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W. Pavicic · SciRah

Researcher profile · Semantic Scholar

W. Pavicic

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W. Pavicic — researcher profile on SciRah

h-index: 12
Works: 31
Citations: 538

Most-cited papers

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 prospective Lynch syndrome database
M. Dominguez-Valentin, Saskia Haupt, T. Seppälä, J. Sampson +112 more
2023EClinicalMedicine110 citations Open access
Semantic Scholar
Altered Methylation at MicroRNA-Associated CpG Islands in Hereditary and Sporadic Carcinomas: A Methylation-Specific Multiplex Ligation-Dependent Probe Amplification (MS-MLPA)-Based Approach
W. Pavicic, Esa Perkiö, S. Kaur, P. Peltomäki
2011Molecular Medicine60 citations Open access
Semantic Scholar
LINE-1 hypomethylation in familial and sporadic cancer
W. Pavicic, E. Joensuu, T. Nieminen, P. Peltomäki
2012Journal of molecular medicine55 citations Open access
Semantic Scholar
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, J. Dowty, Saskia Haupt +153 more
2022Hereditary Cancer in Clinical Practice53 citations Open access
Semantic Scholar
Promoter‐specific alterations of APC are a rare cause for mutation‐negative familial adenomatous polyposis
W. Pavicic, T. Nieminen, A. Gylling, Juha-Pekka Pursiheimo +4 more
2014Genes, Chromosomes and Cancer34 citations Open access
Semantic Scholar
Correlation analysis between mtDNA 4977-bp deletion and ageing.
W. Pavicic, S. Richard
2009Mutation research31 citations
Semantic Scholar
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
T. Seppälä, M. Dominguez-Valentin, E. Crosbie, C. Engel +82 more
2021European Journal of Cancer26 citations Open access
Semantic Scholar
Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis
T. Nieminen, W. Pavicic, Noora Porkka, M. Kankainen +3 more
2016OncoTarget26 citations Open access
Semantic Scholar
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study
M. Dominguez-Valentin, J. Plazzer, J. Sampson, C. Engel +85 more
2021Journal of Clinical Medicine18 citations Open access
Semantic Scholar
Y chromosome instability in testicular cancer.
N. Bianchi, S. Richard, W. Pavicic
2006Mutation research18 citations
Semantic Scholar
Methyltransferase expression and tumor suppressor gene methylation in sporadic and familial colorectal cancer
E. Joensuu, T. Nieminen, Johanna E. Lotsari, W. Pavicic +2 more
2015Genes, Chromosomes and Cancer15 citations Open access
Semantic Scholar
Analysis Association between Mitochondrial Genome Instability and Xenobiotic Metabolizing Genes in Human Breast Cancer
W. Pavicic, M. Laguens, S. Richard
2009Molecular Medicine13 citations Open access
Semantic Scholar
Metachronous colorectal cancer risks after extended or segmental resection in MLH1, MSH2, and MSH6 Lynch syndrome: multicentre study from the Prospective Lynch Syndrome Database
K. Zalevskaja, K. Ojala, A. Petrov, S. Haupt +111 more
2025British Journal of Surgery11 citations Open access
Semantic Scholar
Cigarette smoking, dietary habits and genetic polymorphisms in GSTT1, GSTM1 and CYP1A1 metabolic genes: A case-control study in oncohematological diseases
María Belén Cerliani, W. Pavicic, J. Gili, G. Klein +2 more
2016World Journal of Clinical Oncology11 citations Open access
Semantic Scholar
Ethnic variation in the prevalence of AZF deletions in testicular cancer.
Silvina M. Richard, Néstor O. Bianchi, Martha S. Bianchi, P. Peltomäki +2 more
2004Mutation research11 citations
Semantic Scholar
Automatic Integration of Clinical and Genetic Data Using cBioPortal
Mauricio Brunner, L. Mullen, F. Jauk, J. Oliver +8 more
2022Medinfo9 citations Open access
Semantic Scholar
MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing
T. Piñero, O. Soukarieh, Marion Rolain, K. Álvarez +17 more
2020Familial Cancer7 citations Open access
Semantic Scholar
A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin America
P. Esperón, F. Neffa, W. Pavicic, Florencia Spirandelli +9 more
2024Familial Cancer6 citations
Semantic Scholar
Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents
A. Olkinuora, A. C. Mayordomo, Anni K Kauppinen, María Belén Cerliani +15 more
2022Frontiers in Oncology6 citations Open access
Semantic Scholar
Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort
M. González, N. Causada-Calo, J. Santino, M. Dominguez-Valentin +8 more
2018Familial Cancer6 citations Open access
Semantic Scholar
Characterization of screening strategies for Lynch syndrome in Latin America.
Anthony Vladimir Campos-Segura, K. Álvarez, A. G. Murillo Carrasco, B. Rossi +73 more
2025Clinical Gastroenterology and Hepatology4 citations Open access
Semantic Scholar
Association between PER3 length polymorphism and onco-hematological diseases and its influences on patients' functionality
María Belén Cerliani, J. Gili, W. Pavicic, G. Klein +2 more
20153 citations Open access
Semantic Scholar
Analysis of structure and conservation for supporting functional evaluation of PMS2 missense variants
N. Zeuzem, Manon Quilan, M. Dominguez-Valentin, S. Baert-Desurmont +22 more
2026European Journal of Human Genetics2 citations Open access
Semantic Scholar
Association between PER3 length polymorphism and onco-hematological diseases and its influence on patients'
María Belén Cerliani, J. Gili, W. Pavicic, G. Klein +2 more
20152 citations
Semantic Scholar
Editorial: Advances in genetics and molecular diagnosis in colorectal, stomach, and pancreatic cancer
C. Vaccaro, J. Soarez, M. Dominguez-Valentin, W. Pavicic
2022Frontiers in Oncology1 citations Open access
Semantic Scholar
Editorial: Advances in genetics and molecular diagnosis in colorectal, stomach, and pancreatic cancer vol II
J. Soarez, C. A. Vaccaro, M. Dominguez-Valentin, W. Pavicic
2024Frontiers in Oncology0 citations Open access
Semantic Scholar
Maternal ancestry and hematological cancer risk: case-control study in an Argentinean population.
María Belén Cerliani, A. C. Mayordomo, Anaclara Sanchez Dova, J. Soarez +9 more
2021Personalized Medicine0 citations Open access
Semantic Scholar
Síndrome de Lynch: impacto de la caracterización de familias en base a estudios genéticos
C. Vaccaro, Tamara Piñero, A. I. Herrando, Romina A. Cajal +9 more
2018Oncología Clínica0 citations Open access
Semantic Scholar
Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort
M. González, N. Causada-Calo, J. Santino, M. Dominguez-Valentin +8 more
2017Familial Cancer0 citations Open access
Semantic Scholar
Abstract 4491: Pseudoexons may underlie unbalanced expression of APC alleles in familial adenomatous polyposis
T. Nieminen, W. Pavicic, Noora Porkka, H. Järvinen +2 more
20160 citations
Semantic Scholar
LINE-1 hypomethylation in familial and sporadic cancer
W. Pavicic, E. Joensuu, T. Nieminen, P. Peltomäki
2012Journal of molecular medicine0 citations Open access
Semantic Scholar

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