Pawel Wlasienko

17a Kasprzaka Street
Warsaw, MZ 01211, Poland

Last Updated: 09/26/2026

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Found 18 publications

NGS sequencing reveals the cause of hearing loss in a group of Polish patients with an isolated, non-DFNB1 hearing loss.

NGS sequencing reveals the cause of hearing loss in a group of Polish patients with an isolated, non-DFNB1 hearing loss.

Journal: Journal of applied genetics

Published: December 31, 2024

Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

Journal: Kardiologia polska

Published: April 29, 2024

ERRATUM: Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

ERRATUM: Genetic testing for inherited cardiovascular diseases. A position statement of the Polish Cardiac Society endorsed by Polish Society of Human Genetics and Cardiovascular Patient Communities.

Journal: Kardiologia polska

Published: April 29, 2024

Molecular analysis of inherited disorders of cornification in polish patients show novel variants and functional data and provokes questions on the significance of secondary findings.

Molecular analysis of inherited disorders of cornification in polish patients show novel variants and functional data and provokes questions on the significance of secondary findings.

Journal: Orphanet journal of rare diseases

Published: January 04, 2024

Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience.

Implementation of Exome Sequencing in Prenatal Diagnosis and Impact on Genetic Counseling: The Polish Experience.

Journal: Genes

Published: March 31, 2022

Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.

Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.

Journal: Genes

Published: March 19, 2022

Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.

Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.

Journal: Genes

Published: November 08, 2021

The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (P.GLN1981*).

The MED13L haploinsufficiency syndrome associated with de novo nonsense variant (P.GLN1981*).

Journal: Journal of mother and child

Published: April 30, 2021

Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.

Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.

Journal: American journal of human genetics

Published: May 03, 2019

Echocardiographic analysis of left ventricular function in term and preterm neonates at week 40 of postconceptional life.

Echocardiographic analysis of left ventricular function in term and preterm neonates at week 40 of postconceptional life.

Journal: Kardiologia polska

Published: March 06, 2019

Comprehensive genomic analysis of patients with disorders of cerebral cortical development.

Comprehensive genomic analysis of patients with disorders of cerebral cortical development.

Journal: European journal of human genetics : EJHG

Published: April 10, 2017

Evaluation of left ventricular function in preterm infants with bronchopulmonary dysplasia using various echocardiographic techniques.

Evaluation of left ventricular function in preterm infants with bronchopulmonary dysplasia using various echocardiographic techniques.

Journal: Echocardiography (Mount Kisco, N.Y.)

Published: April 04, 2017

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Last Updated: 09/26/2026