David H. Ledbetter

Professor

University of Florida College of Medicine - Jacksonville

United States

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David H. Ledbetter is a Professor at the University of Florida College of Medicine-Jacksonville, USA. His research focuses on monogenic disorders in children, mental health through genomics, and the genetic underpinnings of neurodevelopmental psychiatric conditions. Recent publications include studies on sex chromosome aneuploidies, the diagnostic yield of exome sequencing in cerebral palsy, and the prevalence of rare pathogenic variants in psychiatric genes.

Articles (12)

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2025

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2024

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2020

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2020

Collaborators (1)

Matthew Oetjens

Assistant Professor

Geisinger Medical Center

UNITED STATES

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David H. Ledbetter

Research Interests

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Articles (12)

Monogenic disorders associated with motor speech phenotypes in children and adolescents undergoing clinical exome sequencing.

Advancing Mental Health Research Through Strategic Integration of Transdiagnostic Dimensions and Genomics.

A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases.

Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines: A Systematic Review and Meta-analysis.

Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism.

Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population.

Frequency of truncating FLCN variants and Birt-Hogg-Dubé-associated phenotypes in a health care system population.

Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology.

Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variants.

Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

Feasibility of blood testing combined with PET-CT to screen for cancer and guide intervention

Collaborators (1)

Matthew Oetjens

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