Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 42 Records) |
| Query Trace: Disease and CACNA1C[original query] |
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| Further evidence for genetic association of CACNA1C and schizophrenia: new risk loci in a Han Chinese population and a meta-analysis. Schizophrenia research 2014 Jan 152 (1): 105-10. Zheng Fanfan, Zhang Yanling, Xie Wuxiang, Li Wenqiang, Jin Chao, Mi Weifeng, Wang Fang, Ma Wenbin, Ma Cuicui, Yang Yongfeng, Du Bo, Li Keqing, Liu Chenxing, Wang Lifang, Lu Tianlan, Zhang Hongyan, Wang Yun, Lu Lin, Lv Luxian, Zhang Dai, Yue Weih |
| Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data. Bipolar disorders 2014 Sep 16 (6): 583-91. Fiorentino Alessia, O'Brien Niamh Louise, Locke Devin Paul, McQuillin Andrew, Jarram Alexandra, Anjorin Adebayo, Kandaswamy Radhika, Curtis David, Blizard Robert Alan, Gurling Hugh Malcolm Dougl |
| Functional implications of a psychiatric risk variant within CACNA1C in induced human neurons. Molecular psychiatry 2015 Feb 20 (2): 162-9. Yoshimizu T, Pan J Q, Mungenast A E, Madison J M, Su S, Ketterman J, Ongur D, McPhie D, Cohen B, Perlis R, Tsai L |
| Hippocampal and frontolimbic function as intermediate phenotype for psychosis: evidence from healthy relatives and a common risk variant in CACNA1C. Biological psychiatry 2014 Sep 76 (6): 466-75. Erk Susanne, Meyer-Lindenberg Andreas, Schmierer Phöbe, Mohnke Sebastian, Grimm Oliver, Garbusow Maria, Haddad Leila, Poehland Lydia, Mühleisen Thomas W, Witt Stephanie H, Tost Heike, Kirsch Peter, Romanczuk-Seiferth Nina, Schott Björn H, Cichon Sven, Nöthen Markus M, Rietschel Marcella, Heinz Andreas, Walter Henr |
| Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human molecular genetics 2015 May 24 (10): 2757-63. Le Scouarnec Solena, Karakachoff Matilde, Gourraud Jean-Baptiste, Lindenbaum Pierre, Bonnaud Stéphanie, Portero Vincent, Duboscq-Bidot Laëtitia, Daumy Xavier, Simonet Floriane, Teusan Raluca, Baron Estelle, Violleau Jade, Persyn Elodie, Bellanger Lise, Barc Julien, Chatel Stéphanie, Martins Raphaël, Mabo Philippe, Sacher Frédéric, Haïssaguerre Michel, Kyndt Florence, Schmitt Sébastien, Bézieau Stéphane, Le Marec Hervé, Dina Christian, Schott Jean-Jacques, Probst Vincent, Redon Richa |
| A common risk variant in CACNA1C supports a sex-dependent effect on longitudinal functioning and functional recovery from episodes of schizophrenia-spectrum but not bipolar disorder. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2015 Oct . Heilbronner Urs, Malzahn Dörthe, Strohmaier Jana, Maier Sandra, Frank Josef, Treutlein Jens, Mühleisen Thomas W, Forstner Andreas J, Witt Stephanie H, Cichon Sven, Falkai Peter, Nöthen Markus M, Rietschel Marcella, Schulze Thomas |
| Functional Characterization of Schizophrenia-Associated Variation in CACNA1C. PloS one 2016 11 (6): e0157086. Eckart Nicole, Song Qifeng, Yang Rebecca, Wang Ruihua, Zhu Heng, McCallion Andrew S, Avramopoulos Dimitri |
| DNA variants in CACNA1C modify Parkinson disease risk only when vitamin D level is deficient. Neurology. Genetics 2016 Jun 2 (3): e72. Wang Liyong, Maldonado Lizmarie, Beecham Gary W, Martin Eden R, Evatt Marian L, Ritchie James C, Haines Jonathan L, Zabetian Cyrus P, Payami Haydeh, Pericak-Vance Margaret A, Vance Jeffery M, Scott William |
| Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiology of aging 2016 Feb 38 141-50. Hohman Timothy J, Bush William S, Jiang Lan, Brown-Gentry Kristin D, Torstenson Eric S, Dudek Scott M, Mukherjee Shubhabrata, Naj Adam, Kunkle Brian W, Ritchie Marylyn D, Martin Eden R, Schellenberg Gerard D, Mayeux Richard, Farrer Lindsay A, Pericak-Vance Margaret A, Haines Jonathan L, Thornton-Wells Tricia A, |
| Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
| Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. Molecular psychiatry 2018 03 23 (3): 533-543. Dedic N, Pöhlmann M L, Richter J S, Mehta D, Czamara D, Metzger M W, Dine J, Bedenk B T, Hartmann J, Wagner K V, Jurik A, Almli L M, Lori A, Moosmang S, Hofmann F, Wotjak C T, Rammes G, Eder M, Chen A, Ressler K J, Wurst W, Schmidt M V, Binder E B, Deussing J |
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function.
The Journal of clinical investigation 2017 May 127 (5): 1798-1812. Wild Philipp S, Felix Janine F, Schillert Arne, Teumer Alexander, Chen Ming-Huei, Leening Maarten J G, Völker Uwe, Großmann Vera, Brody Jennifer A, Irvin Marguerite R, Shah Sanjiv J, Pramana Setia, Lieb Wolfgang, Schmidt Reinhold, Stanton Alice V, Malzahn Dörthe, Smith Albert Vernon, Sundström Johan, Minelli Cosetta, Ruggiero Daniela, Lyytikäinen Leo-Pekka, Tiller Daniel, Smith J Gustav, Monnereau Claire, Di Tullio Marco R, Musani Solomon K, Morrison Alanna C, Pers Tune H, Morley Michael, Kleber Marcus E, Aragam Jayashri, Benjamin Emelia J, Bis Joshua C, Bisping Egbert, Broeckel Ulrich, Cheng Susan, Deckers Jaap W, Del Greco M Fabiola, Edelmann Frank, Fornage Myriam, Franke Lude, Friedrich Nele, Harris Tamara B, Hofer Edith, Hofman Albert, Huang Jie, Hughes Alun D, Kähönen Mika, Investigators Knhi, Kruppa Jochen, Lackner Karl J, Lannfelt Lars, Laskowski Rafael, Launer Lenore J, Leosdottir Margrét, Lin Honghuang, Lindgren Cecilia M, Loley Christina, MacRae Calum A, Mascalzoni Deborah, Mayet Jamil, Medenwald Daniel, Morris Andrew P, Müller Christian, Müller-Nurasyid Martina, Nappo Stefania, Nilsson Peter M, Nuding Sebastian, Nutile Teresa, Peters Annette, Pfeufer Arne, Pietzner Diana, Pramstaller Peter P, Raitakari Olli T, Rice Kenneth M, Rivadeneira Fernando, Rotter Jerome I, Ruohonen Saku T, Sacco Ralph L, Samdarshi Tandaw E, Schmidt Helena, Sharp Andrew S P, Shields Denis C, Sorice Rossella, Sotoodehnia Nona, Stricker Bruno H, Surendran Praveen, Thom Simon, Töglhofer Anna M, Uitterlinden André G, Wachter Rolf, Völzke Henry, Ziegler Andreas, Münzel Thomas, März Winfried, Cappola Thomas P, Hirschhorn Joel N, Mitchell Gary F, Smith Nicholas L, Fox Ervin R, Dueker Nicole D, Jaddoe Vincent W V, Melander Olle, Russ Martin, Lehtimäki Terho, Ciullo Marina, Hicks Andrew A, Lind Lars, Gudnason Vilmundur, Pieske Burkert, Barron Anthony J, Zweiker Robert, Schunkert Heribert, Ingelsson Erik, Liu Kiang, Arnett Donna K, Psaty Bruce M, Blankenberg Stefan, Larson Martin G, Felix Stephan B, Franco Oscar H, Zeller Tanja, Vasan Ramachandran S, Dörr Marc |
| Genetic Risk Score Analysis in Early-Onset Bipolar Disorder. The Journal of clinical psychiatry 2017 Feb . Croarkin Paul E, Luby Joan L, Cercy Kelly, Geske Jennifer R, Veldic Marin, Simonson Matthew, Joshi Paramjit T, Wagner Karen Dineen, Walkup John T, Nassan Malik M, Cuellar-Barboza Alfredo B, Casuto Leah, McElroy Susan L, Jensen Peter S, Frye Mark A, Biernacka Joanna |
| Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A. Annals of laboratory medicine 2017 10 38 (1): 54-58. Seo Soo Hyun, Kim So Yeon, Cho Sung Im, Park Hyunwoong, Lee Seungjun, Choi Jong Moon, Kim Man Jin, Lee Jee Soo, Ahn Kyung Jin, Song Mi Kyoung, Bae Eun Jung, Park Sung Sup, Seong Moon W |
| Genome-Wide Supported Risk Variants in MIR137, CACNA1C, CSMD1, DRD2, and GRM3 Contribute to Schizophrenia Susceptibility in Pakistani Population. Psychiatry investigation 2017 Sep 14 (5): 687-692. Fatima Ambrin, Farooq Muhammad, Abdullah Uzma, Tariq Muhammad, Mustafa Tanveer, Iqbal Muhammad, Tommerup Niels, Mahmood Baig Shah |
| The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia? International journal of cardiology 2017 10 250 139-145. Leinonen Jaakko T, Crotti Lia, Djupsjöbacka Aurora, Castelletti Silvia, Junna Nella, Ghidoni Alice, Tuiskula Annukka M, Spazzolini Carla, Dagradi Federica, Viitasalo Matti, Kontula Kimmo, Kotta Maria-Christina, Widén Elisabeth, Swan Heikki, Schwartz Peter |
| Detection of Variants in Patients with Idiopathic Ventricular Fibrillation by Whole-exome Sequencing. Annals of clinical and laboratory science 2018 8 48 (4): 427-434. Chang Ya-Sian, Lee Chien-Chin, Huang Hsi-Yuan, Lin Kuo-Hung, Chen Jan-Yow, Chang Kuan-Cheng, Chang Jan-Gow |
