Philippe Amouyel
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: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W, van der Spek R, Bakker M, Van Vugt J, Hop P, Zwamborn R, de Klein N, Westra H, Bakker O, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker A, Gawor K, Westeneng H, Tazelaar G, van Eijk K, Kooyman M, Byrne R, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, Ticozzi N, Cooper-Knock J, Smith B, Gromicho M, Chandran S, Pal S, Morrison K, Shaw P, Hardy J, Orrell R, Sendtner M, Meyer T, Başak N, van der Kooi A, Ratti A, Fogh I, Gellera C, Lauria G, Corti S, Cereda C, Sproviero D, D'Alfonso S, Sorarù G, Siciliano G, Filosto M, Padovani A, Chio A, Calvo A, Moglia C, Brunetti M, Canosa A, Grassano M, Beghi E, Pupillo E, Logroscino G, Nefussy B, Osmanovic A, Nordin A, Lerner Y, Zabari M, Gotkine M, Baloh R, Bell S, Vourc'h P, Corcia P, Couratier P, Millecamps S, Meininger V, Salachas F, Mora Pardina J, Assialioui A, Rojas-García R, Dion P, Ross J, Ludolph A, Weishaupt J, Brenner D, Freischmidt A, Bensimon G, Brice A, Dürr A, Payan C, Saker-Delye S, Wood N, Topp S, Rademakers R, Tittmann L, Lieb W, Franke A, Ripke S, Braun A, Kraft J, Whiteman D, Olsen C, Uitterlinden A, Hofman A, Rietschel M, Cichon S, Nöthen M, Amouyel P, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor B, Singleton A, Mitne Neto M, Cauchi R, Ophoff R, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin V, Grosskreutz J, Roediger A, Gaur N, Jörk A, Barthel T, Theele E, Ilse B, Stubendorff B, Witte O, Steinbach R, Hübner C, Graff C, Brylev L, Fominykh V, Demeshonok V, Ataulina A, Rogelj B, Koritnik B, Zidar J, Ravnik-Glavač M, Glavač D, Stević Z, Drory V, Povedano M, Blair I, Kiernan M, Benyamin B, Henderson R, Furlong S, Mathers S, McCombe P, Needham M, Ngo S, Nicholson G, Pamphlett R, Rowe D, Steyn F, Williams K, Mather K, Sachdev P, Henders A, Wallace L, de Carvalho M, Pinto S, Petri S, Weber M, Rouleau G, Silani V, Curtis C, Breen G, Glass J, Brown R, Landers J, Shaw C, Andersen P, Groen E, van Es M, Pasterkamp R, Fan D, Garton F, McRae A, Davey Smith G, Gaunt T, Eberle M, Mill J, McLaughlin R, Hardiman O, Kenna K, Wray N, Tsai E, Runz H, Franke L, Al-Chalabi A, Van Damme P, van den Berg L, Veldink J. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nat Genet 2022; 54:361.
01.03.2022Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
01.03.2022Nat Genet 2022; 54:361
van Rheenen Wouter, van der Spek Rick A A, Bakker Mark K, Van Vugt Joke J F A, Hop Paul J, Zwamborn Ramona A J, de Klein Niek, Westra Harm-Jan, Bakker Olivier B, Deelen Patrick, Shireby Gemma, Hannon Eilis, Moisse Matthieu, Baird Denis, Restuadi Restuadi, Dolzhenko Egor, Dekker Annelot M, Gawor Klara, Westeneng Henk-Jan, Tazelaar Gijs H P, van Eijk Kristel R, Kooyman Maarten, Byrne Ross P, Doherty Mark, Heverin Mark, Al Khleifat Ahmad, Iacoangeli Alfredo, Shatunov Aleksey, Ticozzi Nicola, Cooper-Knock Johnathan, Smith Bradley N, Gromicho Marta, Chandran Siddharthan, Pal Suvankar, Morrison Karen E, Shaw Pamela J, Hardy John, Orrell Richard W, Sendtner Michael, Meyer Thomas, Başak Nazli, van der Kooi Anneke J, Ratti Antonia, Fogh Isabella, Gellera Cinzia, Lauria Giuseppe, Corti Stefania, Cereda Cristina, Sproviero Daisy, D'Alfonso Sandra, Sorarù Gianni, Siciliano Gabriele, Filosto Massimiliano, Padovani Alessandro, Chio Adriano, Calvo Andrea, Moglia Cristina, Brunetti Maura, Canosa Antonio, Grassano Maurizio, Beghi Ettore, Pupillo Elisabetta, Logroscino Giancarlo, Nefussy Beatrice, Osmanovic Alma, Nordin Angelica, Lerner Yossef, Zabari Michal, Gotkine Marc, Baloh Robert H, Bell Shaughn, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Millecamps Stéphanie, Meininger Vincent, Salachas François, Mora Pardina Jesus S, Assialioui Abdelilah, Rojas-García Ricardo, Dion Patrick A, Ross Jay P, Ludolph Albert C, Weishaupt Jochen H, Brenner David, Freischmidt Axel, Bensimon Gilbert, Brice Alexis, Dürr Alexandra, Payan Christine A M, Saker-Delye Safa, Wood Nicholas W, Topp Simon, Rademakers Rosa, Tittmann Lukas, Lieb Wolfgang, Franke Andre, Ripke Stephan, Braun Alice, Kraft Julia, Whiteman David C, Olsen Catherine M, Uitterlinden André G, Hofman Albert, Rietschel Marcella, Cichon Sven, Nöthen Markus M, Amouyel Philippe, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor Bryan J, Singleton Andrew B, Mitne Neto Miguel, Cauchi Ruben J, Ophoff Roel A, Wiedau-Pazos Martina, Lomen-Hoerth Catherine, Van Deerlin Vivianna M, Grosskreutz Julian, Roediger Annekathrin, Gaur Nayana, Jörk Alexander, Barthel Tabea, Theele Erik, Ilse Benjamin, Stubendorff Beatrice, Witte Otto W, Steinbach Robert, Hübner Christian A, Graff Caroline, Brylev Lev, Fominykh Vera, Demeshonok Vera, Ataulina Anastasia, Rogelj Boris, Koritnik Blaž, Zidar Janez, Ravnik-Glavač Metka, Glavač Damjan, Stević Zorica, Drory Vivian, Povedano Monica, Blair Ian P, Kiernan Matthew C, Benyamin Beben, Henderson Robert D, Furlong Sarah, Mathers Susan, McCombe Pamela A, Needham Merrilee, Ngo Shyuan T, Nicholson Garth A, Pamphlett Roger, Rowe Dominic B, Steyn Frederik J, Williams Kelly L, Mather Karen A, Sachdev Perminder S, Henders Anjali K, Wallace Leanne, de Carvalho Mamede, Pinto Susana, Petri Susanne, Weber Markus, Rouleau Guy A, Silani Vincenzo, Curtis Charles J, Breen Gerome, Glass Jonathan D, Brown Robert H, Landers John E, Shaw Christopher E, Andersen Peter M, Groen Ewout J N, van Es Michael A, Pasterkamp R Jeroen, Fan Dongsheng, Garton Fleur C, McRae Allan F, Davey Smith George, Gaunt Tom R, Eberle Michael A, Mill Jonathan, McLaughlin Russell L, Hardiman Orla, Kenna Kevin P, Wray Naomi R, Tsai Ellen, Runz Heiko, Franke Lude, Al-Chalabi Ammar, Van Damme Philip, van den Berg Leonard H, Veldink Jan H
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
van Rheenen W, van der Spek R, Bakker M, Farei-Campagna J, Hop P, Zwamborn R, de Klein N, Westra H, Bakker O, Deelen P, Shireby G, Hannon E, Moisse M, Baird D, Restuadi R, Dolzhenko E, Dekker A, Gawor K, Westeneng H, Tazelaar G, van Eijk K, Kooyman M, Byrne R, Doherty M, Heverin M, Al Khleifat A, Iacoangeli A, Shatunov A, Ticozzi N, Cooper-Knock J, Smith B, Gromicho M, Chandran S, Pal S, Morrison K, Openshaw P, Hardy J, Orrell R, Sendtner M, Meyer T, Başak N, van der Kooi A, Ratti A, Fogh I, Gellera C, Lauria G, Corti S, Cereda C, Sproviero D, D'Alfonso S, Sorarù G, Siciliano G, Filosto M, Padovani A, Chio A, Calvo A, Moglia C, Brunetti M, Canosa A, Grassano M, Beghi E, Pupillo E, Logroscino G, Nefussy B, Osmanovic A, Nordin A, Lerner Y, Zabari M, Gotkine M, Baloh R, Bell S, Vourc'h P, Corcia P, Couratier P, Millecamps S, Meininger V, Salachas F, Mora J, Assialioui A, Rojas-García R, Dion P, Ross J, Ludolph A, Weishaupt J, Brenner D, Freischmidt A, Bensimon G, Brice A, Dürr A, Payan C, Saker-Delye S, Wood N, Topp S, Rademakers R, Tittmann L, Lieb W, Klein-Franke A, Ripke S, Braun A, Kraft J, Whiteman D, Olsen C, Uitterlinden A, Hofman A, Rietschel M, Cichon S, Nöthen M, Amouyel P, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor B, Singleton A, Mitne Neto M, Cauchi R, Ophoff R, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin V, Grosskreutz J, Roediger A, Gaur N, Jörk A, Barthel T, Theele E, Ilse B, Stubendorff B, Witte O, Steinbach R, Hübner C, Graff C, Brylev L, Fominykh V, Demeshonok V, Ataulina A, Rogelj B, Koritnik B, Zidar J, Ravnik-Glavač M, Glavač D, Stević Z, Drory V, Povedano M, Blair I, Kiernan M, Benyamin B, Henderson R, Furlong S, Mathers S, McCombe P, Needham M, Ngo S, Nicholson G, Pamphlett R, Rowe D, Steyn F, Williams K, Mather K, Sachdev P, Henders A, Wallace L, de Carvalho M, Pinto S, Petri S, Weber M, Rouleau G, Silani V, Curtis C, Breen G, Glass J, Brown R, Landers J, Shaw C, Andersen P, Groen E, van Es M, Pasterkamp R, Fan D, Garton F, McRae A, Davey Smith G, Gaunt T, Eberle M, Mill J, McLaughlin R, Hardiman O, Kenna K, Wray N, Tsai E, Runz H, Franke L, Al-Chalabi A, Van Damme P, van den Berg L, Veldink J. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nat Genet 2021; 53:1636-1648.
