D-Index & Metrics Best Publications

D-Index & Metrics

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 64 Citations 14,844 218 World Ranking 4237 National Ranking 2118

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

His scientific interests lie mostly in Genetics, Disease, Parkinsonism, Parkinson's disease and Pathology. His Genetics research focuses on Locus, Allele, Genome-wide association study, Haplotype and Mutation. His study in Disease is interdisciplinary in nature, drawing from both Bioinformatics and Medical genetics.

His studies deal with areas such as Missense mutation, Proband, LRRK2, Gene duplication and Penetrance as well as Parkinsonism. His Parkinson's disease research incorporates elements of Neurodegeneration and Kinase activity. His Pathology study deals with Neurology intersecting with Orthostatic vital signs, Anxiety and Severity of illness.

His most cited work include:

  • Diagnosis and management of dementia with Lewy bodies Fourth consensus report of the DLB Consortium (1355 citations)
  • VPS35 Mutations in Parkinson Disease (585 citations)
  • Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study. (482 citations)

What are the main themes of his work throughout his whole career to date?

Owen A. Ross mainly focuses on Genetics, Disease, Parkinson's disease, Parkinsonism and Pathology. His studies in LRRK2, Gene, Haplotype, Mutation and Genome-wide association study are all subfields of Genetics research. His Disease study contributes to a more complete understanding of Internal medicine.

His Internal medicine study combines topics in areas such as Gastroenterology and Oncology. His Parkinson's disease research includes themes of Genetic variation, Neuroscience, Allele frequency and Degenerative disease. His Parkinsonism research is multidisciplinary, incorporating elements of Missense mutation, Proband, Frontotemporal dementia, Family history and Pediatrics.

He most often published in these fields:

  • Genetics (47.68%)
  • Disease (42.54%)
  • Parkinson's disease (32.52%)

What were the highlights of his more recent work (between 2017-2021)?

  • Disease (42.54%)
  • Internal medicine (16.63%)
  • Genetics (47.68%)

In recent papers he was focusing on the following fields of study:

Owen A. Ross mostly deals with Disease, Internal medicine, Genetics, Parkinson's disease and Progressive supranuclear palsy. His study looks at the intersection of Disease and topics like Gene with Computational biology. His work in Internal medicine covers topics such as Oncology which are related to areas like Genetic association, Cognitive decline and Tau protein.

His research in Parkinson's disease focuses on subjects like Parkinsonism, which are connected to Apathy, Pediatrics and Mitochondrion. The study incorporates disciplines such as Neuropathology, Tau pathology, Frontotemporal dementia and Tauopathy in addition to Progressive supranuclear palsy. As a part of the same scientific family, Owen A. Ross mostly works in the field of LRRK2, focusing on Family history and, on occasion, Psychiatry.

Between 2017 and 2021, his most popular works were:

  • Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines. (234 citations)
  • Age and Age-Related Diseases: Role of Inflammation Triggers and Cytokines. (234 citations)
  • Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study (105 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Internal medicine

Owen A. Ross focuses on Disease, Dementia with Lewy bodies, Progressive supranuclear palsy, Genome-wide association study and Internal medicine. His work deals with themes such as Inflammation, Inflammasome and Missense mutation, which intersect with Disease. His biological study spans a wide range of topics, including Parkinson's disease and Medical genetics.

Owen A. Ross interconnects Frontotemporal dementia and Tauopathy in the investigation of issues within Progressive supranuclear palsy. His study with Genome-wide association study involves better knowledge in Genetics. Owen A. Ross does research in Genetics, focusing on Genetic variation specifically.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

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.
Neurology (2017)

1504 Citations

VPS35 Mutations in Parkinson Disease

Carles Vilariño-Güell;Christian Wider;Owen A. Ross;Justus C. Dachsel.
American Journal of Human Genetics (2011)

803 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.
Lancet Neurology (2011)

614 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.
BMJ (2014)

612 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.
American Journal of Human Genetics (2005)

571 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.
Nature Genetics (2011)

461 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.
Science Translational Medicine (2012)

448 Citations

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

J Fuchs;Christer Nilsson;J Kachergus;M Munz.
Neurology (2007)

416 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.
Nature Genetics (2012)

405 Citations

Genomic investigation of alpha-synuclein multiplication and parkinsonism

Owen A. Ross;Adam T. Braithwaite;Lisa M. Skipper;Jennifer Kachergus.
Annals of Neurology (2008)

319 Citations

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