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

Diane D. Shao

Broad Institute

ORCID: 0000-0003-2087-4082

Also affiliated with Boston Children's Hospital, Howard Hughes Medical Institute, Harvard University, Boston Children's Museum

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 5%percentile
0.373Author 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.

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 8 papers — median percentile 52. Top paper: “The Somatic Mosaicism across Human Tissues Network”.

The Somatic Mosaicism across Human Tissues Network

Nature(2025)10.1038/s41586-025-09096-7
N/A
0.672DataRank · unranked
43 citations

Ji Won Oh, Yujin Angelina Choi, Nam Seop Lim, Boxun Zhao, Adam Voshall +365 more

Spatial transcriptomics reveals human cortical layer and area specification

Nature(2025)10.1038/s41586-025-09010-1
N/A
0.648DataRank · unranked
74 citations

Kyle Coleman, Shunzhou Jiang, Andrea J. Kriz, Jack H. Marciano, Chunyu Luo +22 more

A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features

Genetics in Medicine(2021)10.1038/s41436-021-01097-x
N/A
0.510DataRank · unranked
29 citations

Rachel Straussberg, Hind Ahmed, Amjad Khan, Songhai Tian, R. Sean Hill +28 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008
N/A
0.489DataRank · unranked
25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

A recurrent de novo variant in NUSAP1 escapes nonsense‐mediated decay and leads to microcephaly, epilepsy, and developmental delay

Clinical Genetics(2023)10.1111/cge.14335
N/A
0.396DataRank · unranked
13 citations

Emuna Paz‐Ebstein, Shira Yanovsky‐Dagan, Abbe Lai, Hagar Mor‐Shaked, Tal Gilboa +5 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

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595
N/A
0.104DataRank · unranked
1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Cell-type-specific patterns and consequences of somatic mutation in development and aging brain

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.30.656844
N/A
0DataRank · unranked
0 citations

Shulin Mao, Diane D. Shao, Daniel Snellings, Rebecca Andersen, Guanlan Dong +6 more