Bryan Winchester - Concepedia

Author

Bryan Winchester

Also Known As

B G Winchester, B WINCHESTER, B Winchester, B. G. WINCHESTER, B. G. Winchester, B. WINCHESTER, B. Winchester, B.G. Winchester, BRYAN G. WINCHESTER, BRYAN WINCHESTER

280

Publications

10.7K

Citations

H-Index

144

Concepts

All Affiliations

University College London Great Ormond Street Hospital University of London Institute of Child Health University of Oxford

About

Bryan Winchester is an author at University College London specializing in medicine, biochemistry, and glycobiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	88	5K
2	Natural Sciences	29	47	2K
3	Engineering	13	14	504
4	Health Sciences	2	2	103
5	Education	1	1	99

Bryan Winchester

160

Publications

8.7K

Citations

H-Index

Page 1

	Year	Citations
Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study Arndt Rolfs, Tobias Böttcher, Marlies Zschiesche, The Lancet ThrombosisFabry DiseaseCryptogenic StrokeCardiovascular DiseaseMedicine	2005	466
Prevention of Lysosomal Storage in Tay-Sachs Mice Treated with <i>N</i> -Butyldeoxynojirimycin Frances M. Platt, Gabrielle R. Neises, Gabriele Reinkensmeier, Science	1997	342
Anderson–Fabry disease: Clinical manifestations of disease in female heterozygotes Catharina Whybra, C. Kampmann, I. Willers, Journal of Inherited Metabolic Disease	2001	274
Bone marrow transplantation for mucopolysaccharidosis type I: experience of two British centres Ashok Vellodi, Elisabeth Young, Alan Cooper, Archives of Disease in Childhood Hla Identical RelativeTransplantationMarrow TransplantationMucopolysaccharidosis TypeBone Marrow Failure	1997	207
Iminosugars: from botanical curiosities to licensed drugs Bryan Winchester Tetrahedron Asymmetry BotanyMedicineDrug DiscoveryHerbal MedicinePharmacology	2009	193
Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II François Foulquier, Eliza Vasile, Els Schollen, Proceedings of the National Academy of Sciences Uncharacterized Congenital DisorderGeneticsGlycobiologyMolecular BiologyMolecular Genetics	2006	181
Long‐term follow‐up following bone marrow transplantation for Hunter disease Ashok Vellodi, E. Young, Alan Cooper, Journal of Inherited Metabolic Disease	1999	166
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia) Gert Matthijs, Els Schollen, Cecilia Bjursell, Human Mutation	2000	159
Methods for a prompt and reliable laboratory diagnosis of Pompe disease: Report from an international consensus meeting Bryan Winchester, Deeksha Bali, Olaf A. Bodamer, Molecular Genetics and Metabolism Medical DiagnosticsPompe DiseaseInternational Consensus MeetingEngineeringMedicine	2007	155
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, Molecular Genetics and Metabolism Fabry DiseaseImmunologyPathologyMedicineAntibody Formation	2008	134

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