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

Elizabeth C. Engle

Boston Children's Hospital

ORCID: 0000-0001-8194-7738

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 3%percentile

1.5Author 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 →

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

Genotypic and Phenotypic Spectrum of Foveal Hypoplasia

Ophthalmology(2022)10.1016/j.ophtha.2022.02.010

Top 14%

1.5DataRank

Top 14%74 citations

Gail Maconachie, Jinu Han, Line Kessel, Maria M. van Genderen, Rebecca J. McLean +34 more

Papers

Driven by 12 papers — median percentile 86. Top paper: “Genotypic and Phenotypic Spectrum of Foveal Hypoplasia”.

Genotypic and Phenotypic Spectrum of Foveal Hypoplasia

Ophthalmology(2022)10.1016/j.ophtha.2022.02.010

Top 14%

1.5DataRank

Top 14%74 citations

Gail Maconachie, Jinu Han, Line Kessel, Maria M. van Genderen, Rebecca J. McLean +34 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

Inability to move one's face dampens facial expression perception

Cortex(2023)10.1016/j.cortex.2023.08.014

N/A

0.467DataRank · unranked

12 citations

Jessica Jordan, Judith Licht, Savannah Lokey, Gang Chen, Joseph Snow +7 more

Nuclear IMPDH Filaments in Human Gliomas

Journal of Neuropathology & Experimental Neurology(2021)10.1093/jnen/nlab090

N/A

0.406DataRank · unranked

14 citations

David G. Muñoz, Josée Coulombe, Douglas A. Gray, Elizabeth C. Engle, Long Cheng +2 more

A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders

Nature Communications(2024)10.1038/s41467-024-52463-7

N/A

0.389DataRank · unranked

9 citations

Lauren J. Ayers, Michael Kosicki, Wai‐Man Chan, Lydia Fozo, Brandon M. Pratt +22 more

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

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

medRxiv(2025)10.1101/2025.05.06.25326635

N/A

0.165DataRank · unranked

2 citations

Eirny Tholl Thorolfsdottir, Ilana M. Nodelman, Sara Tholl Halldorsdottir, Stefania Benónísdóttir, Malak Alghamdi +64 more

Inability to make facial expressions dampens emotion perception

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.11.510399

N/A

0DataRank · unranked

3 citations

Jessica Jordan, Judith Licht, Savannah Lokey, Gang Chen, Joseph Snow +7 more

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

0DataRank · unranked

37 citations

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

Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness

International Journal of Environmental Research and Public Health(2024)10.3390/ijerph21050615

N/A

0DataRank · unranked

2 citations

Konstantinia Almpani, Rashmi Mishra, Carol W. Bassim, Carol Van Ryzin, Bryn D. Webb +6 more

A framework for the evaluation of patients with congenital facial weakness

Orphanet Journal of Rare Diseases(2021)10.1186/s13023-021-01736-1

N/A

0DataRank · unranked

13 citations

Irini Manoli, Elizabeth C. Engle, Ethylin Wang Jabs, Bryn D. Webb