Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 29 (of 29 Records) |
Query Trace: Amyotrophic Lateral Sclerosis[original query] |
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ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.
The Lancet. Neurology 2007 Oct 6 (10): 869-77. van Es Michael A, Van Vught Paul W, Blauw Hylke M, Franke Lude, Saris Christiaan G, Andersen Peter M, Van Den Bosch Ludo, de Jong Sonja W, van 't Slot Ruben, Birve Anna, Lemmens Robin, de Jong Vianney, Baas Frank, Schelhaas Helenius J, Sleegers Kristel, Van Broeckhoven Christine, Wokke John H J, Wijmenga Cisca, Robberecht Wim, Veldink Jan H, Ophoff Roel A, van den Berg Leonard |
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.
The Lancet. Neurology 2007 Apr 6 (4): 322-8. Schymick Jennifer C, Scholz Sonja W, Fung Hon-Chung, Britton Angela, Arepalli Sampath, Gibbs J Raphael, Lombardo Federica, Matarin Mar, Kasperaviciute Dalia, Hernandez Dena G, Crews Cynthia, Bruijn Lucie, Rothstein Jeffrey, Mora Gabriele, Restagno Gabriella, Chiò Adriano, Singleton Andrew, Hardy John, Traynor Bryan |
A genome-wide association study of sporadic ALS in a homogenous Irish population.
Human molecular genetics 2008 Mar 17 (5): 768-74. Cronin Simon, Berger Stephen, Ding Jinhui, Schymick Jennifer C, Washecka Nicole, Hernandez Dena G, Greenway Matthew J, Bradley Daniel G, Traynor Bryan J, Hardiman Or |
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
Nature genetics 2008 Jan 40 (1): 29-31. van Es Michael A, van Vught Paul W J, Blauw Hylke M, Franke Lude, Saris Christiaan G J, Van den Bosch Ludo, de Jong Sonja W, de Jong Vianney, Baas Frank, van't Slot Ruben, Lemmens Robin, Schelhaas Helenius J, Birve Anna, Sleegers Kristel, Van Broeckhoven Christine, Schymick Jennifer C, Traynor Bryan J, Wokke John H J, Wijmenga Cisca, Robberecht Wim, Andersen Peter M, Veldink Jan H, Ophoff Roel A, van den Berg Leonard |
Screening for replication of genome-wide SNP associations in sporadic ALS.
European journal of human genetics : EJHG 2009 Feb 17 (2): 213-8. Cronin Simon, Tomik Barbara, Bradley Daniel G, Slowik Agnieszka, Hardiman Or |
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
Nature genetics 2009 Oct 41 (10): 1083-7. van Es Michael A, Veldink Jan H, Saris Christiaan G J, Blauw Hylke M, van Vught Paul W J, Birve Anna, Lemmens Robin, Schelhaas Helenius J, Groen Ewout J N, Huisman Mark H B, van der Kooi Anneke J, de Visser Marianne, Dahlberg Caroline, Estrada Karol, Rivadeneira Fernando, Hofman Albert, Zwarts Machiel J, van Doormaal Perry T C, Rujescu Dan, Strengman Eric, Giegling Ina, Muglia Pierandrea, Tomik Barbara, Slowik Agnieszka, Uitterlinden Andre G, Hendrich Corinna, Waibel Stefan, Meyer Thomas, Ludolph Albert C, Glass Jonathan D, Purcell Shaun, Cichon Sven, Nöthen Markus M, Wichmann H-Erich, Schreiber Stefan, Vermeulen Sita H H M, Kiemeney Lambertus A, Wokke John H J, Cronin Simon, McLaughlin Russell L, Hardiman Orla, Fumoto Katsumi, Pasterkamp R Jeroen, Meininger Vincent, Melki Judith, Leigh P Nigel, Shaw Christopher E, Landers John E, Al-Chalabi Ammar, Brown Robert H, Robberecht Wim, Andersen Peter M, Ophoff Roel A, van den Berg Leonard |
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
Proceedings of the National Academy of Sciences of the United States of America 2009 Jun 106 (22): 9004-9. Landers John E, Melki Judith, Meininger Vincent, Glass Jonathan D, van den Berg Leonard H, van Es Michael A, Sapp Peter C, van Vught Paul W J, McKenna-Yasek Diane M, Blauw Hylke M, Cho Ting-Jan, Polak Meraida, Shi Lijia, Wills Anne-Marie, Broom Wendy J, Ticozzi Nicola, Silani Vincenzo, Ozoguz Aslihan, Rodriguez-Leyva Ildefonso, Veldink Jan H, Ivinson Adrian J, Saris Christiaan G J, Hosler Betsy A, Barnes-Nessa Alayna, Couture Nicole, Wokke John H J, Kwiatkowski Thomas J, Ophoff Roel A, Cronin Simon, Hardiman Orla, Diekstra Frank P, Leigh P Nigel, Shaw Christopher E, Simpson Claire L, Hansen Valerie K, Powell John F, Corcia Philippe, Salachas François, Heath Simon, Galan Pilar, Georges Franck, Horvitz H Robert, Lathrop Mark, Purcell Shaun, Al-Chalabi Ammar, Brown Robert |
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.
