Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: RBMS3[original query] |
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Gene-gene interaction between RBMS3 and ZNF516 influences bone mineral density. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2012 Oct . Yang TL, Guo Y, Li J, Zhang L, Shen H, Li SM, Li SK, Tian Q, Liu YJ, Papasian CJ, Deng HW |
Genomewide pharmacogenetics of bisphosphonate-induced osteonecrosis of the jaw: the role of RBMS3. The oncologist 2012 17 (2): 279-87. Nicoletti Paola, Cartsos Vassiliki M, Palaska Penelope K, Shen Yufeng, Floratos Aris, Zavras Athanasios |
Genetic mapping with multiple levels of phenotypic information reveals determinants of lymphocyte glucocorticoid sensitivity. American journal of human genetics 2013 Sep . Maranville JC, Baxter SS, Witonsky DB, Chase MA, Di Rienzo A |
Polymorphisms in C-reactive protein and Glypican-5 are associated with lung cancer risk and Gartrokine-1 influences Cisplatin-based chemotherapy response in a Chinese Han population. Disease markers 2015 2015 824304. Zhang Shuo, Thakur Asmitananda, Liang Yiqian, Wang Ting, Gao Lei, Yang Tian, Li Yang, Geng Tingting, Jin Tianbo, Chen Tianjun, Liu Johnson J, Chen Mingw |
Head injury, potential interaction with genes, and risk for Parkinson's disease. Parkinsonism & related disorders 2015 Mar 21 (3): 292-6. Gao Jianjun, Liu Rui, Zhao Edward, Huang Xuemei, Nalls Michael A, Singleton Andrew B, Chen Hongl |
Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study.
Human genetics 2016 Aug . Song I-Wen, Chen Hsiang-Cheng, Lin Yuh-Feng, Yang Jenn-Hwai, Chang Chi-Ching, Chou Chung-Tei, Lee Ming-Ta Michael, Chou Yi-Chun, Chen Chien-Hsiun, Chen Yuan-Tsong, Chen Chen-Hung, Wu Jer-Yua |
Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.
Human molecular genetics 2016 May 25 (10): 2113-2129. Offenbacher Steven, Divaris Kimon, Barros Silvana P, Moss Kevin L, Marchesan Julie T, Morelli Thiago, Zhang Shaoping, Kim Steven, Sun Lu, Beck James D, Laudes Matthias, Munz Matthias, Schaefer Arne S, North Kari |
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nature genetics 2017 May . Aung Tin, Ozaki Mineo, Lee Mei Chin, Schlötzer-Schrehardt Ursula, Thorleifsson Gudmar, Mizoguchi Takanori, Igo Robert P, Haripriya Aravind, Williams Susan E, Astakhov Yury S, Orr Andrew C, Burdon Kathryn P, Nakano Satoko, Mori Kazuhiko, Abu-Amero Khaled, Hauser Michael, Li Zheng, Prakadeeswari Gopalakrishnan, Bailey Jessica N Cooke, Cherecheanu Alina Popa, Kang Jae H, Nelson Sarah, Hayashi Ken, Manabe Shin-Ichi, Kazama Shigeyasu, Zarnowski Tomasz, Inoue Kenji, Irkec Murat, Coca-Prados Miguel, Sugiyama Kazuhisa, Järvelä Irma, Schlottmann Patricio, Lerner S Fabian, Lamari Hasnaa, Nilgün Yildirim, Bikbov Mukharram, Park Ki Ho, Cha Soon Cheol, Yamashiro Kenji, Zenteno Juan C, Jonas Jost B, Kumar Rajesh S, Perera Shamira A, Chan Anita S Y, Kobakhidze Nino, George Ronnie, Vijaya Lingam, Do Tan, Edward Deepak P, de Juan Marcos Lourdes, Pakravan Mohammad, Moghimi Sasan, Ideta Ryuichi, Bach-Holm Daniella, Kappelgaard Per, Wirostko Barbara, Thomas Samuel, Gaston Daniel, Bedard