Jonathan Sebat

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

32.7Author DataRank

Indexed papers

9in 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 9 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 36 papers — median percentile 94. Top paper: “A global reference for human genetic variation”.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

An integrated map of structural variation in 2,504 human genomes

Nature(2015)10.1038/nature15394

Top 2%

9.1DataRank

Top 2%2686 citations

Tobias Rausch, Marianne K. DeGorter, Robert E. Handsaker, Alexej Abyzov, Joanna M. M. Howson +75 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

Frequency and Complexity of De Novo Structural Mutation in Autism

The American Journal of Human Genetics(2016)10.1016/j.ajhg.2016.02.018

Top 6%

3.6DataRank

Top 6%112 citations

Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R. Chapman +34 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

Control-independent mosaic single nucleotide variant detection with DeepMosaic

Nature Biotechnology(2023)10.1038/s41587-022-01559-w

N/A

1.1DataRank · unranked

40 citations

Xin Xu, Martin W. Breuss, Danny Antaki, Laurel Ball, Changuk Chung +95 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725

N/A

1.1DataRank · unranked

1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 more

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

Cell(2012)10.1016/j.cell.2012.02.039

N/A

1.0DataRank · unranked

884 citations

Jonathan Sebat, Dheeraj Malhotra

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

Nature Communications(2020)10.1038/s41467-020-19669-x

N/A

1.0DataRank · unranked

830 citations

Jorge Urresti, Jose Lugo-Martinez, Kymberleigh A. Pagel, Guan Ning Lin, Hyun‐Jun Nam +7 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

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

Trends in Genetics(2009)10.1016/j.tig.2009.10.004

N/A

0.836DataRank · unranked

263 citations

Deborah L. Levy, Wellcome Trust Case Control Consortium, Shane McCarthy, Jonathan Sebat

A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats

Cell Genomics(2024)10.1016/j.xgen.2024.100527

Top 29%

0.687DataRank

Top 29%30 citations

Yanchao Pan, Pasi Rastas, Daniel Munro, Monika Tutaj, Huda Akil +46 more

The Psychiatric Genomics Consortium: discoveries and directions

The Lancet Psychiatry(2025)10.1016/s2215-0366(25)00124-5

N/A

0.505DataRank · unranked

28 citations

Cynthia M. Bulik, Dawit Abebe, Ole A. Andreassen, Elizabeth G. Atkinson, Karmel W. Choi +34 more

Effects of genetically predicted posttraumatic stress disorder on autoimmune phenotypes

Translational Psychiatry(2024)10.1038/s41398-024-02869-0

N/A

0.406DataRank · unranked

14 citations

Andrew Ratanatharathorn, Sian Hemmings, Karen H. Costenbader, Vasiliki Michopoulos, Renato Polimanti +16 more

A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.13.536694

Top 51%

0.344DataRank

Top 51%8 citations

Yanchao Pan, Pasi Rastas, Daniel Munro, Monika Tutaj, Huda Akil +46 more

Rare copy number variation in posttraumatic stress disorder

Molecular Psychiatry(2022)10.1038/s41380-022-01776-4

N/A

0.292DataRank · unranked

6 citations

Worrawat Engchuan, Guillaume Huguet, Marieke Klein, Jeffrey R. MacDonald, Omar Shanta +87 more

DeepMosaic: Control-independent mosaic single nucleotide variant detection using deep convolutional neural networks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.14.382473

N/A

0.241DataRank · unranked

4 citations

Xin Xu, Martin W. Breuss, Danny Antaki, Laurel Ball, Changuk Chung +10 more

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

medRxiv(2022)10.1101/2022.05.05.22274031

Top 65%

0.208DataRank

Top 65%3 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Determinants of functional burden pleiotropy and gene dosage responses across human traits

medRxiv(2025)10.1101/2025.02.25.25322833

N/A

0.208DataRank · unranked

3 citations

Kuldeep Kumar, Guillaume Huguet, Florian Benitiere, Josephine Mollon, Thomas Renne +12 more

CHARACTERIZATION OF THE COMBINED EFFECTS OF RARE VARIANTS AND POLYGENIC RISK BY WHOLE GENOME ANALYSIS OF PSYCHIATRIC DISORDERS AND QUANTITATIVE TRAITS

