Embed

Academic

Authors

Jonathan A. Beck

Jonathan A. Beck,University College London,Neuroscience,Genetics & Genealogy,Oncology

Edit

Jonathan A. Beck

University College London

Publications: 44 | Citations: 807

Fields: Neuroscience, Genetics & Genealogy, Oncology

Collaborated with 163 co-authors from 1995 to 2011 | Cited by 3045 authors

Cumulative Annual

Sort by:

Publications (44)

BibTeX | RIS | RefWorks Download

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay (Citations: 6)

, , , , , , , , , ,

Journal: Lancet , vol. 377, no. 9764, pp. 487-493, 2011

Progressive logopenic/phonological aphasia: erosion of the language network (Citations: 13)

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=6711777&selfId1=53452761&selfId2=0&maxNumber=12&query=

Journal: Neuroimage , vol. 49, no. 1, pp. 984-993, 2010

PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit (Citations: 4)

, , , , , , , , , ,

Journal: Human Mutation - HUM MUTAT , vol. 31, no. 7, pp. E1551-E1563, 2010

Relationship of a dominant advanced glycation end product, serum carboxymethyl-lysine, and abnormal glucose metabolism in adults: The baltimore longitudinal study of aging (Citations: 1)

, , , , , ,

Journal: Journal of Nutrition Health & Aging - J NUTR HEALTH AGING , vol. 14, no. 7, pp. 507-513, 2010

Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained (Citations: 1)

, , , , , , ,

Journal: Journal of Neurology Neurosurgery and Psychiatry - J NEUROL NEUROSURG PSYCHIAT , vol. 82, no. 9, pp. 1054-1057, 2010

Sort by:

Citations (807 times by 702 publications)

Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=57402373&selfId1=53452761&selfId2=0&maxNumber=12&query=

Journal: PLOS One , vol. 7, no. 2, 2012

Dietary intake associated with serum versus urinary carboxymethyl-lysine, a major advanced glycation end product, in adults: the Energetics Study

, , , , , , , ,

Journal: European Journal of Clinical Nutrition - EUR J CLIN NUTR , vol. 66, no. 1, pp. 3-9, 2012

Biochemical Properties of Highly Neuroinvasive Prion Strains

, , , , , , ,

Journal: PLOS Pathogens - PLOS PATHOG , vol. 8, no. 2, 2012

Gerstmann–Sträussler–Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt–Jakob disease: a case report and review of the literature

, , , , , , ,

Journal: Neurocase , vol. ahead-of-p, no. ahead-of-p, pp. 1-13, 2012

Dominant-negative effects in prion diseases: insights from molecular dynamics simulations on mouse prion protein chimeras

, , , , ,

Journal: Journal of Biomolecular Structure & Dynamics - J BIOMOL STRUCT DYN , vol. ahead-of-p, no. ahead-of-p, pp. 1-12, 2012

Comments

Co-authors (163)

Journals (28)

Keywords (112)

Jonathan A. Beck,University College London,Neuroscience,Genetics & Genealogy,Oncology

Publications (44)

BibTeX | RIS | RefWorks Download

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay (Citations: 6)

Progressive logopenic/phonological aphasia: erosion of the language network (Citations: 13)

PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit (Citations: 4)

Relationship of a dominant advanced glycation end product, serum carboxymethyl-lysine, and abnormal glucose metabolism in adults: The baltimore longitudinal study of aging (Citations: 1)

Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained (Citations: 1)

Citations (807 times by 702 publications)

Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

Dietary intake associated with serum versus urinary carboxymethyl-lysine, a major advanced glycation end product, in adults: the Energetics Study

Biochemical Properties of Highly Neuroinvasive Prion Strains

Gerstmann–Sträussler–Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt–Jakob disease: a case report and review of the literature

Dominant-negative effects in prion diseases: insights from molecular dynamics simulations on mouse prion protein chimeras


	View FAQ about top research areas and Fields of study

Jonathan A. Beck,University College London,Neuroscience,Genetics & Genealogy,Oncology

Publications (44) BibTeX | RIS | RefWorks Download

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay (Citations: 6)

Progressive logopenic/phonological aphasia: erosion of the language network (Citations: 13)

PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit (Citations: 4)

Relationship of a dominant advanced glycation end product, serum carboxymethyl-lysine, and abnormal glucose metabolism in adults: The baltimore longitudinal study of aging (Citations: 1)

Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained (Citations: 1)

Publications (44)

BibTeX | RIS | RefWorks Download