Jirat Chenbhanich

Medical Genetics

11100 Euclid Ave
Cleveland, OH 44106

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 25 publications

Aberrant right renal perfusion from right internal mammary artery.

Aberrant right renal perfusion from right internal mammary artery.

Journal: Journal of vascular surgery cases and innovative techniques

Published: September 29, 2024

Atypical Femoral Fracture in Hypophosphatasia: A Systematic Review.

Atypical Femoral Fracture in Hypophosphatasia: A Systematic Review.

Journal: International journal of endocrinology

Published: April 18, 2023

Bone Mineral Density in Neurofibromatosis Type 1: A Systematic Review and Meta-Analysis.

Bone Mineral Density in Neurofibromatosis Type 1: A Systematic Review and Meta-Analysis.

Journal: Calcified tissue international

Published: March 10, 2023

Inpatient epidemiology, healthcare utilization, and association with comorbidities of Turner syndrome: A National Inpatient Sample study.

Inpatient epidemiology, healthcare utilization, and association with comorbidities of Turner syndrome: A National Inpatient Sample study.

Journal: American journal of medical genetics. Part A

Published: July 12, 2022

Impact of the COVID-19 pandemic on medical genetics and genomics training: Perspective from clinical trainees.

Impact of the COVID-19 pandemic on medical genetics and genomics training: Perspective from clinical trainees.

Journal: American journal of medical genetics. Part A

Published: October 20, 2021

An adult male with SHANK2 variant with epilepsy and obsessive-compulsive disorder: Expanding the shankopathy phenotypic spectrum.

An adult male with SHANK2 variant with epilepsy and obsessive-compulsive disorder: Expanding the shankopathy phenotypic spectrum.

Journal: Clinical genetics

Published: September 10, 2021

Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program.

Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program.

Journal: Journal of community genetics

Published: February 03, 2021

Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.

Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.

Journal: Genome medicine

Published: September 02, 2020

Segmental overgrowth and aneurysms due to mosaic PDGFRB p.(Tyr562Cys).

Segmental overgrowth and aneurysms due to mosaic PDGFRB p.(Tyr562Cys).

Journal: American journal of medical genetics. Part A

Published: June 19, 2020

Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy.

Activating variants in PDGFRB result in a spectrum of disorders responsive to imatinib monotherapy.

Journal: American journal of medical genetics. Part A

Published: January 21, 2020

Effects of denosumab on bone metabolism and bone mineral density in kidney transplant patients: a systematic review and meta-analysis.

Effects of denosumab on bone metabolism and bone mineral density in kidney transplant patients: a systematic review and meta-analysis.

Journal: Archives of osteoporosis

Published: October 22, 2018

C-peptide as a key risk factor for non-alcoholic fatty liver disease in the United States population.

C-peptide as a key risk factor for non-alcoholic fatty liver disease in the United States population.

Journal: World journal of gastroenterology

Published: May 30, 2018

Showing 1-12 of 25

Last Updated: 09/26/2026