Karen, Greer Wenda L, Yang Zhenglin, Chen Xueyi, Huang Lulin, Sang Jinghong, Jia Hongyan, Jia Liyun, Qiao Chunyan, Zhang Hui, Liu Xuyang, Zhao Bowen, Wang Ya-Xing, Xu Liang, Leruez Stéphanie, Reynier Pascal, Chichua George, Tabagari Sergo, Uebe Steffen, Zenkel Matthias, Berner Daniel, Mossböck Georg, Weisschuh Nicole, Hoja Ursula, Welge-Luessen Ulrich-Christoph, Mardin Christian, Founti Panayiota, Chatzikyriakidou Anthi, Pappas Theofanis, Anastasopoulos Eleftherios, Lambropoulos Alexandros, Ghosh Arkasubhra, Shetty Rohit, Porporato Natalia, Saravanan Vijayan, Venkatesh Rengaraj, Shivkumar Chandrashekaran, Kalpana Narendran, Sarangapani Sripriya, Kanavi Mozhgan R, Beni Afsaneh Naderi, Yazdani Shahin, Lashay Alireza, Naderifar Homa, Khatibi Nassim, Fea Antonio, Lavia Carlo, Dallorto Laura, Rolle Teresa, Frezzotti Paolo, Paoli Daniela, Salvi Erika, Manunta Paolo, Mori Yosai, Miyata Kazunori, Higashide Tomomi, Chihara Etsuo, Ishiko Satoshi, Yoshida Akitoshi, Yanagi Masahide, Kiuchi Yoshiaki, Ohashi Tsutomu, Sakurai Toshiya, Sugimoto Takako, Chuman Hideki, Aihara Makoto, Inatani Masaru, Miyake Masahiro, Gotoh Norimoto, Matsuda Fumihiko, Yoshimura Nagahisa, Ikeda Yoko, Ueno Morio, Sotozono Chie, Jeoung Jin Wook, Sagong Min, Park Kyu Hyung, Ahn Jeeyun, Cruz-Aguilar Marisa, Ezzouhairi Sidi M, Rafei Abderrahman, Chong Yaan Fun, Ng Xiao Yu, Goh Shuang Ru, Chen Yueming, Yong Victor H K, Khan Muhammad Imran, Olawoye Olusola O, Ashaye Adeyinka O, Ugbede Idakwo, Onakoya Adeola, Kizor-Akaraiwe Nkiru, Teekhasaenee Chaiwat, Suwan Yanin, Supakontanasan Wasu, Okeke Suhanya, Uche Nkechi J, Asimadu Ifeoma, Ayub Humaira, Akhtar Farah, Kosior-Jarecka Ewa, Lukasik Urszula, Lischinsky Ignacio, Castro Vania, Grossmann Rodolfo Perez, Megevand Gordana Sunaric, Roy Sylvain, Dervan Edward, Silke Eoin, Rao Aparna, Sahay Priti, Fornero Pablo, Cuello Osvaldo, Sivori Delia, Zompa Tamara, Mills Richard A, Souzeau Emmanuelle, Mitchell Paul, Wang Jie Jin, Hewitt Alex W, Coote Michael, Crowston Jonathan G, Astakhov Sergei Y, Akopov Eugeny L, Emelyanov Anton, Vysochinskaya Vera, Kazakbaeva Gyulli, Fayzrakhmanov Rinat, Al-Obeidan Saleh A, Owaidhah Ohoud, Aljasim Leyla Ali, Chowbay Balram, Foo Jia Nee, Soh Raphael Q, Sim Kar Seng, Xie Zhicheng, Cheong Augustine W O, Mok Shi Qi, Soo Hui Meng, Chen Xiao Yin, Peh Su Qin, Heng Khai Koon, Husain Rahat, Ho Su-Ling, Hillmer Axel M, Cheng Ching-Yu, Escudero-Domínguez Francisco A, González-Sarmiento Rogelio, Martinon-Torres Frederico, Salas Antonio, Pathanapitoon Kessara, Hansapinyo Linda, Wanichwecharugruang Boonsong, Kitnarong Naris, Sakuntabhai Anavaj, Nguyn Hip X, Nguyn Giang T T, Nguyn Trình V, Zenz Werner, Binder Alexander, Klobassa Daniela S, Hibberd Martin L, Davila Sonia, Herms Stefan, Nöthen Markus M, Moebus Susanne, Rautenbach Robyn M, Ziskind Ari, Carmichael Trevor R, Ramsay Michele, Álvarez Lydia, García Montserrat, González-Iglesias Héctor, Rodríguez-Calvo Pedro P, Cueto Luis Fernández-Vega, Oguz Çilingir, Tamcelik Nevbahar, Atalay Eray, Batu Bilge, Aktas Dilek, Kas?m Burcu, Wilson M Roy, Coleman Anne L, Liu Yutao, Challa Pratap, Herndon