
Jacie M. Ihinger
Pediatrics | Medical Genetics
2512 South 7th Street
Floor 3
Minneapolis, MN 55454
Floor 3
Minneapolis, MN 55454
Last Updated: 09/26/2026
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Found 6 publications
Genetic phenotypic characteristics and inheritance patterns of patients with achromatopsia at a large academic institution and a review of the literature and gene therapies.
Journal: Molecular vision
Published: April 20, 2025
The Clinical Findings, Pathogenic Variants, and Gene Therapy Qualifications Found in a Leber Congenital Amaurosis Phenotypic Spectrum Patient Cohort.
Journal: International journal of molecular sciences
Published: December 15, 2023
Clinical Characteristics and Genetic Variants of a Large Cohort of Patients with Retinitis Pigmentosa Using Multimodal Imaging and Next Generation Sequencing.
Journal: International journal of molecular sciences
Published: April 13, 2023
Pathogenic gene variants identified in patients with retinitis pigmentosa at the referral center clinic of the University of Minnesota (UMN).
Journal: Ophthalmic genetics
Published: November 13, 2022
Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy.
Journal: Acta neuropathologica
Published: December 23, 2019
Environmental Regulation of Heterosis in the Allopolyploid Arabidopsis suecica.
Journal: Plant physiology
Published: January 20, 2016
Showing 1-6 of 6
Last Updated: 09/26/2026