Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and CACNA1E[original query] |
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| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Association Study of CACNA1D, KCNJ11, KCNQ1, and CACNA1E Single-Nucleotide Polymorphisms with Type 2 Diabetes Mellitus. International journal of molecular sciences 2024 9 25 (17): . Juan Daniel Díaz-García, Margarita Leyva-Leyva, Fabiola Sánchez-Aguillón, Mercedes Piedad de León-Bautista, Abel Fuentes-Venegas, Alfredo Torres-Viloria, Erika Karina Tenorio-Aguirre, Sara Luz Morales-Lázaro, Angélica Olivo-Díaz, Ricardo González-Ramír |
| Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 Diabetes. Diabetes care 2024 4 . Soo Heon Kwak, Ryan B Hernandez-Cancela, Daniel A DiCorpo, David E Condon, Jordi Merino, Peitao Wu, Jennifer A Brody, Jie Yao, Xiuqing Guo, Fariba Ahmadizar, Mariah Meyer, Murat Sincan, Josep M Mercader, Sujin Lee, Jeffrey Haessler, Ha My T Vy, Zhaotong Lin, Nicole D Armstrong, Shaopeng Gu, Noah L Tsao, Leslie A Lange, Ningyuan Wang, Kerri L Wiggins, Stella Trompet, Simin Liu, Ruth J F Loos, Renae Judy, Philip H Schroeder, Natalie R Hasbani, Maxime M Bos, Alanna C Morrison, Rebecca D Jackson, Alexander P Reiner, JoAnn E Manson, Ninad S Chaudhary, Lynn K Carmichael, Yii-Der Ida Chen, Kent D Taylor, Mohsen Ghanbari, Joyce van Meurs, Achilleas N Pitsillides, Bruce M Psaty, Raymond Noordam, Ron Do, Kyong Soo Park, J Wouter Jukema, Maryam Kavousi, Adolfo Correa, Stephen S Rich, Scott M Damrauer, Catherine Hajek, Nam H Cho, Marguerite R Irvin, James S Pankow, Girish N Nadkarni, Robert Sladek, Mark O Goodarzi, Jose C Florez, Daniel I Chasman, Susan R Heckbert, Charles Kooperberg, Josée Dupuis, Rajeev Malhotra, Paul S de Vries, Ching-Ti Liu, Jerome I Rotter, James B Meigs, |
| Uncovering novel pathogenic variants and pathway mutations in triple-negative breast cancer among the endogamous mizo tribe. Breast cancer research and treatment 2024 10 . Lalawmpuii Pachuau, H Lalremmawia, Lalengkimi Ralte, Johan Vanlalpeka, Jeremy Lalrinsanga Pautu, Saia Chenkual, Thomas Zomuana, Sailo Tlau Lalruatfela, John Zohmingthanga, Lalchhandama Chhakchhuak, Ashok K Varma, Nachimuthu Senthil Kum |
- Page last reviewed:Feb 1, 2024
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