His main research concerns Frontotemporal dementia, Frontotemporal lobar degeneration, Pathology, Semantic dementia and C9orf72. His Frontotemporal dementia study necessitates a more in-depth grasp of Dementia. His Frontotemporal lobar degeneration research incorporates themes from Corticobasal degeneration, Neuroscience and Age of onset.
His studies in Pathology integrate themes in fields like Magnetic resonance imaging, Temporal lobe, Voxel-based morphometry and Gene mutation. His Semantic dementia research includes themes of Primary progressive aphasia, Progressive nonfluent aphasia and Aphasia. His C9orf72 research is multidisciplinary, incorporating elements of C9orf72 Protein and Boston Naming Test.
Jonathan D. Rohrer mostly deals with Frontotemporal dementia, Neuroscience, Dementia, Pathology and Frontotemporal lobar degeneration. His work is dedicated to discovering how Frontotemporal dementia, Atrophy are connected with Magnetic resonance imaging and other disciplines. His Neuroscience study combines topics in areas such as Neurodegeneration and Motor neurone disease.
Jonathan D. Rohrer has included themes like Cognition and Bioinformatics in his Dementia study. The study incorporates disciplines such as White matter, Neurology, Frontal lobe and Gene mutation in addition to Pathology. His research integrates issues of Semantic dementia, Aphasia and Audiology in his study of Primary progressive aphasia.
His primary scientific interests are in Frontotemporal dementia, Disease, Atrophy, Internal medicine and C9orf72. His study in Primary progressive aphasia and Frontotemporal lobar degeneration is done as part of Frontotemporal dementia. Jonathan D. Rohrer interconnects Text mining and Grey matter in the investigation of issues within Primary progressive aphasia.
Jonathan D. Rohrer has researched Atrophy in several fields, including Stage, Magnetic resonance imaging, Gene and Parkinsonism. His Internal medicine research integrates issues from Oncology and Genotype. His C9orf72 research includes elements of Cerebrospinal fluid, Cohort study, Gastroenterology, Asymptomatic carrier and Temporal lobe.
Jonathan D. Rohrer spends much of his time researching Frontotemporal dementia, Atrophy, C9orf72, Pathology and Frontotemporal lobar degeneration. His Frontotemporal dementia research is included under the broader classification of Dementia. The concepts of his Atrophy study are interwoven with issues in Young adult, Magnetic resonance imaging, Disease and Motor neurone disease.
His C9orf72 research is multidisciplinary, relying on both Cerebrospinal fluid, Pediatrics, Asymptomatic carrier and Cardiology. His Pathology research is multidisciplinary, incorporating perspectives in White matter and Senescence. His work carried out in the field of Frontotemporal lobar degeneration brings together such families of science as Apathy, Mood, First-degree relatives, Primary progressive aphasia and Genetic heterogeneity.
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.
Classification of primary progressive aphasia and its variants
M L Gorno-Tempini;M L Gorno-Tempini;A E Hillis;S Weintraub;A Kertesz.
Neurology (2011)
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.
Katya Rascovsky;John R. Hodges;David Knopman;Mario F. Mendez.
Brain (2011)
Automatic classification of MR scans in Alzheimer's disease
Stefan Klöppel;Cynthia M. Stonnington;Carlton Chu;Bogdan Draganski.
Brain (2008)
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie;Alan E. Renton;Kin Mok;Elise G. P. Dopper;Elise G. P. Dopper.
Lancet Neurology (2012)
Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
Harro Seelaar;Jonathan D Rohrer;Yolande A L Pijnenburg;Nick C Fox.
Journal of Neurology, Neurosurgery, and Psychiatry (2011)
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)
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M. Van Deerlin;Patrick M A Sleiman;Maria Martinez-Lage;Maria Martinez-Lage;Alice Chen-Plotkin.
Nature Genetics (2010)
The heritability and genetics of frontotemporal lobar degeneration
J.D. Rohrer;R. Guerreiro;J. Vandrovcova;J. Uphill.
Neurology (2009)
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
Jonathan D Rohrer;Jennifer M Nicholas;Jennifer M Nicholas;David M Cash;John van Swieten.
Lancet Neurology (2015)
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
Colin J. Mahoney;Jon Beck;Jonathan D. Rohrer;Tammaryn Lashley.
Brain (2012)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University College London
University College London
University College London
Karolinska University Hospital
Erasmus University Rotterdam
University of Milan
University of Cambridge
Sunnybrook Health Science Centre
King's College London
University of Brescia
Harvard University
North Carolina Agricultural and Technical State University
Pukyong National University
Polytechnic University of Milan
Natural Resources Canada
Hong Kong University of Science and Technology
F1 Genomics
Hokkaido University
Mendel University Brno
Old Dominion University
Institut National de la Recherche Scientifique
Johns Hopkins University
Memorial Sloan Kettering Cancer Center
Mayo Clinic
University of Granada
McGill University