| Association of CACNA1C with bipolar disorder among the Pakistani population. Gene 2018 Apr . Khalid Madiha, Driessen Terri M, Lee Jong Seo, Tejwani Leon, Rasool Asad, Saqlain Muhammad, Shiaq Pakeeza Arzoo, Hanif Muhammad, Nawaz Amber, DeWan Andrew T, Raja Ghazala Kaukab, Lim Jangh |
| Exploring different impaired speed of genetic-related brain function and structures in schizophrenic progress using multimodal analysis. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2018 11 2018 4126-4129. Luo Na, Tian Lin, Calhoun Vince D, Chen Jiayu, Lin Dongdong, Vergara Victor M, Rao Shuquan, Zhang Fuquan, Sui Ji |
| Genes Involved in Neurodevelopment, Neuroplasticity and Major Depression: No Association for CACNA1C, CHRNA7 and MAPK1. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2019 Aug 17 (3): 364-368. Calabrò Marco, Mandelli Laura, Crisafulli Concetta, Lee Soo-Jung, Jun Tae-Youn, Wang Sheng-Min, Patkar Ashwin A, Masand Prakash S, Han Changsu, Pae Chi-Un, Serretti Alessand |
| Interaction of the Psychiatric Risk Gene Cacna1c With Post-weaning Social Isolation or Environmental Enrichment Does Not Affect Brain Mitochondrial Bioenergetics in Rats. Frontiers in cellular neuroscience 2019 13 483. Michels Susanne, Dolga Amalia M, Braun Moria D, Kisko Theresa M, Sungur A Özge, Witt Stephanie H, Rietschel Marcella, Dempfle Astrid, Wöhr Markus, Schwarting Rainer K W, Culmsee Carst |
| Long-term environmental impact on object recognition, spatial memory and reversal learning capabilities in Cacna1c-haploinsufficient rats. Human molecular genetics 2019 10 28 (24): 4113-4131. Braun Moria D, Kisko Theresa M, Witt Stephanie H, Rietschel Marcella, Schwarting Rainer K W, Wöhr Mark |
| Clinical characterization and outcome of prolonged heart rate-corrected QT interval among children with syndactyly. Medicine 2020 10 99 (42): e22740. Han Hao, Chen Youzhou, Li Songnan, Ren Lan, Zhang Jianqiang, Sun Huayi, Dong Jianzeng, Zhao Xingsh |
| The association of polymorphisms in related circadian rhythm genes and clopidogrel resistance susceptibility. Basic & clinical pharmacology & toxicology 2021 6 129 (3): 196-209. Su Jia, Yu Qinglin, Yang Jin, Zheng Nan, Zhong Jinyan, Ji Lindan, Li Jiyi, Chen Xiaom |
| The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms. Neurobiology of disease 2021 May 155 105394. Hidalgo Sergio, Campusano Jorge M, Hodge James J |
| Diverse genetic causes of polymicrogyria with epilepsy. Epilepsia 2021 Apr 62 (4): 973-983. Authors are not available |
| Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population. Genes 2021 Oct 12 (10): . Bocharova Anna, Vagaitseva Kseniya, Marusin Andrey, Zhukova Natalia, Zhukova Irina, Minaycheva Larisa, Makeeva Oksana, Stepanov Vad |
| Can an Investigation of a Single Gene be Effective in Differentiating Certain Features of the Bipolar Disorder Profile? Clinical practice and epidemiology in mental health : CP & EMH 2022 2 17 187-189. Piras Martina, Scano Alessandra, Orrù Germano, Preti Antonio, Marchese Cinzia, Kalcev Go |
| Pleiotropic Association of CACNA1C Variants With Neuropsychiatric Disorders. Schizophrenia bulletin 2023 6 . Zuxing Wang, Xiandong Lin, Xinqun Luo, Jun Xiao, Yong Zhang, Jianying Xu, Shibin Wang, Fen Zhao, Huifen Wang, Hangxiao Zheng, Wei Zhang, Chen Lin, Zewen Tan, Liping Cao, Zhiren Wang, Yunlong Tan, Wenzhong Chen, Yuping Cao, Xiaoyun Guo, Christopher Pittenger, Xingguang L |
| Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome. Heart rhythm 2023 2 . Christiansen Morten Krogh, Kjær-Sørensen Kasper, Clavsen Natacha C, Dittmann Sven, Jensen Maja Fuhlendorff, Guldbrandsen Halvor Østerby, Pedersen Lisbeth Nørum, Sørensen Rikke Hasle, Lildballe Dorte Launholt, Müller Klara, Müller Patrick, Vogel Kira, Rudic Boris, Borggrefe Martin, Oxvig Claus, Aalkjær Christian, Schulze-Bahr Eric, Matchkov Vladimir, Bundgaard Henning, Jensen Henrik Kjæru |
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