Kim L. McBride
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
189
Citations
5,452
Est. group size
~6
Recurring co-author estimate
Active years
41
Publishing since 1986
Kim L. McBride's research focuses on the genetics of congenital heart defects, particularly bicuspid aortic valve disease, and its overlap with connective tissue disorders like Ehlers-Danlos syndrome and osteogenesis imperfecta. The work combines clinical genetics, genomics (identifying rare gene variants and chromosomal copy number changes), and cardiac imaging to understand inherited heart and vascular conditions, including rare metabolic and genetic syndromes. This research aims to improve diagnosis and genetic counseling for patients with congenital and structural heart disease.
Publication output rose to a peak around 2021 but has generally slowed over the past few years, dropping from about 20 papers in 2021 to roughly 5-10 per year recently.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Response to Burgard et al
Genetics in Medicine · 2026
- Phenomics Based CMR Characterization of Muscular Dystrophy Subtypes With Comparison to Healthy Cohorts
Journal of Cardiovascular Magnetic Resonance · 2026
- A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B
The American Journal of Human Genetics · 2026
- 26-A-12318-ACC RARE TYPE 1 COLLAGEN GENE VARIANTS IMPLICATED IN A NOVEL OVERLAP PHENOTYPE OF BICUSPID AORTIC VALVE, EHLERS-DANLOS SYNDROME, AND OSTEOGENESIS IMPERFECTA
Journal of the American College of Cardiology · 2026
- Rare type I collagen variants in early-onset bicuspid aortic valve disease: Overlap with Ehlers-Danlos syndrome and osteogenesis imperfecta
Human Genetics and Genomics Advances · 2026
- Utility of genetic testing in heart transplant recipients: a systematic review and meta-analysis
Transplantation Reviews · 2026
- P321: Identifying new genotype/phenotype correlations for individuals carrying deleterious RERE variants
Genetics in Medicine Open · 2025
- Leveraging facial shape and connective tissue disorders for genetic insights into thoracic aortic aneurysms and dissections
Lirias · 2025
- Understanding the face of thoracic aortic aneurysms and dissections in the general population
Lirias · 2025
- Phenylalanine hydroxylase deficiency diagnosis and management: A 2023 evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Genetics in Medicine · 2024
- Contribution of rare chromosome 22q11.2 copy number variants to non-syndromic bicuspid aortic valve
Heart · 2024
- Longitudinal echocardiography in pediatric patients with hypermobile Ehlers‐Danlos syndrome
American Journal of Medical Genetics Part A · 2024
- Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve
PLoS ONE · 2024
- Bicuspid Aortic Valve Disease With Early Onset Complications: Characteristics And Aortic Outcomes
medRxiv · 2024
- Bicuspid Aortic Valve Disease with Early-Onset Complications: Characteristics and Aortic Outcomes
Hearts · 2024
- Molecular Genetics and Metabolism×17
- Genetics in Medicine×8
- Molecular Case Studies×6
- Circulation×5
- Human Genetics and Genomics Advances×3
- Manyan Huang
Biochemistry, Genetics and Molecular Biology · Indiana University
- Matthew D. Durbin
Biochemistry, Genetics and Molecular Biology · Indiana University
- Stephanie M. Ware
Biochemistry, Genetics and Molecular Biology · Indiana University
- Vidu Garg
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Yang Yu
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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