Yoichiro Kamatani
Genetic variants for head size share genes and pathways with cancer.
Knol M, Poot R, Evans T, Satizabal C, Mishra A, Sargurupremraj M, van der Auwera S, Duperron M, Jian X, Hostettler I, van Dam-Nolen D, Lamballais S, Pawlak M, Lewis C, Carrion-Castillo A, van Erp T, Reinbold C, Shin J, Scholz M, Håberg A, Kämpe A, Li G, Avinun R, Atkins J, Hsu F, Amod A, Lam M, Tsuchida A, Teunissen M, Aygün N, Patel Y, Liang D, Beiser A, Beyer F, Bis J, Bos D, Bryan R, Bülow R, Caspers S, Catheline G, Cecil C, Dalvie S, Dartigues J, DeCarli C, Enlund-Cerullo M, Ford J, Franke B, Freedman B, Friedrich N, Green M, Haworth S, Helmer C, Hoffmann P, Homuth G, Ikram M, Jack C, Jahanshad N, Jockwitz C, Kamatani Y, Knodt A, Li S, Lim K, Longstreth W, Macciardi F, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Mäkitie O, Mazoyer B, Medland S, Miyamoto S, Moebus S, Mosley T, Muetzel R, Mühleisen T, Nagata M, Nakahara S, Palmer N, Pausova Z, Preda A, Quidé Y, Reay W, Roshchupkin G, Schmidt R, Schreiner P, Setoh K, Shapland C, Sidney S, St Pourcain B, Stein J, Tabara Y, Teumer A, Uhlmann A, van der Lugt A, Vernooij M, Werring D, Windham B, Witte A, Wittfeld K, Yang Q, Yoshida K, Brunner H, Le Grand Q, Sim K, Stein D, Bowden D, Cairns M, Hariri A, Cheung C, Andersson S, Villringer A, Paus T, Cichon S, Calhoun V, Crivello F, Launer L, White T, Koudstaal P, Houlden H, Fornage M, Matsuda F, Grabe H, Debette S, Thompson P, Seshadri S, Adams H. Genetic variants for head size share genes and pathways with cancer. Cell Rep Med 2024:101529.
03.05.2024Genetic variants for head size share genes and pathways with cancer.
03.05.2024Cell Rep Med 2024:101529
Knol Maria J, Poot Raymond A, Evans Tavia E, Satizabal Claudia L, Mishra Aniket, Sargurupremraj Muralidharan, van der Auwera Sandra, Duperron Marie-Gabrielle, Jian Xueqiu, Hostettler Isabel, van Dam-Nolen Dianne H K, Lamballais Sander, Pawlak Mikolaj A, Lewis Cora E, Carrion-Castillo Amaia, van Erp Theo G M, Reinbold Céline S, Shin Jean, Scholz Markus, Håberg Asta K, Kämpe Anders, Li Gloria H Y, Avinun Reut, Atkins Joshua R, Hsu Fang-Chi, Amod AlyR, Lam Max, Tsuchida Ami, Teunissen Mariël W A, Aygün Nil, Patel Yash, Liang Dan, Beiser Alexa S, Beyer Frauke, Bis Joshua C, Bos Daniel, Bryan R Nick, Bülow Robin, Caspers Svenja, Catheline Gwenaëlle, Cecil Charlotte A M, Dalvie Shareefa, Dartigues Jean-François, DeCarli Charles, Enlund-Cerullo Maria, Ford Judith M, Franke Barbara, Freedman Barry I, Friedrich Nele, Green MeliJ, Haworth Simon, Helmer Catherine, Hoffmann Per, Homuth Georg, Ikram Mohammad Arfan, Jack Clifford R, Jahanshad Neda, Jockwitz Christiane, Kamatani Yoichiro, Knodt Annchen R, Li Shuo, Lim Keane, Longstreth W T, Macciardi Fabio, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Mäkitie Outi, Mazoyer Bernard, Medland Sarah E, Miyamoto Susumu, Moebus Susanne, Mosley Thomas H, Muetzel Ryan, Mühleisen Thomas W, Nagata Manabu, Nakahara Soichiro, Palmer Nicholette D, Pausova Zdenka, Preda Adrian, Quidé Yann, Reay William R, Roshchupkin Gennady V, Schmidt Reinhold E, Schreiner Pamela J, Setoh Kazuya, Shapland Chin Yang, Sidney Stephen, St Pourcain Beate, Stein Jason L, Tabara Yasuharu, Teumer Alexander, Uhlmann Anne, van der Lugt Aad, Vernooij Meike W, Werring David J, Windham B Gwen, Witte A Veronica, Wittfeld Katharina, Yang Qiong, Yoshida Kazumichi, Brunner Han G, Le Grand Quentin, Sim Kang, Stein Dan J, Bowden Donald W, Cairns Murray J, Hariri Ahmad R, Cheung Ching-Lung, Andersson Sture, Villringer Arno, Paus Tomas, Cichon Sven, Calhoun Vince D, Crivello Fabrice, Launer Lenore J, White Tonya, Koudstaal Peter J, Houlden Henry, Fornage Myriam, Matsuda Fumihiko, Grabe Hans Jörgen, Debette Stephanie, Thompson Paul M, Seshadri Sudha, Adams Hieab H H
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Rahmioglu N, Mortlock S, Ghiasi M, Møller P, Stefansdottir L, Galarneau G, Turman C, Danning R, Law M, Sapkota Y, Christofidou P, Skarp S, Giri A, Banasik K, Krassowski M, Lepamets M, Marciniak B, Nõukas M, Perro D, Sliz E, Sobalska-Kwapis M, Thorleifsson G, Topbas-Selcuki N, Vitonis A, Westergaard D, Arnadottir R, Burgdorf K, Campbell A, Cheuk C, Clementi C, Cook J, De Vivo I, DiVasta A, Dorien O, Donoghue J, Edwards T, Fontanillas P, Fung J, Geirsson R, Girling J, Harkki P, Harris H, Healey M, Heikinheimo O, Holdsworth-Carson S, Hostettler I, Houlden H, Houshdaran S, Irwin J, Jarvelin M, Kamatani Y, Kennedy S, Kepka E, Kettunen J, Kubo M, Kulig B, Kurra V, Laivuori H, Laufer M, Lindgren C, MacGregor S, Mangino M, Martin N, Matalliotaki C, Matalliotakis M, Murray A, Ndungu A, Nezhat C, Olsen C, Opoku-Anane J, Padmanabhan S, Paranjpe M, Peters M, Polak G, Porteous D, Rabban J, Rexrode K, Romanowicz H, Saare M, Saavalainen L, Schork A, Sen S, Shafrir A, Siewierska-Górska A, Słomka M, Smith B, Smolarz B, Szaflik T, Szyłło K, Takahashi A, Terry K, Tomassetti C, Treloar S, Vanhie A, Vincent K, Vo K, Werring D, Zeggini E, Zervou M, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi S, Buring J, Ridker P, D'Hooghe T, Goulielmos G, Hapangama D, Hayward C, Horne A, Low S, Martikainen H, Chasman D, Rogers P, Saunders P, Sirota M, Spector T, Strapagiel D, Tung J, Whiteman D, Giudice L, Velez Edwards D, Uimari O, Kraft P, Salumets A, Nyholt D, Mägi R, Stefansson K, Becker C, Yurttas-Beim P, Steinthorsdottir V, Nyegaard M, Missmer S, Montgomery G, Morris A, Zondervan K. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nat Genet 2023; 55:423-436.
