Gerome Breen
Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival.
Adey B, Cooper-Knock J, Al Khleifat A, Fogh I, Van Damme P, Corcia P, Couratier P, Hardiman O, McLaughlin R, Gotkine M, Drory V, Silani V, Ticozzi N, Veldink J, van den Berg L, de Carvalho M, Pinto S, Mora J, Povedano Panades M, Andersen P, Weber M, Başak N, Shaw C, Openshaw P, Morrison K, Landers J, Glass J, Vourc'h P, Dobson R, Breen G, Al-Chalabi A, Jones A, Iacoangeli A. Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival. Front Cell Neurosci 2023; 17:1112405.
02.03.2023Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival.
02.03.2023Front Cell Neurosci 2023; 17:1112405
Adey Brett N, Cooper-Knock Johnathan, Al Khleifat Ahmad, Fogh Isabella, Van Damme Philip, Corcia Philippe, Couratier Philippe, Hardiman Orla, McLaughlin Russell L, Gotkine Marc, Drory Vivian E, Silani Vincenzo, Ticozzi Nicola, Veldink Jan H, van den Berg Leonard H, de Carvalho Mamede, Pinto Susana, Mora Jesus S, Povedano Panades Mónica, Andersen Peter Munch, Weber Markus, Başak Nazli A, Shaw Christopher E, Openshaw Peter J M, Morrison Karen E, Landers John E, Glass Jonathan D, Vourc'h Patrick, Dobson Richard J B, Breen Gerome, Al-Chalabi Ammar, Jones Ashley R, Iacoangeli Alfredo
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
Rare and low-frequency coding variants alter human adult height
Ntalla I, Peissig P, Peloso G, Pennell C, Perola M, Perry J, Perry J, Person T, Pirie A, Polasek O, Pedersen O, Pattie A, Patel A, O'Connel J, Oksa H, Loohuis L, Ophoff R, Owen K, Packard C, Padmanabhan S, Palmer C, Pasterkamp G, Posthuma D, Raitakari O, Saleheen D, Salomaa V, Samani N, Sandow K, Sapkota Y, Sattar N, Schmidt M, Schreiner P, Schulze M, Ruth K, Rudan I, Rolandsson O, Rasheed A, Rauramaa R, Reilly D, Reiner A, Renström F, Ridker P, Rioux J, Robertson N, Robino A, Scott R, Nordestgaard B, Langefeld C, Lindström J, Linneberg A, Liu Y, Liu Y, Lophatananon A, Luan J, Lubitz S, Lyytikäinen L, Mackey D, Lind L, Lin X, Lin L, Langenberg C, Larson E, Lee I, Lehtimäki T, Lewis C, Li H, Li J, Li-Gao R, Lin H, Madden P, Manning A, Morris A, Müller-Nurasyid M, Munroe P, Nalls M, Nauck M, Nelson C, Neville M, Nielsen S, Nikus K, Morris A, Morgan A, Mook-Kanamori D, Männistö S, Marenne G, Marten J, Martin N, Mazul A, Meidtner K, Metspalu A, Mitchell P, Mohlke K, Njølstad P, Walker M, Yaghootkar H, Yao J, Yao P, Yerges-Armstrong L, Young R, Zeggini E, Zhan X, Zhang W, Zhao J, Wu Y, Woods M, Witte D, Wang F, Wang C, Wang S, Wang Y, Wareham N, Warren H, Wessel J, Willems S, Wilson J, Zhao W, Zheng H, Pers T, Lindgren C, Oxvig C, Kutalik Z, Rivadeneira F, Loos R, Frayling T, Hirschhorn J, Deloukas P, Heard-Costa N, North K, Liu D, Zhou W, Rotter J, Boehnke