Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 34 Records) |
| Query Trace: Disease and DISC1[original query] |
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| Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample. Schizophrenia research 2008 Dec 106 (2-3): 237-41. Saetre Peter, Agartz Ingrid, De Franciscis Alessandra, Lundmark Per, Djurovic Srdjan, Kähler Anna, Andreassen Ole A, Jakobsen Klaus D, Rasmussen Henrik B, Werge Thomas, Hall Håkan, Terenius Lars, Jönsson Erik |
| Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding. Human molecular genetics 2008 Aug 17 (16): 2462-73. Burdick Katherine E, Kamiya Atsushi, Hodgkinson Colin A, Lencz Todd, DeRosse Pamela, Ishizuka Koko, Elashvili Sarah, Arai Hiroyuki, Goldman David, Sawa Akira, Malhotra Anil |
| Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes, brain, and behavior 2009 Mar 8 (2): 238-47. Houlihan L M, Harris S E, Luciano M, Gow A J, Starr J M, Visscher P M, Deary I |
| Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia. Biological psychiatry 2009 Dec 66 (11): 990-6. Wessman Jaana, Paunio Tiina, Tuulio-Henriksson Annamari, Koivisto Mikko, Partonen Timo, Suvisaari Jaana, Turunen Joni A, Wedenoja Juho, Hennah William, Pietiläinen Olli P H, Lönnqvist Jouko, Mannila Heikki, Peltonen Lee |
| The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. Human molecular genetics 2009 Jul 18 (14): 2719-27. Schumacher Johannes, Laje Gonzalo, Abou Jamra Rami, Becker Tim, Mühleisen Thomas W, Vasilescu Catalina, Mattheisen Manuel, Herms Stefan, Hoffmann Per, Hillmer Axel M, Georgi Alexander, Herold Christine, Schulze Thomas G, Propping Peter, Rietschel Marcella, McMahon Francis J, Nöthen Markus M, Cichon Sv |
| Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. PloS one 2011 6 (8): e23450. Moens Lotte N, De Rijk Peter, Reumers Joke, Van den Bossche Maarten J A, Glassee Wim, De Zutter Sonia, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, Medina Castello Ignacio, Norrback Karl-Fredrik, Goossens Dirk, Van Steen Kristel, Adolfsson Rolf, Del-Favero Jurg |
Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes.
Molecular psychiatry 2011 Nov 16 (11): 1096-104, 1063. Carless M A, Glahn D C, Johnson M P, Curran J E, Bozaoglu K, Dyer T D, Winkler A M, Cole S A, Almasy L, MacCluer J W, Duggirala R, Moses E K, Göring H H H, Blangero |
| Association study between Disrupted-in-Schizophrenia-1 (DISC1) and Japanese patients with treatment-resistant schizophrenia (TRS). Progress in neuro-psychopharmacology & biological psychiatry 2011 Mar 35 (2): 636-9. Hotta Yuri, Ohnuma Tohru, Hanzawa Ryo, Shibata Nobuto, Maeshima Hitoshi, Baba Hajime, Hatano Tokiko, Takebayashi Yuto, Kitazawa Maiko, Higa Motoyuki, Suzuki Toshihito, Arai He |
| Most reported genetic associations with general intelligence are probably false positives. Psychological science 2012 23 (11): 1314-23. Chabris Christopher F, Hebert Benjamin M, Benjamin Daniel J, Beauchamp Jonathan, Cesarini David, van der Loos Matthijs, Johannesson Magnus, Magnusson Patrik K E, Lichtenstein Paul, Atwood Craig S, Freese Jeremy, Hauser Taissa S, Hauser Robert M, Christakis Nicholas, Laibson Dav |
| Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology. Translational psychiatry 2012 7 1 (7): e22. Braunewell K H, Dwary A D, Richter F, Trappe K, Zhao C, Giegling I, Schönrath K, Rujescu |
| Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. PLoS computational biology 2012 8 (7): e1002587. Jia Peilin, Wang Lily, Fanous Ayman H, Pato Carlos N, Edwards Todd L, , Zhao Zhongmi |
| Genetic copy number variants in myocardial infarction patients with hyperlipidemia. BMC genomics 2011 Nov 12 Suppl 3 S23. Shia Wei-Chung, Ku Tien-Hsiung, Tsao Yu-Ming, Hsia Chien-Hsun, Chang Yung-Ming, Huang Ching-Hui, Chung Yeh-Ching, Hsu Shih-Lan, Liang Kae-Woei, Hsu Fang-Ro |
| Effects of a mis-sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Apr 159B (3): 343-53. Whalley Heather C, Sussmann Jessika E, Johnstone Mandy, Romaniuk Liana, Redpath Holly, Chakirova Goultchira, Mukherjee Prerona, Hall Jeremy, Johnstone Eve C, Lawrie Stephen M, McIntosh Andrew |
| 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. Molecular psychiatry 2014 Jun 19 (6): 668-75. Thomson P A, Parla J S, McRae A F, Kramer M, Ramakrishnan K, Yao J, Soares D C, McCarthy S, Morris S W, Cardone L, Cass S, Ghiban E, Hennah W, Evans K L, Rebolini D, Millar J K, Harris S E, Starr J M, MacIntyre D J, , McIntosh A M, Watson J D, Deary I J, Visscher P M, Blackwood D H, McCombie W R, Porteous D |
| The DAO gene is associated with schizophrenia and interacts with other genes in the Taiwan Han Chinese population. PloS one 2013 8 (3): e60099. Yang Hsin-Chou, Liu Chih-Min, Liu Yu-Li, Chen Chia-Wei, Chang Chien Ching, Fann Cathy S J, Chiou Jen-Jie, Yang Ueng-Cheng, Chen Chun-Houh, Faraone Stephen V, Tsuang Ming T, Hwu Hai-G |
| DISC1-TSNAX and DAOA genes in major depression and citalopram efficacy. Journal of affective disorders 2014 Oct 168 91-7. Arias Bárbara, Fabbri Chiara, Serretti Alessandro, Drago Antonio, Mitjans Marina, Gastó Cristóbal, Catalán Rosa, Fañanás Lourd |
| Association between 5q23.2-located polymorphism of CTXN3 gene (Cortexin 3) and schizophrenia in European-Caucasian males; implications for the aetiology of schizophrenia. Behavioral and brain functions : BBF 2015 11 10. Šerý Omar, Lochman Jan, Povová Jana, Janout Vladimír, Plesník Ji?í, Balcar Vladimir |
| NAT2 polymorphisms and risk for Parkinson's disease: a systematic review and meta-analysis. Expert opinion on drug metabolism & toxicology 2016 May . Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, García-Martín Elena, Agúndez José A |
| Association of DISC1 Polymorphisms with Late-Onset Alzheimer's Disease in Northern Han Chinese. Molecular neurobiology 2017 05 54 (4): 2922-2927. Zhang Xiao-Yan, Wang Hui-Fu, Tan Meng-Shan, Wan Yu, Kong Ling-Li, Zheng Zhan-Jie, Tan Chen-Chen, Zhang Wei, Wang Zi-Xuan, Tan Lin, Jiang Teng, Tan Lan, Yu Jin-T |
| Secondary association of PDLIM5 with paranoid schizophrenia in Emirati patients. Meta gene 2015 Sep 5 135-9. Moselhy Hamdy, Eapen Valsamma, Akawi Nadia A, Younis Ali, Salih Badr, Othman Aws R, Yousef Said, Clarke Raymond A, Ali Bassam |
| The association between gene variants and longitudinal structural brain changes in psychosis: a systematic review of longitudinal neuroimaging genetics studies. NPJ schizophrenia 2017 Nov 3 (1): 40. Harari Julia H, Díaz-Caneja Covadonga M, Janssen Joost, Martínez Kenia, Arias Bárbara, Arango Cel |
| DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness. Translational psychiatry 2018 9 8 (1): 184. Malavasi Elise L V, Economides Kyriakos D, Grünewald Ellen, Makedonopoulou Paraskevi, Gautier Philippe, Mackie Shaun, Murphy Laura C, Murdoch Hannah, Crummie Darragh, Ogawa Fumiaki, McCartney Daniel L, O'Sullivan Shane T, Burr Karen, Torrance Helen S, Phillips Jonathan, Bonneau Marion, Anderson Susan M, Perry Paul, Pearson Matthew, Constantinides Costas, Davidson-Smith Hazel, Kabiri Mostafa, Duff Barbara, Johnstone Mandy, Polites H Greg, Lawrie Stephen M, Blackwood Douglas H, Semple Colin A, Evans Kathryn L, Didier Michel, Chandran Siddharthan, McIntosh Andrew M, Price David J, Houslay Miles D, Porteous David J, Millar J Kirs |
| Alcohol consumption and risk for Parkinson's disease: a systematic review and meta-analysis. Journal of neurology 2018 8 266 (8): 1821-1834. Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, García-Martín Elena, Agúndez José A |
| Gene expression over the course of schizophrenia: from clinical high-risk for psychosis to chronic stages. NPJ schizophrenia 2019 Mar 5 (1): 5. Ota Vanessa Kiyomi, Moretti Patricia Natalia, Santoro Marcos Leite, Talarico Fernanda, Spindola Leticia Maria, Xavier Gabriela, Carvalho Carolina Muniz, Marques Diogo Ferri, Costa Giovany Oliveira, Pellegrino Renata, de Jong Simone, Cordeiro Quirino, Hakonarson Hakon, Breen Gerome, Noto Cristiano, Bressan Rodrigo Affonseca, Gadelha Ary, Jesus Mari Jair de, Belangero Sintia |
| Screening of Graves' disease susceptibility genes by whole exome sequencing in a three-generation family. BMC medical genomics 2021 Feb 14 (1): 46. Hu Zhuoqing, Li Wei, Li Miaosheng, Wei Hao, Hu Zhihui, Chen Yanting, Luo Ai, Li Wang |
| Combining fMRI and DISC1 gene haplotypes to understand working memory-related brain activity in schizophrenia. Scientific reports 2022 5 12 (1): 7351. Guardiola-Ripoll Maria, Sotero-Moreno Alejandro, Almodóvar-Payá Carmen, Hostalet Noemí, Guerrero-Pedraza Amalia, Ramiro Núria, Ortiz-Gil Jordi, Arias Bárbara, Madre Mercè, Soler-Vidal Joan, Salvador Raymond, McKenna Peter J, Pomarol-Clotet Edith, Fatjó-Vilas M |
| Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia. Archives of medical research 2022 4 53 (4): 388-398. Fricke-Galindo Ingrid, Pérez-Aldana Blanca E, Macías-Kauffer Luis R, González-Arredondo Susana, Dávila-Ortiz de Montellano David, Aviña-Cervantes Carlos L, López-López Marisol, Rodríguez-Agudelo Yaneth, Monroy-Jaramillo Nan |
| The variants in PTPRB, TRAF3IP3, and DISC1 genes were associated with Graves' disease in the Chinese population. Medicine 2022 11 101 (45): e31501. Li Wei, Jiang Haidong, Chen Xu, Yang Kevin, Deng Xindan, Tang Zheng, Hu Zhihui, Zhang Xiaodan, Lin Shihan, Zou Yuanlin, Wu H |
| Association Between Wnt Target Genes and Cortical Volumes in Alzheimer's Disease. Journal of molecular neuroscience : MN 2023 12 73 (11-12): 1010-1016. Liling Dong, Bo Hou, Caiyan Liu, Chenhui Mao, Xinying Huang, Li Shang, Shanshan Chu, Bin Peng, Liying Cui, Feng Feng, Jing G |
| Structural Variants and Implicated Processes Associated with Familial Tourette Syndrome. International journal of molecular sciences 2024 6 25 (11): . Jakub P Fichna, Mateusz Chili?ski, Anup Kumar Halder, Pawe? Ci?szczyk, Dariusz Plewczynski, Cezary ?ekanowski, Piotr Jan |
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