David Beeson

Research.com Recognitions

• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom
• Fellow of The Academy of Medical Sciences, United Kingdom

Overview

Best Publications

• N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes

  Sarosh R. Irani;Katarzyna Bera;Patrick Waters;Luigi Zuliani

  1142
  Citations

• Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

  Johannes N. Spelbrink;Fang Yuan Li;Valeria Tiranti;Kaisu Nikali

  988
  Citations

• IgG1 antibodies to acetylcholine receptors in 'seronegative' myasthenia gravis.

  Maria Isabel Leite;Saiju Jacob;Stuart Viegas;Judy Cossins

  571
  Citations

• Detection and characterization of MuSK antibodies in seronegative myasthenia gravis

  John McConville;Maria Elena Farrugia;David Beeson;Uday Kishore

  500
  Citations

• Autoantibodies detected to expressed K+ channels are implicated in neuromyotonia.

  Ian K. Hart;Caroline Waters;Angela Vincent;Claire Newland

  420
  Citations

• Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

  Jenny C. Taylor;Jenny C. Taylor;Hilary C. Martin;Stefano Lise;John Broxholme

  418
  Citations

• Aquaporin-4 antibodies in neuromyelitis optica and longitudinally extensive transverse myelitis.

  Patrick Waters;Sven Jarius;Edward Littleton;Maria Isabel Leite

  348
  Citations

• Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy

  David Beeson;Osamu Higuchi;Jackie Palace;Judy Cossins

  299
  Citations

• An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus

  Matthieu Giraud;Richard Taubert;Claire Vandiedonck;Xiayi Ke

  222
  Citations

• Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen

  A. Vincent;C. Newland;D. Beeson;S. Riemersma

  205
  Citations

• Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome

  Rebecca Croxen;Claire Newland;David Beeson;Hans Oosterhuis

  203
  Citations

• Mutation history of the Roma/Gypsies

  Bharti Morar;David Gresham;David Gresham;Dora Angelicheva;Ivailo Tournev

  202
  Citations

• Antibodies to GABAA receptor α1 and γ2 subunits Clinical and serologic characterization

  Philippa Pettingill;Holger B. Kramer;Jan Adriaan Coebergh;Rosie Pettingill

  199
  Citations

• Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.

  Jan Senderek;Jan Senderek;Juliane S. Müller;Marina Dusl;Tim M. Strom

  194
  Citations

• Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.

  Katsiaryna Belaya;Sarah Finlayson;Sarah Finlayson;Clarke R. Slater;Judith Cossins

  187
  Citations

• Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes

  Juliane S. Müller;Agnes Herczegfalvi;Juan J. Vilchez;Jaume Colomer

  182
  Citations

• MuSK Myasthenia Gravis IgG4 Disrupts the Interaction of LRP4 with MuSK but Both IgG4 and IgG1-3 Can Disperse Preformed Agrin-Independent AChR Clusters

  Inga Koneczny;Judith Cossins;Patrick Waters;David Beeson

  174
  Citations

• Rapsyn mutations in hereditary myasthenia Distinct early- and late-onset phenotypes

  G Burke;J Cossins;S Maxwell;G Owens

  171
  Citations

• Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function.

  S Riemersma;A Vincent;D Beeson;C Newland

  169
  Citations

• Clinical features of the DOK7 neuromuscular junction synaptopathy.

  Jacqueline Palace;Daniel Lashley;John Newsom-Davis;Judy Cossins

  166
  Citations