Human Genome Epidemiology Literature Finder

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Records 1 - 7 (of 7 Records)

Query Trace: Disease and ESRRB[original query]
Evidence of genetic variations associated with rotator cuff disease. Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2014 Feb 23 (2): 227-35. Motta Geraldo da Rocha, Amaral Marcus Vinícius, Rezende Eduardo, Pitta Rafael, Vieira Thays Cristine dos Santos, Duarte Maria Eugenia Leite, Vieira Alexandre Rezende, Casado Priscila Ladei Similar articles in PubMed
Significant association of full-thickness rotator cuff tears and estrogen-related receptor-ß (ESRRB). Journal of shoulder and elbow surgery / American Shoulder and Elbow Surgeons ... [et al.] 2015 Feb 24 (2): e31-5. Teerlink Craig C, Cannon-Albright Lisa A, Tashjian Robert Similar articles in PubMed
ESRRB polymorphisms are associated with comorbidity of temporomandibular disorders and rotator cuff disease. International journal of oral and maxillofacial surgery 2015 Nov . Bonato L L, Quinelato V, Pinheiro A daR, Amaral M V G, de Souza F N, Lobo J C, Aguiar D P, Augusto L M M, Vieira A R, Salles J I, Cossich V R A, Guimarães J A M, de Gouvêa C V D, Granjeiro J M, Casado P Similar articles in PubMed
Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese. Nature communications 2018 Oct 9 (1): 4072. Zheng Ruijuan, Li Zhiqiang, He Fusheng, Liu Haipeng, Chen Jianhua, Chen Jiayu, Xie Xuefeng, Zhou Juan, Chen Hao, Wu Xiangyang, Wu Juehui, Chen Boyu, Liu Yahui, Cui Haiyan, Fan Lin, Sha Wei, Liu Yin, Wang Jiqiang, Huang Xiaochen, Zhang Linfeng, Xu Feifan, Wang Jie, Feng Yonghong, Qin Lianhua, Yang Hua, Liu Zhonghua, Cui Zhenglin, Liu Feng, Chen Xinchun, Gao Shaorong, Sun Silong, Shi Yongyong, Ge Baox Similar articles in PubMed
Genetic basis of rotator cuff injury: a systematic review. BMC medical genetics 2019 9 20 (1): 149. Longo Umile Giuseppe, Candela Vincenzo, Berton Alessandra, Salvatore Giuseppe, Guarnieri Andrea, DeAngelis Joseph, Nazarian Ara, Denaro Vincen Similar articles in PubMed
Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease. Frontiers in genetics 2019 10 76. Gallego-Martinez Alvaro, Requena Teresa, Roman-Naranjo Pablo, Lopez-Escamez Jose Similar articles in PubMed
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax Similar articles in PubMed