06.12.2021Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
06.12.2021Nat Genet 2021; 53:1636-1648
van Rheenen Wouter, van der Spek Rick A A, Bakker Mark K, Farei-Campagna Jan Marino, Hop Paul J, Zwamborn Ramona A J, de Klein Niek, Westra Harm-Jan, Bakker Olivier B, Deelen Patrick, Shireby Gemma, Hannon Eilis, Moisse Matthieu, Baird Denis, Restuadi Restuadi, Dolzhenko Egor, Dekker Annelot M, Gawor Klara, Westeneng Henk-Jan, Tazelaar Gijs H P, van Eijk Kristel R, Kooyman Maarten, Byrne Ross P, Doherty Mark, Heverin Mark, Al Khleifat Ahmad, Iacoangeli Alfredo, Shatunov Aleksey, Ticozzi Nicola, Cooper-Knock Johnathan, Smith Bradley N, Gromicho Marta, Chandran Siddharthan, Pal Suvankar, Morrison Karen E, Openshaw Peter J M, Hardy John, Orrell Richard W, Sendtner Michael, Meyer Thomas, Başak Nazli A, van der Kooi Anneke J, Ratti Antonia, Fogh Isabella, Gellera Cinzia, Lauria Giuseppe, Corti Stefania, Cereda Cristina, Sproviero Daisy, D'Alfonso Sandra, Sorarù Gianni, Siciliano Gabriele, Filosto Massimiliano, Padovani Alessandro, Chio Adriano, Calvo Andrea, Moglia Cristina, Brunetti Maura, Canosa Antonio, Grassano Maurizio, Beghi Ettore, Pupillo Elisabetta, Logroscino Giancarlo, Nefussy Beatrice, Osmanovic Alma, Nordin Angelica, Lerner Yossef, Zabari Michal, Gotkine Marc, Baloh Robert H, Bell Shaughn, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Millecamps Stéphanie, Meininger Vincent, Salachas François, Mora Jesus S, Assialioui Abdelilah, Rojas-García Ricardo, Dion Patrick A, Ross Jay P, Ludolph Albert C., Weishaupt Jochen H, Brenner David, Freischmidt Axel, Bensimon Gilbert, Brice Alexis, Dürr Alexandra, Payan Christine A M, Saker-Delye Safaa, Wood Nicholas W, Topp Simon, Rademakers Rosa, Tittmann Lukas, Lieb Wolfgang, Klein-Franke Andreas, Ripke Stephan, Braun Alice, Kraft Julia, Whiteman David C, Olsen Catherine M, Uitterlinden André G, Hofman Albert, Rietschel Marcella, Cichon Sven, Nöthen Markus M, Amouyel Philippe, SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Traynor Bryan J, Singleton Andrew B, Mitne Neto Miguel, Cauchi Ruben J, Ophoff Roel A, Wiedau-Pazos Martina, Lomen-Hoerth Catherine, Van Deerlin Vivianna M, Grosskreutz Julian, Roediger Annekathrin, Gaur Nayana, Jörk Alexander, Barthel Tabea, Theele Erik, Ilse Benjamin, Stubendorff Beatrice, Witte Otto W, Steinbach Robert, Hübner Christian A, Graff Caroline, Brylev Lev, Fominykh Vera, Demeshonok Vera, Ataulina Anastasia, Rogelj Boris, Koritnik Blaž, Zidar Janez, Ravnik-Glavač Metka, Glavač Damjan, Stević Zorica, Drory Vivian E, Povedano Monica, Blair Ian P, Kiernan Matthew C, Benyamin Beben, Henderson Robert D, Furlong Sarah, Mathers Susan, McCombe Pamela A, Needham Merrilee, Ngo Shyuan T, Nicholson Garth A, Pamphlett Roger, Rowe Dominic B, Steyn Frederik J, Williams Kelly L, Mather Karen A, Sachdev Perminder S, Henders Anjali K, Wallace Leanne, de Carvalho Mamede, Pinto Susana, Petri Susanne, Weber Markus, Rouleau Guy A, Silani Vincenzo, Curtis Charles J, Breen Gerome, Glass Jonathan D, Brown Robert H, Landers John E, Shaw Christopher E, Andersen Peter Munch, Groen Ewout J N, van Es Michael A, Pasterkamp R Jeroen, Fan Dongsheng, Garton Fleur C, McRae Allan F, Davey Smith George, Gaunt Tom R, Eberle Michael A, Mill Jonathan, McLaughlin Russell L, Hardiman Orla, Kenna Kevin P, Wray Naomi R, Tsai Ellen, Runz Heiko, Franke Lude, Al-Chalabi Ammar, Van Damme Philip, van den Berg Leonard H, Veldink Jan H
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
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Packard C, Pers T, Person T, Peters A, Petersen E, Peyser P, Pirie A, Polasek O, Polderman T, Puolijoki H, Raitakari O, Perry J, Perry J, Perola M, Padmanabhan S, Palmer C, Palmer N, Pasterkamp G, Patel A, Pattie A, Pedersen O, Peissig P, Peloso G, Pennell C, Rasheed A, Rauramaa R, Reilly D, Samani N, Sapkota Y, Sattar N, Schoen R, Schreiner P, Schulze M, Scott R, Segura-Lepe M, Shah S, Sheu W, Salomaa V, Saleheen D, Ruth K, Renström F, Rheinberger M, Ridker P, Rioux J, Rivas M, Roberts D, Robertson N, Robino A, Rolandsson O, Rudan I, Sim X, Lin K, Lubitz S, Lyytikäinen L, Männistö S, Marenne G, Mazul A, McCarthy M, McKean-Cowdin R, Medland S, Meidtner K, Milani L, Luan J, Loukola A, Lotery A, Lin L, Lin X, Lind L, Lindström J, Linneberg A, Liu C, Liu D, Liu Y, Lo K, Lophatananon A, Mistry V, Mitchell P, Mohlke K, Neville M, Nielsen S, Nikus K, Njølstad P, Nordestgaard B, Nyholt D, O'Connel J, O'Donoghue M, Olde Loohuis L, Ophoff R, Nelson C, Narisu N, Nalls M, Moilanen L, Moitry M, Montgomery G, Mook-Kanamori D, Moore C, Mori T, Morris A, Morris A, Müller-Nurasyid M, Munroe P, Owen K, Slater A, Walker M, Witte D, Wood A, Wu Y, Yaghootkar H, Yao J, Yao P, Yerges-Armstrong L, Young R, Zeggini E, Zhan X, Wilson J, Willer C, White H, Wallentin L, Wang F, Wang C, Wang S, Wang Y, Ware E, Wareham N, Warren H, Waterworth D, Wessel J, Zhang W, Zhao J, Zhao W, CHD Exome+ Consortium, EPIC-CVD Consortium, ExomeBP Consortium, Global Lipids Genetic Consortium, GoT2D Genes Consortium, EPIC InterAct Consortium, INTERVAL Study, ReproGen Consortium, T2D-Genes Consortium, MAGIC Investigators, Loos R, Hirschhorn J, Lindgren C, Zhou W, Zondervan K, Rotter J, Pospisilik J, Rivadeneira F, Borecki I, Deloukas P, Frayling T, Lettre G, North K, Understanding Society Scientific Group, Small K, Swift A, Tada H, Tansey K, Tardif J, Taylor K, Teumer A, Thompson D, Thorleifsson G, Thorsteinsdottir U, Thuesen B, Surendran P, Sun L, Stumvoll M, Smith A, Southam L, Spector T, Speliotes E, Starr J, Stefansson K, Steinthorsdottir V, Stirrups K, Strauch K, Stringham H, Tönjes A, Tromp G, Trompet S, Varga T, Varma R, Velez Edwards D, Vermeulen S, Veronesi G, Vestergaard H, Vitart V, Vogt T, Völker U, Vuckovic D, Varbo A, Vanhala M, van Setten J, Tsafantakis E, Tuomilehto J, Tybjaerg-Hansen A, Tyrer J, Uher R, Uitterlinden A, Uusitupa M, Laan S, Duijn C, Leeuwen N, Wagenknecht L, Lin H, Bots M, Caulfield M, Chambers J, Chasman D, Chen