Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: Attention and BRCA2[original query] |
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Evaluation of the needs of male carriers of mutations in BRCA1 or BRCA2 who have undergone genetic counseling. American journal of human genetics 2000 Dec 67 (6): 1494-504. Liede A, Metcalfe K, Hanna D, Hoodfar E, Snyder C, Durham C, Lynch H T, Narod S |
CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers. British journal of cancer 2001 Jul 85 (1): 36-40. Kadouri L, Easton D F, Edwards S, Hubert A, Kote-Jarai Z, Glaser B, Durocher F, Abeliovich D, Peretz T, Eeles R |
Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients. American journal of medical genetics. Part A 2003 Jan 116A (1): 11-9. Claes Erna, Evers-Kiebooms Gerry, Boogaerts Andrea, Decruyenaere Marleen, Denayer Lieve, Legius Er |
Male BRCA1 and BRCA2 mutation carriers: a pilot study investigating medical characteristics of patients participating in a prostate cancer prevention clinic. The Prostate 2005 Oct 65 (2): 124-9. Horsburgh Sheri, Matthew Andrew, Bristow Robert, Trachtenberg Jo |
Variation of breast cancer risk among BRCA1/2 carriers. JAMA 2008 Jan 299 (2): 194-201. Begg Colin B, Haile Robert W, Borg Ake, Malone Kathleen E, Concannon Patrick, Thomas Duncan C, Langholz Bryan, Bernstein Leslie, Olsen Jørgen H, Lynch Charles F, Anton-Culver Hoda, Capanu Marinela, Liang Xiaolin, Hummer Amanda J, Sima Cami, Bernstein Jonine |
Association between hsa-mir-146a genotype and tumor age-of-onset in BRCA1/BRCA2-negative familial breast and ovarian cancer patients. Carcinogenesis 2010 Dec 31 (12): 2124-6. Pastrello Chiara, Polesel Jerry, Della Puppa Lara, Viel Alessandra, Maestro Rober |
Non-cancer endpoints in BRCA1/2 carriers after risk-reducing salpingo-oophorectomy. Familial cancer 2012 Mar 11 (1): 69-75. Cohen J V, Chiel L, Boghossian L, Jones M, Stopfer J E, Powers J, Rebbeck T R, Nathanson K L, Domchek S |
Molecular analysis of the breast cancer genes BRCA1 and BRCA2 using amplicon-based massive parallel pyrosequencing. The Journal of molecular diagnostics : JMD 2012 Nov 14 (6): 6. Michils G, Hollants S, Dehaspe L, Van Houdt J, Bidet Y, Uhrhammer N, Bignon YJ, Vermeesch JR, Cuppens H, Matthijs G |
TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families. Hereditary cancer in clinical practice 2014 12 (1): 8. Cury Nathalia M, Ferraz Victor Ef, Silva Wilson |
Adjuvant radiotherapy for primary breast cancer in BRCA1 and BRCA2 mutation carriers and risk of contralateral breast cancer with special attention to patients irradiated at younger age. Breast cancer research and treatment 2015 Oct . Drooger Jan C, Akdeniz Delal, Pignol Jean-Philippe, Koppert Linetta B, McCool Danielle, Seynaeve Caroline M, Hooning Maartje J, Jager Agn |
Aurora A is a prognostic marker for breast cancer arising in BRCA2 mutation carriers. The journal of pathology. Clinical research 2016 8 1 (1): 33-40. Aradottir Margret, Reynisdottir Sigridur T, Stefansson Olafur A, Jonasson Jon G, Sverrisdottir Asgerdur, Tryggvadottir Laufey, Eyfjord Jorunn E, Bodvarsdottir Sigridur |
Prioritizing Variants in Complete Hereditary Breast and Ovarian Cancer Genes in Patients Lacking Known BRCA Mutations. Human mutation 2016 Feb . Caminsky Natasha G, Mucaki Eliseos J, Perri Ami M, Lu Ruipeng, Knoll Joan H M, Rogan Peter |
Synchronous Onset of Breast and Pancreatic Cancers: Results of Germline and Somatic Genetic Analysis. Case reports in oncology 0 9 (2): 387-394. Castro Michael, Vierkoetter Koah, Prager Douglas, Montgomery Shasta, Sedgwick Krist |
Mutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study. European journal of human genetics : EJHG 2016 Jan . Garcia Amandine I, Buisson Monique, Damiola Francesca, Tessereau Chloé, Barjhoux Laure, Verny-Pierre Carole, Sornin Valérie, Dondon Marie-Gabrielle, Eon-Marchais Séverine, , Caron Olivier, Gautier-Villars Marion, Coupier Isabelle, Buecher Bruno, Vennin Philippe, Belotti Muriel, Lortholary Alain, Gesta Paul, Dugast Catherine, Noguès Catherine, Fricker Jean-Pierre, Faivre Laurence, Stoppa-Lyonnet Dominique, Andrieu Nadine, Sinilnikova Olga M, Mazoyer Sylv |
Germline Mutations in Cancer Predisposition Genes are Frequent in Sporadic Sarcomas. Scientific reports 2017 9 7 (1): 10660. Chan Sock Hoai, Lim Weng Khong, Ishak Nur Diana Binte, Li Shao-Tzu, Goh Wei Lin, Tan Gek San, Lim Kiat Hon, Teo Melissa, Young Cedric Ng Chuan, Malik Simeen, Tan Mann Hong, Teh Jonathan Yi Hui, Chin Francis Kuok Choon, Kesavan Sittampalam, Selvarajan Sathiyamoorthy, Tan Patrick, Teh Bin Tean, Soo Khee Chee, Farid Mohamad, Quek Richard, Ngeow Joan |
Somatic BRCA1 mutations in clinically sporadic breast cancer with medullary histological features. Journal of cancer research and clinical oncology 2018 2 144 (5): 865-874. Rechsteiner Markus, Dedes Konstantin, Fink Daniel, Pestalozzi Bernhard, Sobottka Bettina, Moch Holger, Wild Peter, Varga Zsuzsan |
Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia. Scientific reports 2020 9 10 (1): 14297. Kim Borahm, Yun Woobin, Lee Seung-Tae, Choi Jong Rok, Yoo Keon Hee, Koo Hong Hoe, Jung Chul Won, Kim Sun H |
[Targeted Therapy in Metastatic Breast Cancer-Which Molecular Tests Are Necessary?]. Journal fur gynakologische Endokrinologie (Osterreichische Ausg.) 2020 8 30 (2): 64-66. Schmidt Marc |
DNA Repair and Ovarian Carcinogenesis: Impact on Risk, Prognosis and Therapy Outcome. Cancers 2020 Jun 12 (7): . Tomasova Kristyna, Cumova Andrea, Seborova Karolina, Horak Josef, Koucka Kamila, Vodickova Ludmila, Vaclavikova Radka, Vodicka Pav |
A clearer view on ovarian clear cell carcinoma. Acta clinica Belgica 2021 8 77 (4): 792-804. De Pauw Aglaja, Naert Eline, Van de Vijver Koen, Philippe Tummers, Vandecasteele Katrien, Denys Hannelo |
Pathogenic BRCA Variants as Biomarkers for Risk in Prostate Cancer. Cancers 2021 11 13 (22): . McNevin Ciara S, Cadoo Karen, Baird Anne-Marie, Murchan Pierre, Sheils Orla, McDermott Ray, Finn Steph |
Detection of germline variants in Brazilian breast cancer patients using multigene panel testing. Scientific reports 2022 3 12 (1): 4190. Guindalini Rodrigo Santa Cruz, Viana Danilo Vilela, Kitajima João Paulo Fumio Whitaker, Rocha Vinícius Marques, López Rossana Verónica Mendoza, Zheng Yonglan, Freitas Érika, Monteiro Fabiola Paoli Mendes, Valim André, Schlesinger David, Kok Fernando, Olopade Olufunmilayo I, Folgueira Maria Aparecida Azevedo Koi |
Study on TFF1 and PALB2 gene variants associated with gastric carcinoma risk in the Chinese Han population. Cancer epidemiology 2023 2 83 102333. Zou Wenjing, Zhang Qian, Sun Ruifang, Li Xu, He Shuixia |
Estrogen receptor-positive breast cancer and adverse outcome in BRCA2 mutation carriers and young non-carrier patients. NPJ breast cancer 2023 11 9 (1): 95. Linda Vidarsdottir, Elinborg J Olafsdottir, Rosa B Barkardottir, Olöf Bjarnadottir, Jon G Jonasson, Stefan Sigurdsson, Laufey Tryggvadott |
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- Page last updated:Apr 16, 2024
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