Leon, Kuchtey Rachel W, Kuchtey John, Curtin Karen, Chaya Craig J, Crandall Alan, Zangwill Linda M, Wong Tien Yin, Nakano Masakazu, Kinoshita Shigeru, den Hollander Anneke I, Vesti Eija, Fingert John H, Lee Richard K, Sit Arthur J, Shingleton Bradford J, Wang Ningli, Cusi Daniele, Qamar Raheel, Kraft Peter, Pericak-Vance Margaret A, Raychaudhuri Soumya, Heegaard Steffen, Kivelä Tero, Reis André, Kruse Friedrich E, Weinreb Robert N, Pasquale Louis R, Haines Jonathan L, Thorsteinsdottir Unnur, Jonasson Fridbert, Allingham R Rand, Milea Dan, Ritch Robert, Kubota Toshiaki, Tashiro Kei, Vithana Eranga N, Micheal Shazia, Topouzis Fotis, Craig Jamie E, Dubina Michael, Sundaresan Periasamy, Stefansson Kari, Wiggs Janey L, Pasutto Francesca, Khor Chiea Chu |
Pharmacogenomics of osteonecrosis of the jaw. Bone 2019 4 124 75-82. Yang Guang, Singh Sonal, Chen Yiqing, Hamadeh Issam S, Langaee Taimour, McDonough Caitrin W, Holliday L Shannon, Lamba Jatinder K, Moreb Jan S, Katz Joseph, Gong Y |
NEW GENETIC MARKERS ASSOCIATED WITH SUSCEPTIBILITY TO EXFOLIATION SYNDROME AMONG GEORGIAN POPULATION. Georgian medical news 2019 Sep (294): 41-45. Kobakhidze N, Tabagari S, Chichua |
Host genetics influences the relationship between the gut microbiome and psychiatric disorders. Progress in neuro-psychopharmacology & biological psychiatry 2020 11 106 110153. Martins-Silva Thais, Salatino-Oliveira Angélica, Genro Júlia Pasqualini, Meyer Fernando D T, Li Yan, Rohde Luís Augusto, Hutz Mara Helena, Tovo-Rodrigues Lucia |
Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury.
Journal of personalized medicine 2022 May 12 (6): . Klumpers Marije J, Witte Ward De, Gattuso Giovanna, Schiavello Elisabetta, Terenziani Monica, Massimino Maura, Gidding Corrie E M, Vermeulen Sita H, Driessen Chantal M, Van Herpen Carla M, Van Meerten Esther, Guchelaar Henk-Jan, Coenen Marieke J H, Te Loo D Maroeska W |
Genome-wide Association Study of Methotrexate-Induced Liver Injury in Rheumatoid Arthritis Patients.
Clinical pharmacology and therapeutics 2023 1 . Eektimmerman Frank, Swen Jesse J, den Broeder Alfons A, Hazes Johanna M W, Kurreeman Fina S, Verstappen Suzanne M M, Nair Nisha, Pawlik Andrzej, Nurmohamed Mike T, Dolžan Vita, Böhringer Stefan, Allaart Cornelia F, Guchelaar Henk-J |
Proteo-genomics of soluble TREM2 in cerebrospinal fluid provides novel insights and identifies novel modulators for Alzheimer's disease. Molecular neurodegeneration 2024 1 19 (1): 1. Lihua Wang, Niko-Petteri Nykänen, Daniel Western, Priyanka Gorijala, Jigyasha Timsina, Fuhai Li, Zhaohua Wang, Muhammad Ali, Chengran Yang, Menghan Liu, William Brock, Marta Marquié, Mercè Boada, Ignacio Alvarez, Miquel Aguilar, Pau Pastor, Agustín Ruiz, Raquel Puerta, Adelina Orellana, Jarod Rutledge, Hamilton Oh, Michael D Greicius, Yann Le Guen, Richard J Perrin, Tony Wyss-Coray, Angela Jefferson, Timothy J Hohman, Neill Graff-Radford, Hiroshi Mori, Alison Goate, Johannes Levin, Yun Ju Sung, Carlos Crucha |
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- Page last updated:May 20, 2024
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