Managing hereditary gastrointestinal cancer syndromes: the partnership between genetic counselors and gastroenterologists

scientific article published on 16 September 2008

Managing hereditary gastrointestinal cancer syndromes: the partnership between genetic counselors and gastroenterologists is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1038/NCPGASTHEP1235
P698PubMed publication ID18797444

P2093author name stringWendy S Rubinstein
Scott M Weissman
P2860cites workRevised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instabilityQ24618618
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type XQ24618839
The frequency of Muir-Torre syndrome among Lynch syndrome familiesQ28268532
Genetic testing and counseling for hereditary forms of colorectal cancerQ33814001
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 geneQ33904639
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndromeQ33904733
Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2Q33910123
MLH1 and MSH2 protein expression as a pre-screening marker in hereditary and non-hereditary endometrial hyperplasia and cancerQ57200538
Accuracy of Colorectal Polyp Self-Reports: Findings from the Colon Cancer Family RegistryQ57268364
Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22Q57742300
Early Gastric Cancer in Young, Asymptomatic Carriers of Germ-Line E-Cadherin MutationsQ59182691
Keeping Pace with the Times — The Genetic Information Nondiscrimination Act of 2008Q60016790
Prophylactic Surgery to Reduce the Risk of Gynecologic Cancers in the Lynch SyndromeQ60167349
Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomasQ61195948
Progress in Genetic Testing, Classification, and Identification of Lynch SyndromeQ62978207
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)Q62978412
Breast cancer susceptibility genes: current challenges and future promisesQ71086291
Phenotypic and molecular characteristics of hyperplastic polyposisQ74127278
American Gastroenterological Association medical position statement: hereditary colorectal cancer and genetic testingQ74139327
MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancersQ74455966
Practice parameters for the identification and testing of patients at risk for dominantly inherited colorectal cancerQ74615205
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patientsQ80050907
Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patientsQ80539040
The "duty to warn" a patient's family members about hereditary disease risksQ80597182
Microsatellite instability is frequently observed in rectal cancer and influenced by neoadjuvant chemoradiationQ80734818
Molecular screening for the Lynch syndrome--better than family history?Q81716567
Hereditary colorectal cancer: risk assessment and managementQ34045183
Deficient DNA mismatch repair: a common etiologic factor for colon cancerQ34189020
AGA technical review on hereditary colorectal cancer and genetic testing.Q34299705
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).Q34306976
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).Q34557362
Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancersQ35022384
American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer SusceptibilityQ35105968
Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancerQ35443388
Attenuated familial adenomatous polyposis (AFAP). A review of the literatureQ35566208
Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instabilityQ35747961
The multiple colorectal adenoma phenotype and MYH, a base excision repair geneQ35854432
Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer historyQ35895179
Phenotypic characteristics and risk of cancer development in hyperplastic polyposis: case series and literature reviewQ35901489
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselorsQ35986971
Hereditary cancer predisposition syndromesQ36002146
The hamartomatous polyposis syndromes: a clinical and molecular reviewQ36018533
Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutationsQ36338216
Familial gastric polyposis revisited. Autosomal dominant inheritance confirmedQ36384186
Genetics, pathology, and clinics of familial gastric cancerQ36406529
The genetics of FAP and FAP-like syndromesQ36602699
Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic reviewQ36604730
Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patientsQ36890349
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?Q36905417
New issues in genetic counseling of hereditary colon cancerQ37002381
Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancerQ39582129
Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defectQ41852209
American founder mutation for attenuated familial adenomatous polyposisQ42100555
Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of functionQ43146864
Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutationsQ43915120
Gynecologic cancer prevention in Lynch syndrome/hereditary nonpolyposis colorectal cancer familiesQ46153060
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United StatesQ46655105
Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCC-like families: Problems in diagnosis, surveillance, and managementQ47301537
ASCO/SSO review of current role of risk-reducing surgery in common hereditary cancer syndromes.Q50789980
Banning genetic discrimination.Q52981673
Hyperplastic polyposis and diffuse carcinoma of the stomach. A study of a family.Q53479321
Standards of care in diagnosis and testing for hereditary colon cancer.Q54436204
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.Q55033068
The concise handbook of family cancer syndromes. Mayo Familial Cancer Program.Q55067670
P433issue10
P407language of work or nameEnglishQ1860
P921main subjectgastroenterologyQ120569
P304page(s)569-582
P577publication date2008-09-16
P1433published inNature Reviews Gastroenterology & HepatologyQ2108255
P1476titleManaging hereditary gastrointestinal cancer syndromes: the partnership between genetic counselors and gastroenterologists
P478volume5

Reverse relations

cites work (P2860)
Q38106642100 years Lynch syndrome: what have we learned about psychosocial issues?
Q38441095Candidate DNA repair susceptibility genes identified by exome sequencing in high-risk pancreatic cancer
Q21261903Duodenal carcinoma at the ligament of Treitz. A molecular and clinical perspective
Q55717557Frontiers in Gastrointestinal Oncology: Advances in Multi-Disciplinary Patient Care.
Q42434480Signs and genetics of rare cancer syndromes with gastroenterological features
Q34081267The genetic basis of Lynch syndrome and its implications for clinical practice and risk management

Search more.