C
Carissa Rodriquez
Assistant Professor
faculty
COM | Peds Hospital Medicine
1 h-index
3 pubs
2 cited
Research Areas
Links
Biography and Research Information
OverviewAI-generated summary
Carissa Rodriquez's research focuses on pediatric hospital medicine, with recent publications detailing cases of profound hypotonia in infants. These publications investigate the genetic underpinnings of conditions like δ-aminolevulinic acid dehydratase deficient porphyria. Rodriquez has published three total works, with her most recent in 2025. Her scholarship metrics include an h-index of 1 and a total of 3 citations. Rodriquez collaborates with several researchers at the University of Arkansas for Medical Sciences, including T. Burrow and Hannah Barkley, with whom she shares three co-authored publications.
Metrics
- h-index: 1
- Publications: 3
- Citations: 2
Selected Publications
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Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria (2025)
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Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria (2024)
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04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations (2024)
Collaboration Network
Top Collaborators
Hannah Barkley
University of Arkansas for Medical Sciences
3 shared publications
In database
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
T. Burrow
Arkansas Children's Hospital
3 shared publications
In database
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
Karl E. Anderson
The University of Texas Medical Branch at Galveston (US)
3 shared publications
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
Alexis N. Roach
Arkansas Children's Hospital (US)
2 shared publications
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
Ankita Shukla
Arkansas Children's Hospital (US)
2 shared publications
- Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
- Correction: Profound hypotonia in an infant with δ-aminolevulinic acid dehydratase deficient porphyria
Alexis N. Roach
University of Arkansas for Medical Sciences
1 shared publication
In database
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
Ankita Shukla
University of Arkansas for Medical Sciences (US)
1 shared publication
- 04145 Profound hypotonia in a newborn with Biallelic δ-Aminolevulinic Acid Dehydratase (ALAD) mutations
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