Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 36 Records) |
Query Trace: GIGYF2[original query] |
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GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients. Neuroscience letters 2009 Oct 463 (3): 172-5. Zhang Yu, Zheng Lan, Zhang Ting, Wang Ying, Xiao Qin, Fei Qin-Zhou, Cui Pei-Jing, Cao Li, Chen Sheng- |
GIGYF2 mutations are not a frequent cause of familial Parkinson's disease. Parkinsonism & related disorders 2009 Nov 15 (9): 703-5. Di Fonzo Alessio, Fabrizio Edito, Thomas Astrid, Fincati Emiliana, Marconi Roberto, Tinazzi Michele, Breedveld Guido J, Simons Erik J, Chien Hsin F, Ferreira Joaquim J, Horstink Martin W, Abbruzzese Giovanni, Borroni Barbara, Cossu Giovanni, Dalla Libera Alessio, Fabbrini Giovanni, Guidi Marco, De Mari Michele, Lopiano Leonardo, Martignoni Emilia, Marini Paolo, Onofrj Marco, Padovani Alessandro, Stocchi Fabrizio, Toni Vincenzo, Sampaio Cristina, Barbosa Egberto R, Meco Giuseppe, , Oostra Ben A, Bonifati Vincen |
Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations. Human genetics 2009 Sep 126 (3): 425-30. Tan Eng-King, Lin Chin-Hslen, Tai Chun-Hwei, Tan Louis C, Chen Meng-Ling, Li R, Lim Hui-Qin, Pavanni Ratnagopal, Yuen Yih, Prakash K M, Zhao Yi, Wu Ruey-Me |
GIGYF2 Asn56Ser and Asn457Thr mutations in Parkinson disease patients. Neuroscience letters 2009 May 454 (3): 209-11. Guo Yi, Jankovic Joseph, Zhu Shaihong, Le Weidong, Song Zhi, Xie Wenjie, Liao Daoguang, Yang Huarong, Deng H |
GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population. Neurobiology of aging 2009 Mar . Meeus B, Nuytemans K, Crosiers D, Engelborghs S, Pals P, Pickut B, Peeters K, Mattheijssens M, Corsmit E, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C |
Follow-up study of the GIGYF2 gene in French families with Parkinson's disease. Neurobiology of aging 2010 Jun 31 (6): 1069-71; discussion 1072-4. Lesage Suzanne, Condroyer Christel, Lohman Ebba, Troiano André, Tison François, Viallet François, Damier Philippe, Tranchant Christine, Vidhaillet Marie, Ouvrard-Hernandez Anne-Marie, Dürr Alexandra, Brice Alexis, |
Analysis of the GIGYF2 gene in familial and sporadic Parkinson disease in the Spanish population. European journal of neurology : the official journal of the European Federation of Neurological Societies 2010 Feb 17 (2): 321-5. Samaranch L, Lorenzo E, Pastor M A, Riverol M, Luquin M R, Rodríguez-Oroz M C, Obeso J A, Pastor |
Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease. Neuroscience letters 2010 Nov 485 (2): 121-4. Dos Santos Adriana Vaz, Pestana Cristiane Pinheiro, Diniz Karen Rafaella da Silva, Campos Mário, Abdalla-Carvalho Cláudia Bueno, de Rosso Ana Lúcia Zuma, Pereira João Santos, Nicaretta Denise Hack, de Carvalho William Luciano, Dos Santos Jussara Mendonça, Santos-Rebouças Cíntia Barros, Pimentel Márcia Mattos Gonçalv |
No evidence for pathogenic role of GIGYF2 mutation in Parkinson disease in Japanese patients. Neuroscience letters 2010 (3): 245-8. Li Lin, Funayama Manabu, Tomiyama Hiroyuki, Li Yuanzhe, Yoshino Hiroyo, Sasaki Ryogen, Kokubo Yasumasa, Kuzuhara Shigeki, Mizuno Yoshikuni, Hattori Nobuta |
Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population. Neuroscience letters 2010 Apr 473 (2): 131-5. Wang Lei, Guo Ji-feng, Zhang Wen-wen, Xu Qian, Zuo Xing, Shi Chang-he, Luo Lin-zi, Liu Jia, Hu Liang, Hu Ya-cen, She Lu, Jiang Hong, Yan Xin-xiang, Xia Kun, Pan Qian, Tang Bei-s |
The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese population. Parkinsonism & related disorders 2009 Dec . Cao L, Zhang T, Zheng L, Wang Y, Wang G, Zhang J, Fei Q Z, Cui P J, Wang X J, Ma J F, Xiao Q, Chen S |
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene. Neurobiology of aging 2011 Nov 32 (11): 1994-2005. Guella Ilaria, Pistocchi Anna, Asselta Rosanna, Rimoldi Valeria, Ghilardi Anna, Sironi Francesca, Trotta Luca, Primignani Paola, Zini Michela, Zecchinelli Anna, Coviello Domenico, Pezzoli Gianni, Del Giacco Luca, Duga Stefano, Goldwurm Stefa |
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease. Neuroscience letters 2012 May 516 (2): 207-11. Tian Jin-yong, Guo Ji-feng, Wang Lei, Sun Qi-ying, Yao Ling-yan, Luo Lin-zi, Shi Chang-he, Hu Ya-cen, Yan Xin-xiang, Tang Bei-s |
Copy number variation in Han Chinese individuals with autism spectrum disorder. Journal of neurodevelopmental disorders 2014 6 (1): 34. Gazzellone Matthew J, Zhou Xue, Lionel Anath C, Uddin Mohammed, Thiruvahindrapuram Bhooma, Liang Shuang, Sun Caihong, Wang Jia, Zou Mingyang, Tammimies Kristiina, Walker Susan, Selvanayagam Thanuja, Wei John, Wang Zhuozhi, Wu Lijie, Scherer Stephen |
Meta-analyses of seven GIGYF2 polymorphisms with Parkinson's disease. Biomedical reports 2014 Nov 2 (6): 886-892. Dai Dongjun, Wang Yunliang, Zhou Xingyu, Tao Jianmin, Jiang Danjie, Zhou Hanlin, Jiang Yi, Pan Guanghui, Ru Ping, Ji Huihui, Li Jinfeng, Zhang Yuzheng, Yin Honglei, Xu Mingqing, Duan Shiw |
Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels. Molecular diagnosis & therapy 2016 Jun . Gorostidi Ana, Martí-Massó José Félix, Bergareche Alberto, Rodríguez-Oroz Mari Cruz, de Munain Adolfo López, Ruiz-Martínez Javi |
De novo genic mutations among a Chinese autism spectrum disorder cohort. Nature communications 2016 Nov 7 13316. Wang Tianyun, Guo Hui, Xiong Bo, Stessman Holly A F, Wu Huidan, Coe Bradley P, Turner Tychele N, Liu Yanling, Zhao Wenjing, Hoekzema Kendra, Vives Laura, Xia Lu, Tang Meina, Ou Jianjun, Chen Biyuan, Shen Yidong, Xun Guanglei, Long Min, Lin Janice, Kronenberg Zev N, Peng Yu, Bai Ting, Li Honghui, Ke Xiaoyan, Hu Zhengmao, Zhao Jingping, Zou Xiaobing, Xia Kun, Eichler Evan |
Genetic analysis of indel markers in three loci associated with Parkinson's disease. PloS one 2017 12 (9): e0184269. Huo Zhixin, Luo Xiaoguang, Zhan Xiaoni, Chu Qiaohong, Xu Qin, Yao Jun, Pang H |