Y, Chowdhury R, Christensen C, Chu A, Cocca M, Collins F, Cook J, Catamo E, Carey D, Cappellani S, Bottinger E, Bowden D, Brandslund I, Breen G, Brilliant M, Broer L, Brumat M, Burt A, Butterworth A, Campbell P, Corley J, Corominas Galbany J, Cox A, Ruijter H, Dennis J, Denny J, Di Angelantonio E, Drenos F, Du M, Dubé M, Dunning A, Easton D, Edwards T, Hollander A, Heijer M, Demerath E, Crosslin D, Cuellar-Partida G, D'Eustacchio A, Danesh J, Davies G, Bakker P, Groot M, Mutsert R, Deary I, Dedoussis G, Ellinghaus D, Turcot V, Locke A, Mahajan A, Marouli E, Sivapalaratnam S, Young K, Alfred T, Feitosa M, Masca N, Manning A, Medina-Gomez C, Lempradl A, Karaderi T, Hendricks A, Lu Y, Highland H, Schurmann C, Justice A, Fine R, Bradfield J, Esko T, Giri A, Graff M, Guo X, Mudgal P, Ng M, Reiner A, Barroso I, Bastarache L, Benn M, Bergmann S, Bielak L, Blüher M, Boehnke M, Boeing H, Boerwinkle E, Böger C, Bang L, Balkau B, Auer P, Vedantam S, Willems S, Winkler T, Abecasis G, Aben K, Alam D, Alharthi S, Allison M, Amouyel P, Asselbergs F, Bork-Jensen J, Ellinor P, Howson J, Jukema J, Kahali B, Kahn R, Kähönen M, Kamstrup P, Kanoni S, Kaprio J, Karaleftheri M, Kardia S, Karpe F, Jørgensen T, Jørgensen M, Johansson S, Hu Y, Huang P, Huffman J, Ikram M, Ingelsson E, Jackson A, Jansson J, Jarvik G, Jensen G, Jia Y, Kathiresan S, Kee F, Kiemeney L, Lamparter D, Lange E, Lange L, Langenberg C, Larson E, Lee N, Lehtimäki T, Lewis C, Li H, Li J, Lakka T, Laakso M, Kuusisto J, Kim E, Kitajima H, Komulainen P, Kooner J, Kooperberg C, Korhonen T, Kovacs P, Kuivaniemi H, Kutalik Z, Kuulasmaa K, Li-Gao R, Elliott P, Franks P, Friedrich N, Frikke-Schmidt R, Galesloot T, Gan W, Gandin I, Gasparini P, Gibson J, Giedraitis V, Gjesing A, Franke A, Franco O, Fornage M, Evangelou E, Farmaki A, Farooqi I, Faul J, Fauser S, Feng S, Ferrannini E, Ferrieres J, Florez J, Ford I, Gordon-Larsen P, Gorski M, Grabe H, Have C, Hayward C, He L, Heard-Costa N, Heath A, Heid I, Helgeland Ø, Hernesniemi J, Hewitt A, Holmen O, Hattersley A, Harris T, Harris K, Grant S, Grarup N, Griffiths H, Grove M, Gudnason V, Gustafsson S, Haessler J, Hakonarson H, Hammerschlag A, Hansen T, Hovingh G. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nat Genet 2017; 50:26-41.
22.12.2017Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
22.12.2017Nat Genet 2017; 50:26-41
Packard Chris J, Pers Tune H, Person Thomas N, Peters Annette, Petersen Eva R B, Peyser Patricia A, Pirie Ailith, Polasek Ozren, Polderman Tinca J, Puolijoki Hannu, Raitakari Olli T, Perry John R B, Perry James A, Perola Markus, Padmanabhan Sandosh, Palmer Colin N A, Palmer Nicholette D, Pasterkamp Gerard, Patel Aniruddh P, Pattie Alison, Pedersen Oluf, Peissig Peggy L, Peloso Gina M, Pennell Craig E, Rasheed Asif, Rauramaa Rainer, Reilly Dermot F, Samani Nilesh J, Sapkota Yadav, Sattar Naveed, Schoen Robert E, Schreiner Pamela J, Schulze Matthias B, Scott Robert A, Segura-Lepe Marcelo P, Shah Svati H, Sheu Wayne H-H, Salomaa Veikko, Saleheen Danish, Ruth Katherine S, Renström Frida, Rheinberger Myriam, Ridker Paul M, Rioux John D, Rivas Manuel A, Roberts David J, Robertson Neil R, Robino Antonietta, Rolandsson Olov, Rudan Igor, Sim Xueling, Lin Keng-Hung, Lubitz Steven A, Lyytikäinen Leo-Pekka, Männistö Satu, Marenne Gaëlle, Mazul Angela L, McCarthy Mark I, McKean-Cowdin Roberta, Medland Sarah E, Meidtner Karina, Milani Lili, Luan Jian'an, Loukola Anu, Lotery Andrew J, Lin Li-An, Lin Xu, Lind Lars, Lindström Jaana, Linneberg Allan, Liu Ching-Ti, Liu Dajiang J, Liu Yongmei, Lo Ken S, Lophatananon Artitaya, Mistry Vanisha, Mitchell Paul, Mohlke Karen L, Neville Matt, Nielsen Sune F, Nikus Kjell, Njølstad Pål R, Nordestgaard Børge G, Nyholt Dale R, O'Connel Jeffrey R, O'Donoghue Michelle L, Olde Loohuis Loes M, Ophoff Roel A, Nelson Christopher P, Narisu Narisu, Nalls Mike A, Moilanen Leena, Moitry Marie, Montgomery Grant W, Mook-Kanamori Dennis O, Moore Carmel, Mori Trevor A, Morris Andrew D, Morris Andrew P, Müller-Nurasyid Martina, Munroe Patricia B, Owen Katharine R, Slater Andrew J, Walker Mark, Witte Daniel R, Wood Andrew R, Wu Ying, Yaghootkar Hanieh, Yao Jie, Yao Pang, Yerges-Armstrong Laura M, Young Robin, Zeggini Eleftheria, Zhan Xiaowei, Wilson James G, Willer Cristen J, White Harvey D, Wallentin Lars, Wang Feijie, Wang Carol A, Wang Shuai, Wang Yiqin, Ware Erin B, Wareham Nicholas J, Warren Helen R, Waterworth Dawn M, Wessel Jennifer, Zhang Weihua, Zhao Jing Hua, Zhao Wei, CHD Exome+ Consortium, EPIC-CVD Consortium, ExomeBP Consortium, Global Lipids Genetic Consortium, GoT2D Genes Consortium, EPIC InterAct Consortium, INTERVAL Study, ReproGen Consortium, T2D-Genes Consortium, MAGIC Investigators, Loos Ruth J F, Hirschhorn Joel N, Lindgren Cecilia M, Zhou Wei, Zondervan Krina T, Rotter Jerome I, Pospisilik John A, Rivadeneira Fernando, Borecki Ingrid B, Deloukas Panos, Frayling Timothy M, Lettre Guillaume, North Kari E, Understanding Society Scientific Group, Small Kerrin S, Swift Amy J, Tada Hayato, Tansey Katherine E, Tardif Jean-Claude, Taylor Kent D, Teumer Alexander, Thompson Deborah J, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Thuesen Betina H, Surendran Praveen, Sun Liang, Stumvoll Michael, Smith Albert V, Southam Lorraine, Spector Timothy D, Speliotes Elizabeth K, Starr John M, Stefansson Kari, Steinthorsdottir Valgerdur, Stirrups Kathleen E, Strauch Konstantin, Stringham Heather M, Tönjes Anke, Tromp Gerard, Trompet Stella, Varga Tibor V, Varma Rohit, Velez Edwards Digna R, Vermeulen Sita H, Veronesi Giovanni, Vestergaard Henrik, Vitart Veronique, Vogt Thomas F, Völker Uwe, Vuckovic Dragana, Varbo Anette, Vanhala Mauno, van Setten Jessica, Tsafantakis Emmanouil, Tuomilehto Jaakko, Tybjaerg-Hansen Anne, Tyrer Jonathan P, Uher Rudolf, Uitterlinden André G, Uusitupa Matti, Laan Sander W, Duijn Cornelia M, Leeuwen Nienke, Wagenknecht Lynne E, Lin Honghuang, Bots Michiel L, Caulfield Mark J, Chambers John C, Chasman Daniel I, Chen