13.03.2023The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
13.03.2023Nat Genet 2023; 55:423-436
Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak Błażej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James P, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd L, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode KathyM, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, Słomka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szyłło Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Timothy D, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina T
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
Bakker M, Kanning J, Abraham G, Martinsen A, Winsvold B, Zwart J, Bourcier R, Sawada T, Koido M, Kamatani Y, Morel S, Amouyel P, Debette S, Bijlenga P, Berrandou T, Ganesh S, Bouatia-Naji N, Jones G, Bown M, Rinkel G, Veldink J, Ruigrok Y, Hostettler I. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke 2023
19.01.2023Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity.
19.01.2023Stroke 2023
Bakker Mark K, Kanning Jos P, Abraham Gad, Martinsen Amy E, Winsvold Bendik S, Zwart John-Anker, Bourcier Romain, Sawada Tomonobu, Koido Masaru, Kamatani Yoichiro, Morel Sandrine, Amouyel Philippe, Debette Stephanie, Bijlenga Philippe, Berrandou Takiy, Ganesh Santhi K, Bouatia-Naji Nabila, Jones Gregory T, Bown Matthew, Rinkel Gabriel J E, Veldink Jan H, Ruigrok Ynte M, Hostettler Isabel C
Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Ruigrok Y, Sargurupremraj M, Dichgans M, Malik R, Klijn C, Zaroff J, Breen G, Coleman J, Kim H, Ko N, Bown M, Jones G, Martin O, Dauvillier J, Schilling S, Hirsch S, Tatlisumak T, Amouyel P, Debette S, Veldink J, Kamatani Y, Bijlenga P, Redon R, Woo D, Werring D, Broderick J, Lindgren A, von Und Zu Fraunberg M, Jaaskelainen J, Niemelä M, Gaal-Paavola E, Slowik A, Pera J, Worrall B, Rinkel G, Friedrich C, Verschuren W, Zwart J, Chen Z, Millwood I, Liang L, Lin K, Walters R, Matsuda K, Terao C, Akiyama M, Koido M, van Eijk K, Alg V, Hostettler I, Bourcier R, Morel S, van Rheenen W, van der Spek R, Rouleau G, Zhou S, Rannikmäe K, Hveem K, Willer C, Sandvei M, Brumpton B, Johnsen M, Børte S, Winsvold B, Desal H, Eugène F, Shotar E, Gentric J, Naggara O, Dina C, van den Berg L, Houlden H, Sudlow C, Bakker M. Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet 2021; 53:254.
01.02.2021Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
01.02.2021Nat Genet 2021; 53:254
Ruigrok Ynte M, Sargurupremraj Muralidharan, Dichgans Martin, Malik Rainer, Klijn Catharina J M, Zaroff Jonathan G, Breen Gerome, Coleman Jonathan R I, Kim Helen, Ko NeriU, Bown Matthew, Jones Gregory T, Martin Olivier, Dauvillier Jerome, Schilling Sabine, Hirsch Sven, Tatlisumak Turgut, Amouyel Philippe, Debette Stephanie, Veldink Jan H, Kamatani Yoichiro, Bijlenga Philippe, Redon Richard, Woo Daniel, Werring David J, Broderick Joseph P, Lindgren Antti, von Und Zu Fraunberg Mikael, Jaaskelainen Juha E, Niemelä Mika, Gaal-Paavola Emilia I, Slowik Agnieszka, Pera Joanna, Worrall Bradford B, Rinkel Gabriel J E, Friedrich Christoph M, Verschuren W M Monique, Zwart