Kết quả tìm kiếm - Aliki‐Eleni Farmaki

Tinh chỉnh kết quả
  1. 1
    HbA1c and brain health across the entire glycaemic spectrum

    HbA1c and brain health across the entire glycaemic spectrum Bằng Victoria Garfield, Aliki‐Eleni Farmaki, Sophie V. Eastwood, Rohini Mathur, Christopher T. Rentsch, Krishnan Bhaskaran, Liam Smeeth, Nish Chaturvedi

    Được phát hành 2021
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  2. 2
    Risk of 16 cancers across the full glycemic spectrum: a population-based cohort study using the UK Biobank

    Risk of 16 cancers across the full glycemic spectrum: a population-based cohort study using the UK Biobank Bằng Christopher T. Rentsch, Ruth Farmer, Sophie V. Eastwood, Rohini Mathur, Victoria Garfield, Aliki‐Eleni Farmaki, Krishnan Bhaskaran, Nish Chaturvedi, Liam Smeeth

    Được phát hành 2020
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  3. 3
    Relationship Between Glycemia and Cognitive Function, Structural Brain Outcomes, and Dementia: A Mendelian Randomization Study in the UK Biobank

    Relationship Between Glycemia and Cognitive Function, Structural Brain Outcomes, and Dementia: A Mendelian Randomization Study in the UK Biobank Bằng Victoria Garfield, Aliki‐Eleni Farmaki, Ghazaleh Fatemifar, Sophie V. Eastwood, Rohini Mathur, Christopher T. Rentsch, Spiros Denaxas, Krishnan Bhaskaran, Liam Smeeth, Nish Chaturvedi

    Được phát hành 2021
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  4. 4
    Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits

    Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits Bằng Lorraine Southam, Arthur Gilly, Dániel Süveges, Aliki‐Eleni Farmaki, Jeremy Schwartzentruber, Ioanna Tachmazidou, Angela Matchan, Nigel W. Rayner, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini

    Được phát hành 2017
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  5. 5
    Very low-depth whole-genome sequencing in complex trait association studies

    Very low-depth whole-genome sequencing in complex trait association studies Bằng Arthur Gilly, Lorraine Southam, Dániel Süveges, Karoline Kuchenbaecker, Rachel Moore, Giorgio Melloni, Konstantinos Hatzikotoulas, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Jeremy Schwartzentruber, Petr Danecek, Britt Kilian, Martin Pollard, Xiangyu Ge, Emmanouil Tsafantakis, George Dedoussis, Eleftheria Zeggini

    Được phát hành 2018
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  6. 6
    Social, economic and demographic correlates of overweight and obesity in primary-school children: preliminary data from the Healthy Growth Study

    Social, economic and demographic correlates of overweight and obesity in primary-school children: preliminary data from the Healthy Growth Study Bằng George Moschonis, Sofia Tanagra, Anastasia Vandorou, Aikaterini Kyriakou, Vasiliki Dede, Paraskevi E Siatitsa, Alexandra Koumpitski, Odysseas Androutsos, Evangelia Grammatikaki, Maria Kantilafti, Anthi Naoumi, Aliki Eleni Farmaki, Aikaterini Siopi, Eleni Papadopoulou, Elpida Voutsadaki, Fanouria Chlouveraki, Konstantina Maragkopoulou, Efstathoula Argyri, Aggeliki Giannopoulou, Yannis Μanios

    Được phát hành 2010
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  7. 7
    A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates

    A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates Bằng Ioanna Tachmazidou, George Dedoussis, Lorraine Southam, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Dionysia K. Xifara, Angela Matchan, Konstantinos Hatzikotoulas, Nigel W. Rayner, Yuan Chen, Toni I. Pollin, Jeffrey R. O’Connell, Laura M. Yerges-Armstrong, Chrysoula Kiagiadaki, Kalliope Panoutsopoulou, Jeremy Schwartzentruber, Loukas Moutsianas, Emmanouil Tsafantakis, Chris Tyler‐Smith, Gil McVean, Yali Xue, Eleftheria Zeggini

    Được phát hành 2013
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  8. 8
    Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants

    Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants Bằng Kalliope Panoutsopoulou, Konstantinos Hatzikotoulas, Dionysia K. Xifara, Vincenza Colonna, Aliki‐Eleni Farmaki, Graham R. S. Ritchie, Lorraine Southam, Arthur Gilly, Ioanna Tachmazidou, Segun Fatumo, Angela Matchan, Nigel W. Rayner, Ιωάννα Ντάλλα, Massimo Mezzavilla, Yuan Chen, Chrysoula Kiagiadaki, Eleni Zengini, Vasiliki Mamakou, Antonis Athanasiadis, Μαργαρίτα Γιαννακοπούλου, Vassiliki-Eirini Kariakli, Rebecca N. Nsubuga, Alex Karabarinde, Manjinder S. Sandhu, Gil McVean, Chris Tyler‐Smith, Emmanouil Tsafantakis, Maria Karaleftheri, Yali Xue, George Dedoussis, Eleftheria Zeggini

    Được phát hành 2014
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  9. 9
    Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

    Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps Bằng Valentina Iotchkova, Jie Huang, John Morris, Deepti Jain, Caterina Barbieri, Klaudia Walter, Josine L. Min, Lu Chen, William J. Astle, Massimiliano Cocca, Patrick Deelen, Heather Elding, Aliki‐Eleni Farmaki, Christopher S. Franklin, Mattias Frånberg, Tom R. Gaunt, Albert Hofman, Tao Jiang, Marcus E. Kleber, Geneviève Lachance, Jian’an Luan, Giovanni Malerba, Angela Matchan, Daniel G. Mead, Yasin Memari, Ιωάννα Ντάλλα, Kalliope Panoutsopoulou, Raha Pazoki, John R. B. Perry, Fernando Rivadeneira, Maria Sabater‐Lleal, Bengt Sennblad, So–Youn Shin, Lorraine Southam, Michela Traglia, Freerk van Dijk, Jin‐Moo Lee, Gianluigi Zaza, Weihua Zhang, Najaf Amin, Adam S. Butterworth, John C. Chambers, George Dedoussis, Abbas Dehghan, Oscar H. Franco, Lude Franke, Mattia Frontini, Giovanni Gambaro, Paolo Gasparini, Anders Hamsten, Aaron Issacs, Jaspal S. Kooner, Charles Kooperberg, Claudia Langenberg, Winfried März, Robert A. Scott, Morris A. Swertz, Daniela Toniolo, André G. Uitterlinden, Cornelia M. van Duijn, Hugh Watkins, Eleftheria Zeggini, Mathew T Maurano, Nicholas J. Timpson, Alexander P. Reiner, Paul L. Auer, Nicole Soranzo

    Được phát hành 2016
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  10. 10
    A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

    A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans Bằng Nicholas J. Timpson, Klaudia Walter, Josine L. Min, Ioanna Tachmazidou, Giovanni Malerba, So–Youn Shin, Lu Chen, Marta Futema, Lorraine Southam, Valentina Iotchkova, Massimiliano Cocca, Jie Huang, Yasin Memari, Shane McCarthy, Petr Danecek, Dawn Muddyman, Massimo Mangino, Cristina Menni, John R. B. Perry, Susan M. Ring, Amadou Gaye, George Dedoussis, Aliki‐Eleni Farmaki, Paul R. Burton, Philippa J. Talmud, Giovanni Gambaro, Tim D. Spector, George Davey Smith, Richard Durbin, J. Brent Richards, Steve E. Humphries, Eleftheria Zeggini, Nicole Soranzo, Saeed Al Turki, Carl A. Anderson, Richard Anney, Dinu Antony, María Soler Artigas, Muhammad Ayub, Senduran Balasubramaniam, Jeffrey C. Barrett, Inês Barroso, Phil Beales, Jamie Bentham, Shoumo Bhattacharya, Ewan Birney, Douglas Blackwood, Martin Bobrow, Elena G. Bochukova, Patrick Bolton, Rebecca Bounds, Chris Boustred, Gerome Breen, Mattia Calissano, Keren Carss, Krishna Chatterjee, Lu Chen, Antonio Ciampi, Sebhattin Cirak, Peter Clapham, Gail Clement, Guy Coates, David Collier, Catherine Cosgrove, Tony Cox, Nick Craddock, Lucy Crooks, Sarah Curran, David Curtis, Allan Daly, Petr Danecek, George Davey Smith, Aaron Day-Williams, Ian N.M. Day, Thomas A. Down, Yuanping Du, Ian Dunham, Richard Durbin, Sarah Edkins, Peter Ellis, David M. Evans, Sadaf Faroogi, Ghazaleh Fatemifar, David Fitzpatrick, Paul Flicek, James Flyod, A. Reghan Foley, Christopher S. Franklin, Marta Futema, Louise Gallagher, Tom R. Gaunt, Matthias Geihs, Daniel Geschwind, Celia M.T. Greenwood, Heather Griffin, Detelina Grozeva, Xueqin Guo, Xiaosen Guo, Hugh Gurling, Deborah Hart

    Được phát hành 2014
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  11. 11
    Directional dominance on stature and cognition in diverse human populations

    Directional dominance on stature and cognition in diverse human populations Bằng 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

    Được phát hành 2015
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  12. 12
    Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

    Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility Bằng Jennifer Wessel, Audrey Y. Chu, Sara M. Willems, Shuai Wang, Hanieh Yaghootkar, Jennifer A. Brody, Marco Dauriz, Marie‐France Hivert, Sridharan Raghavan, Leonard Lipovich, Bertha Hidalgo, Keolu Fox, Jennifer E. Huffman, Ping An, Yingchang Lu, Laura J. Rasmussen‐Torvik, Niels Grarup, Margaret G. Ehm, Li Li, Abigail S. Baldridge, Alena Stančáková, Ravinder Abrol, Céline Besse, Anne Boland, Jette Bork‐Jensen, Myriam Fornage, Daniel F. Freitag, Melissa E. Garcia, Xiuqing Guo, Kazuo Hara, Aaron Isaacs, Jóhanna Jakobsdóttir, Leslie A. Lange, Jill Layton, Man Li, Wei Zhao, Karina Meidtner, Alanna C. Morrison, Mike A. Nalls, Marjolein J. Peters, Maria Sabater‐Lleal, Claudia Schurmann, Angela Silveira, Albert V. Smith, Lorraine Southam, Marcus H. Stoiber, Rona J. Strawbridge, Kent D. Taylor, Tibor V. Varga, Kristine H. Allin, Najaf Amin, Jennifer L. Aponte, Tin Aung, Caterina Barbieri, Nathan A. Bihlmeyer, Michael Boehnke, Cristina Bombieri, Donald W. Bowden, Sean M. Burns, Yuning Chen, Yii-DerI Chen, Ching‐Yu Cheng, Adolfo Correa, Jacek Czajkowski, Abbas Dehghan, Georg Ehret, Guðný Eiríksdóttir, Stefan Andersson Escher, Aliki-Eleni Farmaki, Mattias Frånberg, Giovanni Gambaro, Franco Giulianini, William A. Goddard, Anuj Goel, Omri Gottesman, Megan L. Grove, Stefan Gustafsson, Yang Hai, Göran Hallmans, Jiyoung Heo, Per Hoffmann, M. Kamran Ikram, Richard A. Jensen, Marit E. Jørgensen, Torben Jørgensen, Maria Karaleftheri, Chiea Chuen Khor, Andrea Kirkpatrick, Aldi T. Kraja, Johanna Kuusisto, Ethan M. Lange, I. T. Lee, Wen‐Jane Lee, Aaron Leong, Jiemin Liao, Chunyu Liu, Yongmei Liu, Cecilia M. Lindgren, Allan Linneberg, Giovanni Malerba

    Được phát hành 2015
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  13. 13
    A reference panel of 64,976 haplotypes for genotype imputation

    A reference panel of 64,976 haplotypes for genotype imputation Bằng Shane McCarthy, Sayantan Das, Warren W. Kretzschmar, Olivier Delaneau, Andrew R. Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp, Yang Luo, Carlo Sidore, Alan Kwong, Nicholas J. Timpson, Seppo Koskinen, Scott Vrieze, Laura J. Scott, He Zhang, Anubha Mahajan, Jan H. Veldink, Ulrike Peters, Carlos N. Pato, Cornelia M. van Duijn, Christopher E. Gillies, Ilaria Gandin, Massimo Mezzavilla, Arthur Gilly, Massimiliano Cocca, Michela Traglia, Andrea Angius, Jeffrey C. Barrett, Dorrett Boomsma, Kari Branham, Gerome Breen, Chad M. Brummett, Fabio Busonero, Harry Campbell, Andrew T. Chan, Sai Chen, Emily Y. Chew, Francis S. Collins, Laura J. Corbin, George Davey Smith, George Dedoussis, Marcus Dörr, Aliki-Eleni Farmaki, Luigi Ferrucci, Lukas Forer, Ross M. Fraser, Stacey Gabriel, Shawn Levy, Leif Groop, Tabitha A. Harrison, Andrew T. Hattersley, Oddgeir L. Holmen, Kristian Hveem, Matthias Kretzler, James Lee, Matt McGue, Thomas Meitinger, David Melzer, Josine L. Min, Karen L. Mohlke, John B. Vincent, Matthias Nauck, Deborah A. Nickerson, Aarno Palotie, Michele T. Pato, Nicola Pirastu, Melvin G. McInnis, J. Brent Richards, Cinzia Sala, Veikko Salomaa, David Schlessinger, Sebastian Schoenherr, P. Eline Slagboom, Kerrin S. Small, Timothy D. Spector, Dwight Stambolian, Marcus A. Tuke, Jaakko Tuomilehto, Leonard H. van den Berg, Wouter van Rheenen, Uwe Völker, Cisca Wijmenga, Daniela Toniolo, Eleftheria Zeggini, Paolo Gasparini, Matthew G. Sampson, James F. Wilson, Timothy M. Frayling, Paul I. W. de Bakker, Morris A. Swertz, Steven A. McCarroll, Charles Kooperberg, Annelot M. Dekker, David Altshuler, Cristen J. Willer, William G. Iacono, Samuli Ripatti

    Được phát hành 2016
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  14. 14
    Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

    Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension Bằng Praveen Surendran, Fotios Drenos, Robin Young, Helen R. Warren, James P. Cook, Alisa K. Manning, Niels Grarup, Xueling Sim, Daniel R. Barnes, Kate Witkowska, James R Staley, Vinicius Tragante, Taru Tukiainen, Hanieh Yaghootkar, Nicholas G. D. Masca, Daniel F. Freitag, Teresa Ferreira, Olga Giannakopoulou, Andrew Tinker, Magdaléna Harakaľová, Evelin Mihailov, Chunyu Liu, Aldi T. Kraja, Yan V. Sun, Asif Rasheed, Maria Samuel, Wei Zhao, Lori L. Bonnycastle, Anne Jackson, Narisu Narisu, Amy J. Swift, Lorraine Southam, Jonathan Marten, Jeroen R. Huyghe, Alena Stančáková, Cristiano Fava, Therese Ohlsson, Angela Matchan, Kathleen Stirrups, Jette Bork‐Jensen, Anette P. Gjesing, Jukka Kontto, Markus Perola, Susan Shaw-Hawkins, Aki S. Havulinna, He Zhang, Louise A. Donnelly, Christopher J. Groves, Nigel W. Rayner, Matt J. Neville, Neil R. Robertson, Andrianos M. Yiorkas, Karl‐Heinz Herzig, Eero Kajantie, Weihua Zhang, Sara M. Willems, Lars Lannfelt, Giovanni Malerba, Nicole Soranzo, Elisabetta Trabetti, Niek Verweij, Εvangelos Εvangelou, Alireza Moayyeri, Anne‐Claire Vergnaud, Christopher P. Nelson, Alaitz Poveda, Tibor V. Varga, Muriel Caslake, Anton J. M. de Craen, Stella Trompet, Jian’an Luan, Robert A. Scott, Sarah E. Harris, David C. Liewald, Riccardo E. Marioni, Cristina Menni, Aliki-Eleni Farmaki, Göran Hallmans, Frida Renström, Jennifer E. Huffman, Maija Hassinen, Stephen Burgess, Ramachandran S. Vasan, Janine F. Felix, Maria Uria-Nickelsen, Anders Mälarstig, Dermot F. Reilly, Maarten Hoek, Thomas Vogt, Honghuang Lin, Wolfgang Lieb, Matthew Traylor, Hugh S. Markus, Heather M. Highland, Anne E. Justice, Eirini Marouli, Jaana Lindström, Matti Uusitupa, Pirjo Komulainen, Timo A. Lakka

    Được phát hành 2016
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  15. 15
    A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

    A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape Bằng Janina S. Ried, Janina Jeff M., Audrey Y. Chu, Jennifer L. Bragg‐Gresham, Jenny van Dongen, Jennifer E. Huffman, Tarunveer S. Ahluwalia, Gemma Cadby, Niina Eklund, Joel Eriksson, Tõnu Esko, Mary F. Feitosa, Anuj Goel, Mathias Gorski, Caroline Hayward, Nancy L. Heard‐Costa, Anne Jackson, Eero Jokinen, Stavroula Kanoni, Kati Kristiansson, Zoltán Kutalik, Jari Lahti, Jian’an Luan, Reedik Mägi, Anubha Mahajan, Massimo Mangino, Carolina Medina‐Gómez, Keri L. Monda, Ilja M. Nolte, Louis Pérusse, Inga Prokopenko, Lu Qi, Lynda M. Rose, Erika Salvi, Megan Therese Smith, Harold Snieder, Alena Stančáková, Yan V. Sun, Ioanna Tachmazidou, Alexander Teumer, Guðmar Þorleifsson, Pim van der Harst, Ryan W. Walker, Sophie R. Wang, Sarah H. Wild, Sara M. Willems, Andrew Wong, Weihua Zhang, Eva Albrecht, Alexessander Couto Alves, Stephan J. L. Bakker, Cristina Barlassina, Traci M. Bartz, John Beilby, Claire Bellis, Richard N. Bergman, Sven Bergmann, John Blangero, Matthias Blüher, Eric Boerwinkle, Lori L. Bonnycastle, Stefan R. Bornstein, Marcel Bruinenberg, Harry Campbell, Yii-Der Ida Chen, Charleston W. K. Chiang, Peter S. Chines, Francis S. Collins, Francesco Cucca, L. Adrienne Cupples, Francesca D’Avila, Eco J. C. de Geus, George Dedoussis, Maria Dimitriou, Angela Döring, Johan G. Eriksson, Aliki-Eleni Farmaki, Martin Farrall, Teresa Ferreira, Krista Fischer, Nita G. Forouhi, Nele Friedrich, Anette P. Gjesing, Nicola Glorioso, Mariaelisa Graff, Harald Grallert, Niels Grarup, Jürgen Gräßler, Jagvir Grewal, Anders Hamsten, Marie Neergaard Harder, Catharina A. Hartman, Maija Hassinen, Nicholas D. Hastie, Andrew T. Hattersley, Aki S. Havulinna, Markku Heliövaara, Hans L. Hillege, Albert Hofman, Oddgeir L. Holmen

    Được phát hành 2016
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  16. 16
    Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

    Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits Bằng Ioanna Tachmazidou, Dániel Süveges, Josine L. Min, Graham R. S. Ritchie, Julia Steinberg, Klaudia Walter, Valentina Iotchkova, Jeremy Schwartzentruber, Jie Huang, Yasin Memari, Shane McCarthy, Andrew Crawford, Cristina Bombieri, Massimiliano Cocca, Aliki-Eleni Farmaki, Tom R. Gaunt, Jari Lahti, Marjolein N. Kooijman, Benjamin Lehne, Giovanni Malerba, Satu Männistö, Angela Matchan, Carolina Medina‐Gómez, Sarah Metrustry, Abhishek Nag, Ιωάννα Ντάλλα, Lavinia Paternoster, Nigel W. Rayner, Cinzia Sala, William R. Scott, Hashem A. Shihab, Lorraine Southam, Beaté St Pourcain, Michela Traglia, Katerina Trajanoska, Gianluigi Zaza, Weihua Zhang, María Soler Artigas, Narinder Bansal, Marianne Benn, Zhongsheng Chen, Petr Danecek, Wei‐Yu Lin, Adam E. Locke, Jian’an Luan, Alisa K. Manning, Antonella Mulas, Carlo Sidore, Anne Tybjærg‐Hansen, Anette Varbo, Magdalena Żołędziewska, Chris Finan, Konstantinos Hatzikotoulas, Audrey E. Hendricks, John P. Kemp, Alireza Moayyeri, Kalliope Panoutsopoulou, Michał Szpak, Scott G. Wilson, Michael Boehnke, Francesco Cucca, Emanuele Di Angelantonio, Claudia Langenberg, Cecilia M. Lindgren, Mark I. McCarthy, Andrew P. Morris, Børge G. Nordestgaard, Robert A. Scott, Martin D. Tobin, Nicholas J. Wareham, Paul R. Burton, John C. Chambers, George Davey Smith, George Dedoussis, Janine F. Felix, Oscar H. Franco, Giovanni Gambaro, Paolo Gasparini, Christopher J. Hammond, Albert Hofman, Vincent W. V. Jaddoe, Marcus E. Kleber, Jaspal S. Kooner, Markus Perola, Caroline L. Relton, Susan M. Ring, Fernando Rivadeneira, Veikko Salomaa, Timothy D. Spector, Oliver Stegle, Daniela Toniolo, André G. Uitterlinden, Inês Barroso, Celia M.T. Greenwood, John R. B. Perry, Brian R. Walker, Adam S. Butterworth, Yali Xue, Richard Durbin, Kerrin S. Small

    Được phát hành 2017
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  17. 17
    Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

    Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution Bằng Anne E. Justice, Tugce Karaderi, Heather M. Highland, Kristin L. Young, Mariaelisa Graff, Yingchang Lu, Valérie Turcot, Paul L. Auer, Rebecca S. Fine, Xiuqing Guo, Claudia Schurmann, Adelheid Lempradl, Eirini Marouli, Anubha Mahajan, Thomas Winkler, Adam E. Locke, Carolina Medina‐Gómez, Tõnu Esko, Sailaja Vedantam, Ayush Giri, Ken Sin Lo, Tamuno Alfred, Poorva Mudgal, Maggie C. Y. Ng, Nancy L. Heard‐Costa, Mary F. Feitosa, Alisa K. Manning, Sara M. Willems, Suthesh Sivapalaratnam, Gonçalo R. Abecasis, Dewan S Alam, Matthew Allison, Philippe Amouyel, Zorayr Arzumanyan, Beverley Balkau, Lisa Bastarache, Sven Bergmann, Lawrence F. Bielak, Matthias Blüher, Michael Boehnke, Heiner Boeing, Eric Boerwinkle, Carsten A. Böger, Jette Bork‐Jensen, Erwin P. Böttinger, Donald W. Bowden, Ivan Brandslund, Linda Broer, Amber Burt, Adam S. Butterworth, Mark J. Caulfield, Giancarlo Cesana, John C. Chambers, Daniel I. Chasman, Yii‐Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y. Chu, Francis S. Collins, James P. Cook, Amanda J. Cox, David S. Crosslin, John Danesh, Paul I. W. de Bakker, Simon de Denus, Renée de Mutsert, George Dedoussis, Ellen W. Demerath, Joe Dennis, Joshua C. Denny, Emanuele Di Angelantonio, Marcus Dörr, Fotios Drenos, Marie‐Pierre Dubé, Alison M. Dunning, Douglas F. Easton, Paul Elliott, Εvangelos Εvangelou, Aliki‐Eleni Farmaki, Shuang Feng, Ele Ferrannini, Jean Ferrières, José C. Florez, Myriam Fornage, Caroline S. Fox, Paul W. Franks, Nele Friedrich, Wei Gan, Ilaria Gandin, Paolo Gasparini, Vilmantas Giedraitis, Giorgia Girotto, Mathias Gorski, Harald Grallert, Niels Grarup, Megan L. Grove, Stefan Gustafsson, Jeff Haessler, Torben Hansen, Andrew T. Hattersley

    Được phát hành 2019
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  18. 18
    A reference panel of 64,976 haplotypes for genotype imputation

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    Được phát hành 2015
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  19. 19
    New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals

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    Được phát hành 2017
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  20. 20
    A saturated map of common genetic variants associated with human height

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