Oznur Yilmaz

Bonn, NW 53115, Germany

Last Updated: 09/26/2026

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Found 14 publications

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Evidence that disruption of Discoidin domain receptor 2 contributes to palate malformations through effects on the extracellular matrix.

Journal: Human molecular genetics

Published: November 20, 2025

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Journal: Scientific reports

Published: November 16, 2025

Haploinsufficiency of ABL1 is associated with dominant isolated omphalocele.

Haploinsufficiency of ABL1 is associated with dominant isolated omphalocele.

Journal: Frontiers in cell and developmental biology

Published: May 18, 2025

EZH2 specifically regulates ISL1 during embryonic urinary tract formation.

EZH2 specifically regulates ISL1 during embryonic urinary tract formation.

Journal: Scientific reports

Published: June 24, 2024

Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish models.

Role of ZFHX4 in orofacial clefting based on human genetic data and zebrafish models.

Journal: European journal of human genetics : EJHG

Published: March 11, 2024

TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies.

TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies.

Journal: Journal of medical genetics

Published: December 06, 2023

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.

Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.

Journal: NPJ genomic medicine

Published: August 16, 2023

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.

Journal: Journal of medical genetics

Published: May 30, 2022

Effect of modulating glutamate signaling on myelinating oligodendrocytes and their development-A study in the zebrafish model.

Effect of modulating glutamate signaling on myelinating oligodendrocytes and their development-A study in the zebrafish model.

Journal: Journal of neuroscience research

Published: December 06, 2020

Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies.

Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 02, 2020

SLC20A1 Is Involved in Urinary Tract and Urorectal Development.

SLC20A1 Is Involved in Urinary Tract and Urorectal Development.

Journal: Frontiers in cell and developmental biology

Published: February 10, 2020

CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch.

CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch.

Journal: Glia

Published: July 03, 2019

Showing 1-12 of 14

Last Updated: 09/26/2026