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

Mary C. Whitman

Boston Children's Hospital

ORCID: 0000-0001-6297-7499

Also affiliated with Harvard University

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 5%percentile
0.373Author DataRank

Indexed papers

3in 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 3 indexed papers 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.

Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes

npj Genomic Medicine(2024)10.1038/s41525-024-00441-9
Top 48%
0.373DataRank
Top 48%11 citations

Nancy C. Andrews, Alan H. Beggs, Philip M. Boone, Catherine A. Brownstein, Maya Chopra +32 more

Papers

Driven by 9 papers — median percentile 52. Top paper: “Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis”.

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis

Nature Genetics(2023)10.1038/s41588-023-01424-9
N/A
0.550DataRank · unranked
38 citations

Silvio Alessandro Di Gioia, Bryn D. Webb, Wai‐Man Chan, Elke de Boer, Sarah J. Garnai +53 more

TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy

Human Genetics(2021)10.1007/s00439-021-02379-9
N/A
0.510DataRank · unranked
29 citations

Brenda J. Barry, Caroline D. Robson, Flavia M. Facio, Carol Van Ryzin, Wai‐Man Chan +31 more

Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes

npj Genomic Medicine(2024)10.1038/s41525-024-00441-9
Top 48%
0.373DataRank
Top 48%11 citations

Nancy C. Andrews, Alan H. Beggs, Philip M. Boone, Catherine A. Brownstein, Maya Chopra +32 more

Chromosome 4 Duplication Associated with Strabismus Leads to Gene Expression Changes in iPSC-Derived Cortical Neurons

Genes(2025)10.3390/genes16010080
N/A
0.312DataRank · unranked
7 citations

William C. Skarnes, Ashish Jain, Sampath Kumar Vemula, Liang Sun, Shira Rockowitz +2 more

Genome-Wide Association Study and Rare Variant Association Studies of Strabismus in the All of Us Research Program

Ophthalmology Science(2025)10.1016/j.xops.2025.100873
N/A
0.208DataRank · unranked
3 citations

Corey Tesdahl, Inas F. Aboobakar, Ashish Jain, Mayra Martinez Sanchez, Kimberly Jin +3 more

Strabismus in Genetic Syndromes: A Review

Clinical & Experimental Ophthalmology(2025)10.1111/ceo.14507
N/A
0.208DataRank · unranked
3 citations

Jillian Bove, Bethany Nahri So, Mary C. Whitman, Seyda Kilic

Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.12.612713
N/A
0.165DataRank · unranked
2 citations

Paola M. Matos Ruiz, Jessica King, Emma E. Foster, Lindsay Berube, Wai‐Man Chan +23 more

Genome-Wide and Rare Variant Association Studies of Amblyopia in the All of Us Research Program

Ophthalmology(2025)10.1016/j.ophtha.2025.01.013
N/A
0DataRank · unranked
3 citations

Inas F. Aboobakar, Ashish Jain, Corey Tesdahl, Kimberly Jin, Isdin Oke +2 more

Systematic phenotype and genotype characterization of Moebius syndrome

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103437
N/A
0DataRank · unranked
1 citations

Julie A. Jurgens, Narisu Narisu, Zhongyang Zhang, Brenda J. Barry, Carol Van Ryzin +37 more