Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 43 Records) |
| Query Trace: Disease and PPARGC1A[original query] |
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| A follow-up case-control association study of tractable (druggable) genes in recurrent major depression. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Sep 156B (6): 640-50. Schosser A, Gaysina D, Cohen-Woods S, Domenici E, Perry J, Tozzi F, Korszun A, Gunasinghe C, Gray J, Jones L, Binder E B, Holsboer F, Craddock N, Owen M J, Craig I W, Farmer A E, Muglia P, McGuffin |
| Pathway analysis of a genome-wide association study of ileal Crohn's disease. DNA and cell biology 2012 Oct 31 (10): 1549-54. Lee Young Ho, Song Gwan G |
| Population stratification may bias analysis of PGC-1a as a modifier of age at Huntington disease motor onset. Human genetics 2012 Dec 131 (12): 1833-40. Ramos Eliana Marisa, Latourelle Jeanne C, Lee Ji-Hyun, Gillis Tammy, Mysore Jayalakshmi S, Squitieri Ferdinando, Di Pardo Alba, Di Donato Stefano, Hayden Michael R, Morrison Patrick J, Nance Martha, Ross Christopher A, Margolis Russell L, Gomez-Tortosa Estrella, Ayuso Carmen, Suchowersky Oksana, Trent Ronald J, McCusker Elizabeth, Novelletto Andrea, Frontali Marina, Jones Randi, Ashizawa Tetsuo, Frank Samuel, Saint-Hilaire Marie-Helene, Hersch Steven M, Rosas Herminia D, Lucente Diane, Harrison Madaline B, Zanko Andrea, Marder Karen, Gusella James F, Lee Jong-Min, Alonso Isabel, Sequeiros Jorge, Myers Richard H, Macdonald Marcy |
| A common variant in the peroxisome proliferator-activated receptor-? coactivator-1a gene is associated with nonalcoholic fatty liver disease in obese children. The American journal of clinical nutrition 2012 Dec . Lin YC, Chang PF, Chang MH, Ni YH |
| Mitochondriogenesis genes and extreme longevity. Rejuvenation research 2013 Feb 16 (1): 67-73. Santiago Catalina, Garatachea Nuria, Yvert Thomas, Rodríguez-Romo Gabriel, Santos-Lozano Alejandro, Fiuza-Luces Carmen, Lucia Alejand |
| Association of genes involved in bile acid synthesis with the progression of primary biliary cirrhosis in Japanese patients. Journal of gastroenterology 2013 Oct 48 (10): 1160-70. Inamine Tatsuo, Higa Shingo, Noguchi Fumie, Kondo Shinji, Omagari Katsuhisa, Yatsuhashi Hiroshi, Tsukamoto Kazuhiro, Nakamura Mino |
| Genetic variants in ICAM1, PPARGC1A and MTHFR are potentially associated with different phenotypes of diabetic retinopathy. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift für Augenheilkunde 2014 232 (3): 156-62. Simões Maria José, Lobo Conceição, Egas Conceição, Nunes Sandrina, Carmona Susana, Costa Miguel Ângelo, Duarte Tânia, Ribeiro Luísa, Faro Carlos, Cunha-Vaz José |
| A single nucleotide polymorphism in the coding region of PGC-1a is a male-specific modifier of Huntington disease age-at-onset in a large European cohort. BMC neurology 2014 14 1. Weydt Patrick, Soyal Selma M, Landwehrmeyer G Bernhard, Patsch Wolfgang, |
| Variants in Genes Controlling Oxidative Metabolism Contribute to Lower Hepatic ATP Independent of Liver Fat Content in Type 1 Diabetes. Diabetes 2016 Apr . Gancheva Sofiya, Bierwagen Alessandra, Kaul Kirti, Herder Christian, Nowotny Peter, Kahl Sabine, Giani Guido, Klueppelholz Birgit, Knebel Birgit, Begovatz Paul, Strassburger Klaus, Al-Hasani Hadi, Lundbom Jesper, Szendroedi Julia, Roden Michael, |
| Interactions of a PPARGC1A Variant and a PNPLA3 Variant Affect Nonalcoholic Steatohepatitis in Severely Obese Taiwanese Patients. Medicine 2016 Mar 95 (12): e3120. Tai Chi-Ming, Huang Chih-Kun, Tu Hung-Pin, Hwang Jau-Chung, Yeh Ming-Lun, Huang Chung-Feng, Huang Jee-Fu, Dai Chia-Yen, Chuang Wan-Long, Yu Ming-Lu |
Genome-wide association study in essential tremor identifies three new loci.
