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Genetics

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

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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