Jeshurun C. Kalanithy
Bonn, NW, Germany
Last Updated: 09/26/2026
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Found 9 publications
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.
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
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax.
Journal: American journal of medical genetics. Part A
Published: March 17, 2021
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.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 02, 2020
Showing 1-9 of 9
Last Updated: 09/26/2026