Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: EGR2[original query] |
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Genetic and functional analyses of early growth response (EGR) family genes in schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry 2012 Oct 39 (1): 149-55. Cheng Min-Chih, Chuang Yang-An, Lu Chao-Lin, Chen Yu-Jung, Luu Sy-Ueng, Li Jun-Ming, Hsu Shih-Hsin, Chen Chia-Hsia |
Family-based association study of early growth response gene 3 with child bipolar I disorder. Journal of affective disorders 2012 May 138 (3): 387-96. Gallitano Amelia L, Tillman Rebecca, Dinu Valentin, Geller Barba |
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.
Nature genetics 2012 Mar 44 (3): 323-7. Postel-Vinay Sophie, Véron Amélie S, Tirode Franck, Pierron Gaelle, Reynaud Stéphanie, Kovar Heinrich, Oberlin Odile, Lapouble Eve, Ballet Stelly, Lucchesi Carlo, Kontny Udo, González-Neira Anna, Picci Piero, Alonso Javier, Patino-Garcia Ana, de Paillerets Brigitte Bressac, Laud Karine, Dina Christian, Froguel Philippe, Clavel-Chapelon Françoise, Doz Francois, Michon Jean, Chanock Stephen J, Thomas Gilles, Cox David G, Delattre Olivi |
Lack of association of EGR2 variants with bipolar disorder in Japanese population. Gene 2013 Sep 526 (2): 246-50. Balan Shabeesh, Yamada Kazuo, Iwayama Yoshimi, Toyota Tomoko, Ohnishi Tetsuo, Maekawa Motoko, Toyoshima Manabu, Iwata Yasuhide, Suzuki Katsuaki, Kikuchi Mitsuru, Ujike Hiroshi, Inada Toshiya, Kunugi Hiroshi, Ozaki Norio, Iwata Nakao, Nanko Shinichiro, Kato Tadafumi, Yoshikawa Tak |
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
Nature genetics 2014 Sep 46 (9): 1007-11. Hou Shengping, Du Liping, Lei Bo, Pang Chi Pui, Zhang Meifen, Zhuang Wenjuan, Zhang Minglian, Huang Lulin, Gong Bo, Wang Meilin, Zhang Qi, Hu Ke, Zhou Qingyun, Qi Jian, Wang Chaokui, Tian Yuan, Ye Zi, Liang Liang, Yu Hongsong, Li Hong, Zhou Yan, Cao Qingfeng, Liu Yunjia, Bai Lin, Liao Dan, Kijlstra Aize, Xu Jianfeng, Yang Zhenglin, Yang Peize |
Resequencing of early growth response 2 (EGR2) gene revealed a recurrent patient-specific mutation in schizophrenia. Psychiatry research 2015 Aug 228 (3): 958-60. Hu Tsung-Ming, Chen Chia-Hsiang, Chuang Yang-An, Hsu Shih-Hsin, Cheng Min-Ch |
Investigation of the association of Vogt-Koyanagi-Harada syndrome with IL23R-C1orf141 in Han Chinese Singaporean and ADO-ZNF365-EGR2 in Thai. The British journal of ophthalmology 2015 Dec . Cao Shuang, Chee Soon Phaik, Yu Hyeong Gon, Sukavatcharin Somsiri, Wu Lili, Kijlstra Aize, Hou Shengping, Yang Peize |
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 |
Genomic Profile of Chronic Lymphocytic Leukemia in Korea Identified by Targeted Sequencing. PloS one 2016 11 (12): e0167641. Kim Jung-Ah, Hwang Byungjin, Park Si Nae, Huh Sunghoon, Im Kyongok, Choi Sungbin, Chung Hye Yoon, Huh JooRyung, Seo Eul-Ju, Lee Je-Hwan, Bang Duhee, Lee Dong So |
EGR2 mutations define a new clinically aggressive subgroup of chronic lymphocytic leukemia. Leukemia 2017 Jan . Young E, Noerenberg D, Mansouri L, Ljungström V, Frick M, Sutton L-A, Blakemore S J, Galan-Sousa J, Plevova K, Baliakas P, Rossi D, Clifford R, Roos-Weil D, Navrkalova V, Dörken B, Schmitt C A, Smedby K E, Juliusson G, Giacopelli B, Blachly J S, Belessi C, Panagiotidis P, Chiorazzi N, Davi F, Langerak A W, Oscier D, Schuh A, Gaidano G, Ghia P, Xu W, Fan L, Bernard O A, Nguyen-Khac F, Rassenti L, Li J, Kipps T J, Stamatopoulos K, Pospisilova S, Zenz T, Oakes C C, Strefford J C, Rosenquist R, Damm |
Multiple Gene-Environment Interactions on the Angiogenesis Gene-Pathway Impact Rectal Cancer Risk and Survival. International journal of environmental research and public health 2017 Sep 14 (10): . Sharafeldin Noha, Slattery Martha L, Liu Qi, Franco-Villalobos Conrado, Caan Bette J, Potter John D, Yasui Yuta |
