Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: PCM1[original query] |
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Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia. Archives of general psychiatry 2006 Aug 63 (8): 844-54. Gurling Hugh M D, Critchley Hugo, Datta Susmita R, McQuillin Andrew, Blaveri Ekaterina, Thirumalai Srinivasa, Pimm Jonathan, Krasucki Robert, Kalsi Gursharan, Quested Digby, Lawrence Jacob, Bass Nicholas, Choudhury Khalid, Puri Vinay, O'Daly Owen, Curtis David, Blackwood Douglas, Muir Walter, Malhotra Anil K, Buchanan Robert W, Good Catriona D, Frackowiak Richard S J, Dolan Raymond |
A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular psychiatry 2010 Jun 15 (6): 615-28. Datta S R, McQuillin A, Rizig M, Blaveri E, Thirumalai S, Kalsi G, Lawrence J, Bass N J, Puri V, Choudhury K, Pimm J, Crombie C, Fraser G, Walker N, Curtis D, Zvelebil M, Pereira A, Kandaswamy R, St Clair D, Gurling H M |
PCM1 and schizophrenia: a replication study in the Northern Swedish population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Sep 153B (6): 1240-3. Moens Lotte N, Ceulemans Shana, Alaerts Maaike, Van Den Bossche Maarten J A, Lenaerts An-Sofie, De Zutter Sonia, Norrback Karl-Fredrik, Adolfsson Rolf, Del-Favero Jurg |
The DISC1 Ser704Cys substitution affects centrosomal localization of its binding partner PCM1 in glia in human brain. Human molecular genetics 2010 Jun 19 (12): 2487-96. Eastwood Sharon L, Walker Mary, Hyde Thomas M, Kleinman Joel E, Harrison Paul |
No association between the PCM1 gene and schizophrenia: a multi-center case-control study and a meta-analysis. Schizophrenia research 2011 Jun 129 (1): 80-4. Hashimoto Ryota, Ohi Kazutaka, Yasuda Yuka, Fukumoto Motoyuki, Yamamori Hidenaga, Kamino Kouzin, Morihara Takashi, Iwase Masao, Kazui Hiroaki, Numata Shusuke, Ikeda Masashi, Ueno Shu-Ichi, Ohmori Tetsuro, Iwata Nakao, Ozaki Norio, Takeda Masatos |
Targeted resequencing of the microRNAome and 3'UTRome reveals functional germline DNA variants with altered prevalence in epithelial ovarian cancer. Oncogene 2015 Apr 34 (16): 2125-37. Chen X, Paranjape T, Stahlhut C, McVeigh T, Keane F, Nallur S, Miller N, Kerin M, Deng Y, Yao X, Zhao H, Weidhaas J B, Slack F |
RACK1 is a candidate gene associated with the prognosis of patients with early stage non-small cell lung cancer. Oncotarget 2015 Feb 6 (6): 4451-66. Choi Yi-Young, Lee Shin Yup, Lee Won Kee, Jeon Hyo-Sung, Lee Eung Bae, Lee Hyun Cheol, Choi Jin Eun, Kang Hyo-Gyoung, Lee Eun Jin, Bae Eun Young, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Kim In-San, Lee Myung Hoon, Kim Young Tae, Jheon Sanghoon, Park Jae Yo |
Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency. BioMed research international 2016 3 2015 862039. Sandgren Johanna, Holm Stefan, Marino Ana Maria, Asmundsson Jurate, Grillner Pernilla, Nistér Monica, Díaz de Ståhl Teresi |
The utilization of next-generation sequencing to detect somatic mutations and predict clinical prognosis of Chinese non-small cell lung cancer patients. OncoTargets and therapy 2018 11 2637-2646. Cao Liming, Long Long, Li Min, Yang Huaping, Deng Pengbo, Mao Xinru, Xiang Jianxing, Li Bing, Zhang Tengfei, Hu Chengpi |
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. Circulation research 2019 Feb 124 (4): 553-563. Page Donna J, Miossec Matthieu J, Williams Simon G, Monaghan Richard M, Fotiou Elisavet, Cordell Heather J, Sutcliffe Louise, Topf Ana, Bourgey Mathieu, Bourque Guillaume, Eveleigh Robert, Dunwoodie Sally L, Winlaw David S, Bhattacharya Shoumo, Breckpot Jeroen, Devriendt Koenraad, Gewillig Marc, Brook J David, Setchfield Kerry J, Bu'Lock Frances A, O'Sullivan John, Stuart Graham, Bezzina Connie R, Mulder Barbara J M, Postma Alex V, Bentham James R, Baron Martin, Bhaskar Sanjeev S, Black Graeme C, Newman William G, Hentges Kathryn E, Lathrop G Mark, Santibanez-Koref Mauro, Keavney Bernard |
PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia. Nature communications 2020 11 11 (1): 5903. Monroe Tanner O, Garrett Melanie E, Kousi Maria, Rodriguiz Ramona M, Moon Sungjin, Bai Yushi, Brodar Steven C, Soldano Karen L, Savage Jeremiah, Hansen Thomas F, Muzny Donna M, Gibbs Richard A, Barak Lawrence, Sullivan Patrick F, Ashley-Koch Allison E, Sawa Akira, Wetsel William C, Werge Thomas, Katsanis Nichol |
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
MET gene alterations predict poor survival following chemotherapy in patients with advanced cancer. Pathology oncology research : POR 2022 12 28 1610697. Ko Jihoon, Jung Jaeyun, Kim Seung Tae, Hong Jung Yong, Park Sehhoon, Park Joon Oh, Park Young Suk, Lim Ho Yeong, Ahn Soomin, Kim Kyoung-Mee, Kang Won Ki, Lee Jeey |
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- Page last updated:Apr 22, 2024
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