Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and ANK3[original query] |
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| Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Sep 144B (6): 762-70. Morgan A R, Turic D, Jehu L, Hamilton G, Hollingworth P, Moskvina V, Jones L, Lovestone S, Brayne C, Rubinsztein D C, Lawlor B, Gill M, O'Donovan M C, Owen M J, Williams |
| Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Sep 147B (6): 727-31. Morgan A R, Hamilton G, Turic D, Jehu L, Harold D, Abraham R, Hollingworth P, Moskvina V, Brayne C, Rubinsztein D C, Lynch A, Lawlor B, Gill M, O'Donovan M, Powell J, Lovestone S, Williams J, Owen M |
| Is Ankyrin a genetic risk factor for psychiatric phenotypes? BMC psychiatry 2011 11 (1): 103. Gella Alejandro, Segura Mònica, Durany Núria, Pfuhlmann Bruno, Stöber Gerald, Gawlik Mic |
| Cross-disorder analysis of bipolar risk genes: further evidence of DGKH as a risk gene for bipolar disorder, but also unipolar depression and adult ADHD. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2011 Sep 36 (10): 2076-85. Weber Heike, Kittel-Schneider Sarah, Gessner Alexandra, Domschke Katharina, Neuner Maria, Jacob Christian P, Buttenschon Henriette N, Boreatti-Hümmer Andrea, Volkert Julia, Herterich Sabine, Baune Bernhard T, Gross-Lesch Silke, Kopf Juliane, Kreiker Susanne, Nguyen Thuy Trang, Weissflog Lena, Arolt Volker, Mors Ole, Deckert Jürgen, Lesch Klaus-Peter, Reif Andre |
| A genetic variant in the seed region of miR-4513 shows pleiotropic effects on lipid and glucose homeostasis, blood pressure, and coronary artery disease. Human mutation 2014 Dec 35 (12): 1524-31. Ghanbari Mohsen, de Vries Paul S, de Looper Hans, Peters Marjolein J, Schurmann Claudia, Yaghootkar Hanieh, Dörr Marcus, Frayling Timothy M, Uitterlinden Andre G, Hofman Albert, van Meurs Joyce B J, Erkeland Stefan J, Franco Oscar H, Dehghan Abb |
| 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 |
Genome-wide association study reveals two new risk loci for bipolar disorder.
Nature communications 2014 5 3339. Mühleisen Thomas W, Leber Markus, Schulze Thomas G, Strohmaier Jana, Degenhardt Franziska, Treutlein Jens, Mattheisen Manuel, Forstner Andreas J, Schumacher Johannes, Breuer René, Meier Sandra, Herms Stefan, Hoffmann Per, Lacour André, Witt Stephanie H, Reif Andreas, Müller-Myhsok Bertram, Lucae Susanne, Maier Wolfgang, Schwarz Markus, Vedder Helmut, Kammerer-Ciernioch Jutta, Pfennig Andrea, Bauer Michael, Hautzinger Martin, Moebus Susanne, Priebe Lutz, Czerski Piotr M, Hauser Joanna, Lissowska Jolanta, Szeszenia-Dabrowska Neonila, Brennan Paul, McKay James D, Wright Adam, Mitchell Philip B, Fullerton Janice M, Schofield Peter R, Montgomery Grant W, Medland Sarah E, Gordon Scott D, Martin Nicholas G, Krasnow Valery, Chuchalin Alexander, Babadjanova Gulja, Pantelejeva Galina, Abramova Lilia I, Tiganov Alexander S, Polonikov Alexey, Khusnutdinova Elza, Alda Martin, Grof Paul, Rouleau Guy A, Turecki Gustavo, Laprise Catherine, Rivas Fabio, Mayoral Fermin, Kogevinas Manolis, Grigoroiu-Serbanescu Maria, Propping Peter, Becker Tim, Rietschel Marcella, Nöthen Markus M, Cichon Sv |
| Genome-wide association study of behavioural and psychiatric features in human prion disease.
Translational psychiatry 2015 5 e552. Thompson A G B, Uphill J, Lowe J, Porter M-C, Lukic A, Carswell C, Rudge P, MacKay A, Collinge J, Mead |
| Shared and unique common genetic determinants between pediatric and adult celiac disease. BMC medical genomics 2016 07 9 (1): 44. Senapati Sabyasachi, Sood Ajit, Midha Vandana, Sood Neena, Sharma Suresh, Kumar Lalit, Thelma B |
| 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 |
| 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 |
| Spatial correlations exploitation based on nonlocal voxel-wise GWAS for biomarker detection of AD.
NeuroImage. Clinical 2019 21 101642. Huang Meiyan, Deng Chunyan, Yu Yuwei, Lian Tao, Yang Wei, Feng Qianjin, |
| Genome-wide association study of an unusual dolphin mortality event reveals candidate genes for susceptibility and resistance to cetacean morbillivirus. Evolutionary applications 2019 4 12 (4): 718-732. Batley Kimberley C, Sandoval-Castillo Jonathan, Kemper Catherine M, Attard Catherine R M, Zanardo Nikki, Tomo Ikuko, Beheregaray Luciano B, Möller Luciana |
| Age-related atrophy of cortical thickness and genetic effect of ANK3 gene in first episode MDD patients. NeuroImage. Clinical 2020 Aug 28 102384. Cheng Yuqi, Xu Jian, Dong Chenglong, Shen Zonglin, Zhou Cong, Li Na, Lu Yi, Ran Liuyi, Xu Lin, Shan Baoci, Xu Xiufe |
| A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21. Journal of psychiatry & neuroscience : JPN 2021 Mar 46 (2): E247-E257. Toma Claudio, Shaw Alex D, Heath Anna, Pierce Kerrie D, Mitchell Philip B, Schofield Peter R, Fullerton Janice |
| Identification of distinct genomic features reveals frequent somatic AHNAK and PTEN mutations predominantly in primary malignant melanoma presenting in the ureter. Japanese journal of clinical oncology 2022 5 52 (8): 930-943. Huang Yan, Wei Lai, Huang Yuanbin, Wen Shuang, Liu Tianqing, Duan Xu, Wang Yutong, Zhang Hongshuo, Fan Bo, Hu B |
| Genome-wide association analysis of cystatin-C kidney function in continental Africa. EBioMedicine 2023 8 95 104775. Richard Mayanja, Tafadzwa Machipisa, Opeyemi Soremekun, Abram B Kamiza, Christopher Kintu, Allan Kalungi, Robert Kalyesubula, Obondo J Sande, Daudi Jjingo, June Fabian, Cassianne Robinson-Cohen, Nora Franceschini, Dorothea Nitsch, Moffat Nyirenda, Eleftheria Zeggini, Andrew P Morris, Tinashe Chikowore, Segun Fatu |
| Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer's-type dementia. Acta neuropathologica 2024 10 148 (1): 55. Celeste Laureyssen, Fahri Küçükali, Jasper Van Dongen, Klara Gawor, Sandra O Tomé, Alicja Ronisz, Markus Otto, Christine A F von Arnim, Philip Van Damme, Rik Vandenberghe, Dietmar Rudolf Thal, Kristel Sleege |
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