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

Taehwan Shin

Boston Children's Hospital

ORCID: 0000-0003-3604-8594

Also affiliated with Harvard University

Biochemistry, Genetics and Molecular BiologyNeuroscienceAgricultural and Biological Sciences

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
1.1Author 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.

Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder

Mobile DNA(2021)10.1186/s13100-021-00256-w
Top 19%
1.1DataRank
Top 19%34 citations

Chong Chu, Caroline Dias, Jaejoon Choi, Soohyun Lee, Yue Gao +5 more

Papers

Driven by 7 papers — median percentile 81. Top paper: “Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder”.

Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder

Mobile DNA(2021)10.1186/s13100-021-00256-w
Top 19%
1.1DataRank
Top 19%34 citations

Chong Chu, Caroline Dias, Jaejoon Choi, Soohyun Lee, Yue Gao +5 more

Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions

Neuron(2021)10.1016/j.neuron.2021.08.005
N/A
0.803DataRank · unranked
210 citations

Andrew B. Stergachis, Ellen M. DeGennaro, Ryan N. Doan, Xuyu Qian, Matthew B. Johnson +20 more

Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk

medRxiv(2023)10.1101/2023.09.19.23295780
N/A
0DataRank · unranked
5 citations

Janet Song, Michael Kosicki, Connor Kenny, Samantha G. Beck, Lily Kelley +13 more

Somatic mosaicism in amyotrophic lateral sclerosis and frontotemporal dementia identifies focal mutations associated with widespread degeneration

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.30.569436
N/A
0DataRank · unranked
3 citations

Jun‐Ho Kim, August Yue Huang, Matthew Nolan, Junseok Park, Ryan N. Doan +19 more

Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder risk

Cell Genomics(2024)10.1016/j.xgen.2024.100609
N/A
0DataRank · unranked
32 citations

Janet Song, Michael Kosicki, Connor Kenny, Samantha G. Beck, Lily Kelley +13 more

Whole-genome analysis of de novo and polymorphic retrotransposon insertions in Autism Spectrum Disorder

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.29.428895
N/A
0DataRank · unranked
4 citations

Chong Chu, Caroline Dias, Jaejoon Choi, Soohyun Lee, Gao Yue +5 more

Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human Brain

Cancer Discovery(2021)10.1158/2159-8290.cd-21-0245
N/A
0DataRank · unranked
48 citations

Eduardo A. Maury, Basheer Becerra, Sara Bizzotto, Ryan N. Doan, Connor Kenny +7 more