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Lista de obras de Henricus Franciscus Antonius Vasen

8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.

artículo científico publicado en 2011

A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.

artículo científico publicado en 2010

A cost-effectiveness analysis of colorectal screening of hereditary nonpolyposis colorectal carcinoma gene carriers

scientific article published on 01 May 1998

A cost‐effectiveness analysis of colorectal screening for hereditary nonpolyposis colorectal carcinoma gene carriers

article

A genome wide linkage search for breast cancer susceptibility genes

artículo científico publicado en 2006

A hundred years of Lynch syndrome research (1913-2013).

artículo científico publicado en 2013

A nation-wide study comparing sporadic and familial adenomatous polyposis-related desmoid-type fibromatoses.

artículo científico publicado en 2010

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis.

artículo científico publicado en 1991

A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families

artículo científico publicado en 2018

A pooled analysis of the outcome of prospective colonoscopic surveillance for familial colorectal cancer

artículo científico publicado en 2013

A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer

artículo científico publicado en 2007

A prospective study on predictive factors linked to the presence of BRCA1 and BRCA2 mutations in breast cancer patients

artículo científico publicado en 2005

A randomized placebo-controlled prevention trial of aspirin and/or resistant starch in young people with familial adenomatous polyposis

artículo científico publicado en 2011

A thirty-year follow-up surveillance study for neoplasia of a dutch ulcerative colitis cohort

artículo científico publicado en 2013

APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis.

artículo científico publicado en 1995

APC mutations are associated with increased bone mineral density in patients with familial adenomatous polyposis

artículo científico publicado en 2010

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

artículo científico publicado en 2007

Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families

artículo científico publicado en 2019

Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

artículo científico publicado en 1995

An Evidence-Based Review on Surveillance for Lynch Syndrome

article

An Overview of the Lynch Syndrome (Hereditary Non-polyposis Colorectal Cancer)

An alternative to prophylactic colectomy for colon cancer prevention in HNPCC syndrome.

artículo científico publicado en 2005

Analysis of MUTYH Genotypes and Colorectal Phenotypes in Patients With MUTYH-Associated Polyposis

scientific article published on 30 October 2008

Application of a Serum Protein Signature for Pancreatic Cancer to Separate Cases from Controls in a Pancreatic Surveillance Cohort.

artículo científico publicado en 2016

Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome

scientific article published on 08 January 2020

Attitudes toward genetic testing in childhood and reproductive decision-making for familial adenomatous polyposis.

artículo científico publicado en 2009

Author reply

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

artículo científico publicado en 1997

Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.

artículo científico publicado en 2003

Benefit of Surveillance for Pancreatic Cancer in High-Risk Individuals: Outcome of Long-Term Prospective Follow-Up Studies From Three European Expert Centers

artículo científico publicado en 2016

Body mass index increases risk of colorectal adenomas in men with Lynch syndrome: the GEOLynch cohort study

artículo científico publicado en 2010

Body weight and risk of breast cancer in BRCA1/2 mutation carriers ⬇️

artículo científico publicado el 21 de agosto de 2010

CHEK2 1100delC Is a Susceptibility Allele for HNPCC-Related Colorectal Cancer

scientific article published on 01 August 2008

CM-Score: a validated scoring system to predict CDKN2A germline mutations in melanoma families from Northern Europe

artículo científico publicado en 2018

Can the identification of high risk groups increase the effectiveness of colon cancer screening programmes?

artículo científico publicado en 2008

Cancer Risks for PMS2-Associated Lynch Syndrome

artículo científico publicado en 2018

Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

artículo científico publicado en 2015

Cancer occurrence during follow-up of the CAPP2 study -aspirin use for up to four years significantly reduces Lynch syndrome cancers for up to several years after completion of therapy.

artículo científico publicado en 2010

Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome

artículo científico publicado en 2014

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

artículo científico publicado en 2017

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

artículo científico publicado en 1996

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

artículo científico publicado en 2004

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

scientific article published on 24 July 2019

Cancer risks in BRCA2 families: estimates for sites other than breast and ovary.

artículo científico publicado en 2005

Cancer: Lynch syndrome--how should colorectal cancer be managed?

artículo científico publicado en 2011

Characteristics of Lynch syndrome associated ovarian cancer

artículo científico publicado en 2018

Characteristics of small bowel carcinoma in hereditary nonpolyposis colorectal carcinoma. International Collaborative Group on HNPCC.

artículo científico publicado en 1998

Characterization of Familial Non-BRCA1/2 Breast Tumors by Loss of Heterozygosity and Immunophenotyping

artículo científico publicado en 2006

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

artículo científico publicado en 2008

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

article by Juul T. Wijnen et al published 20 August 1998 in The New England Journal of Medicine

Clinical Utility Gene Card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP)--update 2014.

artículo científico publicado en 2014

Clinical and histologic characteristics of malignant melanoma in families with a germline mutation in CDKN2A.

artículo científico publicado en 2011

Clinical evidence for an association between familial adenomatous polyposis and type II diabetes.

artículo científico publicado en 2012

Clinical heterogeneity of familial colorectal cancer and its influence on screening protocols.

artículo científico publicado en 1994

Clinical heterogeneity of hereditary breast cancer and its impact on screening protocols: The dutch experience on 24 families under surveillance

artículo científico publicado en 1993

Clinical management of hereditary colorectal cancer syndromes

artículo científico publicado en 2015

Clinical utility gene card for: familial adenomatous polyposis (FAP) and attenuated FAP (AFAP).

artículo científico publicado en 2011

Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22.

artículo científico publicado en 1988

Colectomy and ileorectal anastomosis is still an option for selected patients with familial adenomatous polyposis

artículo científico publicado en 2008

Colonoscopy in Lynch syndrome: the need for a new quality score.

artículo científico publicado en 2017

Colorectal cancer and family history.

artículo científico publicado en 2000

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2017

Colorectal cancer risk in HNPCC families: Development during lifetime and in successive generations

article

Colorectal cancer risk in HNPCC families: development during lifetime and in successive generations. National Collaborative Group on HNPCC

scientific article published on 01 July 1997

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.

artículo científico publicado en 2016

Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis

artículo científico publicado en 2013

Colorectal carcinomas in MUTYH-associated polyposis display histopathological similarities to microsatellite unstable carcinomas

artículo científico publicado en 2009

Colorectal surveillance in Lynch syndrome families.

artículo científico publicado en 2013

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

artículo científico publicado en 2012

Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer

article

Consequences of CT colonography in stenosing colorectal cancer

scientific article published on 25 October 2016

Consequences of testing for mismatch repair deficiency of colorectal cancer in clinical practice

artículo científico publicado en 2017

Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy

artículo científico publicado en 2018

Constitutional or biallelic? Settling on a name for a recessively inherited cancer susceptibility syndrome.

artículo científico publicado en 2015

Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors

artículo científico publicado en 2003

Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

artículo científico publicado en 2020

Correction: Dietary Supplement Use and Colorectal Adenoma Risk in Individuals with Lynch Syndrome: The GEOLynch Cohort Study.

artículo científico publicado en 2014

Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.

artículo científico publicado en 2006

Correspondence re: A. Müller et al., Exclusion of breast cancer as an integral tumor of hereditary nonpolyposis colorectal cancer. Cancer Res., 62: 1014-1019, 2002

artículo científico publicado en 2003

Cost-utility analysis of genetic screening in families of patients with germline MUTYH mutations

artículo científico publicado en 2007

Cumulative risk of developing polyps or malignancy at the ileal pouch—anal anastomosis in patients with familial adenomatous polyposis

scientific article published on 01 May 1999

Decision analysis in the management of duodenal adenomatosis in familial adenomatous polyposis.

artículo científico publicado en 1997

Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect

artículo científico publicado en 2003

Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy

scientific article published on 16 September 2019

Decrease in mortality in Lynch syndrome families because of surveillance.

artículo científico publicado en 2006

Desmoid tumors in a dutch cohort of patients with familial adenomatous polyposis

artículo científico publicado en 2008

Desmoid tumors in patients with familial adenomatous polyposis

artículo científico publicado en 2002

Detection of pancreatic cancer using serum protein profiling.

artículo científico publicado en 2012

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

artículo científico publicado en 2015

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

artículo científico publicado en 2006

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD).

artículo científico

Diagnostic value of targeted next-generation sequencing in patients with suspected pancreatic or periampullary cancer.

artículo científico publicado en 2017

Diet quality and colorectal tumor risk in persons with Lynch syndrome

scientific article published on 15 September 2020

Dietary B vitamin and methionine intake and MTHFR C677T genotype on risk of colorectal tumors in Lynch syndrome: the GEOLynch cohort study

artículo científico publicado en 2014

Dietary Supplement Use and Colorectal Adenoma Risk in Individuals with Lynch Syndrome: The GEOLynch Cohort Study

artículo científico publicado en 2013

Dietary patterns and colorectal adenomas in Lynch syndrome: the GEOLynch cohort study

artículo científico publicado en 2012

Dilatation of the main pancreatic duct as first manifestation of small pancreatic ductal adenocarcinomas detected in a hereditary pancreatic cancer surveillance program

scientific article published on 22 March 2019

Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer

artículo científico publicado en 2016

Disease expression in juvenile polyposis syndrome: a retrospective survey on a cohort of 221 European patients and comparison with a literature-derived cohort of 473 SMAD4/BMPR1A pathogenic variant carriers

artículo científico publicado en 2020

Do lifestyle factors influence colorectal cancer risk in Lynch syndrome?

