World's Best Scientists 2026 revealed!
Emmanuel Barillot

Emmanuel Barillot

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Computer Science
France
2025
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Genetics
France
2024

D-Index & Metrics

Genetics

D-Index
75
Citations
24639
World Ranking
1890
National Ranking
82

Computer Science

D-Index
58
Citations
18002
World Ranking
3561
National Ranking
59

Emmanuel Barillot publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Emmanuel Barillot sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 261 publications — 69th percentile

69% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Emmanuel Barillot D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Emmanuel Barillot sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 75 D-Index — 57th percentile

57% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

Research.com Recognitions

  • 2025 - Research.com Computer Science in France Leader Award
  • 2024 - Research.com Genetics in France Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in France Leader Award
  • 2022 - Research.com Computer Science in France Leader Award

Overview

Emmanuel Barillot is affiliated with the Institute Curie in France. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a focused subfield presence in Molecular Biology, Computational Theory and Mathematics, Modeling and Simulation, Oncology, and Pulmonary and Respiratory Medicine.

Their work covers a variety of main topics, such as Bioinformatics and Genomic Networks, Gene Regulatory Network Analysis, Computational Drug Discovery Methods, Mathematical Biology Tumor Growth, Single-cell and Spatial Transcriptomics, Microbial Metabolic Engineering and Bioproduction, and Cell Image Analysis Techniques.

Frequent publication venues for Emmanuel Barillot include bioRxiv (Cold Spring Harbor Laboratory), Cancers, Bioinformatics, Nature Communications, and PLoS Computational Biology.

Several recent papers reflect the scope of their research:

  • COVID-19 Disease Map, building a computational repository of SARS-CoV-2 virus-host interaction mechanisms (2020, Scientific Data)
  • Transcriptional Programs Define Intratumoral Heterogeneity of Ewing Sarcoma at Single-Cell Resolution (2020, Cell Reports)
  • Interpreting pathways to discover cancer driver genes with Moonlight (2020, Nature Communications)
  • A high-risk retinoblastoma subtype with stemness features, dedifferentiated cone states and neuronal/ganglion cell gene expression (2021, Nature Communications)
  • Patient-specific Boolean models of signalling networks guide personalised treatments (2022, eLife)

Emmanuel Barillot often collaborates with colleagues such as Laurence Calzone, Andreï Zinovyev, Vincent Noël, Inna Kuperstein, and Alfonso Valencia. These frequent co-authors have contributed to various publications alongside Barillot, reflecting a collaborative research approach.

Best Publications

  • Spatial partitioning of the regulatory landscape of the X-inactivation centre

    Elphège P. Nora;Bryan R. Lajoie;Edda G. Schulz;Luca Giorgetti;Luca Giorgetti;Luca Giorgetti

  • HiC-Pro: an optimized and flexible pipeline for Hi-C data processing

    Nicolas Servant;Nelle Varoquaux;Nelle Varoquaux;Nelle Varoquaux;Bryan R. Lajoie;Eric Viara

  • Control-FREEC

    Valentina Boeva;Tatiana Popova;Kevin Bleakley;Pierre Chiche

  • A critical function for transforming growth factor-beta, interleukin 23 and proinflammatory cytokines in driving and modulating human T(H)-17 responses.

    Elisabetta Volpe;Nicolas Servant;Nicolas Servant;Nicolas Servant;Raphaël Zollinger;Raphaël Zollinger;Sofia I Bogiatzi;Sofia I Bogiatzi

  • Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

    Philippe Hupé;Nicolas Stransky;Jean-Paul Thiery;François Radvanyi

  • Continuum of overlapping clones spanning the entire human chromosome 21q.

    Ilya Chumakov;Philippe Rigault;Sophie Guillou;Pierre Ougen

  • Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries

    Valentina Boeva;Valentina Boeva;Caroline Louis-Brennetot;Agathe Peltier;Simon Durand

  • LINE-1 Activity in Facultative Heterochromatin Formation during X Chromosome Inactivation

    Jennifer C. Chow;Constance Ciaudo;Melissa J. Fazzari;Nathan Mise;Nathan Mise

  • XML, bioinformatics and data integration.

    Frédéric Achard;Guy Vaysseix;Emmanuel Barillot

  • miR-181a and miR-630 Regulate Cisplatin-Induced Cancer Cell Death

    Lorenzo Galluzzi;Eugenia Morselli;Ilio Vitale;Oliver Kepp

  • Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization

    Valentina Boeva;Andrei Zinovyev;Kevin Bleakley;Jean-Philippe Vert

  • Classification of microarray data using gene networks

    Franck Rapaport;Franck Rapaport;Andrei Yu. Zinovyev;Marie Dutreix;Emmanuel Barillot

  • Germline BAP1 mutations predispose to renal cell carcinomas.

    Tatiana Popova;Lucie Hebert;Virginie Jacquemin;Sophie Gad

  • Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

    Tatiana Popova;Elodie Manié;Dominique Stoppa-Lyonnet;Guillem Rigaill;Guillem Rigaill

  • Frequent PTEN genomic alterations and activated phosphatidylinositol 3-kinase pathway in basal-like breast cancer cells.

    Bérengère Marty;Virginie Maire;Eléonore Gravier;Guillem Rigaill;Guillem Rigaill

  • Mathematical Modelling of Cell-Fate Decision in Response to Death Receptor Engagement

    Laurence Calzone;Laurence Calzone;Laurence Calzone;Laurent Tournier;Laurent Tournier;Laurent Tournier;Simon Fourquet;Simon Fourquet;Simon Fourquet;Denis Thieffry;Denis Thieffry

  • SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data

    Bruno Zeitouni;Valentina Boeva;Isabelle Janoueix-Lerosey;Sophie Loeillet

  • Mapping the whole human genome by fingerprinting yeast artificial chromosomes.

    Christine Bellanné-Chantelot;Bruno Lacroix;Pierre Ougen;Alain Billault

  • Beta-catenin status in paediatric medulloblastomas: correlation of immunohistochemical expression with mutational status, genetic profiles, and clinical characteristics.

    Sarah Fattet;Sarah Fattet;Sarah Fattet;Christine Haberler;Christine Haberler;Christine Haberler;Patricia Legoix;Pascale Varlet

  • The oncogenic EWS-FLI1 protein binds in vivo GGAA microsatellite sequences with potential transcriptional activation function.

    Noëlle Guillon;Noëlle Guillon;Franck Tirode;Franck Tirode;Valentina Boeva;Valentina Boeva;Andrei Zynovyev;Andrei Zynovyev

Frequent Co-Authors

Andrei Zinovyev
Andrei Zinovyev Institute Curie
Laurence Calzone
Laurence Calzone PSL University
Olivier Delattre
Olivier Delattre PSL University
Edith Heard
Edith Heard Collège de France
Jean-Philippe Vert
Jean-Philippe Vert Google (United States)
Xavier Sastre-Garau
Xavier Sastre-Garau Institute Curie
Sergio Roman-Roman
Sergio Roman-Roman Institute Curie
Bernard Asselain
Bernard Asselain Institute Curie
Vassili Soumelis
Vassili Soumelis Université Paris Cité

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