Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: NBEAL1[original query] |
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Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.
Neurology 2015 Dec . Traylor Matthew, Zhang Cathy R, Adib-Samii Poneh, Devan William J, Parsons Owen E, Lanfranconi Silvia, Gregory Sarah, Cloonan Lisa, Falcone Guido J, Radmanesh Farid, Fitzpatrick Kaitlin, Kanakis Allison, Barrick Thomas R, Moynihan Barry, Lewis Cathryn M, Boncoraglio Giorgio B, Lemmens Robin, Thijs Vincent, Sudlow Cathie, Wardlaw Joanna, Rothwell Peter M, Meschia James F, Worrall Bradford B, Levi Christopher, Bevan Steve, Furie Karen L, Dichgans Martin, Rosand Jonathan, Markus Hugh S, Rost Natalia, |
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Molecular psychiatry 2016 May . Hinney A, Kesselmeier M, Jall S, Volckmar A-L, Föcker M, Antel J, , , Heid I M, Winkler T W, , Grant S F A, , Guo Y, Bergen A W, Kaye W, Berrettini W, Hakonarson H, , , Herpertz-Dahlmann B, de Zwaan M, Herzog W, Ehrlich S, Zipfel S, Egberts K M, Adan R, Brandys M, van Elburg A, Boraska Perica V, Franklin C S, Tschöp M H, Zeggini E, Bulik C M, Collier D, Scherag A, Müller T D, Hebebrand |
Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons. Scientific reports 2017 Jun 7 (1): 4091. Hixson James E, Jun Goo, Shimmin Lawrence C, Wang Yizhi, Yu Guoqiang, Mao Chunhong, Warren Andrew S, Howard Timothy D, Heide Richard S Vander, Van Eyk Jennifer, Wang Yue, Herrington David |
Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
Stroke 2018 Jul . Jian Xueqiu, Satizabal Claudia L, Smith Albert V, Wittfeld Katharina, Bis Joshua C, Smith Jennifer A, Hsu Fang-Chi, Nho Kwangsik, Hofer Edith, Hagenaars Saskia P, Nyquist Paul A, Mishra Aniket, Adams Hieab H H, Li Shuo, Teumer Alexander, Zhao Wei, Freedman Barry I, Saba Yasaman, Yanek Lisa R, Chauhan Ganesh, van Buchem Mark A, Cushman Mary, Royle Natalie A, Bryan R Nick, Niessen Wiro J, Windham Beverly G, DeStefano Anita L, Habes Mohamad, Heckbert Susan R, Palmer Nicholette D, Lewis Cora E, Eiriksdottir Gudny, Maillard Pauline, Mathias Rasika A, Homuth Georg, Valdés-Hernández Maria Del C, Divers Jasmin, Beiser Alexa S, Langner Sönke, Rice Kenneth M, Bastin Mark E, Yang Qiong, Maldjian Joseph A, Starr John M, Sidney Stephen, Risacher Shannon L, Uitterlinden André G, Gudnason Vilmundur G, Nauck Matthias, Rotter Jerome I, Schreiner Pamela J, Boerwinkle Eric, van Duijn Cornelia M, Mazoyer Bernard, von Sarnowski Bettina, Gottesman Rebecca F, Levy Daniel, Sigurdsson Sigurdur, Vernooij Meike W, Turner Stephen T, Schmidt Reinhold, Wardlaw Joanna M, Psaty Bruce M, Mosley Thomas H, DeCarli Charles S, Saykin Andrew J, Bowden Donald W, Becker Diane M, Deary Ian J, Schmidt Helena, Kardia Sharon L R, Ikram M Arfan, Debette Stéphanie, Grabe Hans J, Longstreth W T, Seshadri Sudha, Launer Lenore J, Fornage Myriam, |
Genome-wide association study of cerebral small vessel disease reveals established and novel loci.
Brain : a journal of neurology 2019 Oct 142 (10): 3176-3189. Chung Jaeyoon, Marini Sandro, Pera Joanna, Norrving Bo, Jimenez-Conde Jordi, Roquer Jaume, Fernandez-Cadenas Israel, Tirschwell David L, Selim Magdy, Brown Devin L, Silliman Scott L, Worrall Bradford B, Meschia James F, Demel Stacie, Greenberg Steven M, Slowik Agnieszka, Lindgren Arne, Schmidt Reinhold, Traylor Matthew, Sargurupremraj Muralidharan, Tiedt Steffen, Malik Rainer, Debette Stéphanie, Dichgans Martin, Langefeld Carl D, Woo Daniel, Rosand Jonathan, Anderson Christopher |
Ancestral characterization of 1018 cancer cell lines highlights disparities and reveals gene expression and mutational differences. Cancer 2019 3 125 (12): 2076-2088. Kessler Michael D, Bateman Nicholas W, Conrads Thomas P, Maxwell George L, Dunning Hotopp Julie C, O'Connor Timothy |
Exome Sequencing in BRCA1- and BRCA2-Negative Greek Families Identifies MDM1 and NBEAL1 as Candidate Risk Genes for Hereditary Breast Cancer. Frontiers in genetics 2019 10 1005. Glentis Stavros, Dimopoulos Alexandros C, Rouskas Konstantinos, Ntritsos George, Evangelou Evangelos, Narod Steven A, Mes-Masson Anne-Marie, Foulkes William D, Rivera Barbara, Tonin Patricia N, Ragoussis Jiannis, Dimas Antigone |
NBEAL1 controls SREBP2 processing and cholesterol metabolism and is a susceptibility locus for coronary artery disease. Scientific reports 2020 3 10 (1): 4528. Bindesbøll Christian, Aas Aleksander, Ogmundsdottir Margret Helga, Pankiv Serhiy, Reine Trine, Zoncu Roberto, Simonsen An |
Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease. Computational and mathematical methods in medicine 2021 8 2021 7036592. Hu Yang, Qiu Shizheng, Cheng Lia |
Mutations of METTL3 predict response to neoadjuvant chemotherapy in muscle-invasive bladder cancer. Journal of clinical and translational research 2021 7 7 (3): 386-413. Yang Zhao, Shen Zongyi, Jin Di, Zhang Nan, Wang Yue, Lei Wanjun, Zhang Zhiming, Chen Haige, Naz Faiza, Xu Lida, Wang Lei, Wang Shihui, Su Xin, Yu Changyuan, Li Cho |
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
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