Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: DGKQ[original query] |
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Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Human genetics 2009 Jan 124 (6): 593-605. Pankratz Nathan, Wilk Jemma B, Latourelle Jeanne C, DeStefano Anita L, Halter Cheryl, Pugh Elizabeth W, Doheny Kimberly F, Gusella James F, Nichols William C, Foroud Tatiana, Myers Richard H, |
Genome-wide association study confirms extant PD risk loci among the Dutch. European journal of human genetics : EJHG 2011 Jun 19 (6): 655-61. Simón-Sánchez Javier, van Hilten Jacobus J, van de Warrenburg Bart, Post Bart, Berendse Henk W, Arepalli Sampath, Hernandez Dena G, de Bie Rob M A, Velseboer Daan, Scheffer Hans, Bloem Bas, van Dijk Karin D, Rivadeneira Fernando, Hofman Albert, Uitterlinden André G, Rizzu Patrizia, Bochdanovits Zoltan, Singleton Andrew B, Heutink Pet |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Annals of neurology 2012 Mar 71 (3): 3. Pankratz N, Beecham GW, Destefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T |
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS genetics 2012 8 (3): e1002548. Lill Christina M, Roehr Johannes T, McQueen Matthew B, Kavvoura Fotini K, Bagade Sachin, Schjeide Brit-Maren M, Schjeide Leif M, Meissner Esther, Zauft Ute, Allen Nicole C, Liu Tian, Schilling Marcel, Anderson Kari J, Beecham Gary, Berg Daniela, Biernacka Joanna M, Brice Alexis, DeStefano Anita L, Do Chuong B, Eriksson Nicholas, Factor Stewart A, Farrer Matthew J, Foroud Tatiana, Gasser Thomas, Hamza Taye, Hardy John A, Heutink Peter, Hill-Burns Erin M, Klein Christine, Latourelle Jeanne C, Maraganore Demetrius M, Martin Eden R, Martinez Maria, Myers Richard H, Nalls Michael A, Pankratz Nathan, Payami Haydeh, Satake Wataru, Scott William K, Sharma Manu, Singleton Andrew B, Stefansson Kari, Toda Tatsushi, Tung Joyce Y, Vance Jeffery, Wood Nick W, Zabetian Cyrus P, , , , , Young Peter, Tanzi Rudolph E, Khoury Muin J, Zipp Frauke, Lehrach Hans, Ioannidis John P A, Bertram La |
GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2013 Jun 20 (6): 880-3. Chen Yong Ping, Song Wei, Huang Rui, Chen Ke, Zhao Bi, Li Jianpeng, Yang Yuan, Shang Hui-Fa |
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome.
Nature genetics 2013 Nov 45 (11): 1284-92. Lessard Christopher J, Li He, Adrianto Indra, Ice John A, Rasmussen Astrid, Grundahl Kiely M, Kelly Jennifer A, Dozmorov Mikhail G, Miceli-Richard Corinne, Bowman Simon, Lester Sue, Eriksson Per, Eloranta Maija-Leena, Brun Johan G, Gøransson Lasse G, Harboe Erna, Guthridge Joel M, Kaufman Kenneth M, Kvarnström Marika, Jazebi Helmi, Cunninghame Graham Deborah S, Grandits Martha E, Nazmul-Hossain Abu N M, Patel Ketan, Adler Adam J, Maier-Moore Jacen S, Farris A Darise, Brennan Michael T, Lessard James A, Chodosh James, Gopalakrishnan Rajaram, Hefner Kimberly S, Houston Glen D, Huang Andrew J W, Hughes Pamela J, Lewis David M, Radfar Lida, Rohrer Michael D, Stone Donald U, Wren Jonathan D, Vyse Timothy J, Gaffney Patrick M, James Judith A, Omdal Roald, Wahren-Herlenius Marie, Illei Gabor G, Witte Torsten, Jonsson Roland, Rischmueller Maureen, Rönnblom Lars, Nordmark Gunnel, Ng Wan-Fai, , Mariette Xavier, Anaya Juan-Manuel, Rhodus Nelson L, Segal Barbara M, Scofield R Hal, Montgomery Courtney G, Harley John B, Sivils Kathy |
