Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: RS1[original query] |
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Musical aptitude is associated with AVPR1A-haplotypes. PloS one 2009 4 (5): e5534. Ukkola Liisa T, Onkamo Päivi, Raijas Pirre, Karma Kai, Järvelä Ir |
Molecular genetic characteristics of X-linked retinoschisis in Koreans. Molecular vision 2009 15 833-43. Kim So Yeon, Ko Hyun Soo, Yu Young Suk, Hwang Jeong-Min, Lee Jong Joo, Kim Sung Yeun, Kim Ji Yeon, Seong Moon-Woo, Park Kyu Hyung, Park Sung S |
Family-based association study of microsatellites in the 5' flanking region of AVPR1A with autism spectrum disorder in the Korean population. Psychiatry research 2010 Jun 178 (1): 199-201. Yang So Young, Cho Soo-Churl, Yoo Hee Jeong, Cho In Hee, Park Mira, Yoe Jin, Kim Soon |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism. Molecular autism 2011 2 (1): 3. Tansey Katherine E, Hill Matthew J, Cochrane Lynne E, Gill Michael, Anney Richard Jl, Gallagher Loui |
Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music. Journal of human genetics 2011 Apr 56 (4): 324-9. Ukkola-Vuoti Liisa, Oikkonen Jaana, Onkamo Päivi, Karma Kai, Raijas Pirre, Järvelä Ir |
Association of heat shock proteins with all-cause mortality. Age (Dordrecht, Netherlands) 2013 Aug 35 (4): 1367-76. Broer L, Demerath E W, Garcia M E, Homuth G, Kaplan R C, Lunetta K L, Tanaka T, Tranah G J, Walter S, Arnold A M, Atzmon G, Harris T B, Hoffmann W, Karasik D, Kiel D P, Kocher T, Launer L J, Lohman K K, Rotter J I, Tiemeier H, Uitterlinden A G, Wallaschofski H, Bandinelli S, Dörr M, Ferrucci L, Franceschini N, Gudnason V, Hofman A, Liu Y, Murabito J M, Newman A B, Oostra B A, Psaty B M, Smith A V, van Duijn C |
The neurogenetics of nice: receptor genes for oxytocin and vasopressin interact with threat to predict prosocial behavior. Psychological science 2012 Mar . Poulin MJ, Holman EA, Buffone A |
AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. PloS one 2012 7 (2): e31763. Morley Andrew P, Narayanan Madan, Mines Rebecca, Molokhia Ashraf, Baxter Sebastian, Craig Gavin, Lewis Cathryn M, Craig I |
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight. American journal of human genetics 2012 Apr 90 (4): 715-9. Ishida Miho, Monk David, Duncan Andrew J, Abu-Amero Sayeda, Chong Jiehan, Ring Susan M, Pembrey Marcus E, Hindmarsh Peter C, Whittaker John C, Stanier Philip, Moore Gudrun |
Single-nucleotide polymorphisms of TNFA and IL1 in allergic rhinitis. Journal of investigational allergology & clinical immunology 2013 23 (7): 455-61. Nasiri R, Amirzargar A Akbar, Movahedi M, Hirbod-Mobarakeh A, Farhadi E, Behniafard N, Tavakkol M, Ansaripour B, Moradi B, Zare A, Rezaei |
Common variants in PCSK1 influence blood pressure and body mass index. Journal of human hypertension 2015 Feb 29 (2): 82-6. Gu Q, Yazdanpanah M, van Hoek M, Hofman A, Gao X, de Rooij F W M, Sijbrands E J |
Oxytocin and vasopressin receptor polymorphisms interact with circulating neuropeptides to predict human emotional reactions to stress. Emotion (Washington, D.C.) 2014 Jun 14 (3): 562-72. Moons Wesley G, Way Baldwin M, Taylor Shelley |
Clinical and molecular characterization of females affected by X-linked retinoschisis. Clinical & experimental ophthalmology 2015 Apr . Staffieri Sandra E, Rose Loreto, Chang Andrew, De Roach John N, McLaren Terri L, Mackey David A, Hewitt Alex W, Lamey Tina |
Association and Promoter Analysis of AVPR1A in Finnish Autism Families. Autism research : official journal of the International Society for Autism Research 2015 Feb . Kantojärvi Katri, Oikkonen Jaana, Kotala Ilona, Kallela Jenni, Vanhala Raija, Onkamo Päivi, Järvelä Ir |
[THE INFLUENCE OF TUMOR NECROSIS FACTOR ALPHA AND POLYMORPHISM OF ITS GENE (RS1800629) ON THE SEVERITY AND PROGRESSION OF CHRONIC HEPATITIS AND ULCERATIVE COLITIS]. E?ksperimental'nai?a? i klinicheskai?a? gastroe?nterologii?a? = Experimental & clinical gastroenterology 2016 (3): 9-14. Bulatova I A, Tretyakova Y I, Shchekotova A P, Shchekotov V V, Krivtsov A V, Nasibullina N |
