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

Chelsea Barrows

Children’s Institute

ORCID: 0009-0007-8106-9446

Also affiliated with University of California San Diego

Biochemistry, Genetics and Molecular BiologyMedicine

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 4%percentile
0.763Author DataRank

Indexed papers

2in 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 2 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.

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401
Top 37%
0.522DataRank
Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

Papers

Driven by 11 papers — median percentile 51. Top paper: “Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain”.

Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain

Nature(2024)10.1038/s41586-024-07292-5
N/A
1.3DataRank · unranked
55 citations

Xiaoxu Yang, Robert F. Hevner, Katie Kennedy, Keng Ioi Vong, Yang Liu +12 more

Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

Nature Genetics(2023)10.1038/s41588-022-01276-9
N/A
0.709DataRank · unranked
112 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +76 more

TMEM161B modulates radial glial scaffolding in neocortical development

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2209983120
N/A
0.632DataRank · unranked
16 citations

Caleb Heffner, Keng Ioi Vong, Chelsea Barrows, Yoo-Jin Ha, Sangmoon Lee +15 more

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401
Top 37%
0.522DataRank
Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624
N/A
0.464DataRank · unranked
21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

The contribution of de novo coding mutations to meningomyelocele

Nature(2025)10.1038/s41586-025-08676-x
N/A
0.396DataRank · unranked
13 citations

Ashna Nisal, Isaac Tang, Chanjae Lee, Ishani Jhamb, Cassidy Wallace +74 more

A phenotypic brain organoid atlas and biobank for neurodevelopmental disorders

Cell stem cell(2025)10.1016/j.stem.2025.10.006
Top 61%
0.241DataRank
Top 61%4 citations

Y. Nakamura, Junhao Li, David Sievert, Yang Liu, Toan D. Nguyen +16 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

medRxiv(2024)10.1101/2024.12.22.24319370
N/A
0.104DataRank · unranked
1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +30 more

Cell-type-resolved somatic mosaicism reveals clonal dynamics of the human forebrain

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.24.563814
N/A
0DataRank · unranked
4 citations

Xiaoxu Yang, Robert F. Hevner, Katie Kennedy, Keng Ioi Vong, Yang Liu +10 more

Novel association of Dandy–Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63363
N/A
0DataRank · unranked
11 citations

Lucia Guidugli, Monia Hammer, Chelsea Barrows, Anne Gregor, Sangmoon Lee +9 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100441
N/A
0DataRank · unranked
1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +31 more