(Q34120176)

English

Effect of genome-wide association studies, direct-to-consumer genetic testing, and high-speed sequencing technologies on predictive genetic counselling for cancer risk

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

Europe PubMed Central

Effect of genome-wide association studies, direct-to-consumer genetic testing, and high-speed sequencing technologies on predictive genetic counselling for cancer risk (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

genome-wide association study

0 references

Michael R. Speicher

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

Jochen B Geigl

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Ian P Tomlinson

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

25 May 2010

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

Lancet Oncology Commission

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

890-898

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

BRCA1 and BRCA2: 1994 and beyond

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic predisposition to colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited susceptibility to common cancers

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Testing guidelines for hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Who should be sent for genetic testing in hereditary colorectal cancer syndromes?

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Standards of care in diagnosis and testing for hereditary colon cancer.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

"Genetic exceptionalism" in medicine: clarifying the differences between genetic and nongenetic tests

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic testing for colon cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of the gene for familial adenomatous polyposis on chromosome 5.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic mapping of a locus predisposing to human colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for clinicians

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Management of extracolonic tumours in patients with Lynch syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Results of national registration of familial adenomatous polyposis

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Feasibility of screening for Lynch syndrome among patients with colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Comprehensive Screening for Lynch Syndrome: Who Can Be the Driving Force in Daily Clinical Practice?

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Beyond odds ratios — communicating disease risk based on genetic profiles

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic mapping in human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of rising chemotherapy costs on the cost savings of colorectal cancer screening

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Apolipoprotein E and its receptors in Alzheimer's disease: pathways, pathogenesis and therapy

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Assessing New Biomarkers and Predictive Models for Use in Clinical Practice

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A common genetic risk factor for colorectal and prostate cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

WNT signaling in the normal intestine and colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mapping and sequencing of structural variation from eight human genomes

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Fine-scale structural variation of the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Copy number variation at 1q21.1 associated with neuroblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Copy number variations and cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The regulation of direct-to-consumer genetic tests

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic tests for common diseases: new insights, old concerns

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic horoscopes: is it all in the genes? Points for regulatory control of direct-to-consumer genetic testing

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Common vs. rare allele hypotheses for complex diseases

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Next-generation DNA sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The complete genome of an individual by massively parallel DNA sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Accurate whole human genome sequencing using reversible terminator chemistry

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The diploid genome sequence of an Asian individual

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A highly annotated whole-genome sequence of a Korean individual

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Single-molecule sequencing of an individual human genome

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The potential and challenges of nanopore sequencing

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation of consumer genomic tests remains in limbo

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Modifier genes and HNPCC: variable phenotypic expression in HNPCC and the search for modifier genes

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2809%2970359-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1470-2045(09)70359-6

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34120176&oldid=1766426698"