| Altered methylation at microRNA-associated CpG islands in hereditary and sporadic carcinomas: a methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA … W Pavicic, E Perkiö, S Kaur, P Peltomäki Molecular Medicine 17, 726-735, 2011 | 67 | 2011 |
| LINE-1 hypomethylation in familial and sporadic cancer W Pavicic, EI Joensuu, T Nieminen, P Peltomäki Journal of molecular medicine 90, 827-835, 2012 | 62 | 2012 |
| Effects of the pesticide chlorpyrifos on breast cancer disease. Implication of epigenetic mechanisms C Ventura, CD Zappia, M Lasagna, W Pavicic, S Richard, AD Bolzan, ... The Journal of steroid biochemistry and molecular biology 186, 96-104, 2019 | 49 | 2019 |
| Promoter‐specific alterations of APC are a rare cause for mutation‐negative familial adenomatous polyposis W Pavicic, TT Nieminen, A Gylling, JP Pursiheimo, A Laiho, A Gyenesei, ... Genes, Chromosomes and Cancer 53 (10), 857-864, 2014 | 34 | 2014 |
| Correlation analysis between mtDNA 4977-bp deletion and ageing WH Pavicic, SM Richard Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 670 (1 …, 2009 | 33 | 2009 |
| Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium P Møller, T Seppälä, JG Dowty, S Haupt, M Dominguez-Valentin, L Sunde, ... Hereditary cancer in clinical practice 20 (1), 36, 2022 | 31 | 2022 |
| Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the … M Dominguez-Valentin, S Haupt, TT Seppälä, JR Sampson, L Sunde, ... EClinicalMedicine 58, 2023 | 27 | 2023 |
| Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis TT Nieminen, W Pavicic, N Porkka, M Kankainen, HJ Järvinen, A Lepistö, ... Oncotarget 7 (43), 70685, 2016 | 22 | 2016 |
| Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer EI Joensuu, TT Nieminen, JE Lotsari, W Pavicic, WM Abdel‐Rahman, ... Genes, Chromosomes and Cancer 54 (12), 776-787, 2015 | 22 | 2015 |
| Y chromosome instability in testicular cancer NO Bianchi, SM Richard, W Pavicic Mutation Research/Reviews in Mutation Research 612 (3), 172-188, 2006 | 21 | 2006 |
| Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report TT Seppälä, M Dominguez-Valentin, EJ Crosbie, C Engel, S Aretz, ... European Journal of Cancer 148, 124-133, 2021 | 16 | 2021 |
| Cigarette smoking, dietary habits and genetic polymorphisms in GSTT1, GSTM1 and CYP1A1 metabolic genes: a case-control study in oncohematological diseases MB Cerliani, W Pavicic, JA Gili, G Klein, S Saba, S Richard World journal of clinical oncology 7 (5), 395, 2016 | 15 | 2016 |
| Analysis association between mitochondrial genome instability and xenobiotic metabolizing genes in human breast cancer WH Pavicic, M Laguens, SM Richard Molecular Medicine 15, 160-165, 2009 | 15 | 2009 |
| No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome … M Dominguez-Valentin, JP Plazzer, JR Sampson, C Engel, S Aretz, ... Journal of clinical medicine 10 (13), 2856, 2021 | 14 | 2021 |
| Ethnic variation in the prevalence of AZF deletions in testicular cancer SM Richard, NO Bianchi, MS Bianchi, P Peltomäki, RA Lothe, W Pavicic Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 554 (1 …, 2004 | 14 | 2004 |
| Automatic integration of clinical and genetic data using cBioPortal M Brunner, L Mullen, F Jauk, J Oliver, F Cayol, J Minata, V Herrera, ... MEDINFO 2021: One World, One Health–Global Partnership for Digital …, 2022 | 7 | 2022 |
| Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort ML González, N Causada-Calo, JP Santino, M Dominguez-Valentin, ... Familial Cancer 17, 395-402, 2018 | 7 | 2018 |
| MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing TA Piñero, O Soukarieh, M Rolain, K Alvarez, F López-Köstner, ... Familial Cancer 19, 323-336, 2020 | 6 | 2020 |
| Hereditary Cancer Program (ProCanHe): 21-years of experience at a referral registry in Argentina TA Piñero, I Herrando, PG Kalfayan, M Gonzales, A Ferro, JP Santino, ... BioMed Central, 2019 | 3 | 2019 |
| Association between PER3 length polymorphism and onco-hematological diseases and its influence on patients’ functionality MB Cerliani, JA Gili, WH Pavicic, GE Klein, S Saba, SM Richard PiscoMed Publishing Pte Ltd, 2015 | 3 | 2015 |
