World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
47
Citations
25590
World Ranking
4078
National Ranking
1758

Serge Batalov 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 Serge Batalov 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: 70 publications — 1st percentile

1% of scientists in this discipline score the same or lower.

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

Serge Batalov 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 Serge Batalov 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: 47 D-Index — 6th percentile

6% of scientists in this discipline score the same or lower.

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

Overview

Serge Batalov is affiliated with the Genomics Institute of the Novartis Research Foundation in the United States. Their research focuses on a range of subjects within biochemistry, genetics, and molecular biology, with significant contributions to medicine.

The main fields of study include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Specific subfields where Serge Batalov has contributed are:

  • Genetics
  • Molecular Biology
  • Cancer Research
  • Pediatrics, Perinatology and Child Health
  • Epidemiology

The scientist's work covers several main topics, such as:

  • Genomics and Rare Diseases
  • Genomic variations and chromosomal abnormalities
  • Cancer Genomics and Diagnostics
  • Neurogenetic and Muscular Disorders Research
  • Congenital heart defects research
  • Congenital Heart Disease Studies
  • RNA modifications and cancer

Serge Batalov has contributed publications in the following venues with respective frequency:

  • npj Genomic Medicine (5 publications)
  • The American Journal of Human Genetics (4 publications)
  • bioRxiv (Cold Spring Harbor Laboratory) (2 publications)
  • New England Journal of Medicine (1 publication)
  • Nature Communications (1 publication)

Recent papers by Serge Batalov include:

  • "An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm" (2020, The American Journal of Human Genetics)
  • "A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases" (2022, The American Journal of Human Genetics)
  • "Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease" (2021, npj Genomic Medicine)
  • "Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction Syndrome" (2021, New England Journal of Medicine)
  • "An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases" (2022, Nature Communications)

Frequent coauthors collaborating with Serge Batalov are:

  • Stephen F. Kingsmore
  • Yan Ding
  • Narayanan Veeraraghavan
  • Shimul Chowdhury
  • Charlotte A. Hobbs

Best Publications

  • The Transcriptional Landscape of the Mammalian Genome

    P. Carninci;T. Kasukawa;S. Katayama;J. Gough

  • A gene atlas of the mouse and human protein-encoding transcriptomes

    Andrew I. Su;Tim Wiltshire;Serge Batalov;Hilmar Lapp

  • Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs

    Y. Okazaki;M. Furuno;T. Kasukawa;J. Adachi

  • Antisense Transcription in the Mammalian Transcriptome

    S. Katayama;Y. Tomaru;T. Kasukawa;K. Waki

  • Discovery of Gene Function by Expression Profiling of the Malaria Parasite Life Cycle

    Karine G. Le Roch;Yingyao Zhou;Peter L. Blair;Muni Grainger

  • BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources.

    Chunlei Wu;Camilo Orozco;Jason Boyer;Marc Leglise

  • Genome-Wide and Functional Annotation of Human E3 Ubiquitin Ligases Identifies MULAN, a Mitochondrial E3 that Regulates the Organelle's Dynamics and Signaling

    Wei Li;Mario H. Bengtson;Axel Ulbrich;Akio Matsuda

  • Functional annotation of a full-length mouse cDNA collection

    J. Kawai;A. Shinagawa;K. Shibata;M. Yoshino

  • A strategy for probing the function of noncoding RNAs finds a repressor of NFAT.

    A. T. Willingham;A. P. Orth;S. Batalov;E. C. Peters

  • Identification of modulators of TRAIL-induced apoptosis via RNAi-based phenotypic screening.

    Pedro Aza-Blanc;Christopher L. Cooper;Klaus Wagner;Serge Batalov

  • Complex Loci in Human and Mouse Genomes

    Par G Engstrom;Harukazu Suzuki;Noriko Ninomiya;Altuna Akalin

  • Do aligned sequences share the same fold

    Ruben A. Abagyan;Serge Batalov

  • Ubiquitin-mediated sequestration of normal cellular proteins into polyglutamine aggregates

    Kathryn M. Donaldson;Wei Li;Keith A. Ching;Serge Batalov

  • Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

    Tim Wiltshire;Mathew T. Pletcher;Serge Batalov;S. Whitney Barnes

  • A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.

    Stephen F. Kingsmore;Julie A. Cakici;Julie A. Cakici;Michelle M. Clark;Mary Gaughran

  • Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse.

    Mathew T Pletcher;Philip McClurg;Serge Batalov;Andrew I Su

  • A Systematic Map of Genetic Variation in Plasmodium falciparum

    Claire Kidgell;Sarah K Volkman;Johanna Daily;Justin O Borevitz

  • A Comparison of the Celera and Ensembl Predicted Gene Sets Reveals Little Overlap in Novel Genes

    John B. Hogenesch;Keith A. Ching;Serge Batalov;Andrew I. Su

  • Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation

    Michelle M. Clark;Amber Hildreth;Amber Hildreth;Amber Hildreth;Sergey Batalov;Yan Ding

  • Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAs.

    Norihiro Maeda;Takeya Kasukawa;Rieko Oyama;Julian Gough

Frequent Co-Authors

Elizabeth A. Winzeler
Elizabeth A. Winzeler University of California, San Diego
Tim Wiltshire
Tim Wiltshire University of North Carolina at Chapel Hill
Andrew I. Su
Andrew I. Su Scripps Research Institute
Boris Lenhard
Boris Lenhard Imperial College London
Christine A. Wells
Christine A. Wells University of Melbourne
Claes Wahlestedt
Claes Wahlestedt University of Miami

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