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. Journal of the American College of Cardiology 2017 Feb 69 (7): 823-836. Webb Thomas R, Erdmann Jeanette, Stirrups Kathleen E, Stitziel Nathan O, Masca Nicholas G D, Jansen Henning, Kanoni Stavroula, Nelson Christopher P, Ferrario Paola G, König Inke R, Eicher John D, Johnson Andrew D, Hamby Stephen E, Betsholtz Christer, Ruusalepp Arno, Franzén Oscar, Schadt Eric E, Björkegren Johan L M, Weeke Peter E, Auer Paul L, Schick Ursula M, Lu Yingchang, Zhang He, Dube Marie-Pierre, Goel Anuj, Farrall Martin, Peloso Gina M, Won Hong-Hee, Do Ron, van Iperen Erik, Kruppa Jochen, Mahajan Anubha, Scott Robert A, Willenborg Christina, Braund Peter S, van Capelleveen Julian C, Doney Alex S F, Donnelly Louise A, Asselta Rosanna, Merlini Pier A, Duga Stefano, Marziliano Nicola, Denny Josh C, Shaffer Christian, El-Mokhtari Nour Eddine, Franke Andre, Heilmann Stefanie, Hengstenberg Christian, Hoffmann Per, Holmen Oddgeir L, Hveem Kristian, Jansson Jan-Håkan, Jöckel Karl-Heinz, Kessler Thorsten, Kriebel Jennifer, Laugwitz Karl L, Marouli Eirini, Martinelli Nicola, McCarthy Mark I, Van Zuydam Natalie R, Meisinger Christa, Esko Tõnu, Mihailov Evelin, Escher Stefan A, Alver Maris, Moebus Susanne, Morris Andrew D, Virtamo Jarma, Nikpay Majid, Olivieri Oliviero, Provost Sylvie, AlQarawi Alaa, Robertson Neil R, Akinsansya Karen O, Reilly Dermot F, Vogt Thomas F, Yin Wu, Asselbergs Folkert W, Kooperberg Charles, Jackson Rebecca D, Stahl Eli, Müller-Nurasyid Martina, Strauch Konstantin, Varga Tibor V, Waldenberger Melanie, , Zeng Lingyao, Chowdhury Rajiv, Salomaa Veikko, Ford Ian, Jukema J Wouter, Amouyel Philippe, Kontto Jukka, , Nordestgaard Børge G, Ferrières Jean, Saleheen Danish, Sattar Naveed, Surendran Praveen, Wagner Aline, Young Robin, Howson Joanna M M, Butterworth Adam S, Danesh John, Ardissino Diego, Bottinger Erwin P, Erbel Raimund, Franks Paul W, Girelli Domenico, Hall Alistair S, Hovingh G Kees, Kastrati Adnan, Lieb Wolfgang, Meitinger Thomas, Kraus William E, Shah Svati H, McPherson Ruth, Orho-Melander Marju, Melander Olle, Metspalu Andres, Palmer Colin N A, Peters Annette, Rader Daniel J, Reilly Muredach P, Loos Ruth J F, Reiner Alex P, Roden Dan M, Tardif Jean-Claude, Thompson John R, Wareham Nicholas J, Watkins Hugh, Willer Cristen J, Samani Nilesh J, Schunkert Heribert, Deloukas Panos, Kathiresan Sekar, |
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model. Molecular autism 2018 12 9 64. Guo Hui, Wang Tianyun, Wu Huidan, Long Min, Coe Bradley P, Li Honghui, Xun Guanglei, Ou Jianjun, Chen Biyuan, Duan Guiqin, Bai Ting, Zhao Ningxia, Shen Yidong, Li Yun, Wang Yazhe, Zhang Yu, Baker Carl, Liu Yanling, Pang Nan, Huang Lian, Han Lin, Jia Xiangbin, Liu Cenying, Ni Hailun, Yang Xinyi, Xia Lu, Chen Jingjing, Shen Lu, Li Ying, Zhao Rongjuan, Zhao Wenjing, Peng Jing, Pan Qian, Long Zhigao, Su Wei, Tan Jieqiong, Du Xiaogang, Ke Xiaoyan, Yao Meiling, Hu Zhengmao, Zou Xiaobing, Zhao Jingping, Bernier Raphael A, Eichler Evan E, Xia K |
SETD2, GIGYF2, FGFR3, BCR, KMT2C, and TSC2 as candidate genes for differentiating multilocular cystic renal neoplasm of low malignant potential from clear cell renal cell carcinoma with cystic change. Investigative and clinical urology 2019 May 60 (3): 148-155. Kim Sung Han, Park Weon Seo, Chung Jins |
