Fumihiko Urano

19PUBLICATIONS
45CO-AUTHORS
Genome structure and regulationGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsGene mappingNeurology and neuromuscular diseases
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Publications (19)

|Oct 10, 2026
Hyperexcitable but seizure-free: hippocampal network dysfunction in a Wolfram syndrome model.

|Jul 10, 2026
Consensus Recommendations for the Clinical Management of Wolfram syndrome Using a Delphi Method.

|Apr 18, 2026
Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy.

|Apr 10, 2026
Evaluating the Use of GLP-1 Receptor Agonists in Wolfram syndrome Patients.

Laura Lee, Abby F Tang, Anna Asako

|Apr 03, 2026
Genotype-Based Severity Scoring System in Wolfram Syndrome: Correlation with Onset of Cardinal Symptoms and WFS1 Gene Variant Types.

Liam Oiknine, Abby F Tang, Fumihiko Urano

|Apr 03, 2026
Synaptic Alterations Are Preceding the Axonal Loss in Optic Atrophy of Wolfram Syndrome Mouse Model.

Venu Gurram, William An, Shrinivas Bimal

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Frequent Collaborators

3 joint publications

Shuntaro Morikawa

2 joint publications

Kristina G Maxwell

2 joint publications

Punn Augsornworawat

2 joint publications

Ying Maggie Chen