Search Results - Suthesh Sivapalaratnam

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  1. 1
    Diagnosis of inherited bleeding disorders in the genomic era

    Diagnosis of inherited bleeding disorders in the genomic era by Suthesh Sivapalaratnam, Janine Collins, Keith Gomez

    Published 2017
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  2. 2
    Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study

    Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study by Suthesh Sivapalaratnam, S. Matthijs Boekholdt, Mieke D. Trip, Manjinder S. Sandhu, Robert Luben, J.J.P. Kastelein, Nicholas J. Wareham, Kay‐Tee Khaw

    Published 2010
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  3. 3
    Lupus Anticoagulant and Abnormal Coagulation Tests in Patients with Covid-19

    Lupus Anticoagulant and Abnormal Coagulation Tests in Patients with Covid-19 by Louise Bowles, Sean Platton, Nada Yartey, Minal Dave, Kurtis Lee, Daniel P. Hart, Vickie MacDonald, Laura Green, Suthesh Sivapalaratnam, John Pasi, Peter MacCallum

    Published 2020
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  4. 4
    Platelets in Patients with Premature Coronary Artery Disease Exhibit Upregulation of miRNA340* and miRNA624*

    Platelets in Patients with Premature Coronary Artery Disease Exhibit Upregulation of miRNA340* and miRNA624* by Brigitte M. Sondermeijer, Annemieke Bakker, Amalia Halliani, Maurice W.J. de Ronde, Arnoud A. Marquart, Anke J. Tijsen, Ties A. Mulders, M. G. M. Kok, Suzanne Battjes, S. Maiwald, Suthesh Sivapalaratnam, Mieke D. Trip, Perry D. Moerland, Joost C.M. Meijers, Esther E. Creemers, Sara‐Joan Pinto‐Sietsma

    Published 2011
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  5. 5
    Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome

    Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome by Cornelis A. Albers, Ana Cvejic, Rémi Favier, Evelien E. Bouwmans, Marie‐Christine Alessi, Paul Bertone, Gregory E. Jordan, Ross Kettleborough, Graham Kiddle, Myrto Kostadima, Randy J. Read, Botond Sipos, Suthesh Sivapalaratnam, Peter A. Smethurst, Jonathan Stephens, Katrin Voß, Alan T. Nurden, Augusto Rendon, Paquita Nurden, Willem H. Ouwehand

    Published 2011
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  6. 6
    High-throughput elucidation of thrombus formation reveals sources of platelet function variability

    High-throughput elucidation of thrombus formation reveals sources of platelet function variability by Johanna P. van Geffen, Sanne L. N. Brouns, Joana Batista, Harriet McKinney, Carly Kempster, Magdolna Nagy, Suthesh Sivapalaratnam, Constance C. F. M. J. Baaten, Nikki Bourry, Mattia Frontini, Kerstin Jurk, Manuela Krause, Daniele Pillitteri, Frauke Swieringa, Remco Verdoold, Rachel Cavill, Marijke J. E. Kuijpers, Willem H. Ouwehand, Kate Downes, Johan W. M. Heemskerk

    Published 2018
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  7. 7
    Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

    Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia by Suthesh Sivapalaratnam, Sarah K. Westbury, Jonathan Stephens, Daniel Greene, Kate Downes, Anne M. Kelly, Claire Lentaigne, William J. Astle, Eric G. Huizinga, Paquita Nurden, Sofia Papadia, Kathelijne Peerlinck, Christopher J. Penkett, David J. Perry, Catherine Roughley, Ilenia Simeoni, Kathleen Stirrups, Daniel P. Hart, Robert C. Tait, Andrew Mumford, Michael Laffan, Kathleen Freson, Willem H. Ouwehand, Shinji Kunishima, Ernest Turro

    Published 2016
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  8. 8
    Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

    Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders by Kate Downes, Karyn Mégy, Daniel Duarte, Minka J. A. Vries, Johanna Gebhart, Stefanie Hofer, Olga Shamardina, Sri V. V. Deevi, Jonathan Stephens, Rutendo Mapeta, Salih Tuna, Namir Al Hasso, Martin Besser, Nichola Cooper, Louise C. Daugherty, Nick Gleadall, Daniel Greene, Matthias Haimel, Howard Martin, Sofia Papadia, Shoshana Revel‐Vilk, Suthesh Sivapalaratnam, Emily Symington, Will Thomas, Chantal Thys, Alexander Tolios, Christopher J. Penkett, Willem H. Ouwehand, Stephen Abbs, Michael Laffan, Ernest Turro, Ilenia Simeoni, Andrew Mumford, Yvonne Henskens, Ingrid Pabinger, Keith Gomez, Kathleen Freson

    Published 2019
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  9. 9
    The Impact of Partial and Complete Loss-of-Function Mutations in Endothelial Lipase on High-Density Lipoprotein Levels and Functionality in Humans

    The Impact of Partial and Complete Loss-of-Function Mutations in Endothelial Lipase on High-Density Lipoprotein Levels and Functionality in Humans by Roshni R. Singaraja, Suthesh Sivapalaratnam, Kees Hovingh, Marie‐Pierre Dubé, José Castro‐Perez, Heidi L. Collins, Steven J. Adelman, Meliana Riwanto, Jasmin Manz, Brian K. Hubbard, Ian Tietjen, Kenny K. Wong, Lyndon J. Mitnaul, Margaret van Heek, Linus Lin, Thomas A. Roddy, Jason McEwen, Geesje M. Dallinge-Thie, Leonie van Vark‐van der Zee, Germaine C. Verwoert, Michael D. Winther, Cornelia M. van Duijn, Albert Hofman, Mieke D. Trip, A. David Marais, Bela F. Asztalos, Ulf Landmesser, Eric J.G. Sijbrands, John J.P. Kastelein, Michael R. Hayden

    Published 2012
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  10. 10
    Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia

    Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia by Nathan O. Stitziel, Sigrid W. Fouchier, Barbara Sjouke, Gina M. Peloso, Alessa M. Moscoso, Paul L. Auer, Anuj Goel, Bruna Gigante, Timothy Barnes, Olle Melander, Marju Orho‐Melander, Stefano Duga, Suthesh Sivapalaratnam, Majid Nikpay, Nicola Martinelli, Domenico Girelli, Rebecca D. Jackson, Charles Kooperberg, Leslie A. Lange, Diego Ardissino, Ruth McPherson, Martin Farrall, Hugh Watkins, Muredach P. Reilly, Daniel J. Rader, Ulf dé Fairé, Heribert Schunkert, Jeanette Erdmann, Mark M. Iles, Lawrence Charnas, David Altshuler, Stacey Gabriel, John J.P. Kastelein, Joep C. Defesche, Aart J. Nederveen, Sekar Kathiresan, G. Kees Hovingh

    Published 2013
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  11. 11
    Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

    Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome by Matthew C. Sims, Louisa Mayer, Janine Collins, Tadbir K. Bariana, Karyn Mégy, Cécile Lavenu‐Bombled, Denis Seyres, Laxmikanth Kollipara, Frances Burden, Daniel Greene, Dave Lee, Antonio Rodriguez-Romera, Marie‐Christine Alessi, William J. Astle, Wadie F. Bahou, Loredana Bury, Elizabeth Chalmers, Rachael Da Silva, Erica De Candia, Sri V. V. Deevi, Samantha Farrow, Keith Gomez, Luigi Grassi, Andreas Greinacher, Paolo Gresele, Dan Hart, Marie-Françoise Hurtaud, Anne M. Kelly, Ron Kerr, Sandra Le Quellec, Thierry Leblanc, Eva Leinøe, Rutendo Mapeta, Harriet McKinney, Alan D. Michelson, Sara Moráis, Diane J. Nugent, Sofia Papadia, Soo Jung Park, John Pasi, Gian Marco Podda, Man‐Chiu Poon, Rachel Reed, Mallika Sekhar, Hanna Shalev, Suthesh Sivapalaratnam, Orna Steinberg‐Shemer, Jonathan Stephens, Robert C. Tait, Ernest Turro, John K. Wu, Barbara Zieger, Taco W. Kuijpers, Anthony D. Whetton, Albert Sickmann, Kathleen Freson, Kate Downes, Wendy N. Erber, Mattia Frontini, Paquita Nurden, Willem H. Ouwehand, Rémi Favier, José A. Guerrero

