World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
63
Citations
12228
World Ranking
10370
National Ranking
789

Overview

Bryan Winchester is affiliated with University College London in the United Kingdom. Their academic contributions reflect a focus aligned with the research environment of this institution.

While no specific recent papers are listed, the absence of detailed publication data on papers, co-authors, and frequent publication venues suggests a profile that may be either emerging or oriented towards other academic activities beyond high-output paper publishing.

The scientist's areas of expertise are not explicitly detailed, as no main fields of study, subfields, or principal research topics are provided. Similarly, there are no records of book publications or awards won, indicating either a focus on non-book academic outputs or a career stage where such details have not yet been cataloged in this data.

The lack of recent papers or specified collaboration networks also means there are no insights into typical co-authors or recurring publication platforms. This may imply a specialization in research types, roles, or institutional responsibilities that do not center on frequent publication or broad collaborative projects.

Nonetheless, the affiliation with University College London positions Bryan Winchester within a well-established research community, potentially engaged in interdisciplinary or emerging field contributions not yet extensively documented in the available sources.

The profile reflects a neutral and factual overview grounded strictly in the supplied data. Without additional publication or award information, the focus remains on institutional association and the potential scope of scientific involvement at University College London.

Best Publications

  • Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study.

    Arndt Rolfs;Tobias Böttcher;Marlies Zschiesche;Peter Morris

  • Prevention of Lysosomal Storage in Tay-Sachs Mice Treated with N-Butyldeoxynojirimycin

    F M Platt;G R Neises;G Reinkensmeier;M J Townsend

  • Anderson-Fabry disease: Clinical manifestations of disease in female heterozygotes

    C. Whybra;Chr. Kampmann;I. Willers;J. Davies

  • Lysosomal metabolism of glycoproteins.

    Bryan Winchester

  • The molecular basis of lysosomal storage diseases and their treatment

    Bryan Winchester;Ashok Vellodi;Elisabeth Young

  • Iminosugars: from botanical curiosities to licensed drugs

    Bryan G. Winchester

  • Mammalian alpha-mannosidases--multiple forms but a common purpose?

    Peter F. Daniel;Bryan Winchester;Christopher D. Warren

  • Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres

    A Vellodi;E P Young;A Cooper;J E Wraith

  • Long‐term follow‐up following bone marrow transplantation for Hunter disease

    A. Vellodi;E. Young;A. Cooper;V. Lidchi

  • Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II

    François Foulquier;Eliza Vasile;Els Schollen;Nico Callewaert

  • Methods for a prompt and reliable laboratory diagnosis of Pompe disease: Report from an international consensus meeting

    B. Winchester;D. Bali;O.A. Bodamer;C. Caillaud

  • Treatment of Fabry disease with different dosing regimens of agalsidase: effects on antibody formation and GL-3.

    Anouk C. Vedder;Frank Breunig;Wilma E. Donker-Koopman;Kevin Mills

  • Is globotriaosylceramide a useful biomarker in Fabry disease

    E Young;K Mills;P Morris;A Vellodi

  • Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia).

    Gert Matthijs;E Schollen;C Bjursell;A Erlandson

  • A Rapid Fluorogenic Palmitoyl-Protein Thioesterase Assay: Pre- and Postnatal Diagnosis of INCL

    O.P. van Diggelen;J.L.M. Keulemans;B. Winchester;I.L. Hofman

  • Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations.

    Clare E. Beesley;Cathy A. Meaney;Gavin Greenland;Vanessa Adams

  • Defective galactosylation of serum transferrin in galactosemia

    Joanne Charlwood;Peter Clayton;Geoffrey Keir;Nasi Mian

  • Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG. First International Workshop on CDGS.

    M Aebi;A Helenius;B Schenk;R Barone

  • Lysosomal membrane proteins

    Bryan G. Winchester

  • A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation

    François Foulquier;Daniel Ungar;Ellen Reynders;Renate Zeevaert

Frequent Co-Authors

Peter E. Clayton
Peter E. Clayton University of Manchester
George W. J. Fleet
George W. J. Fleet University of Oxford
Andreas Gal
Andreas Gal Universität Hamburg
Roberto Giugliani
Roberto Giugliani Federal University of Rio Grande do Sul
Benjamin G. Davis
Benjamin G. Davis University of Oxford
Gert Matthijs
Gert Matthijs KU Leuven
Robert J. Nash
Robert J. Nash Aberystwyth University
John J. Hopwood
John J. Hopwood University of Adelaide
Simon J. R. Heales
Simon J. R. Heales University College London
Hudson H. Freeze
Hudson H. Freeze Discovery Institute

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