Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: RAI1[original query] |
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Search on chromosome 17 centromere reveals TNFRSF13B as a susceptibility gene for intracranial aneurysm: a preliminary study. Circulation 2006 Apr 113 (16): 2002-10. Inoue Kayoko, Mineharu Youhei, Inoue Sumiko, Yamada Shigeki, Matsuda Fumihiko, Nozaki Kazuhiko, Takenaka Katsunobu, Hashimoto Nobuo, Koizumi Ak |
Gender, genotype, and phenotype differences in Smith-Magenis syndrome: a meta-analysis of 105 cases. Clinical genetics 2007 Jun 71 (6): 540-50. Edelman E A, Girirajan S, Finucane B, Patel P I, Lupski J R, Smith A C M, Elsea S |
Gene-network analysis identifies susceptibility genes related to glycobiology in autism. PloS one 2009 4 (5): e5324. van der Zwaag Bert, Franke Lude, Poot Martin, Hochstenbach Ron, Spierenburg Henk A, Vorstman Jacob A S, van Daalen Emma, de Jonge Maretha V, Verbeek Nienke E, Brilstra Eva H, van 't Slot Ruben, Ophoff Roel A, van Es Michael A, Blauw Hylke M, Veldink Jan H, Buizer-Voskamp Jacobine E, Beemer Frits A, van den Berg Leonard H, Wijmenga Cisca, van Amstel Hans Kristian Ploos, van Engeland Herman, Burbach J Peter H, Staal Wouter |
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
PLoS genetics 2011 Jun 7 (6): e1002141. Do Chuong B, Tung Joyce Y, Dorfman Elizabeth, Kiefer Amy K, Drabant Emily M, Francke Uta, Mountain Joanna L, Goldman Samuel M, Tanner Caroline M, Langston J William, Wojcicki Anne, Eriksson Nichol |
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Stroke; a journal of cerebral circulation 2014 Jan 45 (1): 24-36. Dichgans Martin, Malik Rainer, König Inke R, Rosand Jonathan, Clarke Robert, Gretarsdottir Solveig, Thorleifsson Gudmar, Mitchell Braxton D, Assimes Themistocles L, Levi Christopher, O'Donnell Christopher J, Fornage Myriam, Thorsteinsdottir Unnur, Psaty Bruce M, Hengstenberg Christian, Seshadri Sudha, Erdmann Jeanette, Bis Joshua C, Peters Annette, Boncoraglio Giorgio B, März Winfried, Meschia James F, Kathiresan Sekar, Ikram M Arfan, McPherson Ruth, Stefansson Kari, Sudlow Cathie, Reilly Muredach P, Thompson John R, Sharma Pankaj, Hopewell Jemma C, Chambers John C, Watkins Hugh, Rothwell Peter M, Roberts Robert, Markus Hugh S, Samani Nilesh J, Farrall Martin, Schunkert Heribert, , , , |
Association of premenstrual/menstrual symptoms with perinatal depression and a polymorphic repeat in the polyglutamine tract of the retinoic acid induced 1 gene. Journal of affective disorders 2014 Jun 161 43-6. Tan Ene-Choo, Tan Hui-San, Chua Tze-Ern, Lee Theresa, Ng Jasmine, Ch'ng Ying-Chia, Choo Chih-Huei, Chen Helen |
ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America. Cerebellum (London, England) 2015 Apr . Pereira Fernanda S, Monte Thais L, Locks-Coelho Lucas D, Silva Amanda S P, Barsottini Orlando, Pedroso José L, Cornejo-Olivas Mario, Mazzetti Pilar, Godeiro Clecio, Vargas Fernando R, Lima Maria-Angélica F D, van der Linden Hélio, Toralles Maria Betânia Pereira, Medeiros Paula F V, Ribeiro Erlane, Braga-Neto Pedro, Salarini Diego, Castilhos Raphael M, Saraiva-Pereira Maria-Luiza, Jardim Laura Bannach, |
Genome-wide assessment of Parkinson's disease in a Southern Spanish population. Neurobiology of aging 2016 Jun . Bandrés-Ciga Sara, Price Timothy Ryan, Barrero Francisco Javier, Escamilla-Sevilla Francisco, Pelegrina Javier, Arepalli Sampath, Hernández Dena, Gutiérrez Blanca, Cervilla Jorge, Rivera Margarita, Rivera Alberto, Ding Jing-Hui, Vives Francisco, Nalls Michael, Singleton Andrew, Durán Raqu |
Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia). PloS one 2016 11 (4): e0153841. ?hurbanov Alexander Y, Karafet Tatiana M, Morozov Igor V, Mikhalskaia Valeriia Yu, Zytsar Marina V, Bondar Alexander A, Posukh Olga |
Evidence for genetic regulation of mRNA expression of the dosage-sensitive gene retinoic acid induced-1 (RAI1) in human brain. Scientific reports 2016 6 19010. Chen Li, Tao Yu, Song Fan, Yuan Xi, Wang Jian, Saffen Dav |
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors. Parkinsonism & related disorders 2017 Jun . Monte Thais Lampert, Pereira Fernanda Santos, Reckziegel Estela da Rosa, Augustin Marina Coutinho, Locks-Coelho Lucas Dorídio, Santos Amanda Senna P, Pedroso José Luiz, Barsottini Orlando, Vargas Fernando Regla, Saraiva-Pereira Maria-Luiza, Jardim Laura Bannach, |
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men.
