Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: GLB1[original query] |
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| Population analysis of the GLB1 gene in South Brazil. Genetics and molecular biology 2011 Jan 34 (1): 45-8. Baiotto Cléia, Sperb Fernanda, Matte Ursula, da Silva Cláudia Dornelles, Sano Renata, Coelho Janice Carneiro, Giugliani Rober |
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
Nature genetics 2012 Nov 44 (11): 1222-6. Hirota Tomomitsu, Takahashi Atsushi, Kubo Michiaki, Tsunoda Tatsuhiko, Tomita Kaori, Sakashita Masafumi, Yamada Takechiyo, Fujieda Shigeharu, Tanaka Shota, Doi Satoru, Miyatake Akihiko, Enomoto Tadao, Nishiyama Chiharu, Nakano Nobuhiro, Maeda Keiko, Okumura Ko, Ogawa Hideoki, Ikeda Shigaku, Noguchi Emiko, Sakamoto Tohru, Hizawa Nobuyuki, Ebe Koji, Saeki Hidehisa, Sasaki Takashi, Ebihara Tamotsu, Amagai Masayuki, Takeuchi Satoshi, Furue Masutaka, Nakamura Yusuke, Tamari Mayu |
| Prevalence and Novel Mutations of Lysosomal Storage Disorders in United Arab Emirates : LSD in UAE. JIMD reports 2013 10 1-9. Al-Jasmi Fatma A, Tawfig Nafisa, Berniah Ans, Ali Bassam R, Taleb Mahmoud, Hertecant Jozef L, Bastaki Fatma, Souid Abdul-Kad |
| Recurrent and novel GLB1 mutations in India. Gene 2015 Aug 567 (2): 173-81. Bidchol Abdul Mueed, Dalal Ashwin, Trivedi Rakesh, Shukla Anju, Nampoothiri Sheela, Sankar V H, Danda Sumita, Gupta Neerja, Kabra Madhulika, Hebbar Shrikiran A, Bhat Ramesh Y, Matta Divya, Ekbote Alka V, Puri Ratna Dua, Phadke Shubha R, Gowrishankar Kalpana, Aggarwal Shagun, Ranganath Prajnya, Sharda Sheetal, Kamate Mahesh, Datar Chaitanya A, Bhat Kamalakshi, Kamath Nutan, Shah Hitesh, Krishna Shuba, Gopinath Puthiya Mundyat, Verma Ishwar C, Nagarajaram H A, Satyamoorthy Kapaettu, Girisha Katta Moh |
| Replication the association of 2q32.2-q32.3 and 14q32.11 with hepatocellular carcinoma. Gene 2015 Apr 561 (1): 63-7. Chen Wei, Wang Mingquan, Zhang Zhen, Tang Huayang, Zuo Xianbo, Meng Xiangling, Xiong Maoming, Zhou Fusheng, Liang Bo, Dai Fen, Fang Jun, Gao Jinping, Zhu Jun, Zhu Yong, Wan Hong, Wang Miaofeng, Chan Shixin, Sun Liangd |
| Association of the GLB1 rs4678680 genetic variant with risk of HBV-related hepatocellular carcinoma. Oncotarget 2016 Aug 7 (35): 56501-56507. Wang Wen-Tao, Li Ziqiang, Shi Meng, Zhu Hui, Xiong Xiangyu, Shang Jinhua, Liu Jibing, Teng Mujian, Yang Mi |
| Rapid Targeted Genomics in Critically Ill Newborns. Pediatrics 2017 9 140 (4): . van Diemen Cleo C, Kerstjens-Frederikse Wilhelmina S, Bergman Klasien A, de Koning Tom J, Sikkema-Raddatz Birgit, van der Velde Joeri K, Abbott Kristin M, Herkert Johanna C, Löhner Katharina, Rump Patrick, Meems-Veldhuis Martine T, Neerincx Pieter B T, Jongbloed Jan D H, van Ravenswaaij-Arts Conny M, Swertz Morris A, Sinke Richard J, van Langen Irene M, Wijmenga Cis |
| Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients. PloS one 2018 2 13 (2): e0188869. Ji Haoran, Li Dongxiao, Wu Ye, Zhang Quanli, Gu Qiang, Xie Han, Ji Taoyun, Wang Huifang, Zhao Lu, Zhao Haijuan, Yang Yanling, Feng Hongchun, Xiong Hui, Ji Jinhua, Yang Zhixian, Kou Liping, Li Ming, Bao Xinhua, Chang Xingzhi, Zhang Yuehua, Li Li, Li Huijuan, Niu Zhengping, Wu Xiru, Xiao Jiangxi, Jiang Yuwu, Wang Jingm |
| Genotype, phenotype and in silico pathogenicity analysis of HEXB mutations: Panel based sequencing for differential diagnosis of gangliosidosis. Clinical neurology and neurosurgery 2018 2 167 43-53. Mahdieh Nejat, Mikaeeli Sahar, Tavasoli Ali Reza, Rezaei Zahra, Maleki Majid, Rabbani Bahar |
| Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.
