Thierry van de Wetering
Overview
Explore the profile of Thierry van de Wetering including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
314
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Recent Articles
1.
Kostrzewa-Nowak D, Trzeciak-Ryczek A, Lewandowska K, van de Wetering T, Ciechanowicz A, Nowak R
Int J Mol Sci
. 2025 Jan;
26(1.
PMID: 39796092
The transport of biological materials must protect samples from degradation and ensure courier safety. The main goal of this study was to evaluate the usefulness of a new type of...
2.
Lisman D, Drath J, Zielinska G, van de Wetering T, Bukowski K, Ossowski A
Arch Med Sadowej Kryminol
. 2024 Apr;
73(4):294-307.
PMID: 38662482
The purpose of this paper is to formulate recommendations for the disclosure of biological traces in the laboratory and the handling of forensic evidence submitted for identification tests, recommended by...
3.
Lisman D, Drath J, Zielinska G, Zacharczuk J, Piatek J, van de Wetering T, et al.
Sci Rep
. 2023 Dec;
13(1):21666.
PMID: 38066060
DNA analysis-based identification is by far the gold standard in forensic genetics and it should be performed in every case involving human remains or unidentified bodies. Bones and teeth are...
4.
Clark J, Podsiadlo K, Sobalska-Kwapis M, Marciniak B, Rydzewska K, Ciechanowicz A, et al.
Sci Rep
. 2023 Oct;
13(1):17118.
PMID: 37816715
There is now substantial evidence that zinc-finger proteins are implicated in adiposity. Aims were to datamine for high-frequency (near-neutral selection) pretermination-codon (PTC) single-nucleotide polymorphisms (SNPs; n = 141) from a...
5.
Clark J, van de Wetering T, Marciniak B, Zadzinska E, Ciechanowicz A, Kaczmarczyk M, et al.
Sci Rep
. 2022 Nov;
12(1):18923.
PMID: 36344606
Number of children is an important human trait and studies have indicated associations with single-nucleotide polymorphisms (SNPs). Aim: to give further evidence for four associations using a large sample of...
6.
Zlowocka-Perlowska E, van de Wetering T, Toloczko-Grabarek A, Scott R, Lubinski J
Oncotarget
. 2022 Apr;
13:628-640.
PMID: 35478773
Purpose: The association between the c.3020insC allele and missense variant c.442G>A (p.P.A148T) and survival of patients with bladder or kidney cancer remains controversial. Materials And Methods: We compared the allele...
7.
Zlowocka-Perlowska E, Debniak T, Slojewski M, van de Wetering T, Toloczko-Grabarek A, Cybulski C, et al.
PLoS One
. 2021 Sep;
16(9):e0257132.
PMID: 34499690
Purpose: The purpose of this study was to compare the clinical characteristics and the survival of CHEK2 mutation positive and CHEK2 mutation negative patients diagnosed with bladder or kidney cancer....
8.
Zlowocka-Perlowska E, Debniak T, Slojewski M, Leminski A, Soczawa M, van de Wetering T, et al.
Hered Cancer Clin Pract
. 2021 Jan;
19(1):6.
PMID: 33419454
Introduction: The role of PALB2 in carcinogenesis remains to be clarified. Our main goal was to determine the prevalence of PALB2 (509_510delGA and 172_175delTTGT) mutations in bladder and kidney cancer...
9.
Kazmierczak-Siedlecka K, Daca A, Fic M, van de Wetering T, Folwarski M, Makarewicz W
Gut Microbes
. 2020 May;
11(6):1518-1530.
PMID: 32453670
The link between gut microbiota and the development of colorectal cancer has been investigated. An imbalance in the gut microbiota promotes the progress of colorectal carcinogenesis multiple mechanisms, including inflammation,...
10.
Paszkowska-Szczur K, Scott R, Gorski B, Cybulski C, Kurzawski G, Dymerska D, et al.
Mol Biol Rep
. 2014 Nov;
42(3):755-64.
PMID: 25391773
Xeroderma pigmentosum (XP) is a rare autosomal recessive disease that is associated with a severe deficiency in nucleotide excision repair. Genetic polymorphisms in XP genes may be associated with a...