Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and DGCR8[original query] |
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| Common genetic polymorphisms of microRNA biogenesis pathway genes and breast cancer survival. BMC cancer 2012 12 (1): 195. Sung Hyuna, Jeon Sujee, Lee Kyoung-Mu, Han Sohee, Song Minkyo, Choi Ji-Yeob, Park Sue K, Yoo Keun-Young, Noh Dong-Young, Ahn Sei-Hyun, Kang Daeh |
| Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications. JAMA neurology 2013 Nov 70 (11): 1359-66. Butcher Nancy J, Kiehl Tim-Rasmus, Hazrati Lili-Naz, Chow Eva W C, Rogaeva Ekaterina, Lang Anthony E, Bassett Anne |
| Ambient particulate air pollution and microRNAs in elderly men. Epidemiology (Cambridge, Mass.) 2014 Jan 25 (1): 68-78. Fossati Serena, Baccarelli Andrea, Zanobetti Antonella, Hoxha Mirjam, Vokonas Pantel S, Wright Robert O, Schwartz Jo |
| Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
| SNP Variation in MicroRNA Biogenesis Pathway Genes as a New Innovation Strategy for Alzheimer Disease Diagnostics: A Study of 10 Candidate Genes in an Understudied Population From the Eastern Mediterranean. Alzheimer disease and associated disorders 2016 Jan . Görücü Yilmaz ?enay, Erdal Mehmet E, Avci Özge Aynur, Sungur Mehmet |
| Polymorphisms and expression of genes encoding Argonautes 1 and 2 in autoimmune thyroid diseases. Autoimmunity 2017 Dec 1-8. Tokiyoshi Ena, Watanabe Mikio, Inoue Naoya, Hidaka Yoh, Iwatani Yoshino |
| Correlation analysis between SNPs in microRNA-machinery genes and tuberculosis susceptibility in the Chinese Uygur population. Medicine 2018 Dec 97 (52): e13637. Cheng Hong, Li Haixia, Feng Yangchun, Zhang Zhaox |
| Gene expression over the course of schizophrenia: from clinical high-risk for psychosis to chronic stages. NPJ schizophrenia 2019 Mar 5 (1): 5. Ota Vanessa Kiyomi, Moretti Patricia Natalia, Santoro Marcos Leite, Talarico Fernanda, Spindola Leticia Maria, Xavier Gabriela, Carvalho Carolina Muniz, Marques Diogo Ferri, Costa Giovany Oliveira, Pellegrino Renata, de Jong Simone, Cordeiro Quirino, Hakonarson Hakon, Breen Gerome, Noto Cristiano, Bressan Rodrigo Affonseca, Gadelha Ary, Jesus Mari Jair de, Belangero Sintia |
| Race disparities in genetic alterations within Wilms tumor specimens. Journal of pediatric surgery 2021 Feb . Apple Annie N, Neuzil Kevin E, Phelps Hannah M, Li Bingshan, Lovvorn Iii Harold |
| Whole-Exome Sequencing Among Chinese Patients With Hereditary Diffuse Gastric Cancer. JAMA network open 2022 Dec 5 (12): e2245836. Liu Ze-Xian, Zhang Xiao-Long, Zhao Qi, Chen Yungchang, Sheng Hui, He Cai-Yun, Sun Yu-Ting, Lai Ming-Yu, Wu Min-Qing, Zuo Zhi-Xiang, Wang Wei, Zhou Zhi-Wei, Wang Feng-Hua, Li Yu-Hong, Xu Rui-Hua, Qiu Miao-Zh |
| DGCR8 Microprocessor Subunit Mutation and Expression Deregulation in Thyroid Lesions. International journal of molecular sciences 2022 12 23 (23): . Rodrigues Lia, Canberk Sule, Macedo Sofia, Soares Paula, Vinagre Jo |
| Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003510. Saacks Nicole A, Eales James, Spracklen Timothy F, Aldersley Thomas, Human Paul, Verryn Mark, Lawrenson John, Cupido Blanche, Comitis George, De Decker Rik, Fourie Barend, Swanson Lenise, Joachim Alexia, Brooks Andre, Ramesar Raj, Shaboodien Gasnat, Keavney Bernard D, Zühlke Liesl |
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