Yii-Der I, Chowdhury Rajiv, Christensen Cramer, Chu Audrey Y, Cocca Massimiliano, Collins Francis S, Cook James P, Catamo Eulalia, Carey David J, Cappellani Stefania, Bottinger Erwin P, Bowden Donald W, Brandslund Ivan, Breen Gerome, Brilliant Murray H, Broer Linda, Brumat Marco, Burt Amber A, Butterworth Adam S, Campbell Peter T, Corley Janie, Corominas Galbany Jordi, Cox Amanda J, Ruijter Hester M, Dennis Joe G, Denny Josh C, Di Angelantonio Emanuele, Drenos Fotios, Du Mengmeng, Dubé Marie-Pierre, Dunning Alison M, Easton Douglas F, Edwards Todd L, Hollander Anneke I, Heijer Martin, Demerath Ellen W, Crosslin David S, Cuellar-Partida Gabriel, D'Eustacchio Angela, Danesh John, Davies Gail, Bakker Paul I W, Groot Mark C H, Mutsert Renée, Deary Ian J, Dedoussis George, Ellinghaus David, Turcot Valérie, Locke Adam E, Mahajan Anubha, Marouli Eirini, Sivapalaratnam Suthesh, Young Kristin L, Alfred Tamuno, Feitosa Mary F, Masca Nicholas G D, Manning Alisa K, Medina-Gomez Carolina, Lempradl Adelheid, Karaderi Tugce, Hendricks Audrey E, Lu Yingchang, Highland Heather M, Schurmann Claudia, Justice Anne E, Fine Rebecca S, Bradfield Jonathan P, Esko Tõnu, Giri Ayush, Graff Mariaelisa, Guo Xiuqing, Mudgal Poorva, Ng Maggie C Y, Reiner Alex P, Barroso Inês, Bastarache Lisa, Benn Marianne, Bergmann Sven, Bielak Lawrence F, Blüher Matthias, Boehnke Michael, Boeing Heiner, Boerwinkle Eric, Böger Carsten A, Bang Lia E, Balkau Beverley, Auer Paul L, Vedantam Sailaja, Willems Sara M, Winkler Thomas W, Abecasis Goncalo, Aben Katja K, Alam Dewan S, Alharthi Sameer E, Allison Matthew, Amouyel Philippe, Asselbergs Folkert W, Bork-Jensen Jette, Ellinor Patrick T, Howson Joanna M M, Jukema J Wouter, Kahali Bratati, Kahn René S, Kähönen Mika, Kamstrup Pia R, Kanoni Stavroula, Kaprio Jaakko, Karaleftheri Maria, Kardia Sharon L R, Karpe Fredrik, Jørgensen Torben, Jørgensen Marit E, Johansson Stefan, Hu Yao, Huang Paul L, Huffman Jennifer E, Ikram M Arfan, Ingelsson Erik, Jackson Anne U, Jansson Jan-Håkan, Jarvik Gail P, Jensen Gorm B, Jia Yucheng, Kathiresan Sekar, Kee Frank, Kiemeney Lambertus A, Lamparter David, Lange Ethan M, Lange Leslie A, Langenberg Claudia, Larson Eric B, Lee Nanette R, Lehtimäki Terho, Lewis Cora E, Li Huaixing, Li Jin, Lakka Timo A, Laakso Markku, Kuusisto Johanna, Kim Eric, Kitajima Hidetoshi, Komulainen Pirjo, Kooner Jaspal S, Kooperberg Charles, Korhonen Tellervo, Kovacs Peter, Kuivaniemi Helena, Kutalik Zoltán, Kuulasmaa Kari, Li-Gao Ruifang, Elliott Paul, Franks Paul W, Friedrich Nele, Frikke-Schmidt Ruth, Galesloot Tessel E, Gan Wei, Gandin Ilaria, Gasparini Paolo, Gibson Jane, Giedraitis Vilmantas, Gjesing Anette P, Franke Andre, Franco Oscar H, Fornage Myriam, Evangelou Evangelos, Farmaki Aliki-Eleni, Farooqi I Sadaf, Faul Jessica D, Fauser Sascha, Feng Shuang, Ferrannini Ele, Ferrieres Jean, Florez Jose C, Ford Ian, Gordon-Larsen Penny, Gorski Mathias, Grabe Hans-Jörgen, Have Christian T, Hayward Caroline, He Liang, Heard-Costa Nancy L, Heath Andrew C, Heid Iris M, Helgeland Øyvind, Hernesniemi Jussi, Hewitt Alex W, Holmen Oddgeir L, Hattersley Andrew T, Harris Tamara B, Harris Kathleen Mullan, Grant Struan F A, Grarup Niels, Griffiths Helen L, Grove Megan L, Gudnason Vilmundur, Gustafsson Stefan, Haessler Jeff, Hakonarson Hakon, Hammerschlag Anke R, Hansen Torben, Hovingh G Kees
Exome-wide association study of plasma lipids in >300,000 individuals
Sim X, Ridker P, Rich S, Renström F, Reiner A, Reilly D, Rauramaa R, Rasheed A, Rader D, Psaty B, Poulter N, Polasek O, Pistis G, Rioux J, Robertson N, Shaffer C, Sevilla R, Sever P, Scott R, Schmidt E, Sattar N, Sanna S, Samani N, Salomaa V, Rudan I, Rotter J, Roden D, Pisinger C, Peters A, Perola M, Neville M, Munroe P, Müller-Nurasyid M, Mulas A, Morrison A, Morris A, Metspalu A, Melander O, Meigs J, Maschio A, Masca N, Marouli E, Nielsen J, Nielsen S, Pedersen O, Patel A, Pasko D, Palmer C, Padmanabhan S, Muntendam P, Molony C, Orho-Melander M, O'Donnell C, Mehran R, Ordovas J, Nordestgaard B, Mäntyselkä P, Kathiresan S, Zheng N, Zhang H, Zeggini E, Young R, Yaghootkar H, Xu M, Wilson P, Wilson J, Wessel J, Weinstock J, Weeke P, Warren H, Zhang W, Zhang Y, Willer C, Musunuru K, Deloukas P, Abecasis G, Cowan C, McCarthy M, Danesh J, Howson J, Zoledziewska M, Zhou Y, Zhou W, Wareham N, Wang N, Waldenberger M, Stringham H, Strauch K, Stitziel N, Stirrups K, Starr J, Speliotes E, Spector T, Southam L, Somayajula S, Smith B, Smith A, Small K, Surendran P, Tada H, Virtamo J, Varga T, Varbo A, van Zuydam N, Tybjaerg-Hansen A, Tuomilehto J, Tsao P, Trompet S, Taylor K, Tardif J, Tang H, Tall A, Sivapalaratnam S, Frikke-Schmidt R, Dedoussis G, Deary I, Davies G, Damrauer S, Cupples L, Cucca F, Connell J, Chu A, Christensen C, Chowdhury R, Chen Y, Chen Y, Denny J, Dominiczak A, Frayling T, Franks P, Fornage M, Ford I, Ferrieres J, Ferrario M, Feitosa M, Farmaki A, Esko T, Eiriksdottir G, Ebeling T, Dubé M, Chasman D, Chambers J, Caulfield M, Arveiler D, Di Angelantonio E, Amouyel P, Alves A, Alam D, Emdin C, Saleheen D, Mahajan A, Wang X, Butterworth A, Yu H, Peloso G, Assimes T, Auer P, Busonero F, Brown M, Brandslund I, Bottinger E, Bork-Jensen J, Boerwinkle E, Boehnke M, Bis J, Benn M, Bang L, Ballantyne C, Baber U, Liu D, Manning A, Laakso M, Kuusisto J, Kuulasmaa K, Kooperberg C, Kooner J, Koistinen H, Klarin D, Khera A, Kee F, Karpe F, Kanoni S, Kamstrup P, Lakka T, Langenberg C, Manichaikul A, Malarstig A, Mägi R, Lu X, Lu Y, Loos R, Linneberg A, Lin L, Liewald D, Lauritzen T, Launer L, Langsted A, Justesen J, Jukema J, Jørgensen M, Grove M, Groop L, Grarup N, Grallert H, Goodarzi M, Giulianini F, Gieger C, Garcia M, Gao W, Ganesh S, Fuster V, Frossard P, Gudnason V, Hansen T, Jensen G, Jarvelin M, Jakobsdottir J, Jackson A, Jabeen S, Hveem K, Huo Y, Huffman J, Holmen O, Hirschhorn J, Hayward C, Harris T, Fritsche L. Exome-wide association study of plasma lipids in >300,000 individuals. Nat Genet 2017; 49:1758-1766.
