Bozsik A - Search Results

1

Case Report: A Novel Pathomechanism in PEComa by the Loss of Heterozygosity of TP53.

Butz H, Lövey J, Szentkereszty M, Bozsik A, Tóth E, Patócs A. Butz H, et al. Among authors: bozsik a. Front Oncol. 2022 Mar 28;12:849004. doi: 10.3389/fonc.2022.849004. eCollection 2022. Front Oncol. 2022. PMID: 35419288 Free PMC article.

2

Complex Characterization of Germline Large Genomic Rearrangements of the BRCA1 and BRCA2 Genes in High-Risk Breast Cancer Patients-Novel Variants from a Large National Center.

Bozsik A, Pócza T, Papp J, Vaszkó T, Butz H, Patócs A, Oláh E. Bozsik A, et al. Int J Mol Sci. 2020 Jun 30;21(13):4650. doi: 10.3390/ijms21134650. Int J Mol Sci. 2020. PMID: 32629901 Free PMC article.

3

Application of Multilayer Evidence for Annotation of C-Terminal BRCA2 Variants.

Butz H, Papp J, Bozsik A, Krokker L, Pócza T, Oláh E, Patócs A. Butz H, et al. Among authors: bozsik a. Cancers (Basel). 2021 Feb 20;13(4):881. doi: 10.3390/cancers13040881. Cancers (Basel). 2021. PMID: 33672545 Free PMC article.

4

Germline Genetic Variants of Viral Entry and Innate Immunity May Influence Susceptibility to SARS-CoV-2 Infection: Toward a Polygenic Risk Score for Risk Stratification.

Grolmusz VK, Bozsik A, Papp J, Patócs A. Grolmusz VK, et al. Among authors: bozsik a. Front Immunol. 2021 Mar 8;12:653489. doi: 10.3389/fimmu.2021.653489. eCollection 2021. Front Immunol. 2021. PMID: 33763088 Free PMC article. Review.

5

Germline Structural Variations in Cancer Predisposition Genes.

Pócza T, Grolmusz VK, Papp J, Butz H, Patócs A, Bozsik A. Pócza T, et al. Among authors: bozsik a. Front Genet. 2021 Apr 14;12:634217. doi: 10.3389/fgene.2021.634217. eCollection 2021. Front Genet. 2021. PMID: 33936164 Free PMC article. Review.

6

Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of PTCH1 in Gorlin-Goltz syndrome.

Igaz P, Toth G, Nagy P, Dezső K, Turai PI, Medvecz M, Wikonkal N, Huszty G, Piros L, Toth E, Bozsik A, Likó I, Patócs A, Butz H. Igaz P, et al. Among authors: bozsik a. J Med Genet. 2022 Sep;59(9):916-919. doi: 10.1136/jmedgenet-2021-108082. Epub 2021 Dec 16. J Med Genet. 2022. PMID: 34916233

7

Reclassification of Five BRCA1/2 Variants with Unknown Significance Using Complex Functional Study.

Bozsik A, Papp J, Grolmusz VK, Patócs A, Oláh E, Butz H. Bozsik A, et al. Cancer Res Treat. 2022 Oct;54(4):970-984. doi: 10.4143/crt.2021.1078. Epub 2022 Feb 8. Cancer Res Treat. 2022. PMID: 35167739 Free PMC article.

8

Genome sequencing-based discovery of a novel deep intronic APC pathogenic variant causing exonization.

Bozsik A, Butz H, Grolmusz VK, Polgár C, Patócs A, Papp J. Bozsik A, et al. Eur J Hum Genet. 2023 Jul;31(7):841-845. doi: 10.1038/s41431-023-01322-y. Epub 2023 Feb 24. Eur J Hum Genet. 2023. PMID: 36828923 Free PMC article.

9

A common genetic variation in GZMB may associate with cancer risk in patients with Lynch syndrome.

Grolmusz VK, Nagy P, Likó I, Butz H, Pócza T, Bozsik A, Papp J, Oláh E, Patócs A. Grolmusz VK, et al. Among authors: bozsik a. Front Oncol. 2023 Feb 20;13:1005066. doi: 10.3389/fonc.2023.1005066. eCollection 2023. Front Oncol. 2023. PMID: 36890824 Free PMC article.

10

Challenging interpretation of germline TP53 variants based on the experience of a national comprehensive cancer centre.

Butz H, Bozsik A, Grolmusz V, Szőcs E, Papp J, Patócs A. Butz H, et al. Among authors: bozsik a. Sci Rep. 2023 Aug 31;13(1):14259. doi: 10.1038/s41598-023-41481-y. Sci Rep. 2023. PMID: 37653074 Free PMC article.

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