Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and CAV3[original query] |
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| Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease. Gastroenterology 2010 Jul 139 (1): 130-9.e24. Roberts Kari E, Kawut Steven M, Krowka Michael J, Brown Robert S, Trotter James F, Shah Vijay, Peter Inga, Tighiouart Hocine, Mitra Nandita, Handorf Elizabeth, Knowles James A, Zacks Steven, Fallon Michael B, |
| Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics. The Canadian journal of cardiology 0 28 (2): 196-200. Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac |
| Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
| Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data. The Canadian journal of cardiology 2013 Sep 29 (9): 1104-9. Andreasen Charlotte, Refsgaard Lena, Nielsen Jonas B, Sajadieh Ahmad, Winkel Bo G, Tfelt-Hansen Jacob, Haunsø Stig, Holst Anders G, Svendsen Jesper H, Olesen Morten |
| Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). Rare diseases (Austin, Tex.) 2013 Dec 1 (1): 1. Xie Zhihui, Nagarajan Vijayaraj, Sturdevant Daniel E, Iwaki Shoko, Chan Eunice, Wisch Laura, Young Michael, Nelson Celeste M, Porcella Stephen F, Druey Kirk |
| A Next-Generation Sequencing Approach to Identify Gene Mutations in Early- and Late-Onset Hypertrophic Cardiomyopathy Patients of an Italian Cohort. International journal of molecular sciences 2016 17 (8): . Rubattu Speranza, Bozzao Cristina, Pennacchini Ermelinda, Pagannone Erika, Musumeci Beatrice Maria, Piane Maria, Germani Aldo, Savio Camilla, Francia Pietro, Volpe Massimo, Autore Camillo, Chessa Lucia |
| [Correlation between Genetic Variants and Polymorphism of Caveolin and Sudden Unexplained Death]. Fa yi xue za zhi 2017 Apr 33 (2): 114-119. Wu F Y, Tang X H, Gai L L, Kong X P, Hao B, Huang E W, Shi H, Sheng L H, Quan L, Liu S P, Luo |
| Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
| Whole genome sequencing and rare variant analysis in essential tremor families. PloS one 2019 8 14 (8): e0220512. Odgerel Zagaa, Sonti Shilpa, Hernandez Nora, Park Jemin, Ottman Ruth, Louis Elan D, Clark Lorraine |
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population.
Frontiers in genetics 2021 3 12 588452. Irvin Marguerite R, Aggarwal Praful, Claas Steven A, de Las Fuentes Lisa, Do Anh N, Gu C Charles, Matter Andrea, Olson Benjamin S, Patki Amit, Schwander Karen, Smith Joshua D, Srinivasasainagendra Vinodh, Tiwari Hemant K, Turner Amy J, Nickerson Deborah A, Rao Dabeeru C, Broeckel Ulrich, Arnett Donna |
| Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort. Brain : a journal of neurology 2021 12 145 (5): 1839-1853. Baez-Nieto David, Allen Andrew, Akers-Campbell Seth, Yang Lingling, Budnik Nikita, Pupo Amaury, Shin Young-Cheul, Genovese Giulio, Liao Maofu, Pérez-Palma Eduardo, Heyne Henrike, Lal Dennis, Lipscombe Diane, Pan Jen |
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