Brain : a journal of neurology 2016 Dec 139 (Pt 12): 3163-3169. Müller Stefanie H, Girard Simon L, Hopfner Franziska, Merner Nancy D, Bourassa Cynthia V, Lorenz Delia, Clark Lorraine N, Tittmann Lukas, Soto-Ortolaza Alexandra I, Klebe Stephan, Hallett Mark, Schneider Susanne A, Hodgkinson Colin A, Lieb Wolfgang, Wszolek Zbigniew K, Pendziwiat Manuela, Lorenzo-Betancor Oswaldo, Poewe Werner, Ortega-Cubero Sara, Seppi Klaus, Rajput Alex, Hussl Anna, Rajput Ali H, Berg Daniela, Dion Patrick A, Wurster Isabel, Shulman Joshua M, Srulijes Karin, Haubenberger Dietrich, Pastor Pau, Vilariño-Güell Carles, Postuma Ronald B, Bernard Geneviève, Ladwig Karl-Heinz, Dupré Nicolas, Jankovic Joseph, Strauch Konstantin, Panisset Michel, Winkelmann Juliane, Testa Claudia M, Reischl Eva, Zeuner Kirsten E, Ross Owen A, Arzberger Thomas, Chouinard Sylvain, Deuschl Günther, Louis Elan D, Kuhlenbäumer Gregor, Rouleau Guy |
| The role of single-nucleotide variants of the energy metabolism-linked genes SIRT3, PPARGC1A and APOE in amyotrophic lateral sclerosis risk. Genes & genetic systems 2017 Feb . Albani Diego, Pupillo Elisabetta, Bianchi Elisa, Chierchia Armando, Martines Rosalba, Forloni Gianluigi, Beghi Etto |
| Analysis of Single Nucleotide Polymorphisms of STK32B, PPARGC1A and CTNNA3 Gene With Sporadic Parkinson's Disease Susceptibility in Chinese Han Population. Frontiers in neurology 2018 9 387. Shi Chang-He, Cheng Yuan, Tang Mi-Bo, Liu Yu-Tao, Yang Zhi-Hua, Li Fang, Fan Yu, Yang Jing, Xu Yu-Mi |
| The ADRA2A rs553668 variant is associated with type 2 diabetes and five variants were associated at nominal significance levels in a population-based case-control study from Mexico City. Gene 2018 May . Totomoch-Serra Armando, Muñoz María de Lourdes, Burgueño Juan, Revilla-Monsalve María Cristina, Perez-Muñoz Ashael, Diaz-Badillo Álva |
| Expression of the gene coading for PGC-1? in peripheral blood leukocytes and related gene variants in patients with Parkinson's disease. Parkinsonism & related disorders 2018 Feb . Yang Xiao-Dong, Qian Yi-Wei, Xu Shao-Qing, Wan Da-Yong, Sun Feng-Hua, Chen Sheng-Di, Xiao Q |
| A logical relationship for schizophrenia, bipolar, and major depressive disorder. Part 4: Evidence from chromosome 4 high-density association screen. The Journal of comparative neurology 2019 Feb 527 (2): 392-405. Tang Jian, Chen Xing, Cai Bin, Chen Ga |
| Association between PPARGC1A single nucleotide polymorphisms and increased risk of nonalcoholic fatty liver disease among Iranian patients with type 2 diabetes mellitus. Turkish journal of medical sciences 2019 08 49 (4): 1089-1094. Saremi Leila, Lotf?panah Shirin, Mohammadi Masumeh, Hosseinzadeh Hassan, Hosseini-Khah Zahra, Johari Behrooz, Saltanatpour Zohr |
| Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease. PloS one 2019 7 14 (7): e0218111. Baker Emily, Sims Rebecca, Leonenko Ganna, Frizzati Aura, Harwood Janet C, Grozeva Detelina, , , , , , Morgan Kevin, Passmore Peter, Holmes Clive, Powell John, Brayne Carol, Gill Michael, Mead Simon, Bossù Paola, Spalletta Gianfranco, Goate Alison M, Cruchaga Carlos, Maier Wolfgang, Heun Reinhard, Jessen Frank, Peters Oliver, Dichgans Martin, FröLich Lutz, Ramirez Alfredo, Jones Lesley, Hardy John, Ivanov Dobril, Hill Matthew, Holmans Peter, Allen Nicholas D, Morgan B Paul, Seshadri Sudha, Schellenberg Gerard D, Amouyel Philippe, Williams Julie, Escott-Price Valenti |
| Assessment of three essential tremor genetic loci in sporadic Parkinson's disease in Eastern China. CNS neuroscience & therapeutics 2019 Nov . Gao Ting, Wu Jiong, Zheng Ran, Fang Yi, Jin Chong-Yao, Ruan Yang, Cao Jin, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
| Prevalence, clinical characteristics, risk factors, and indicators for lean Chinese adults with nonalcoholic fatty liver disease. World journal of gastroenterology 2020 Apr 26 (15): 1792-1804. Zeng Jing, Yang Rui-Xu, Sun Chao, Pan Qin, Zhang Rui-Nan, Chen Guang-Yu, Hu Ying, Fan Jian-G |
| Effect of Peroxisome Proliferator-Activated Receptor-? Coactivator-1 Alpha Variants on Spontaneous Clearance and Fibrosis Progression during Hepatitis C Virus Infection in Moroccan Patients. Virologica Sinica 2020 Apr . ElFihry Raouia, Elmessaoudi-Idrissi Mohcine, Jadid Fatima-Zahra, Zaidane Imane, Chihab Hajar, Tahiri Mohamed, Kabine Mostafa, Badre Wafaa, Chemin Isabelle, Marchio Agnes, Pineau Pascal, Ezzikouri Sayeh, Benjelloun Souma |
| Gene-environment interaction in chronic kidney disease among people with type 2 diabetes from The Malaysian Cohort project: a case-control study. Diabetic medicine : a journal of the British Diabetic Association 2020 Feb . Ahmad N, Shah S A, Abdul Gafor A H, Abdul Murad N A, Kamaruddin M A, Abd Jalal N, Ismail N, Alias M R, Jamal |
| PPARGC1A rs8192678 G>A polymorphism affects the severity of hepatic histological features and nonalcoholic steatohepatitis in patients with nonalcoholic fatty liver disease. World journal of gastroenterology 2021 Jul 27 (25): 3863-3876. Zhang Rui-Nan, Shen Feng, Pan Qin, Cao Hai-Xia, Chen Guang-Yu, Fan Jian-G |
| Association of rare PPARGC1A variants with Parkinson's disease risk. Journal of human genetics 2022 Aug . Li Li-Zhi, Zhao Yu-Wen, Pan Hong-Xu, Xiang Ya-Qin, Wang Yi-Ge, Xu Qian, Yan Xin-Xiang, Tan Jie-Qiong, Li Jin-Chen, Tang Bei-Sha, Guo Ji-Fe |
| Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis. Frontiers in physiology 2022 13 909870. Schillemans Tessa, Tragante Vinicius, Maitusong Buamina, Gigante Bruna, Cresci Sharon, Laguzzi Federica, Vikström Max, Richards Mark, Pilbrow Anna, Cameron Vicky, Foco Luisa, Doughty Robert N, Kuukasjärvi Pekka, Allayee Hooman, Hartiala Jaana A, Tang W H Wilson, Lyytikäinen Leo-Pekka, Nikus Kjell, Laurikka Jari O, Srinivasan Sundararajan, Mordi Ify R, Trompet Stella, Kraaijeveld Adriaan, van Setten Jessica, Gijsberts Crystel M, Maitland-van der Zee Anke H, Saely Christoph H, Gong Yan, Johnson Julie A, Cooper-DeHoff Rhonda M, Pepine Carl J, Casu Gavino, Leiherer Andreas, Drexel Heinz, Horne Benjamin D, van der Laan Sander W, Marziliano Nicola, Hazen Stanley L, Sinisalo Juha, Kähönen Mika, Lehtimäki Terho, Lang Chim C, Burkhardt Ralph, Scholz Markus, Jukema J Wouter, Eriksson Niclas, Åkerblom Axel, James Stefan, Held Claes, Hagström Emil, Spertus John A, Algra Ale, de Faire Ulf, Åkesson Agneta, Asselbergs Folkert W, Patel Riyaz S, Leander Kar |
| Unraveling Gut Microbiota Signatures Associated with PPARD and PARGC1A Genetic Polymorphisms in a Healthy Population. Genes 2022 Feb 13 (2): . Bailén María, Tabone Mariangela, Bressa Carlo, Lominchar María Gregoria Montalvo, Larrosa Mar, González-Soltero Roc |
| Implications of genetic variations, differential gene expression, and allele-specific expression on metformin response in drug-naïve type 2 diabetes. Journal of endocrinological investigation 2022 12 . Vohra M, Sharma A R, Mallya S, Prabhu N B, Jayaram P, Nagri S K, Umakanth S, Rai P |
| The peroxisome proliferator-activated receptor ? coactivator-1 alpha rs8192678 (Gly482Ser) variant and hepatitis B virus clearance. Infectious diseases (London, England) 2023 6 1-11. Karima Abounouh, Ikram-Allah Tanouti, Ahd Ouladlahsen, Mohamed Tahiri, Wafaa Badre, Hind Dehbi, M'hammed Sarih, Soumaya Benjelloun, Pascal Pineau, Sayeh Ezzikou |
| Recent Progress in Genetics and Epigenetics Research on Diabetic Nephropathy in Malaysia. Journal of diabetes research 2023 5 2023 9053580. Norhashimah Abu Seman, Siti Haslina Othm |
| Deletion of the Murine Ortholog of the Human 9p21.3 Locus Leads to Insulin Resistance and Obesity in Hypercholesterolemic Mice. Cells 2024 6 13 (11): . Sanna Kettunen, Tuisku Suoranta, Sadegh Beikverdi, Minja Heikkilä, Anna Slita, Iida Räty, Elias Ylä-Herttuala, Katariina Öörni, Anna-Kaisa Ruotsalainen, Seppo Ylä-Herttua |
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