Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: ACMSD[original query] |
---|
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Lancet (London, England) 2011 Feb 377 (9766): 641-9. , Nalls Michael A, Plagnol Vincent, Hernandez Dena G, Sharma Manu, Sheerin Una-Marie, Saad Mohamad, Simón-Sánchez J, Schulte Claudia, Lesage Suzanne, Sveinbjörnsdóttir Sigurlaug, Stefánsson Kári, Martinez Maria, Hardy John, Heutink Peter, Brice Alexis, Gasser Thomas, Singleton Andrew B, Wood Nicholas |
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.
Diabetes 2012 Dec . Tabassum R, Chauhan G, Dwivedi OP, Mahajan A, Jaiswal A, Kaur I, Bandesh K, Singh T, Mathai BJ, Pandey Y, Chidambaram M, Sharma A, Chavali S, Sengupta S, Ramakrishnan L, Venkatesh P, Aggarwal SK, Ghosh S, Prabhakaran D, Srinath RK, Saxena M, Banerjee M, Mathur S, Bhansali A, Shah VN, Madhu SV, Marwaha RK, Basu A, Scaria V, McCarthy MI, Venkatesan R, Mohan V, Tandon N, Bharadwaj D |
Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease. Neurobiology of aging 2012 Nov . Pihlstrøm L, Axelsson G, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Ohman E, Dietrichs E, Toft M |
Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease. PloS one 2013 8 (11): e79211. Li Nan-Nan, Tan Eng-King, Chang Xue-Li, Mao Xue-Ye, Zhang Jin-Hong, Zhao Dong-Mei, Liao Qiao, Yu Wen-Juan, Peng Ro |
Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han population. Neuroscience letters 2014 Apr 566 206-9. Wang Ya-qin, Tang Bei-sha, Yu Ri-li, Li Kai, Liu Zhen-hua, Xu Qian, Sun Qi-ying, Yan Xin-xiang, Guo Ji-fe |
Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma.
Toxicological sciences : an official journal of the Society of Toxicology 2015 Jul 146 (1): 192-201. Yucesoy Berran, Kaufman Kenneth M, Lummus Zana L, Weirauch Matthew T, Zhang Ge, Cartier André, Boulet Louis-Philippe, Sastre Joaquin, Quirce Santiago, Tarlo Susan M, Cruz Maria-Jesus, Munoz Xavier, Harley John B, Bernstein David |
Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression. Neurobiology of aging 2015 Sep . Davis Albert A, Andruska Kristin M, Benitez Bruno A, Racette Brad A, Perlmutter Joel S, Cruchaga Carl |
An enzyme in the kynurenine pathway that governs vulnerability to suicidal behavior by regulating excitotoxicity and neuroinflammation. Translational psychiatry 2016 6 (8): e865. Brundin L, Sellgren C M, Lim C K, Grit J, Pålsson E, Landén M, Samuelsson M, Lundgren K, Brundin P, Fuchs D, Postolache T T, Traskman-Bendz L, Guillemin G J, Erhardt |
Genome-wide assessment of Parkinson's disease in a Southern Spanish population. Neurobiology of aging 2016 Jun . Bandrés-Ciga Sara, Price Timothy Ryan, Barrero Francisco Javier, Escamilla-Sevilla Francisco, Pelegrina Javier, Arepalli Sampath, Hernández Dena, Gutiérrez Blanca, Cervilla Jorge, Rivera Margarita, Rivera Alberto, Ding Jing-Hui, Vives Francisco, Nalls Michael, Singleton Andrew, Durán Raqu |
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 |
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 |
A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population. Neuroscience letters 2019 Aug 134425. Tejera-Parrado Cristina, Jesús Silvia, Periñán María Teresa, Buiza-Rueda Dolores, Oliva-Ariza Guillermo, Adarmes-Gómez Astrid D, Macías-García Daniel, Gómez-Garre Pilar, Mir Pab |
Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK /STX1B with sporadic Parkinson's disease in Han Chinese. Neuroscience letters 2019 Mar 703 45-48. Wang Ling, Li Nan-Nan, Lu Zhong-Jiao, Li Jun-Ying, Peng Jia-Xin, Duan Li-Ren, Peng Ro |
Polymorphisms of ACMSD-TMEM163, MCCC1, and BCKDK-STX1B Are Not Associated with Parkinson's Disease in Taiwan. Parkinson's disease 2019 2019 3489638. Chang Kuo-Hsuan, Chen Chiung-Mei, Chen Yi-Chun, Fung Hon-Chung, Wu Yih- |
Central levels of tryptophan metabolites in subjects with bipolar disorder. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2020 12 43 52-62. Trepci Ada, Sellgren Carl M, Pålsson Erik, Brundin Lena, Khanlarkhani Neda, Schwieler Lilly, Landén Mikael, Erhardt Soph |
Atremorine in Parkinson's disease: From dopaminergic neuroprotection to pharmacogenomics. Medicinal research reviews 2021 6 41 (5): 2841-2886. Cacabelos Ramón, Carrera Iván, Martínez Olaia, Alejo Ramón, Fernández-Novoa Lucía, Cacabelos Pablo, Corzo Lola, Rodríguez Susana, Alcaraz Margarita, Nebril Laura, Tellado Iván, Cacabelos Natalia, Pego Rocío, Naidoo Vinogran, Carril Juan |
Identification of Genetic Variations in the NAD-Related Pathways for Patients with Major Depressive Disorder: A Case-Control Study in Taiwan. Journal of clinical medicine 2022 7 11 (13): . Chen Daniel Tzu-Li, Cheng Szu-Wei, Chen Tiffany, Chang Jane Pei-Chen, Hwang Bing-Fang, Chang Hen-Hong, Chuang Eric Y, Chen Che-Hong, Su Kuan-P |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: