Hilary J. Vernon

Also affiliated with Johns Hopkins Medicine

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 15 papers. Top paper: “Diverse mitochondrial abnormalities in a new cellular model of TAFFAZZIN deficiency are remediated by cardiolipin-interacting small molecules”.

Diverse mitochondrial abnormalities in a new cellular model of TAFFAZZIN deficiency are remediated by cardiolipin-interacting small molecules

Journal of Biological Chemistry(2021)10.1016/j.jbc.2021.101005

N/A

0.672DataRank · unranked

21 citations

Olivia Sniezek Carney, Alexandra Pado, Veronica F. Busa, Frédéric M. Vaz, Simion Kreimer +7 more

Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.06.007

N/A

0.457DataRank · unranked

20 citations

Nicholas Ah Mew, Hilary J. Vernon, Rebecca Ganetzky, Ryan H. Peretz

AGAP1-associated endolysosomal trafficking abnormalities link gene–environment interactions in neurodevelopmental disorders

Disease Models & Mechanisms(2023)10.1242/dmm.049838

N/A

0.444DataRank · unranked

11 citations

Somayeh Bakhtiari, Jacob Forstrom, Allan Bayat, Frédéric Bilan, Gwenaël Le Guyader +5 more

Lipodystrophy in methylmalonic acidemia associated with elevated FGF21 and abnormal methylmalonylation

JCI Insight(2024)10.1172/jci.insight.174097

N/A

0.345DataRank · unranked

6 citations

Justin R. Sysol, PamelaSara E. Head, Madeline Epping, Oksana Gavrilova, Melissa K. Crocker +22 more

AGAP1-associated endolysosomal trafficking abnormalities link gene-environment interactions in a neurodevelopmental disorder

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.31.526497

N/A

0.165DataRank · unranked

2 citations

Somayeh Bakhtiari, Jacob Forstrom, Allan Bayat, Frédéric Bilan, Gwenaël Le Guyader +5 more

Granulopoietic Dysregulation in a Patient-Tailored Mouse Model of Barth Syndrome

Stem Cell Reviews and Reports(2025)10.1007/s12015-025-10945-1

N/A

0.165DataRank · unranked

2 citations

Maegan L. Capitano, Donna M. Edwards, Baskar Ramdas, Scott Cooper, James Ropa +8 more

Barth syndrome cellular models have dysregulated respiratory chain complex I and mitochondrial quality control due to abnormal cardiolipin

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.06.425502

N/A

0.165DataRank · unranked

2 citations

Olivia Sniezek Carney, Alexandra Pado, Veronica F. Busa, Frédéric M. Vaz, Simion Kreimer +6 more

A Prospective Birth Cohort Study on the Association Between Cord Blood Acylcarnitine Profile and Childhood Risk of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder

Journal of the American Academy of Child & Adolescent Psychiatry(2025)10.1016/j.jaac.2025.10.002

N/A

0.104DataRank · unranked

1 citations

Mengmeng Li, Marilyn Augustyn, Colleen Pearson, Hilary J. Vernon, Guoying Wang +4 more

The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem

JIMD Reports(2023)10.1002/jmd2.12361

N/A

0DataRank · unranked

1 citations

Ryan H. Peretz, Angela Pipitone Dempsey, Jacquelyn Britton, Lisa E. Kratz, Ada Hamosh +4 more

Arginine kinetics are altered in a pilot sample of adolescents and young adults with Barth syndrome

Molecular Genetics and Metabolism Reports(2020)10.1016/j.ymgmr.2020.100675

N/A

0DataRank · unranked

4 citations

Kathryn L. Bohnert, Adam J. Bittel, Shaji Chacko, Bruce W. Patterson, Christina A. Pacak +4 more

Accurate assignment of disease liability to genetic variants using only population data

Genetics in Medicine(2021)10.1016/j.gim.2021.08.012

N/A

0DataRank · unranked

5 citations

Karen S. Raraigh, Joshua Betz, Melis A. Aksit, Nenad Blau, Jordan Brown +9 more

Mitochondrial disease disrupts hepatic allostasis and lowers the threshold for immune-mediated liver toxicity

Molecular Metabolism(2020)10.1016/j.molmet.2020.100981

N/A

0DataRank · unranked

17 citations

Senta M. Kapnick, Т. Н. Тарасенко, Cassidy T. Burke, Patricia M. Zerfas, Francisca Díaz +5 more

Lipid metabolism drives allele-specific early-stage hypertrophic cardiomyopathy

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.10.564562

N/A

0DataRank · unranked

1 citations

Anja Karlstaedt, Damla Ates Gulkok, Tilo Thottakara, Yamin Liu, Sili Fan +6 more

Stem cell models of TAFAZZIN deficiency reveal novel tissue-specific pathologies in Barth syndrome

Human Molecular Genetics(2024)10.1093/hmg/ddae152

N/A

0DataRank · unranked

8 citations

Kodi William Harris, Yvonne Wohlfarter, Kyuna Lee, Grant J. Butschek, Arianna F. Anzmann +4 more

Allele-specific dysregulation of lipid and energy metabolism in early-stage hypertrophic cardiomyopathy

Journal of Molecular and Cellular Cardiology Plus(2024)10.1016/j.jmccpl.2024.100073

N/A

0DataRank · unranked

2 citations

Anja Karlstaedt, Damla Ates Gulkok, Tilo Thottakara, Yamin Liu, Sili Fan +7 more