Jon Beck

National Cancer Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

22h-index3.6kcitations45works3.52yr avg
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Research Topics

Prion Diseases and Protein Misfolding(16), Neurological diseases and metabolism(16), Amyotrophic Lateral Sclerosis Research(13), Trace Elements in Health(8), Alzheimer's disease research and treatments(7)

Publications45 total

Immunological responses and clinical outcomes in dogs with osteosarcoma receiving standard therapy and a Listeria vaccine expressing HER2
Molecular Therapy·2025· 7 cited
Cognitive dysfunction rapidly improves after closure of spinal CSF leaks - A treatable "spinal dementia"?
Brain and Spine·2024Open Access
Familial Creutzfeldt-Jakob disease in an Indian kindred
Annals of Indian Academy of Neurology·2019· 9 citedOpen Access
High prevalence of focal and multi-focal somatic genetic variants in the human brain
Nature Communications·2018· 75 citedOpen Access
Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series
Molecular Psychiatry·2018· 59 citedOpen Access
RARE STRUCTURAL GENETIC VARIATION IN HUMAN PRION DISEASES
Journal of Neurology Neurosurgery & Psychiatry·2016
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series
The Lancet Neurology·2016· 240 citedOpen Access
Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease
Neurobiology of Aging·2015· 71 citedOpen Access
K11 C9orf72 Expansions Are The Most Common Genetic Cause Of Huntington's Disease Phenocopy Presentations In A Uk Cohort
Journal of Neurology Neurosurgery & Psychiatry·2014· 2 cited
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion
Neurobiology of Aging·2014· 62 citedOpen Access
Predictive testing for inherited prion disease: report of 22 years experience
European Journal of Human Genetics·2014· 27 citedOpen Access
<i>C9orf72</i> expansions are the most common genetic cause of Huntington disease phenocopies
Neurology·2013· 200 citedOpen Access
A pathogenic <i>progranulin</i> mutation and <scp><i>C9orf72</i></scp> repeat expansion in a family with frontotemporal dementia
Neuropathology and Applied Neurobiology·2013· 40 citedOpen Access
A Novel Prion Disease Presenting with Diarrhea and Autonomic Neuropathy
UCL Discovery (University College London)·2013
A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy
New England Journal of Medicine·2013· 158 citedOpen Access
Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia
Acta Neuropathologica·2013· 133 citedOpen Access
O3–01–06: TREM2 variants and young‐onset Alzheimer's disease: A study of clinical phenotype
Alzheimer s & Dementia·2013Open Access
P1–182: Validation of next‐generation sequencing technologies to radically change dementia genetic diagnosis
Alzheimer s & Dementia·2013
The Presenilin 1 P264L Mutation Presenting as non-Fluent/Agrammatic Primary Progressive Aphasia
Journal of Alzheimer s Disease·2013· 18 citedOpen Access
Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population
The American Journal of Human Genetics·2013· 343 citedOpen Access
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Frequent Co-authors

Simon Mead(34), Nick C. Fox(16), Martin N. Rossor(16), John Collinge(16), Jason D. Warren(15), Jonathan D. Rohrer(12), Mark Poulter(11), Colin Mahoney(10), Tammaryn Lashley(10), Tamás Révész(9), Tracy Campbell(9), Jonathan M. Schott(8), James Uphill(7), John Hardy(7), Gary Adamson(7), Henry Houlden(7), James M. Polke(6), Adrian M. Isaacs(5), Sarah J. Tabrizi(5), John Collinge(5)