SET domain containing 1B gene is mutated in primary hepatic neuroendocrine tumors. International journal of cancer 2019 4 145 (11): 2986-2995. Yang Penghui, Huang Xuanlin, Lai Chengcai, Li Lin, Li Tieling, Huang Peide, Ouyang Songying, Yan Jin, Cheng Sijie, Lei Guanglin, Wang Zhaohai, Yu Linxiang, Hong Zhixian, Li Ruisheng, Dong Hui, Wang Cheng, Yu Yinghao, Wang Xuan, Li Xianghong, Wang Liming, Lv Fudong, Yin Ye, Yang Huanming, Song Jianxun, Gao Qiang, Wang Xiliang, Zhang Shaoge |
Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patients. Blood 2019 1 133 (10): 1140-1151. Christen Friederike, Hoyer Kaja, Yoshida Kenichi, Hou Hsin-An, Waldhueter Nils, Heuser Michael, Hills Robert K, Chan Willy, Hablesreiter Raphael, Blau Olga, Ochi Yotaro, Klement Piroska, Chou Wen-Chien, Blau Igor-Wolfgang, Tang Jih-Luh, Zemojtel Tomasz, Shiraishi Yuichi, Shiozawa Yusuke, Thol Felicitas, Ganser Arnold, Löwenberg Bob, Linch David C, Bullinger Lars, Valk Peter J M, Tien Hwei-Fang, Gale Rosemary E, Ogawa Seishi, Damm Freder |
Systematically analyzing rare variants of autosomal-dominant genes for sporadic Parkinson's disease in a Chinese cohort. Neurobiology of aging 2019 1 76 215.e1-215.e7. Yang Nannan, Zhao Yuwen, Liu Zhenhua, Zhang Rui, He Yan, Zhou Yangjie, Xu Qian, Sun Qiying, Yan Xinxiang, Guo Jifeng, Tang Beis |
A genetic analysis of a Spanish population with early onset Parkinson's disease. PloS one 2020 15 (9): e0238098. Cristina Tejera-Parrado, Pablo Mir, Teresa Periñán María, Lydia Vela-Desojo, Irene Abreu-Rodríguez, Araceli Alonso-Cánovas, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Dolores Buiza-Rueda, José Catalán-Alonso María, Rocío García-Ramos, José García-Ruiz Pedro, Ismael Huertas-Fernández, Silvia Jesús, Labrador Miguel A-Espinosa, Lydia López-Manzanares, Carlos Martínez-Castrillo Juan, Posada Ignacio J, Ana Rojo-Sebastián, Cristina Ruiz-Huete, Javier Del Val, Gómez-Garre Pil |
Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease. Molecular genetics & genomic medicine 2020 Aug e1449. Zheng Ran, Jin Chong-Yao, Chen Ying, Ruan Yang, Gao Ting, Lin Zhi-Hao, Dong Jia-Xian, Yan Ya-Ping, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease. Neurobiology of aging 2020 Oct . Saini Prabhjyot, Rudakou Uladzislau, Yu Eric, Ruskey Jennifer A, Asayesh Farnaz, Laurent Sandra B, Spiegelman Dan, Fahn Stanley, Waters Cheryl, Monchi Oury, Dauvilliers Yves, Dupré Nicolas, Greenbaum Lior, Hassin-Baer Sharon, Espay Alberto J, Rouleau Guy A, Alcalay Roy N, Fon Edward A, Postuma Ronald B, Gan-Or Z |
High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic. Life (Basel, Switzerland) 2022 1 12 (1): . Kolarikova Kristyna, Vodicka Radek, Vrtel Radek, Stellmachova Julia, Prochazka Martin, Mensikova Katerina, Bartonikova Tereza, Furst Tomas, Kanovsky Petr, Geryk J |
Identification of potential susceptibility genes in patients with primary Sjögren's syndrome-associated pulmonary arterial hypertension through whole exome sequencing. Arthritis research & therapy 2023 9 25 (1): 175. Mucong Li, Yue Shi, Jiuliang Zhao, Qian Wang, Mengtao Li, Xiuli Zh |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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- Page last updated:Apr 22, 2024
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