Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and EGR2[original query] |
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| Mutation frequency for Charcot-Marie-Tooth disease type 1 in the Chinese population is similar to that in the global ethnic patients. Genetics in medicine : official journal of the American College of Medical Genetics 2006 Aug 8 (8): 532-5. Song Shujuan, Zhang Yuanzhi, Chen Biao, Zhang Yuanjin, Wang Manjie, Wang Yueying, Yan Ming, Zou Junhua, Huang Yu, Zhong Nanbe |
| Regulatory polymorphisms in EGR2 are associated with susceptibility to systemic lupus erythematosus. Human molecular genetics 2010 Jun 19 (11): 2313-20. Myouzen Keiko, Kochi Yuta, Shimane Kenichi, Fujio Keishi, Okamura Tomohisa, Okada Yukinori, Suzuki Akari, Atsumi Tatsuya, Ito Satoshi, Takada Kazuki, Mimori Akio, Ikegawa Shiro, Yamada Ryo, Nakamura Yusuke, Yamamoto Kazuhi |
| Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan. Journal of human genetics 2011 May 56 (5): 364-8. Abe Akiko, Numakura Chikahiko, Kijima Kazuki, Hayashi Makiko, Hashimoto Taeko, Hayasaka Kiyos |
| The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy. Molecular genetics & genomic medicine 2014 Nov 2 (6): 522-9. DiVincenzo Christina, Elzinga Christopher D, Medeiros Adam C, Karbassi Izabela, Jones Jeremiah R, Evans Matthew C, Braastad Corey D, Bishop Crystal M, Jaremko Malgorzata, Wang Zhenyuan, Liaquat Khalida, Hoffman Carol A, York Michelle D, Batish Sat D, Lupski James R, Higgins Joseph |
| Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility. Nature genetics 2017 Feb . Takeuchi Masaki, Mizuki Nobuhisa, Meguro Akira, Ombrello Michael J, Kirino Yohei, Satorius Colleen, Le Julie, Blake Mary, Erer Burak, Kawagoe Tatsukata, Ustek Duran, Tugal-Tutkun Ilknur, Seyahi Emire, Ozyazgan Yilmaz, Sousa Inês, Davatchi Fereydoun, Francisco Vânia, Shahram Farhad, Abdollahi Bahar Sadeghi, Nadji Abdolhadi, Shafiee Niloofar Mojarad, Ghaderibarmi Fahmida, Ohno Shigeaki, Ueda Atsuhisa, Ishigatsubo Yoshiaki, Gadina Massimo, Oliveira Sofia A, Gül Ahmet, Kastner Daniel L, Remmers Elaine |
| Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients. Neuromuscular disorders : NMD 2017 11 28 (1): 38-43. Milley György Máté, Varga Edina Timea, Grosz Zoltán, Nemes Csilla, Arányi Zsuzsanna, Boczán Judit, Diószeghy Péter, Molnár Mária Judit, Gál Ani |
| Association of LACC1, CEBPB-PTPN1, RIPK2 and ADO-EGR2 with ocular Behcet's disease in a Chinese Han population. The British journal of ophthalmology 2018 Jun . Wu Pengcheng, Du Liping, Hou Shengping, Su Guannan, Yang Lu, Hu Jiayue, Deng Jing, Cao Qingfeng, Yuan Gangxiang, Zhou Chunjiang, Kijlstra Aize, Yang Peize |
| Genetic susceptibility to bone and soft tissue sarcomas: a field synopsis and meta-analysis. Oncotarget 2018 5 9 (26): 18607-18626. Benna Clara, Simioni Andrea, Pasquali Sandro, De Boni Davide, Rajendran Senthilkumar, Spiro Giovanna, Colombo Chiara, Virgone Calogero, DuBois Steven G, Gronchi Alessandro, Rossi Carlo Riccardo, Mocellin Simo |
| Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth. Chinese medical journal 2018 Jan 131 (2): 151-155. Zhao Xin, Jiang Ming-Ming, Yan Yi-Zhou, Liu Lei, Xie Yong-Zhi, Li Xiao-Bo, Hu Zheng-Mao, Zi Xiao-Hong, Xia Kun, Tang Bei-Sha, Zhang Ru- |
| Charcot-Marie-Tooth disease with pyramidal features due to a new mutation of EGR2 gene. Acta bio-medica : Atenei Parmensis 2019 3 90 (1): 104-107. Fusco Carlo, Spagnoli Carlotta, Salerno Grazia Gabriella, Pavlidis Elena, Frattini Daniele, Pisani Francesco, Bassi Maria Tere |
| Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population. PloS one 2020 15 (5): e0233464. Sakono Takuto, Meguro Akira, Takeuchi Masaki, Yamane Takahiro, Teshigawara Takeshi, Kitaichi Nobuyoshi, Horie Yukihiro, Namba Kenichi, Ohno Shigeaki, Nakao Kumiko, Sakamoto Taiji, Sakai Tsutomu, Nakano Tadashi, Keino Hiroshi, Okada Annabelle A, Takeda Atsunobu, Ito Takako, Mashimo Hisashi, Ohguro Nobuyuki, Oono Shinichirou, Enaida Hiroshi, Okinami Satoshi, Horita Nobuyuki, Ota Masao, Mizuki Nobuhi |
| Predictive significance of selected gene mutations in relapsed and refractory chronic lymphocytic leukemia patients treated with ibrutinib. European journal of haematology 2020 Nov . Machnicki Marcin M, Górniak Patryk, P?pek Monika, Szymczyk Agnieszka, Iskierka-Ja?d?ewska El?bieta, Steckiewicz Pawe?, Bluszcz Aleksandra, Rydzanicz Ma?gorzata, Hus Marek, P?oski Rafa?, Makuch-?asica Hanna, Nowak Gra?yna, Juszczy?ski Przemys?aw, Jamroziak Krzysztof, Stok?osa Tomasz, Pu?a Barto |
| The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease. Turkish neurosurgery 2021 6 31 (6): 888-895. Yalcintepe Sinem, Gurkan Hakan, Dogan Ipek Gungor, Demir Selma, Sag Sebnem Ozemri, Kabayegit Zehra Manav, Atli Emine Ikbal, Atli Engin, Eker Damla, Temel Sehime Guls |
Eight novel susceptibility loci and putative causal variants in atopic dermatitis.
The Journal of allergy and clinical immunology 2021 Jun . Tanaka Nao, Koido Masaru, Suzuki Akari, Otomo Nao, Suetsugu Hiroyuki, Kochi Yuta, Tomizuka Kouhei, Momozawa Yukihide, Kamatani Yoichiro, , Ikegawa Shiro, Yamamoto Kazuhiko, Terao Chikas |
| Genotype-phenotype characteristics of Vietnamese patients diagnosed with Charcot-Marie-Tooth disease. Brain and behavior 2022 8 12 (9): e2744. Nguyen-Le Trung-Hieu, Do Minh Duc, Le Linh Hoang Gia, Nhat Quynh Nhu Nguyen, Hoang Nghia Trong Tien, Van Le Tuan, Mai Thao Phuo |
| Identification of shared loci associated with both Crohn's disease and leprosy in East Asians.
Human molecular genetics 2022 May . Jung Seulgi, Park Dohoon, Lee Ho-Su, Kim Yongjae, Baek Jiwon, Hwang Sung Wook, Park Sang Hyoung, Yang Suk-Kyun, Ye Byong Duk, Han Buhm, Sun Yonghu, Liu Hong, Zhang Furen, Liu Jianjun, Song Kyuyou |
| Ultra-low-coverage genome-wide association study-insights into gestational age using 17,844 embryo samples with preimplantation genetic testing.
Genome medicine 2023 2 15 (1): 10. Li Shumin, Yan Bin, Li Thomas K T, Lu Jianliang, Gu Yifan, Tan Yueqiu, Gong Fei, Lam Tak-Wah, Xie Pingyuan, Wang Yuexuan, Lin Ge, Luo Ruiba |
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