Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: CACNA1E[original query] |
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Association analysis of chromosome 1 migraine candidate genes. BMC medical genetics 2007 8 (1): 57. Fernandez Francesca, Curtain Robert P, Colson Natalie J, Ovcaric Micky, MacMillan John, Griffiths Lyn |
Variants in the Ca V 2.3 (alpha 1E) subunit of voltage-activated Ca2+ channels are associated with insulin resistance and type 2 diabetes in Pima Indians. Diabetes 2007 Dec 56 (12): 3089-94. Muller Yunhua Li, Hanson Robert L, Zimmerman Collin, Harper Inge, Sutherland Jeff, Kobes Sayuko, , Knowler William C, Bogardus Clifton, Baier Leslie |
Polymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretion. Diabetologia 2007 Dec 50 (12): 2467-75. Holmkvist J, Tojjar D, Almgren P, Lyssenko V, Lindgren C M, Isomaa B, Tuomi T, Berglund G, Renström E, Groop |
A high-density association screen of 155 ion transport genes for involvement with common migraine. Human molecular genetics 2008 Nov 17 (21): 3318-31. Nyholt Dale R, LaForge K Steven, Kallela Mikko, Alakurtti Kirsi, Anttila Verneri, Färkkilä Markus, Hämaläinen Eija, Kaprio Jaakko, Kaunisto Mari A, Heath Andrew C, Montgomery Grant W, Göbel Hartmut, Todt Unda, Ferrari Michel D, Launer Lenore J, Frants Rune R, Terwindt Gisela M, de Vries Boukje, Verschuren W M Monique, Brand Jan, Freilinger Tobias, Pfaffenrath Volker, Straube Andreas, Ballinger Dennis G, Zhan Yiping, Daly Mark J, Cox David R, Dichgans Martin, van den Maagdenberg Arn M J M, Kubisch Christian, Martin Nicholas G, Wessman Maija, Peltonen Leena, Palotie Aar |
CACNA1E variants affect beta cell function in patients with newly diagnosed type 2 diabetes. the Verona newly diagnosed type 2 diabetes study (VNDS) 3. PloS one 2012 7 (3): e32755. Trombetta Maddalena, Bonetti Sara, Boselli Marialinda, Turrini Fabiola, Malerba Giovanni, Trabetti Elisabetta, Pignatti PierFranco, Bonora Enzo, Bonadonna Riccardo |
Association between genetic polymorphisms in Ca(v)2.3 (R-type) Ca2+ channels and fentanyl sensitivity in patients undergoing painful cosmetic surgery. PloS one 2013 8 (8): e70694. Ide Soichiro, Nishizawa Daisuke, Fukuda Ken-ichi, Kasai Shinya, Hasegawa Junko, Hayashida Masakazu, Minami Masabumi, Ikeda Kazuta |
Exploring the associations between genetic variants in genes encoding for subunits of calcium channel and subtypes of bipolar disorder. Journal of affective disorders 2014 Mar 157 80-6. Jan Wen-Chi, Yang Shi-Yi, Chuang Li-Chung, Lu Ru-Band, Lu Ming-Kun, Sun H Sunny, Kuo Po-Hs |
Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer. EBioMedicine 2015 Jun 2 (6): 583-90. Yu Xian-Jun, Yang Min-Jun, Zhou Bo, Wang Gui-Zhen, Huang Yun-Chao, Wu Li-Chuan, Cheng Xin, Wen Zhe-Sheng, Huang Jin-Yan, Zhang Yun-Dong, Gao Xiao-Hong, Li Gao-Feng, He Shui-Wang, Gu Zhao-Hui, Ma Liang, Pan Chun-Ming, Wang Ping, Chen Hao-Bin, Hong Zhi-Peng, Wang Xiao-Lu, Mao Wen-Jing, Jin Xiao-Long, Kang Hui, Chen Shu-Ting, Zhu Yong-Qiang, Gu Wen-Yi, Liu Zi, Dong Hui, Tian Lin-Wei, Chen Sai-Juan, Cao Yi, Wang Sheng-Yue, Zhou Guang-Bi |
Opposite Associations Between the rs3845446 Single-Nucleotide Polymorphism of the CACNA1E Gene and Postoperative Pain-Related Phenotypes in Gastrointestinal Surgery Versus Previously Reported Orthognathic Surgery. The journal of pain : official journal of the American Pain Society 2016 Jul . Amano Kojiro, Nishizawa Daisuke, Mieda Tsutomu, Tsujita Miki, Kitamura Akira, Hasegawa Junko, Inada Eiichi, Hayashida Masakazu, Ikeda Kazuta |
A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors. Scientific reports 2017 Aug 7 (1): 10252. Brænne Ingrid, Willenborg Christina, Tragante Vinicius, Kessler Thorsten, Zeng Lingyao, Reiz Benedikt, Kleinecke Mariana, von Ameln Simon, Willer Cristen J, Laakso Markku, Wild Philipp S, Zeller Tanja, Wallentin Lars, Franks Paul W, Salomaa Veikko, Dehghan Abbas, Meitinger Thomas, Samani Nilesh J, Asselbergs Folkert W, Erdmann Jeanette, Schunkert Heribe |
Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes. Headache 2017 Jun . Ambrosini Anna, D'Onofrio Mara, Buzzi Maria Gabriella, Arisi Ivan, Grieco Gaetano S, Pierelli Francesco, Santorelli Filippo M, Schoenen Je |
Genetic findings in sport-related concussions: potential for individualized medicine? Concussion (London, England) 2017 Mar 2 (1): CNC26. McDevitt Jane, Krynetskiy Evge |
A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers.
