Architecture of inherited susceptibility to common cancer (Q37736259)

22 August 2017

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title

Architecture of inherited susceptibility to common cancer (English)

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22 August 2017

Richard S Houlston

2

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Olivia Fletcher

object named as

Olivia Fletcher

series ordinal

1

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language of work or name

English

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publication date

1 May 2010

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22 August 2017

published in

Nature Reviews Cancer

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22 August 2017

volume

10

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22 August 2017

issue

5

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22 August 2017

page(s)

353-361

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

22 August 2017

cites work

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Linkage of early-onset familial breast cancer to chromosome 17q21

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Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

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

31 March 2020

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Genetic mapping of a locus predisposing to human colorectal cancer

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Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

31 March 2020

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Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22

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Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands

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Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors

31 March 2020

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31 March 2020

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Implications of Familial Colorectal Cancer Risk Profiles and Microsatellite Instability Status

31 March 2020

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Breast cancer susceptibility-A new look at an old model

31 March 2020

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Polygenic susceptibility to breast cancer and implications for prevention

31 March 2020

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Common and rare variants in multifactorial susceptibility to common diseases

31 March 2020

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Breast and other cancers in families with ataxia-telangiectasia

31 March 2020

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Cancer risks in A-T heterozygotes

31 March 2020

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ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

31 March 2020

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Cancer risks and mortality in heterozygous ATM mutation carriers

31 March 2020

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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

31 March 2020

1 reference

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

31 March 2020

1 reference

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

31 March 2020

1 reference

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer

31 March 2020

1 reference

The CHEK2 gene and inherited breast cancer susceptibility

31 March 2020

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A recurrent mutation in PALB2 in Finnish cancer families.

31 March 2020

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Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women

31 March 2020

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Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

31 March 2020

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Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors

31 March 2020

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Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation

31 March 2020

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The future of genetic studies of complex human diseases

31 March 2020

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NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses

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Multiple ADH genes are associated with upper aerodigestive cancers

31 March 2020

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A common coding variant in CASP8 is associated with breast cancer risk

31 March 2020

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Genome-wide association study identifies novel breast cancer susceptibility loci

31 March 2020

1 reference

Multiple newly identified loci associated with prostate cancer susceptibility

31 March 2020

1 reference

A common variant associated with prostate cancer in European and African populations

31 March 2020

1 reference

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

31 March 2020

1 reference

Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

31 March 2020

1 reference

Common 5p15.33 and 6p21.33 variants influence lung cancer risk

31 March 2020

1 reference

Lung cancer susceptibility locus at 5p15.33

31 March 2020

1 reference

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

1 reference

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

31 March 2020

1 reference

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

31 March 2020

1 reference

Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer

31 March 2020

1 reference

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

31 March 2020

1 reference

Genome-wide association study identifies three loci associated with melanoma risk

31 March 2020

1 reference

A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

31 March 2020

1 reference

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

31 March 2020

1 reference

Genome-wide association study identifies five susceptibility loci for glioma

31 March 2020

1 reference

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility

31 March 2020

1 reference

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia

31 March 2020

1 reference

Germline genomic variants associated with childhood acute lymphoblastic leukemia

31 March 2020

1 reference

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia

31 March 2020

1 reference

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

31 March 2020

1 reference

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

31 March 2020

1 reference

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

31 March 2020

1 reference

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

31 March 2020

1 reference

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

1 reference

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

31 March 2020

1 reference

Calibrating the performance of SNP arrays for whole-genome association studies

31 March 2020

1 reference

Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms

31 March 2020

1 reference

A census of human cancer genes

31 March 2020

1 reference

Copy number variations and cancer

31 March 2020

1 reference

Copy number variation at 1q21.1 associated with neuroblastoma

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

1 reference

Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer

31 March 2020

1 reference

Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

31 March 2020

1 reference

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

31 March 2020

1 reference

Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study

31 March 2020

1 reference

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.

31 March 2020

1 reference

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

31 March 2020

1 reference

Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.

31 March 2020

1 reference

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

31 March 2020

1 reference

The strength of selection on ultraconserved elements in the human genome

31 March 2020

1 reference

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

31 March 2020

1 reference

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

31 March 2020

1 reference

The gene for familial polyposis coli maps to the long arm of chromosome 5.

31 March 2020

1 reference

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

31 March 2020

1 reference

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome

31 March 2020

1 reference

Identification of FAP locus genes from chromosome 5q21

31 March 2020

1 reference

Identification of deletion mutations and three new genes at the familial polyposis locus

31 March 2020

1 reference

Identification and characterization of the familial adenomatous polyposis coli gene

31 March 2020

1 reference

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

31 March 2020

1 reference

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

31 March 2020

1 reference

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

31 March 2020

1 reference

Mutation of a mutL homolog in hereditary colon cancer

31 March 2020

1 reference

Germline p16 mutations in familial melanoma

31 March 2020

1 reference

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

31 March 2020

1 reference

Identification of the breast cancer susceptibility gene BRCA2

31 March 2020

1 reference

E-cadherin germline mutations in familial gastric cancer.

31 March 2020

1 reference

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

31 March 2020

1 reference

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

31 March 2020

1 reference

Carcinogenesis in MYH-associated polyposis follows a distinct genetic pathway

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20414203

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20414203

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRC2840

1 reference

22 August 2017

1 reference