Match tier
Listed
Presence
Current · Arkansas
Last published
2026
Sources
OpenAlex · ORCID
Refreshed
2026-09-26
M
Matthew H. Merves
Associate Professor
Also affiliated: Arkansas Children's Hospital (2022–2026); Emory University (2018–2019); University of Florida (2011)
Peds Pediatrics, College of Medicine
3 h-index
7 pubs
26 cited
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Matthew Merves investigates the validity of novel assessment tools for bag-mask ventilation, a critical procedure in emergency and acute care settings. His work contributes to improving medical education and training for healthcare professionals. Merves' research focuses on developing and evaluating methods to enhance the proficiency and effectiveness of clinicians in delivering essential respiratory support.
Metrics
- h-index: 3
- Publications: 7
- Citations: 26
Positions
-
Associate Professor publications 2022–2026University of Arkansas for Medical Sciences Peds Pediatrics, College of Medicine Institutional directory
Selected Publications
-
Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU (2026)
-
Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool (2022)
Collaboration Network
Top Collaborators
Allison Whalen
Medical University of South Carolina (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Priyanka Kharayat
Jefferson Einstein Philadelphia Hospital (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
James S. Barry
University of Colorado Denver (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Kristen Glass
Penn State Milton S. Hershey Medical Center (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Robert A. Berg
Children's Hospital of Philadelphia (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Taylor Sawyer
Seattle Children's Hospital (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Vinay Nadkarni
Children's Hospital of Philadelphia
1 shared publication
In database
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Donald L. Boyer
Children's Hospital of Philadelphia (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Akira Nishisaki
Children's Hospital of Philadelphia (US)
1 shared publication
- Validity Evidence for a Novel, Comprehensive Bag–Mask Ventilation Assessment Tool
Vonita Chawla
Arkansas Children's Hospital
1 shared publication
In database
- Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU
Kumar Shashi
Arkansas Children's Hospital
1 shared publication
In database
- Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU
Makenzie L. Niven
Southwestern Medical Center (US)
1 shared publication
- Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU
Venkatasai Devarapalli
Arkansas Children's Hospital
1 shared publication
In database
- Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU
Prachi Shah
Arkansas Children's Hospital
1 shared publication
In database
- Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU
Andrew Tran
Arkansas Children's Hospital (US)
1 shared publication
- Sirolimus for non-immune hydrops due to vascular and lymphatic anomalies in preterm neonates: an imaging-anchored response phenotype from a level IV NICU
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