Association testing of vasopressin receptor 1a microsatellite polymorphisms in non-clinical autism spectrum phenotypes. Autism research : official journal of the International Society for Autism Research 2016 Nov . Procyshyn Tanya L, Hurd Peter L, Crespi Bernard |
CLINICAL PROGRESS IN INHERITED RETINAL DEGENERATIONS: GENE THERAPY CLINICAL TRIALS AND ADVANCES IN GENETIC SEQUENCING. Retina (Philadelphia, Pa.) 2016 Oct . Hafler Brian |
Replicative genetic association study between functional polymorphisms in AVPR1A and social behavior scales of autism spectrum disorder in the Korean population. Molecular autism 2017 8 44. Yang So Young, Kim Soon Ae, Hur Gang Min, Park Mira, Park Jong-Eun, Yoo Hee Jeo |
Genomic Rearrangement Signatures and Clinical Outcomes in High-Grade Serous Ovarian Cancer. Journal of the National Cancer Institute 2018 3 110 (3): 265-72. Hillman R Tyler, Chisholm Gary B, Lu Karen H, Futreal P Andr |
Neural mechanisms of AVPR1A RS3-RS1 haplotypes that impact verbal learning and memory. NeuroImage 2020 Aug 222 117283. Zhang Yan, Zhu Dan, Zhang Peng, Li Wei, Qin Wen, Liu Feng, Xu Jiayuan, Xu Qiang, Wang Junping, Ye Zhaoxiang, Yu Chunsh |
Influence of Polymorphisms in the Interleukin-18 Gene on Allergic Rhinitis: A Meta-Analysis. International archives of allergy and immunology 2020 Feb 1-10. Tharabenjasin Phuntila, Pabalan Noel, Jarjanazi Hamdi, Poachanukoon Orap |
Comprehensive analysis of genetic and clinical characteristics of 30 patients with X-linked juvenile retinoschisis in China. Acta ophthalmologica 2020 10 99 (4): e470-e479. Gao Feng-Juan, Dong Jian-Hong, Wang Dan-Dan, Chen Fang, Hu Fang-Yuan, Chang Qing, Xu Ping, Liu Wei, Li Jian-Kang, Huang Ying, Wu Ji-Hong, Xu Ge-Z |
Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case series. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2020 1 258 (3): 529-536. Rubinstein Yair, Weiner Chen, Chetrit Noa, Newman Hadas, Hecht Idan, Shoshany Nadav, Pras Er |
(Re-)activity in the caregiving situation: Genetic diversity within Oxytocin-Vasopressin Pathway is associated with salivary oxytocin and vasopressin concentrations in response to contact with a crying infant-simulator. Psychoneuroendocrinology 2021 Jun 131 105294. Rybicka Magda, Ka?mierczak Maria, Pawlicka Paulina, ?ada-Ma?ko Ariadna Beata, Anikiej-Wiczenbach Paulina, Bielawski Krzysztof Pio |
Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort. Genes 2021 5 12 (5): . Kim Yoon-Jeon, Kim You-Na, Yoon Young-Hee, Seo Eul-Ju, Seo Go-Hun, Keum Changwon, Lee Beom-Hee, Lee Joo-Yo |
The role of polymorphisms rs2070744 and rs1799983 eNOS gene in patients with POAG: a systematic review and meta-analysis. International ophthalmology 2021 4 41 (8): 2747-2763. Salari Nader, Bokaee Shadi, Farshchian Nushin, Mohammadi Masoud, Kazeminia Mohs |
Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population. Ophthalmic genetics 2021 Dec 1-8. Cetin Gokhan Ozan, Cetin Ebru Nevin, Akyol Tunahan, Ilhan Hatice Deniz, Pekel Gokh |
Predominant Founder Effect among Recurrent Pathogenic Variants for an X-Linked Disorder. Genes 2022 4 13 (4): . Bender Chelsea, Woo Elizabeth Geena, Guan Bin, Ullah Ehsan, Feng Eric, Turriff Amy, Tumminia Santa J, Sieving Paul A, Cukras Catherine A, Hufnagel Robert |
X-linked retinoschisis: mutation spectrum and genotype-phenotype relationship in an Italian pediatric cohort. Ophthalmic genetics 2022 11 44 (1): 35-42. Fortunato P, Pagliazzi A, Bargiacchi S, Marziali E, Sodi A, Caputo R, Passerini I, Pelo E, Bacci G |
De Novo Mutations Contributes Approximately 7% of Pathogenicity in Inherited Eye Diseases. Investigative ophthalmology & visual science 2023 2 64 (2): 5. Li Wei, He Xiang-Dong, Yang Zheng-Tao, Han Dong-Ming, Sun Yan, Chen Yan-Xian, Han Xiao-Tong, Guo Si-Cheng, Ma Yu-Ting, Jin Xin, Yang Huan-Ming, Gao Ya, Wang Zhuo-Shi, Li Jian-Kang, He W |
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- Page last updated:Mar 25, 2024
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