檢索結果 - Thomas Sparsø

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  1. 1
    Physiologic Characterization of Type 2 Diabetes–Related Loci

    Physiologic Characterization of Type 2 Diabetes–Related Loci 由 Niels Grarup, Thomas Sparsø, Torben Hansen

    出版 2010
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  2. 2
    Combined Analyses of 20 Common Obesity Susceptibility Variants

    Combined Analyses of 20 Common Obesity Susceptibility Variants 由 Camilla H. Sandholt, Thomas Sparsø, Niels Grarup, Anders Albrechtsen, Katrine Almind, Lars Hansen, Ulla Toft, Torben Jørgensen, Torben Hansen, Oluf Pedersen

    出版 2010
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  3. 3
    Type 2 Diabetes Risk Alleles Near <i>BCAR1</i> and in <i>ANK1</i> Associate With Decreased β-Cell Function Whereas Risk Alleles Near <i>ANKRD55</i> and <i>GRB14</i> Associate With Decreased Insulin Sensitivity in the Danish Inter99 Cohort

    Type 2 Diabetes Risk Alleles Near <i>BCAR1</i> and in <i>ANK1</i> Associate With Decreased β-Cell Function Whereas Risk Alleles Near <i>ANKRD55</i> and <i>GRB14</i> Associate With... 由 Marie Neergaard Harder, Rasmus Ribel‐Madsen, Johanne Marie Justesen, Thomas Sparsø, Ehm A. Andersson, Niels Grarup, Torben Jørgensen, Allan Linneberg, Torben Hansen, Oluf Pedersen

    出版 2013
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  4. 4
    Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene–gene interaction

    Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene–gene interaction 由 Thomas Sparsø, Niels Grarup, Camilla Andreasen, Anders Albrechtsen, Johan Holmkvist, Gary L. Andersen, Torben Jørgensen, K. Borch‐Johnsen, Annelli Sandbæk, T. Lauritzen, Sten Madsbad, Torben Hansen, Oluf Pedersen

    出版 2009
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  5. 5
    The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes

    The GCKR rs780094 polymorphism is associated with elevated fasting serum triacylglycerol, reduced fasting and OGTT-related insulinaemia, and reduced risk of type 2 diabetes 由 Thomas Sparsø, Gary L. Andersen, Trine Nielsen, Kristoffer Sølvsten Burgdorf, Anette P. Gjesing, Arne L. Nielsen, Anders Albrechtsen, S. Rasmussen, Torben Jørgensen, K. Borch‐Johnsen, Annelli Sandbæk, T. Lauritzen, Sten Madsbad, Torben Hansen, Oluf Pedersen

    出版 2007
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  6. 6
    A glycogene mutation map for discovery of diseases of glycosylation

    A glycogene mutation map for discovery of diseases of glycosylation 由 Lars Hestbjerg Hansen, Allan Lind-Thomsen, Hiren J. Joshi, Nis Borbye‐Lorenzen, Henri Theil, Yun Kong, Shengjun Wang, Thomas Sparsø, Niels Grarup, Malene Bech Vester-Christensen, Katrine T. Schjoldager, Hudson H. Freeze, Torben Hansen, Oluf Pedersen, Bernard Henrissat, Ulla Mandel, Henrik Clausen, Hans H. Wandall, Eric Bennett

    出版 2014
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  7. 7
    Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes

    Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes 由 Kirk E. Lohmueller, Thomas Sparsø, Qibin Li, Ehm A. Andersson, Thorfinn Sand Korneliussen, Anders Albrechtsen, Karina Banasik, Niels Grarup, Ingileif B. Hallgrímsdóttir, Kristoffer Kiil, Tuomas O. Kilpeläinen, Nikolaj T. Krarup, Tune H. Pers, Gastón Sánchez, Youna Hu, Michael DeGiorgio, Torben Jørgensen, Annelli Sandbæk, Torsten Lauritzen, Søren Brunak, Karsten Kristiansen, Yingrui Li, Torben Hansen, Jun Wang, Rasmus Nielsen, Oluf Pedersen

    出版 2013
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  8. 8
    G-allele of Intronic rs10830963 in<i>MTNR1B</i>Confers Increased Risk of Impaired Fasting Glycemia and Type 2 Diabetes Through an Impaired Glucose-Stimulated Insulin Release

