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

Gregory M. Cooper

HudsonAlpha Institute for Biotechnology

ORCID: 0000-0001-5509-9923
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 1%percentile
16.1Author DataRank

Indexed papers

7in 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 7 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.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874
Top 1%
12.9DataRank
Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Papers

Driven by 23 papers — median percentile 73. Top paper: “Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project”.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874
Top 1%
12.9DataRank
Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Single-cell multi-cohort dissection of the schizophrenia transcriptome

Science(2024)10.1126/science.adg5136
N/A
1.3DataRank · unranked
125 citations

Shahin Mohammadi, José Dávila-Velderrain, Sivan Subburaju, Daniel Reed Tso, Makayla Hourihan +196 more

A data-driven single-cell and spatial transcriptomic map of the human prefrontal cortex

Science(2024)10.1126/science.adh1938
Top 18%
1.2DataRank
Top 18%69 citations

Abby Spangler, Nicholas J. Eagles, Kelsey D. Montgomery, Sang Ho Kwon, Boyi Guo +90 more

Massively parallel characterization of regulatory elements in the developing human cortex

Science(2024)10.1126/science.adh0559
N/A
1.2DataRank · unranked
61 citations

Sean Whalen, Marilyn Steyert, Ryan Ziffra, Pawel F. Przytycki, Fumitaka Inoue +197 more

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

Science(2008)10.1126/science.1155174
N/A
1.1DataRank · unranked
1822 citations

Anjene M Addington, Wellcome Trust Case Control Consortium, Anjené M. Addington, Sarah B. Pierce, Alex S. Nord +39 more

Distribution and intensity of constraint in mammalian genomic sequence

Genome Research(2005)10.1101/gr.3577405
N/A
1.1DataRank · unranked
1438 citations

Eric A. Stone, George Asimenos, Eric D. Green, Serafim Batzoglou, Arend Sidow +1 more

Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain

Science(2024)10.1126/science.adh0829
Top 26%
0.765DataRank
Top 26%50 citations

Michael Margolis, Rujia Dai, Pan Zhang, Pawel F. Przytycki, Daniel Vo +95 more

Transcriptomic sex differences in postmortem brain samples from patients with psychiatric disorders

Science Translational Medicine(2024)10.1126/scitranslmed.adh9974
Top 27%
0.733DataRank
Top 27%22 citations

Cuihua Xia, Yi Jiang, Yu Chen, Jiaqi Zhou, Rujia Dai +95 more

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy

PLoS Genetics(2021)10.1371/journal.pgen.1009195
N/A
0.538DataRank · unranked
35 citations

Gopal Battu, Stephanie A. Felker, J. Nicholas Cochran, M. Newton, Laura Lambert +6 more

Combined bioinformatic and splicing analysis of likely benign intronic and synonymous variants reveals evidence for pathogenicity

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101850
Top 56%
0.292DataRank
Top 56%4 citations

Stephanie A. Felker, Surya P. Rednam, Kelly Vallance, D. Williams Parsons, Angshumoy Roy +3 more

Extensive profiling of transcription factors in postmortem brains defines genomic occupancy in disease-relevant cell types and links TF activities to neuropsychiatric disorders

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.21.545934
Top 59%
0.261DataRank
Top 59%4 citations

Ashlyn G. Anderson, Lindsay F. Rizzardi, Iván Rodríguez-Nunez, Belle Moyers, Katie Trausch‐Lowther +10 more

Aberrant regulation of a poison exon caused by a non-coding variant in Scn1a -associated epileptic encephalopathy

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.21.163428
N/A
0DataRank · unranked
0 citations

Gopal Battu, Stephanie A. Felker, J. Nicholas Cochran, M. Newton, Laura Lambert +6 more

Genome-wide strand asymmetry in massively parallel reporter activity favors genic strands

Genome Research(2021)10.1101/gr.270751.120
N/A
0DataRank · unranked
6 citations

E. Christopher Partridge, Bryan A. Moyers, Vikram Agarwal, Kimberly M. Newberry, Beth Martin +4 more

Learning Adjustment Sets from Observational and Limited Experimental Data

Proceedings of the AAAI Conference on Artificial Intelligence(2021)10.1609/aaai.v35i11.17194
N/A
0DataRank · unranked
1 citations

Gregory M. Cooper, Sofia Triantafillou

Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.06.561245
N/A
0DataRank · unranked
1 citations

Jacob M. Loupe, Stephanie A. Felker, James M.J. Lawlor, Ashlyn G. Anderson, Iván Rodríguez-Nunez +10 more

Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity

medRxiv(2023)10.1101/2023.10.30.23297632
Top 100%
0DataRank
Top 100%0 citations

Stephanie A. Felker, Surya P. Rednam, Kelly Vallance, D. Williams Parsons, Angshumoy Roy +3 more

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature

European Journal of Human Genetics(2020)10.1038/s41431-020-0571-6
N/A
0DataRank · unranked
38 citations

Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, Julien Thévenon, Ange‐Line Bruel +60 more

Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.03.010
N/A
0DataRank · unranked
73 citations

Ethan G. Geier, Luke W. Bonham, J. Scott Newberry, Michelle D. Amaral, Michelle L. Thompson +9 more

Multiomic profiling of transcription factor binding and function in human brain

Nature Neuroscience(2024)10.1038/s41593-024-01658-8
N/A
0DataRank · unranked
23 citations

Ashlyn G. Anderson, Lindsay F. Rizzardi, Iván Rodríguez-Nunez, Belle A. Moyers, Katie Trausch‐Lowther +10 more

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.011
N/A
0DataRank · unranked
112 citations

Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner +25 more

Genome-wide strand asymmetry in massively parallel reporter activity favors genic strands

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.26.269027
N/A
0DataRank · unranked
0 citations

E. Christopher Partridge, Bryan A. Moyers, Vikram Agarwal, Kimberly M. Newberry, Beth Martin +4 more

Allele-specific transcription factor binding across human brain regions offers mechanistic insight into eQTLs

Genome Research(2024)10.1101/gr.278601.123
N/A
0DataRank · unranked
6 citations

Belle A. Moyers, Jacob M. Loupe, Iván Rodríguez-Nunez, Stephanie A. Felker, James M.J. Lawlor +10 more

Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1α are Associated with C-Reactive Protein

UNC Libraries(2020)10.17615/w18n-ks35
N/A
0DataRank · unranked
0 citations

Matthew Stephens, Yongtao Guan, Gregory M. Cooper, J. Peter Durda, Joshua D. Smith +13 more