John-Anker, Chen Zhengming, Millwood Iona Y, Liang Liming, Lin Kuang, Walters Robin G, Matsuda Koichi, Terao Chikashi, Akiyama Masato, Koido Masaru, van Eijk Kristel R, Alg Varinder S, Hostettler Isabel, Bourcier Romain, Morel Sandrine, van Rheenen Wouter, van der Spek Rick A A, Rouleau Guy A, Zhou Sirui, Rannikmäe Kristiina, Hveem Kristian, Willer Cristen J, Sandvei Marie Søfteland, Brumpton Ben M, Johnsen Marianne Bakke, Børte Sigrid, Winsvold Bendik S, Desal Hubert, Eugène François, Shotar Eimad, Gentric Jean-Christophe, Naggara Olivier, Dina Christian, van den Berg Leonard H, Houlden Henry, Sudlow Cathie L M, Bakker Mark K
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
Ruigrok Y, Sargurupremraj M, Dichgans M, Malik R, Klijn C, Zaroff J, Breen G, Coleman J, Kim H, Ko N, Bown M, Jones G, Martin O, Dauvillier J, Schilling S, Hirsch S, Tatlisumak T, Amouyel P, Debette S, Veldink J, Kamatani Y, Bijlenga P, Redon R, Woo D, Werring D, Broderick J, Lindgren A, von Und Zu Fraunberg M, Jaaskelainen J, Niemelä M, Gaal-Paavola E, Slowik A, Pera J, Worrall B, Rinkel G, Friedrich C, Verschuren W, Zwart J, Chen Z, Millwood I, Liang L, Lin K, Walters R, Matsuda K, Terao C, Akiyama M, Koido M, van Eijk K, Alg V, Hostettler I, Bourcier R, Morel S, van Rheenen W, van der Spek R, Rouleau G, Zhou S, Rannikmäe K, Hveem K, Willer C, Sandvei M, Brumpton B, Johnsen M, Børte S, Winsvold B, Desal H, Eugène F, Shotar E, Gentric J, Naggara O, Dina C, van den Berg L, Houlden H, Sudlow C, Bakker M. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nat Genet 2020; 52:1303-1313.
16.11.2020Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.
16.11.2020Nat Genet 2020; 52:1303-1313
Ruigrok Ynte M, Sargurupremraj Muralidharan, Dichgans Martin, Malik Rainer, Klijn Catharina J M, Zaroff Jonathan G, Breen Gerome, Coleman Jonathan R I, Kim Helen, Ko NeriU, Bown Matthew, Jones Gregory T, Martin Olivier, Dauvillier Jerome, Schilling Sabine, Hirsch Sven, Tatlisumak Turgut, Amouyel Philippe, Debette Stephanie, Veldink Jan H, Kamatani Yoichiro, Bijlenga Philippe, Redon Richard, Woo Daniel, Werring David J, Broderick Joseph P, Lindgren Antti, von Und Zu Fraunberg Mikael, Jaaskelainen Juha E, Niemelä Mika, Gaal-Paavola Emilia I, Slowik Agnieszka, Pera Joanna, Worrall Bradford B, Rinkel Gabriel J E, Friedrich Christoph M, Verschuren W M Monique, Zwart John-Anker, Chen Zhengming, Millwood Iona Y, Liang Liming, Lin Kuang, Walters Robin G, Matsuda Koichi, Terao Chikashi, Akiyama Masato, Koido Masaru, van Eijk Kristel R, Alg Varinder S, Hostettler Isabel, Bourcier Romain, Morel Sandrine, van Rheenen Wouter, van der Spek Rick A A, Rouleau Guy A, Zhou Sirui, Rannikmäe Kristiina, Hveem Kristian, Willer Cristen J, Sandvei Marie Søfteland, Brumpton Ben M, Johnsen Marianne Bakke, Børte Sigrid, Winsvold Bendik S, Desal Hubert, Eugène François, Shotar Eimad, Gentric Jean-Christophe, Naggara Olivier, Dina Christian, van den Berg Leonard H, Houlden Henry, Sudlow Cathie L M, Bakker Mark K
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Bowden D, Snieder H, Smith J, Sitlani C, Sever P, Seshadri S, Scott W, Schreiner P, Schmidt C, Sandow K, Salako B, Sabanayagam C, Rudan I, Rose L, Robinson J, Robino A, Ridker P, Starr J, Strauch K, Tang H, Boehnke M, Becker D, Zonderman A, Yuan J, Yao J, Wojczynski M, Wilson G, Williams C, Wei W, Wang Y, Wang L, Waldenberger M, Uitterlinden A, Tham Y, Teo Y, Taylor K, Rice T, Renström F, Raitakari O, Metspalu A, Meitinger T, Mahajan A, Mägi R, Louie T, Long J, Lohman K, Loh M, Liu Y, Liu K, Liu J, Liu J, Liu C, Lin S, Lim S, Lifelines Cohort Study, Milani L, Momozawa Y, Morris A, Polasek O, Peyser P, Peters A, Pedersen N, Pankow J, Palmer N, Palmas W, Padmanabhan S, Ogunniyi A, North K, Norris J, Nasri U, Nalls M, Murray A, Munson P, Mosley T, Li Y, Chasman D, Hayward C, Fox E, Kelly T, Mook-Kanamori D, Arnett D, Sims M, van Dam R, Psaty B, O'Connell J, Levy D, Kritchevsky S, Kardia S, Gudnason V, Evans M, Cooper R, Bouchard C, Fornage M, Rotimi C, Province M, Rao D, Cupples L, Morrison A, Munroe P, Rice K, Elliott P, Caulfield M, Gauderman W, Bierut L, Zhu X, Rotter J, Reiner A, Loos R, Wong T, Tai E, van Duijn C, Laurie C, Kamatani Y, Zheng W, Kooner J, Kato N, Jonas J, Hung Y, Horta B, Gieger C, Gasparini P, Froguel P, Freedman B, Franks P, Forrester T, Farrall M, Esko T, Deary I, de Faire U, Chen Y, Laakso M, Lehtimäki T, Liang K, Wu T, Wickremasinghe A, Weir D, Watkins H, Wareham N, Wagenknecht L, van der Harst P, Shu X, Scott J, Samani N, Rettig R, Redline S, Pereira A, Oldehinkel A, Newman A, Magnusson P, Chambers J, Lewis C, Yanek L, Leander K, Kühnel B, Kasturiratne A, Kähönen M, Jackson A, Hsu F, Horimoto A, Hartwig F, Harris S, Goel A, Giulianini F, Gao C, Gandin I, Divers J, Chen X, Chai J, Lee W, Lin K, 'an Luan J, Wen W, Weiss S, Ware E, Wang Y, Wang H, Varga T, van der Most P, Takeuchi F, Stančáková A, Sheu W, Scott R, Schupf N, Rauramaa R, Nelson C, He M, McKenzie C, Boissel M, Amini M, Alver M, Li C, Musani S, Marten J, Vojinovic D, Sim X, Cheng C, Lu Y, Franceschini N, Guo X, Ntalla I, Schwander K, Kraja A, Brown M, Bentley A, de Las Fuentes L, Winkler T, Feitosa M, Kilpeläinen T, Richard M, Sofer T, Matoba N, Zhou Y, Zhao W, Warren H, Tayo B, Tajuddin S, Smith A, Rankinen T, Manning A, Liu Y, Dorajoo R, Bartz T, Aschard H, Aslibekyan S, Noordam R, Sung Y, Lehne B, Howard B, Hofman A, Hirata M, Heng C, Heikkinen S, He J, Harris T, Hagenaars S, Gupta P, Gu D, Gu C, Graff M, Gigante B, GIANT Consortium, Gao H, Friedlander Y, Hunt S, Irvin M, Jia Y, Launer L, Langenberg C, Langefeld C, Kuusisto J, Kubo M, Krieger J, Kooperberg C, Komulainen P, Koistinen H, Koh W, Khor C, Kerrison N, Kaufman J, Katsuya T, Justice A, Joehanes R, Franco O, Forouhi N, Fisher V, Caizheng Y, Cade B, Cabrera C, Broeckel U, Brody J, Braund P, Bottinger E, Boerwinkle E, Bielak L, Barr R, Aung T, Arking D, Amin N, Alfred T, Afaq S, Zhao J, Campbell A, Canouil M, Chakravarti A, Faul J, Evangelou E, Ehret G, Eaton C, Duan Q, Dörr M, Debette S, de Silva H, de Mutsert R, Connell J, Collins F, COGENT-Kidney Consortium, Cocca M, Christensen K, Chauhan G, CHARGE Neurology Working Group, Zhang W. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Am J Hum Genet 2018; 102:375-400.
