Claudia Soler‐Alfonso

Also affiliated with Cook Children's Medical Center, Texas Children's Hospital

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Clinical trials in mitochondrial disorders, an update”.

Clinical trials in mitochondrial disorders, an update

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.10.002

N/A

0.646DataRank · unranked

73 citations

Ayman W. El‐Hattab, M. Nadir Ali, Claudia Soler‐Alfonso, Fernando Scaglia, Mohammed Almannai

Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients

Genetics in Medicine(2022)10.1016/j.gim.2022.11.020

N/A

0.590DataRank · unranked

50 citations

Erica Julianne Lay, Claudia Soler‐Alfonso, Kevin E. Glinton, Kimberly Houck, Mustafa Tosur +29 more

Case Series of Nizon‐Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid–Triploid Mosaicism

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64233

N/A

0.104DataRank · unranked

1 citations

Kimberly Ezell, Deanna S. Bell, Brian Corner, Ashley McMinn, Joy D. Cogan +16 more

Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants

Genetics in Medicine(2022)10.1016/j.gim.2022.09.015

N/A

0DataRank · unranked

17 citations

Yael Mozer‐Glassberg, Yuval E. Landau, Lea D. Schlieben, Holger Prokisch, René G. Feichtinger +56 more

Reducing Time to Diagnosis of Rare Genetic Diseases in a Medically Underserved Hispanic Population- Lessons Learned for Meaningful Engagement

Research Square(2023)10.21203/rs.3.rs-3699740/v1

N/A

0DataRank · unranked

3 citations

Roberta Sierra, Dan Brooks, Christopher J. Holder, Lauren Urbanski, Keila Rodriguez +19 more

Project GIVE: using a virtual genetics service platform to reduce health inequities and improve access to genomic care in an underserved region of Texas

Journal of Neurodevelopmental Disorders(2024)10.1186/s11689-024-09560-x

N/A

0DataRank · unranked

5 citations

Roberta Sierra, Daniel Brooks, Christopher J. Holder, Lauren Urbanski, Keila Rodriguez +20 more

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

EMBO Molecular Medicine(2025)10.1038/s44321-025-00290-8

N/A

0DataRank · unranked

8 citations

Marisa W. Friederich, Daniella H. Hock, Jessie R. Zhang, Liana Valin, Jill A. Rosenfeld +35 more

Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders

medRxiv(2025)10.1101/2025.07.08.25330848

N/A

0DataRank · unranked

1 citations

Marisa W. Friederich, Daniella H. Hock, Jessie R. Zhang, Liana Valin, Jill A. Rosenfeld +35 more

TRMU deficiency: A broad clinical spectrum responsive to cysteine supplementation

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.01.005

N/A

0DataRank · unranked

26 citations

Claudia Soler‐Alfonso, Kathleen M. Loomes, Amit A. Shah, Danielle Monteil, Carmencita D. Padilla +3 more

Exome sequencing in children with clinically suspected maturity‐onset diabetes of the young

Pediatric Diabetes(2021)10.1111/pedi.13257

N/A

0DataRank · unranked

18 citations

Claudia Soler‐Alfonso, Katie Chan, Michael M. Khayat, Shalini N. Jhangiani, Qingchang Meng +9 more