artículo científico publicado en 2013

Double balloon endoscopy for detection of small-bowel adenomas in familial adenomatous polyposis after pancreaticoduodenectomy according to Whipple

artículo científico publicado en 2008

Duodenal adenomatosis in familial adenomatous polyposis

artículo científico publicado en 1995

Duodenal adenomatosis in familial adenomatous polyposis.

artículo científico publicado en 2004

Duodenal adenomatosis in familial adenomatous polyposis.

artículo científico publicado en 2004

Duodenal surveillance improves the prognosis after duodenal cancer in familial adenomatous polyposis.

artículo científico publicado en 2012

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2003

Early detection of breast and ovarian cancer in families with BRCA mutations.

artículo científico publicado en 2005

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

artículo científico publicado en 2008

Effectiveness and causes for failure of surveillance of CDKN2A-mutated melanoma families.

artículo científico publicado en 2011

Efficacy of early diagnosis and treatment in women with a family history of breast cancer. European Familial Breast Cancer Collaborative Group.

artículo científico publicado en 1999

Endometrial Cancer in Four Sisters: Report of a Kindred with Presumed Cancer Family Syndrome

artículo científico publicado en 1994

Endoscopic full thickness resection for early colon cancer in Lynch syndrome.

artículo científico publicado en 2019

Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort

artículo científico publicado en 2009

Environmental factors and colorectal tumor risk in individuals with hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2007

Equivalent Helicobacter pylori infection rates in Lynch syndrome mutation carriers with and without a first-degree relative with gastric cancer

artículo científico publicado en 2016

Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families.

artículo científico publicado en 2017

Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium

artículo científico publicado en 2002

Evaluation of management of desmoid tumours associated with familial adenomatous polyposis in Dutch patients.

artículo científico publicado en 2010

Evidence for accelerated colorectal adenoma–carcinoma progression inMUTYH-associated polyposis?

artículo científico publicado en 2011

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

artículo científico publicado en 2017

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

artículo científico publicado en 2017

Exome sequencing of germline DNA from non-BRCA1/2 familial breast cancer cases selected on the basis of aCGH tumor profiling

artículo científico publicado en 2013

Expanded extracolonic tumor spectrum in MUTYH-associated polyposis

artículo científico publicado en 2009

Experience of discharge from colonoscopy of mutation negative HNPCC family members.

artículo científico publicado en 2003

Extending the p16-Leiden tumour spectrum by respiratory tract tumours

artículo científico publicado en 2004

Extracolonic Manifestations of Familial Adenomatous Polyposis: Desmoid Tumours, and Upper Gastrointestinal Adenomas and Carcinomas ⬇️

artículo científico publicado el 1 de enero de 1998

Extracolonic cancer risk in Dutch patients with APC (adenomatous polyposis coli)-associated polyposis

artículo científico publicado en 2017

Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives

artículo científico publicado en 2013

Familial Pancreatic Cancer: To Screen or not to Screen?

artículo científico publicado en 2015

Familial adenomatous polyposis and its clinical surveillance.

artículo científico publicado en 1993

Familial adenomatous polyposis: from bedside to bench and vice versa. A tribute to the somatic cell geneticist P. Meera Khan.

artículo científico publicado en 1999

Familial and hereditary non-polyposis colorectal cancer: issues relevant for surgical practice

artículo científico publicado en 1998

Familial endometrial cancer in female carriers of MSH6 germline mutations

artículo científico publicado en 1999

Family history, surgery, and APC mutation are risk factors for desmoid tumors in familial adenomatous polyposis: an international cohort study.

artículo científico publicado en 2011

Female fertility after colorectal surgery for familial adenomatous polyposis: a nationwide cross-sectional study

artículo científico publicado en 2010

From gene to disease; MutYH-associated polyposis coli (MAP)

artículo científico publicado en 2005

From gene to disease; from DNA 'mismatch' repair genes to hereditary non-polyposis colorectal carcinoma

artículo científico publicado en 2001

Gene-environment interaction in hereditary nonpolyposis colorectal cancer with implications for diagnosis and genetic testing.

artículo científico publicado en 1999

Genetic analysis of a breast-ovarian cancer family, with 7 cases of colorectal cancer linked toBRCA1, fails to support a role forBRCA1 in colorectal tumorigenesis

scientific article published on 01 December 2000

Genetic counseling in hereditary nonpolyposis colorectal cancer

scientific article published on 01 January 1996

Genetic testing in familial melanoma: uptake and implications.

artículo científico publicado en 2008

Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome

artículo científico publicado en 2012

Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas.

artículo científico

Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus

artículo científico publicado en 2008

Genome-wide scanning for linkage in 56 Dutch breast cancer families selected for a minimal probability of being due to BRCA1 or BRCA2.

artículo científico publicado en 2005

Genotype predicting phenotype in familial adenomatous polyposis: a practical application to the choice of surgery.

artículo científico publicado en 2009

Genotype-phenotype correlations as a guide in the management of familial adenomatous polyposis.

artículo científico publicado en 2007

Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants

artículo científico publicado en 2020

Genotype-phenotype correlations in 19 Dutch cases with APC gene deletions and a literature review.

artículo científico publicado en 2007

Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study

artículo científico publicado en 2006

Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.

artículo científico publicado en 2007

Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.

artículo científico publicado en 1996

Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer

artículo científico publicado en 2014

Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D)

scientific article published on 20 February 2014

Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).

artículo científico publicado en 2007

Guidelines for the clinical management of familial adenomatous polyposis (FAP).

artículo científico publicado en 2008

Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population.

artículo científico publicado en 2010

Health, life, and disability insurance and hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 1998

Height and Colorectal and Endometrial Cancer Risk for Persons with Lynch Syndrome

scientific article published on 17 August 2020

Hereditary Colorectal Cancer

Hereditary Nonpolyposis Colorectal Cancer

artículo científico publicado en 1994

Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry

artículo científico publicado en 2016

Hereditary medullary thyroid carcinoma

artículo científico publicado en 1995

Hereditary nonpolyposis colorectal cancer: results of long-term surveillance in 50 families

scientific article published on 01 July 1995

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).

artículo científico publicado en 2006

High Growth Rate of Pancreatic Ductal Adenocarcinoma inCDKN2A-p16-LeidenMutation Carriers

scientific article published on 10 July 2018

High detection rate of adenomas in familial colorectal cancer ⬇️

artículo científico publicado el 9 de septiembre de 2010

High frequency of copy-neutral LOH inMUTYH-associated polyposis carcinomas

artículo científico publicado en 2008

High risk of endometrial cancer in colorectal cancer kindred is pathognomonic for MMR-mutation carriers

artículo científico publicado en 2008

High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations.

artículo científico publicado en 2015

History of the International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer

artículo científico publicado en 2003

Identification and management of Lynch syndrome in the Middle East and North African countries: outcome of a survey in 12 countries

artículo científico publicado en 2020

Identification of HNPCC by molecular analysis of colorectal and endometrial tumors.

artículo científico publicado en 2004

Identification of familial colorectal cancer and hereditary colorectal cancer syndromes through the Dutch population-screening program: results ofa pilot study

artículo científico publicado en 2016

Identification of patients with (atypical) MUTYH-associated polyposis by KRAS2 c.34G > T prescreening followed by MUTYH hotspot analysis in formalin-fixed paraffin-embedded tissue.

artículo científico publicado en 2008

Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis

artículo científico publicado en 2000

Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysis

artículo científico publicado en 2014

Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

artículo científico publicado en 2016

Incidence of small bowel neoplasia in Lynch syndrome assessed by video capsule endoscopy

artículo científico publicado en 2017

Inclusion of malignant fibrous histiocytoma in the tumour spectrum associated with hereditary non-polyposis colorectal cancer

article

Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancer

artículo científico publicado en 2010

Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma Families

artículo científico publicado en 2008

Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.

artículo científico publicado en 2009

Increased prevalence of Barrett's esophagus in patients with MUTYH-associated polyposis (MAP)

artículo científico publicado en 2020

Increased prevalence of colonic adenomas in patients with acromegaly.

artículo científico publicado en 1994

Increased risk of colorectal neoplasia in asymptomatic liver-transplant recipients.

artículo científico publicado en 2007

Infiltration of Lynch Colorectal Cancers by Activated Immune Cells Associates with Early Staging of the Primary Tumor and Absence of Lymph Node Metastases

artículo científico publicado en 2012

Inflammatory potential of the diet and colorectal tumor risk in persons with Lynch syndrome

artículo científico publicado en 2017

Informing one's family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study

artículo científico publicado en 2005

Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers

artículo científico publicado en 2019

Interval cancers in hereditary non-polyposis colorectal cancer (Lynch syndrome)

scientific article published on 01 May 1995

Is a colorectal neoplasm diagnosis a trigger to change dietary and other lifestyle habits for persons with Lynch syndrome? A prospective cohort study

artículo científico publicado en 2020

Is breast cancer part of the tumor spectrum of hereditary nonpolyposis colorectal cancer?

