Enrico Mingardo
Bonn, NW, Germany
Last Updated: 09/26/2026
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Found 11 publications
Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.
Journal: Scientific reports
Published: November 16, 2025
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.
Journal: European journal of human genetics : EJHG
Published: March 11, 2024
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.
Journal: NPJ genomic medicine
Published: August 16, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.
Journal: Biomolecules
Published: May 27, 2023
Impact of the Voltage-Gated Calcium Channel Antagonist Nimodipine on the Development of Oligodendrocyte Precursor Cells.
Journal: International journal of molecular sciences
Published: January 02, 2023
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.
Journal: Communications biology
Published: February 23, 2022
Humanized zebrafish as a tractable tool for in vivo evaluation of pro-myelinating drugs.
Journal: Cell chemical biology
Published: December 20, 2021
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
Showing 1-11 of 11
Last Updated: 09/26/2026