The Lancet. Neurology 2010 Oct 9 (10): 978-85. Laaksovirta Hannu, Peuralinna Terhi, Schymick Jennifer C, Scholz Sonja W, Lai Shaoi-Lin, Myllykangas Liisa, Sulkava Raimo, Jansson Lilja, Hernandez Dena G, Gibbs J Raphael, Nalls Michael A, Heckerman David, Tienari Pentti J, Traynor Bryan |
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.
The Lancet. Neurology 2010 Oct 9 (10): 986-94. Shatunov Aleksey, Mok Kin, Newhouse Stephen, Weale Michael E, Smith Bradley, Vance Caroline, Johnson Lauren, Veldink Jan H, van Es Michael A, van den Berg Leonard H, Robberecht Wim, Van Damme Philip, Hardiman Orla, Farmer Anne E, Lewis Cathryn M, Butler Amy W, Abel Olubunmi, Andersen Peter M, Fogh Isabella, Silani Vincenzo, Chiò Adriano, Traynor Bryan J, Melki Judith, Meininger Vincent, Landers John E, McGuffin Peter, Glass Jonathan D, Pall Hardev, Leigh P Nigel, Hardy John, Brown Robert H, Powell John F, Orrell Richard W, Morrison Karen E, Shaw Pamela J, Shaw Christopher E, Al-Chalabi Amm |
Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2012 Mar 13 (3): 211-22. Fliers Ellen A, Vasquez Alejandro Arias, Poelmans Geert, Rommelse Nanda, Altink Marieke, Buschgens Cathelijne, Asherson Philip, Banaschewski Tobias, Ebstein Richard, Gill Michael, Miranda Ana, Mulas Fernando, Oades Robert D, Roeyers Herbert, Rothenberger Aribert, Sergeant Joseph, Sonuga-Barke Edmund, Steinhausen Hans-Christoph, Faraone Stephen V, Buitelaar Jan K, Franke Barba |
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
Neurobiology of aging 2013 Jan 34 (1): 357.e7-19. Ahmeti Kreshnik B, Ajroud-Driss Senda, Al-Chalabi Ammar, Andersen Peter M, Armstrong Jennifer, Birve Anne, Blauw Hylke M, Brown Robert H, Bruijn Lucie, Chen Wenjie, Chio Adriano, Comeau Mary C, Cronin Simon, Diekstra Frank P, Soraya Gkazi Athina, Glass Jonathan D, Grab Josh D, Groen Ewout J, Haines Jonathan L, Hardiman Orla, Heller Scott, Huang Jie, Hung Wu-Yen, , Jaworski James M, Jones Ashley, Khan Humaira, Landers John E, Langefeld Carl D, Leigh P Nigel, Marion Miranda C, McLaughlin Russell L, Meininger Vincent, Melki Judith, Miller Jack W, Mora Gabriele, Pericak-Vance Margaret A, Rampersaud Evadnie, Robberecht Wim, Russell Laurie P, Salachas Francois, Saris Christiaan G, Shatunov Aleksey, Shaw Christopher E, Siddique Nailah, Siddique Teepu, Smith Bradley N, Sufit Robert, Topp Simon, Traynor Bryan J, Vance Caroline, van Damme Philip, van den Berg Leonard H, van Es Michael A, van Vught Paul W, Veldink Jan H, Yang Yi, Zheng J G, |
A high-density genome-wide association screen of sporadic ALS in US veterans.