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Nature genetics 2014 Sep 46 (9): 989-93. Nalls Mike A, Pankratz Nathan, Lill Christina M, Do Chuong B, Hernandez Dena G, Saad Mohamad, DeStefano Anita L, Kara Eleanna, Bras Jose, Sharma Manu, Schulte Claudia, Keller Margaux F, Arepalli Sampath, Letson Christopher, Edsall Connor, Stefansson Hreinn, Liu Xinmin, Pliner Hannah, Lee Joseph H, Cheng Rong, , , , , , , , , , , , , Ikram M Arfan, Ioannidis John P A, Hadjigeorgiou Georgios M, Bis Joshua C, Martinez Maria, Perlmutter Joel S, Goate Alison, Marder Karen, Fiske Brian, Sutherland Margaret, Xiromerisiou Georgia, Myers Richard H, Clark Lorraine N, Stefansson Kari, Hardy John A, Heutink Peter, Chen Honglei, Wood Nicholas W, Houlden Henry, Payami Haydeh, Brice Alexis, Scott William K, Gasser Thomas, Bertram Lars, Eriksson Nicholas, Foroud Tatiana, Singleton Andrew |
Target gene capture sequencing in Chinese population of sporadic Parkinson disease. Medicine 2015 May 94 (20): e836. Li Zhiming, Lin Qing, Huang Wenqing, Tzeng Chi-Me |
Association of Parkinson's Disease GWAS-Linked Loci with Alzheimer's Disease in Han Chinese. Molecular neurobiology 2017 01 54 (1): 308-318. Zhu Xi-Chen, Cao Lei, Tan Meng-Shan, Jiang Teng, Wang Hui-Fu, Lu Huan, Tan Chen-Chen, Zhang Wei, Tan Lan, Yu Jin-T |
Congenital glaucoma and CYP1B1: an old story revisited. Human genetics 2018 3 138 (8-9): 1043-1049. Alsaif Hessa S, Khan Arif O, Patel Nisha, Alkuraya Hisham, Hashem Mais, Abdulwahab Firdous, Ibrahim Niema, Aldahmesh Mohammed A, Alkuraya Fowzan |
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies. Annals of neurology 2019 10 87 (1): 139-153. Krohn Lynne, Öztürk Tu?ba Nur, Vanderperre Benoît, Ouled Amar Bencheikh Bouchra, Ruskey Jennifer A, Laurent Sandra B, Spiegelman Dan, Postuma Ronald B, Arnulf Isabelle, Hu Michele T M, Dauvilliers Yves, Högl Birgit, Stefani Ambra, Monaca Christelle Charley, Plazzi Giuseppe, Antelmi Elena, Ferini-Strambi Luigi, Heidbreder Anna, Rudakou Uladzislau, Cochen De Cock Valérie, Young Peter, Wolf Pavlina, Oliva Petra, Zhang Xiaokui Kate, Greenbaum Lior, Liong Christopher, Gagnon Jean-François, Desautels Alex, Hassin-Baer Sharon, Montplaisir Jacques Y, Dupré Nicolas, Rouleau Guy A, Fon Edward A, Trempe Jean-François, Lamoureux Guillaume, Alcalay Roy N, Gan-Or Z |
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2021 Feb . Lim Jia Lun, Ng Ebonne Yulin, Lim Shen-Yang, Tan Ai Huey, Abdul-Aziz Zariah, Ibrahim Khairul Azmi, Gopalai Aroma Agape, Tay Yi Wen, Vijayanathan Yuganthini, Toh Tzi Shin, Lim Soo Kun, Bee Ping-Chong, Puvanarajah Santhi Datuk, Viswanathan Shanthi, Looi Irene, Lim Thien Thien, Eow Gaik Bee, Cheah Wee Kooi, Tan Eng-King, Ahmad-Annuar Azli |
Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies.
Arthritis & rheumatology (Hoboken, N.J.) 2022 12 . Rothwell Simon, Amos Christopher I, Miller Frederick W, Rider Lisa G, Lundberg Ingrid E, Gregersen Peter K, Vencovsky Jiri, McHugh Neil, Limaye Vidya, Selva-O'Callaghan Albert, Hanna Michael G, Machado Pedro M, Pachman Lauren M, Reed Ann M, Molberg Øyvind, Benveniste Olivier, Mathiesen Pernille, Radstake Timothy, Doria Andrea, De Bleecker Jan L, De Paepe Boel, Maurer Britta, Ollier William E, Padyukov Leonid, O'Hanlon Terrance P, Lee Annette, Wedderburn Lucy R, Chinoy Hector, Lamb Janine A, |
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