Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: RCBTB1[original query] |
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Comprehensive testing of positionally cloned asthma genes in two populations. American journal of respiratory and critical care medicine 2007 Nov 176 (9): 849-57. Hersh Craig P, Raby Benjamin A, Soto-Quirós Manuel E, Murphy Amy J, Avila Lydiana, Lasky-Su Jessica, Sylvia Jody S, Klanderman Barbara J, Lange Christoph, Weiss Scott T, Celedón Juan |
Genome-wide interaction study identifies RCBTB1 as a modifier for smoking effect on carotid intima-media thickness. Arteriosclerosis, thrombosis, and vascular biology 2014 Jan 34 (1): 219-25. Wang Liyong, Rundek Tatjana, Beecham Ashley, Hudson Barry, Blanton Susan H, Zhao Hongyu, Sacco Ralph L, Dong Chuanh |
arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Sep . Van Cauwenbergh Caroline, Van Schil Kristof, Cannoodt Robrecht, Bauwens Miriam, Van Laethem Thalia, De Jaegere Sarah, Steyaert Wouter, Sante Tom, Menten Björn, Leroy Bart P, Coppieters Frauke, De Baere Elfri |
Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study.
Frontiers in genetics 2019 10 1354. Boua Palwende Romuald, Brandenburg Jean-Tristan, Choudhury Ananyo, Hazelhurst Scott, Sengupta Dhriti, Agongo Godfred, Nonterah Engelbert A, Oduro Abraham R, Tinto Halidou, Mathew Christopher G, Sorgho Hermann, Ramsay Michè |
Mutation spectrum in a cohort with familial exudative vitreoretinopathy. Molecular genetics & genomic medicine 2022 Jul e2021. Qu Ning, Li Wei, Han Dong-Ming, Gao Jia-Yu, Yang Zheng-Tao, Jiang Li, Liu Tian-Bin, Chen Yan-Xian, Jiang Xiao-Sen, Zhou Liang, Wu Ji-Hong, Huang X |
Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. Ophthalmic genetics 2022 1 43 (3): 332-339. Catomeris Andrew J, Ballios Brian G, Sangermano Riccardo, Wagner Naomi E, Comander Jason I, Pierce Eric A, Place Emily M, Bujakowska Kinga M, Huckfeldt Rachel |
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