Frontiers in psychiatry 2018 9 290. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yu Younger W-Y, Yang Albert C, Tsai Shih-J |
Novel caries loci in children and adults implicated by genome-wide analysis of families. BMC oral health 2018 6 18 (1): 98. Govil Manika, Mukhopadhyay Nandita, Weeks Daniel E, Feingold Eleanor, Shaffer John R, Levy Steven M, Vieira Alexandre R, Slayton Rebecca L, McNeil Daniel W, Weyant Robert J, Crout Richard J, Marazita Mary |
De novo variants in neurodevelopmental disorders with epilepsy. Nature genetics 2018 6 50 (7): 1048-1053. Heyne Henrike O, Singh Tarjinder, Stamberger Hannah, Abou Jamra Rami, Caglayan Hande, Craiu Dana, De Jonghe Peter, Guerrini Renzo, Helbig Katherine L, Koeleman Bobby P C, Kosmicki Jack A, Linnankivi Tarja, May Patrick, Muhle Hiltrud, Møller Rikke S, Neubauer Bernd A, Palotie Aarno, Pendziwiat Manuela, Striano Pasquale, Tang Sha, Wu Sitao, , Poduri Annapurna, Weber Yvonne G, Weckhuysen Sarah, Sisodiya Sanjay M, Daly Mark J, Helbig Ingo, Lal Dennis, Lemke Johannes |
Somatic mutations in early onset luminal breast cancer. Oncotarget 2018 Apr 9 (32): 22460-22479. Encinas Giselly, Sabelnykova Veronica Y, de Lyra Eduardo Carneiro, Hirata Katayama Maria Lucia, Maistro Simone, de Vasconcellos Valle Pedro Wilson Mompean, de Lima Pereira Gláucia Fernanda, Rodrigues Lívia Munhoz, de Menezes Pacheco Serio Pedro Adolpho, de Gouvêa Ana Carolina Ribeiro Chaves, Geyer Felipe Correa, Basso Ricardo Alves, Pasini Fátima Solange, Del Pilar Esteves Diz Maria, Brentani Maria Mitzi, Guedes Sampaio Góes João Carlos, Chammas Roger, Boutros Paul C, Koike Folgueira Maria Aparecida Azeve |
DNA polymorphisms predict time to progression from uncomplicated to complicated Crohn's disease. European journal of gastroenterology & hepatology 2018 1 30 (4): 447-455. Pernat Drobež Cvetka, Repnik Katja, Gorenjak Mario, Ferkolj Ivan, Weersma Rinse K, Poto?nik Ur |
PPARGC1B Is Associated with Nontraumatic Osteonecrosis of the Femoral Head: A Genomewide Association Study on a Chart-Reviewed Cohort.
The Journal of bone and joint surgery. American volume 2020 Sep 102 (18): 1628-1636. Zhang Yanfei, Bowen Thomas R, Lietman Steven A, Suk Michael, Williams Marc S, Lee Ming Ta Micha |
Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia. Biomedicines 2020 5 8 (5): . Maksemous Neven, Sutherland Heidi G, Smith Robert A, Haupt Larisa M, Griffiths Lyn |
De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures. Molecular autism 2021 10 12 (1): 69. Royer-Bertrand Beryl, Jequier Gygax Marine, Cisarova Katarina, Rosenfeld Jill A, Bassetti Jennifer A, Moldovan Oana, O'Heir Emily, Burrage Lindsay C, Allen Jake, Emrick Lisa T, Eastman Emma, Kumps Camille, Abbas Safdar, Van Winckel Geraldine, , Chabane Nadia, Zackai Elaine H, Lebon Sebastien, Keena Beth, Bhoj Elizabeth J, Umair Muhammad, Li Dong, Donald Kirsten A, Superti-Furga Andr |
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus. NPJ genomic medicine 2022 11 7 (1): 70. Gallego-Martinez Alvaro, Escalera-Balsera Alba, Trpchevska Natalia, Robles-Bolivar Paula, Roman-Naranjo Pablo, Frejo Lidia, Perez-Carpena Patricia, Bulla Jan, Gallus Silvano, Canlon Barbara, Cederroth Christopher R, Lopez-Escamez Jose |
Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes. Molecular neurobiology 2023 2 . Maksemous Neven, Harder Aster V E, Ibrahim Omar, Vijfhuizen Lisanne S, Sutherland Heidi, Pelzer Nadine, de Boer Irene, Terwindt Gisela M, Lea Rodney A, van den Maagdenberg Arn M J M, Griffiths Lyn |
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- Page last updated:Apr 22, 2024
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