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 |
Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing. PloS one 2017 12 (10): e0185602. Lee Jee-Soo, Seo Heewon, Im Kyongok, Park Si Nae, Kim Sung-Min, Lee Eun Kyoung, Kim Jung-Ah, Lee Joon-Hee, Kwon Sunghoon, Kim Miyoung, Koh Insong, Hwang Seungwoo, Park Heung-Woo, Kang Hye-Ryun, Park Kyoung Soo, Kim Ju Han, Lee Dong So |
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 |
An integrated pan-cancer analysis of identifying biomarkers about the EGR family genes in human carcinomas. Computers in biology and medicine 2022 8 148 105889. Hua Youwei, Wang Hetian, Ye Zhiqiang, Zheng Degao, Zhang |
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 |
Subpopulations of cancer-associated fibroblasts link the prognosis and metabolic features of pancreatic ductal adenocarcinoma. Annals of translational medicine 2022 4 10 (5): 262. Hu Beiyuan, Wu Chuntao, Mao Huarong, Gu Haitao, Dong Hanguang, Yan Jiuliang, Qi Zihao, Yuan Lin, Dong Qiongzhu, Long Jia |
Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY. Leukemia 2022 12 37 (2): 339-347. Mansouri Larry, Thorvaldsdottir Birna, Sutton Lesley-Ann, Karakatsoulis Georgios, Meggendorfer Manja, Parker Helen, Nadeu Ferran, Brieghel Christian, Laidou Stamatia, Moia Riccardo, Rossi Davide, Catherwood Mark, Kotaskova Jana, Delgado Julio, Rodríguez-Vicente Ana E, Benito Rocío, Rigolin Gian Matteo, Bonfiglio Silvia, Scarfo Lydia, Mattsson Mattias, Davis Zadie, Gogia Ajay, Rani Lata, Baliakas Panagiotis, Foroughi-Asl Hassan, Jylhä Cecilia, Skaftason Aron, Rapado Inmaculada, Miras Fatima, Martinez-Lopez Joaquín, de la Serna Javier, Rivas Jesús María Hernández, Thornton Patrick, Larráyoz María José, Calasanz María José, Fésüs Viktória, Mátrai Zoltán, Bödör Csaba, Smedby Karin E, Espinet Blanca, Puiggros Anna, Gupta Ritu, Bullinger Lars, Bosch Francesc, Tazón-Vega Bárbara, Baran-Marszak Fanny, Oscier David, Nguyen-Khac Florence, Zenz Thorsten, Terol Maria Jose, Cuneo Antonio, Hernández-Sánchez María, Pospisilova Sarka, Mills Ken, Gaidano Gianluca, Niemann Carsten U, Campo Elias, Strefford Jonathan C, Ghia Paolo, Stamatopoulos Kostas, Rosenquist Richa |
Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing.
Annals of the rheumatic diseases 2023 2 . Ortiz-Fernández Lourdes, Carmona Elio G, Kerick Martin, Lyons Paul, Carmona Francisco David, López Mejías Raquel, Khor Chiea Chuen, Grayson Peter C, Tombetti Enrico, Jiang Lindi, Direskeneli Haner, Saruhan-Direskeneli Guher, Callejas-Rubio José-Luis, Vaglio Augusto, Salvarani Carlo, Hernández-Rodríguez Jose, Cid Maria Cinta, Morgan Ann W, Merkel Peter A, Burgner David, Smith Kenneth Gc, Gonzalez-Gay Miguel Angel, Sawalha Amr H, Martin Javier, Marquez A |
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 |
BTK and PLCG2 remain unmutated in one third of patients with CLL relapsing on ibrutinib. Blood advances 2023 1 . Bonfiglio Silvia, Sutton Lesley-Ann, Ljungström Viktor, Capasso Antonella, Pandzic Tatjana, Weström Simone, Foroughi-Asl Hassan, Skaftason Aron, Gellerbring Anna, Lyander Anna, Gandini Francesca, Gaidano Gianluca, Trentin Livio, Bonello Lisa, Reda Gianluigi, Bödör Csaba, Stavroyianni Niki, Tam Constantine S, Marasca Roberto, Forconi Francesco, Panayiotidis Panayiotis, Ringshausen Ingo, Jaksic Ozren, Frustaci Anna Maria, Iyengar Sunil, Coscia Marta, Mulligan Stephen P, Ysebaert Loïc, Strugov Vladimir, Pavlovsky Carolina, Walewska Renata, Österborg Anders, Cortese Diego, Ranghetti Pamela, Baliakas Panagiotis, Stamatopoulos Kostas, Scarfò Lydia, Rosenquist Richard, Ghia Pao |
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- Page last updated:Apr 22, 2024
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