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

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James S. Sutcliffe

James S. Sutcliffe

Vanderbilt University

ORCID: 0000-0001-5200-6007

NeuroscienceBiochemistry, 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 6%percentile

0.252Author 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.

A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2022)10.1002/ajmg.b.32911

Top 60%

0.252DataRank

Top 60%4 citations

Julia Sealock, Péter Straub, Sandra Sanchez-Roige, James S. Sutcliffe, Lea K. Davis +1 more

Papers

Driven by 12 papers — median percentile 40. Top paper: “Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p”.

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Functional impact of global rare copy number variation in autism spectrum disorders

Nature(2010)10.1038/nature09146

N/A

1.1DataRank · unranked

2044 citations

Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan +204 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474

N/A

0.990DataRank · unranked

733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2022)10.1002/ajmg.b.32911

Top 60%

0.252DataRank

Top 60%4 citations

Julia Sealock, Péter Straub, Sandra Sanchez-Roige, James S. Sutcliffe, Lea K. Davis +1 more

Development and validation of electronic health record-based ascertainment of obsessive-compulsive disorder cases and controls

medRxiv(2025)10.1101/2025.08.05.25332874

N/A

0.104DataRank · unranked

1 citations

Tyne W. Miller‐Fleming, Dongmei Yu, Donald Hucks, Emily Gantz, Rebecca L. Johnston +18 more

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

UNC Libraries(2020)10.17615/dvnt-qn64

N/A

0DataRank · unranked

0 citations

Dexter Hadley, Mingyao Li, Ingrid Lindquist, Brett S. Abrahams, Edward I. Herman +27 more

Characterizing sleep disorders in an autism-specific collection of electronic health records

Sleep Medicine(2022)10.1016/j.sleep.2022.03.009

N/A

0DataRank · unranked

17 citations

Maria Niarchou, Angela Maxwell-Horn, Donald Hucks, Rebecca L. Johnston, James S. Sutcliffe +3 more

Analyses of GWAS and sub-threshold loci lead to the discovery of dendrite development and morphology dysfunction underlying schizophrenia genetic risk

Research Square(2021)10.21203/rs.3.rs-240477/v1

N/A

0DataRank · unranked

0 citations

Quan Wang, Chongchong Xu, Qiang Wei, Hai Yang, James S. Sutcliffe +9 more

Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data

Journal of Neurodevelopmental Disorders(2022)10.1186/s11689-022-09448-8

N/A

0DataRank · unranked

1 citations

Diego R. Mazzotti, Robert T. Schultz, Ted Abel, Jacob J. Michaelson, Edward S. Brodkin +7 more

Analyses of GWAS and Sub‐Threshold Loci Lead to the Discovery of Dendrite Development and Morphology Dysfunction Underlying Schizophrenia Genetic Risk

Advanced Science(2025)10.1002/advs.202508519

N/A

0DataRank · unranked

0 citations

Benjamin Siciliano, Quan Wang, Chongchong Xu, Qiang Wei, Hai Yang +11 more