European Neuropsychopharmacology(2022)10.1016/j.euroneuro.2022.07.563

N/A

0.104DataRank · unranked

1 citations

Jonathan Sebat

Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p

medRxiv(2022)10.1101/2022.03.23.22272826

N/A

0DataRank · unranked

2 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +15 more

Customized de novo mutation detection for any variant calling pipeline: SynthDNM

Bioinformatics(2021)10.1093/bioinformatics/btab225

N/A

0DataRank · unranked

4 citations

James P. Guevara, Kun Xia, Jonathan Sebat, Aojie Lian

Developmental and temporal characteristics of clonal sperm mosaicism

Cell(2021)10.1016/j.cell.2021.07.024

N/A

0DataRank · unranked

57 citations

Martin W. Breuss, Xin Xu, Danny Antaki, Kiely N. James, Valentina Stanley +13 more

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

UNC Libraries(2020)10.17615/8m0s-na92

N/A

0DataRank · unranked

0 citations

John A. McGrath, Pamela Sklar, Gerald Nestadt, David J. Cutler, Paula Wolyniec +25 more

Temporal stability of human sperm mosaic mutations results in life-long threat of transmission to offspring

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.14.339796

N/A

0DataRank · unranked

3 citations

Martin W. Breuss, Xin Xu, Danny Antaki, Kiely N. James, Valentina Stanley +13 more

Genomic architecture of autism from comprehensive whole-genome sequence annotation

Cell(2022)10.1016/j.cell.2022.10.009

N/A

0DataRank · unranked

280 citations

Bhooma Thiruvahindrapuram, Ada J. S. Chan, Worrawat Engchuan, Edward J. Higginbotham, Jennifer Howe +95 more

Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.16.589618

N/A

0DataRank · unranked

3 citations

Thomas Renne, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, Sayeh Kazem +25 more

Common DNA sequence variation influences 3-dimensional conformation of the human genome

UNC Libraries(2024)10.17615/kmnm-q097

N/A

0DataRank · unranked

0 citations

Tristin Liu, Bing Ren, Joshua Chiou, Yun Li, Ming Hu +8 more

Cell type- and factor-specific nonsense-mediated RNA decay

Nucleic Acids Research(2025)10.1093/nar/gkaf395

N/A

0DataRank · unranked

21 citations

Jonathan Sebat, Miles Wilkinson, Kun Tan

Determinants of pleiotropy and monotonic gene dosage responses across human traits

Research Square(2025)10.21203/rs.3.rs-7547111/v1

N/A

0DataRank · unranked

0 citations

Kuldeep Kumar, Guillaume Huguet, Josephine Mollon, Thomas Renne, Laura M. Schultz +13 more

Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex

Research Square(2025)10.21203/rs.3.rs-8099338/v1

N/A

0DataRank · unranked

0 citations

Sayeh Kazem, Guillaume Huguet, Worrawat Engchuan, Jakub Kopál, Thomas Renne +22 more

COLLABORATIVE STUDY OF THE COMBINED EFFECTS OF RARE CNVS AND POLYGENIC RISK ON PSYCHIATRIC TRAITS

European Neuropsychopharmacology(2024)10.1016/j.euroneuro.2024.08.072

N/A

0DataRank · unranked

0 citations

Marieke Klein, Omar Shanta, Mohammad Ahangari, Oanh Hong, Jeff MacDonald +8 more

Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes

Cell Genomics(2024)10.1016/j.xgen.2024.100721

N/A

0DataRank · unranked

6 citations

Thomas Renné, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, Sayeh Kazem +25 more

SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrains

Cell Genomics(2022)10.1016/j.xgen.2022.100102

N/A

0DataRank · unranked

24 citations

Yangsu Ren, Shubham Saini, Danny Antaki, Celine L. St. Pierre, April E. Williams +6 more

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

medRxiv(2021)10.1101/2021.03.30.21254657

N/A

0DataRank · unranked

25 citations

Adam X. Maihofer, Marieke Klein, James P. Guevara, Jakob Grove, Caitlin E. Carey +13 more

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

medRxiv(2022)10.1101/2021.12.24.21268385

N/A

0DataRank · unranked

4 citations

Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Prashanth Rajarajan, Erin Flaherty +14 more

Jonathan Sebat

Indexed papers

Top data-sharing exemplar

Papers