Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: PCNT[original query] |
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Positive association of the pericentrin (PCNT) gene with major depressive disorder in the Japanese population. Journal of psychiatry & neuroscience : JPN 2009 May 34 (3): 195-8. Numata Shusuke, Iga Jun-Ichi, Nakataki Masahito, Tayoshi Shin'ya, Tanahashi Toshihito, Itakura Mitsuo, Ueno Shu-Ichi, Ohmori Tetsu |
Association study between the pericentrin (PCNT) gene and schizophrenia. Neuromolecular medicine 2010 Sep 12 (3): 243-7. Numata Shusuke, Nakataki Masahito, Iga Jun-ichi, Tanahashi Toshihito, Nakadoi Yoshihiro, Ohi Kazutaka, Hashimoto Ryota, Takeda Masatoshi, Itakura Mitsuo, Ueno Shu-ichi, Ohmori Tetsu |
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of human genetics 2015 Jul 60 (7): 399-401. Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo Ht, Peyrard-Janvid Myriam, Kere Ju |
A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report. Biomedical reports 2019 7 1 (1): 1-5. Orru Sandro, Papoulidis Ioannis, Siomou Elisavet, Papadimitriou Dimitrios T, Sotiriou Sotirios, Nikolaidis Petros, Eleftheriades Makarios, Papanikolaou Evaggelos, Thomaidis Loretta, Manolakos Emmanou |
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019 2 180 (3): 223-231. Harold Denise, Connolly Siobhan, Riley Brien P, Kendler Kenneth S, McCarthy Shane E, McCombie William R, Richards Alex, Owen Michael J, O'Donovan Michael C, Walters James, , , Donohoe Gary, Gill Michael, Corvin Aiden, Morris Derek |
Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage. Journal of neurology 2020 May . Sauvigny Thomas, Alawi Malik, Krause Linda, Renner Sina, Spohn Michael, Busch Alice, Kolbe Verena, Altmüller Janine, Löscher Britt-Sabina, Franke Andre, Brockmann Christian, Lieb Wolfgang, Westphal Manfred, Schmidt Nils Ole, Regelsberger Jan, Rosenberger Geo |
Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. American journal of medical genetics. Part A 2020 4 182 (6): 1407-1420. Abdel-Salam Ghada M H, Sayed Inas S M, Afifi Hanan H, Abdel-Ghafar Sherif F, Abouzaid Maha R, Ismail Samira I, Aglan Mona S, Issa Mahmoud Y, El-Bassyouni Hala T, El-Kamah Ghada, Effat Laila K, Eid Maha, Zaki Maha S, Temtamy Samia A, Abdel-Hamid Mohamed |
Family-Based Analysis Combined with Case-Controls Study Implicate Roles of PCNT in Tourette Syndrome. Neuropsychiatric disease and treatment 2020 16 349-354. Liu Wenmiao, Guo Yixia, Liu Xiumei, Zhang Ru, Dong Jicheng, Deng Hao, He Fan, Che Fengyuan, Liu Shiguo, Yi Ming |
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism. EBioMedicine 2021 8 71 103530. Lam Wai-Yee, Tang Clara Sze-Man, So Man-Ting, Yue Haibing, Hsu Jacob Shujui, Chung Patrick Ho-Yu, Nicholls John M, Yeung Fanny, Lee Chun-Wai Davy, Ngo Diem Ngoc, Nguyen Pham Anh Hoa, Mitchison Hannah M, Jenkins Dagan, O'Callaghan Christopher, Garcia-Barceló Maria-Mercè, Lee So-Lun, Sham Pak-Chung, Lui Vincent Chi-Hang, Tam Paul Kwong-Ha |
Coding variants in the PCNT and CEP295 genes contribute to breast cancer risk in Chinese women. Pathology, research and practice 2021 8 225 153581. Zhou Jing, Chen Congcong, Zhao Xiaoyu, Jiang Tao, Jiang Yue, Dai Juncheng, Chen Jiapi |
The mutational landscape and prognostic indicators of pseudomyxoma peritonei originating from the ovary. International journal of cancer 2021 1 148 (8): 2036-2047. Wang Bing, Yao Jianfei, Ma Ruiqing, Liu Danni, Lu Yiyan, Shi Guanjun, An Lubiao, Xia Ao, Chen Feng, Pang Shaojun, Zhai Xichao, Liu Guifeng, Chen Shifu, Xu Mingyan, Song Lele, Xu Hongb |
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. Medicina (Kaunas, Lithuania) 2023 8 59 (8): . Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo, Santina Città, Concetta Federico, Luigi Vetri, Salvatore Saccone, Serafino Buo |
Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses. Frontiers in endocrinology 2023 4 14 1143067. Mansour Afnan, Mousa Mira, Abdelmannan Dima, Tay Guan, Hassoun Ahmed, Alsafar Habi |
Ciliary phenotyping in renal epithelial cells in a cranioectodermal dysplasia patient with WDR35 variants. Frontiers in molecular biosciences 2024 1 10 1285790. Joanna Walczak-Sztulpa, Anna Wawrocka, ?ukasz Kuszel, Paulina Pietras, Marta Le?niczak-Staszak, Miros?aw Andrusiewicz, Maciej R Krawczy?ski, Anna Latos-Biele?ska, Marta Pawlak, Ryszard Grenda, Anna Materna-Kiryluk, Machteld M Oud, Witold Szaflars |
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- Page last updated:Apr 22, 2024
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