30.10.2017Exome-wide association study of plasma lipids in >300,000 individuals
30.10.2017Nat Genet 2017; 49:1758-1766
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Rare and low-frequency coding variants alter human adult height
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01.02.2017Rare and low-frequency coding variants alter human adult height
01.02.2017Nature 2017; 542:186-190
Ntalla Ioanna, Peissig Peggy L, Peloso Gina M, Pennell Craig E, Perola Markus, Perry James A, Perry John R B, Person Thomas N, Pirie Ailith, Polasek Ozren, Pedersen Oluf, Pattie Alison, Patel Aniruddh P, O'Connel Jeffrey R, Oksa Heikki, Loohuis Loes M Olde, Ophoff Roel A, Owen Katharine R, Packard Chris J, Padmanabhan Sandosh, Palmer Colin N A, Pasterkamp Gerard, Posthuma Danielle, Raitakari Olli T, Saleheen Danish, Salomaa Veikko, Samani Nilesh J, Sandow Kevin, Sapkota Yadav, Sattar Naveed, Schmidt Marjanka K, Schreiner Pamela J, Schulze Matthias B, Ruth Katherine S, Rudan Igor, Rolandsson Olov, Rasheed Asif, Rauramaa Rainer, Reilly Dermot F, Reiner Alex P, Renström Frida, Ridker Paul M, Rioux John D, Robertson Neil, Robino Antonietta, Scott Robert A, Nordestgaard Børge G, Langefeld Carl D, Lindström Jaana, Linneberg Allan, Liu Yeheng, Liu Yongmei, Lophatananon Artitaya, Luan Jian'an, Lubitz Steven A, Lyytikäinen Leo-Pekka, Mackey David A, Lind Lars, Lin Xu, Lin Li-An, Langenberg 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Jaakko, Tybjaerg-Hansen Anne, Tyrer Jonathan P, Uher Rudolf, Uitterlinden André G, Ulivi Sheila, Vogt Thomas F, Boeing Heiner, Butterworth Adam S, Carey David J, Caulfield Mark J, Chambers John C, Chasman Daniel I, Chen Yii-Der Ida, Chowdhury Rajiv, Christensen Cramer, Chu Audrey Y, Burt Amber A, Broer Linda, Brilliant Murray H, Boerwinkle Eric, Böger Carsten A, Bonnycastle Lori L, Bork-Jensen Jette, Bots Michiel L, Bottinger Erwin P, Bowden Donald W, Brandslund Ivan, Breen Gerome, Cocca Massimiliano, Collins Francis S, Deary Ian J, Dedoussis George, Demerath Ellen W, den Hollander Anneke I, Dennis Joe G, Di Angelantonio Emanuele, Drenos Fotios, Du Mengmeng, Dunning Alison M, de Mutsert Renée, de Groot Mark C H, de Denus Simon, Cook James P, Corley Janie, Galbany Jordi Corominas, Cox Amanda J, Cuellar-Partida Gabriel, Danesh John, Davies Gail, de Bakker Paul I W, de Borst Gert J, Easton Douglas F, Blüher Matthias, Marouli Eirini, Lamparter David, Stirrups Kathleen E, Turcot Valérie, 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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Palotie A, Linneberg A, Husemoen L, Jarvelin M, Franks S, Blakemore A, Kooner J, Chambers J, Oksa H, Korpi-Hyövälti E, Petersen E, Christensen C, Skaaby T, Thuesen B, Käräjämäki A, Groop L, Tuomi T, Willer C, Hveem K, Holmen O, Palmer C, Morris A, Doney A, Tuomilehto J, Karpe F, Brandslund I, Numans M, Jukema J, Connell J, Dominiczak A, Brown M, Wareham N, Langenberg C, Starr J, Deary I, Männistö S, Jousilahti P, Spector T, Sattar N, Ford I, de Bakker P, Lind L, Ingelsson E, Gambaro G, van der Harst P, van der Meer P, de Boer R, Metspalu A, Mägi R, Esko T, Packard C, Dedoussis G, Ripatti S, Munroe P, Tobin M, Newton-Cheh C, Frossard P, Stringham H, Boehnke M, Pedersen O, Hansen T, Mohlke K, Collins F, Scotland G, Hayward C, Nordestgaard B, Caulfield M, Howson J, Butterworth A, Wain L, Danesh J, Lindgren C, Asselbergs F, Saleheen D, Samani N, Tomaszewski M, Morris A, Mahajan A, Porteous D, Padmanabhan S, Blankenberg S, Arveiler D, Amouyel P, Sever P, Stanton A, Poulter N, McCarthy M, Chowdhury R, Di Angelantonio E, Shafi Majumder A, Alam D, Ferrieres J, Kee F, Laakso M, Kuusisto J, Melander O, Kathiresan S, Zeggini E, Elliott P, Deloukas P, Virtamo J, Veronesi G, Müller-Nurasyid M, Kuulasmaa K, Salomaa V, Franks P, Yiorkas A, Matchan A, Ohlsson T, Fava C, Stančáková A, Huyghe J, Marten J, Southam L, Swift A, Narisu N, Jackson A, Bonnycastle L, Stirrups K, Bork-Jensen J, Robertson N, Neville M, Rayner N, Groves C, Donnelly L, Zhang H, Havulinna A, Shaw-Hawkins S, Perola M, Kontto J, Gjesing A, Zhao W, Samuel M, Tragante V, Staley J, Witkowska K, Barnes D, Sim X, Grarup N, Manning A, Cook J, Warren H, Young R, Drenos F, Tukiainen T, Yaghootkar H, Rasheed A, Fallgaard Nielsen S, Kraja A, Liu C, Mihailov E, Harakalova M, Tinker A, Giannakopoulou O, Ferreira T, Freitag D, Masca N, Surendran P, Herzig K, Rolandsson O, Lin H, Vogt T, Hoek M, Reily D, Malarstig A, Uria-Nickelsen M, Felix J, Vasan R, Burgess S, Hassinen M, Lieb W, Traylor M, Rudan I, Polasek O, Rauramaa R, Lakka T, Komulainen P, Uusitupa M, Lindström J, Marouli E, Justice A, Highland H, Markus H, Huffman J, Renström F, Nelson C, Vergnaud A, Moayyeri A, Evangelou E, Verweij N, Trabetti E, Soranzo N, Malerba G, Lannfelt L, Willems S, Zhang W, Poveda A, Varga T, Hallmans G, Farmaki A, Menni C, Marioni R, Liewald D, Harris S, Scott R, Luan J, Trompet S, de Craen A, Caslake M, Kajantie E. Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nat Genet 2016; 48:1151-1161.
12.09.2016Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
12.09.2016Nat Genet 2016; 48:1151-1161
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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
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25.07.2016Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
25.07.2016Nat Genet 2016; 48:1043-8
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Genetic studies of body mass index yield new insights for obesity biology
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12.02.2015Genetic studies of body mass index yield new insights for obesity biology
12.02.2015Nature 2015; 518:197-206
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Gådin Jesper R, Gharavi Ali G, Goddard Michael E, Handsaker Robert E, Huang Jinyan, Karpe Fredrik, Kathiresan Sekar, Keildson Sarah, Kiryluk Krzysztof, Kubo Michiaki, Lee Jong-Young, Liang Liming, Lifton Richard P, Ma Baoshan, McCarroll Steven A, McKnight Amy J, Min Josine L, Moffatt Miriam F, Montgomery Grant W, Murabito Joanne M, Nicholson George, Nyholt Dale R, Okada Yukinori, Perry John R B, Dorajoo Rajkumar, Reinmaa Eva, Salem Rany M, Sandholm Niina, Scott Robert A, Locke Adam E, Stolk Lisette, Kahali Bratati, Takahashi Atsushi, Berndt Sonja I, Tanaka Toshihiro, Justice Anne E, van 't Hooft Ferdinand M, Pers Tune H, Vinkhuyzen Anna A E, Day Felix R, Westra Harm-Jan, Powell Corey, Zheng Wei, Vedantam Sailaja, Zondervan Krina T, Buchkovich Martin L, Heath Andrew C, Yang Jian, Arveiler Dominique, Winkler Thomas W, Absher Devin, Amin Najaf, Anderson Denise, Beekman Marian, Bolton Jennifer L, Bragg-Gresham Jennifer L, Buyske Steven, Demirkan Ayse, Schmidt Ellen M, Karjalainen Juha, Workalemahu Tsegaselassie, Faul Jessica D, Smith Jennifer A, Zhao Jing Hua, Zhao Wei, Chen Jin, Fehrmann Rudolf, Hedman Åsa K
New genetic loci link adipose and insulin biology to body fat distribution
Hofman A, Kovacs P, Kraja A, Kumari M, Kuulasmaa K, Kuusisto J, Lakka T, Langenberg C, Le Marchand L, Lehtimäki T, Lyssenko V, Kooperberg C, Kooner J, Keinanen-Kiukaanniemi S, Homuth G, Humphries S, Hyppönen E, Illig T, Jarvelin M, Johansen B, Jousilahti P, Jula A, Kaprio J, Kee F, Männistö S, Marette A, Pramstaller P, Raitakari O, Rankinen T, Rao D, Rice T, Ridker P, Ritchie M, Rudan I, Salomaa V, Samani N, Peters A, Penninx B, Palmer L, Matise T, McKenzie C, McKnight B, Musk A, Möhlenkamp S, Morris A, Nelis M, Ohlsson C, Oldehinkel A, Ong K, Saramies J, Hoffmann W, Murabito J, Amouyel P, Arveiler D, Bakker S, Beilby J, Bergman R, Blangero J, Brown M, Burnier M, Campbell H, Zondervan K, Westra H, Vallejo E, Nicholson G, Nyholt D, Olsson C, Perry J, Reinmaa E, Salem R, Sandholm N, Schadt E, Scott R, Stolk L, Chakravarti A, Chines P, Forrester T, Franco O, Gansevoort R, Gieger C, Gudnason V, Haiman C, Harris T, Hattersley A, Heliövaara M, Hicks A, Forouhi N, Ferrieres J, Ferrannini E, Claudi-Boehm S, Collins F, Crawford D, Danesh J, de Faire U, de Geus E, Dörr M, Erbel R, Eriksson J, Farrall M, Hingorani A, Sarzynski M, Sinisalo J, Wichmann H, Abecasis G, Assimes T, Berndt S, Boehnke M, Borecki I, Deloukas P, Franke L, Frayling T, Groop L, Watkins H, Wareham N, Walker M, Slagboom P, Snieder H, Spector T, Stefansson K, Stumvoll M, Tuomilehto J, Uitterlinden A, Uusitupa M, van der Harst P, Veronesi G, Hunter D, Kaplan R, North K, Fox C, Barroso I, Franks P, Ingelsson E, Heid I, Loos R, Cupples L, Morris A, Lindgren C, Speliotes E, McCarthy M, Zillikens M, O'Connell J, Qi L, Schlessinger D, Strachan D, Thorsteinsdottir U, van Duijn C, Willer C, Visscher P, Yang J, Hirschhorn J, Mohlke K, Saleheen D, Schwarz P, Adair L, Bochud M, Boehm B, Bornstein S, Bouchard C, Cauchi S, Caulfield M, Chambers J, Chasman D, Cooper R, Witteman J, Wilson J, Vollenweider P, Shuldiner A, Staessen J, Steinthorsdottir V, Stolk R, Strauch K, Tönjes A, Tremblay A, Tremoli E, Vohl M, Völker U, Dedoussis G, Ferrucci L, Oostra B, Palmer C, Pedersen N, Perola M, Pérusse L, Peters U, Power C, Quertermous T, Rauramaa R, Rivadeneira F, Njølstad I, Munroe P, März W, Froguel P, Grabe H, Hamsten A, Hui J, Hveem K, Jöckel K, Kivimäki M, Kuh D, Laakso M, Liu Y, Saaristo T, Montgomery G, Pasko D, Bandinelli S, Barrett A, Bellis C, Bennett A, Berne C, Blüher M, Böhringer S, Bonnet F, Böttcher Y, Bruinenberg M, Arscott G, Arnlöv J, Albrecht E, Pechlivanis S, Peters M, Prokopenko I, Stančáková A, Sung Y, Tanaka T, Teumer A, van Vliet-Ostaptchouk J, Yengo L, Zhang W, Carba D, Caspersen I, Gigante B, Go A, Golay A, Grallert H, Grammer T, Gräßler J, Grewal J, Groves C, Haller T, Hallmans G, Giedraitis V, Garcia M, Friedrich N, Clarke R, Daw E, Deelen J, Deelman E, Delgado G, Doney A, Eklund N, Erdos M, Estrada K, Eury E, Hartman C, Palmer C, Shungin D, Roman T, Drong A, Song C, Gustafsson S, Day F, Esko T, Fall T, Kutalik Z, Luan J, Randall J, Heard-Costa N, Buchkovich M, Wu J, Winkler T, Croteau-Chonka D, Ferreira T, Locke A, Mägi R, Strawbridge R, Pers T, Fischer K, Justice A, Workalemahu T, Scherag A, Vedantam S, Demirkan A, Ehret G, Feitosa M, Goel A, Jackson A, Johnson T, Kleber M, Kristiansson K, Mangino M, Leach I, Buyske S, Bragg-Gresham J, Beekman M, Wood A, Chen J, Fehrmann R, Karjalainen J, Kahali B, Liu C, Schmidt E, Absher D, Amin N, Anderson D, Medina-Gomez C, Hassinen M, Rose L, Tayo B, Thorand B, Thorleifsson G, Tomaschitz A, Troffa C, van Oort F, Verweij N, Vonk J, Waite L, Wennauer R, Syvänen A, Swift A, Swertz M, Sanna S, Scharnagl H, Scholtens S, Sennblad B, Seufferlein T, Sitlani C, Smith A, Stirrups K, Stringham H, Sundstrom J, Wilsgaard T, Wojczynski M, Karpe F, Keildson S, Kiryluk K, Liang L, Lifton R, Ma B, McKnight A, McPherson R, Metspalu A, Min J, Kanoni S, Huang J, Hivert M, Wong A, Zhang Q, Zhao J, Brennan E, Choi M, Eriksson P, Folkersen L, Franco-Cereceda A, Gharavi A, Hedman Å, Moffatt M, Robertson N, Hayward C, Koenig W, Kooner I, Kratzer W, Lamina C, Leander K, Lee N, Lichtner P, Lind L, Lindström J, Lobbens S, Kinnunen L, Kalafati I, Juliusdottir T, Heikkilä K, Herzig K, Helmer Q, Hillege H, Holmen O, Hunt S, Isaacs A, Ittermann T, James A, Johansson I, Lorentzon M, Mach F, Müller G, Müller-Nurasyid M, Nagaraja R, Nalls M, Narisu N, Glorioso N, Nolte I, Olden M, Rayner N, Renström F, Mulas A, Mühleisen T, Mooijaart S, Magnusson P, Mahajan A, McArdle W, Menni C, Merger S, Mihailov E, Milani L, Mills R, Moayyeri A, Monda K, Ried J. New genetic loci link adipose and insulin biology to body fat distribution. Nature 2015; 518:187-196.
