(Q50483571)

English

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.

scientific article published on 12 November 2013

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scholarly article

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29 February 2020

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer (English)

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29 February 2020

genome-wide association study

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colorectal cancer

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based on heuristic

inferred from title

Ceres Fernández-rozadilla

1

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29 February 2020

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29 February 2020

Antoni Castells

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29 February 2020

Ángel Carracedo

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Maria Jesus Lamas

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29 February 2020

Luis A Lopez-Fernandez

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29 February 2020

Sergi Castellví-Bel

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I Tomlinson

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author name string

J B Cazier

2

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29 February 2020

A Brea-Fernández

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29 February 2020

M Baiget

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29 February 2020

J Clofent

8

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29 February 2020

D Gonzalez

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29 February 2020

L de Castro

11

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29 February 2020

EPICOLON Consortium

12

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29 February 2020

K Hemminki

13

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29 February 2020

X Bessa

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29 February 2020

M Andreu

15

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29 February 2020

R Jover

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29 February 2020

R Xicola

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29 February 2020

X Llor

18

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29 February 2020

C Ruiz-Ponte

23

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29 February 2020

publication date

12 November 2013

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29 February 2020

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29 February 2020

133

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29 February 2020

5

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29 February 2020

525-534

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29 February 2020

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

https://scigraph.springernature.com/pub.10.1007/s00439-013-1390-4

0 references

The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Origins and functional impact of copy number variation in the human genome

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

1 reference

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21 January 2018

Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Structural variants: changing the landscape of chromosomes and design of disease studies

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Influence of obesity on the risk of developing colon cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body mass

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Copy number variation accuracy in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Copy-number variation and association studies of human disease

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Integrated detection and population-genetic analysis of SNPs and copy number variation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Copy-number variation in control population cohorts

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Challenges and standards in integrating surveys of structural variation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Dosage sensitivity shapes the evolution of copy-number varied regions.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Genome-wide association studies: theoretical and practical concerns

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Comparing CNV detection methods for SNP arrays

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1390-4

21 January 2018

Colorectal cancer genetics: from candidate genes to GWAS and back again

1 reference

https://pubmed.ncbi.nlm.nih.gov/24218287

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation is the spice of life

1 reference

https://pubmed.ncbi.nlm.nih.gov/24218287

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The new genomics: global views of biology

1 reference

https://pubmed.ncbi.nlm.nih.gov/24218287

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide polymorphisms in the Wnt and BMP pathways and colorectal cancer risk in a Spanish cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/24218287

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-013-1390-4

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29 February 2020

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24 November 2022

based on heuristic

mapped directly with Wikidata item

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29 February 2020

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