HuGE Literature Finder
Records 1-11
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Functional polymorphisms in FOXC2 gene and Epithelial ovarian Cancer susceptibility in Chinese population.
Journal of ovarian research 2020 Mar 13 (1): 34. Zhou Zhijiao, Ou Xiang, Zou Qiong, Chu Ling, Quan Xiyun, Chen Yong, Liu Ya |
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Identification of a FAS/FASL haplotype associated with endometriosis in Iranian patients.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2019 Sep 1-4. Akhavan Sales Zhima, Tahoori Mohammad Taher, Sheikhha Mohammad Hassan, Seifati Seyed Morteza, Bitaraf Sani Morte |
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Identification of miR-146a and miR-196a-2 single nucleotide polymorphisms at patients with high-grade serous ovarian cancer.
Journal of biotechnology 2019 Mar . Lukács János, Soltész Beáta, Penyige András, Nagy Bálint, Póka Róbe |
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Novel Associations between BRCA1 Variants C.181 T>G (Rs28897672) and Ovarian Crisk in Saudi Females.
Journal of medical biochemistry 2019 Mar 38 (1): 13-21. Alyahri Nora, Abdi Saba, Khan Wajahatullah, Elrobh Mohamed, Addar Mohammed H, Babay Zeneb A, Alanazi Mohamed, Aldaihan Sooad, Shaik Jilani, Arafah Maha, Parine Narasimha Reddy, Warsy Arjuma |
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Benchmarking of Amplicon-Based Next-Generation Sequencing Panels Combined with Bioinformatics Solutions for Germline BRCA1 and BRCA2 Alteration Detection.
The Journal of molecular diagnostics : JMD 2018 Jul . Vendrell Julie A, Vilquin Paul, Larrieux Marion, Van Goethem Charles, Solassol Jérô |
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Evaluation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Mutation Detection.
The Journal of molecular diagnostics : JMD 2018 01 20 (1): 87-94. Capone Gabriele Lorenzo, Putignano Anna Laura, Trujillo Saavedra Sharon, Paganini Irene, Sestini Roberta, Gensini Francesca, De Rienzo Irene, Papi Laura, Porfirio Berardi |
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The status of Her2 amplification and Kras mutations in mucinous ovarian carcinoma.
Human genomics 2016 Dec 10 (1): 40. Chang Kuang-Leei, Lee Ming-Yung, Chao Wan-Ru, Han Chih-Pi |
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A SNaPshot of potentially personalized care: Molecular diagnostics in gynecologic cancer.
Gynecologic oncology 2016 Apr 141 (1): 108-12. Penson R T, Sales E, Sullivan L, Borger D R, Krasner C N, Goodman A K, Del Carmen M G, Growdon W B, Schorge J O, Boruta D M, Castro C M, Dizon D S, Birrer M |
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Profiling cancer gene mutations in longitudinal epithelial ovarian cancer biopsies by targeted next-generation sequencing: a retrospective study.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2015 Jul 26 (7): 1363-71. Beltrame L, Di Marino M, Fruscio R, Calura E, Chapman B, Clivio L, Sina F, Mele C, Iatropoulos P, Grassi T, Fotia V, Romualdi C, Martini P, Noris M, Paracchini L, Craparotta I, Petrillo M, Milani R, Perego P, Ravaggi A, Zambelli A, Ronchetti E, D'Incalci M, Marchini |
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Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes.
European journal of human genetics : EJHG 2012 Dec . Feliubadaló L, Lopez-Doriga A, Castellsagué E, Del Valle J, Menéndez M, Tornero E, Montes E, Cuesta R, Gómez C, Campos O, Pineda M, González S, Moreno V, Brunet J, Blanco I, Serra E, Capellá G, Lázaro C |
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High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2007 Jun 18 Suppl 6 vi86-92. Veschi S, Aceto G, Scioletti A P, Gatta V, Palka G, Cama A, Mariani-Costantini R, Battista P, Calò V, Barbera F, Bazan V, Russo A, Stuppia |
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- Page last updated:Sep 16, 2021
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