Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and COQ2[original query] |
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| Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome. Journal of the American Society of Nephrology : JASN 2010 Jul 21 (7): 1209-17. Machuca Eduardo, Benoit Geneviève, Nevo Fabien, Tête Marie-Josèphe, Gribouval Olivier, Pawtowski Audrey, Brandström Per, Loirat Chantal, Niaudet Patrick, Gubler Marie-Claire, Antignac Corin |
| Mutations in COQ2 in familial and sporadic multiple-system atrophy. The New England journal of medicine 2013 Jul 369 (3): 233-44. Authors are not available |
| Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome. Clinical journal of the American Society of Nephrology : CJASN 2013 Jan . McCarthy HJ, Bierzynska A, Wherlock M, Ognjanovic M, Kerecuk L, Hegde S, Feather S, Gilbert RD, Krischock L, Jones C, Sinha MD, Webb NJ, Christian M, Williams MM, Marks S, Koziell A, Welsh GI, Saleem MA |
| COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population. Neurobiology of aging 2015 Jan 36 (1): 546.e17-8. Lin Chin-Hsien, Lin Hang-I, Chen Meng-Ling, Wu Ruey-Me |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Genetic profiles of multiple system atrophy revealed by exome sequencing, long-read sequencing and spinocerebellar ataxia repeat expansion analysis. European journal of neurology 2024 8 e16441. Xu-Ying Li, Hong Lai, Xian Li, Fanxi Xu, Yang Song, Zhanjun Wang, Qibin Li, Ruichai Lin, Zhiheng Xu, Chaodong Wa |
| Steroid-Resistant Nephrotic Syndrome Is Associated With a Unique Genetic Profile in a Highly Admixed Pediatric Population. Kidney international reports 2024 12 9 (12): 3501-3516. Andreia Watanabe, Precil Diego Miranda de Menezes Neves, Kelly Nunes, Antonio Marcondes Lerario, Elieser Hitoshi Watanabe, Frederico Moraes Ferreira, Denise Maria Avancini Costa Malheiros, Amanda de Moraes Narcizo, Mara Sanches Guaragna, Stanley de Almeida Araujo, Thais Medeiros Cruz, Jussara Soares Fontes, Vera Maria Santoro Belangero, Maria Helena Vaisbich, Friedhelm Hildebrandt, Matthew Gordon Sampson, Luiz Fernando Onuch |
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