World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
45
Citations
15851
World Ranking
4195
National Ranking
81

Mònica Bayés 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 Mònica Bayés 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: 93 publications — 5th percentile

5% of scientists in this discipline score the same or lower.

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

Mònica Bayés 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 Mònica Bayés 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: 45 D-Index — 4th percentile

4% of scientists in this discipline score the same or lower.

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

Overview

Mònica Bayés is affiliated with the Centro Nacional de Análisis Genómico in Spain. Their research spans multiple domains within biochemistry, genetics, molecular biology, and medicine, with a particular focus on genetics and molecular biology. The scientist's work addresses topics such as inflammatory bowel disease, genomics and rare diseases, microscopic colitis, inflammasome and immune disorders, biomedical text mining and ontologies, bioinformatics and genomic networks, and epigenetics and DNA methylation.

Among recent publications, the following papers highlight the scope and focus of their research:

  • "Systemic Inflammation in Preclinical Ulcerative Colitis," 2021, Gastroenterology
  • "The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases," 2022, Human Mutation
  • "Characterisation of the Circulating Transcriptomic Landscape in Inflammatory Bowel Disease Provides Evidence for Dysregulation of Multiple Transcription Factors Including NFE2, SPI1, CEBPB, and IRF2," 2022, Journal of Crohn's and Colitis
  • "Analysis of Systemic Epigenetic Alterations in Inflammatory Bowel Disease: Defining Geographical, Genetic and Immune-Inflammatory influences on the Circulating Methylome," 2022, Journal of Crohn's and Colitis
  • "Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases," 2022, Journal of Molecular Diagnostics

Their frequent collaborators include several researchers who have co-authored multiple papers with them over time:

  • Marta Gut (9 co-authored publications)
  • Mauro D'Amato (4 co-authored publications)
  • Johan D. Söderholm (4 co-authored publications)
  • Nicholas A. Kennedy (4 co-authored publications)
  • Christine Olbjørn (4 co-authored publications)

The scientist regularly publishes in specific venues that reflect their research interests, including:

  • Journal of Crohn's and Colitis (2 publications)
  • Gastroenterology (1 publication)
  • Human Mutation (1 publication)
  • Journal of Molecular Diagnostics (1 publication)
  • NAR Genomics and Bioinformatics (1 publication)

Mònica Bayés's specialization includes subfields such as genetics, molecular biology, immunology, surgery, and epidemiology. Their work engages with complex disease mechanisms and genomic analytics relevant to inflammatory and rare disease research.

Best Publications

  • Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

    S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone

  • International network of cancer genome projects

    Thomas J. Hudson;Thomas J. Hudson;Warwick Anderson;Axel Aretz;Anna D. Barker

  • Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

    Xose S. Puente;Magda Pinyol;Víctor Quesada;Laura Conde

  • Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.

    Víctor Quesada;Laura Conde;Neus Villamor;Gonzalo R Ordóñez

  • Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Colm O'Dushlaine;Lizzy Rossin;Phil H. Lee;Laramie Duncan;Laramie Duncan

  • Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia

    Marta Kulis;Simon Heath;Marina Bibikova;Ana C Queirós

  • Mutational mechanisms of williams-beuren syndrome deletions

    Mònica Bayés;Luis F. Magano;Núria Rivera;Raquel Flores

  • Differential Association of Circadian Genes with Mood Disorders: CRY1 and NPAS2 are Associated with Unipolar Major Depression and CLOCK and VIP with Bipolar Disorder

    Virginia Soria;Èrika Martínez-Amorós;Geòrgia Escaramís;Joaquín Valero

  • A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

    Arcos-Burgos M;Jain M;Acosta Mt;Shively S

  • Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy.

    Cristina Balbás-Martínez;Ana Sagrera;Enrique Carrillo-de-Santa-Pau;Julie Earl

  • Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

    Robert Maier;Gerhard Moser;Guo-Bo Chen;Stephan Ripke

  • Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease

    N. T. Ventham;N. A. Kennedy;A. T. Adams;R. Kalla

  • Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD.

    Barbara Franke;Alejandro Arias Vasquez;Stefan Johansson;Stefan Johansson;Martine Hoogman

  • Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease

    B. Cormand;H. Pihko;M. Bayes;M. Bayes;L. Valanne

  • Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.

    M Ribasés;J A Ramos-Quiroga;A Hervás;R Bosch

  • Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder.

    Marta Ribasés;Amaia Hervás;Josep Antoni Ramos-Quiroga;Rosa Bosch

  • Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1.

    Jie Zhou;Marcel Tawk;Francesco Danilo Tiziano;Julien Veillet

  • Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study.

    M. Ribasés;J. A. Ramos-Quiroga;C. Sánchez-Mora;R. Bosch

  • Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non‐synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment

    M. Gratacòs;J. Costas;R. De Cid;M. Bayés

  • Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations†‡

    C. Sanchez-Mora;M. Ribases;J. A. Ramos-Quiroga;M. Casas

Frequent Co-Authors

Josep Antoni Ramos-Quiroga
Josep Antoni Ramos-Quiroga Autonomous University of Barcelona
Ivo Gut
Ivo Gut Centro Nacional de Análisis Genómico
Stefan Johansson
Stefan Johansson University of Bergen
Jan Haavik
Jan Haavik University of Bergen
José M. Menchón
José M. Menchón University of Barcelona
Andreas Reif
Andreas Reif Goethe University Frankfurt
Barbara Franke
Barbara Franke Radboud University
Klaus-Peter Lesch
Klaus-Peter Lesch University of Würzburg
Marta Gut
Marta Gut Centro Nacional de Análisis Genómico

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