M, Kathiresan S, McCarthy M, Willer C, Stefansson K, Borecki I, Lettre G, Vozzi D, Segura-Lepe M, Stumvoll M, Surendran P, 't Hart L, Tansey K, Tardif J, Taylor K, Teumer A, Thompson D, Thorsteinsdottir U, Stringham H, Steinthorsdottir V, Starr J, Shah S, Sim X, Sivapalaratnam S, Small K, Smith A, Smith J, Southam L, Spector T, Speliotes E, Thuesen B, Tönjes A, van Schoor N, van Setten J, Varbo A, Varga T, Varma R, Edwards D, Vermeulen S, Vestergaard H, Vitart V, van Duijn C, Van Der Leij A, van der Laan S, Tromp G, Trompet S, Tsafantakis E, Tuomilehto J, Tybjaerg-Hansen A, Tyrer J, Uher R, Uitterlinden A, Ulivi S, Vogt T, Boeing H, Butterworth A, Carey D, Caulfield M, Chambers J, Chasman D, Chen Y, Chowdhury R, Christensen C, Chu A, Burt A, Broer L, Brilliant M, Boerwinkle E, Böger C, Bonnycastle L, Bork-Jensen J, Bots M, Bottinger E, Bowden D, Brandslund I, Breen G, Cocca M, Collins F, Deary I, Dedoussis G, Demerath E, den Hollander A, Dennis J, Di Angelantonio E, Drenos F, Du M, Dunning A, de Mutsert R, de Groot M, de Denus S, Cook J, Corley J, Galbany J, Cox A, Cuellar-Partida G, Danesh J, Davies G, de Bakker P, de Borst G, Easton D, Blüher M, Marouli E, Lamparter D, Stirrups K, Turcot V, Young K, Winkler T, Esko T, Karaderi T, Locke A, Masca N, Justice A, Thorleifsson G, Rüeger S, Graff M, Medina-Gomez C, Lo K, Wood A, Kjaer T, Fine R, Lu Y, Schurmann C, Highland H, Ng M, Mudgal P, Appel E, Arveiler D, Asselbergs F, Auer P, Balkau B, Banas B, Bang L, Benn M, Bergmann S, Amouyel P, Allison M, Allin K, Rivas M, Vedantam S, Mahajan A, Guo X, Abecasis G, Aben K, Adair L, Alam D, Albrecht E, Bielak L, Hoyng C, Jørgensen M, Jørgensen T, Jousilahti P, Jukema J, Kahali B, Kahn R, Kähönen M, Kamstrup P, Kanoni S, Johansson S, Jiang X, Jia Y, Huang P, Hveem K, Ikram M, Ingelsson E, Jackson A, Jansson J, Jarvik G, Jensen G, Jhun M, Kaprio J, Karaleftheri M, Kovacs P, Kriebel J, Kuivaniemi H, Küry S, Kuusisto J, La Bianca M, Laakso M, Lakka T, Lange E, Kooperberg C, Kooner J, Kontto J, Kardia S, Karpe F, Kee F, Keeman R, Kiemeney L, Kitajima H, Kluivers K, Kocher T, Komulainen P, Lange L, Howson J, Ebeling T, Ford I, Fornage M, Franks P, Frikke-Schmidt R, Galesloot T, Gan W, Gandin I, Gasparini P, Giedraitis V, Florez J, Ferrieres J, Ferrario M, Edwards T, Ellinor P, Elliott P, Evangelou E, Farmaki A, Faul J, Feitosa M, Feng S, Ferrannini E, Giri A, Girotto G, He L, Heid I, Heikkilä K, Helgeland Ø, Hernesniemi J, Hewitt A, Hocking L, Hollensted M, Holmen O, Hayward C, Hattersley A, Harris T, Gordon S, Gordon-Larsen P, Gorski M, Grarup N, Grove M, Gudnason V, Gustafsson S, Hansen T, Harris K, Hovingh G. Rare and low-frequency coding variants alter human adult height. Nature 2017; 542:186-190.
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 Claudia, Larson Eric B, Lee I-Te, Lehtimäki Terho, Lewis Cora E, Li Huaixing, Li Jin, Li-Gao Ruifang, Lin Honghuang, Madden Pamela A F, Manning Alisa K, Morris Andrew P, Müller-Nurasyid Martina, Munroe Patricia B, Nalls Mike A, Nauck Matthias, Nelson Christopher P, Neville Matt, Nielsen Sune F, Nikus Kjell, Morris Andrew D, Morgan Anna, Mook-Kanamori Dennis O, Männistö Satu, Marenne Gaëlle, Marten Jonathan, Martin Nicholas G, Mazul Angela L, Meidtner Karina, Metspalu Andres, Mitchell Paul, Mohlke Karen L, Njølstad Pål R, Walker Mark, Yaghootkar Hanieh, Yao Jie, Yao Pang, Yerges-Armstrong Laura M, Young Robin, Zeggini Eleftheria, Zhan Xiaowei, Zhang Weihua, Zhao Jing Hua, Wu Ying, Woods Michael O, Witte Daniel R, Wang Feijie, Wang Carol A, Wang Shuai, Wang Yiqin, Wareham Nicholas J, Warren Helen R, Wessel Jennifer, Willems Sara M, Wilson James G, Zhao Wei, Zheng He, Pers Tune H, Lindgren Cecilia M, Oxvig Claus, Kutalik Zoltán, Rivadeneira Fernando, Loos Ruth J F, Frayling Timothy M, Hirschhorn Joel N, Deloukas Panos, Heard-Costa Nancy L, North Kari E, Liu Dajiang J, Zhou Wei, Rotter Jerome I, Boehnke Michael, Kathiresan Sekar, McCarthy Mark I, Willer Cristen J, Stefansson Kari, Borecki Ingrid B, Lettre Guillaume, Vozzi Diego, Segura-Lepe Marcelo P, Stumvoll Michael, Surendran Praveen, 't Hart Leen M, Tansey Katherine E, Tardif Jean-Claude, Taylor Kent D, Teumer Alexander, Thompson Deborah J, Thorsteinsdottir Unnur, Stringham Heather M, Steinthorsdottir Valgerdur, Starr John M, Shah Svati, Sim Xueling, Sivapalaratnam Suthesh, Small Kerrin S, Smith Albert Vernon, Smith Jennifer A, Southam Lorraine, Spector Timothy D, Speliotes Elizabeth K, Thuesen Betina H, Tönjes Anke, van Schoor Natasja M, van Setten Jessica, Varbo Anette, Varga Tibor V, Varma Rohit, Edwards Digna R Velez, Vermeulen Sita H, Vestergaard Henrik, Vitart Veronique, van Duijn Cornelia M, Van Der Leij Andries R, van der Laan Sander W, Tromp Gerard, Trompet Stella, Tsafantakis Emmanouil, Tuomilehto 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, Young Kristin L, Winkler Thomas W, Esko Tõnu, Karaderi Tugce, Locke Adam E, Masca Nicholas G D, Justice Anne E, Thorleifsson Gudmar, Rüeger Sina, Graff Mariaelisa, Medina-Gomez Carolina, Lo Ken Sin, Wood Andrew R, Kjaer Troels R, Fine Rebecca S, Lu Yingchang, Schurmann Claudia, Highland Heather M, Ng Maggie C Y, Mudgal Poorva, Appel Emil V, Arveiler Dominique, Asselbergs Folkert W, Auer Paul L, Balkau Beverley, Banas Bernhard, Bang Lia E, Benn Marianne, Bergmann Sven, Amouyel Philippe, Allison Matthew, Allin Kristine H, Rivas Manuel A, Vedantam Sailaja, Mahajan Anubha, Guo Xiuqing, Abecasis Goncalo, Aben Katja K, Adair Linda S, Alam Dewan S, Albrecht Eva, Bielak Lawrence F, Hoyng Carel B, Jørgensen Marit E, Jørgensen Torben, Jousilahti Pekka, Jukema J Wouter, Kahali Bratati, Kahn René S, Kähönen Mika, Kamstrup Pia R, Kanoni Stavroula, Johansson Stefan, Jiang Xuejuan, Jia Yucheng, Huang Paul L, Hveem Kristian, Ikram M Arfan, Ingelsson Erik, Jackson Anne U, Jansson Jan-Håkan, Jarvik Gail P, Jensen Gorm B, Jhun Min A, Kaprio Jaakko, Karaleftheri Maria, Kovacs Peter, Kriebel Jennifer, Kuivaniemi