(Q34356036)

1 August 2017

title

Detection of disease-associated deletions in case-control studies using SNP genotypes with application to rheumatoid arthritis (English)

1 reference

1 August 2017

1 reference

4

Bo Peng

1 reference

1 August 2017

7

Peter K Gregersen

1 reference

1 August 2017

8

Christopher I Amos

1 reference

1 August 2017

Chih-Chieh Wu

1

1 reference

1 August 2017

Sanjay Shete

2

1 reference

1 August 2017

Wei V Chen

3

1 reference

1 August 2017

Annette T Lee

5

1 reference

1 August 2017

Jianzhong Ma

6

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1 August 2017

publication date

5 May 2009

1 reference

1 August 2017

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1 August 2017

volume

126

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1 August 2017

issue

2

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1 August 2017

page(s)

303-315

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-009-0672-3

1 August 2017

exact match

0 references

cites work

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Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays

6 July 2018

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Association between microdeletion and microduplication at 16p11.2 and autism

6 July 2018

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6 July 2018

1 reference

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Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

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6 July 2018

1 reference

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Strong association of de novo copy number mutations with autism

6 July 2018

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Relative impact of nucleotide and copy number variation on gene expression phenotypes

6 July 2018

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A comprehensive analysis of common copy-number variations in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Global variation in copy number in the human genome

6 July 2018

1 reference

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Copy number variation: new insights in genome diversity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

A complete genetic association scan of the 22q11 deletion region and functional evidence reveal an association between DGCR2 and schizophrenia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

6 July 2018

1 reference

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Calibrating a coalescent simulation of human genome sequence variation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Fine-scale structural variation of the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

The fine-scale structure of recombination rate variation in the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Presence of large deletions in kindreds with autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Chromosomal microdeletions: dissecting del22q11 syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

A method for detecting current temporal clusters of toxic events through data monitoring by poison control centers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

When did the human population size start increasing?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

The genetics revolution and the assault on rheumatoid arthritis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Sequence organisation of the class II region of the human MHC.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Structural organization of the DR subregion of the human major histocompatibility complex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

An approximation for the distribution of the scan statistic

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Statistical methods for anomalous discrete time series based on minimum cell count

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Common deletion polymorphisms in the human genome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Positional Identification of Microdeletions with Genetic Markers

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Whole-genome linkage analysis of rheumatoid arthritis susceptibility loci in 252 affected sibling pairs in the United Kingdom

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Common deletions and SNPs are in linkage disequilibrium in the human genome

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2992885

Probability of detecting disease-associated single nucleotide polymorphisms in case-control genome-wide association studies.

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19415332

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A high-resolution survey of deletion polymorphism in the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19415332

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Disease clusters, exact distributions of maxima, and P-values

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19415332

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-009-0672-3

1 reference

Dimensions Publication ID

1 August 2017

0 references

1 reference

1 August 2017

1 reference