2023 - Research.com Medicine in France Leader Award
2023 - Research.com Genetics in France Leader Award
2022 - Research.com Best Female Scientist Award
2022 - Research.com Genetics and Molecular Biology in France Leader Award
Alexandra Durr mostly deals with Genetics, Ataxia, Spinocerebellar ataxia, Age of onset and Mutation. Many of her studies on Genetics involve topics that are commonly interrelated, such as Parkin. Her Ataxia research is multidisciplinary, relying on both Pediatrics and Frataxin.
The concepts of her Spinocerebellar ataxia study are interwoven with issues in Cerebellum, Physical therapy and Autosomal dominant cerebellar ataxia. Her Age of onset research is multidisciplinary, incorporating perspectives in Cohort study, Cohort and Degenerative disease. Gene mutation is closely connected to Genotype in her research, which is encompassed under the umbrella topic of Internal medicine.
Her primary scientific interests are in Genetics, Ataxia, Spinocerebellar ataxia, Disease and Huntington's disease. Her study involves Locus, Gene, Mutation, Genetic linkage and Allele, a branch of Genetics. Her Ataxia study integrates concerns from other disciplines, such as Internal medicine, Physical therapy and Pediatrics.
Her Spinocerebellar ataxia research incorporates themes from Age of onset and Autosomal dominant cerebellar ataxia, Trinucleotide repeat expansion. Her Disease research includes themes of Psychiatry and Bioinformatics. Her Huntington's disease study incorporates themes from White matter, Physical medicine and rehabilitation, Cognition, Neuroscience and Atrophy.
Alexandra Durr mainly focuses on Ataxia, Disease, Internal medicine, Huntington's disease and Spinocerebellar ataxia. Her Ataxia research incorporates elements of Movement disorders and Pediatrics. Her studies deal with areas such as Gastroenterology, Trinucleotide repeat expansion, Oncology and Cardiology as well as Internal medicine.
Her Huntington's disease research integrates issues from White matter, Cognition, Neuroscience, Neurodegeneration and Atrophy. Her research on Spinocerebellar ataxia concerns the broader Pathology. Autosomal recessive cerebellar ataxia is a subfield of Genetics that she explores.
Alexandra Durr focuses on Huntington's disease, Internal medicine, Neuroscience, Spinocerebellar ataxia and Neurodegeneration. Alexandra Durr combines subjects such as Progenitor cell and White matter with her study of Huntington's disease. Her Internal medicine research includes elements of Gastroenterology, Ataxia, Cerebellar ataxia and Oncology.
Cerebellar ataxia is closely attributed to Genetics in her work. The Genetics study combines topics in areas such as Frontotemporal lobar degeneration, Dementia and Frontotemporal dementia. Her Spinocerebellar ataxia study combines topics in areas such as Purkinje cell, Age of onset, Genetic counseling, Genetic variation and NAD+ kinase.
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Second consensus statement on the diagnosis of multiple system atrophy
S. Gilman;G. K. Wenning;P. A. Low;D. J. Brooks.
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Ellen Sidransky;Michael A. Nalls;Jan O. Aasly;Judith Aharon-Peretz.
The New England Journal of Medicine (2009)
Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
CB Lucking;A Durr;Bonifati;J Vaughan.
The New England Journal of Medicine (2000)
Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch;S Tezenas du Montcel;L Baliko;J Berciano.
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
Daniel G Healy;Mario Falchi;Sean S O'Sullivan;Vincenzo Bonifati.
Lancet Neurology (2008)
Causal relation between α-synuclein locus duplication as a cause of familial Parkinson's disease
P Ibáñez;A-M Bonnet;B Débarges;E Lohmann.
The Lancet (2004)
Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
Alexandra Dürr;Mireille Cossee;Yves Agid;Victoria Campuzano.
The New England Journal of Medicine (1996)
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
Georges Imbert;Frédéric Saudou;Frédéric Saudou;Gaël Yvert;Gaël Yvert;Didier Devys;Didier Devys.
Nature Genetics (1996)
Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data.
Sarah J Tabrizi;Douglas R Langbehn;Blair R Leavitt;Raymund A C Roos.
Lancet Neurology (2009)
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
Gilles David;Nacer Abbas;Giovanni Stevanin;Alexandra Dürr.
Nature Genetics (1997)
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