Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: COQ2[original query] |
---|
Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis. PloS one 2015 10 (6): e0130970. Yang Xinglong, Xi Jing, Zhao Quanzhen, Jia Hua, An Ran, Liu Zhuolin, Xu Yanmi |
Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy. CNS neuroscience & therapeutics 2015 Aug 21 (8): 626-30. Wen Xiao-Dan, Li Hong-Fu, Wang Hong-Xia, Ni Wang, Dong Yi, Wu Zhi-Yi |
Association Analysis of COQ2 Variant in Dementia and Essential Tremor. Parkinson's disease 2015 2015 926280. Chao Yin Xia, Ng Ebonne Yu Lin, Li Huihua, Nagaendran Kandiah, Yih Yuen, Chong Mei Sian, Prakash Kumar M, Tan Louis, Au Wing Lok, Zhao Yi, Zhou Zhi Dong, Tio Murni, Pavanni Ratnagopal, Tan Eng Ki |
Brain energy metabolism in early MSA-P: A phosphorus and proton magnetic resonance spectroscopy study. Parkinsonism & related disorders 2015 May 21 (5): 533-5. Stamelou M, Pilatus U, Reuss A, Respondek G, Knake S, Oertel W H, Höglinger G |
[Susceptibility gene in multiple system atrophy (MSA)]. Rinsh? shinkeigaku = Clinical neurology 2014 54 (12): 969-71. Tsuji Sho |
Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Nov . Zhao QuanZhen, Yang Xinglong, Tian SiJia, An Ran, Zheng JinHua, Xu Yanmi |
Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Jul 36 (7): 1211-5. Yang Xinglong, Xi Jing, An Ran, Yu Lihua, Lin Zhenfang, Zhou Huayong, Xu Yanmi |
The COQ2 genotype predicts the severity of coenzyme Q10 deficiency. Human molecular genetics 2016 Aug . Andrea Desbats Maria, Morbidoni Valeria, Silic-Benussi Micol, Doimo Mara, Ciminale Vincenzo, Cassina Matteo, Sacconi Sabrina, Hirano Michio, Basso Giuseppe, Pierrel Fabien, Navas Placido, Salviati Leonardo, Trevisson E |
MAPT haplotype diversity in multiple system atrophy. Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
Mutational analysis of COQ2 in patients with MSA in Italy. Neurobiology of aging 2016 Jun . Ronchi Dario, Di Biase Ernesto, Franco Giulia, Melzi Valentina, Del Sorbo Francesca, Elia Antonio, Barzaghi Chiara, Garavaglia Barbara, Bergamini Christian, Fato Romana, Mora Gabriele, Del Bo Roberto, Fortunato Francesco, Borellini Linda, Trezzi Ilaria, Compagnoni Giacomo Monzio, Monfrini Edoardo, Frattini Emanuele, Bonato Sara, Cogiamanian Filippo, Ardolino Gianluca, Priori Alberto, Bresolin Nereo, Corti Stefania, Comi Giacomo Pietro, Di Fonzo Aless |
Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy. JAMA neurology 2016 Jun . Mitsui Jun, Matsukawa Takashi, Yasuda Tsutomu, Ishiura Hiroyuki, Tsuji Sho |
New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophy. Neurology. Genetics 2016 Apr 2 (2): e54. Sun Zhuoran, Ohta Yasuyuki, Yamashita Toru, Sato Kota, Takemoto Mami, Hishikawa Nozomi, Abe Ko |
A genome-wide association study in multiple system atrophy.
