🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Penelope E. Bonnen

Baylor College of Medicine

ORCID: 0000-0001-5581-5301

Also affiliated with Baylor Genetics

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

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Systematic Review of Parkinsonism in Cerebrotendinous Xanthomatosis

Neurology International(2025)10.3390/neurolint17080117
Top 100%
0DataRank
Top 100%0 citations

Penelope E. Bonnen, Jennifer Hanson

Papers

Driven by 8 papers — median percentile 0. Top paper: “Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia”.

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015
N/A
0.604DataRank · unranked
55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Bi-allelic KICS2 mutations impair KICSTOR complex-mediated mTORC1 regulation, causing intellectual disability and epilepsy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.019
N/A
0.269DataRank · unranked
5 citations

Martin D. Burkhalter, Chrisovalantou Huridou, Linda Sofan, Timo Roser, Kirsten Cremer +29 more

POLRMT mutations impair mitochondrial transcription causing neurological disease

Nature Communications(2021)10.1038/s41467-021-21279-0
N/A
0DataRank · unranked
60 citations

Bradley Peter, Zsolt Szilágyi, Héctor Díaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville +34 more

RRM1 variants cause a mitochondrial DNA maintenance disorder via impaired de novo nucleotide synthesis

Journal of Clinical Investigation(2022)10.1172/jci145660
N/A
0DataRank · unranked
15 citations

Wolfgang M. Pernice, Wafaa Eyaid, B. Jeevan, Zuben P. Brown, Martí Juanola‐Falgarona +19 more

Leveraging Clinical, Functional, Molecular and Population Genetic Data Reveals Genotype Phenotype Association and Health Disparity in a Monogenic Disorder, CTX

medRxiv(2024)10.1101/2024.04.15.24305853
N/A
0DataRank · unranked
1 citations

Penelope E. Bonnen, Jennifer Hanson

Cerebrotendinous Xanthomatosis occurs at high frequency in Ashkenazi Jews

Molecular Genetics and Metabolism(2025)10.1016/j.ymgme.2025.109041
N/A
0DataRank · unranked
5 citations

Penelope E. Bonnen, Jennifer Hanson

Systematic Review of Parkinsonism in Cerebrotendinous Xanthomatosis

Neurology International(2025)10.3390/neurolint17080117
Top 100%
0DataRank
Top 100%0 citations

Penelope E. Bonnen, Jennifer Hanson

LONP1 de novo dominant mutation causes mitochondrial encephalopathy with loss of LONP1 chaperone activity and excessive LONP1 proteolytic activity

Mitochondrion(2020)10.1016/j.mito.2020.01.004
N/A
0DataRank · unranked
28 citations

Daniel Brezavar, Jennifer Hanson, Austin Larson, Penelope E. Bonnen, Arnaud Besse