    G-allele of Intronic rs10830963 in<i>MTNR1B</i>Confers Increased Risk of Impaired Fasting Glycemia and Type 2 Diabetes Through an Impaired Glucose-Stimulated Insulin Release 由 Thomas Sparsø, Amélie Bonnefond, Ehm A. Andersson, Nabila Bouatia‐Naji, Johan Holmkvist, Lise Wegner, Niels Grarup, Anette P. Gjesing, Karina Banasik, Christine Cavalcanti-Proença, Marion Marchand, Martine Vaxillaire, G. Charpentier, Marjo‐Riitta Järvelin, Jean Tichet, Beverley Balkau, Michel Marre, Claire Lévy‐Marchal, Kristine Færch, Knut Borch‐Johnsen, Torben Jørgensen, Sten Madsbad, Pernille Poulsen, Allan Vaag, Christian Dina, Torben Hansen, Oluf Pedersen, Philippe Froguel

    出版 2009
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  9. 9
    Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets

    Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets 由 Niels Grarup, Patrick Sulem, Camilla H. Sandholt, Guðmar Þorleifsson, Tarunveer S. Ahluwalia, Valgerður Steinthórsdóttir, Helgi Bjarnason, Daníel F. Guðbjartsson, Ólafur Þ. Magnússon, Thomas Sparsø, Anders Albrechtsen, Augustine Kong, Gísli Másson, Geng Tian, Hongzhi Cao, Chao Nie, Karsten Kristiansen, Lise Lotte N. Husemoen, Betina H. Thuesen, Yingrui Li, Rasmus Nielsen, Allan Linneberg, Ísleifur Ólafsson, Guðmundur I. Eyjólfsson, Torben Jørgensen, Jun Wang, Torben Hansen, Unnur Þorsteinsdóttir, Kāri Stefánsson, Oluf Pedersen

    出版 2013
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  10. 10
    Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

    Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study 由 Line Olsen, Thomas Sparsø, Shantel Weinsheimer, Marcelo Bertalan Quintanilha Dos Santos, Wiktor Mazin, Anders Rosengren, Xabier Calle Sánchez, Louise K. Hoeffding, Henriette Schmock, Marie Bækvad‐Hansen, Jonas Bybjerg‐Grauholm, Mark J. Daly, Benjamin M. Neale, Marianne G. Pedersen, Esben Agerbo, Ole Mors, Anders D. Børglum, Merete Nordentoft, David M. Hougaard, Preben Bo Mortensen, Daniel H. Geschwind, Carsten Bøcker Pedersen, Wesley K. Thompson, Thomas Werge

    出版 2018
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  11. 11
    Transcriptomic analysis links diverse hypothalamic cell types to fibroblast growth factor 1-induced sustained diabetes remission

    Transcriptomic analysis links diverse hypothalamic cell types to fibroblast growth factor 1-induced sustained diabetes remission 由 Marie A. Bentsen, Dylan M. Rausch, Zaman Mirzadeh, Kenjiro Muta, Jarrad M. Scarlett, Jenny M. Brown, Vicente Herranz‐Pérez, Arian F. Baquero, Jonatan J. Thompson, Kimberly M. Alonge, Chelsea L. Faber, Karl J. Kaiyala, Camdin M. Bennett, Charles Pyke, Cecilia Ratner, Kristoffer L. Egerod, Birgitte Holst, Thomas H. Meek, Burak Kutlu, Yu Zhang, Thomas Sparsø, Kevin L. Grove, Gregory J. Morton, Birgitte Rahbek Kornum, José Manuel García‐Verdugo, Anna Secher, Rasmus Jørgensen, Michael W. Schwartz, Tune H. Pers

    出版 2020
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  12. 12
    Subclassification of obesity for precision prediction of cardiometabolic diseases

    Subclassification of obesity for precision prediction of cardiometabolic diseases 由 Daniel Coral, Femke Smit, Ali Farzaneh, Alexander Gieswinkel, Juan Fernández Tajes, Thomas Sparsø, Carl Delfin, Pierre Bauvin, Kan Wang, Marinella Temprosa, Diederik De Cock, Jordi Blanch, José Manuel Fernández‐Real, Rafel Ramos, M. Kamran Ikram, Maria F. Gomez, Maryam Kavousi, Marina Panova‐Noeva, Philipp S. Wild, Carla Kallen, Michiel Adriaens, Marleen M. J. van Greevenbroek, Ilja C.W. Arts, Carel W. le Roux, Fariba Ahmadizar, Timothy M. Frayling, Giuseppe N. Giordano, Ewan R. Pearson, Paul W. Franks

