Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer

scientific article published on 02 August 2019

Mutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.3389/FONC.2019.00673
P932PMC publication ID6688539
P698PubMed publication ID31428572

P2093author name stringDilyara Kaidarova
Leyla Djansugurova
Gulnur Zhunussova
Abai Jumanov
Anastassiya Perfilyeva
Georgiy Afonin
Saltanat Abdikerim
P2860cites workA map of human genome variation from population-scale sequencingQ24617794
Interplay between Fanconi anemia and homologous recombination pathways in genome integrityQ26753126
Epigenetic modifications in colorectal cancer: molecular insights and therapeutic challengesQ26823070
Integrative Genomics Viewer (IGV): high-performance genomics data visualization and explorationQ28264933
Hereditary and familial colon cancerQ28280647
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithmQ29547194
Integrative genomics viewerQ29547446
Peutz-Jeghers syndrome with germline mutation of STK11.Q33773686
Carcinoma of the anal canalQ33862619
Familial colorectal cancer: eleven years of data from a registry program in SwitzerlandQ33931803
Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory.Q34022144
BRCA-associated ovarian cancer: from molecular genetics to risk managementQ34032766
Deficient DNA mismatch repair: a common etiologic factor for colon cancerQ34189020
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular PathologyQ34465792
Mutation analysis of the adenomatous polyposis coli (APC) gene in Danish patients with familial adenomatous polyposis (FAP).Q50578226
Cancer Susceptibility Gene Mutations in Individuals With Colorectal CancerQ51162850
Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.Q52633302
BRCA1 mutations and colorectal cancer in PolandQ54409850
Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methodsQ57797237
Frequency of BRCA1 and BRCA2 Mutations in Unselected Ashkenazi Jewish Patients With Colorectal CancerQ57908288
Novel genetic mutations detected by multigene panel are associated with hereditary colorectal cancer predispositionQ58695957
Detection of five novel germline mutations of the APC gene in Irish familial adenomatous polyposis familiesQ74127887
Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutationQ74643959
APC gene mutations causing familial adenomatous polyposis in Polish patientsQ82706701
Colorectal Cancer Epidemiology: Incidence, Mortality, Survival, and Risk FactorsQ34624887
Ulcerative colitis and colorectal cancer. A population-based studyQ34634203
Hereditary colorectal cancer syndromes: molecular genetics, genetic counseling, diagnosis and management.Q34713100
Spectrum of AIDS-associated malignant disordersQ34748862
Genetics, Cytogenetics, and Epigenetics of Colorectal CancerQ34758641
Aetiology of colorectal cancer and relevance of monogenic inheritanceQ35596248
Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family RegistryQ35735103
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch SyndromeQ35998356
Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk ManagementQ36101775
BRCA1/2 associated hereditary breast cancerQ36426858
The frequency of the predominant Jewish mutations in BRCA1 and BRCA2 in unselected Ashkenazi colorectal cancer patientsQ36622655
Colorectal cancer carcinogenesis: a review of mechanismsQ36849645
Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancerQ36946787
Deficient DNA mismatch repair is common in Lynch syndrome-associated colorectal adenomasQ37164481
Hereditary colorectal cancer syndromes: familial adenomatous polyposis and lynch syndromeQ37232269
Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up studyQ37507426
ClinVar: public archive of relationships among sequence variation and human phenotypeQ37661886
Multigene Panel Testing Provides a New Perspective on Lynch SyndromeQ38780723
Global patterns and trends in colorectal cancer incidence and mortality.Q38915351
Update on Hereditary Colorectal Cancer.Q38954873
The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancerQ39778179
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal CancerQ40423712
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.Q41625837
Predicting functional effect of human missense mutations using PolyPhen-2.Q42406410
Association of DCC, MLH1, GSTT1, GSTM1, and TP53 gene polymorphisms with colorectal cancer in KazakhstanQ44991537
Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.Q45985357
Germline Genetic Features of Young Individuals with Colorectal CancerQ46385586
The colon cancer burden of genetically defined hereditary nonpolyposis colon cancerQ46652176
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P921main subjectcolorectal cancerQ188874
P304page(s)673
P577publication date2019-08-02
P1433published inFrontiers in OncologyQ26839986
P1476titleMutation Spectrum of Cancer-Associated Genes in Patients With Early Onset of Colorectal Cancer
P478volume9

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cites work (P2860)
Q98771176A Multiple Primary Malignancy Patient With FANCA Gene Mutation: A Case Report and Literature Review
Q132041261In Silico Deciphering of the Potential Impact of Variants of Uncertain Significance in Hereditary Colorectal Cancer Syndromes

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