(Q53010655)

English

Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.

scientific article published on 25 September 2006

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scholarly article

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Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives. (English)

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

colorectal cancer

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based on heuristic

inferred from title

colorectal carcinoma

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based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Richard Houlston

15

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Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

object named as

Lara Bethke

5

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object named as

Richard Gray

13

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Olivia Fletcher

object named as

Olivia Fletcher

7

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14

object named as

Julian Peto

1 reference

Europe PubMed Central

10 May 2018

12

object named as

Ian Tomlinson

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Nichola Johnson

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object named as

Nichola Johnson

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

6

object named as

Wendy Wood

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Gabrielle S Sellick

3

object named as

Gabrielle S Sellick

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

author name string

Matthew F Rudd

2

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Rachid El Galta

4

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Steven Penegar

8

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Laura Withey

9

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

Mobshra Qureshi

10

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

publication date

25 September 2006

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Europe PubMed Central

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http://europepmc.org/abstract/MED/17000706

Human Molecular Genetics

1 reference

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http://europepmc.org/abstract/MED/17000706

15

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http://europepmc.org/abstract/MED/17000706

3263-3271

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http://europepmc.org/abstract/MED/17000706

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10 May 2018

http://europepmc.org/abstract/MED/17000706

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

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Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

1 reference

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The future of genetic studies of complex human diseases

1 reference

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21 January 2018

Polymorphisms and colorectal tumor risk

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

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Many amino acid substitution variants identified in DNA repair genes during human population screenings are predicted to impact protein function.

1 reference

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Functional consequences of ATM sequence variants for chromosomal radiosensitivity

1 reference

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21 January 2018

An allelic variant at the ATM locus is implicated in breast cancer susceptibility.

1 reference

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Functional impact of concomitant versus alternative defects in the Chk2-p53 tumour suppressor pathway.

1 reference

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Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2

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Cancer risks and mortality in heterozygous ATM mutation carriers

1 reference

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21 January 2018

CHEK2 is a multiorgan cancer susceptibility gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype

1 reference

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21 January 2018

Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage

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Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

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21 January 2018

Database resources of the National Center for Biotechnology Information: 2002 update

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Comparison of self-reported and database-linked family history of cancer data in a case-control study

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

The predicted impact of coding single nucleotide polymorphisms database

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Gene ontology: tool for the unification of biology

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

The KEGG resource for deciphering the genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Entrez Gene: gene-centered information at NCBI

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Human non-synonymous SNPs: server and survey

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Predicting deleterious amino acid substitutions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Identification of single nucleotide polymorphisms in human DNA repair genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Variants in DNA double-strand break repair genes and breast cancer susceptibility

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Genomic control for association studies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Genome-wide strategies for detecting multiple loci that influence complex diseases.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

A comparison of bayesian methods for haplotype reconstruction from population genotype data

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

A marginal likelihood approach for estimating penetrance from kin-cohort designs

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL401

21 January 2018

Identifiers

10.1093/HMG/DDL401

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

1 reference

Europe PubMed Central

10 May 2018

http://europepmc.org/abstract/MED/17000706

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