artículo científico publicado en 2001

Is colorectal surveillance indicated in patients with PTEN mutations?

artículo científico publicado en 2012

Is surveillance of the small bowel indicated for Lynch syndrome families?

artículo científico publicado en 2007

Kluwer Academic Publishers: Familial Cancer

announcement of journal

Known susceptibility SNPs for sporadic prostate cancer show a similar association with “hereditary” prostate cancer

scientific article published on 05 January 2015

Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report

scientific article published on 28 February 2019

Limited resection of pancreatic cancer in high-risk patients can result in a second primary: Table 1

scientific article published on 02 April 2015

Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures

article

Long-term compliance with endoscopic surveillance for familial adenomatous polyposis.

artículo científico publicado en 2010

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

artículo científico publicado en 2011

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

article

Loss of ARID1A expression and its relationship with PI3K-Akt pathway alterations, TP53 and microsatellite instability in endometrial cancer.

artículo científico publicado en 2013

Loss-of-Function Mutations in the Cell-Cycle Control Gene CDKN2A Impact on Glucose Homeostasis in Humans. ⬇️

artículo científico publicado en 2015

Low frequency of POLD1 and POLE exonuclease domain variants in patients with multiple colorectal polyps

artículo científico publicado en 2019

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk

artículo científico publicado en 2014

MSH2 genomic deletions are a frequent cause of HNPCC

article

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

artículo científico publicado en 2001

MUTYH-associated polyposis (MAP)

artículo científico publicado en 2011

MUTYH-associated polyposis carcinomas frequently lose HLA class I expression - a common event amongst DNA-repair-deficient colorectal cancers

artículo científico publicado en 2009

Magnetic resonance imaging surveillance detects early-stage pancreatic cancer in carriers of a p16-Leiden mutation

artículo científico publicado en 2010

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

artículo científico publicado en 1996

Management of patients with increased risk for familial pancreatic cancer: updated recommendations from the International Cancer of the Pancreas Screening (CAPS) Consortium

artículo científico publicado en 2019

Massive gastric polyposis associated with a germline SMAD4 gene mutation

artículo científico publicado en 2015

Meat consumption and meat preparation in relation to colorectal adenomas among sporadic and HNPCC family patients in The Netherlands

artículo científico publicado en 2002

Meat consumption and preparation, and genetic susceptibility in relation to colorectal adenomas

scientific article published on 01 March 1997

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2004

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

article

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

artículo científico publicado en 1997

Molecular characterization of the spectrum of genomic deletions in the mismatch repair genesMSH2,MLH1,MSH6, andPMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)

article

Molecular genetic tests as a guide to surgical management of familial adenomatous polyposis

artículo científico publicado en 1996

Molecular genetic tests in surgical management of familial adenomatous polyposis

artículo científico publicado en 1998

Multiple endocrine neoplasia syndrome type 2: The value of screening and central registration

artículo científico publicado en 1987

Multiple endocrine neoplasia syndromes

artículo científico publicado en 1984

Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors

article

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

artículo científico publicado en 2004

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

artículo científico publicado en 1997

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

artículo científico publicado en 1999

No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

artículo científico publicado en 2018

No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in and : A Prospective Lynch Syndrome Database Study

artículo científico publicado en 2021

No major difference in K-ras and p53 abnormalities in sporadic and hereditary nonpolyposis colorectal adenomas.

artículo científico publicado en 2000

Non-allelic heterogeneity of familial adenomatous polyposis.

artículo científico publicado en 1993

Nonpolypoid colorectal neoplasms: a challenge in endoscopic surveillance of patients with Lynch syndrome.

artículo científico publicado en 2013

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

artículo científico publicado en 2015

Occurrence of thyroid carcinoma in Dutch patients with familial adenomatous polyposis. An epidemiological study and report of new cases

artículo científico publicado en 1998

One to 2-year surveillance intervals reduce risk of colorectal cancer in families with Lynch syndrome

artículo científico publicado en 2010

Optimizing the timing of colorectal surgery in patients with familial adenomatous polyposis in clinical practice

scientific article published on 01 June 2019

Outcome of ovarian cancer after breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2016

Ovarian cancer in Lynch syndrome; a systematic review.

