Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: FOXF2[original query] |
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De novo copy number variants are associated with congenital diaphragmatic hernia. Journal of medical genetics 2012 Oct 49 (10): 650-9. Yu Lan, Wynn Julia, Ma Lijiang, Guha Saurav, Mychaliska George B, Crombleholme Timothy M, Azarow Kenneth S, Lim Foong Yen, Chung Dai H, Potoka Douglas, Warner Brad W, Bucher Brian, LeDuc Charles A, Costa Katherine, Stolar Charles, Aspelund Gudrun, Arkovitz Marc S, Chung Wendy |
Genome-wide interaction study of smoking and bladder cancer risk.
Carcinogenesis 2014 Aug 35 (8): 1737-44. Figueroa Jonine D, Han Summer S, Garcia-Closas Montserrat, Baris Dalsu, Jacobs Eric J, Kogevinas Manolis, Schwenn Molly, Malats Nuria, Johnson Alison, Purdue Mark P, Caporaso Neil, Landi Maria Teresa, Prokunina-Olsson Ludmila, Wang Zhaoming, Hutchinson Amy, Burdette Laurie, Wheeler William, Vineis Paolo, Siddiq Afshan, Cortessis Victoria K, Kooperberg Charles, Cussenot Olivier, Benhamou Simone, Prescott Jennifer, Porru Stefano, Bueno-de-Mesquita H Bas, Trichopoulos Dimitrios, Ljungberg Börje, Clavel-Chapelon Françoise, Weiderpass Elisabete, Krogh Vittorio, Dorronsoro Miren, Travis Ruth, Tjønneland Anne, Brenan Paul, Chang-Claude Jenny, Riboli Elio, Conti David, Gago-Dominguez Manuela, Stern Mariana C, Pike Malcolm C, Van Den Berg David, Yuan Jian-Min, Hohensee Chancellor, Rodabough Rebecca, Cancel-Tassin Geraldine, Roupret Morgan, Comperat Eva, Chen Constance, De Vivo Immaculata, Giovannucci Edward, Hunter David J, Kraft Peter, Lindstrom Sara, Carta Angela, Pavanello Sofia, Arici Cecilia, Mastrangelo Giuseppe, Karagas Margaret R, Schned Alan, Armenti Karla R, Hosain G M Monawar, Haiman Chris A, Fraumeni Joseph F, Chanock Stephen J, Chatterjee Nilanjan, Rothman Nathaniel, Silverman Debra |
Novel evidence of association with nonsyndromic cleft lip with or without cleft palate was shown for single nucleotide polymorphisms in FOXF2 gene in an Asian population. Birth defects research. Part A, Clinical and molecular teratology 2015 Aug . Bu Lingxue, Chen Qianqian, Wang Hong, Zhang Tianxiao, Hetmanski Jacqueline B, Schwender Holger, Parker Margaret, Chou Yah-Huei Wu, Yeow Vincent, Chong Samuel S, Zhang Bo, Jabs Ethylin Wang, Scott Alan F, Beaty Terri |
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.
The Lancet. Neurology 2016 06 15 (7): 695-707. Authors are not available |
Polymorphisms in Epithelial-Mesenchymal Transition-Related Genes and the Prognosis of Surgically Treated Non-small Cell Lung Cancer. Annals of surgical oncology 2017 Aug . Seok Yangki, Kang Hyo-Gyoung, Lee Shin Yup, Jeong Ji Yun, Choi Jin Eun, Jung Deuk Kju, Jin Cheng Cheng, Hong Mi Jeong, Do Sook Kyung, Lee Won Kee, Park Ji Young, Shin Kyung Min, Yoo Seung Soo, Lee Jaehee, Cho Sukki, Cha Seung Ick, Kim Chang Ho, Jheon Sanghoon, Lee Eung Bae, Park Jae Yo |
Association of FOXF2 gene polymorphisms with ischemic stroke in Chinese Han population. Oncotarget 2017 Oct 8 (52): 89867-89875. Shi Chang-He, Tang Mi-Bo, Li Shao-Hua, Wang Zhi-Jie, Liu Xin-Jing, Zhao Lu, Gao Yuan, Li Yu-Sheng, Sun Shi-Lei, Wu Jun, Song Bo, Xu Yu-Mi |
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
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