15.02.2018A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
15.02.2018Am J Hum Genet 2018; 102:375-400
Bowden Donald W, Snieder Harold, Smith Jennifer A, Sitlani Colleen M, Sever Peter, Seshadri Sudha, Scott William R, Schreiner Pamela J, Schmidt Carsten O, Sandow Kevin, Salako Babatunde L, Sabanayagam Charumathi, Rudan Igor, Rose Lynda M, Robinson Jennifer G, Robino Antonietta, Ridker Paul M, Starr John M, Strauch Konstantin, Tang Hua, Boehnke Michael, Becker Diane M, Zonderman Alan B, Yuan Jian-Min, Yao Jie, Wojczynski Mary K, Wilson Gregory, Williams Christine, Wei Wen Bin, Wang Ya X, Wang Lihua, Waldenberger Melanie, Uitterlinden André G, Tham Yih Chung, Teo Yik Ying, Taylor Kent D, Rice Treva K, Renström Frida, Raitakari Olli T, Metspalu Andres, Meitinger Thomas, Mahajan Anubha, Mägi Reedik, Louie Tin, Long Jirong, Lohman Kurt K, Loh Marie, Liu Yeheng, Liu Kiang, Liu Jingmin, Liu Jianjun, Liu Ching-Ti, Lin Shiow, Lim Sing Hui, Lifelines Cohort Study, Milani Lili, Momozawa Yukihide, Morris Andrew P, Polasek Ozren, Peyser Patricia A, Peters Annette, Pedersen Nancy L, Pankow James S, Palmer Nicholette D, Palmas Walter R, Padmanabhan Sandosh, Ogunniyi Adesola, North Kari, Norris Jill M, Nasri Ubaydah, Nalls Mike A, Murray Alison D, Munson Peter, Mosley Thomas H, Li Yize, Chasman Daniel I, Hayward Caroline, Fox Ervin R, Kelly Tanika N, Mook-Kanamori Dennis O, Arnett Donna K, Sims Mario, van Dam Rob M, Psaty Bruce M, O'Connell Jeff R, Levy Daniel, Kritchevsky Stephen B, Kardia Sharon L R, Gudnason Vilmundur, Evans Michele K, Cooper Richard S, Bouchard Claude, Fornage Myriam, Rotimi Charles N, Province Michael A, Rao Dabeeru C, Cupples L Adrienne, Morrison Alanna C, Munroe Patricia B, Rice Kenneth, Elliott Paul, Caulfield Mark J, Gauderman W James, Bierut Laura J, Zhu Xiaofeng, Rotter Jerome I, Reiner Alex P, Loos Ruth J F, Wong Tien Yin, Tai E Shyong, van Duijn Cornelia M, Laurie Cathy C, Kamatani Yoichiro, Zheng Wei, Kooner Jaspal S, Kato Norihiro, Jonas Jost B, Hung Yi-Jen, Horta Bernardo Lessa, Gieger Christian, Gasparini Paolo, Froguel Philippe, Freedman Barry I, Franks Paul W, Forrester Terrence, Farrall Martin, Esko Tõnu, Deary Ian J, de Faire Ulf, Chen Yii-Der Ida, Laakso Markku, Lehtimäki Terho, Liang Kae-Woei, Wu Tangchun, Wickremasinghe Ananda R, Weir David R, Watkins Hugh, Wareham Nicholas J, Wagenknecht Lynne E, van der Harst Pim, Shu Xiao-Ou, Scott James, Samani Nilesh J, Rettig Rainer, Redline Susan, Pereira Alexandre C, Oldehinkel Albertine