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

Bernie Devlin

University of Pittsburgh

ORCID: 0000-0003-2524-4290
Biochemistry, Genetics and Molecular BiologyNeuroscience

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
6.9Author DataRank

Indexed papers

8in 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 8 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.

Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions

Scientific Data(2020)10.1038/s41597-020-00642-8
Top 3%
6.5DataRank
Top 3%331 citations

Thanneer M. Perumal, Minerva M. Carrasquillo, Mariet Allen, Joseph S. Reddy, Gabriel E. Hoffman +95 more

Papers

Driven by 36 papers — median percentile 26. Top paper: “Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions”.

Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions

Scientific Data(2020)10.1038/s41597-020-00642-8
Top 3%
6.5DataRank
Top 3%331 citations

Thanneer M. Perumal, Minerva M. Carrasquillo, Mariet Allen, Joseph S. Reddy, Gabriel E. Hoffman +95 more

Functional annotation of rare structural variation in the human brain

Nature Communications(2020)10.1038/s41467-020-16736-1
N/A
1.7DataRank · unranked
54 citations

Xuefang Zhao, Mary Lauren Benton, Thanneer M. Perumal, Ryan L. Collins, Gabriel E. Hoffman +65 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
1.4DataRank · unranked
57 citations

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

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

Population-level variation in enhancer expression identifies disease mechanisms in the human brain

Nature Genetics(2022)10.1038/s41588-022-01170-4
N/A
1.1DataRank · unranked
53 citations

Gabriel E. Hoffman, Pasha Apontes, Jaroslav Bendl, Samir Rahman, Michael B. Fernando +48 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

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

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Nature Genetics(2017)10.1038/ng.3863
N/A
0.950DataRank · unranked
562 citations

Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki +18 more

Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia

Biological Psychiatry(2021)10.1016/j.biopsych.2021.03.020
N/A
0.722DataRank · unranked
122 citations

Yixuan Ma, Kelsey S. Montgomery, Jaroslav Bendl, Manoj K. Jaiswal, Alexey Kozlenkov +8 more

De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.012
N/A
0.722DataRank · unranked
122 citations

Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier +10 more

Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum

Biological Psychiatry(2021)10.1016/j.biopsych.2020.12.028
N/A
0.700DataRank · unranked
105 citations

Hanrui Wu, Phil H. Lee, Fotis Tsetsos, Lea K. Davis, Dongmei Yu +20 more

Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease

Molecular Psychiatry(2021)10.1038/s41380-021-01152-8
N/A
0.637DataRank · unranked
69 citations

Lambertus Klei, Byron Creese, Janet Harwood, Elise A. Weamer, Lora McClain +39 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

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

Translational Psychiatry(2021)10.1038/s41398-021-01290-1
N/A
0.524DataRank · unranked
32 citations

Lora McClain, Lambertus Klei, Jiebiao Wang, Brittany L. Chamberlain, Sara A. Springer +4 more

Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development

Cell Reports(2022)10.1016/j.celrep.2022.111585
N/A
0.520DataRank · unranked
31 citations

Xuanjia Fan, Laura Sloofman, Lindsay Liang, Enrico Mossotto, Kendall Moore +11 more

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

Translational Psychiatry(2022)10.1038/s41398-022-02071-0
N/A
0.510DataRank · unranked
29 citations

Lora McClain, Christopher Hensler, Yue Wei, Lambertus Klei, David A. Lewis +5 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

Genetic associations with psychosis and affective disturbance in Alzheimer's disease

Alzheimer s & Dementia Translational Research & Clinical Interventions(2024)10.1002/trc2.12472
Top 48%
0.371DataRank
Top 48%6 citations

Byron Creese, Lambertus Klei, Mary Ann A. DeMichele‐Sweet, Elise A. Weamer, Pablo García-González +27 more

Comparison of gene expression in living and postmortem human brain

medRxiv(2023)10.1101/2023.11.08.23298172
N/A
0.345DataRank · unranked
9 citations