artículo científico publicado en 2016

Ovarian metastases of colorectal and duodenal cancer in familial adenomatous polyposis

artículo científico publicado en 2012

Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study

artículo científico publicado en 2015

Pancreatic carcinoma in carriers of a specific 19 base pair deletion of CDKN2A/p16 (p16-leiden).

artículo científico publicado en 2003

Pheochromocytoma in multiple endocrine neoplasia type 2: European study

scientific article published on 01 October 1995

Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers

artículo científico publicado en 2009

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

article

Preface

Prevalence of adenomas among young individuals at average risk for colorectal cancer.

artículo científico publicado en 2005

Prevalence of small-bowel neoplasia in Lynch syndrome assessed by video capsule endoscopy

scientific article published on 10 September 2014

Progress in Genetic Testing, Classification, and Identification of Lynch Syndrome

artículo científico publicado en 2005

Prospective results of surveillance colonoscopy in dominant familial colorectal cancer with and without Lynch syndrome

artículo científico publicado en 2006

Prospective risk of cancer and the influence of tobacco use in carriers of the p16-Leiden germline variant

artículo científico publicado en 2014

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

artículo científico publicado en 2018

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

artículo científico publicado en 2018

Psychological distress and quality of life following positive fecal occult blood testing in colorectal cancer screening

artículo científico publicado en 2020

Psychological distress and quality of life of partners of individuals with familial adenomatous polyposis.

artículo científico publicado en 2011

Psychological distress and use of psychosocial support in familial adenomatous polyposis.

artículo científico publicado en 2010

Psychosocial issues in genetic testing for familial adenomatous polyposis: a review of the literature.

artículo científico publicado en 2008

Quality colonoscopy and risk of interval cancer in Lynch syndrome

artículo científico publicado en 2013

Quality of colonoscopy in Lynch syndrome

artículo científico publicado en 2014

Quality of life after surgery for colon cancer in patients with Lynch syndrome: partial versus subtotal colectomy

artículo científico publicado en 2012

Quality of life after total colectomy with ileorectal anastomosis or proctocolectomy and ileal pouch-anal anastomosis for familial adenomatous polyposis.

artículo científico publicado en 2000

Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients

artículo científico publicado en 2010

Randomized Comparison of Surveillance Intervals in Familial Colorectal Cancer

artículo científico publicado en 2015

Rapid detection of BRCA1 mutations by the protein truncation test

artículo científico publicado en 1995

Rapid detection of translation-terminating mutations at the adenomatous polyposis coli (APC) gene by direct protein truncation test.

artículo científico publicado en 1994

Recommendations for the management of women with an increased genetic risk of gynaecological cancer

artículo científico publicado en 2002

Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

artículo científico publicado en 2009

Rectal Cancer Risk in Hereditary Nonpolyposis Colorectal Cancer After Abdominal Colectomy

artículo científico publicado en 1997

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ⬇️

artículo científico publicado en 2015

Refinement of screening for familial pancreatic cancer.

artículo científico publicado en 2016

Reply

Reply

Reply to V. Bonadona et al

artículo científico publicado en 2013

Reply to Win and Jenkins

artículo científico publicado en 2013

Review article: The Lynch syndrome (hereditary nonpolyposis colorectal cancer).

artículo científico publicado en 2007

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability ⬇️

artículo científico publicado en 2004

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts

artículo científico publicado en 2013

Risk and epidemiological time trends of gastric cancer in Lynch syndrome carriers in the Netherlands

artículo científico publicado en 2009

Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and hMSH2 gene: correction for ascertainment

artículo científico publicado en 2005

Risk of developing adenomas and carcinomas in the ileal pouch in patients with familial adenomatous polyposis

artículo científico publicado en 2008

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion ofp16 (p16-Leiden)

artículo científico publicado en 2000

Risk of multiple pancreatic cancers in CDKN2A-p16-Leiden mutation carriers

artículo científico publicado en 2018

Risk reducing mastectomy: outcomes in 10 European centres.

artículo científico publicado en 2008

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2020

Risks of Lynch syndrome cancers for MSH6 mutation carriers

artículo científico publicado en 2009

Risks of less common cancers in proven mutation carriers with lynch syndrome

artículo científico publicado en 2012

Safety of endoscopic mucosal resection (EMR) of large non-pedunculated colorectal adenomas in the elderly.

artículo científico publicado en 2017

Screening behavior of individuals at high risk for colorectal cancer

artículo científico publicado en 2005

Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families

artículo científico publicado en 2000

Screening for hereditary non-polyposis colorectal cancer: A study of 22 kindreds in The Netherlands

artículo científico publicado en 1989

Screening for prostate cancer in Dutch hereditary prostate cancer families

artículo científico publicado en 2008

Screening for the multiple endocrine neoplasia syndrome type I. A study of 11 kindreds in The Netherlands

artículo científico publicado en 1989

Screening in breast cancer families: is it useful?