12.02.2015New genetic loci link adipose and insulin biology to body fat distribution
12.02.2015Nature 2015; 518:187-196
Hofman Albert, Kovacs Peter, Kraja Aldi T, Kumari Meena, Kuulasmaa Kari, Kuusisto Johanna, Lakka Timo A, Langenberg Claudia, Le Marchand Loic, Lehtimäki Terho, Lyssenko Valeriya, Kooperberg Charles, Kooner Jaspal S, Keinanen-Kiukaanniemi Sirkka M, Homuth Georg, Humphries Steve E, Hyppönen Elina, Illig Thomas, Jarvelin Marjo-Riitta, Johansen Berit, Jousilahti Pekka, Jula Antti M, Kaprio Jaakko, Kee Frank, Männistö Satu, Marette André, Pramstaller Peter P, Raitakari Olli T, Rankinen Tuomo, Rao D C, Rice Treva K, Ridker Paul M, Ritchie Marylyn D, Rudan Igor, Salomaa Veikko, Samani Nilesh J, Peters Annette, Penninx Brenda W, Palmer Lyle J, Matise Tara C, McKenzie Colin A, McKnight Barbara, Musk Arthur W, Möhlenkamp Stefan, Morris Andrew D, Nelis Mari, Ohlsson Claes, Oldehinkel Albertine J, Ong Ken K, Saramies Jouko, Hoffmann Wolfgang, Murabito Joanne M, Amouyel Philippe, Arveiler Dominique, Bakker Stephan Jl, Beilby John, Bergman Richard N, Blangero John, Brown Morris J, Burnier Michel, Campbell Harry, Zondervan Krina T, Westra Harm-Jan, Vallejo Edgar E, Nicholson George, Nyholt Dale R, Olsson Christian, Perry John Rb, Reinmaa Eva, Salem Rany M, Sandholm Niina, Schadt Eric E, Scott Robert A, Stolk Lisette, Chakravarti Aravinda, Chines Peter S, Forrester Terrence, Franco Oscar H, Gansevoort Ron T, Gieger Christian, Gudnason Vilmundur, Haiman Christopher A, Harris Tamara B, Hattersley Andrew T, Heliövaara Markku, Hicks Andrew A, Forouhi Nita G, Ferrieres Jean, Ferrannini Ele, Claudi-Boehm Simone, Collins Francis S, Crawford Dana C, Danesh John, de Faire Ulf, de Geus Eco Jc, Dörr Marcus, Erbel Raimund, Eriksson Johan G, Farrall Martin, Hingorani Aroon D, Sarzynski Mark A, Sinisalo Juha, Wichmann H-Erich, Abecasis Gonçalo R, Assimes Themistocles L, Berndt Sonja I, Boehnke Michael, Borecki Ingrid B, Deloukas Panos, Franke Lude, Frayling Timothy M, Groop Leif C, Watkins Hugh, Wareham Nicholas J, Walker Mark, Slagboom P Eline, Snieder Harold, Spector Tim D, Stefansson Kari, Stumvoll Michael, Tuomilehto Jaakko, Uitterlinden André G, Uusitupa Matti, van der Harst Pim, Veronesi Giovanni, Hunter David J, Kaplan Robert C, North Kari E, Fox Caroline S, Barroso Inês, Franks Paul W, Ingelsson Erik, Heid Iris M, Loos Ruth Jf, Cupples L Adrienne, Morris Andrew P, Lindgren Cecilia M, Speliotes Elizabeth K, McCarthy Mark I, Zillikens M Carola, O'Connell Jeffrey R, Qi Lu, Schlessinger David, Strachan David P, Thorsteinsdottir Unnur, van Duijn Cornelia M, Willer Cristen J, Visscher Peter M, Yang Jian, Hirschhorn Joel N, Mohlke Karen L, Saleheen Danish, Schwarz Peter Eh, Adair Linda S, Bochud Murielle, Boehm Bernhard O, Bornstein Stefan R, Bouchard Claude, Cauchi Stéphane, Caulfield Mark J, Chambers John C, Chasman Daniel I, Cooper Richard S, Witteman Jacqueline C, Wilson James F, Vollenweider Peter, Shuldiner Alan R, Staessen Jan A, Steinthorsdottir Valgerdur, Stolk Ronald P, Strauch Konstantin, Tönjes Anke, Tremblay Angelo, Tremoli Elena, Vohl Marie-Claude, Völker Uwe, Dedoussis George, Ferrucci Luigi, Oostra Ben A, Palmer Colin Na, Pedersen Nancy L, Perola Markus, Pérusse Louis, Peters Ulrike, Power Chris, Quertermous Thomas, Rauramaa Rainer, Rivadeneira Fernando, Njølstad Inger, Munroe Patricia B, März Winfried, Froguel Philippe, Grabe Hans-Jörgen, Hamsten Anders, Hui Jennie, Hveem Kristian, Jöckel Karl-Heinz, Kivimäki Mika, Kuh Diana, Laakso Markku, Liu Yongmei, Saaristo Timo E, Montgomery Grant W, Pasko Dorota, Bandinelli Stefania, Barrett Amy, Bellis Claire, Bennett Amanda J, Berne Christian, Blüher Matthias, Böhringer Stefan, Bonnet Fabrice, Böttcher Yvonne, Bruinenberg Marcel, Arscott Gillian M, Arnlöv Johan, Albrecht Eva, Pechlivanis Sonali, Peters Marjolein J, Prokopenko Inga, Stančáková Alena, Sung Yun Ju, Tanaka Toshiko, Teumer Alexander, van Vliet-Ostaptchouk Jana V, Yengo Loic, Zhang Weihua, Carba Delia B, Caspersen Ida H, Gigante Bruna, Go Alan S, Golay Alain, Grallert Harald, Grammer Tanja B, Gräßler Jürgen, Grewal Jagvir, Groves Christopher J, Haller Toomas, Hallmans Göran, Giedraitis Vilmantas, Garcia Melissa E, Friedrich Nele, Clarke Robert, Daw E Warwick, Deelen Joris, Deelman Ewa, Delgado Graciela, Doney Alex Sf, Eklund Niina, Erdos Michael R, Estrada Karol, Eury Elodie, Hartman Catharina A, Palmer Cameron D, Shungin Dmitry, Roman Tamara S, Drong Alexander W, Song Ci, Gustafsson Stefan, Day Felix R, Esko Tõnu, Fall Tove, Kutalik Zoltán, Luan Jian'an, Randall Joshua C, Heard-Costa Nancy L, Buchkovich Martin L, Wu Joseph M W, Winkler Thomas W, Croteau-Chonka Damien C, Ferreira Teresa, Locke Adam E, Mägi Reedik, Strawbridge Rona J, Pers Tune H, Fischer Krista, Justice Anne E, Workalemahu Tsegaselassie, Scherag André, Vedantam Sailaja, Demirkan Ayse, Ehret Georg B, Feitosa Mary F, Goel Anuj, Jackson Anne U, Johnson Toby, Kleber Marcus E, Kristiansson Kati, Mangino Massimo, Leach Irene Mateo, Buyske Steven, Bragg-Gresham Jennifer L, Beekman Marian, Wood Andrew R, Chen Jin, Fehrmann Rudolf, Karjalainen Juha, Kahali Bratati, Liu Ching-Ti, Schmidt Ellen M, Absher Devin, Amin Najaf, Anderson Denise, Medina-Gomez Carolina, Hassinen Maija, Rose Lynda M, Tayo Bamidele O, Thorand Barbara, Thorleifsson Gudmar, Tomaschitz Andreas, Troffa Chiara, van Oort Floor Va, Verweij Niek, Vonk Judith M, Waite Lindsay L, Wennauer Roman, Syvänen Ann-Christine, Swift Amy J, Swertz Morris A, Sanna Serena, Scharnagl Hubert, Scholtens Salome, Sennblad Bengt, Seufferlein Thomas, Sitlani Colleen M, Smith Albert Vernon, Stirrups Kathleen, Stringham Heather M, Sundstrom Johan, Wilsgaard Tom, Wojczynski Mary K, Karpe Fredrik, Keildson Sarah, Kiryluk Krzysztof, Liang Liming, Lifton Richard P, Ma Baoshan, McKnight Amy J, McPherson Ruth, Metspalu Andres, Min Josine L, Kanoni Stavroula, Huang Jinyan, Hivert Marie-France, Wong Andrew, Zhang Qunyuan, Zhao Jing Hua, Brennan Eoin P, Choi Murim, Eriksson Per, Folkersen Lasse, Franco-Cereceda Anders, Gharavi Ali G, Hedman Åsa K, Moffatt Miriam F, Robertson Neil R, Hayward Caroline, Koenig Wolfgang, Kooner Ishminder K, Kratzer Wolfgang, Lamina Claudia, Leander Karin, Lee Nanette R, Lichtner Peter, Lind Lars, Lindström Jaana, Lobbens Stephane, Kinnunen Leena, Kalafati Ioanna-Panagiota, Juliusdottir Thorhildur, Heikkilä Kauko, Herzig Karl-Heinz, Helmer Quinta, Hillege Hans L, Holmen Oddgeir, Hunt Steven C, Isaacs Aaron, Ittermann Till, James Alan L, Johansson Ingegerd, Lorentzon Mattias, Mach François, Müller Gabriele, Müller-Nurasyid Martina, Nagaraja Ramaiah, Nalls Michael A, Narisu Narisu, Glorioso Nicola, Nolte Ilja M, Olden Matthias, Rayner Nigel W, Renström Frida, Mulas Antonella, Mühleisen Thomas W, Mooijaart Simon P, Magnusson Patrik Ke, Mahajan Anubha, McArdle Wendy L, Menni Cristina, Merger Sigrun, Mihailov Evelin, Milani Lili, Mills Rebecca, Moayyeri Alireza, Monda Keri L, Ried Janina S
