Walter Pavicic
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Explore the profile of Walter Pavicic including associated specialties, affiliations and a list of published articles.
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12
Citations
138
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Recent Articles
1.
Esperon P, Neffa F, Pavicic W, Spirandelli F, Alvarez K, Mullins M, et al.
Fam Cancer
. 2024 Apr;
23(4):507-513.
PMID: 38687439
MUTYH-Associated Polyposis (MAP) is caused by biallelic pathogenic germline variants in the MUTYH gene. However, individuals harboring monoallelic MUTYH pathogenic variants in the presence of a positive family history have...
2.
Dominguez-Valentin M, Haupt S, Seppala T, Sampson J, Sunde L, Bernstein I, et al.
EClinicalMedicine
. 2023 May;
58:101909.
PMID: 37181409
Background: The Prospective Lynch Syndrome Database (PLSD) collates information on carriers of pathogenic or likely pathogenic MMR variants () who are receiving medical follow-up, including colonoscopy surveillance, which aims to...
3.
Brunner M, Mullen L, Jauk F, Oliver J, Cayol F, Minata J, et al.
Stud Health Technol Inform
. 2022 Jun;
290:799-803.
PMID: 35673128
Precision medicine seeks to improve the prevention, diagnosis and treatment of patients based on genetic characteristics unique to each person. In oncology, therapeutic decisions have been established based on the...
4.
Seppala T, Dominguez-Valentin M, Crosbie E, Engel C, Aretz S, Macrae F, et al.
Eur J Cancer
. 2021 Mar;
148:124-133.
PMID: 33743481
Purpose: This study aimed to report the uptake of hysterectomy and/or bilateral salpingo-oophorectomy (BSO) to prevent gynaecological cancers (risk-reducing surgery [RRS]) in carriers of pathogenic MMR (path_MMR) variants. Methods: The...
5.
Gonzalez M, Causada-Calo N, Santino J, Dominguez-Valentin M, Ferro F, Sammartino I, et al.
Fam Cancer
. 2017 Nov;
17(3):395-402.
PMID: 29128931
Microsatellite instability (MSI) is a hallmark tool for Lynch syndrome (LS) screening and a prognostic marker for sporadic colorectal cancer (CRC). In regions with limited resources and scarce CRC molecular...
6.
Cerliani M, Pavicic W, Gili J, Klein G, Saba S, Richard S
World J Clin Oncol
. 2016 Oct;
7(5):395-405.
PMID: 27777882
Aim: To analyze the association between oncohematological diseases and // polymorphisms, dietary habits and smoking, in an argentine hospital-based case-control study. Methods: This hospital-based case-control study involved 125 patients with...
7.
Nieminen T, Pavicic W, Porkka N, Kankainen M, Jarvinen H, Lepisto A, et al.
Oncotarget
. 2016 Sep;
7(43):70685-70698.
PMID: 27683109
Allele-specific expression (ASE) of the Adenomatous Polyposis Coli (APC) gene occurs in up to one-third of families with adenomatous polyposis (FAP) that have screened mutation-negative by conventional techniques. To advance...
8.
Joensuu E, Nieminen T, Lotsari J, Pavicic W, Abdel-Rahman W, Peltomaki P
Genes Chromosomes Cancer
. 2015 Aug;
54(12):776-87.
PMID: 26305882
Molecular mechanisms underlying coordinated hypermethylation of multiple CpG islands in cancer remain unclear and studies of methyltransferase enzymes have arrived at conflicting results. We focused on DNMT1 and DNMT3B, DNA...
9.
Pavicic W, Nieminen T, Gylling A, Pursiheimo J, Laiho A, Gyenesei A, et al.
Genes Chromosomes Cancer
. 2014 Jun;
53(10):857-64.
PMID: 24946964
n familial adenomatous polyposis (FAP), 20% of classical and 70% of attenuated/atypical (AFAP) cases remain mutation-negative after routine testing; yet, allelic expression imbalance may suggest an APC alteration. Our aim...
10.
Pavicic W, Joensuu E, Nieminen T, Peltomaki P
J Mol Med (Berl)
. 2012 Jan;
90(7):827-35.
PMID: 22228215
Increased and decreased methylation at specific sequences (hypermethylation and hypomethylation, respectively) is characteristic of tumor DNA compared to normal DNA and promotes carcinogenesis in multiple ways including genomic instability. Long...