Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: DGCR8[original query] |
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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 |
Association between SNPs in miRNA-machinery genes and chronic hepatitis B in the Chinese Han population. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2014 Dec 28 113-7. Shang Mengqiao, Huang Yanchun, Hu Xuejiao, Wang Jun, Song Xingbo, Zhou Yi, Zhou Juan, Ye Yuanxin, Lu Xiaojun, Tao Chuanmin, Wang Lanlan, Ying Bin |
Noncoding RNA-related polymorphisms in pediatric acute lymphoblastic leukemia susceptibility. Pediatric research 2014 Jun 75 (6): 767-73. Gutierrez-Camino Angela, Lopez-Lopez Elixabet, Martin-Guerrero Idoia, Piñan Maria A, Garcia-Miguel Purificacion, Sanchez-Toledo Jose, Carbone Bañeres Ana, Uriz Javier, Navajas Aurora, Garcia-Orad Afri |
Association of microRNA biogenesis pathway gene variants and alcohol dependence risk. DNA and cell biology 2015 Mar 34 (3): 220-6. Gedik Huseyin, Erdal Mehmet Emin, Yilmaz Senay Gorucu, Sengul Cem, Sengul Ceyhan Balci, Herken Has |
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 |
Association of Polymorphic Variants of miRNA Processing Genes with Larynx Cancer Risk in a Polish Population. BioMed research international 2015 2015 298378. Osuch-Wojcikiewicz Ewa, Bruzgielewicz Antoni, Niemczyk Kazimierz, Sieniawska-Buccella Olga, Nowak Alicja, Walczak Anna, Majsterek Ireneu |
Impact of polymorphisms in microRNA biogenesis genes on colon cancer risk and microRNA expression levels: a population-based, case-control study. BMC medical genomics 2016 9 (1): 21. Mullany Lila E, Herrick Jennifer S, Wolff Roger K, Buas Matthew F, Slattery Martha |
MiRNA-Related Genetic Variations Associated with Radiotherapy-Induced Toxicities in Patients with Locally Advanced Non-Small Cell Lung Cancer. PloS one 2016 11 (3): e0150467. Li Rong, Pu Xia, Chang Joe Y, Ye Yuanqing, Komaki Ritsuko, Minna John D, Roth Jack A, Han Baohui, Wu Xife |
Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review. Cancer science 2016 Feb . Deng Changkai, Dai Rong, Li Xuliang, Liu Fe |
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 |
Genetic variants of microRNA processing genes and risk of non-syndromic orofacial clefts. Oral diseases 2017 Aug . Xu M, Ma L, Lou S, Du Y, Yin X, Zhang C, Fan L, Wang H, Wang Z, Zhang W, Wang L, Pan |
Evaluation of polymorphisms in microRNA biosynthesis genes and risk of laryngeal cancer in the Polish population. Polish journal of pathology : official journal of the Polish Society of Pathologists 2016 67 (3): 283-290. Bruzgielewicz Antoni, Osuch-Wójcikiewicz Ewa, Walczak Anna, Nowak Alicja, Uczkowski Helen, Majsterek Ireneu |
Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan . Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy |
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 |
Association of miRNA biosynthesis genes DROSHA and DGCR8 polymorphisms with cancer susceptibility: a systematic review and meta-analysis. Bioscience reports 2018 Apr . Wen Jing, Lv Zhi, Ding Hanxi, Fang Xinxin, Sun Mingj |
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 |
Genetic polymorphism in DGCR8 is associated with late onset of preeclampsia. BMC medical genetics 2019 Sep 20 (1): 151. Huang Xin, Li Zuodong, Lei Jun, Wang Dapeng, Zhang Yuji |
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 |
Association between microRNA machinery gene polymorphisms and recurrent implantation failure. Experimental and therapeutic medicine 2020 Apr 19 (4): 3113-3123. Lee Yubin, Ahn Eun Hee, Ryu Chang Soo, Kim Jung Oh, An Hui Jeong, Cho Sung Hwan, Kim Ji Hyang, Kim Young Ran, Lee Woo Sik, Kim Nam Ke |
Pathogenic noncoding variants in the neurofibromatosis and schwannomatosis predisposition genes. Human mutation 2021 7 42 (10): 1187-1207. Perez-Becerril Cristina, Evans D Gareth, Smith Miriam |
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 |
MicroRNAs in the Onset of Schizophrenia. Cells 2021 Oct 10 (10): . Thomas Kristen T, Zakharenko Stanislav |
Screening of potential novel candidate genes in schwannomatosis patients. Human mutation 2022 Jun . Perez-Becerril Cristina, Wallace Andrew J, Schlecht Helene, Bowers Naomi L, Smith Philip T, Gokhale Carolyn, Eaton Helen, Charlton Chris, Robinson Rachel, Charlton Ruth S, Evans D Gareth, Smith Miriam |
Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome. Frontiers in genetics 2022 5 13 812183. Ying Shengjie, Heung Tracy, Zhang Zhaolei, Yuen Ryan K C, Bassett Anne |
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 |
Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect. Genes 2023 4 14 (4): . Caiyun Zhu, Yang Yang, Bo Pan, Hui Wei, Jiahang Ju, Nuo Si, Qi |
Single nucleotide variants in microRNA biosynthesis genes in Mexican individuals. Frontiers in genetics 2023 3 14 1022912. Juárez-Luis Jesús, Canseco-Ocaña Moisés, Cid-Soto Miguel Angel, Castro-Martínez Xochitl H, Martínez-Hernández Angélica, Orozco Lorena, Hernández-Zavala Araceli, Córdova Emilio |
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- Page last updated:Apr 22, 2024
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