    Published 2020
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  12. 12
    Mendelian randomization of blood lipids for coronary heart disease

    Mendelian randomization of blood lipids for coronary heart disease by Michael V. Holmes, Folkert W. Asselbergs, Tom Palmer, Fotios Drenos, Matthew B. Lanktree, Christopher P. Nelson, Caroline Dale, Sandosh Padmanabhan, Chris Finan, Daniel I. Swerdlow, Vinicius Tragante, Erik P.A. van Iperen, Suthesh Sivapalaratnam, Sonia Shah, Clara C. Elbers, Tina Shah, Jorgen Engmann, Claudia Giambartolomei, Jon White, Delilah Zabaneh, Reecha Sofat, Stela McLachlan, Pieter A. Doevendans, Anthony J. Balmforth, Alistair S. Hall, Kari E. North, Berta Almoguera, Ron C. Hoogeveen, Mary Cushman, Myriam Fornage, Sanjay R. Patel, Susan Redline, David S. Siscovick, Michael Y. Tsai, Konrad J. Karczewski, Marten H. Hofker, W. M. Monique Verschuren, Michiel L. Bots, Yvonne T. van der Schouw, Olle Melander, Anna F. Dominiczak, Richard Morris, Yoav Ben‐Shlomo, Jackie F. Price, Meena Kumari, Jens Baumert, Annette Peters, Barbara Thorand, Wolfgang Köenig, Tom R. Gaunt, Steve E. Humphries, Robert Clarke, Hugh Watkins, Martin Farrall, James G. Wilson, Stephen S. Rich, Paul I. W. de Bakker, Leslie A. Lange, George Davey Smith, Alex P. Reiner, Philippa J. Talmud, Mika Kivimäki, Debbie A. Lawlor, Frank Dudbridge, Nilesh J. Samani, Brendan J. Keating, Aroon D. Hingorani, Juan P. Casas

    Published 2014
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  13. 13
    The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

    The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease by William J. Astle, Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice Mann, Daniel G. Mead, Heleen Bouman, Fernando Riveros-Mckay, Myrto Kostadima, John Lambourne, Suthesh Sivapalaratnam, Kate Downes, Kousik Kundu, Lorenzo Bomba, Kim Berentsen, John R. Bradley, Louise C. Daugherty, Olivier Delaneau, Kathleen Freson, Stephen F. Garner, Luigi Grassi, José A. Guerrero, Matthias Haimel, Eva M. Janssen‐Megens, Anita Kaan, Mihir Kamat, Bowon Kim, Amit Mandoli, Jonathan Marchini, Joost H.A. Martens, Stuart Meacham, Karyn Mégy, Jared O’Connell, R. Petersen, Nilofar Sharifi, Simon Sheard, James R Staley, Salih Tuna, Martijn van der Ent, Klaudia Walter, Shuang-Yin Wang, Eleanor Wheeler, Steven P. Wilder, Valentina Iotchkova, Carmel Moore, Jennifer Sambrook, Hendrik G. Stunnenberg, Emanuele Di Angelantonio, Stephen Kaptoge, Taco W. Kuijpers, Enrique Carrillo de Santa Pau, David Juan, Daniel Rico, Alfonso Valencia, Lu Chen, Bing Ge, Louella Vasquez, Tony Kwan, Diego Garrido-Martín, Stephen Watt, Ying Yang, Roderic Guigó, Stephan Beck, Dirk S. Paul, Tomi Pastinen, David Bujold, Guillaume Bourque, Mattia Frontini, John Danesh, David J. Roberts, Willem H. Ouwehand, Adam S. Butterworth, Nicole Soranzo

    Published 2016
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  14. 14
    Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations

    Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations by Clara C. Elbers, Yiran Guo, Vinicius Tragante, Erik P.A. van Iperen, Matthew B. Lanktree, Berta Almoguera Castillo, Fang Chen, Lisa R. Yanek, Mary K. Wojczynski, Leslie A. Lange, Bart Ferwerda, Christie M. Ballantyne, Sarah G. Buxbaum, Yii-Der Ida Chen, Wei‐Min Chen, L. Adrienne Cupples, Mary Cushman, Yanan Duan, David Duggan, Michele K. Evans, Jyotika K. Fernandes, Myriam Fornage, Melissa García, W. Timothy Garvey, Nicole L. Glazer, Felicia Gomez, Tamara B. Harris, Indrani Halder, Virginia J. Howard, Margaux F. Keller, M. Ilyas Kamboh, Charles Kooperberg, Stephen B. Kritchevsky, Andrea Z. LaCroix, Kiang Liu, Yongmei Liu, Kiran Musunuru, Anne B. Newman, N. Charlotte Onland‐Moret, José M. Ordovás, Inga Peter, Wendy S. Post, Susan Redline, Steven E. Reís, Richa Saxena, Pamela J. Schreiner, Kelly A. Volcik, Xingbin Wang, Salim Yusuf, Alan B. Zonderland, Sonia S. Anand, Diane M. Becker, Bruce M. Psaty, Daniel J. Rader, Alex P. Reiner, Stephen S. Rich, Jerome I. Rotter, Michèle M. Sale, Michael Y. Tsai, Ingrid B. Borecki, Robert A. Hegele, Sekar Kathiresan, Michael A. Nalls, Herman A. Taylor, Hákon Hákonarson, Suthesh Sivapalaratnam, Folkert W. Asselbergs, Fotios Drenos, James G. Wilson, Brendan J. Keating

    Published 2012
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  15. 15
    A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

    A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders by Ilenia Simeoni, Jonathan Stephens, Fengyuan Hu, Sri V. V. Deevi, Karyn Mégy, Tadbir K. Bariana, Claire Lentaigne, Sol Schulman, Suthesh Sivapalaratnam, Minka J. A. Vries, Sarah K. Westbury, Daniel Greene, Sofia Papadia, Marie‐Christine Alessi, Antony Attwood, Matthias Ballmaier, Gareth Baynam, Emilsé Bermejo, Marta Bértoli, Paul F. Bray, Loredana Bury, Marco Cattaneo, Peter Collins, Louise C. Daugherty, Rémi Favier, Deborah L. French, Bruce Furie, Michael Gattens, Manuela Germeshausen, Cédric Ghevaert, Anne Goodeve, José A. Guerrero, Daniel J. Hampshire, Daniel P. Hart, Johan W. M. Heemskerk, Yvonne Henskens, Marian Hill, Nancy Hogg, Jennifer D. Jolley, Walter H.A. Kahr, Anne M. Kelly, Ron Kerr, Myrto Kostadima, Shinji Kunishima, Michele P. Lambert, Ri Liesner, José A. López, Rutendo Mapeta, Mary Mathias, Carolyn M. Millar, Amit Nathwani, Marguerite Neerman‐Arbez, Alan T. Nurden, Paquita Nurden, Maha Othman, Kathelijne Peerlinck, David J. Perry, Pawan Poudel, Pieter H. Reitsma, Matthew T. Rondina, Peter A. Smethurst, William Stevenson, Artur Szkotak, Salih Tuna, Chris Van Geet, Deborah Whitehorn, David A. Wilcox, Bin Zhang, Shoshana Revel‐Vilk, Paolo Gresele, Daniel B. Bellissimo, Christopher J. Penkett, Michael Laffan, Andrew Mumford, Augusto Rendon, Keith Gomez, Kathleen Freson, Willem H. Ouwehand, Ernest Turro

    Published 2016
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  16. 16
    Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

    Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis by Eveline Nüesch, Caroline Dale, Tom Palmer, Jon White, Brendan J. Keating, Erik P.A. van Iperen, Anuj Goel, Sandosh Padmanabhan, Folkert W. Asselbergs, W. M. Monique Verschuren, Cisca Wijmenga, Yvonne T. van der Schouw, N. Charlotte Onland‐Moret, Leslie A. Lange, GK Hovingh, Suthesh Sivapalaratnam, Richard Morris, Peter H. Whincup, Goya S Wannamethe, Tom R. Gaunt, Shah Ebrahim, Laura Steel, Nikhil Nair, Alexander P. Reiner, Charles Kooperberg, James F. Wilson, Jennifer L. Bolton, Stela McLachlan, Jackie F. Price, Mark W. J. Strachan, C. Robertson, Marcus E. Kleber, Graciela Delgado, Winfried März, Olle Melander, Anna F. Dominiczak, Martin Farrall, Hugh Watkins, Maarten Leusink, Anke H. Maitland‐van der Zee, Mark de Groot, Frank Dudbridge, Aroon D. Hingorani, Yoav Ben‐Shlomo, Debbie A. Lawlor, Antoinette Amuzu, M Caufield, Alana Cavadino, D. James Cooper, TL Davies, Fotios Drenos, Jorgen Engmann, Chris Finan, Claudia Giambartolomei, Rebecca Hardy, Steve E. Humphries, Elina Hyppönen, Mika Kivimäki, Diana Kuh, Meena Kumari, Ken K. Ong, Vincent Plagnol, Chris Power, Marcus Richards, Svati H. Shah, Tina Shah, Reecha Sofat, Philippa J. Talmud, Nicholas J. Wareham, Helen R. Warren, John C. Whittaker, Andrew Wong, Delilah Zabaneh, George Davey Smith, Jonathan C. K. Wells, David A. Leon, Michael V. Holmes, Juan P. Casas

    Published 2015
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  17. 17
    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes by Andrew P. Morris, Benjamin F. Voight, Tanya M. Teslovich, Teresa Ferreira, Ayellet V. Segrè, Valgerður Steinthórsdóttir, Rona J. Strawbridge, Hassan Khan, Harald Grallert, Anubha Mahajan, Inga Prokopenko, Hyun Min Kang, Christian Dina, Tõnu Esko, Ross M. Fraser, Stavroula Kanoni, Ashish Kumar, Vasiliki Lagou, Claudia Langenberg, Jian’an Luan, Cecilia M. Lindgren, Martina Müller‐Nurasyid, Sonali Pechlivanis, Nigel W. Rayner, Laura J. Scott, Steven Wiltshire, Loïc Yengo, Leena Kinnunen, Elizabeth J. Rossin, Soumya Raychaudhuri, Andrew D. Johnson, Antigone S. Dimas, Ruth J. F. Loos, Sailaja Vedantam, Han Chen, José C. Florez, Caroline S. Fox, Yongmei Liu, Denis Rybin, David Couper, Wen Hong Linda Kao, Man Li, Marilyn C. Cornelis, Peter Kraft, Qi Sun, Rob M. van Dam, Heather M. Stringham, Peter S. Chines, Krista Fischer, Pierre Fontanillas, Oddgeir L. Holmen, Sarah Hunt, Anne Jackson, Augustine Kong, Robert Lawrence, Julia Meyer, John R. B. Perry, Carl Platou, Simon Potter, Emil Rehnberg, Neil Robertson, Suthesh Sivapalaratnam, Alena Stančáková, Kathleen Stirrups, Guðmar Þorleifsson, Emmi Tikkanen, Andrew R. Wood, Peter Almgren, Mustafa Atalay, Rafn Benediktsson, Lori L. Bonnycastle, Noël P. Burtt, Jason Carey, G. Charpentier, Andrew Crenshaw, Alex S. F. Doney, Mozhgan Dorkhan, Sarah Edkins, Valur Emilsson, Elodie Eury, Tom Forsén, Karl Gertow, Bruna Gigante, George Grant, Christopher J. Groves, Candace Guiducci, Christian Herder, Ástráður B. Hreiðarsson, Jennie Hui, Anthony James, Anna Jonsson, Wolfgang Rathmann, Norman Klopp, Jasmina Kravić, Kaarel Krjutškov, Cordelia Langford, Karin Leander, Eero Lindholm, Stéphane Lobbens, Satu Männistö

    Published 2012
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  18. 18
    A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