PloS one 2012 7 (3): e32768. Kwee Lydia Coulter, Liu Yutao, Haynes Carol, Gibson Jason R, Stone Annjanette, Schichman Steven A, Kamel Freya, Nelson Lorene M, Topol Barbara, Van den Eeden Stephen K, Tanner Caroline M, Cudkowicz Merit E, Grasso Daniela L, Lawson Robert, Muralidhar Sumitra, Oddone Eugene Z, Schmidt Silke, Hauser Michael |
Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis.
Nature genetics 2013 Jun 45 (6): 697-700. Deng Min, Wei Ling, Zuo Xianbo, Tian Yanghua, Xie Fei, Hu Panpan, Zhu Chunyan, Yu Fengqiong, Meng Yu, Wang Honghao, Zhang Fangfang, Ma Huijuan, Ye Rong, Cheng Huaidong, Du Jing, Dong Wenwen, Zhou Shanshan, Wang Changqing, Wang Yu, Wang Jingye, Chen Xianwen, Sun Zhongwu, Zhou Nong, Jiang Yubao, Liu Xiuxiu, Li Xiaogang, Zhang Nan, Liu Na, Guan Yingjun, Han Yongsheng, Han Yongzhu, Lv Xinyi, Fu Yu, Yu Hui, Xi Chunhua, Xie Dandan, Zhao Qiyuan, Xie Peng, Wang Xin, Zhang Zhijun, Shen Lu, Cui Yong, Yin Xianyong, Cheng Hui, Liang Bo, Zheng Xiaodong, Lee Tatia M C, Chen Gang, Zhou Fusheng, Veldink Jan H, Robberecht Wim, Landers John E, Andersen Peter M, Al-Chalabi Ammar, Shaw Chris, Liu Chunfeng, Tang Beisha, Xiao Shangxi, Robertson Janice, Zhang Fengyu, van den Berg Leonard H, Sun Liangdan, Liu Jianjun, Yang Sen, Ju Xiaodong, Wang Kai, Zhang Xuej |
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
Human molecular genetics 2013 Nov . Fogh I, Ratti A, Gellera C, Lin K, Tiloca C, Moskvina V, Corrado L, Sorarù G, Cereda C, Corti S, Gentilini D, Calini D, Castellotti B, Mazzini L, Querin G, Gagliardi S, Del Bo R, Conforti FL, Siciliano G, Inghilleri M, Saccà F, Bongioanni P, Penco S, Corbo M, Sorbi S, Filosto M, Ferlini A, Di Blasio AM, Signorini S, Shatunov A, Jones A, Shaw PJ, Morrison KE, Farmer AE, Van Damme P, Robberecht W, Chiò A, Traynor BJ, Sendtner M, Melki J, Meininger V, Hardiman O, Andersen PM, Leigh NP, Glass JD, Overste D, Diekstra FP, Veldink JH, van Es MA, Shaw CE, Weale ME, Lewis CM, Williams J, Brown RH, Landers JE, Ticozzi N, Ceroni M, Pegoraro E, Comi GP, D'Alfonso S, van den Berg LH, Taroni F, Al-Chalabi A, Powell J, Silani V |
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.
Human molecular genetics 2014 Apr 23 (7): 1916-22. Goris An, van Setten Jessica, Diekstra Frank, Ripke Stephan, Patsopoulos Nikolaos A, Sawcer Stephen J, , van Es Michael, , Andersen Peter M, Melki Judith, Meininger Vincent, Hardiman Orla, Landers John E, Brown Robert H, Shatunov Aleksey, Leigh Nigel, Al-Chalabi Ammar, Shaw Christopher E, Traynor Bryan J, Chiò Adriano, Restagno Gabriella, Mora Gabriele, Ophoff Roel A, Oksenberg Jorge R, Van Damme Philip, Compston Alastair, Robberecht Wim, Dubois Bénédicte, van den Berg Leonard H, De Jager Philip L, Veldink Jan H, de Bakker Paul I |
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.
Annals of neurology 2014 Jul 76 (1): 120-33. Diekstra Frank P, Van Deerlin Vivianna M, van Swieten John C, Al-Chalabi Ammar, Ludolph Albert C, Weishaupt Jochen H, Hardiman Orla, Landers John E, Brown Robert H, van Es Michael A, Pasterkamp R Jeroen, Koppers Max, Andersen Peter M, Estrada Karol, Rivadeneira Fernando, Hofman Albert, Uitterlinden André G, van Damme Philip, Melki Judith, Meininger Vincent, Shatunov Aleksey, Shaw Christopher E, Leigh P Nigel, Shaw Pamela J, Morrison Karen E, Fogh Isabella, Chiò Adriano, Traynor Bryan J, Czell David, Weber Markus, Heutink Peter, de Bakker Paul I W, Silani Vincenzo, Robberecht Wim, van den Berg Leonard H, Veldink Jan |
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Neurobiology of aging 2014 Jul 35 (7): 1778.e9-1778.e23. Xie Tong, Deng Libin, Mei Puming, Zhou Yiyi, Wang Bo, Zhang Jie, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens |
Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis.
