D. Hensman

发表

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

L. Petrucelli, S. Mead, J. Collinge, 2013, Acta Neuropathologica.

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

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

Nick C Fox, Colin J. Mahoney, J. Hardy, 2013, American journal of human genetics.

ORIGINAL ARTICLE: Assessment of cardiac valve dysfunction in patients receiving cabergoline treatment for hyperprolactinaemia

P. Nihoyannopoulos, N. Martin, W. Dhillo, 2010, Clinical endocrinology.

Role of neuroimaging in the evaluation of tremor.

P. Bain, D. Hensman, 2010, Neuroimaging clinics of North America.

POPULATION FREQUENCY OF REPEAT EXPANSIONS INDICATES INCREASED DISEASE PREVALENCE ESTIMATES ACROSS DIFFERENT POPULATIONS

M. Caulfield, A. Sharp, M. Shoai, 2023, medRxiv.

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

Nick C Fox, Colin J. Mahoney, J. Hodges, 2013, American journal of human genetics.

Assessment of cardiac valve dysfunction in patients receiving cabergoline treatment for hyperprolactinaemia.

P. Nihoyannopoulos, N. Martin, W. Dhillo, 2010, Clinical endocrinology.

Intellectual enrichment and genetic modifiers of cognitive function in Huntington's disease

Langbehn, P. Holmans, D. Langbehn, 2022, medRxiv.