(Q28943533)

David J. Balding

18

0 references

Vincent Plagnol

Vincent Plagnol

13

0 references

John Whittaker

John Whittaker

17

0 references

Norman Klopp

9

Norman Klopp

1 reference

14 March 2017

19

Inga Zerr

1 reference

14 March 2017

8

Holger Hummerich

1 reference

14 March 2017

21

John Collinge

1 reference

14 March 2017

Simon Mead

1

1 reference

14 March 2017

James Uphill

2

1 reference

14 March 2017

John Beck

3

1 reference

14 March 2017

Mark Poulter

4

1 reference

14 March 2017

Tracy Campbell

5

1 reference

14 March 2017

Jessica Lowe

6

1 reference

14 March 2017

Gary Adamson

7

1 reference

14 March 2017

Ina-Maria Rückert

10

1 reference

14 March 2017

H.-Erich Wichmann

11

1 reference

14 March 2017

Wandagi H. Pako

14

1 reference

14 March 2017

Jerome Whitfield

15

1 reference

14 March 2017

Michael P. Alpers

16

1 reference

14 March 2017

Hans Kretzschmar

describes a project that uses

20

1 reference

14 March 2017

15 April 2012

1 reference

14 March 2017

Human Molecular Genetics

1 reference

14 March 2017

21

1 reference

14 March 2017

1897–1906

1 reference

14 March 2017

8

1 reference

14 March 2017

genome-wide association study

1 reference

A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Genome-wide association study reveals genetic risk underlying Parkinson's disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Genetic susceptibility, evolution and the kuru epidemic

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Many sequence variants affecting diversity of adult human height

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

A general model of prion strains and their pathogenicity

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

PLINK: a tool set for whole-genome association and population-based linkage analyses

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Exogenous induction of cerebral beta-amyloidogenesis is governed by agent and host

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Prion diseases of humans and animals: their causes and molecular basis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

A new multipoint method for genome-wide association studies by imputation of genotypes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Genomic control for association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Avoiding the high Bonferroni penalty in genome-wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

HECTD2 is associated with susceptibility to mouse and human prion disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Molecular neurology of prion disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Identification of multiple quantitative trait loci linked to prion disease incubation period in mice

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3313791

Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent

3 June 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

PRNP contains both intronic and upstream regulatory regions that may influence susceptibility to Creutzfeldt-Jakob Disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

Molecular classification of sporadic Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

First report of Creutzfeldt-Jakob disease occurring in 2 siblings unexplained by PRNP mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

Risk factors for sporadic Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

The same prion strain causes vCJD and BSE

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

Age of onset and death in inherited prion disease are heritable

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR607

Neurodegeneration. Could they all be prion diseases?

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22210626

12 December 2020

inferred from PubMed ID database lookup

Quantitative trait loci affecting prion incubation time in mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22210626

12 December 2020

inferred from PubMed ID database lookup

Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22210626

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1093/HMG/DDR607

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2428871

OpenCitations bibliographic resource ID

2428871

1 reference