Number of the records: 1  

Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families

  1. TitleAshkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families
    Author Čierniková Soňa 1978- SAVEXONK - Ústav experimentálnej onkológie SAV
    Co-authors Tomka Miroslav 1974- SAVEXONK - Ústav experimentálnej onkológie SAV

    Kováč Michal 1977- SAVEXONK - Ústav experimentálnej onkológie SAV

    Števurková Viola SAVEXONK - Ústav experimentálnej onkológie SAV

    Zajac Vladimír 1943- SAVEXONK - Ústav experimentálnej onkológie SAV

    Source document Neoplasma. Vol. 53, no. 2 (2006), p. 97-102. - Bratislava : Ústav experimentálnej onkológie, Biomedicínske centrum SAV, 1954-
    Languageeng - English
    CountrySK - Slovak Republic
    Document kindrozpis článkov z periodík (rbx)
    CitationsDUFFY, David L. - ANTILL, Yoland C. - STEWART, Colin J. - YOUNG, Joanne R. - SPURDLE, Amanda B. Report of Endometrial Cancer in Australian BRCA1 and BRCA2 Mutation-Positive Families. In TWIN RESEARCH AND HUMAN GENETICS. ISSN 1832-4274, 2011, vol. 14, no. 2, pp. 111.
    FEDOROVA, O. E. - LYUBCHENKO, L. N. - PAYANIDI, Yu. G. - KAZUBSKAYA, T. P. - AMOSENKO, F. A. - GARKAVTSEVA, R. F. - ZASEDATELEV, A. S. - NASEDKINA, T. V. Biochip analysis of BRCA1/2 and CHEK2 common mutations in ovarian cancer and primary multiple tumors involving the ovaries (Russian population). In MOLECULAR BIOLOGY. ISSN 0026-8933, 2007, vol. 41, no. 1, pp. 32.
    KARAMI, Fatemeh - MEHDIPOUR, Parvin. A Comprehensive Focus on Global Spectrum of BRCA1 and BRCA2 Mutations in Breast Cancer. In BIOMED RESEARCH INTERNATIONAL. ISSN 2314-6133, 2013, vol., no., pp.
    NEGURA, Lucian - CARASEVICI, Eugen - NEGURA, Anca - UHRHAMMER, Nancy - BIGNON, Yves-Jean. Identification of a recurrent BRCA1 mutation in two breast/ovarian cancer predisposition families with distinct phenotypes, by using allele-specific multiplex-PCR. In REVISTA ROMANA DE MEDICINA DE LABORATOR. ISSN 1841-6624, 2010, vol. 18, no. 2, pp. 53.
    MATEJU, M. - STRIBRNA, J. - ZIKAN, M. - KLEIBL, Z. - JANATOVA, M. - KORMUNDA, S. - NOVOTNY, J. - SOUCEK, P. - PETRUZELKA, L. - POHLREICH, P. Population-based study of BRCA1/2 mutations: Family history based criteria identify minority of mutation carriers. In NEOPLASMA. ISSN 0028-2685, 2010, vol. 57, no. 3, pp. 280.
    LAITMAN, Yael - FENG, Bing-Jian - ZAMIR, Itay M. - WEITZEL, Jeffrey N. - DUNCAN, Paul - PORT, Danielle - THIRTHAGIRI, Eswary - TEO, Soo-Hwang - EVANS, Gareth - LATIF, Ayse - NEWMAN, William G. - GERSHONI-BARUCH, Ruth - ZIDAN, Jamal - SHIMON-PALUCH, Shani - GOLDGAR, David - FRIEDMAN, Eitan. Haplotype analysis of the 185delAG BRCA1 mutation in ethnically diverse populations. In EUROPEAN JOURNAL OF HUMAN GENETICS. ISSN 1018-4813, 2013, vol. 21, no. 2, pp. 212.
    ZAVODNA, K. - BUJALKOVA, M. - KRIVULCIK, T. - ALEMAYEHU, A. - SKORVAGA, M. - MARRA, G. - FRIDRICHOVA, I. - JIRICNY, J. - BARTOSOVA, Z. Novel and recurrent germline alterations in the MLH1 and MSH2 genes identified in hereditary nonpolyposis colorectal cancer patients in Slovakia. In NEOPLASMA. ISSN 0028-2685, 2006, vol. 53, no. 4, pp. 269.
    BARTOSOVA, Z. - ZAVODNA, K. - KRIVULCIK, T. - USAK, J. - MLKVA, I. - KRUZLIAK, T. - HROMEC, J. - USAKOVA, V. - KOPECKA, I. - VERES, P. - BARTOSOVA, Z. - BUJALKOVA, M. STK11/LKB1 germline mutations in the first Peutz-Jeghers syndrome patients identified in Slovakia. In NEOPLASMA. ISSN 0028-2685, 2007, vol. 54, no. 2, pp. 101.
    MLADOSIEVICOVA, B. - CARTER, A. - KRISTOVA, V. Genetic tests for predicting the toxicity and efficacy of anticancer chemotherapy. In NEOPLASMA. ISSN 0028-2685, 2007, vol. 54, no. 3, pp. 181.
    NEGURA, Lucian - UHRHAMMER, Nancy - NEGURA, Anca - ARTENIE, Vlad - CARASEVICI, Eugen - BIGNON, Yves-Jean. Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population. In FAMILIAL CANCER. ISSN 1389-9600, 2010, vol. 9, no. 4, pp. 519.
    CECENER, Gulsah - EGELI, Unal - TUNCA, Berrin - ERTURK, Elif - AK, Secil - GOKGOZ, Sehsuvar - TASDELEN, Ismet - TEZCAN, Gulcin - DEMIRDOGEN, Elif - BAYRAM, Nuran - AVCI, Nilufer - EVRENSEL, Turkkan. BRCA1/2 Germline Mutations and Their Clinical Importance in Turkish Breast Cancer Patients. In CANCER INVESTIGATION. ISSN 0735-7907, 2014, vol. 32, no. 8, pp. 375.
    SPURDLE, Amanda B. - BOWMAN, Michael A. - SHAMSANI, Jannah - KIRK, Judy. Endometrial cancer gene panels: clinical diagnostic vs research germline DNA testing. In MODERN PATHOLOGY. ISSN 0893-3952, 2017, vol. 30, no. 8, pp. 1048-1068.
    SHARMA, Babita - KAUR, Raman Preet - RAUT, Sonali - MUNSHI, Anjana. BRCA1 mutation spectrum, functions, and therapeutic strategies: The story so far. In CURRENT PROBLEMS IN CANCER. ISSN 0147-0272, 2018, vol. 42, no. 2, pp. 189-207.
    CategoryADDA - Scientific papers in domestic journals registered in Current Contents Connect with IF (impacted)
    Category of document (from 2022)V3 - Vedecký výstup publikačnej činnosti z časopisu
    Type of documentčlánok
    Year2006
    Registered inWOS
    Registered inSCOPUS
    Registered inCCC
    article

    article

    rokCCIFIF Q (best)JCR Av Jour IF PercSJRSJR Q (best)CiteScore
    A
    rok vydaniarok metrikyIFIF Q (best)SJRSJR Q (best)
    200620050.731Q40.325Q4
Number of the records: 1  

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