artículo científico publicado en 1994

Screening of Individuals at High Risk for Pancreatic Cancer

artículo científico publicado en 2019

Screening of families predisposed to cancer development in The Netherlands.

artículo científico publicado en 1990

Serum peptide signatures for pancreatic cancer based on mass spectrometry: a comparison to CA19-9 levels and routine imaging techniques.

artículo científico publicado en 2014

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

artículo científico publicado en 1995

Skin self-examination of persons from families with familial atypical multiple mole melanoma (FAMMM).

artículo científico publicado en 2008

Small-bowel cancer in Lynch syndrome: is it time for surveillance?

artículo científico publicado en 2008

Smoking increases the risk for colorectal adenomas in patients with Lynch syndrome

artículo científico publicado en 2011

Somatic APC mosaicism: an underestimated cause of polyposis coli.

artículo científico publicado en 2007

Surgical management for advanced duodenal adenomatosis and duodenal cancer in Dutch patients with familial adenomatous polyposis: A nationwide retrospective cohort study

artículo científico publicado en 2012

Surveillance colonoscopy practice in Lynch syndrome in the Netherlands: A nationwide survey.

artículo científico publicado en 2007

Surveillance for Hereditary Nonpolyposis Colorectal Cancer

artículo científico publicado en 2002

Surveillance for familial melanoma: recommendations from a national centre of expertise

artículo científico publicado en 2019

Surveillance for familial pancreatic cancer.

artículo científico publicado en 2003

Surveillance for hereditary cancer: does the benefit outweigh the psychological burden?--A systematic review.

artículo científico

Surveillance in hereditary nonpolyposis colorectal cancer

scientific article published on 01 January 1993

Surveillance of Second-Degree Relatives from Melanoma Families with a CDKN2A Germline Mutation

artículo científico publicado en 2013

Survival after adjuvant 5-FU treatment for stage III colon cancer in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2004

Survival analysis of endometrial carcinoma associated with hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2002

Survival in prospectively ascertained familial breast cancer: Analysis of a series stratified by tumour characteristics,BRCAmutations and oophorectomy

article

Survival in women with MMR mutations and ovarian cancer: a multicentre study in Lynch syndrome kindreds

artículo científico publicado en 2009

Survival of MUTYH-associated polyposis patients with colorectal cancer and matched control colorectal cancer patients

artículo científico publicado en 2010

Survival of Patients with Ovarian Cancer due to a Mismatch Repair Defect

scientific article published on 01 January 2005

Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study.

artículo científico publicado en 2002

Suspected hereditary nonpolyposis colorectal cancer

artículo científico publicado en 1999

TGFBR1*6A may contribute to hereditary colorectal cancer

artículo científico publicado en 2005

Targeted next-generation sequencing of FNA-derived DNA in pancreatic cancer

artículo científico publicado en 2016

Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study

artículo científico publicado en 2014

The "unnatural" history of colorectal cancer in Lynch syndrome: lessons from colonoscopy surveillance

artículo científico publicado en 2020

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

artículo científico publicado en 2003

The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families

artículo científico publicado en 2003

The International Collaborative Group on HNPCC

scientific article published on 01 July 1994

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

artículo científico publicado en 1991

The Natural Course of Multiple Endocrine Neoplasia Type iib

artículo científico publicado en 1992

The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2001

The clinical phenotype of hereditary versus sporadic prostate cancer: HPC definition revisited

artículo científico publicado en 2016

The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers

artículo científico publicado en 2015

The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 1994

The establishment of a polyposis register.

artículo científico publicado en 1993

The familial dysplastic nevus syndrome. Natural history and the impact of screening on prognosis. A study of nine families in the Netherlands

artículo científico publicado en 1989

The frequency of a positive family history for colorectal cancer: a population-based study in the Netherlands

artículo científico publicado en 2006

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients

artículo científico publicado en 2013

The importance of a well-structured pancreatic screening program for familial and hereditary pancreatic cancer

artículo científico publicado en 2017

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2

artículo científico publicado en 1996

The natural history of a combined defect in MSH6 and MUTYH in a HNPCC family

artículo científico publicado en 2007

The outcome of endometrial carcinoma surveillance by ultrasound scan in women at risk of hereditary nonpolyposis colorectal carcinoma and familial colorectal carcinoma

artículo científico publicado en 2002

The protocol for a european double-blind trial of aspirin and resistant starch in familial adenomatous polyposis: The capp study

artículo científico publicado en 1995

The risk of endometrial cancer in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 1994

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.

artículo científico publicado en 2008

The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC

scientific article published on 01 January 2004

The role of the prostate cancer gene 3 urine test in addition to serum prostate-specific antigen level in prostate cancer screening among breast cancer, early-onset gene mutation carriers

artículo científico publicado en 2015

The tumour spectrum in hereditary non-polyposis colorectal cancer: A study of 24 kindreds in the netherlands

artículo científico publicado en 1990

The value of screening and central registration of families with familial adenomatous polyposis. A study of 82 families in The Netherlands.

artículo científico publicado en 1990

Three germline mutations in the TP53 gene

artículo científico publicado en 1997

Thyroid C-cell hyperplasia and micronodules in close relatives of MEN-2A patients: pitfalls in early diagnosis and reevaluation of criteria for surgery

artículo científico publicado en 1987

Thyroid carcinoma as first manifestation of familial adenomatous polyposis.

artículo científico publicado en 1996

Transanal minimally invasive surgery (TAMIS) versus endoscopic submucosal dissection (ESD) for resection of non-pedunculated rectal lesions (TRIASSIC study): study protocol of a European multicenter randomised controlled trial

artículo científico publicado en 2020

Transsphenoidal microsurgery as primary treatment in 25 acromegalic patients: results and follow-up ⬇️

artículo científico publicado el 1 de febrero de 1988

Treatment of mesenteric desmoid tumours with the anti-oestrogenic agent toremifene: case histories and an overview of the literature.

artículo científico publicado en 1999

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

artículo científico publicado en 2021

Urologists' and GPs' knowledge of hereditary prostate cancer is suboptimal for prostate cancer counseling: a nation-wide survey in The Netherlands

artículo científico publicado en 2012

Value-based healthcare in Lynch syndrome

artículo científico publicado en 2013

Variation in mutation spectrum partly explains regional differences in the breast cancer risk of female BRCA mutation carriers in the Netherlands

artículo científico publicado en 2014

Variation in precursor lesions of pancreatic cancer among high-risk groups

artículo científico publicado en 2012

What is hereditary nonpolyposis colorectal cancer (HNPCC).

artículo científico publicado en 1994

What is the appropriate screening protocol in Lynch syndrome?

artículo científico publicado en 2006

When should endoscopic screening in familial adenomatous polyposis be started?

artículo científico publicado en 2000

Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.

artículo científico publicado en 2016

Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles

artículo científico publicado en 2013

Worldwide survey among polyposis registries of surgical management of severe duodenal adenomatosis in familial adenomatous polyposis.

artículo científico publicado en 2003

[Characterisation of families with hereditary prostate cancer in the Netherlands]

artículo científico publicado en 2002

[Desmoid tumour as indication of familial adenomatous polyposis].

artículo científico publicado en 2010

[Familial gastric cancer: diagnosis, treatment and periodic surveillance].

artículo científico publicado en 2011

[Frequency of duodenal adenomas in patients with familial adenomatous polyposis].

artículo científico publicado en 2001

[From gene to disease; the APC gene and familial adenomatous polyposis coli]

artículo científico publicado en 2000

[Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer]

scientific article published on 01 June 1999

[Genetics of colorectal cancer. II. Hereditary background of sporadic and familial colorectal cancer]

scientific article published on 01 June 1999

[Hemolytic anemia associated with severe liver insufficiency as an initial symptom of Wilson's disease]

artículo científico publicado en 1982

[Hereditary mutations in the p53 tumor suppressor gene; significance for clinical practice. National Work Group Hereditary Mamma Carcinoma]

scientific article published on 01 June 1996

[Hereditary prostate carcinoma. National Work Group Hereditary Urological tumors. Foundation Tracing Hereditary Tumors]

scientific article published on 01 May 1996

[Indications for surgery of incidentally detected adrenal gland tumors]

artículo científico publicado en 1984

[Intraocular tumor metastases]

artículo científico publicado en 1982

[Periodic colonoscopic examinations of persons with a positive family history for colorectal cancer. Work Group 'Hereditary non-polyposis- colon-rectum cancers']

artículo científico publicado en 1999

[Periodic examination of families with hereditary nonpolyposis colorectal carcinoma in The Netherlands: a study of 41 families]

artículo científico publicado en 1994

[Periodical screening of families with a hereditary predisposition for breast carcinoma]

artículo científico publicado en 1993

[The doctor and the yellow girl]

artículo científico publicado en 1988

[The value of screening and the national registration of hereditary tumors]

artículo científico publicado en 1988

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