Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: KRT18[original query] |
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| Keratin variants predispose to acute liver failure and adverse outcome: race and ethnic associations. Gastroenterology 2010 Sep 139 (3): 828-35, 835.e1-3. Strnad Pavel, Zhou Qin, Hanada Shinichiro, Lazzeroni Laura C, Zhong Bi Hui, So Phillip, Davern Timothy J, Lee William M, , Omary M Bis |
| An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion. BMC medical genetics 2011 12 (1): 62. Stanke Frauke, Hedtfeld Silke, Becker Tim, Tümmler Burkha |
Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.
Nature communications 2017 Feb 8 14364. Yu Yanqin, Zuo Xianbo, He Miao, Gao Jinping, Fu Yuchuan, Qin Chuanqi, Meng Liuyan, Wang Wenjun, Song Yaling, Cheng Yong, Zhou Fusheng, Chen Gang, Zheng Xiaodong, Wang Xinhuan, Liang Bo, Zhu Zhengwei, Fu Xiazhou, Sheng Yujun, Hao Jiebing, Liu Zhongyin, Yan Hansong, Mangold Elisabeth, Ruczinski Ingo, Liu Jianjun, Marazita Mary L, Ludwig Kerstin U, Beaty Terri H, Zhang Xuejun, Sun Liangdan, Bian Zhu |
| Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
Human genetics 2017 Mar 136 (3): 275-286. Leslie Elizabeth J, Carlson Jenna C, Shaffer John R, Butali Azeez, Buxó Carmen J, Castilla Eduardo E, Christensen Kaare, Deleyiannis Fred W B, Leigh Field L, Hecht Jacqueline T, Moreno Lina, Orioli Ieda M, Padilla Carmencita, Vieira Alexandre R, Wehby George L, Feingold Eleanor, Weinberg Seth M, Murray Jeffrey C, Beaty Terri H, Marazita Mary |
| Comprehensive Cohort Analysis of Mutational Spectrum in Early Onset Breast Cancer Patients. Cancers 2020 Jul 12 (8): . Midha Mohit K, Huang Yu-Feng, Yang Hsiao-Hsiang, Fan Tan-Chi, Chang Nai-Chuan, Chen Tzu-Han, Wang Yu-Tai, Kuo Wen-Hung, Chang King-Jen, Shen Chen-Yang, Yu Alice L, Chiu Kuo-Ping, Chen Chien-J |
| The landscape of RNA polymerase II-associated chromatin interactions in prostate cancer. The Journal of clinical investigation 2020 4 130 (8): 3987-4005. Ramanand Susmita G, Chen Yong, Yuan Jiapei, Daescu Kelly, Lambros Maryou Bk, Houlahan Kathleen E, Carreira Suzanne, Yuan Wei, Baek GuemHee, Sharp Adam, Paschalis Alec, Kanchwala Mohammed, Gao Yunpeng, Aslam Adam, Safdar Nida, Zhan Xiaowei, Raj Ganesh V, Xing Chao, Boutros Paul C, de Bono Johann, Zhang Michael Q, Mani Ram |
| Whole exome sequencing identifies the novel putative gene variants related with type 2 diabetes in Mizo population, northeast India. Gene 2020 10 769 145229. Lalrohlui Freda, Zohmingthanga John, Hruaii Vanlal, Vanlallawma Andrew, Senthil Kumar Nachimut |
| Associations between pancreatic expression quantitative traits and risk of pancreatic ductal adenocarcinoma.
Carcinogenesis 2021 Jul . Pistoni Laura, Gentiluomo Manuel, Lu Ye, López de Maturana Evangelina, Hlavac Viktor, Vanella Giuseppe, Darvasi Erika, Milanetto Anna Caterina, Oliverius Martin, Vashist Yogesh, Di Leo Milena, Mohelnikova-Duchonova Beatrice, Talar-Wojnarowska Renata, Gheorghe Cristian, Petrone Maria Chiara, Strobel Oliver, Arcidiacono Paolo Giorgio, Vodickova Ludmila, Szentesi Andrea, Capurso Gabriele, Gajdán László, Malleo Giuseppe, Theodoropoulos George E, Basso Daniela, Soucek Pavel, Brenner Hermann, Lawlor Rita T, Morelli Luca, Ivanauskas Audrius, , Kauffmann Emanuele Federico, Macauda Angelica, Gazouli Maria, Archibugi Livia, Nentwich Michael, Love?ek Martin, Cavestro Giulia Martina, Vodicka Pavel, Landi Stefano, Tavano Francesca, Sperti Cosimo, Hackert Thilo, Kupcinskas Juozas, Pezzilli Raffaele, Andriulli Angelo, Pollina Luca, Kreivenaite Edita, Gioffreda Domenica, Jamroziak Krzysztof, Hegyi Péter, Izbicki Jakob R, Testoni Sabrina Gloria Giulia, Zuppardo Raffaella Alessia, Bozzato Dania, Neoptolemos John P, Malats Núria, Canzian Federico, Campa Danie |
| Molecular characterization of vascular intestinal obstruction using whole-exome sequencing. Annals of translational medicine 2022 5 10 (8): 442. Ji Zhong, Du Zhaohui, Zheng Chuanming, Dou Hehe, Jiang Hai, Wang Xing, Wang Zhenj |
| Identification of Potentially Pathogenic Variants Associated with Recurrence in Medication-Related Osteonecrosis of the Jaw (MRONJ) Patients Using Whole-Exome Sequencing. Journal of clinical medicine 2022 4 11 (8): . Kim Songmi, Mun Seyoung, Shin Wonseok, Han Kyudong, Kim Moon-You |
| Impact of keratins 8 and 18 genetic variants on the severity of alcoholic liver disease. Laboratory investigation; a journal of technical methods and pathology 2024 9 102133. Matthieu Tihy, Nathalie Lin-Marq, Thierry Berney, Laurent Spahr, Laura Rubbia-Brandt, Laure Elkri |
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