American journal of respiratory cell and molecular biology 2017 Oct . Chen Han, Cade Brian E, Gleason Kevin J, Bjonnes Andrew C, Stilp Adrienne M, Sofer Tamar, Conomos Matthew P, Ancoli-Israel Sonia, Arens Raanan, Azarbarzin Ali, Bell Graeme I, Below Jennifer E, Chun Sung, Evans Daniel S, Ewert Ralf, Frazier-Wood Alexis C, Gharib Sina A, Haba-Rubio José, Hagen Erika W, Heinzer Raphael, Hillman David R, Johnson W Craig, Kutalik Zoltan, Lane Jacqueline M, Larkin Emma K, Lee Seung Ku, Liang Jingjing, Loredo Jose S, Mukherjee Sutapa, Palmer Lyle J, Papanicolaou George J, Penzel Thomas, Peppard Paul E, Post Wendy S, Ramos Alberto R, Rice Ken, Rotter Jerome I, Sands Scott A, Shah Neomi A, Shin Chol, Stone Katie L, Stubbe Beate, Sul Jae Hoon, Tafti Mehdi, Taylor Kent D, Teumer Alexander, Thornton Timothy A, Tranah Gregory J, Wang Chaolong, Wang Heming, Warby Simon C, Wellman D Andrew, Zee Phyllis C, Hanis Craig L, Laurie Cathy C, Gottlieb Daniel J, Patel Sanjay R, Zhu Xiaofeng, Sunyaev Shamil R, Saxena Richa, Lin Xihong, Redline Sus |
Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American-specific associations. Sleep 2019 May . Barfield Richard, Wang Heming, Liu Yongmei, Brody Jennifer A, Swenson Brenton, Li Ruitong, Bartz Traci M, Sotoodehnia Nona, Chen Yii-der I, Cade Brian E, Chen Han, Patel Sanjay R, Zhu Xiaofeng, Gharib Sina A, Johnson W Craig, Rotter Jerome I, Saxena Richa, Purcell Shaun, Lin Xihong, Redline Susan, Sofer Tam |
(CAG) loci as genetic modifiers of age at onset in patients with spinocerebellar ataxia type 1 from mainland China. European journal of neurology 2019 Mar . Wang P, Chen Z, Peng Y, Cao L, Li X, Wang C, Yang H, Peng H, Shi Y, Zhou X, Li T, Feng L, Wu C, Qiu R, Xia K, Tang B, Jiang |
Effect of CAG repeats on the age at onset of patients with spinocerebellar ataxia type 2 in China. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2021 9 46 (8): 793-799. Li Yu, Liu Zhen, Hou Xiaorong, Chen Zhao, Shen Lu, Xia Kun, Tang Beisha, Jiang Hong, Wang Junli |
Supratentorial Sporadic Hemangioblastoma: A Case Report With Mutation Profiling Using Next-Generation DNA Sequencing. Cureus 2023 6 15 (6): e39818. Mohiuddin M Taher, Najwa A Bantan, Mustafa H Alwalily, Muhammad Saeed, Nuha M Taher, Meriem Bouzidi, Raid A Jastania, Kamal B Balkhoyo |
Understanding the genetics of early onset obesity in a cohort of children from Qatar. The Journal of clinical endocrinology and metabolism 2023 6 . Idris Mohammed, Basma Haris, Tara Al-Barazenji, Dhanya Vasudeva, Sara Tomei, Iman Al Azwani, Hajar Dauleh, Saira Shehzad, Shiga Chirayath, Ghassan Mohamadsalih, Goran Petrovski, Amel Khalifa, Donald R Love, Mashael Al-Shafai, Khalid Hussa |
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