Jonathan Sebat

68.7k citations
62 papers · 7.7k · 5 hit papers · h-index 32

Impact in

  • Genetics top 0.1%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Autism Spectrum Disorder Research

Papers in

    • Genomic variations and chromosomal abnormalities 29
    • Genomics and Rare Diseases 18
    • Genetics and Neurodevelopmental Disorders 15
    • Genetic Associations and Epidemiology 6
    • Congenital heart defects research 12
    • Genomics and Phylogenetic Studies 10

Jonathan Sebat

61 papers receiving 7.5k citations

Jonathan Sebat's Hit Papers

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2 2020 · 426 citations
4260+7+14Years since publication50010001.5k

Peers

Jonathan Sebat
Comparison fields: 5 of 144
  • Genetics 4.7k
  • Cognitive Neuroscience 1.4k
  • Molecular Biology 4.3k
  • Developmental Neuroscience 260
  • Cancer Research 681
Replace Gudrun Rappold with:
Gudrun Rappold Germany
T. Conrad Gilliam United States
Janine M. LaSalle United States
Santhosh Girirajan United States
Jonathan Pevsner United States
R. Frank Kooy Belgium
Xinsheng Nan United Kingdom
Rob Willemsen Netherlands
Yong‐hui Jiang United States
Maja Bućan United States
Jonathan Sebat relative to Gudrun Rappold Germany Gudrun Rappold's profile →
Citations per field
00.5×1.5×2.1×
Gudrun Rappold · 1×
Citations per year

Countries citing papers authored by Jonathan Sebat

Since Specialization
Citations

This map shows the geographic impact of Jonathan Sebat's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jonathan Sebat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan Sebat more than expected).

Fields of papers citing papers by Jonathan Sebat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jonathan Sebat. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jonathan Sebat. The network helps show where Jonathan Sebat may publish in the future.

Co-authors

The 25 scholars most cited alongside Jonathan Sebat, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jonathan Sebat Line = papers co-authored together Jonathan Sebat links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 62 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Large-Scale Copy Number Polymorphism in the Human Genome
Hit paper breakdown →
20041763
2
Modelling schizophrenia using human induced pluripotent stem cells
Hit paper breakdown →
2011985
3
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
Hit paper breakdown →
2008603
4
CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
Hit paper breakdown →
2012551
5
Inferring the molecular and phenotypic impact of amino acid variants with MutPred2
Hit paper breakdown →
2020426
6 2009424
7 2003309
8 2007223
9 2009180
10 2012161
11 2019160
12 2007146
13 2017123
14 2022110
15 2015103
16 200997
17 201189
18 201887
19 200781
20 200381

About Jonathan Sebat

Jonathan Sebat is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Pediatrics, Perinatology and Child Health, having authored 62 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (29 papers), Genomics and Rare Diseases (18 papers), Genetics and Neurodevelopmental Disorders (15 papers), Congenital heart defects research (12 papers), Genomics and Phylogenetic Studies (10 papers), Autism Spectrum Disorder Research (10 papers), Chromosomal and Genetic Variations (7 papers) and Genetic Associations and Epidemiology (6 papers). The work is most often cited by research in Genetics (4.7k citations), Cognitive Neuroscience (1.4k citations), Molecular Biology (4.3k citations), Developmental Neuroscience (260 citations) and Cancer Research (681 citations). Jonathan Sebat has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Dheeraj Malhotra, Kenny Ye, Michael Wigler, Shane McCarthy, Lilia M. Iakoucheva, Jennifer Troge, John Healy, Robert Lucito, Andrew H. Reiner and Joan Alexander. Their work appears in journals such as Bioinformatics, The American Journal of Human Genetics, European Neuropsychopharmacology, Cell and Molecular Psychiatry.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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