Victor A. Pienkowski-Murcia

Krakow, MA, Poland

Last Updated: 09/26/2026

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Found 15 publications

Computational identification of cross-reactive TCR epitopes with ARDitox.

Computational identification of cross-reactive TCR epitopes with ARDitox.

Journal: Journal of cancer research and clinical oncology

Published: May 27, 2025

Harnessing the power of AI in precision medicine: NGS-based therapeutic insights for colorectal cancer cohort.

Harnessing the power of AI in precision medicine: NGS-based therapeutic insights for colorectal cancer cohort.

Journal: Frontiers in oncology

Published: March 26, 2024

Cryptic MYC insertions in Burkitt lymphoma: New data and a review of the literature.

Cryptic MYC insertions in Burkitt lymphoma: New data and a review of the literature.

Journal: PloS one

Published: September 03, 2021

Gene Expression Profile of Human Mesenchymal Stromal Cells Exposed to Hypoxic and Pseudohypoxic Preconditioning-An Analysis by RNA Sequencing.

Gene Expression Profile of Human Mesenchymal Stromal Cells Exposed to Hypoxic and Pseudohypoxic Preconditioning-An Analysis by RNA Sequencing.

Journal: International journal of molecular sciences

Published: June 30, 2021

Developmental delay with hypotrophy associated with homozygous functionally relevant REV3L variant.

Developmental delay with hypotrophy associated with homozygous functionally relevant REV3L variant.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: July 10, 2020

Breakpoint Mapping of Symptomatic Balanced Translocations Links the EPHA6, KLF13 and UBR3 Genes to Novel Disease Phenotype.

Breakpoint Mapping of Symptomatic Balanced Translocations Links the EPHA6, KLF13 and UBR3 Genes to Novel Disease Phenotype.

Journal: Journal of clinical medicine

Published: March 26, 2020

De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy.

De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy.

Journal: Brain : a journal of neurology

Published: March 03, 2020

Syndromic chorioretinal coloboma associated with heterozygous de novo RARA mutation affecting an amino acid critical for retinoic acid interaction.

Syndromic chorioretinal coloboma associated with heterozygous de novo RARA mutation affecting an amino acid critical for retinoic acid interaction.

Journal: Clinical genetics

Published: May 02, 2019

Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy.

Novel COL12A1 variant as a cause of mild familial extracellular matrix-related myopathy.

Journal: Clinical genetics

Published: February 11, 2019

Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines.

Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines.

Journal: Clinical genetics

Published: July 26, 2018

Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders.

Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders.

Journal: Journal of medical genetics

Published: June 10, 2018

Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation.

Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation.

Journal: Clinical genetics

Published: April 29, 2018

Showing 1-12 of 15

Last Updated: 09/26/2026