Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: EPHA3[original query] |
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Exploring the link between germline and somatic genetic alterations in breast carcinogenesis. PloS one 2010 5 (11): e14078. Bonifaci Núria, Górski Bohdan, Masoj? Bartlomiej, Woko?orczyk Dominika, Jakubowska Anna, D?bniak Tadeusz, Berenguer Antoni, Serra Musach Jordi, Brunet Joan, Dopazo Joaquín, Narod Steven A, Lubi?ski Jan, Lázaro Conxi, Cybulski Cezary, Pujana Miguel Ang |
Copy number variations of EphA3 are associated with multiple types of hematologic malignancies. Clinical lymphoma, myeloma & leukemia 2011 Feb 11 (1): 50-3. Guan Ming, Liu Li, Zhao Xiaosu, Wu Qi, Yu Bo, Shao Yong, Yang Hong, Fu Xinrong, Wan Jun, Zhang W |
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human genetics 2012 Apr 131 (4): 565-79. Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid, Ennis Se |
Association of Ephrin receptor A3 gene polymorphism with susceptibility to chronic severe hepatitis B. Hepatology research : the official journal of the Japan Society of Hepatology 2012 Aug 42 (8): 790-7. Yang Hong, He Xing-Xing, Song Qi-Long, Chen Man, Li Jin, Wang Meng-Yi, Yu Jin-Ling, Yao Jin-Jian, Liu Li-Feng, Lin Ju-She |
Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor. PloS one 2013 8 (8): e72381. Uyan Özgün, Ömür Özgür, A??m Zeynep Sena, Özo?uz Asl?han, Li Hong, Parman Ye?im, Deymeer Feza, Oflazer Piraye, Koç Filiz, Tan Ersin, Özçelik Hilmi, Ba?ak A Naz |
copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer. PloS one 2013 8 (8): e71802. Kuusisto Kirsi M, Akinrinade Oyediran, Vihinen Mauno, Kankuri-Tammilehto Minna, Laasanen Satu-Leena, Schleutker Johan |
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors. Cancer causes & control : CCC 2014 Jun 25 (6): 759-69. Huhn Stefanie, Bevier Melanie, Pardini Barbara, Naccarati Alessio, Vodickova Ludmila, Novotny Jan, Vodicka Pavel, Hemminki Kari, Försti As |
Clonal architectures and driver mutations in metastatic melanomas. PloS one 2014 9 (11): e111153. Ding Li, Kim Minjung, Kanchi Krishna L, Dees Nathan D, Lu Charles, Griffith Malachi, Fenstermacher David, Sung Hyeran, Miller Christopher A, Goetz Brian, Wendl Michael C, Griffith Obi, Cornelius Lynn A, Linette Gerald P, McMichael Joshua F, Sondak Vernon K, Fields Ryan C, Ley Timothy J, Mulé James J, Wilson Richard K, Weber Jeffrey |
Association of EPHA3 Gene Polymorphisms with Nonsyndromic Cleft Lip With or Without Cleft Palate. Genetic testing and molecular biomarkers 2018 Jun . Chen Renji, Guo Siyuan, Wang Xin, Mu Yue, Duan Erling, Xu |
EphA3 Downregulation by Hypermethylation Associated with Lymph Node Metastasis and TNM Stage in Colorectal Cancer. Digestive diseases and sciences 2018 12 64 (6): 1514-1522. Wang Yong, Xuan Zhuoqi, Wang Baocheng, Zhang Dongsheng, Zhang Chuan, Wang Jiandong, Sun Yuemi |
Pathway analysis of a genome-wide gene by air pollution interaction study in asthmatic children.
Journal of exposure science & environmental epidemiology 2019 Jun 29 (4): 539-547. Ierodiakonou Despo, Coull Brent A, Zanobetti Antonella, Postma Dirkje S, Boezen H Marike, Vonk Judith M, McKone Edward F, Schildcrout Jonathan S, Koppelman Gerard H, Croteau-Chonka Damien C, Lumley Thomas, Koutrakis Petros, Schwartz Joel, Gold Diane R, Weiss Scott |
Comparison of genomic landscapes of large cell neuroendocrine carcinoma, small cell lung carcinoma, and large cell carcinoma. Thoracic cancer 2019 2 10 (4): 839-847. Zhou Zhen, Zhu Lei, Niu Xiaomin, Shen Shengping, Zhao Yi, Zhang Jie, Ye Junyi, Han-Zhang Han, Liu Junjun, Liu Chenglin, Lu Sh |
Survival Benefit and Genetic Profile of Pemetrexed as Initial Chemotherapy in Selected Chinese Patients With Advanced Lung Adenocarcinoma. Frontiers in oncology 2020 10 10 1568. Guo Long-Hua, Zhang Ming-Feng, Zhang He-Long, Zhou Jian-Ying, Cai Xiao-Hong, Long Yu, Guo Qi-Sen, Yang Nong, Zhao Jun, Xie Zhan-Hong, Jiang Bo, Zhu Ying, Fan Yun, Xie Cong-Ying, Hu Yi, Yao Yu, Jia Jun, Li Xiao-Ling, Cui Jiu-Wei, Sui Xi-Zhao, Lin Wen, Cheng Ying, Wang Hui-Juan, Wang Chang-Li, Zhao Ming-Fang, Qiao Gui-Bin, Peng Li-Jun, Yang Lin, Chen Gong-Yan, Cai Kai-Can, Xu Xin-Hua, Zhang Liang-Ming, Feng Guo-Sheng, Zhou Jing-Min, Wu Guo-Wu, Dong Xiao-Rong, Wang Li-Feng, Zhang Hong-Mei, Gao Ya-Jie, Jiang Qiu-Ying, Cang Shun-Dong, Yang Zhi-Xiong, Song Xia, Liu Xiao-Qing, Zhu Bo, Chen Feng-Xia, Hu Chun-Hong, Chen Xi, Wu Yi-Long, Zhou Qi |
Two progressed malignant phyllodes tumors of the breast harbor alterations in genes frequently involved in other advanced cancers. Orphanet journal of rare diseases 2021 Aug 16 (1): 363. Reinisch Mattea, Kuemmel Sherko, Breit Elisabeth, Theuerkauf Ingo, Harrach Hakima, Schindowski Dorothea, Moka Detlef, Bettstetter Marcus, Bruzas Simona, Chiari Ouaf |
Longitudinal change of genetic variations in cetuximab-treated metastatic colorectal cancer. Cancer genetics 2021 7 258-259 27-36. Kim Sun Young, Kim Kwoneel, Cho Su Han, Chun Sung-Min, Tak Eunyoung, Hong Yong Sang, Kim Jeong Eun, Kim Tae W |
Novel targetable FGFR2 and FGFR3 alterations in glioblastoma associate with aggressive phenotype and distinct gene expression programs. Acta neuropathologica communications 2021 04 9 (1): 69. Georgescu Maria-Magdalena, Islam Mohammad Zahidul, Li Yan, Traylor James, Nanda An |
The genetic architecture of language functional connectivity.
NeuroImage 2021 12 249 118795. Mekki Yasmina, Guillemot Vincent, Lemaître Hervé, Carrión-Castillo Amaia, Forkel Stephanie, Frouin Vincent, Philippe Cat |
Genomic features of Chinese small cell lung cancer. BMC medical genomics 2022 May 15 (1): 117. Liu Jun, Zhao Zhuxiang, Wei Shuquan, Li Binkai, Zhao Ziw |
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- Page last updated:Apr 22, 2024
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