(Q28943413)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

title

Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe (English)

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

genome-wide association study

9 February 2020

main subject

0 references

Stevens–Johnson syndrome

1 reference

toxic epidermal necrolysis

inferred from title

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Luigi Naldi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Peggy Sekula

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Alain Hovnanian

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

author name string

Martin Schumacher

2

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Jean-Claude Roujeau

3

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Yvonne Liss

5

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Rémi Kazma

6

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Maja Mockenhaupt

9

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

publication date

29 July 2011

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

Orphanet Journal of Rare Diseases

9 February 2020

published in

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

volume

6

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

page(s)

52

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

9 February 2020

genome-wide association study

1 reference

https://scigraph.springernature.com/pub.10.1186/1750-1172-6-52

inferred from title

exact match

0 references

cites work

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Strong association between HLA-B*5801 and allopurinol-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in a Thai population

16 March 2017

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A European study of HLA-B in Stevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs

16 March 2017

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Principal components analysis corrects for stratification in genome-wide association studies

16 March 2017

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16 March 2017

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HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol

16 March 2017

1 reference

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Medical genetics: a marker for Stevens-Johnson syndrome

16 March 2017

1 reference

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

16 March 2017

1 reference

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A human genome diversity cell line panel

16 March 2017

1 reference

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Population genetic structure of variable drug response

16 March 2017

1 reference

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Genomic control for association studies

16 March 2017

1 reference

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Common and rare variants in multifactorial susceptibility to common diseases

7 April 2017

1 reference

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A HapMap harvest of insights into the genetics of common disease

7 April 2017

1 reference

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On the allelic spectrum of human disease

7 April 2017

1 reference

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Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies

7 April 2017

1 reference

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Optimizing the power of genome-wide association studies by using publicly available reference samples to expand the control group

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

Exploring the unknown: assumptions about allelic architecture and strategies for susceptibility variant discovery

3 June 2018

1 reference

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Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies

3 June 2018

1 reference

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Of race, ethnicity, and rash: the genetics of antiepileptic drug-induced skin reactions

3 June 2018

1 reference

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Toxic epidermal necrolysis and Stevens-Johnson syndrome: soluble Fas ligand involvement in the pathomechanisms of these diseases

3 June 2018

1 reference

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Assessing the evolutionary impact of amino acid mutations in the human genome

3 June 2018

1 reference

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fdrtool: a versatile R package for estimating local and tail area-based false discovery rates

3 June 2018

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On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

3 June 2018

1 reference

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Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

3 June 2018

1 reference

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A statistical method for predicting classical HLA alleles from SNP data

3 June 2018

1 reference

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Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

3 June 2018

1 reference

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A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

Genetic factors in the predisposition to drug-induced hypersensitivity reactions

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

A marker for Stevens-Johnson syndrome ...: ethnicity matters

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

Correlations between clinical patterns and causes of erythema multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis: results of an international prospective study

3 June 2018

1 reference

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3 June 2018

1 reference

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Genetic susceptibility to adverse drug reactions

3 June 2018

1 reference

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Update on cutaneous drug reactions.

3 June 2018

1 reference

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Severe adverse cutaneous reactions to drugs

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

Allopurinol is the most common cause of Stevens-Johnson syndrome and toxic epidermal necrolysis in Europe and Israel.

3 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-6-52

Stevens-Johnson syndrome and toxic epidermal necrolysis: assessment of medication risks with emphasis on recently marketed drugs. The EuroSCAR-study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-6-52

Investigation into the multidimensional genetic basis of drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-6-52

Investigation of the fine structure of European populations with applications to disease association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-6-52

High-resolution HLA genotyping and severe cutaneous adverse reactions in lamotrigine-treated patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-6-52

Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

HLA phenotypes and bullous cutaneous reactions to drugs.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173287

Epidemiology of erythema exsudativum multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis in Germany (1990-1992): structure and results of a population-based registry

26 November 2018

1 reference

12 December 2020

Familial hypersensitivity to allopurinol with subsequent desensitization

1 reference

12 December 2020

Familial occurrence of fixed drug eruptions

1 reference

12 December 2020

Genetic susceptibility to toxic epidermal necrolysis

1 reference

12 December 2020

Identifiers

DOI

10.1186/1750-1172-6-52

2 references

14 March 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

9 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21801394%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

2 references

14 March 2017