Helena, Küry Sébastien, Kuusisto Johanna, La Bianca Martina, Laakso Markku, Lakka Timo A, Lange Ethan M, Kooperberg Charles, Kooner Jaspal S, Kontto Jukka, Kardia Sharon L R, Karpe Fredrik, Kee Frank, Keeman Renske, Kiemeney Lambertus A, Kitajima Hidetoshi, Kluivers Kirsten B, Kocher Thomas, Komulainen Pirjo, Lange Leslie A, Howson Joanna M M, Ebeling Tapani, Ford Ian, Fornage Myriam, Franks Paul W, Frikke-Schmidt Ruth, Galesloot Tessel E, Gan Wei, Gandin Ilaria, Gasparini Paolo, Giedraitis Vilmantas, Florez Jose C, Ferrieres Jean, Ferrario Marco M, Edwards Todd L, Ellinor Patrick T, Elliott Paul, Evangelou Evangelos, Farmaki Aliki-Eleni, Faul Jessica D, Feitosa Mary F, Feng Shuang, Ferrannini Ele, Giri Ayush, Girotto Giorgia, He Liang, Heid Iris M, Heikkilä Kauko, Helgeland Øyvind, Hernesniemi Jussi, Hewitt Alex W, Hocking Lynne J, Hollensted Mette, Holmen Oddgeir L, Hayward Caroline, Hattersley Andrew T, Harris Tamara B, Gordon Scott D, Gordon-Larsen Penny, Gorski Mathias, Grarup Niels, Grove Megan L, Gudnason Vilmundur, Gustafsson Stefan, Hansen Torben, Harris Kathleen Mullan, Hovingh G Kees
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Zhang K, Arcuti S, Brunetti M, Moglia C, Calvo A, Ratti A, Tiloca C, Gellera C, Pensato V, Mazzini L, Capozzo R, Zecca C, Blair I, Stuit R, Muller B, Filosto M, Padovani A, Riva N, Penco S, Lunetta C, Sorarù G, Bertolin C, Blauw H, Curtis C, Hofman A, Estrada K, Rivadeneira F, Uitterlinden A, Dartigues J, Tzourio C, Amouyel P, van der Kooi A, de Visser M, D'Alfonso S, Comi G, Del Bo R, Cereda C, Pansarasa O, Smith B, Shaw C, Weber M, Goris A, Nöthen M, McCann E, Veldink J, Corcia P, Andersen P, Hardiman O, Landers J, Glass J, Brown R, Pers T, Franke L, Van Damme P, Vourc'h P, Silani V, van den Berg L, Al-Chalabi A, Breen G, Lewis C, Pasterkamp R, van Es M, de Bakker P, Visscher P, Wray N, Robberecht W, Weishaupt J, Stubendorff B, Prell T, Ringer T, Witte O, Grosskreutz J, Kiernan M, Pamphlett R, Rowe D, Nicholson G, Kurth I, Hübner C, Ludolph A, Powell J, Logroscino G, Tortelli R, Pupillo E, Beghi E, Chio A, Casale F, Leigh P, Fifita J, Chandran S, Koritnik B, Ravnik-Glavač M, Vrabec K, Rogelj B, Lin K, Ticozzi N, Vajda A, Menelaou A, Medic J, Zidar J, Leonardis L, Polak M, Rojas-García R, Mora J, Pinto S, de Carvalho M, Meininger V, Salachas F, Millecamps S, Grošelj L, Brands W, Schellevis R, Robinson M, de Jong S, Võsa U, van der Spek R, Pulit S, Diekstra F, McLaughlin R, Dekker A, Shatunov A, Yang J, Fogh I, Harschnitz O, van Eijk K, Kenna K, Jones A, Sproviero W, Blokhuis A, Koppers M, Tazelaar G, van Doormaal P, van Rheenen W, Colville S, Cichon S, Maurel C, Andres C, Radivojkov-Blagojevic M, Lichtner P, Meitinger T, Parman Y, Hamzeiy H, Tunca C, Basak A, Bensimon G, Landwehrmeyer B, Rietschel M, Franke A, Lieb W, Tittmann L, Wood N, Dürr A, Saker-Delye S, Payan C, Brice A, McCluskey L, Elman L, Topp S, Malaspina A, Fratta P, Sidle K, Pittman A, Orrell R, Hardy J, Shaw P, Morrison K, Petri S, Abdulla S, Trojanowski J, Van Deerlin V, Lomen-Hoerth C, Wiedau-Pazos M, Staats K, Ophoff R, Meyer T, Sendtner M, Drepper C, Swingler R. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet 2016; 48:1043-8.
