(Q80434469)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17551518%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families (English)

1 reference

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31 December 2019

4

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31 December 2019

10

Benedicte A Lie

1 reference

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31 December 2019

author name string

Silja Svanstrøm Amundsen

1

1 reference

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31 December 2019

Svetlana Adamovic

2

1 reference

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31 December 2019

Asa Hellqvist

3

1 reference

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31 December 2019

Audur H Gudjónsdóttir

5

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31 December 2019

Henry Ascher

6

1 reference

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31 December 2019

Johan Ek

7

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31 December 2019

Kristina Larsson

8

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31 December 2019

Jan Wahlström

9

1 reference

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31 December 2019

Ludvig M Sollid

11

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31 December 2019

Asa Torinsson Naluai

12

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31 December 2019

publication date

6 June 2007

1 reference

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European Journal of Human Genetics

31 December 2019

published in

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31 December 2019

volume

15

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31 December 2019

issue

9

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31 December 2019

page(s)

980-987

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201870

31 December 2019

exact match

0 references

cites work

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7 January 2021

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Genome search in celiac disease.

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Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

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7 January 2021

Genomewide linkage analysis of celiac disease in Finnish families

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7 January 2021

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201870

7 January 2021

An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland

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7 January 2021

Meta and pooled analysis of European coeliac disease data

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7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

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7 January 2021

The risk of celiac disease in 107 families with at least two affected siblings

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7 January 2021

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7 January 2021

Management of infantile gastroenteritis

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7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

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7 January 2021

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

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7 January 2021

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

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7 January 2021

Efficient multipoint linkage analysis through reduction of inheritance space

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7 January 2021

The family based association test method: strategies for studying general genotype--phenotype associations.

1 reference

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7 January 2021

Haplotype-based quantitative trait mapping using a clustering algorithm.

1 reference

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7 January 2021

Haplotype-based linkage disequilibrium mapping via direct data mining

1 reference

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7 January 2021

An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201870

7 January 2021

An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets

1 reference

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7 January 2021

Efficiency and consistency of haplotype tagging of dense SNP maps in multiple samples.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201870

7 January 2021

A haplotype map of the human genome

1 reference

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7 January 2021

Global variation in copy number in the human genome

1 reference

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7 January 2021

What a difference copy number variation makes

1 reference

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7 January 2021

1 reference

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7 January 2021

Will the real disease gene please stand up?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201870

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201870

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17551518%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference