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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome

Journal of clinical oncology, 2012-12, Vol.30 (35), p.4409-4415

2012

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CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling

International journal of cancer, 2012-07, Vol.131 (2), p.367-376

2012

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Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence

European journal of human genetics : EJHG, 2015-09, Vol.23 (9), p.1151-1157

2015

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Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences

Journal of clinical oncology, 2010-06, Vol.28 (18), p.3008-3014

2010

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International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer

Gut, 2013-03, Vol.62 (3), p.339-347

2013

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An α-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer

The Journal of pathology, 2013-03, Vol.229 (4), p.621-629

2013

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Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

The lancet oncology, 2011, Vol.12 (1), p.49-55

2011

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A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

Hereditary cancer in clinical practice, 2010-08, Vol.8 (1), p.7-7, Article 7

2010

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Pregnancies, Breast-Feeding, and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study (IBCCS)

JNCI : Journal of the National Cancer Institute, 2006-04, Vol.98 (8), p.535-544

2006

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Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

Cancer research (Chicago, Ill.), 2003-04, Vol.63 (7), p.1449-1453

2003

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Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance

Familial cancer, 2012-09, Vol.11 (3), p.363-369

2012

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Colorectal cancer in the family: psychosocial distress and social issues in the years following genetic counselling

Hereditary cancer in clinical practice, 2007-06, Vol.5 (2), p.59-66

2007

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CHEK21100delC homozygosity is associated with a high breast cancer risk in women

Journal of medical genetics, 2011-12, Vol.48 (12), p.860-863

2011

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The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing

American journal of human genetics, 1999-08, Vol.65 (2), p.413-419

1999

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Hereditary causes of kidney tumours

European journal of clinical investigation, 2010-05, Vol.40 (5), p.433-439

2010

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Specific Psychosocial Issues of Individuals Undergoing Genetic Counseling for Cancer – A Literature Review

Journal of genetic counseling, 2014-04, Vol.23 (2), p.133-146

2014

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Feasibility of a pancreatic cancer surveillance program from a psychological point of view

Genetics in medicine, 2011-12, Vol.13 (12), p.1015-1024

2011

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Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated

European journal of human genetics : EJHG, 2012-05, Vol.20 (5), p.577-579

2012

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

Breast cancer research and treatment, 2011-02, Vol.126 (1), p.193-202

2011

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Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas

Journal of medical genetics, 2012-06, Vol.49 (6), p.362-365

2012

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Screening behavior of individuals at high risk for colorectal cancer

Gastroenterology (New York, N.Y. 1943), 2005-02, Vol.128 (2), p.280-287

2005

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Atypical familial presentation of FAMMM syndrome with a high incidence of pancreatic cancer: case finding of asymptomatic individuals by EUS surveillance

Journal of clinical gastroenterology, 2009-10, Vol.43 (9), p.853-857

2009

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A family with complement factor D deficiency

The Journal of clinical investigation, 2001-07, Vol.108 (2), p.233-240

2001

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An [alpha]-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer

The Journal of pathology, 2013-03, Vol.229 (4), p.621-629

2013

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The efficacy of a standardized questionnaire in facilitating personalized communication about problems encountered in cancer genetic counseling: design of a randomized controlled trial

BMC cancer, 2014-01, Vol.14 (1), p.26-26, Article 26

2014

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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome

CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling

Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence

Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences

International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer

An α-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

Pregnancies, Breast-Feeding, and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study (IBCCS)

Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance

Colorectal cancer in the family: psychosocial distress and social issues in the years following genetic counselling

CHEK21100delC homozygosity is associated with a high breast cancer risk in women

The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing

Hereditary causes of kidney tumours

Specific Psychosocial Issues of Individuals Undergoing Genetic Counseling for Cancer – A Literature Review

Feasibility of a pancreatic cancer surveillance program from a psychological point of view

Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated

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

Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas

Screening behavior of individuals at high risk for colorectal cancer

Atypical familial presentation of FAMMM syndrome with a high incidence of pancreatic cancer: case finding of asymptomatic individuals by EUS surveillance

A family with complement factor D deficiency

An [alpha]-E-catenin (CTNNA1) mutation in hereditary diffuse gastric cancer

The efficacy of a standardized questionnaire in facilitating personalized communication about problems encountered in cancer genetic counseling: design of a randomized controlled trial

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