Translational psychiatry 2018 Jan 8 (1): 9. Hall Lynsey S, Adams Mark J, Arnau-Soler Aleix, Clarke Toni-Kim, Howard David M, Zeng Yanni, Davies Gail, Hagenaars Saskia P, Maria Fernandez-Pujals Ana, Gibson Jude, Wigmore Eleanor M, Boutin Thibaud S, Hayward Caroline, Scotland Generation, , Porteous David J, Deary Ian J, Thomson Pippa A, Haley Chris S, McIntosh Andrew |
| Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes. Parkinsonism & related disorders 2019 11 69 111-118. Kumar Kishore R, Davis Ryan L, Tchan Michel C, Wali G M, Mahant Neil, Ng Karl, Kotschet Katya, Siow Sue-Faye, Gu Jason, Walls Zachary, Kang Ce, Wali Gautam, Levy Stan, Phua Chung Sen, Yiannikas Con, Darveniza Paul, Chang Florence C F, Morales-Briceño Hugo, Rowe Dominic B, Drew Alex, Gayevskiy Velimir, Cowley Mark J, Minoche Andre E, Tisch Stephen, Hayes Michael, Kummerfeld Sarah, Fung Victor S C, Sue Carolyn |
| Mongolian spots in GM1 gangliosidosis: a pictorial report. Clinical dysmorphology 2020 10 30 (1): 6-9. Mishra Shivani, Pai Pranita, Uttarilli Anusha, Girisha Katta Moh |
| Genetic Associations and Architecture of Asthma-COPD Overlap.
Chest 2022 Jan . John Catherine, Guyatt Anna L, Shrine Nick, Packer Richard, Olafsdottir Thorunn A, Liu Jiangyuan, Hayden Lystra P, Chu Su H, Koskela Jukka T, Luan Jian'an, Li Xingnan, Terzikhan Natalie, Xu Hanfei, Bartz Traci M, Petersen Hans, Leng Shuguang, Belinsky Steven A, Cepelis Aivaras, Hernández Cordero Ana I, Obeidat Ma'en, Thorleifsson Gudmar, Meyers Deborah A, Bleecker Eugene R, Sakoda Lori C, Iribarren Carlos, Tesfaigzi Yohannes, Gharib Sina A, Dupuis Josée, Brusselle Guy, Lahousse Lies, Ortega Victor E, Jonsdottir Ingileif, Sin Don D, Bossé Yohan, van den Berge Maarten, Nickle David, Quint Jennifer K, Sayers Ian, Hall Ian P, Langenberg Claudia, Ripatti Samuli, Laitinen Tarja, Wu Ann C, Lasky-Su Jessica, Bakke Per, Gulsvik Amund, Hersh Craig P, Hayward Caroline, Langhammer Arnulf, Brumpton Ben, Stefansson Kari, Cho Michael H, Wain Louise V, Tobin Martin |
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