Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and ATP2A2[original query] |
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| Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Molecular psychiatry 2001 Jan 6 (1): 92-7. Jacobsen N J, Franks E K, Elvidge G, Jones I, McCandless F, O'Donovan M C, Owen M J, Craddock |
| Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease. Basic research in cardiology 2013 Nov 108 (6): 387. Fedele Francesco, Mancone Massimo, Chilian William M, Severino Paolo, Canali Emanuele, Logan Suzanna, De Marchis Maria Laura, Volterrani Maurizio, Palmirotta Raffaele, Guadagni Fiorel |
| Intellectual disability and cognitive ability in Darier disease: Swedish nation-wide study. The British journal of dermatology 2015 Jul 173 (1): 155-8. Cederlöf M, Karlsson R, Larsson H, Almqvist C, Magnusson P K E, Nordlind K, Landén M, Lichtenstein |
| Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects. The British journal of dermatology 2015 Oct . Dodiuk-Gad R P, Cohen-Barak E, Khayat M, Milo H, Amariglio-Diskin L, Danial-Faran N, Sah M, Ziv M, Shani-Adir A, Amichai B, Zlotogorski A, Borochowitz Z, Rozenman D, Shalev |
| Novel mutations in Darier disease and association to self-reported disease severity. PloS one 2017 10 12 (10): e0186356. Leong Ivone U S, Stuckey Alexander, Ahanian Tara, Cederlöf Martin, Wikstrom Jakob |
| Genotype-phenotype correlations in Darier disease: A focus on the neuropsychiatric phenotype. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 10 177 (8): 717-726. Gordon-Smith Katherine, Green Elaine, Grozeva Detelina, Tavadia Sherine, Craddock Nick, Jones Li |
| Mitochondrial Energetics and Ca2-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy. Journal of clinical medicine 2020 6 9 (6): . Lombardi Maria, Lazzeroni Davide, Pisano Annalinda, Girolami Francesca, Alfieri Ottavio, La Canna Giovanni, d'Amati Giulia, Olivotto Iacopo, Rimoldi Ornella E, Foglieni Chiara, Camici Paolo |
| Whole exome sequencing improves mutation detection in Hailey-Hailey disease. The Journal of dermatology 2021 4 48 (7): 989-992. Wang Zhe, Wang Zhenzhen, Sun Lele, Yu Xueping, Pang Zheng, Liu Hong, Zhang Fur |
| Subcellular compartmentalization of STIM1 for the distinction of Darier disease from Hailey-Hailey disease. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2022 11 20 (12): 1613-1619. Stanisz Hedwig, Mitteldorf Christina, Janning Helena, Bennemann Anette, Schön Michael P, Frank Jor |
| Association of Somatic ATP2A2 Damaging Variants With Grover Disease. JAMA dermatology 2023 5 . Devin Seli, Katharine T Ellis, Mohamad Goldust, Khadim Shah, Ronghua Hu, Jing Zhou, Jennifer M McNiff, Keith A Choa |
| Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. Advanced genetics (Hoboken, N.J.) 2023 3 4 (1): 2200013. Estrella Elicia, Rockowitz Shira, Thorne Marielle, Smith Pressley, Petit Jeanette, Zehnder Veronica, Yu Richard N, Bauer Stuart, Berde Charles, Agrawal Pankaj B, Beggs Alan H, Gharavi Ali G, Kunkel Louis, Brownstein Catherine |
| Whole-Exome Sequencing Reveals Mutational Signature of Hypertrophic Cardiomyopathy. International journal of general medicine 2023 10 16 4617-4628. Xi-Qin Wang, Fang Yuan, Bao-Rui |
- Page last reviewed:Feb 1, 2024
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