Bertoni, A G, Bombieri, C, Bork-Jensen, J, Brandslund, I, Brody, J A, Burtt, N P, Canouil, M, Chen, Y-D I, Cho, Y S, Christensen, C, Eastwood, S V, Eckardt, K-U, Fischer, K, Gambaro, G, Giedraitis, V, Grove, M L, de Haan, H G, Hackinger, S, Hai, Y, Han, S, Tybjærg-Hansen, A, Hivert, M-F, Isomaa, B, Jäger, S, Jørgensen, M E, Jørgensen, T, Käräjämäki, A, Kim, B-J, Kim, S S, Koistinen, H A, Kovacs, P, Kriebel, J, Kronenberg, F, Läll, K, Lange, L A, Lee, J-J, Lehne, B, Li, H, Lin, K-H, Linneberg, A, Liu, C-T, Liu, J, Loh, M, Mägi, R, Mamakou, V, McKean-Cowdin, R, Nadkarni, G, Neville, M, Nielsen, S F, Ntalla, I, Peyser, P A, Rathmann, W, Rice, K, Rich, S S, Rode, L, Rolandsson, O, Schönherr, S, Selvin, E, Small, K S, Stančáková, A, Surendran, P, Taylor, K D, Teslovich, T M, Thorand, B, Thorleifsson, G, Tin, A, Tönjes, A, Varbo, A, Witte, D R, Wood, A R, Yajnik, P, Yao, J, Yengo, L, Young, R, Amouyel, P, Boeing, H, Boerwinkle, E, Bottinger, E P, Chowdhury, R, Collins, F S, Dedoussis, G, Dehghan, A, Deloukas, P, Ferrario, M M, Ferrieres, J, Florez, J C, Frossard, P, Gudnason, V, Harris, T B, Heckbert, S R, Howson, J M M, Ingelsson, M, Kathiresan, S, Kee, F, Kuusisto, J, Langenberg, C, Launer, L J, Lindgren, C M, Männistö, S, Meitinger, T, Melander, O, Mohlke, K L, Moitry, M, Morris, A P, Murray, A D, de Mutsert, R, Orho-Melander, M, Owen, K R, Perola, M, Peters, A, Province, M A, Rasheed, A, Ridker, P M, Rivadineira, F, Rosendaal, F R, Rosengren, A H, Salomaa, V, Sheu, W H-H, Sladek, R, Willer, C J, Blüher, M, Butterworth, A S, Chambers, J C, Chasman, D I, Danesh, J, van Duijn, C M, Dupuis, J, Franco, O H, Franks, P W, Froguel, P, Grallert, H, Groop, L, Kardia, S L R, Karpe, F, Kooner, J S, Köttgen, A, Kuulasmaa, K, Laakso, M, Lin, X, Lind, L, Liu, Y, Loos, R J F, Marchini, J, Metspalu, A, Mook-Kanamori, D O, Nordestgaard, B G, Palmer, C N A, Pankow, J S, Pedersen, O, Psaty, B M, Rauramaa, R, Sattar, N, Schulze, M B, Soranzo, N, Spector, T D, Stefansson, K, Stumvoll, M, Thorsteinsdottir, U, Tuomi, T, Tuomilehto, J, Wareham, N J, Wilson, J G, Zeggini, E, Scott, R A, Barroso, I, Frayling, T M, Goodarzi, M O, Meigs, J B, Boehnke, M, Saleheen, D, Morris, A P, Rotter, J I & McCarthy, M I 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
ExomeBP Consortium 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Nature Genetics
Nat. Genet. 50, 559-571 (2018)
NATURE GENETICS
ExomeBP Consortium, MAGIC Consortium, GIANT Consortium, Witte, D R & Hansen, T 2018, ' Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ', Nature Genetics, vol. 50, no. 4, pp. 559-571 . https://doi.org/10.1038/s41588-018-0084-1
Nature genetics
Nature Genetics, 50(4), 559-+. Nature Publishing Group
Nature Genetics, 50(4), 559
Identification of coding variant associations for complex diseases offers a direct route to biological insight, but is dependent on appropriate inference concerning the causal impact of those variants on disease risk. We aggregated coding variant dat
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