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Molecular Biology

D-Index
50
Citations
23128
World Ranking
2526
National Ranking
196

Overview

Caleb Webber is affiliated with the University of Oxford in the United Kingdom. Their research spans several intersecting scientific fields, including Biochemistry, Genetics and Molecular Biology, Medicine, and Neuroscience. Within these main domains, their work notably focuses on subfields such as Neurology, Molecular Biology, Cellular and Molecular Neuroscience, Physiology, and Psychiatry and Mental Health.

The scientist's research interests are reflected in several major topics including Single-cell and spatial transcriptomics, Neuroinflammation and Neurodegeneration Mechanisms, Parkinson's Disease Mechanisms and Treatments, RNA Research and Splicing, Migraine and Headache Studies, Neurological Disease Mechanisms and Treatments, and Alzheimer's disease research and treatments.

Some of Caleb Webber's most recent publications include:

  • Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution, 2021, Kent Academic Repository (University of Kent)
  • Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility, 2020, Disease Models & Mechanisms
  • A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders, 2020, Nature Communications
  • Pro-maturational Effects of Human iPSC-Derived Cortical Astrocytes upon iPSC-Derived Cortical Neurons, 2020, Stem Cell Reports
  • The Parkinson's Disease Genome-Wide Association Study Locus Browser, 2020, Movement Disorders

Webber frequently collaborates with a number of colleagues, including Jimena Monzón-Sandoval, Viola Volpato, Cynthia Sandor, M. Zameel Cader, and Frank Wessely. These collaborators have worked with Webber in multiple publications.

The primary venues where Webber's work appears include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature Communications
  • Disease Models & Mechanisms
  • Stem Cell Reports
  • Movement Disorders

Best Publications

  • Genome sequence, comparative analysis and haplotype structure of the domestic dog

    Kerstin Lindblad-Toh;Claire M Wade;Claire M Wade;Tarjei S. Mikkelsen;Tarjei S. Mikkelsen;Elinor K. Karlsson;Elinor K. Karlsson

  • Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution

    Ladeana W. Hillier;Webb Miller;Ewan Birney;Wesley Warren

  • Genome sequence of the Brown Norway rat yields insights into mammalian evolution

    Richard A. Gibbs;George M. Weinstock;Michael L. Metzker;Donna M. Muzny

  • Functional impact of global rare copy number variation in autism spectrum disorders

    Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney

  • Analysis of shared heritability in common disorders of the brain

    Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters

  • A Physical Map of 30,000 Human Genes

    P. Deloukas;G. D. Schuler;G. Gyapay;E. M. Beasley

  • Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences

    Tarjei S. Mikkelsen;Tarjei S. Mikkelsen;Matthew J. Wakefield;Bronwen Aken;Chris T. Amemiya

  • Genome analysis of the platypus reveals unique signatures of evolution

    Wesley C. Warren;La Deana W. Hillier;Jennifer A. Marshall Graves;Ewan Birney

  • Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

    Padhraig Gormley;Verneri Anttila;Verneri Anttila;Bendik S. Winsvold;Bendik S. Winsvold;Priit Palta

  • A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms

    Gane Ka Shu Wong;Gane Ka Shu Wong;Gane Ka Shu Wong;Bin Liu;Jun Wang;Jun Wang;Yong Zhang;Yong Zhang

  • Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules

    Korinna Kochinke;Christiane Zweier;Bonnie Nijhof;Michaela Fenckova

  • Bias of selection on human copy-number variants.

    Duc-Quang Nguyen;Caleb Webber;Chris P Ponting

  • Natural genetic variation caused by small insertions and deletions in the human genome

    Ryan E. Mills;W. Stephen Pittard;Julienne M. Mullaney;Umar Farooq

  • Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility.

    Viola Volpato;Caleb Webber

  • A radiation hybrid map of the rat genome containing 5,255 markers.

    Takeshi K. Watanabe;Marie Therese Bihoreau;Linda C. McCarthy;Susanna L. Kiguwa

  • A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders

    Devika Agarwal;Devika Agarwal;Cynthia Sandor;Viola Volpato;Tara M. Caffrey;Tara M. Caffrey

  • GAT: a simulation framework for testing the association of genomic intervals

    Andreas Heger;Caleb Webber;Martin Goodson;Chris P. Ponting

  • CSF1R inhibitor JNJ-40346527 attenuates microglial proliferation and neurodegeneration in P301S mice

    Renzo Mancuso;Gemma Fryatt;Madeleine Cleal;Juliane Obst

  • Diagnostically relevant facial gestalt information from ordinary photos

    Quentin Ferry;Julia Steinberg;Caleb Webber;David R FitzPatrick

  • Tumour invasion and metastasis initiated by microRNA-10b in breast cancer (Nature (2007) 449, (682-688))

    Li Ma;Julie Teruya-Feldstein;Robert A. Weinberg

Frequent Co-Authors

Chris P. Ponting
Chris P. Ponting University of Edinburgh
Thomas Werge
Thomas Werge University of Copenhagen
Mark J. Daly
Mark J. Daly Massachusetts General Hospital
Hailiang Huang
Hailiang Huang Harvard Medical School
Rory Bowden
Rory Bowden Walter and Eliza Hall Institute of Medical Research
Julie E. Buring
Julie E. Buring Brigham and Women's Hospital
Daniel I. Chasman
Daniel I. Chasman Brigham and Women's Hospital
Tobias Kurth
Tobias Kurth Charité - University Medicine Berlin
Benjamin M. Neale
Benjamin M. Neale Harvard University
Grant W. Montgomery
Grant W. Montgomery University of Queensland

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