Neurology 2016 Sep . Sailer Anna, Scholz Sonja W, Nalls Michael A, Schulte Claudia, Federoff Monica, Price T Ryan, Lees Andrew, Ross Owen A, Dickson Dennis W, Mok Kin, Mencacci Niccolo E, Schottlaender Lucia, Chelban Viorica, Ling Helen, O'Sullivan Sean S, Wood Nicholas W, Traynor Bryan J, Ferrucci Luigi, Federoff Howard J, Mhyre Timothy R, Morris Huw R, Deuschl Günther, Quinn Niall, Widner Hakan, Albanese Alberto, Infante Jon, Bhatia Kailash P, Poewe Werner, Oertel Wolfgang, Höglinger Günter U, Wüllner Ullrich, Goldwurm Stefano, Pellecchia Maria Teresa, Ferreira Joaquim, Tolosa Eduardo, Bloem Bastiaan R, Rascol Olivier, Meissner Wassilios G, Hardy John A, Revesz Tamas, Holton Janice L, Gasser Thomas, Wenning Gregor K, Singleton Andrew B, Houlden Henry, |
Serum Levels of Coenzyme Q10 in Patients with Multiple System Atrophy. PloS one 2016 11 (1): e0147574. Kasai Takashi, Tokuda Takahiko, Ohmichi Takuma, Ishii Ryotaro, Tatebe Harutsugu, Nakagawa Masanori, Mizuno Toshi |
Lack of association of mortalin (HSPA9) and other mitochondria-related genes with risk of Parkinson's and Alzheimer's diseases. Neurobiology of aging 2017 Jan 49 215.e9-215.e10. Chung Sun Ju, Kim Mi-Jung, Ryu Ho-Sung, Kim Juyeon, Kim Young Jin, Kim Kiju, You Sooyeoun, Kim Seong Yoon, Lee Jae-Ho |
COQ2 polymorphisms are not associated with increased risk of statin-induced myalgia/myopathy in the Czech population. Drug metabolism and personalized therapy 2017 Dec . Hubacek Jaroslav A, Adamkova Vera, Zlatohlavek Lukas, Steiner-Mrazova Lenka, Vrablik Mich |
Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function. Human mutation 2017 12 39 (3): 406-414. Vazquez Fonseca Luis, Doimo Mara, Calderan Cristina, Desbats Maria Andrea, Acosta Manuel J, Cerqua Cristina, Cassina Matteo, Ashraf Shazia, Hildebrandt Friedhelm, Sartori Geppo, Navas Placido, Trevisson Eva, Salviati Leonar |
Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93. Pediatric nephrology (Berlin, Germany) 2018 Jun . Bezdí?ka Martin, Štolbová Šárka, Seeman Tomáš, Cinek Ond?ej, Malina Michal, Šimánková Nad?žda, Pr?hová Št?pánka, Zieg Jak |
COQ2 variants in Parkinson's disease and multiple system atrophy. Journal of neural transmission (Vienna, Austria : 1996) 2018 4 125 (6): 937-944. Mikasa Michitaka, Kanai Kazuaki, Li Yuanzhe, Yoshino Hiroyo, Mogushi Kaoru, Hayashida Arisa, Ikeda Aya, Kawajiri Sumihiro, Okuma Yasuyuki, Kashihara Kenichi, Sato Tatsuya, Kondo Hiroshi, Funayama Manabu, Nishioka Kenya, Hattori Nobuta |
Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome. BMC nephrology 2018 12 19 (1): 382. Li Guo-Min, Cao Qi, Shen Qian, Sun Li, Zhai Yi-Hui, Liu Hai-Mei, An Yu, Xu Ho |
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy. Gene 2019 Aug 144037. Procopio Radha, Gagliardi Monica, Brighina Laura, Nicoletti Giuseppe, Morelli Maurizio, Ferrarese Carlo, Annesi Grazia, Quattrone Al |
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 |
Association of SLCO1B1 and ABCB1 Genetic Variants with Atorvastatin-induced Myopathy in Patients with Acute Ischemic Stroke. Current pharmaceutical design 2019 Jul . Zhang Limin, Lv Hong, Zhang Qian, Wang Dongzhi, Kang Xixiong, Zhang Guojun, Li Xinga |
Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease. Scientific reports 2019 4 9 (1): 6559. Foti Sandrine C, Hargreaves Iain, Carrington Stephanie, Kiely Aoife P, Houlden Henry, Holton Janice |
Reductions in COQ2 Expression Relate to Reduced ATP Levels in Multiple System Atrophy Brain. Frontiers in neuroscience 2019 13 1187. Hsiao Jen-Hsiang T, Purushothuman Sivaraman, Jensen Poul H, Halliday Glenda M, Kim Woojin Sco |
Missense PDSS1 mutations in CoenzymeQ10 synthesis cause optic atrophy and sensorineural deafness. Annals of clinical and translational neurology 2020 12 8 (1): 247-251. Nardecchia Francesca, De Giorgi Agnese, Palombo Flavia, Fiorini Claudio, De Negri Anna M, Carelli Valerio, Caporali Leonardo, Leuzzi Vincen |
COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population. Journal of the neurological sciences 2021 8 429 117623. Porto Kristine Joyce, Hirano Makito, Mitsui Jun, Chikada Ayaka, Matsukawa Takashi, Ishiura Hiroyuki, , Toda Tatsushi, Kusunoki Susumu, Tsuji Sho |
Integrated genomic analysis identifies novel low-frequency cis-regulatory variant rs2279658 associated with VSD risk in Chinese children. Frontiers in cell and developmental biology 2022 12 10 1062403. Jin Lihui, Han Zhenyuan, Jiang Zhongli, Lu Jieru, Wu Yizhuo, Yan Bingqian, Zhang Weibin, Lin Xuedong, Jiang Lvyan, Zhao Pengjun, Sun K |
COQ2 and SNCA polymorphisms interact with environmental factors to modulate the risk of multiple system atrophy and subtype disposition. European journal of neurology 2022 Jun . Kuo Ming-Che, Lu Ying-Che, Tai Chun-Hwei, Soong Bing-Wen, Hu Fu-Chang, Chen Meng-Ling, Lin Chin-Hsien, Wu Ruey-Me |
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: