Pawel Skiba

Pasteur Street 10
Wroclaw, DS 50367, Poland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

The results of CNVs analysis in patients with neurodevelopmental delay, dysmorphic features and congenital defects.

The results of CNVs analysis in patients with neurodevelopmental delay, dysmorphic features and congenital defects.

Journal: Journal of applied genetics

Published: December 18, 2025

Epigenetic Findings in Twins with Esophageal Atresia.

Epigenetic Findings in Twins with Esophageal Atresia.

Journal: Genes

Published: July 09, 2023

The Moderating Role of the FKBP5 Gene Polymorphisms in the Relationship between Attachment Style, Perceived Stress and Psychotic-like Experiences in Non-Clinical Young Adults.

The Moderating Role of the FKBP5 Gene Polymorphisms in the Relationship between Attachment Style, Perceived Stress and Psychotic-like Experiences in Non-Clinical Young Adults.

Journal: Journal of clinical medicine

Published: February 07, 2022

The Impact of the FKBP5 Gene Polymorphisms on the Relationship between Traumatic Life Events and Psychotic-Like Experiences in Non-Clinical Adults.

The Impact of the FKBP5 Gene Polymorphisms on the Relationship between Traumatic Life Events and Psychotic-Like Experiences in Non-Clinical Adults.

Journal: Brain sciences

Published: April 13, 2021

The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes.

The Role of the Reanalysis of Genetic Test Results in the Diagnosis of Dysmorphic Syndrome Caused by Inherited xq24 Deletion including the UBE2A and CXorf56 Genes.

Journal: Genes

Published: February 06, 2021

Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia.

Broad phenotypic spectrum of germ line 7p12.1 microdeletions encompassing the IKZF1 gene includes predisposition to acute lymphoblastic leukemia.

Journal: Genes, chromosomes & cancer

Published: July 12, 2020

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit.

Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit.

Journal: Journal of clinical medicine

Published: June 09, 2020

Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders.

Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders.

Journal: Advances in clinical and experimental medicine : official organ Wroclaw Medical University

Published: January 29, 2020

Limited Long-Term Impact of Insect Venom Immunotherapy on the Micro-RNA Landscape in Whole Blood.

Limited Long-Term Impact of Insect Venom Immunotherapy on the Micro-RNA Landscape in Whole Blood.

Journal: Journal of investigational allergology & clinical immunology

Published: September 06, 2018

Genome-wide analysis of gene expression after one year of venom immunotherapy.

Genome-wide analysis of gene expression after one year of venom immunotherapy.

Journal: Immunology letters

Published: July 17, 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

Polymorphisms in immune-inflammatory response genes and the risk of deficit schizophrenia.

Polymorphisms in immune-inflammatory response genes and the risk of deficit schizophrenia.

Journal: Schizophrenia research

Published: April 04, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026