Neurobiology of aging 2015 Feb 36 (2): 1221.e7-13. McLaughlin Russell L, Kenna Kevin P, Vajda Alice, Bede Peter, Elamin Marwa, Cronin Simon, Donaghy Colette G, Bradley Daniel G, Hardiman Or |
A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population.
Biomarkers in medicine 2016 Jun 10 (6): 597-611. Chen Chi-Jim, Chen Chien-Ming, Pai Tun-Wen, Chang Hao-Teng, Hwang Chi-Sh |
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Nature genetics 2016 Jul . van Rheenen Wouter, Shatunov Aleksey, Dekker Annelot M, McLaughlin Russell L, Diekstra Frank P, Pulit Sara L, van der Spek Rick A A, Võsa Urmo, de Jong Simone, Robinson Matthew R, Yang Jian, Fogh Isabella, van Doormaal Perry Tc, Tazelaar Gijs H P, Koppers Max, Blokhuis Anna M, Sproviero William, Jones Ashley R, Kenna Kevin P, van Eijk Kristel R, Harschnitz Oliver, Schellevis Raymond D, Brands William J, Medic Jelena, Menelaou Androniki, Vajda Alice, Ticozzi Nicola, Lin Kuang, Rogelj Boris, Vrabec Katarina, Ravnik-Glava? Metka, Koritnik Blaž, Zidar Janez, Leonardis Lea, Grošelj Leja Dolenc, Millecamps Stéphanie, Salachas François, Meininger Vincent, de Carvalho Mamede, Pinto Susana, Mora Jesus S, Rojas-García Ricardo, Polak Meraida, Chandran Siddharthan, Colville Shuna, Swingler Robert, Morrison Karen E, Shaw Pamela J, Hardy John, Orrell Richard W, Pittman Alan, Sidle Katie, Fratta Pietro, Malaspina Andrea, Topp Simon, Petri Susanne, Abdulla Susanne, Drepper Carsten, Sendtner Michael, Meyer Thomas, Ophoff Roel A, Staats Kim A, Wiedau-Pazos Martina, Lomen-Hoerth Catherine, Van Deerlin Vivianna M, Trojanowski John Q, Elman Lauren, McCluskey Leo, Basak A Nazli, Tunca Ceren, Hamzeiy Hamid, Parman Yesim, Meitinger Thomas, Lichtner Peter, Radivojkov-Blagojevic Milena, Andres Christian R, Maurel Cindy, Bensimon Gilbert, Landwehrmeyer Bernhard, Brice Alexis, Payan Christine A M, Saker-Delye Safaa, Dürr Alexandra, Wood Nicholas W, Tittmann Lukas, Lieb Wolfgang, Franke Andre, Rietschel Marcella, Cichon Sven, Nöthen Markus M, Amouyel Philippe, Tzourio Christophe, Dartigues Jean-François, Uitterlinden Andre G, Rivadeneira Fernando, Estrada Karol, Hofman Albert, Curtis Charles, Blauw Hylke M, van der Kooi Anneke J, de Visser Marianne, Goris An, Weber Markus, Shaw Christopher E, Smith Bradley N, Pansarasa Orietta, Cereda Cristina, Del Bo Roberto, Comi Giacomo P, D'Alfonso Sandra, Bertolin Cinzia, Sorarù Gianni, Mazzini Letizia, Pensato Viviana, Gellera Cinzia, Tiloca Cinzia, Ratti Antonia, Calvo Andrea, Moglia Cristina, Brunetti Maura, Arcuti Simona, Capozzo Rosa, Zecca Chiara, Lunetta Christian, Penco Silvana, Riva Nilo, Padovani Alessandro, Filosto Massimiliano, Muller Bernard, Stuit Robbert Jan, , , , , , , Blair Ian, Zhang Katharine, McCann Emily P, Fifita Jennifer A, Nicholson Garth A, Rowe Dominic B, Pamphlett Roger, Kiernan Matthew C, Grosskreutz Julian, Witte Otto W, Ringer Thomas, Prell Tino, Stubendorff Beatrice, Kurth Ingo, Hübner Christian A, Leigh P Nigel, Casale Federico, Chio Adriano, Beghi Ettore, Pupillo Elisabetta, Tortelli Rosanna, Logroscino Giancarlo, Powell John, Ludolph Albert C, Weishaupt Jochen H, Robberecht Wim, Van Damme Philip, Franke Lude, Pers Tune H, Brown Robert H, Glass Jonathan D, Landers John E, Hardiman Orla, Andersen Peter M, Corcia Philippe, Vourc'h Patrick, Silani Vincenzo, Wray Naomi R, Visscher Peter M, de Bakker Paul I W, van Es Michael A, Pasterkamp R Jeroen, Lewis Cathryn M, Breen Gerome, Al-Chalabi Ammar, van den Berg Leonard H, Veldink Jan |
