Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study

QR Code

Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study

Bibliographic Details
Main Authors:	Mead, S., Poulter, M., Uphill, J., Beck, J., Whitfield, Jerome, Webb, T., Campbell, T., Adamson, G., Deriziotis, P., Tabrizi, S., Hummerich, H., Verzilli, C., Alpers, Michael Philip, Whittaker, J., Collinge, J.
Format:	Journal Article
Published:	The Lancet Publishing Group 2009
Online Access:	http://hdl.handle.net/20.500.11937/44701

Similar Items

A novel protective prion protein variant that colocalizes with Kuru exposure
by: Mead, S., et al.
Published: (2009)

Creutzfeldt-Jakob Disease (CJD) in Southeast Asia: a diagnostic challenge
by: Abdul Rashid, Anna Misya'il, et al.
Published: (2017)

Genetic susceptibility, evolution and the kuru epidemic
by: Mead, S., et al.
Published: (2008)

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
by: Mead, S., et al.
Published: (2012)

HECTD2 is associated with susceptibility to mouse and human prion disease
by: Lloyd, S., et al.
Published: (2009)

Mortuary rites of the South Fore and kuru
by: Whitfield, Jerome, et al.
Published: (2008)

Cultural factors that affected the spatial and temporal epidemiology of kuru
by: Whitfield, J., et al.
Published: (2017)

A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea
by: Collinge, J., et al.
Published: (2008)

Applying Jakob Nielsen's rules on Kor Suksis UMP portal (KSUP)
by: Noor Shafika Syuhada, Rosli
Published: (2012)

Philosophical Transactions of the Royal Society B: Biological Sciences - Introduction
by: Collinge, J., et al.
Published: (2008)

Reminiscences and reflections on kuru, personal and scientific
by: Collinge, J., et al.
Published: (2008)

Introduction
by: Collinge, J., et al.
Published: (2008)

Singapore English. Structure, variation and usage. Studies in English Language. By Jakob R. E. Leimgruber
by: Ansaldo, Umberto
Published: (2016)

Implementing Jakob Nielsenâ��s 10 Heuristics of usability in development of web based dental system (WEBDENT)
by: Nur Fadhilah, Che Nordin
Published: (2012)

Ergonomic study on eye discomfort for using ump website homepage by applying Jakob Nielsen’s heuristics
by: Iza Nor Afinie, Mohd Samuri
Published: (2013)

Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease
by: Brandner, S., et al.
Published: (2008)

Metaphysical personhood and traditional South Fore mortuary rites
by: Whitfield, J., et al.
Published: (2016)

Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study
by: Allen, Richard J., et al.
Published: (2017)

Genome-wide association scan of neuropathic pain symptoms post total joint replacement highlights a variant in the protein-kinase C gene
by: Warner, Sophie C., et al.
Published: (2017)

Disruption of diphenylalanine assembly by a Boc-modified variant
by: Creasey, Rhiannon, et al.
Published: (2016)

Joint Identification of Genetic Variants for Physical Activity inKorean Population
by: Kim, J., et al.
Published: (2014)

Structural and Functional Characterization of Ubiquitin Variant Inhibitors of USP15
by: Teyra, J., et al.
Published: (2019)

Exome array analysis suggests an increased variant burden in families with schizophrenia
by: McCarthy, N., et al.
Published: (2016)

The spitzer deep, wide-field survey
by: Ashby, M., et al.
Published: (2009)

Planned stage endovascular treatment for complex wide neck aneurysm
by: Ahmad Sobri M,, et al.
Published: (2011)

Findings in genome-wide association studies on asthma lack generalisation
by: Zhang, Guicheng, et al.
Published: (2010)

FRB Event Rate Predictions for the Ooty Wide Field Array
by: Bhattacharyya, S., et al.
Published: (2017)

The era of genome-wide association studies: Opportunities and challenges for asthma genetics
by: Zhang, Guicheng, et al.
Published: (2009)

A study on the validity of a four-variant diagnostic learning styles questionnaire
by: Goulding, J.S., et al.
Published: (2014)

A molecular tool to assess the pathological relevance of alpha-globin DNA variants
by: Qadah, T., et al.
Published: (2012)

SPACA3gene variants in a New Zealand cohort of infertile and fertile couples
by: Prendergast, Deborah, et al.
Published: (2014)

Genome-wide genetic investigation of serological measures of common infections
by: Rubicz, R., et al.
Published: (2015)

Identification of common variants associated with human hippocampal and intracranial volumes
by: Stein, J., et al.
Published: (2012)

Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens
by: Rubicz, R., et al.
Published: (2014)

Wide-band spectral variability of peaked spectrum sources
by: Ross, Kat, et al.
Published: (2022)

Interferometric Imaging with the 32 Element Murchison Wide-Field Array
by: Ord, S., et al.
Published: (2010)

Investigation of genetic variants, birthweight and hypothalamic-pituitary- adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the Western Australia Pregnancy Cohort (Raine) study
by: Anderson, L., et al.
Published: (2014)

Individual common variants exert weak effects on the risk for autism spectrum disorders
by: Anney, R., et al.
Published: (2012)

A genome-wide association study for malignant mesothelioma risk
by: Cadby, G., et al.
Published: (2013)

Genome-wide analysis in three Fusarium pathogens identifies rapidly evolving chromosomes and genes associated with pathogenicity
by: Sperschneider, J., et al.
Published: (2015)

Cannot write session to /tmp/vufind_sessions/sess_jeo8cke0tp8fk0flkgc8vqn4df