Owen A. Ross

Overview

Best Publications

• Diagnosis and management of dementia with Lewy bodies Fourth consensus report of the DLB Consortium

  Ian G. McKeith;Bradley F. Boeve;Dennis W. DIckson;Glenda Halliday

  4225
  Citations

• Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study.

  Melissa E Murray;Neill R Graff-Radford;Owen A Ross;Ronald C Petersen

  1067
  Citations

• VPS35 Mutations in Parkinson Disease

  Carles Vilariño-Güell;Christian Wider;Owen A. Ross;Justus C. Dachsel

  1056
  Citations

• Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines.

  Irene Maeve Rea;Irene Maeve Rea;Irene Maeve Rea;David S. Gibson;Victoria McGilligan;Susan E. McNerlan

  1025
  Citations

• Association between alcohol and cardiovascular disease:Mendelian randomisation analysis based on individual participant data

  Michael V Holmes;Michael V Holmes;Caroline E Dale;Luisa Zuccolo;Richard J Silverwood

  854
  Citations

• Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

  Günter U. Höglinger;Nadine M. Melhem;Dennis W. Dickson;Patrick M A Sleiman

  688
  Citations

• Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

  Jennifer Kachergus;Ignacio F. Mata;Mary Hulihan;Julie P. Taylor

  621
  Citations

• Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease

  Oliver Cooper;Hyemyung Seo;Shaida Andrabi;Cristina Guardia-Laguarta

  560
  Citations

• Mutations in the colony stimulating factor 1 receptor ( CSF1R ) gene cause hereditary diffuse leukoencephalopathy with spheroids

  Rosa Rademakers;Matt Baker;Alexandra M Nicholson;Nicola J Rutherford

  555
  Citations

• Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.

  J Fuchs;Christer Nilsson;J Kachergus;M Munz

  503
  Citations

• TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease

  Sruti Rayaprolu;Bianca Mullen;Matt Baker;Timothy Lynch

  450
  Citations

• Clinical correlations with Lewy body pathology in LRRK2-related Parkinson disease

  Lorraine V. Kalia;Anthony E. Lang;Lili Naz Hazrati;Shinsuke Fujioka

  402
  Citations

• Translation initiator EIF4G1 mutations in familial Parkinson disease

  Marie Christine Chartier-Harlin;Marie Christine Chartier-Harlin;Justus C. Dachsel;Carles Vilariño-Güell;Sarah J. Lincoln

  389
  Citations

• Genomic investigation of alpha-synuclein multiplication and parkinsonism

  Owen A. Ross;Adam T. Braithwaite;Lisa M. Skipper;Jennifer Kachergus

  386
  Citations

• Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.

  Owen A. Ross;Alexandra I. Soto-Ortolaza;Michael G. Heckman;Jan O. Aasly

  365
  Citations

• DCTN1 mutations in Perry syndrome

  Matthew J. Farrer;Mary M. Hulihan;Jennifer M. Kachergus;Justus C Dächsel

  363
  Citations

• DNAJC13 mutations in Parkinson disease

  Carles Vilariño-Güell;Alex Rajput;Austen J. Milnerwood;Brinda Shah

  348
  Citations

• Clinicopathologic and 11C-Pittsburgh compound B implications of Thal amyloid phase across the Alzheimer’s disease spectrum

  Melissa E. Murray;Val J. Lowe;Neill R. Graff-Radford;Amanda M. Liesinger

  330
  Citations

• Meta-analysis of Parkinson's Disease: Identification of a Novel Locus, RIT2

  Nathan Pankratz;Gary W. Beecham;Anita L. Destefano;Ted M. Dawson

  330
  Citations

• Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank

  Kevin F. Bieniek;Owen A. Ross;Kerry A. Cormier;Ronald L. Walton

  320
  Citations