Scahill, Rachael I.

Huntington disease

Bates, G. P., Dorsey, R., Gusella, J. F., Hayden, M. R., Kay, C., Leavitt, B. R., Nance, M., Ross, C. A., Scahill, R. I., Wetzel, R., et al. (2015) · Nature Reviews Disease Primers

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

Cited by 1,641

Automatic classification of MR scans in Alzheimer’s disease.

Kloppel, S., Stonnington, C. M., Chu, C., Draganski, B., Scahill, R. I., Rohrer, J. D., Fox, N. C., Jack, C. R., Ashburner, J., & Frackowiak, R. S. J. (2008) · Brain

Dementia and Cognitive Impairment ResearchArtificial Intelligence in Healthcare

Cited by 1,170

Huntington disease: natural history, biomarkers and prospects for therapeutics

Ross, C. A., Aylward, E. H., Wild, E. J., Langbehn, D. R., Long, J. D., Warner, J. H., Scahill, R. I., Leavitt, B. R., Stout, J. C., Paulsen, J. S., et al. (2014) · Nature Reviews Neurology

Genetic Neurodegenerative DiseasesDeep Brain Stimulation and Movement Disorders

Cited by 1,016

Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: cross-sectional analysis of baseline data

Tabrizi, S. J., Langbehn, D. R., Leavitt, B. R., Roos, R. A., Durr, A., Craufurd, D., Kennard, C., Hicks, S. L., Fox, N. C., Scahill, R. I., et al. (2009) · The Lancet Neurology

Genetic Neurodegenerative DiseasesDeep Brain Stimulation and Movement Disorders

Cited by 984

Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease

Chan, D., Fox, N. C., Scahill, R. I., Crum, W. R., Whitwell, J. L., Leschziner, G., Rossor, A. M., Stevens, J. M., Cipolotti, L., & Rossor, M. N. (2001) · Annals of Neurology

Dementia and Cognitive Impairment ResearchNeurobiology of Language and Bilingualism

Cited by 749

Imaging of onset and progression of Alzheimer's disease with voxel-compression mapping of serial magnetic resonance images

Fox, N. C., Crum, W. R., Scahill, R. I., Stevens, J. M., Janssen, J. C., & Rossor, M. N. (2001) · The Lancet

Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments

Cited by 455

The clinical profile of right temporal lobe atrophy

Chan, D., Anderson, V., Pijnenburg, Y., Whitwell, J., Barnes, J., Scahill, R., Stevens, J. M., Barkhof, F., Scheltens, P., Rossor, M. N., et al. (2009) · Brain

Dementia and Cognitive Impairment ResearchNeurobiology of Language and Bilingualism

Cited by 377

Neurofilament light protein in blood as a potential biomarker of neurodegeneration in Huntington's disease: a retrospective cohort analysis

Byrne, L. M., Rodrigues, F. B., Blennow, K., Durr, A., Leavitt, B. R., Roos, R. A. C., Scahill, R. I., Tabrizi, S. J., Zetterberg, H., Langbehn, D., et al. (2017) · The Lancet Neurology

Genetic Neurodegenerative DiseasesHereditary Neurological Disorders

Cited by 364

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Moss, D. J. H., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., Coleman, A., Santos, R. D., et al. (2017) · The Lancet Neurology

Genetic Neurodegenerative DiseasesGenetic Associations and Epidemiology

Cited by 312

In vivo characterization of white matter pathology in premanifest huntington's disease

Zhang, J., Gregory, S., Scahill, R. I., Durr, A., Thomas, D. L., Lehericy, S., Rees, G., Tabrizi, S. J., Zhang, H., & the TrackOn‐HD investigators (2018) · Annals of Neurology

Advanced Neuroimaging Techniques and ApplicationsGenetic Neurodegenerative Diseases

Cited by 80

Embodied emotion impairment in Huntington’s disease

Trinkler, I., Devignevielle, S., Achaibou, A., Ligneul, R. V., Brugières, P., Cleret de Langavant, L., De Gelder, B., Scahill, R., Schwartz, S., & Bachoud-Lévi, A.-C. (2017) · Cortex

Genetic Neurodegenerative DiseasesAction Observation and Synchronization

Cited by 33