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
JAMA neurology 2016 May . Fogh Isabella, Lin Kuang, Tiloca Cinzia, Rooney James, Gellera Cinzia, Diekstra Frank P, Ratti Antonia, Shatunov Aleksey, van Es Michael A, Proitsi Petroula, Jones Ashley, Sproviero William, Chiò Adriano, McLaughlin Russell Lewis, Sorarù Gianni, Corrado Lucia, Stahl Daniel, Del Bo Roberto, Cereda Cristina, Castellotti Barbara, Glass Jonathan D, Newhouse Steven, Dobson Richard, Smith Bradley N, Topp Simon, van Rheenen Wouter, Meininger Vincent, Melki Judith, Morrison Karen E, Shaw Pamela J, Leigh P Nigel, Andersen Peter M, Comi Giacomo P, Ticozzi Nicola, Mazzini Letizia, D'Alfonso Sandra, Traynor Bryan J, Van Damme Philip, Robberecht Wim, Brown Robert H, Landers John E, Hardiman Orla, Lewis Cathryn M, van den Berg Leonard H, Shaw Christopher E, Veldink Jan H, Silani Vincenzo, Al-Chalabi Ammar, Powell Jo |
A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN.
Journal of neurology, neurosurgery, and psychiatry 2016 Jan . Watanabe Hazuki, Atsuta Naoki, Hirakawa Akihiro, Nakamura Ryoichi, Nakatochi Masahiro, Ishigaki Shinsuke, Iida Aritoshi, Ikegawa Shiro, Kubo Michiaki, Yokoi Daichi, Watanabe Hirohisa, Ito Mizuki, Katsuno Masahisa, Izumi Yuishin, Morita Mitsuya, Kanai Kazuaki, Taniguchi Akira, Aiba Ikuko, Abe Koji, Mizoguchi Koichi, Oda Masaya, Kano Osamu, Okamoto Koichi, Kuwabara Satoshi, Hasegawa Kazuko, Imai Takashi, Kawata Akihiro, Aoki Masashi, Tsuji Shoji, Nakashima Kenji, Kaji Ryuji, Sobue G |
Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.
Nature communications 2017 Sep 8 (1): 611. Benyamin Beben, He Ji, Zhao Qiongyi, Gratten Jacob, Garton Fleur, Leo Paul J, Liu Zhijun, Mangelsdorf Marie, Al-Chalabi Ammar, Anderson Lisa, Butler Timothy J, Chen Lu, Chen Xiang-Ding, Cremin Katie, Deng Hong-Weng, Devine Matthew, Edson Janette, Fifita Jennifer A, Furlong Sarah, Han Ying-Ying, Harris Jessica, Henders Anjali K, Jeffree Rosalind L, Jin Zi-Bing, Li Zhongshan, Li Ting, Li Mengmeng, Lin Yong, Liu Xiaolu, Marshall Mhairi, McCann Emily P, Mowry Bryan J, Ngo Shyuan T, Pamphlett Roger, Ran Shu, Reutens David C, Rowe Dominic B, Sachdev Perminder, Shah Sonia, Song Sharon, Tan Li-Jun, Tang Lu, van den Berg Leonard H, van Rheenen Wouter, Veldink Jan H, Wallace Robyn H, Wheeler Lawrie, Williams Kelly L, Wu Jinyu, Wu Xin, Yang Jian, Yue Weihua, Zhang Zong-Hong, Zhang Dai, Noakes Peter G, Blair Ian P, Henderson Robert D, McCombe Pamela A, Visscher Peter M, Xu Huji, Bartlett Perry F, Brown Matthew A, Wray Naomi R, Fan Dongshe |
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.
