Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 34 Records) |
| Query Trace: Disease and DICER1[original query] |
|---|
| Germline mutations of DICER1 in Chinese women with BRCA1/BRCA2-negative familial breast cancer. Genetics and molecular research : GMR 2014 13 (4): 10754-60. Cao W-M, Gao Y, Yang H-J, Xie S-N, Meng X-L, Pan Z-W, Chen Z-H, Huang J, Ye W-W, Shao X-Y, Wang X |
| Genetic variants in miRNA processing genes and pre-miRNAs are associated with the risk of chronic lymphocytic leukemia. PloS one 2015 10 (3): e0118905. Martin-Guerrero Idoia, Gutierrez-Camino Angela, Lopez-Lopez Elixabet, Bilbao-Aldaiturriaga Nerea, Pombar-Gomez Maria, Ardanaz Maite, Garcia-Orad Afri |
| Increased co-expression of genes harboring the damaging de novo mutations in Chinese schizophrenic patients during prenatal development. Scientific reports 2015 5 18209. Wang Qiang, Li Miaoxin, Yang Zhenxing, Hu Xun, Wu Hei-Man, Ni Peiyan, Ren Hongyan, Deng Wei, Li Mingli, Ma Xiaohong, Guo Wanjun, Zhao Liansheng, Wang Yingcheng, Xiang Bo, Lei Wei, Sham Pak C, Li T |
| A novel somatic MAPK1 mutation in primary ovarian mixed germ cell tumors. Oncology reports 2015 Nov . Zou Yang, Deng Wei, Wang Feng, Yu Xiao-Hong, Liu Fa-Ying, Yang Bi-Cheng, Huang Mei-Zhen, Guo Jiu-Bai, Xie Qiu-Hua, He Ming, Huang Ou-Pi |
| MicroRNA biogenesis pathway genes polymorphisms and cancer risk: a systematic review and meta-analysis. PeerJ 2016 4 e2706. He Jieyu, Zhao Jun, Zhu Wenbo, Qi Daxun, Wang Lina, Sun Jinfang, Wang Bei, Ma Xu, Dai Qiaoyun, Yu Xiaoj |
| 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 |
| High-grade Müllerian Adenosarcoma: Genomic and Clinicopathologic Characterization of a Distinct Neoplasm With Prevalent TP53 Pathway Alterations and Aggressive Behavior. The American journal of surgical pathology 2017 Aug . Hodgson Anjelica, Amemiya Yutaka, Seth Arun, Djordjevic Bojana, Parra-Herran Carl |
| Targeted Genomic Profiling of Female Adnexal Tumors of Probable Wolffian Origin (FATWO). International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2018 Aug . Mirkovic Jelena, Dong Fei, Sholl Lynette M, Garcia Elizabeth, Lindeman Neal, MacConaill Laura, Crum Christopher P, Nucci Marisa R, McCluggage W Glenn, Howitt Brooke |
| Comprehensive Genetic Analysis of Follicular Thyroid Carcinoma Predicts Prognosis Independent of Histology. The Journal of clinical endocrinology and metabolism 2018 07 103 (7): 2640-2650. Nicolson Norman G, Murtha Timothy D, Dong Weilai, Paulsson Johan O, Choi Jungmin, Barbieri Andrea L, Brown Taylor C, Kunstman John W, Larsson Catharina, Prasad Manju L, Korah Reju, Lifton Richard P, Juhlin C Christofer, Carling Tobi |
| 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 |
| Analysis of the Association Between MicroRNA Biogenesis Gene Polymorphisms and Venous Thromboembolism in Koreans. International journal of molecular sciences 2019 8 20 (15): . Ko Eun Ju, Kim Eo Jin, Kim Jung Oh, Sung Jung Hoon, Park Han Sung, Ryu Chang Soo, Oh Jisu, Chong So Young, Oh Doyeun, Kim Nam Ke |
| Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer. Frontiers in oncology 2019 8 9 673. Zhunussova Gulnur, Afonin Georgiy, Abdikerim Saltanat, Jumanov Abai, Perfilyeva Anastassiya, Kaidarova Dilyara, Djansugurova Ley |
| Recurrent hotspot SF3B1 mutations at codon 625 in vulvovaginal mucosal melanoma identified in a study of 27 Australian mucosal melanomas. Oncotarget 2019 3 10 (9): 930-941. Quek Camelia, Rawson Robert V, Ferguson Peter M, Shang Ping, Silva Ines, Saw Robyn P M, Shannon Kerwin, Thompson John F, Hayward Nicholas K, Long Georgina V, Mann Graham J, Scolyer Richard A, Wilmott James |
