Tomoyasu Higashimoto
Medical Genetics
1540 E Hospital Dr
Floor 6 Reception C
Ann Arbor, MI 48109
Floor 6 Reception C
Ann Arbor, MI 48109
Last Updated: 09/26/2026
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Found 9 publications
From Multiple Congenital Anomalies to Pituitary Gland Malformation: Wide Spectrum of Clinical Features in a Family With FOXA2 Variant.
Journal: American journal of medical genetics. Part A
Published: November 12, 2025
Atypical Presentation of Congenital Insensitivity to Pain With Anhidrosis Leading to Diagnostic Odyssey.
Journal: Molecular genetics & genomic medicine
Published: June 14, 2024
Primary amenorrhea in myotonic dystrophy type 1: Initial presentation versus incidental finding on whole genome sequencing.
Journal: American journal of medical genetics. Part A
Published: March 05, 2024
Maple syrup urine disease decompensation misdiagnosed as a psychotic event.
Journal: Molecular genetics and metabolism reports
Published: April 19, 2022
Case report of bilateral ovarian fibromas associated with de novo germline variants in PTCH1 and SMARCA4.
Journal: Molecular genetics & genomic medicine
Published: April 11, 2022
A method for overcoming plasma protein inhibition of tyrosine kinase inhibitors.
Journal: Blood cancer discovery
Published: September 30, 2021
Epigenetic downregulation of Socs2 contributes to mutant N-Ras-mediated hematopoietic dysregulation.
Epigenetic downregulation of Socs2 contributes to mutant N-Ras-mediated hematopoietic dysregulation.
Journal: Disease models & mechanisms
Published: April 30, 2021
High-dose hydroxocobalamin achieves biochemical correction and improvement of neuropsychiatric deficits in adults with late onset cobalamin C deficiency.
Journal: JIMD reports
Published: August 25, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026