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
Zhang Katharine, Arcuti Simona, Brunetti Maura, Moglia Cristina, Calvo Andrea, Ratti Antonia, Tiloca Cinzia, Gellera Cinzia, Pensato Viviana, Mazzini Letizia, Capozzo Rosa, Zecca Chiara, Blair Ian, Stuit Robbert Jan, Muller Bernard, Filosto Massimiliano, Padovani Alessandro, Riva Nilo, Penco Silvana, Lunetta Christian, Sorarù Gianni, Bertolin Cinzia, Blauw Hylke M, Curtis Charles, Hofman Albert, Estrada Karol, Rivadeneira Fernando, Uitterlinden André G, Dartigues Jean-François, Tzourio Christophe, Amouyel Philippe, van der Kooi Anneke J, de Visser Marianne, D'Alfonso Sandra, Comi Giacomo P, Del Bo Roberto, Cereda Cristina, Pansarasa Orietta, Smith Bradley N, Shaw Christopher E, Weber Markus, Goris An, Nöthen Markus M, McCann Emily P, Veldink Jan H, Corcia Philippe, Andersen Peter M, Hardiman Orla, Landers John E, Glass Jonathan D, Brown Robert H, Pers Tune H, Franke Lude, Van Damme Philip, Vourc'h Patrick, Silani Vincenzo, van den Berg Leonard H, Al-Chalabi Ammar, Breen Gerome, Lewis Cathryn M, Pasterkamp R Jeroen, van Es Michael A, de Bakker Paul I W, Visscher Peter M, Wray Naomi R, Robberecht Wim, Weishaupt Jochen H, Stubendorff Beatrice, Prell Tino, Ringer Thomas, Witte Otto W, Grosskreutz Julian, Kiernan Matthew C, Pamphlett Roger, Rowe Dominic B, Nicholson Garth A, Kurth Ingo, Hübner Christian A, Ludolph Albert C, Powell John, Logroscino Giancarlo, Tortelli Rosanna, Pupillo Elisabetta, Beghi Ettore, Chio Adriano, Casale Federico, Leigh P Nigel, Fifita Jennifer A, Chandran Siddharthan, Koritnik Blaž, Ravnik-Glavač Metka, Vrabec Katarina, Rogelj Boris, Lin Kuang, Ticozzi Nicola, Vajda Alice, Menelaou Androniki, Medic Jelena, Zidar Janez, Leonardis Lea, Polak Meraida, Rojas-García Ricardo, Mora Jesus S, Pinto Susana, de Carvalho Mamede, Meininger Vincent, Salachas François, Millecamps Stéphanie, Grošelj Leja Dolenc, Brands William J, Schellevis Raymond D, Robinson Matthew R, de Jong Simone, Võsa Urmo, van der Spek Rick A A, Pulit Sara L, Diekstra Frank P, McLaughlin Russell L, Dekker Annelot M, Shatunov Aleksey, Yang Jian, Fogh Isabella, Harschnitz Oliver, van Eijk Kristel R, Kenna Kevin P, Jones Ashley R, Sproviero William, Blokhuis Anna M, Koppers Max, Tazelaar Gijs H P, van Doormaal Perry Tc, van Rheenen Wouter, Colville Shuna, Cichon Sven, Maurel Cindy, Andres Christian R, Radivojkov-Blagojevic Milena, Lichtner Peter, Meitinger Thomas, Parman Yesim, Hamzeiy Hamid, Tunca Ceren, Basak A Nazli, Bensimon Gilbert, Landwehrmeyer Bernhard, Rietschel Marcella, Franke Andre, Lieb Wolfgang, Tittmann Lukas, Wood Nicholas W, Dürr Alexandra, Saker-Delye Safaa, Payan Christine A M, Brice Alexis, McCluskey Leo, Elman Lauren, Topp Simon, Malaspina Andrea, Fratta Pietro, Sidle Katie, Pittman Alan, Orrell Richard W, Hardy John, Shaw Pamela J, Morrison Karen E, Petri Susanne, Abdulla Susanne, Trojanowski John Q, Van Deerlin Vivianna M, Lomen-Hoerth Catherine, Wiedau-Pazos Martina, Staats Kim A, Ophoff Roel A, Meyer Thomas, Sendtner Michael, Drepper Carsten, Swingler Robert