Jean-François Dartigues
Genetic variants for head size share genes and pathways with cancer.
Knol M, Poot R, Evans T, Satizabal C, Mishra A, Sargurupremraj M, van der Auwera S, Duperron M, Jian X, Hostettler I, van Dam-Nolen D, Lamballais S, Pawlak M, Lewis C, Carrion-Castillo A, van Erp T, Reinbold C, Shin J, Scholz M, Håberg A, Kämpe A, Li G, Avinun R, Atkins J, Hsu F, Amod A, Lam M, Tsuchida A, Teunissen M, Aygün N, Patel Y, Liang D, Beiser A, Beyer F, Bis J, Bos D, Bryan R, Bülow R, Caspers S, Catheline G, Cecil C, Dalvie S, Dartigues J, DeCarli C, Enlund-Cerullo M, Ford J, Franke B, Freedman B, Friedrich N, Green M, Haworth S, Helmer C, Hoffmann P, Homuth G, Ikram M, Jack C, Jahanshad N, Jockwitz C, Kamatani Y, Knodt A, Li S, Lim K, Longstreth W, Macciardi F, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Mäkitie O, Mazoyer B, Medland S, Miyamoto S, Moebus S, Mosley T, Muetzel R, Mühleisen T, Nagata M, Nakahara S, Palmer N, Pausova Z, Preda A, Quidé Y, Reay W, Roshchupkin G, Schmidt R, Schreiner P, Setoh K, Shapland C, Sidney S, St Pourcain B, Stein J, Tabara Y, Teumer A, Uhlmann A, van der Lugt A, Vernooij M, Werring D, Windham B, Witte A, Wittfeld K, Yang Q, Yoshida K, Brunner H, Le Grand Q, Sim K, Stein D, Bowden D, Cairns M, Hariri A, Cheung C, Andersson S, Villringer A, Paus T, Cichon S, Calhoun V, Crivello F, Launer L, White T, Koudstaal P, Houlden H, Fornage M, Matsuda F, Grabe H, Debette S, Thompson P, Seshadri S, Adams H. Genetic variants for head size share genes and pathways with cancer. Cell Rep Med 2024:101529.
May 3, 2024Genetic variants for head size share genes and pathways with cancer.
May 3, 2024Cell Rep Med 2024:101529
Knol Maria J, Poot Raymond A, Evans Tavia E, Satizabal Claudia L, Mishra Aniket, Sargurupremraj Muralidharan, van der Auwera Sandra, Duperron Marie-Gabrielle, Jian Xueqiu, Hostettler Isabel, van Dam-Nolen Dianne H K, Lamballais Sander, Pawlak Mikolaj A, Lewis Cora E, Carrion-Castillo Amaia, van Erp Theo G M, Reinbold Céline S, Shin Jean, Scholz Markus, Håberg Asta K, Kämpe Anders, Li Gloria H Y, Avinun Reut, Atkins Joshua R, Hsu Fang-Chi, Amod AlyR, Lam Max, Tsuchida Ami, Teunissen Mariël W A, Aygün Nil, Patel Yash, Liang Dan, Beiser Alexa S, Beyer Frauke, Bis Joshua C, Bos Daniel, Bryan R Nick, Bülow Robin, Caspers Svenja, Catheline Gwenaëlle, Cecil Charlotte A M, Dalvie Shareefa, Dartigues Jean-François, DeCarli Charles, Enlund-Cerullo Maria, Ford Judith M, Franke Barbara, Freedman Barry I, Friedrich Nele, Green MeliJ, Haworth Simon, Helmer Catherine, Hoffmann Per, Homuth Georg, Ikram Mohammad Arfan, Jack Clifford R, Jahanshad Neda, Jockwitz Christiane, Kamatani Yoichiro, Knodt Annchen R, Li Shuo, Lim Keane, Longstreth W T, Macciardi Fabio, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium, Mäkitie Outi, Mazoyer Bernard, Medland Sarah E, Miyamoto Susumu, Moebus Susanne, Mosley Thomas H, Muetzel Ryan, Mühleisen Thomas W, Nagata Manabu, Nakahara Soichiro, Palmer Nicholette D, Pausova Zdenka, Preda Adrian, Quidé Yann, Reay William R, Roshchupkin Gennady V, Schmidt Reinhold E, Schreiner Pamela J, Setoh Kazuya, Shapland Chin Yang, Sidney Stephen, St Pourcain Beate, Stein Jason L, Tabara Yasuharu, Teumer Alexander, Uhlmann Anne, van der Lugt Aad, Vernooij Meike W, Werring David J, Windham B Gwen, Witte A Veronica, Wittfeld Katharina, Yang Qiong, Yoshida Kazumichi, Brunner Han G, Le Grand Quentin, Sim Kang, Stein Dan J, Bowden Donald W, Cairns Murray J, Hariri Ahmad R, Cheung Ching-Lung, Andersson Sture, Villringer Arno, Paus Tomas, Cichon Sven, Calhoun Vince D, Crivello Fabrice, Launer Lenore J, White Tonya, Koudstaal Peter J, Houlden Henry, Fornage Myriam, Matsuda Fumihiko, Grabe Hans Jörgen, Debette Stephanie, Thompson Paul M, Seshadri Sudha, Adams Hieab H H
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.
Jul 25, 2016Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Jul 25, 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