J, Newman Anne B, Magnusson Patrik K E, Chambers John C, Lewis Cora E, Yanek Lisa R, Leander Karin, Kühnel Brigitte, Kasturiratne Anuradhani, Kähönen Mika, Jackson Anne U, Hsu Fang-Chi, Horimoto Andrea R V R, Hartwig Fernando Pires, Harris Sarah E, Goel Anuj, Giulianini Franco, Gao Chuan, Gandin Ilaria, Divers Jasmin, Chen Xu, Chai Jin Fang, Lee Wen-Jane, Lin Keng-Hung, 'an Luan Jian, Wen Wanqing, Weiss Stefan, Ware Erin B, Wang Yajuan, Wang Heming, Varga Tibor V, van der Most Peter J, Takeuchi Fumihiko, Stančáková Alena, Sheu Wayne H H, Scott Robert A, Schupf Nicole, Rauramaa Rainer, Nelson Christopher P, He Meian, McKenzie Colin A, Boissel Mathilde, Amini Marzyeh, Alver Maris, Li Changwei, Musani Solomon K, Marten Jonathan, Vojinovic Dina, Sim Xueling, Cheng Ching-Yu, Lu Yingchang, Franceschini Nora, Guo Xiuqing, Ntalla Ioanna, Schwander Karen, Kraja Aldi T, Brown Michael R, Bentley Amy R, de Las Fuentes Lisa, Winkler Thomas W, Feitosa Mary F, Kilpeläinen Tuomas O, Richard Melissa A, Sofer Tamar, Matoba Nana, Zhou Yanhua, Zhao Wei, Warren Helen R, Tayo Bamidele O, Tajuddin Salman M, Smith Albert Vernon, Rankinen Tuomo, Manning Alisa K, Liu Yongmei, Dorajoo Rajkumar, Bartz Traci M, Aschard Hugues, Aslibekyan Stella, Noordam Raymond, Sung Yun J, Lehne Benjamin, Howard Barbara V, Hofman Albert, Hirata Makoto, Heng Chew-Kiat, Heikkinen Sami, He Jiang, Harris Tamara B, Hagenaars Saskia P, Gupta Preeti, Gu Dongfeng, Gu C Charles, Graff Misa, Gigante Bruna, GIANT Consortium, Gao He, Friedlander Yechiel, Hunt Steven, Irvin Marguerite R, Jia Yucheng, Launer Lenore J, Langenberg Claudia, Langefeld Carl D, Kuusisto Johanna, Kubo Michiaki, Krieger Jose E, Kooperberg Charles, Komulainen Pirjo, Koistinen Heikki A, Koh Woon-Puay, Khor Chiea Chuen, Kerrison Nicola D, Kaufman Joel, Katsuya Tomohiro, Justice Anne E, Joehanes Roby, Franco Oscar H, Forouhi Nita G, Fisher Virginia A, Caizheng Yu, Cade Brian, Cabrera Claudia P, Broeckel Ulrich, Brody Jennifer A, Braund Peter S, Bottinger Erwin P, Boerwinkle Eric, Bielak Lawrence F, Barr R Graham, Aung Tin, Arking Dan, Amin Najaf, Alfred Tamuno, Afaq Saima, Zhao Jing Hua, Campbell Archie, Canouil Mickaël, Chakravarti Aravinda, Faul Jessica D, Evangelou Evangelos, Ehret Georg, Eaton Charles B, Duan Qing, Dörr Marcus, Debette Stephanie, de Silva H Janaka, de Mutsert Renée, Connell John M, Collins Francis S, COGENT-Kidney Consortium, Cocca Massimiliano, Christensen Kaare, Chauhan Ganesh, CHARGE Neurology Working Group, Zhang Weihua