Defining the role of common variation in the genomic and biological architecture of adult human height
Jousilahti P, Lakka T, Langenberg C, Le Marchand L, Lehtimäki T, Lupoli S, Madden P, Männistö S, Manunta P, Marette A, Matise T, McKnight B, Kuusisto J, Kumari M, Kraja A, Jula A, Kaprio J, Kastelein J, Kayser M, Kee F, Keinanen-Kiukaanniemi S, Kiemeney L, Kooner J, Kooperberg C, Koskinen S, Kovacs P, Meitinger T, Moll F, Montgomery G, Rankinen T, Rao D, Rice T, Ritchie M, Rudan I, Salomaa V, Samani N, Saramies J, Sarzynski M, Schwarz P, Sebert S, Raitakari O, Qi L, Price J, Morris A, Morris A, Murray J, Nelis M, Ohlsson C, Oldehinkel A, Ong K, Ouwehand W, Pasterkamp G, Peters A, Pramstaller P, Sever P, Jarvelin M, Wright A, Caulfield M, Chakravarti A, Collins R, Collins F, Crawford D, Cupples L, Danesh J, de Faire U, den Ruijter H, Erbel R, Erdmann J, Campbell H, Brown M, Brambilla P, Zhang Q, Arveiler D, Bakker S, Beilby J, Bergman R, Bergmann S, Biffar R, Blangero J, Boomsma D, Bornstein S, Bovet P, Eriksson J, Farrall M, Ferrannini E, Hattersley A, Heath A, Hengstenberg C, Hicks A, Hindorff L, Hingorani A, Hofman A, Hovingh G, Humphries S, Hunt S, Hyppönen E, Harris T, Hall A, Haas D, Ferrieres J, Ford I, Forouhi N, Forrester T, Gansevoort R, Gejman P, Gieger C, Golay A, Gottesman O, Gudnason V, Gyllensten U, Jacobs K, Shuldiner A, Reinmaa E, Völzke H, Walker M, Wareham N, Watkins H, Wichmann H, Wilson J, Zanen P, Deloukas P, Heid I, Lindgren C, Mohlke K, van der Harst P, Uusitupa M, Tuomilehto J, Ridker P, Rivadeneira F, Rotter J, Saaristo T, Saleheen D, Schlessinger D, Slagboom P, Snieder H, Spector T, Strauch K, Stumvoll M, Speliotes E, Thorsteinsdottir U, Barroso I, Price A, Lettre G, Loos R, Weedon M, Ingelsson E, O'Connell J, Abecasis G, Chasman D, Goddard M, Visscher P, Hirschhorn J, Willer C, Franke L, van Duijn C, Fox C, North K, Strachan D, Beckmann J, Berndt S, Boehnke M, Borecki I, McCarthy M, Metspalu A, Stefansson K, Uitterlinden A, Frayling T, Rauramaa R, Sinisalo J, Boerwinkle E, Bottinger E, Bouchard C, Cauchi S, Chambers J, Chanock S, Cooper R, de Bakker P, Dedoussis G, Ferrucci L, Franks P, Boehm B, Bochud M, Assimes T, Steinthorsdottir V, Stolk R, Tardif J, Tönjes A, Tremblay A, Tremoli E, Virtamo J, Vohl M, Amouyel P, Asselbergs F, Froguel P, Groop L, Haiman C, Moebus S, Munroe P, Njølstad I, Oostra B, Palmer C, Pedersen N, Perola M, Pérusse L, Peters U, Powell J, Power C, Melbye M, März W, Martin N, Hamsten A, Hayes M, Hui J, Hunter D, Hveem K, Jukema J, Kaplan R, Kivimäki M, Kuh D, Laakso M, Liu Y, Quertermous T, Nyholt D, van Setten J, van Vliet-Ostaptchouk J, Wang Z, Yengo L, Zhang W, Afzal U, Arnlöv J, Arscott G, Bandinelli S, Barrett A, Bellis C, van der Laan S, Trompet S, Teumer A, Palmer C, Pasko D, Pechlivanis S, Prokopenko I, Ried J, Ripke S, Shungin D, Stančáková A, Strawbridge R, Sung Y, Tanaka T, Bennett A, Berne C, Blüher M, Delgado G, Denny J, Dhonukshe-Rutten R, Dimitriou M, Doney A, Dörr M, Eklund N, Eury E, Folkersen L, Garcia M, Geller F, Deelen J, De Jong P, Daw E, Bolton J, Böttcher Y, Boyd H, Bruinenberg M, Buckley B, Buyske S, Caspersen I, Chines P, Clarke R, Claudi-Boehm S, Cooper M, Giedraitis V, Nalls M, Wood A, Fall T, Fehrmann R, Ferreira T, Jackson A, Karjalainen J, Lo K, Locke A, Mägi R, Mihailov E, Porcu E, Randall J, Duan Y, Day F, Croteau-Chonka D, Esko T, Yang J, Vedantam S, Pers T, Gustafsson S, Chu A, Estrada K, Luan J, Kutalik Z, Amin N, Buchkovich M, Scherag A, Vinkhuyzen A, Westra H, Goel A, Gong J, Justice A, Kanoni S, Kleber M, Kristiansson K, Lim U, Lotay V, Lui J, Mangino M, Mateo Leach I, Fraser R, Fischer K, Feitosa M, Winkler T, Workalemahu T, Zhao J, Absher D, Albrecht E, Anderson D, Baron J, Beekman M, Demirkan A, Ehret G, Feenstra B, Medina-Gomez C, Go A, Monda K, Roussel R, Sanna S, Scharnagl H, Scholtens S, Schumacher F, Schunkert H, Scott R, Sehmi J, Seufferlein T, Shi J, Silventoinen K, Rose L, Robertson N, Renström F, Morken M, Müller G, Müller-Nurasyid M, Musk A, Narisu N, Nauck M, Nolte I, Nöthen M, Oozageer L, Pilz S, Rayner N, Smit J, Smith A, Smolonska J, van Oort F, Vermeulen S, Verweij N, Vonk J, Waite L, Waldenberger M, Wennauer R, Wilkens L, Willenborg C, Wilsgaard T, Wojczynski M, van Heemst D, van der Velde N, van Schoor N, Stanton A, Stirrups K, Stott D, Stringham H, Sundstrom J, Swertz M, Syvänen A, Tayo B, Thorleifsson G, Tyrer J, van Dijk S, Wong A, Moayyeri A, Grallert H, Helmer Q, Hemani G, Henders A, Hillege H, Hlatky M, Hoffmann W, Hoffmann P, Holmen O, Houwing-Duistermaat J, Illig T, Isaacs A, Heard-Costa N, Hayward C, Hassinen M, Grammer T, Gräßler J, Grönberg H, de Groot L, Groves C, Haessler J, Hall P, Haller T, Hallmans G, Hannemann A, Hartman C, James A, Jeff J, Johansen B, Lu Y, Lyssenko V, Magnusson P, Mahajan A, Maillard M, McArdle W, McKenzie C, McLachlan S, McLaren P, Menni C, Merger S, Lorentzon M, Lobbens S, Lindström J, Johansson Å, Jolley J, Juliusdottir T, Junttila J, Kho A, Kinnunen L, Klopp N, Kocher T, Kratzer W, Lichtner P, Lind L, Milani L. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat Genet 2014; 46:1173-86.
05.10.2014Defining the role of common variation in the genomic and biological architecture of adult human height
05.10.2014Nat Genet 2014; 46:1173-86
Jousilahti Pekka, Lakka Timo A, Langenberg Claudia, Le Marchand Loic, Lehtimäki Terho, Lupoli Sara, Madden Pamela A F, Männistö Satu, Manunta Paolo, Marette André, Matise Tara C, McKnight Barbara, Kuusisto Johanna, Kumari Meena, Kraja Aldi T, Jula Antti M, Kaprio Jaakko, Kastelein John J P, Kayser Manfred, Kee Frank, Keinanen-Kiukaanniemi Sirkka M, Kiemeney Lambertus A, Kooner Jaspal S, Kooperberg Charles, Koskinen Seppo, Kovacs Peter, Meitinger Thomas, Moll Frans L, Montgomery Grant W, Rankinen Tuomo, Rao D C, Rice Treva K, Ritchie Marylyn, Rudan Igor, Salomaa Veikko, Samani Nilesh J, Saramies Jouko, Sarzynski Mark A, Schwarz Peter E H, Sebert Sylvain, Raitakari Olli T, Qi Lu, Price Jackie F, Morris Andrew D, Morris Andrew P, Murray Jeffrey C, Nelis Mari, Ohlsson Claes, Oldehinkel Albertine J, Ong Ken K, Ouwehand Willem H, Pasterkamp Gerard, Peters Annette, Pramstaller Peter P, Sever Peter, Jarvelin Marjo-Riitta, Wright Alan F, Caulfield Mark J, Chakravarti Aravinda, Collins Rory, 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