Lambertus Klei, Chunyu Liu, Joel E. Kleinman, Thomas M. Hyde, Daniel H. Geschwind +4 more

The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

medRxiv10.1101/2021.01.26.21250409
N/A
0.233DataRank · unranked
3 citations

Lambertus Klei, Manuel Mattheisen, Matthew W. Halvorsen, Abraham Reichenberg, Kathryn Roeder +15 more

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

medRxiv(2025)10.1101/2024.12.27.24319460
N/A
0.208DataRank · unranked
3 citations

Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura G Sloofman +49 more

Selection of eating-disorder phenotypes for linkage analysis

UNC Libraries(2020)10.17615/w8hx-6t53
N/A
0DataRank · unranked
0 citations

Silviu‐Alin Bacanu, Wade H. Berrettini, Bernie Devlin, Pamela K. Keel, Andrew W. Bergen +13 more

CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder

UNC Libraries(2024)10.17615/jxgd-8293
Top 100%
0DataRank
Top 100%0 citations

Shah H.R, Montgomery K.S, Stefano Marenco, Sieberts S.K, Patrick F. Sullivan +25 more

Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia

UNC Libraries(2024)10.17615/w913-sr13
N/A
0DataRank · unranked
0 citations

Jianwei Wang, A Charney, Vahram Haroutunian, Nancy Francoeur, Gil S.E +60 more

Transcriptomes of higher order thalamic nuclei in obsessive compulsive disorder

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.22.650032
N/A
0DataRank · unranked
0 citations

Rishi Deshmukh, Lambertus Klei, Bernie Devlin, Jill R. Glausier, David A. Lewis +2 more

PACS1 syndrome variant alters proteomic landscape of developing cortical organoids

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.23.650290
N/A
0DataRank · unranked
0 citations

Lauren Rylaarsdam, Ashley Woo, Annika Schroder, Jennifer Rakotomamonjy, Clare L Bossert +8 more

Age dependent association of inbreeding with risk for schizophrenia in Egypt

Schizophrenia Research(2020)10.1016/j.schres.2019.10.039
N/A
0DataRank · unranked
5 citations

Hader Mansour, Ibtihal Ibrahim, Lambertus Klei, Warda Fathi, Joel Wood +19 more

Evaluating and improving health equity and fairness of polygenic scores

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100280
N/A
0DataRank · unranked
3 citations

Geyu Zhou, Lambertus Klei, Peng Liu, Alexandra Chouldechova, Hongyu Zhao +4 more

Gene expression elucidates functional impact of polygenic risk for schizophrenia

UNC Libraries(2020)10.17615/k6wj-s665
N/A
0DataRank · unranked
0 citations

Edwin C. Oh, Eli A. Stahl, David A. Bennett, Nicholas Katsanis, Tymor Hamamsy +53 more

The genetics of anorexia nervosa collaborative study: Methods and sample description

UNC Libraries(2020)10.17615/ns80-mj75
Top 100%
0DataRank
Top 100%0 citations

Michael Strober, Manfred M. Fichter, Katherine A. Halmi, Harry Brandt, Ian Jones +12 more

Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data

Genome Research(2021)10.1101/gr.268722.120
N/A
0DataRank · unranked
115 citations

Kathryn Roeder, Bernie Devlin, Jiebiao Wang

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.23.216697
N/A
0DataRank · unranked
3 citations

Lora McClain, Lambertus Klei, Jiebiao Wang, Brittany L. Chamberlain, Sara A. Springer +4 more

De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.06.329011
N/A
0DataRank · unranked
5 citations

Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier +9 more

Sex differences in the human brain transcriptome of cases with schizophrenia

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.05.326405
N/A
0DataRank · unranked
11 citations

Yixuan Ma, Kelsey S. Montgomery, Jaroslav Bendl, Manoj K. Jaiswal, Alexey Kozlenkov +8 more