Molecular neurodegeneration 2018 Aug 13 (1): 41. Chen Jason A, Chen Zhongbo, Won Hyejung, Huang Alden Y, Lowe Jennifer K, Wojta Kevin, Yokoyama Jennifer S, Bensimon Gilbert, Leigh P Nigel, Payan Christine, Shatunov Aleksey, Jones Ashley R, Lewis Cathryn M, Deloukas Panagiotis, Amouyel Philippe, Tzourio Christophe, Dartigues Jean-Francois, Ludolph Albert, Boxer Adam L, Bronstein Jeff M, Al-Chalabi Ammar, Geschwind Daniel H, Coppola Giovan |
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis.
Scientific reports 2019 Apr 9 (1): 5931. Dekker Annelot M, Diekstra Frank P, Pulit Sara L, Tazelaar Gijs H P, van der Spek Rick A, van Rheenen Wouter, van Eijk Kristel R, Calvo Andrea, Brunetti Maura, Damme Philip Van, Robberecht Wim, Hardiman Orla, McLaughlin Russell, Chiò Adriano, Sendtner Michael, Ludolph Albert C, Weishaupt Jochen H, Pardina Jesus S Mora, van den Berg Leonard H, Veldink Jan |
Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis.
Neurology. Genetics 2019 Dec 5 (6): e375. Wei Ling, Tian Yanghua, Chen Yongping, Wei Qianqian, Chen Fangfang, Cao Bei, Wu Ying, Zhao Bi, Chen Xueping, Xie Chengjuan, Xi Chunhua, Yu Xu'en, Wang Juan, Lv Xinyi, Du Jing, Wang Yu, Shen Lu, Wang Xin, Shen Bin, Guo Qihao, Guo Li, Xia Kun, Xie Peng, Zhang Xuejun, Zuo Xianbo, Shang Huifang, Wang K |
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis.
Communications biology 2020 Sep 3 (1): 526. Nakamura Ryoichi, Misawa Kazuharu, Tohnai Genki, Nakatochi Masahiro, Furuhashi Sho, Atsuta Naoki, Hayashi Naoki, Yokoi Daichi, Watanabe Hazuki, Watanabe Hirohisa, Katsuno Masahisa, Izumi Yuishin, Kanai Kazuaki, Hattori Nobutaka, Morita Mitsuya, Taniguchi Akira, Kano Osamu, Oda Masaya, Shibuya Kazumoto, Kuwabara Satoshi, Suzuki Naoki, Aoki Masashi, Ohta Yasuyuki, Yamashita Toru, Abe Koji, Hashimoto Rina, Aiba Ikuko, Okamoto Koichi, Mizoguchi Kouichi, Hasegawa Kazuko, Okada Yohei, Ishihara Tomohiko, Onodera Osamu, Nakashima Kenji, Kaji Ryuji, Kamatani Yoichiro, Ikegawa Shiro, Momozawa Yukihide, Kubo Michiaki, Ishida Noriko, Minegishi Naoko, Nagasaki Masao, Sobue G |
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
Translational psychiatry 2021 9 11 (1): 451. Reus Lianne M, Jansen Iris E, Mol Merel O, van Ruissen Fred, van Rooij Jeroen, van Schoor Natasja M, Tesi Niccolò, Reinders Marcel J T, Huisman Martijn A, Holstege Henne, Visser Pieter Jelle, de Boer Sterre C M, Hulsman Marc, Ahmad Shahzad, Amin Najaf, Uitterlinden Andre G, Ikram Arfan, van Duijn Cornelia M, Seelaar Harro, Ramakers Inez H G B, Verhey Frans R J, van der Lugt Aad, Claassen Jurgen A H R, Jan Biessels Geert, De Deyn Peter Paul, Scheltens Philip, van der Flier Wiesje M, van Swieten John C, Pijnenburg Yolande A L, van der Lee Sven |
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology.
Nature genetics 2021 12 53 (12): 1636-1648. 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, Ba?ak 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, Chiò 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, Durr 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 Andre G, Hofman Albert, Rietschel Marcella, Cichon Sven, Nöthen Markus M, Amouyel Philippe, , , , , 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-Glava? Metka, Glava? Damjan, Stevi? 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 |
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