Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: SCARB2[original query] |
---|
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
PLoS genetics 2011 Jun 7 (6): e1002141. Do Chuong B, Tung Joyce Y, Dorfman Elizabeth, Kiefer Amy K, Drabant Emily M, Francke Uta, Mountain Joanna L, Goldman Samuel M, Tanner Caroline M, Langston J William, Wojcicki Anne, Eriksson Nichol |
Association study of SCARB2 rs6812193 polymorphism with Parkinson's disease in Han Chinese. Neuroscience letters 2012 May 516 (1): 21-3. Chen Shuai, Zhang Yu, Chen Wei, Wang Ying, Liu Jun, Rong Tian-Yi, Ma Jian-Fang, Wang Gang, Zhang Jing, Pan Jing, Xiao Qin, Chen Sheng- |
Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2012 Mar 27 (3): 400-5. Michelakakis Helen, Xiromerisiou Georgia, Dardiotis Efthimios, Bozi Maria, Vassilatis Demetrios, Kountra Persa-Maria, Patramani Gianna, Moraitou Marina, Papadimitriou Dimitra, Stamboulis Eleftherios, Stefanis Leonidas, Zintzaras Elias, Hadjigeorgiou Georgios |
Is Parkinson disease associated with lysosomal integral membrane protein type-2?: challenges in interpreting association data. Molecular genetics and metabolism 2013 Apr 108 (4): 269-71. Maniwang Emerson, Tayebi Nahid, Sidransky Ell |
The role of SCARB2 as susceptibility factor in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2013 Apr 28 (4): 538-40. Hopfner Franziska, Schulte Eva C, Mollenhauer Brit, Bereznai Benjamin, Knauf Franziska, Lichtner Peter, Zimprich Alexander, Haubenberger Dietrich, Pirker Walter, Brücke Thomas, Peters Annette, Gieger Christian, Kuhlenbäumer Gregor, Trenkwalder Claudia, Winkelmann Julia |
Association analysis of polymorphisms in OAS1 with susceptibility and severity of hand, foot and mouth disease. International journal of immunogenetics 2014 Oct 41 (5): 384-92. Cai Y, Chen Q, Zhou W, Chu C, Ji W, Ding Y, Xu J, Ji Z, You H, Wang |
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human molecular genetics 2014 Dec 23 (23): 6139-46. Bras Jose, Guerreiro Rita, Darwent Lee, Parkkinen Laura, Ansorge Olaf, Escott-Price Valentina, Hernandez Dena G, Nalls Michael A, Clark Lorraine N, Honig Lawrence S, Marder Karen, Van Der Flier Wiesje M, Lemstra Afina, Scheltens Philip, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Ortega-Cubero Sara, Pastor Pau, Ferman Tanis J, Graff-Radford Neill R, Ross Owen A, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Maetzler Walter, Berg Daniela, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Compta Yaroslau, Revesz Tamas, Lees Andrew, Cairns Nigel, Halliday Glenda M, Mann David, Pickering-Brown Stuart, Dickson Dennis W, Singleton Andrew, Hardy Jo |
No association of FAM47E rs6812193, SCARB2 rs6825004 and STX1B rs4889603 polymorphisms with Parkinson's disease in a Chinese Han population. Journal of neural transmission (Vienna, Austria : 1996) 2015 Jul . Chen YongPing, Yuan XiaoQin, Cao Bei, Wei QianQian, Ou RuWei, Yang Jing, Chen XuePing, Zhao Bi, Song Wei, Wu Ying, Shang HuiFa |
Hyperprolactinemia in Children and Adolescents with Use of Risperidone: Clinical and Molecular Genetics Aspects. Journal of child and adolescent psychopharmacology 2015 Dec 25 (10): 738-48. Dos Santos Júnior Amilton, Henriques Taciane Barbosa, de Mello Maricilda Palandi, Neto Adriana Perez Ferreira, Paes Lúcia Arisaka, Torre Osmar Henrique Della, Sewaybricker Letícia Esposito, Fontana Thiago Salum, Celeri Eloisa Helena Rubello Valler, Júnior Gil Guerra, Dalgalarrondo Pau |
Polymorphisms in enterovirus 71 receptors associated with susceptibility and clinical severity. PloS one 2018 13 (11): e0206769. Yen Ting-Yu, Shih Wei-Liang, Huang Yi-Chuan, Lee Jian-Te, Huang Li-Min, Chang Luan-Y |
A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and ?-synuclein mechanisms.
Movement disorders : official journal of the Movement Disorder Society 2019 Jun 34 (6): 866-875. Blauwendraat Cornelis, Heilbron Karl, Vallerga Costanza L, Bandres-Ciga Sara, von Coelln Rainer, Pihlstrøm Lasse, Simón-Sánchez Javier, Schulte Claudia, Sharma Manu, Krohn Lynne, Siitonen Ari, Iwaki Hirotaka, Leonard Hampton, Noyce Alastair J, Tan Manuela, Gibbs J Raphael, Hernandez Dena G, Scholz Sonja W, Jankovic Joseph, Shulman Lisa M, Lesage Suzanne, Corvol Jean-Christophe, Brice Alexis, van Hilten Jacobus J, Marinus Johan, , Eerola-Rautio Johanna, Tienari Pentti, Majamaa Kari, Toft Mathias, Grosset Donald G, Gasser Thomas, Heutink Peter, Shulman Joshua M, Wood Nicolas, Hardy John, Morris Huw R, Hinds David A, Gratten Jacob, Visscher Peter M, Gan-Or Ziv, Nalls Mike A, Singleton Andrew B, |
Genetic Polymorphisms on 4q21.1 Contributed to the Risk of Hashimoto's Thyroiditis. Genetic testing and molecular biomarkers 2019 Nov . Mo Dachao, Li Junjiu, Peng Liang, Liu Zhiyuan, Wang Jieyun, Yuan Ji |
Genetics variants and expression of the SCARB2 gene in the pathogenesis of Parkinson's disease in Russia. Neuroscience letters 2020 Nov 135509. Usenko T S, Bezrukova A I, Bogdanova D A, Kopytova A E, Senkevich K A, Gracheva E V, Timofeeva A A, Miliukhina I V, Zakharova E Y, Emelyanov A K, Pchelina S |
Genetic Interactions with Intrauterine Diabetes Exposure in Relation to Obesity: The EPOCH and Project Viva Studies. Pediatric reports 2021 Jun 13 (2): 279-288. Stanislawski Maggie A, Litkowski Elizabeth, Fore Ruby, Rifas-Shiman Sheryl L, Oken Emily, Hivert Marie-France, Lange Ethan M, Lange Leslie A, Dabelea Dana, Raghavan Sridhar |
Rare Variants Analysis of Lysosomal Related Genes in Early-Onset and Familial Parkinson's Disease in a Chinese Cohort. Journal of Parkinson's disease 2021 7 11 (4): 1845-1855. Chen Yong-Ping, Gu Xiao-Jing, Song Wei, Hou Yan-Bing, Ou Ru-Wei, Zhang Ling-Yu, Liu Kun-Cheng, Su Wei-Ming, Cao Bei, Wei Qian-Qian, Zhao Bi, Wu Ying, Shang Hui-Fa |
Relationship between polymorphism of receptor SCARB2 gene and clinical severity of enterovirus-71 associated hand-foot-mouth disease. Virology journal 2021 7 18 (1): 132. Wang Xia, Liu Hong, Li Ying, Su Rui, Liu Yamin, Qiao Kuny |
The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population. Frontiers in aging neuroscience 2021 12 13 749109. Zhao Yu-Wen, Pan Hong-Xu, Liu Zhenhua, Wang Yige, Zeng Qian, Fang Zheng-Huan, Luo Teng-Fei, Xu Kun, Wang Zheng, Zhou Xun, He Runcheng, Li Bin, Zhao Guihu, Xu Qian, Sun Qi-Ying, Yan Xin-Xiang, Tan Jie-Qiong, Li Jin-Chen, Guo Ji-Feng, Tang Bei-S |
Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects.
Nature communications 2022 12 13 (1): 7496. Krohn Lynne, Heilbron Karl, Blauwendraat Cornelis, Reynolds Regina H, Yu Eric, Senkevich Konstantin, Rudakou Uladzislau, Estiar Mehrdad A, Gustavsson Emil K, Brolin Kajsa, Ruskey Jennifer A, Freeman Kathryn, Asayesh Farnaz, Chia Ruth, Arnulf Isabelle, Hu Michele T M, Montplaisir Jacques Y, Gagnon Jean-François, Desautels Alex, Dauvilliers Yves, Gigli Gian Luigi, Valente Mariarosaria, Janes Francesco, Bernardini Andrea, Högl Birgit, Stefani Ambra, Ibrahim Abubaker, Šonka Karel, Kemlink David, Oertel Wolfgang, Janzen Annette, Plazzi Giuseppe, Biscarini Francesco, Antelmi Elena, Figorilli Michela, Puligheddu Monica, Mollenhauer Brit, Trenkwalder Claudia, Sixel-Döring Friederike, Cochen De Cock Valérie, Monaca Christelle Charley, Heidbreder Anna, Ferini-Strambi Luigi, Dijkstra Femke, Viaene Mineke, Abril Beatriz, Boeve Bradley F, , Scholz Sonja W, Ryten Mina, Bandres-Ciga Sara, Noyce Alastair, Cannon Paul, Pihlstrøm Lasse, Nalls Mike A, Singleton Andrew B, Rouleau Guy A, Postuma Ronald B, Gan-Or Z |
Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine 2022 10 85 104290. Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: