Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 54 Records) |
| Query Trace: Disease and PGC[original query] |
|---|
| Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2015 Mar 40 (4): 915-26. Sánchez-Mora Cristina, Ramos-Quiroga Josep A, Bosch Rosa, Corrales Montse, Garcia-Martínez Iris, Nogueira Mariana, Pagerols Mireia, Palomar Gloria, Richarte Vanesa, Vidal Raquel, Arias-Vasquez Alejandro, Bustamante Mariona, Forns Joan, Gross-Lesch Silke, Guxens Monica, Hinney Anke, Hoogman Martine, Jacob Christian, Jacobsen Kaya K, Kan Cornelis C, Kiemeney Lambertus, Kittel-Schneider Sarah, Klein Marieke, Onnink Marten, Rivero Olga, Zayats Tetyana, Buitelaar Jan, Faraone Stephen V, Franke Barbara, Haavik Jan, Johansson Stefan, Lesch Klaus-Peter, Reif Andreas, Sunyer Jordi, Bayés Mònica, Casas Miguel, Cormand Bru, Ribasés Mar |
| Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct 168 (7): 617-29. Fullerton Janice M, Koller Daniel L, Edenberg Howard J, Foroud Tatiana, Liu Hai, Glowinski Anne L, McInnis Melvin G, Wilcox Holly C, Frankland Andrew, Roberts Gloria, Schofield Peter R, Mitchell Philip B, Nurnberger John I, |
| Polymorphic rs9471643 and rs6458238 upregulate PGC transcription and protein expression in overdominant or dominant models. Molecular carcinogenesis 2015 Apr . He Caiyun, Xu Qian, Tu Huakang, Sun Liping, Gong Yuehua, Liu Jingwei, Yuan Yu |
| Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis. Nature genetics 2015 Nov . Loh Po-Ru, Bhatia Gaurav, Gusev Alexander, Finucane Hilary K, Bulik-Sullivan Brendan K, Pollack Samuela J, , de Candia Teresa R, Lee Sang Hong, Wray Naomi R, Kendler Kenneth S, O'Donovan Michael C, Neale Benjamin M, Patterson Nick, Price Alkes |
| A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder. Biological psychiatry 2017 02 81 (4): 336-346. Zeng Yanni, Navarro Pau, Fernandez-Pujals Ana M, Hall Lynsey S, Clarke Toni-Kim, Thomson Pippa A, Smith Blair H, Hocking Lynne J, Padmanabhan Sandosh, Hayward Caroline, MacIntyre Donald J, Wray Naomi R, , Deary Ian J, Porteous David J, Haley Chris S, McIntosh Andrew |
| Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Translational psychiatry 2016 6 e768. Costas J, Carrera N, Alonso P, Gurriarán X, Segalàs C, Real E, López-Solà C, Mas S, Gassó P, Domènech L, Morell M, Quintela I, Lázaro L, Menchón J M, Estivill X, Carracedo |
| Association of combined genetic variations in PPAR?, PGC-1a, and LXRa with coronary artery disease and severity in Thai population. Atherosclerosis 2016 Mar 248 140-148. Yongsakulchai Pratthana, Settasatian Chatri, Settasatian Nongnuch, Komanasin Nantarat, Kukongwiriyapan Upa, Cote Michele L, Intharapetch Pongsak, Senthong Vich |
| SNP-SNP interactions of three new pri-miRNAs with the target gene PGC and multidimensional analysis of H. pylori in the gastric cancer/atrophic gastritis risk in a Chinese population. Oncotarget 2016 Apr 7 (17): 23700-14. Xu Qian, Wu Ye-Feng, Li Ying, He Cai-Yun, Sun Li-Ping, Liu Jing-Wei, Yuan Yu |
| No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study. PLoS genetics 2016 Oct 12 (10): e1006343. Johnson Emma C, Bjelland Douglas W, Howrigan Daniel P, Abdellaoui Abdel, Breen Gerome, Borglum Anders, Cichon Sven, Degenhardt Franziska, Forstner Andreas J, Frank Josef, Genovese Giulio, Heilmann-Heimbach Stefanie, Herms Stefan, Hoffman Per, Maier Wolfgang, Mattheisen Manuel, Morris Derek, Mowry Bryan, Müller-Mhysok Betram, Neale Benjamin, Nenadic Igor, Nöthen Markus M, O'Dushlaine Colm, Rietschel Marcella, Ruderfer Douglas M, Rujescu Dan, Schulze Thomas G, Simonson Matthew A, Stahl Eli, Strohmaier Jana, Witt Stephanie H, , Sullivan Patrick F, Keller Matthew |
| Common variants in the chromosome 2p23 region containing the SLC30A3 (ZnT3) gene are associated with schizophrenia in female but not male individuals in a large collection of European samples. Psychiatry research 2016 Dec 246 335-340. Perez-Becerril C, Morris A G, Mortimer A, McKenna P J, de Belleroche |
| Role of 108 schizophrenia-associated loci in modulating psychopathological dimensions in schizophrenia and bipolar disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 8 174 (7): 757-764. Fabbri Chiara, Serretti Alessand |
| Polygenic risk for schizophrenia and neurocognitive performance in patients with schizophrenia. Genes, brain, and behavior 2017 Jul . Wang Shi-Heng, Hsiao Po-Chang, Yeh Ling-Ling, Liu Chih-Min, Liu Chen-Chung, Hwang Tzung-Jeng, Hsieh Ming H, Chien Yi-Ling, Lin Yi-Ting, Chandler Sharon D, Faraone Stephen V, Laird Nan, Neale Benjamin, McCarroll Steve A, Glatt Stephen J, Tsuang Ming T, Hwu Hai-Gwo, Chen Wei |
| Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder. Biological psychiatry 2016 Dec . Zeng Yanni, Navarro Pau, Shirali Masoud, Howard David M, Adams Mark J, Hall Lynsey S, Clarke Toni-Kim, Thomson Pippa A, Smith Blair H, Murray Alison, Padmanabhan Sandosh, Hayward Caroline, Boutin Thibaud, MacIntyre Donald J, Lewis Cathryn M, Wray Naomi R, Mehta Divya, Penninx Brenda W J H, Milaneschi Yuri, Baune Bernhard T, Air Tracy, Hottenga Jouke-Jan, Mbarek Hamdi, Castelao Enrique, Pistis Giorgio, Schulze Thomas G, Streit Fabian, Forstner Andreas J, Byrne Enda M, Martin Nicholas G, Breen Gerome, Müller-Myhsok Bertram, Lucae Susanne, Kloiber Stefan, Domenici Enrico, , Deary Ian J, Porteous David J, Haley Chris S, McIntosh Andrew |
| Association of PGC-1? gene with type 2 diabetes in three unrelated endogamous groups of North-West India (Punjab): a case-control and meta-analysis study. Molecular genetics and genomics : MGG 2017 Oct . Sharma Rubina, Matharoo Kawaljit, Kapoor Rohit, Bhanwer A J |
| Variability of 128 schizophrenia-associated gene variants across distinct ethnic populations. Translational psychiatry 2017 Jan 7 (1): e988. Ohi K, Shimada T, Yasuyama T, Uehara T, Kawasaki |
| SNP interactions of PGC with its neighbor lncRNAs enhance the susceptibility to gastric cancer/atrophic gastritis and influence the expression of involved molecules. Cancer medicine 2018 Aug . Lv Zhi, Sun Liping, Xu Qian, Gong Yuehua, Jing Jingjing, Dong Nannan, Xing Chengzhong, Yuan Yu |
| 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 |
| Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders. PLoS genetics 2018 12 14 (12): e1007535. Toma Claudio, Pierce Kerrie D, Shaw Alex D, Heath Anna, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
| 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 |
Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.
Translational psychiatry 2019 02 9 (1): 14. Arnau-Soler Aleix, Macdonald-Dunlop Erin, Adams Mark J, Clarke Toni-Kim, MacIntyre Donald J, Milburn Keith, Navrady Lauren, , , Hayward Caroline, McIntosh Andrew M, Thomson Pippa |
| Association of Candidate Gene Polymorphism with Metabolic Syndrome among Mongolian Subjects: A Case-Control Study. Medical sciences (Basel, Switzerland) 2020 Sep 8 (3): . Chuluun-Erdene Ariunbold, Sengeragchaa Orgil, Altangerel Tsend-Ayush, Sanjmyatav Purevjal, Dagdan Batnaran, Battulga Solongo, Enkhbat Lundiamaa, Byambasuren Nyamjav, Malchinkhuu Munkhzol, Janlav Munkhtstets |
| Impact of glucose on risk of dementia: Mendelian randomisation studies in 115,875 individuals. Diabetologia 2020 3 63 (6): 1151-1161. Benn Marianne, Nordestgaard Børge G, Tybjærg-Hansen Anne, Frikke-Schmidt Ru |
| Plasma high-density lipoprotein cholesterol and risk of dementia: observational and genetic studies. Cardiovascular research 2021 5 118 (5): 1330-1343. Kjeldsen Emilie W, Thomassen Jesper Q, Juul Rasmussen Ida, Nordestgaard Børge G, Tybjærg-Hansen Anne, Frikke-Schmidt Ru |
| Causal effect of insulin resistance on small vessel stroke and Alzheimer's disease: A Mendelian randomization analysis. European journal of neurology 2021 11 29 (3): 698-706. Zhou Mengyuan, Li Hao, Wang Yongjun, Pan Yuesong, Wang Yilo |
| [Neurogenetics of schizophrenia: findings from studies based on data sharing and global partnerships]. Der Nervenarzt 2021 1 92 (3): 199-207. Adorjan K, Schulze T G, Budde M, Heilbronner U, Tessema F, Mekonnen Z, Falkai |
| 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 |
| Exercise modulates APOE expression in brain cortex of female APOE3 and APOE4 targeted replacement mice. Neuropeptides 2022 11 97 102307. Mulgrave Verona E, Alsayegh Abdulrahman A, Jaldi Aida, Omire-Mayor DianneMarie T, James Niaya, Ntekim Oyonumo, Walters Eric, Akala Emanuel O, Allard Joanne |
| Major depressive disorder plays a vital role in the pathway from gastroesophageal reflux disease to chronic obstructive pulmonary disease: a Mendelian randomization study. Frontiers in genetics 2023 7 14 1198476. Menglong Zou, Wei Zhang, Lele Shen, Yin Xu, Ying Z |
| Heterogeneity analysis provides evidence for a genetically homogeneous subtype of bipolar-disorder. ArXiv 2024 5 . Caroline C McGrouther, Aaditya V Rangan, Arianna Di Florio, Jeremy A Elman, Nicholas J Schork, John Kelsoe, |
| Causal relationship between IgA nephropathy and common neuropsychiatric disorders: A two-sample Mendelian randomization analysis. Journal of affective disorders 2024 10 369 782-788. Xu Lin, Gui-Bing Chen, Ke-Yi Li, Ya-Juan |
- Page last reviewed:Feb 1, 2024
- Content source: