Oana V. Amarie
Neuherberg, BY, Germany
Last Updated: 09/26/2026
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Found 36 publications
Searching for New Genes That Cause Usher Syndrome.
Journal: American journal of ophthalmology
Published: January 21, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME.
Journal: American journal of ophthalmology
Published: January 21, 2026
REECAP: Contrastive learning of retinal aging reveals genetic loci linking morphology to eye disease.
Journal: medRxiv : the preprint server for health sciences
Published: December 03, 2025
Ocular Phenotyping of Knockout Mice Identifies Genes Associated With Late Adult Retinal Phenotypes.
Journal: Investigative ophthalmology & visual science
Published: June 23, 2025
Systematic Ocular Phenotyping of Knockout Mouse Lines Identifies Genes Associated With Age-Related Corneal Dystrophies.
Journal: Investigative ophthalmology & visual science
Published: May 05, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita.
Journal: Science advances
Published: April 11, 2025
Opa1 processing is dispensable in mouse development but is protective in mitochondrial cardiomyopathy.
Journal: Science advances
Published: August 02, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes.
Journal: Nature communications
Published: January 26, 2024
Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Journal: medRxiv : the preprint server for health sciences
Published: March 30, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Journal: Kidney international
Published: March 16, 2023
Last Updated: 09/26/2026