Caleb P. Bupp

Caleb P. Bupp

Pediatrics | Medical Genetics

25 Michigan Street Northeast
Suite 2100
Grand Rapids, MI 49503

Last Updated: 09/26/2026

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Found 72 publications

An Interesting Case of Sulphonylurea-Responsive Permanent Neonatal Diabetes Mellitus With Potassium Channel Mutation.

An Interesting Case of Sulphonylurea-Responsive Permanent Neonatal Diabetes Mellitus With Potassium Channel Mutation.

Journal: Cureus

Published: April 30, 2026

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.

Journal: American journal of human genetics

Published: February 06, 2026

Opportunities for RNA sequencing in physiology: from big data to understanding homeostasis and heterogeneity.

Opportunities for RNA sequencing in physiology: from big data to understanding homeostasis and heterogeneity.

Journal: Function (Oxford, England)

Published: December 16, 2025

The molecular architecture of severe pediatric traumatic brain injury: integrated omics reveal therapeutic pathways.

The molecular architecture of severe pediatric traumatic brain injury: integrated omics reveal therapeutic pathways.

Journal: Critical care (London, England)

Published: September 04, 2025

Role of CAMK2D in neurodevelopment and associated conditions.

Role of CAMK2D in neurodevelopment and associated conditions.

Journal: American journal of human genetics

Published: August 12, 2025

Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review.

Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review.

Journal: American journal of medical genetics. Part A

Published: July 31, 2025

Methyl-CpG-binding domain as a protein interaction partner in promoter regulation and neurodevelopment through evolutionary expanded entanglement.

Methyl-CpG-binding domain as a protein interaction partner in promoter regulation and neurodevelopment through evolutionary expanded entanglement.

Journal: American journal of physiology. Cell physiology

Published: July 25, 2025

Collection, preparation, and biobanking of clinical specimens for analysis in polyaminopathies.

Collection, preparation, and biobanking of clinical specimens for analysis in polyaminopathies.

Journal: Methods in enzymology

Published: May 17, 2025

Monitoring ODC activity and polyamines in Bachmann-Bupp syndrome patient biological samples.

Monitoring ODC activity and polyamines in Bachmann-Bupp syndrome patient biological samples.

Journal: Methods in enzymology

Published: May 17, 2025

From castaways to discoveries: unveiling treasures in skin RNAseq using a novel multidimensional data processing workflow including infection-host dynamics.

From castaways to discoveries: unveiling treasures in skin RNAseq using a novel multidimensional data processing workflow including infection-host dynamics.

Journal: Physiological genomics

Published: March 12, 2025

Repurposing With Purpose: Treatment of Bachmann-Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies.

Repurposing With Purpose: Treatment of Bachmann-Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: January 15, 2025

Implementation of Rapid Whole Genome Sequencing in Pediatric Acute Care is Associated with Positive Shifts in Health Care Professionals' Perspectives Toward Testing.

Implementation of Rapid Whole Genome Sequencing in Pediatric Acute Care is Associated with Positive Shifts in Health Care Professionals' Perspectives Toward Testing.

Journal: The Journal of pediatrics

Published: January 08, 2025

Showing 1-12 of 72

Last Updated: 09/26/2026