Mateusz Sypniewski
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Explore the profile of Mateusz Sypniewski including associated specialties, affiliations and a list of published articles.
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11
Citations
63
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Recent Articles
1.
Borowczyk M, Sypniewski M, Szyda J, Braszka M, Ziemnicka K, Ruchala M, et al.
Pol Arch Intern Med
. 2024 Jan;
134(3).
PMID: 38165228
Introduction: Genome sequencing technologies reveal molecular mechanisms of differentiated thyroid cancer (DTC). Unlike somatic mutation analysis from thyroidectomy samples, germline mutations showing genetic susceptibility to DTC are less understood. Objectives:...
2.
Sypniewski M, Szydlowski M
Vet Sci
. 2023 Jun;
10(6).
PMID: 37368776
Obesity and overweight are common conditions in dogs, but individual susceptibility varies with numerous risk factors, including diet, age, sterilization, and gender. In addition to environmental and biological factors, genetic...
3.
Mroczek M, Liu J, Sypniewski M, Pienkowski T, Itrych B, Stojak J, et al.
Front Oncol
. 2023 Feb;
13:1045817.
PMID: 36845707
Introduction: Population-based cancer screening has raised many controversies in recent years, not only regarding the costs but also regarding the ethical nature and issues related to variant interpretation. Nowadays, genetic...
4.
Slomian D, Szyda J, Dobosz P, Stojak J, Michalska-Foryszewska A, Sypniewski M, et al.
PLoS One
. 2023 Jan;
18(1):e0279356.
PMID: 36662838
Undoubtedly, genetic factors play an important role in susceptibility and resistance to COVID-19. In this study, we conducted the GWAS analysis. Out of 15,489,173 SNPs, we identified 18,191 significant SNPs...
5.
Sypniewski M, Kresa D, Dobosz P, Topolski P, Kotula L, Sztromwasser P, et al.
J Appl Genet
. 2022 Nov;
64(1):135-139.
PMID: 36417168
Spinal muscular atrophy is a severe neuromuscular disorder with an autosomal recessive inheritance pattern. The disease-causing gene is SMN1, and its paralogue, SMN2, is a disease course modifier. Both genes...
6.
Butler-Laporte G, Povysil G, Kosmicki J, Cirulli E, Drivas T, Furini S, et al.
PLoS Genet
. 2022 Nov;
18(11):e1010367.
PMID: 36327219
Host genetics is a key determinant of COVID-19 outcomes. Previously, the COVID-19 Host Genetics Initiative genome-wide association study used common variants to identify multiple loci associated with COVID-19 outcomes. However,...
7.
Sypniewski M, Krol Z, Szyda J, Kaja E, Mroczek M, Suchocki T, et al.
Int J Mol Sci
. 2022 Aug;
23(15).
PMID: 35955824
Severe outcomes of COVID-19 account for up to 15% of all cases. The study aims to check if any gene variants related to cardiovascular (CVD) and pulmonary diseases (PD) are...
8.
Mroczek M, Inashkina I, Stavusis J, Zayakin P, Khrunin A, Micule I, et al.
Hum Mutat
. 2022 Jun;
43(10):1347-1353.
PMID: 35731190
The investigated intronic CAPN3 variant NM_000070.3:c.1746-20C>G occurs in the Central and Eastern Europe with a frequency of >1% and there are conflicting interpretations on its pathogenicity. We collected data on...
9.
Szyda J, Dobosz P, Stojak J, Sypniewski M, Suchocki T, Kotlarz K, et al.
Int J Mol Sci
. 2022 Jun;
23(11).
PMID: 35682950
COVID-19 infections pose a serious global health concern so it is crucial to identify the biomarkers for the susceptibility to and resistance against this disease that could help in a...
10.
Kaja E, Lejman A, Sielski D, Sypniewski M, Gambin T, Dawidziuk M, et al.
Int J Mol Sci
. 2022 May;
23(9).
PMID: 35562925
Although Slavic populations account for over 4.5% of world inhabitants, no centralised, open-source reference database of genetic variation of any Slavic population exists to date. Such data are crucial for...