    出版 2024
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  13. 13
    A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

    A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk 由 Nabila Bouatia‐Naji, Amélie Bonnefond, Christine Cavalcanti-Proença, Thomas Sparsø, Johan Holmkvist, Marion Marchand, Jérôme Delplanque, Stéphane Lobbens, Ghislain Rocheleau, Emmanuelle Durand, Franck De Graeve, Jean-Claude Chèvre, Knut Borch‐Johnsen, Anna‐Liisa Hartikainen, Aimo Ruokonen, Jean Tichet, Michel Marre, Jacques Weill, Barbara Heude, Maïthé Tauber, Katleen Lemaire, Frans Schuit, Paul Elliott, Torben Jørgensen, G. Charpentier, Samy Hadjadj, Stéphane Cauchi, Martine Vaxillaire, Robert Sladek, Sophie Visvikis‐Siest, Beverley Balkau, Claire Lévy‐Marchal, François Pattou, Stephen Eyre, Alexandra I. F. Blakemore, Marjo‐Riitta Järvelin, Andrew J. Walley, Torben Hansen, Christian Dina, Oluf Pedersen, Philippe Froguel

    出版 2008
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  14. 14
    Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes

    Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes 由 John R. B. Perry, Michael N. Weedon, Claudia Langenberg, Anne Jackson, Valeriya Lyssenko, Thomas Sparsø, Guðmar Þorleifsson, Harald Grallert, Luigi Ferrucci, Marcello Maggio, Giuseppe Paolisso, Mark Walker, Colin N. A. Palmer, Felicity Payne, Elizabeth Young, Christian Herder, Narisu Narisu, Mario A. Morken, Lori L. Bonnycastle, Katharine R. Owen, Beverley M. Shields, Beatrice Knight, Amanda J. Bennett, Christopher J. Groves, Aimo Ruokonen, Marjo‐Riitta Järvelin, Ewan R. Pearson, Laura Pascoe, Ele Ferrannini, Stefan R. Bornstein, Heather M. Stringham, Laura J. Scott, Johanna Kuusisto, Peter M. Nilsson, Malin Neptin, Anette P. Gjesing, Charlotta Pisinger, Torsten Lauritzen, Annelli Sandbæk, Mike Sampson, Eleftheria Zeggini, Cecilia M. Lindgren, Valgerður Steinthórsdóttir, Unnur Þorsteinsdóttir, Torben Hansen, Peter Schwarz, Thomas Illig, Markku Laakso, Hreinn Stefánsson, Andrew D. Morris, Leif Groop, Oluf Pedersen, Michael Boehnke, Inês Barroso, Nicholas J. Wareham, Andrew T. Hattersley, Mark I. McCarthy, Timothy M. Frayling

    出版 2009
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  15. 15
    Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

    Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes 由 Anders Albrechtsen, Niels Grarup, Y. Li, Thomas Sparsø, Geng Tian, Hongzhi Cao, Tao Jiang, Steven Kim, Thorfinn Sand Korneliussen, Qi Li, Chao Nie, Renhua Wu, Line Skotte, Andrew P. Morris, Claes Ladenvall, Stéphane Cauchi, Alena Stančáková, Gary L. Andersen, Arne Astrup, Karina Banasik, Amanda J. Bennett, Lars Bolund, G. Charpentier, Y. Chen, Jordy Dekker, Alex S. F. Doney, Mozhgan Dorkhan, Tom Forsén, Timothy M. Frayling, Chris Groves, Yaoting Gui, Göran Hallmans, Andrew T. Hattersley, Kunlun He, G. A. Hitman, Johan Holmkvist, Shujia Huang, Hui Jiang, Xin Jin, Johanne Marie Justesen, Karsten Kristiansen, Johanna Kuusisto, Maria Lajer, Olivier Lantieri, W. Li, Hui Liang, Qijun Liao, X. Liu, Teng Ma, Xin Ma, M. P. Manijak, Michel Marre, Jacek Mokrosiński, Andrew D. Morris, Baiyang Mu, Aneta Aleksandra Nielsen, Giel Nijpels, Peter M. Nilsson, Colin N. A. Palmer, Nigel W. Rayner, Frida Renström, Rasmus Ribel‐Madsen, Neil Robertson, Olov Rolandsson, Peter Rossing, Thue W. Schwartz, P. Eline Slagboom, Maria Sterner, Tang Meifang, Lise Tarnow, Jaakko Tuomilehto, E. van’t Riet, Nienke van Leeuwen, Tibor V. Varga, M. A. Vestmar, Mark Walker, Beier Wang, Y. Wang, Honglong Wu, Feng Xi, Loïc Yengo, Chang Yu, X. Zhang, J. Zhang, Q. Zhang, Wei Zhang, Hancheng Zheng, Yi‐Hui Zhou, David Altshuler, Leen M. ’t Hart, Paul W. Franks, Beverley Balkau, Philippe Froguel, Mark I. McCarthy, Markku Laakso, Leif Groop, C Christensen, Ivan Brandslund, T. Lauritzen, Daniel R. Witte

    出版 2012
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  16. 16
    Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

    Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis 由 Benjamin F. Voight, Laura J. Scott, Valgerður Steinthórsdóttir, Andrew P. Morris, Christian Dina, Ryan Welch, Eleftheria Zeggini, Cornelia Huth, Yurii S. Aulchenko, Guðmar Þorleifsson, Laura McCulloch, Teresa Ferreira, Harald Grallert, Najaf Amin, Guanming Wu, Cristen J. Willer, Soumya Raychaudhuri, Steve McCarroll, Claudia Langenberg, Oliver Hofmann, Josée Dupuis, Lu Qi, Ayellet V. Segrè, Mandy van Hoek, Pau Navarro, Kristin Ardlie, Beverley Balkau, Rafn Benediktsson, Amanda J. Bennett, Roza Blagieva, Eric Boerwinkle, Lori L. Bonnycastle, Kristina Bengtsson Boström, Bert Bravenboer, Suzannah Bumpstead, Noisël P Burtt, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Gabe Crawford, Alex S. F. Doney, Katherine S. Elliott, Amanda L. Elliott, Michael R. Erdos, Caroline S. Fox, Christopher S. Franklin, Martha Ganser, Christian Gieger, Niels Grarup, Todd J. Green, Simon J. Griffin, Christopher J. Groves, Candace Guiducci, Samy Hadjadj, Neelam Hassanali, Christian Herder, Bo Isomaa, Anne Jackson, Paul R V Johnson, Torben Jørgensen, Wen H. Kao, Norman Klopp, Augustine Kong, Peter Kraft, Johanna Kuusisto, Torsten Lauritzen, Man Li, Aloysius G. Lieverse, Cecilia M. Lindgren, Valeriya Lyssenko, Michel Marre, Thomas Meitinger, Kristian Midthjell, Mario A. Morken, Narisu Narisu, Peter M. Nilsson, Katharine R. Owen, Felicity Payne, John R. B. Perry, Ann-Kristin Petersen, Carl G. P. Platou, Christine Proença, Inga Prokopenko, Wolfgang Rathmann, Nigel W. Rayner, Neil R. Robertson, Ghislain Rocheleau, Michael Roden, Michael Sampson, Richa Saxena, Beverley M. Shields, Peter Shrader, Gunnar Sigurðsson, Thomas Sparsø, Klaus Straßburger, Heather M. Stringham, Qi Sun, Amy J. Swift, Barbara Thorand

    出版 2010
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  17. 17
    Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

    Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge 由 Richa Saxena, Marie‐France Hivert, Claudia Langenberg, Toshiko Tanaka, James S. Pankow, Péter Vollenweider, Valeriya Lyssenko, Nabila Bouatia‐Naji, Josée Dupuis, Anne Jackson, W.H. Linda Kao, Man Li, Nicole L. Glazer, Man Li, Jian’an Luan, Heather M. Stringham, Inga Prokopenko, Toby Johnson, Niels Grarup, Trine Welløv Boesgaard, Cécile Lecœur, Peter Shrader, Jeffrey R. O’Connell, Erik Ingelsson, David Couper, Kenneth Rice, Kijoung Song, Camilla Andreasen, Christian Dina, Anna Köttgen, Olivier Le Bacquer, François Pattou, Jalal Taneera, Valgerður Steinthórsdóttir, Denis Rybin, Kristin Ardlie, Michael Sampson, Lu Qi, Mandy van Hoek, Michael N. Weedon, Yurii S. Aulchenko, Benjamin F. Voight, Harald Grallert, Beverley Balkau, Richard N. Bergman, Suzette J. Bielinski, Amélie Bonnefond, Lori L. Bonnycastle, Knut Borch‐Johnsen, Yvonne Böttcher, Eric J. Brunner, Thomas A. Buchanan, Suzannah J. Bumpstead, Christine Cavalcanti-Proença, G. Charpentier, Yii-Der Ida Chen, Peter S. Chines, Francis S. Collins, Marilyn C. Cornelis, Gabriel Crawford, Jérôme Delplanque, Alex S. F. Doney, Josephine M. Egan, Michael R. Erdos, Mathieu Firmann, Nita G. Forouhi, Caroline S. Fox, Mark O. Goodarzi, J. Graessler, Aroon D. Hingorani, Bo Isomaa, Torben Jørgensen, Mika Kivimäki, Péter Kovács, Knut Krohn, Meena Kumari, Torsten Lauritzen, Claire Lévy‐Marchal, Vladimir Mayor, Jarred B. McAteer, Stephen Eyre, Braxton D. Mitchell, Karen L. Mohlke, Mario A. Morken, Narisu Narisu, Colin N. A. Palmer, Ruth Pakyz, Laura Pascoe, Felicity Payne, Daniel S. Pearson, Wolfgang Rathmann, Annelli Sandbæk, Avan Aihie Sayer, Laura J. Scott, Stephen J. Sharp, Eric J.G. Sijbrands, Andrew B. Singleton, David S. Siscovick, Nicholas L. Smith, Thomas Sparsø

    出版 2010
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  18. 18
    Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

    Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci 由 Kyle J. Gaulton, Teresa Ferreira, Yeji Lee, Anne Raimondo, Reedik Mägi, Michael E. Reschen, Anubha Mahajan, Adam E. Locke, Nigel W. Rayner, Neil Robertson, Robert A. Scott, Inga Prokopenko, Laura J. Scott, Todd Green, Thomas Sparsø, Dorothée Thuillier, Loïc Yengo, Harald Grallert, Simone Wahl, Mattias Frånberg, Rona J. Strawbridge, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Valgerður Steinthórsdóttir, Guðmar Þorleifsson, Lu Qi, Lennart C. Karssen, Jin‐Moo Lee, Sara M. Willems, Man Li, Han Chen, Christian Fuchsberger, Phoenix Kwan, Clement Ma, Michael D. Linderman, Yingchang Lu, Soren K. Thomsen, Jana K. Rundle, Nicola L. Beer, Martijn van de Bunt, Anil Chalisey, Hyun Min Kang, Benjamin F. Voight, Gonçalo R. Abecasis, Peter Almgren, Damiano Baldassarre, Beverley Balkau, Rafn Benediktsson, Matthias Blüher, Heiner Boeing, Lori L. Bonnycastle, Erwin P. Böttinger, Noël P. Burtt, Jason Carey, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Andrew Crenshaw, Rob M. van Dam, Alex S. F. Doney, Mozhgan Dorkhan, Sarah Edkins, Johan G. Eriksson, Tõnu Esko, Elodie Eury, João Fadista, Jason Flannick, Pierre Fontanillas, Caroline S. Fox, Paul W. Franks, Karl Gertow, Christian Gieger, Bruna Gigante, Omri Gottesman, George Grant, Niels Grarup, Christopher J. Groves, Maija Hassinen, Henri Theil, Christian Herder, Oddgeir L. Holmen, Ástráður B. Hreiðarsson, Steve E. Humphries, Sarah Hunt, Anne Jackson, Anna Jonsson, Marit E. Jørgensen, Torben Jørgensen, Wen‐Hong L. Kao, Nicola D. Kerrison, Leena Kinnunen, Norman Klopp, Augustine Kong, Péter Kovács, Peter Kraft, Jasmina Kravić, Cordelia Langford

