Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: MANBA[original query] |
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MANBA polymorphism was related to increased risk of colorectal cancer in Swedish but not in Chinese populations. Acta oncologica (Stockholm, Sweden) 2008 47 (3): 372-8. Gao Jingfang, Arbman Gunnar, He Lujun, Qiao Fang, Zhang Zhiyong, Zhao Zengren, Rosell Johan, Sun Xiao-Fe |
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain : a journal of neurology 2013 Jun 136 (Pt 6): 1778-82. , Lill Christina M, Schjeide Brit-Maren M, Graetz Christine, Ban Maria, Alcina Antonio, Ortiz Miguel A, Pérez Jennifer, Damotte Vincent, Booth David, Lopez de Lapuente Aitzkoa, Broer Linda, Schilling Marcel, Akkad Denis A, Aktas Orhan, Alloza Iraide, Antigüedad Alfredo, Arroyo Rafa, Blaschke Paul, Buttmann Mathias, Chan Andrew, Compston Alastair, Cournu-Rebeix Isabelle, Dörner Thomas, Epplen Joerg T, Fernández Óscar, Gerdes Lisa-Ann, Guillot-Noël Léna, Hartung Hans-Peter, Hoffjan Sabine, Izquierdo Guillermo, Kemppinen Anu, Kroner Antje, Kubisch Christian, Kümpfel Tania, Li Shu-Chen, Lindenberger Ulman, Lohse Peter, Lubetzki Catherine, Luessi Felix, Malhotra Sunny, Mescheriakova Julia, Montalban Xavier, Papeix Caroline, Paredes Lidia F, Rieckmann Peter, Steinhagen-Thiessen Elisabeth, Winkelmann Alexander, Zettl Uwe K, Hintzen Rogier, Vandenbroeck Koen, Stewart Graeme, Fontaine Bertrand, Comabella Manuel, Urcelay Elena, Matesanz Fuencisla, Sawcer Stephen, Bertram Lars, Zipp Frau |
Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk.
American journal of respiratory and critical care medicine 2015 Sep 192 (6): 727-36. Fischer Annegret, Ellinghaus David, Nutsua Marcel, Hofmann Sylvia, Montgomery Courtney G, Iannuzzi Michael C, Rybicki Benjamin A, Petrek Martin, Mrazek Frantisek, Pabst Stefan, Grohé Christian, Grunewald Johan, Ronninger Marcus, Eklund Anders, Padyukov Leonid, Mihailovic-Vucinic Violeta, Jovanovic Dragana, Sterclova Martina, Homolka Jiri, Nöthen Markus M, Herms Stefan, Gieger Christian, Strauch Konstantin, Winkelmann Juliane, Boehm Bernhard O, Brand Stephan, Büning Carsten, Schürmann Manfred, Ellinghaus Eva, Baurecht Hansjörg, Lieb Wolfgang, Nebel Almut, Müller-Quernheim Joachim, Franke Andre, Schreiber Stefan, |
Fine-mapping of antipsychotic response genome-wide association studies reveals novel regulatory mechanisms. Pharmacogenomics 2017 Jan 18 (2): 105-120. Ovenden Ellen S, Drögemöller Britt I, van der Merwe Lize, Chiliza Bonginkosi, Asmal Laila, Emsley Robin A, Warnich Loui |
NFKB1 and MANBA Confer Disease Susceptibility to Primary Biliary Cholangitis via Independent Putative Primary Functional Variants. Cellular and molecular gastroenterology and hepatology 2018 Dec . Hitomi Yuki, Nakatani Ken, Kojima Kaname, Nishida Nao, Kawai Yosuke, Kawashima Minae, Aiba Yoshihiro, Nagasaki Masao, Nakamura Minoru, Tokunaga Katsus |
A meta-analysis of genome-wide association studies of epigenetic age acceleration.
PLoS genetics 2019 11 15 (11): e1008104. Gibson Jude, Russ Tom C, Clarke Toni-Kim, Howard David M, Hillary Robert F, Evans Kathryn L, Walker Rosie M, Bermingham Mairead L, Morris Stewart W, Campbell Archie, Hayward Caroline, Murray Alison D, Porteous David J, Horvath Steve, Lu Ake T, McIntosh Andrew M, Whalley Heather C, Marioni Riccardo |
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant. Orphanet journal of rare diseases 2020 8 15 (1): 222. Safka Brozkova Dana, Varga Lukas, Uhrova Meszarosova Anna, Slobodova Zuzana, Skopkova Martina, Soltysova Andrea, Ficek Andrej, Jencik Jan, Lastuvkova Jana, Gasperikova Daniela, Seeman Pav |
Association between MANBA Gene Variants and Chronic Kidney Disease in a Korean Population. Journal of clinical medicine 2021 6 10 (11): . Kim Hye-Rim, Jin Hyun-Seok, Eom Yong-B |
A novel genetic variant potentially altering the expression of MANBA in the cerebellum associated with attention deficit hyperactivity disorder in Han Chinese children. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2021 Dec 1-39. Chen Xinzhen, Yao Ting, Cai Jinliang, Zhang Qi, Li Shanyawen, Li Huiru, Fu Xihang, Wu Ji |
Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation. International journal of molecular sciences 2022 Jul 23 (15): . González-Jiménez Adela, López-Cotarelo Pilar, Agudo-Jiménez Teresa, Casanova Ignacio, Silanes Carlos López de, Martín-Requero Ángeles, Matesanz Fuencisla, Urcelay Elena, Espino-Paisán Lau |
Association between plasma proteome and childhood neurodevelopmental disorders: A two-sample Mendelian randomization analysis. EBioMedicine 2022 3 78 103948. Yang Jian, He Xiaoyan, Qian Li, Zhao Binbin, Fan Yajuan, Gao Fengjie, Yan Bin, Zhu Feng, Ma Xianca |
Correlation research of susceptibility single nucleotide polymorphisms and the severity of clinical symptoms in attention deficit hyperactivity disorder. Frontiers in psychiatry 2022 10 13 1003542. Xu Yunyu, Lin Shuangxiang, Tao Jiejie, Liu Xinmiao, Zhou Ronghui, Chen Shuangli, Vyas Punit, Yang Chuang, Chen Bicheng, Qian Andan, Wang Meih |
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention. Genes 2021 12 13 (1): . Fernàndez-Castillo Noèlia, Cabana-Domínguez Judit, Kappel Djenifer B, Torrico Bàrbara, Weber Heike, Lesch Klaus-Peter, Lao Oscar, Reif Andreas, Cormand B |
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis.
Nature communications 2023 2 14 (1): 1069. Han Younghun, Byun Jinyoung, Zhu Catherine, Sun Ryan, Roh Julia Y, Cordell Heather J, Lee Hyun-Sung, Shaw Vikram R, Kang Sung Wook, Razjouyan Javad, Cooley Matthew A, Hassan Manal M, Siminovitch Katherine A, Folseraas Trine, Ellinghaus David, Bergquist Annika, Rushbrook Simon M, Franke Andre, Karlsen Tom H, Lazaridis Konstantinos N, , McGlynn Katherine A, Roberts Lewis R, Amos Christopher |
eQTL colocalization analysis highlights novel susceptibility genes in Autism Spectrum Disorders (ASD). Translational psychiatry 2023 11 13 (1): 336. S Dominguez-Alonso, A Carracedo, C Rodriguez-Fonten |
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- Page last updated:Apr 22, 2024
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