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

Shan Dong

University of California, San Francisco

ORCID: 0000-0001-9130-0225
NeuroscienceBiochemistry, 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 100%percentile
0Author 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.

Molecular dynamics of Brodmann Area 22 in development and autism

10.64898/2026.03.31.715694
Top 70%
0.165DataRank
Top 70%2 citations

Emilie M. Wigdor, Yuhan Hao, Rachel Leonard, Joseph Asfouri, Michael Griffiths +14 more

Papers

Driven by 10 papers — median percentile 30. Top paper: “Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism”.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Cell(2020)10.1016/j.cell.2019.12.036
N/A
9.5DataRank · unranked
2470 citations

Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An +95 more

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature Genetics(2022)10.1038/s41588-022-01104-0
N/A
0.969DataRank · unranked
638 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +112 more

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

10.1101/2021.12.20.21267194
N/A
0.538DataRank · unranked
35 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +60 more

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.12.248526
N/A
0.385DataRank · unranked
12 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Nr2f1 enhancers have distinct functions in controlling Nr2f1 expression during cortical development

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2402368121
N/A
0.165DataRank · unranked
2 citations

Athéna R. Ypsilanti, Eirene Markenscoff-Papadimitriou, Diane E. Dickel, Stephan Sanders, Shan Dong +4 more

Molecular dynamics of Brodmann Area 22 in development and autism

10.64898/2026.03.31.715694
Top 70%
0.165DataRank
Top 70%2 citations

Emilie M. Wigdor, Yuhan Hao, Rachel Leonard, Joseph Asfouri, Michael Griffiths +14 more

Generation of Mature DENVs via Genetic Modification and Directed Evolution

UNC Libraries(2024)10.17615/xnyg-1b54
N/A
0DataRank · unranked
0 citations

De Silva, Shan Dong, Baric R.S, Adams L.E, Mallory M.L +4 more

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.07.010
N/A
0DataRank · unranked
54 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438
N/A
0DataRank · unranked
10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants

The American Journal of Surgery(2021)10.1016/j.amjsurg.2021.07.016
N/A
0DataRank · unranked
10 citations

Shan Dong, Billie R. Lianoglou, Alessandra F. Aguilar Lucero, Grace Schwartz, Mary E. Norton +3 more