    出版 2015
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  19. 19
    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans 由 Robert A. Scott, Laura J. Scott, Reedik Mägi, Letizia Marullo, Kyle J. Gaulton, Marika Kaakinen, Natalia Pervjakova, Tune H. Pers, Andrew D. Johnson, John D. Eicher, Anne Jackson, Teresa Ferreira, Yeji Lee, Clement Ma, Valgerður Steinthórsdóttir, Guðmar Þorleifsson, Lu Qi, Natalie R. van Zuydam, Anubha Mahajan, Han Chen, Peter Almgren, Benjamin F. Voight, Harald Grallert, Martina Müller‐Nurasyid, Janina S. Ried, Nigel W. Rayner, Neil Robertson, Lennart C. Karssen, Jin‐Moo Lee, Sara M. Willems, Christian Fuchsberger, Phoenix Kwan, Tanya M. Teslovich, Pritam Chanda, Man Li, Yingchang Lu, Christian Dina, Dorothée Thuillier, Loïc Yengo, Longda Jiang, Thomas Sparsø, Hans A. Kestler, Himanshu Chheda, Lewin Eisele, Stefan Gustafsson, Mattias Frånberg, Rona J. Strawbridge, Rafn Benediktsson, Ástráður B. Hreiðarsson, Augustine Kong, Gunnar Sigurðsson, Nicola D. Kerrison, Jian’an Luan, Liming Liang, Thomas Meitinger, Michael Roden, Barbara Thorand, Tõnu Esko, Evelin Mihailov, Caroline S. Fox, Yongmei Liu, Denis Rybin, Bo Isomaa, Valeriya Lyssenko, Jaakko Tuomilehto, David Couper, James S. Pankow, Niels Grarup, Henri Theil, Marit E. Jørgensen, Torben Jørgensen, Allan Linneberg, Marilyn C. Cornelis, Rob M. van Dam, Sarah Hunt, Peter Kraft, Qi Sun, Sarah Edkins, Katharine R. Owen, John R. B. Perry, Andrew R. Wood, Eleftheria Zeggini, Juan Tajes-Fernandes, Gonçalo R. Abecasis, Lori L. Bonnycastle, Peter S. Chines, Heather M. Stringham, Heikki A. Koistinen, Leena Kinnunen, Bengt Sennblad, Hae‐Won Uh, Markus M. Nöthen, Sonali Pechlivanis, Damiano Baldassarre, Karl Gertow, Steve E. Humphries, Elena Tremoli, Norman Klopp, Julia Meyer, Gerald Steinbach

    出版 2017
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  20. 20
    CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

    CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits 由 Aurélien Macé, Marcus A. Tuke, Patrick Deelen, Kati Kristiansson, Hannele Mattsson, Margit Nõukas, Yadav Sapkota, Ursula M. Schick, Eleonora Porcu, Sina Rüeger, Aaron F. McDaid, David J. Porteous, Thomas W. Winkler, Erika Salvi, Nick Shrine, Xueping Liu, Wei Ang, Weihua Zhang, Mary F. Feitosa, Cristina Venturini, Peter J. van der Most, Anders Rosengren, Andrew R. Wood, Robin N. Beaumont, Samuel E. Jones, Katherine S. Ruth, Hanieh Yaghootkar, Jessica Tyrrell, Aki S. Havulinna, Harmen Boers, Reedik Mägi, Jennifer Kriebel, Martina Müller‐Nurasyid, Markus Perola, Markku S. Nieminen, Marja‐Liisa Lokki, Mika Kähönen, Jorma Viikari, Frank Geller, Jari Lahti, Aarno Palotie, Päivikki Koponen, Annamari Lundqvist, Harri Rissanen, Erwin P. Böttinger, Saima Afaq, Mary K. Wojczynski, Petra Lenzini, Ilja M. Nolte, Thomas Sparsø, Nicole Schupf, Kaare Christensen, Thomas T. Perls, Anne B. Newman, Thomas Werge, Harold Snieder, Timothy D. Spector, John C. Chambers, Seppo Koskinen, Mads Melbye, Olli T. Raitakari, Terho Lehtimäki, Martin D. Tobin, Louise V. Wain, Juha Sinisalo, Annette Peters, Thomas Meitinger, Nicholas G. Martin, Naomi R. Wray, Grant W. Montgomery, Sarah E. Medland, Morris A. Swertz, Erkki Vartiainen, Katja Borodulin, Satu Männistö, Anna Murray, Murielle Bochud, Sébastien Jacquemont, Fernando Rivadeneira, Thomas Hansen, Albertine J. Oldehinkel, Massimo Mangino, Michael A. Province, Panos Deloukas, Jaspal S. Kooner, Rachel M. Freathy, Craig E. Pennell, Bjarke Feenstra, David P. Strachan, Guillaume Lettre, Joel N. Hirschhorn, Daniele Cusi, Iris M. Heid, Caroline Hayward, Katrin Männik, J. Beckmann, Ruth J. F. Loos, Dale R. Nyholt, Andres Metspalu, Johan G. Eriksson

    出版 2017
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