Print previewVALIDITY EXPIRED personal data approved: 2015. XII. 17. Publications |
2015
 from data base, 2015. XII. 17. |
Oláh E, Mátrai Z: Herediter emlő- és petefészekrák-szindróma, a gyanútól a rizikócsökkentésig, In: Szerk.: Mátrai Z, Szerk.: Gulyás G, Szerk.: Kásler M Az emlőrák korszerű sebészete. Budapest: Medicina Könyvkiadó Zrt., 2015. pp. 389-408. type of document: Part of book/Könyvfejezet (to be translated) language: Hungarian
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2015
 from data base, 2015. XII. 17. |
Papp J, Kovacs ME, Matrai Z, Orosz E, Kasler M, Borresen-Dale AL, Olah E: Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary, FAMILIAL CANCER 14: pp. 1-13. Paper 10.1007/s10689-015-9845-5. type of document: Journal paper/Article language: English
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2012
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Oláh Edit: A népbetegségek genetikai meghatározottsága: Daganatos betegségek, In: Szerk.: Ádány Róza, Szerk.: Sándor Judit, Szerk.: Angela Brand Népegészségügyi Genomika. Budapest: Medicina Könyvkiadó, 2012. pp. 85-120. type of document: Part of book/Könyvfejezet (to be translated) language: Hungarian
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2011
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Oláh Edit: Örökletes daganatok, In: Szerk.: Tulassay Zs A belgyógyászat alapjai. Budapest: Medicina Könyvkiadó, 2011. pp. 1772-1775. 1-2. kötet type of document: Part of book/Könyvfejezet (to be translated) language: Hungarian
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2011
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Oláh Edit: Molekuláris onkogenetika, In: Szerk.: Kásler M Az onkológia alapjai: Egyetemi tankönyv. Budapest: Medicina Könyvkiadó, 2011. pp. 49-69. type of document: Part of book/Könyvfejezet (to be translated) language: Hungarian
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2010
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Papp J, Kovacs ME, Solyom S, Kasler M, Borresen-Dale AL, Olah E: High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients, BMC MEDICAL GENETICS 11: pp. 169-178. type of document: Journal paper/Article number of independent citations: 11 language: English URL |
2009
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Kovács ME, Papp J, Szentirmay Z, Otto Sz, Oláh E: Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome, HUMAN MUTATION 30: (2) pp. 197-203. type of document: Journal paper/Article number of independent citations: 84 language: English DOI |
2003
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Orban TI, Olah E: Emerging roles of BRCA1 alternative splicing - Invited review, MOLECULAR PATHOLOGY 56: pp. 191-197. type of document: Journal paper/Article number of independent citations: 88 language: English DOI |
1999
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Csokay B, Udvarhelyi N, Sulyok Z, Besznyak I, Ramus S, Ponder B, Olah E: High frequency of germ-line BRCA2 mutations among Hungarian male breast cancer patients without family history, CANCER RESEARCH 59: pp. 995-998. type of document: Journal paper/Article number of independent citations: 72 language: English
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1997
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Ramus SJ, Kote Jarai Z, Friedman LS, van Der Looij M, Gayther SA, Csokay B, Ponder BA, Olah E: Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer, AMERICAN JOURNAL OF HUMAN GENETICS 60: (5) pp. 1242-1246. type of document: Journal paper/Article number of independent citations: 40 language: English
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