    A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease by John F. Peden, Jemma C. Hopewell, Danish Saleheen, John C. Chambers, Jörg Hager, Nicole Soranzo, Rory Collins, John Danesh, Paul Elliott, Martin Farrall, Kathy Stirrups, Weihua Zhang, Anders Hamsten, Sarah Parish, Mark Lathrop, Hugh Watkins, Robert Clarke, Panos Deloukas, Jaspal S. Kooner, Anuj Goel, Halit Ongen, Rona J. Strawbridge, Simon Heath, Anders Mälarstig, Anna Helgadóttir, John Öhrvik, Muhammed Murtaza, Simon Potter, Sarah Hunt, Marc Delépine, Shapour Jalilzadeh, Tomas Axelsson, Ann‐Christine Syvänen, Rhian Gwilliam, Suzannah Bumpstead, Emma Gray, Sarah Edkins, Lasse Folkersen, Theodosios Kyriakou, Anders Franco-Cereceda, Anders Gabrielsen, Udo Seedorf, Per Eriksson, Alison Offer, Louise Bowman, Peter Sleight, Jane Armitage, Richard Peto, Gonçalo R. Abecasis, Nabeel Ahmed, Mark J. Caulfield, Peter Donnelly, Philippe Froguel, Angad S. Kooner, Mark I. McCarthy, N. J. Samani, James Scott, Joban Sehmi, Angela Silveira, Mai‐Lis Hellénius, Ferdinand M. van’t Hooft, Gunnar Olsson, Stephan Rust, Gerd Assmann, Simona Barlera, Gianni Tognoni, Maria Grazia Franzosi, Pamela Linksted, Fiona R. Green, Asif Rasheed, Moazzam Zaidi, Nabi Shah, Maria Samuel, Nadeem Hayyat Mallick, Muhammad Azhar, Khan Shah Zaman, Abdus Samad, Mohammad Ishaq, Ali Raza Gardezi, Fazal-ur-Rehman Memon, Philippe M. Frossard, Tim Spector, Leena Peltonen, Markku S. Nieminen, Juha Sinisalo, Veikko Salomaa, Samuli Ripatti, Derrick Bennett, Karin Leander, Bruna Gigante, Ulf dé Fairé, Silvia De Pietri, F. Gori, Roberto Marchioli, Suthesh Sivapalaratnam, John J.P. Kastelein, Mieke D. Trip, Eirini Theodoraki, George Dedoussis, James C. Engert

    Published 2011
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  19. 19
    Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

    Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction by Ron Do, Nathan O. Stitziel, Hong‐Hee Won, Anders Berg Jørgensen, Stefano Duga, Pier Angelica Merlini, Adam Kieżun, Martin Farrall, Anuj Goel, Or Zuk, I. Guella, Rosanna Asselta, Leslie A. Lange, Gina M. Peloso, Paul L. Auer, Domenico Girelli, Nicola Martinelli, Deborah Farlow, Mark A. DePristo, Robert Roberts, Alexandre F.R. Stewart, Danish Saleheen, John Danesh, Stephen E. Epstein, Suthesh Sivapalaratnam, G. Kees Hovingh, John J.P. Kastelein, Nilesh J. Samani, Heribert Schunkert, Jeanette Erdmann, Svati H. Shah, William E. Kraus, R. W. Davies, Majid Nikpay, Christopher T. Johansen, Jian Wang, Robert A. Hegele, Eliana Hechter, Winfried März, Marcus E. Kleber, Jie Huang, Andrew D. Johnson, Mingyao Li, Greg Burke, Myron D. Gross, Yongmei Liu, Themistocles L. Assimes, Gerardo Heiss, Ethan M. Lange, Aaron R. Folsom, Herman A. Taylor, Oliviero Olivieri, Anders Hamsten, Robert Clarke, Dermot F. Reilly, Yin Wu, Manuel A. Rivas, Peter Donnelly, Jacques E. Rossouw, Bruce M. Psaty, David M. Herrington, James G. Wilson, Stephen S. Rich, Michael J. Bamshad, Russell P. Tracy, L. Adrienne Cupples, Daniel J. Rader, Muredach P. Reilly, John A. Spertus, Sharon Cresci, Jaana Hartiala, W.H. Wilson Tang, Stanley L. Hazen, Hooman Allayee, Alex P. Reiner, Christopher S. Carlson, Charles Kooperberg, Rebecca D. Jackson, Eric Boerwinkle, Eric S. Lander, Stephen M. Schwartz, David S. Siscovick, Ruth McPherson, Anne Tybjærg‐Hansen, Gonçalo R. Abecasis, Hugh Watkins, Deborah A. Nickerson, Diego Ardissino, Shamil Sunyaev, Christopher J. O’Donnell, David Altshuler, Stacey Gabriel, Sekar Kathiresan

    Published 2014
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  20. 20
    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 by 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

    Published 2019
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