Jessica T. Ogawa

Medical Genetics

11100 Euclid Ave
Cleveland, OH 44106

Last Updated: 09/26/2026

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Found 5 publications

Germline de novo alterations of RUNX1T1 in individuals with neurodevelopmental and congenital anomalies.

Germline de novo alterations of RUNX1T1 in individuals with neurodevelopmental and congenital anomalies.

Journal: HGG advances

Published: October 01, 2024

Postnatal Progressive Craniosynostosis: An Unusual Case Presentation Leading to Cascade Diagnosis for Multiple Generations.

Postnatal Progressive Craniosynostosis: An Unusual Case Presentation Leading to Cascade Diagnosis for Multiple Generations.

Journal: American journal of medical genetics. Part A

Published: September 09, 2024

Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition.

Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition.

Journal: bioRxiv : the preprint server for biology

Published: October 09, 2023

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition.

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition.

Journal: Nature genetics

Published: September 26, 2023

Oral Health and Dental Clinic Attendance in Pediatric Refugees.

Oral Health and Dental Clinic Attendance in Pediatric Refugees.

Journal: Pediatric dentistry

Published: February 26, 2019

Showing 1-5 of 5

Last Updated: 09/26/2026