Victor M. Pienkowski

Warsaw, MZ 02106, Poland

Last Updated: 09/26/2026

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Found 12 publications

Identification of MHC Ligands Through Allele-Guided Isolation Combined With Machine Learning for Improved MHC Assignment Using ARDisplay-I.

Identification of MHC Ligands Through Allele-Guided Isolation Combined With Machine Learning for Improved MHC Assignment Using ARDisplay-I.

Journal: Molecular & cellular proteomics : MCP

Published: March 13, 2025

Identification of MHC ligands through allele-guided isolation combined with machine learning for improved MHC assignment using ARDisplay-I.

Identification of MHC ligands through allele-guided isolation combined with machine learning for improved MHC assignment using ARDisplay-I.

Journal: Molecular & cellular proteomics : MCP

Published: March 13, 2025

Long read sequencing identifies complex structural variant landscape and recurrent TERT rearrangements in mucoepidermoid carcinoma.

Long read sequencing identifies complex structural variant landscape and recurrent TERT rearrangements in mucoepidermoid carcinoma.

Journal: Oral oncology

Published: October 15, 2024

Vaccine-induced T cell receptor T cell therapy targeting a glioblastoma stemness antigen.

Vaccine-induced T cell receptor T cell therapy targeting a glioblastoma stemness antigen.

Journal: Nature communications

Published: July 26, 2024

Macrocephaly and developmental delay caused by missense variants in RAB5C.

Macrocephaly and developmental delay caused by missense variants in RAB5C.

Journal: Human molecular genetics

Published: March 30, 2023

TADeus2: a web server facilitating the clinical diagnosis by pathogenicity assessment of structural variations disarranging 3D chromatin structure.

TADeus2: a web server facilitating the clinical diagnosis by pathogenicity assessment of structural variations disarranging 3D chromatin structure.

Journal: Nucleic acids research

Published: March 12, 2022

Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene.

Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene.

Journal: Genes

Published: March 05, 2022

De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy.

De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy.

Journal: American journal of human genetics

Published: October 07, 2020

Answer to Finsterer about "Multisystem presentation of a homozygous POLG2 variant".

Answer to Finsterer about "Multisystem presentation of a homozygous POLG2 variant".

Journal: European journal of medical genetics

Published: February 21, 2020

Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion.

Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion.

Journal: European journal of medical genetics

Published: April 04, 2019

A study in a Polish ataxia cohort indicates genetic heterogeneity and points to MTCL1 as a novel candidate gene.

A study in a Polish ataxia cohort indicates genetic heterogeneity and points to MTCL1 as a novel candidate gene.

Journal: Clinical genetics

Published: October 23, 2018

Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.

Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.

Journal: European journal of medical genetics

Published: February 05, 2018

Showing 1-12 of 12

Last Updated: 09/26/2026