| The molecular landscape of ETMR at diagnosis and relapse. Nature 2019 12 576 (7786): 274-280. Lambo Sander, Gröbner Susanne N, Rausch Tobias, Waszak Sebastian M, Schmidt Christin, Gorthi Aparna, Romero July Carolina, Mauermann Monika, Brabetz Sebastian, Krausert Sonja, Buchhalter Ivo, Koster Jan, Zwijnenburg Danny A, Sill Martin, Hübner Jens-Martin, Mack Norman, Schwalm Benjamin, Ryzhova Marina, Hovestadt Volker, Papillon-Cavanagh Simon, Chan Jennifer A, Landgraf Pablo, Ho Ben, Milde Till, Witt Olaf, Ecker Jonas, Sahm Felix, Sumerauer David, Ellison David W, Orr Brent A, Darabi Anna, Haberler Christine, Figarella-Branger Dominique, Wesseling Pieter, Schittenhelm Jens, Remke Marc, Taylor Michael D, Gil-da-Costa Maria J, ?astowska Maria, Grajkowska Wies?awa, Hasselblatt Martin, Hauser Peter, Pietsch Torsten, Uro-Coste Emmanuelle, Bourdeaut Franck, Masliah-Planchon Julien, Rigau Valérie, Alexandrescu Sanda, Wolf Stephan, Li Xiao-Nan, Schüller Ulrich, Snuderl Matija, Karajannis Matthias A, Giangaspero Felice, Jabado Nada, von Deimling Andreas, Jones David T W, Korbel Jan O, von Hoff Katja, Lichter Peter, Huang Annie, Bishop Alexander J R, Pfister Stefan M, Korshunov Andrey, Kool Marc |
| Analysis of microRNA processing machinery gene (DROSHA, DICER1, RAN, and XPO5) variants association with end-stage renal disease. Journal of clinical laboratory analysis 2020 Aug e23520. Fawzy Manal S, Abu AlSel Baraah T, Toraih Eman |
| Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? Frontiers in endocrinology 2020 7 11 433. Martínez de LaPiscina Idoia, Hernández-Ramírez Laura C, Portillo Nancy, Gómez-Gila Ana L, Urrutia Inés, Martínez-Salazar Rosa, García-Castaño Alejandro, Aguayo Aníbal, Rica Itxaso, Gaztambide Sonia, Faucz Fabio R, Keil Margaret F, Lodish Maya B, Quezado Martha, Pankratz Nathan, Chittiboina Prashant, Lane John, Kay Denise M, Mills James L, Castaño Luis, Stratakis Constantine |
| Novel genetic characteristics in low-grade fetal adenocarcinoma of the lung. Thoracic cancer 2021 8 12 (20): 2789-2795. Zhang Shuyang, Yin Huihui, Zhang Jing, Yang Lu, Yang Guangjian, Jia Jia, Jiao Yuchen, Ying Jianming, Wang Y |
| Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in the Childhood Cancer Survivor Study. JNCI cancer spectrum 2021 7 5 (2): . Kim Jung, Gianferante Matthew, Karyadi Danielle M, Hartley Stephen W, Frone Megan N, Luo Wen, Robison Leslie L, Armstrong Gregory T, Bhatia Smita, Dean Michael, Yeager Meredith, Zhu Bin, Song Lei, Sampson Joshua N, Yasui Yutaka, Leisenring Wendy M, Brodie Seth A, de Andrade Kelvin C, Fortes Fernanda P, Goldstein Alisa M, Khincha Payal P, Machiela Mitchell J, McMaster Mary L, Nickerson Michael L, Oba Leatrisse, Pemov Alexander, Pinheiro Maisa, Rotunno Melissa, Santiago Karina, Wegman-Ostrosky Talia, Diver W Ryan, Teras Lauren, Freedman Neal D, Hicks Belynda D, Zhu Bin, Wang Mingyi, Jones Kristine, Hutchinson Amy A, Dagnall Casey, Savage Sharon A, Tucker Margaret A, Chanock Stephen J, Morton Lindsay M, Stewart Douglas R, Mirabello Li |
| 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 |
| DROSHA rs10719 and DICER1 rs3742330 polymorphisms in endometriosis and different diseases: Case-control and review studies. Experimental and molecular pathology 2021 Jan 104616. Cardoso Jéssica Vilarinho, Medeiros Rui, Dias Francisca, Costa Isabelle Alves, Ferrari Renato, Berardo Plinio Tostes, Perini Jamila Alessand |
| A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype. JAMA network open 2021 2 4 (2): e210112. Mirshahi Uyenlinh L, Kim Jung, Best Ana F, Chen Zongming E, Hu Ying, Haley Jeremy S, Golden Alicia, Stahl Richard, Manickam Kandamurugu, Carr Ann G, Harney Laura A, Field Amanda, Hatton Jessica, Schultz Kris Ann P, Bauer Andrew J, Hill D Ashley, Rosenberg Philip S, Murray Michael F, Carey David J, Stewart Douglas |
| Primary central nervous system sarcoma with DICER1 mutation-treatment results of a novel molecular entity in pediatric Peruvian patients. Cancer 2021 Oct . Diaz Coronado Rosdali Y, Mynarek Martin, Koelsche Christian, Mora Alferez Pamela, Casavilca Zambrano Sandro, Wachtel Aptowitzer Antonio, Sahm Felix, von Deimling Andreas, Schüller Ulrich, Spohn Michael, Sturm Dominik, Pfister Stefan M, Morales La Madrid Andres, Sernaque Quintana Raymundo, Sarria Bardales Gustavo, Negreiros Chinchihuara Tatiana, Ojeda Medina Luis, Garcia-Corrochano Medina Pamela, Campos Sanchez Danny A, Ponce Farfan Jimena, Rutkowski Stefan, Garcia Leon Juan |
| Mullerian adenosarcoma: clinicopathologic and molecular characterization highlighting recurrent BAP1 loss and distinctive features of high-grade tumors. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2022 Sep . Momeni Boroujeni Amir, Kertowidjojo Elizabeth, Wu Xinyu, Soslow Robert A, Chiang Sarah, Da Silva Edaise M, Weigelt Britta, Chui M Herm |
| DICER1 Mutations Occur in More Than One-Third of Follicular-Patterned Pediatric Papillary Thyroid Carcinomas and Correlate with a Low-Risk Disease and Female Gender Predilection. Endocrine pathology 2022 10 33 (4): 437-445. Onder Semen, Mete Ozgur, Yilmaz Ismail, Bayram Aysel, Bagbudar Sidar, Altay Ali Y?lmaz, Issin Gizem, Terzi Neslihan Kaya, Iscan Yal?n, Sormaz Ismail Cem, Tunca Fatih, Senyurek Yasemin Giles, Yegen Gulc |
| The 3' UTR polymorphisms rs3742330 in DICER1 and rs10719 in DROSHA genes are not associated with primary open-angle and angle-closure glaucoma: As case-control study. PloS one 2023 4 18 (4): e0284852. Altaf A Kondkar, Taif A Azad, Tahira Sultan, Essam A Osman, Faisal A Almobarak, Glenn P Lobo, Saleh A Al-Obeid |
| Germline mutations in pediatric cancer cohort with mixed-ancestry Mexicans. Molecular genetics & genomic medicine 2023 12 e2332. Oscar Alonso-Luna, Gabriela E Mercado-Celis, Jorge Melendez-Zajgla, Rodrigo Barquera, Marta Zapata-Tarres, Luis Enrique Juárez-Villegas, Elvia Cristina Mendoza-Caamal, Elianeth Rey-Helo, Socorro Aida Borges-Yañ |
| Identification of novel candidate predisposing genes in familial nonmedullary thyroid carcinoma implicating DNA damage repair pathways. International journal of cancer 2024 9 . Carolina Pires, Inês J Marques, Ana Saramago, Margarida M Moura, Marta Pojo, Rafael Cabrera, Catarina Santos, Francisco Rosário, Diana Lousa, João B Vicente, Tiago M Bandeiras, Manuel R Teixeira, Valeriano Leite, Branca M Cava |
| A genome-first approach to characterize DICER1 pathogenic variant prevalence, penetrance and cancer, thyroid, and other phenotypes in 2 population-scale cohorts. Genetics in medicine open 2024 7 2 . Jung Kim, Jeremy Haley, Jessica N Hatton, Uyenlinh L Mirshahi, H Shanker Rao, Mark F Ramos, Diane Smelser, Gretchen Urban, Kris Ann P Schultz, David J Carey, Douglas R Stewa |
| Atrophic changes in thyroid tumors are strong indicators of underlying DICER1 mutations: a bi-institutional genotype-phenotype correlation study. Virchows Archiv : an international journal of pathology 2024 4 . Vincenzo Condello, James W Roberts, Adam Stenman, Catharina Larsson, Kartik Viswanathan, C Christofer Juhl |
| Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
- Page last reviewed:Feb 1, 2024
- Content source: