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Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

Clinical cancer research, 2006-05, Vol.12 (10), p.3209-3215

2006

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Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer

The Journal of pathology, 2001-11, Vol.195 (4), p.451-456

2001

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Investigation of the Birt–Hogg–Dubé tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer

Journal of medical genetics, 2010-06, Vol.47 (6), p.385-390

2010

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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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Birt-Hogg-Dubé Syndrome: Clinical and Genetic Studies of 20 Families

Journal of investigative dermatology, 2008-01, Vol.128 (1), p.45-49

2008

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Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and Fallopian tube in women at hereditary high risk of breast and ovarian cancer

International journal of cancer, 2006-09, Vol.119 (6), p.1412-1418

2006

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Familial multiple discoid fibromas: A look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus

Journal of the American Academy of Dermatology, 2012-02, Vol.66 (2), p.259.e1-259.e9

2012

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Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study

Journal of the American Academy of Dermatology, 2020-08, Vol.83 (2), p.604-607

2020

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A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

Familial cancer, 2013-09, Vol.12 (3), p.373-379

2013

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An Autosomal Dominant High Bone Mass Phenotype in Association With Craniosynostosis in an Extended Family Is Caused by an LRP5 Missense Mutation

Journal of bone and mineral research, 2005-07, Vol.20 (7), p.1254-1260

2005

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Multifocal and microscopic chromophobe renal cell carcinomatous lesions associated with ‘capsulomas’ without FCLN gene abnormality

Pathology international, 2013-10, Vol.63 (10), p.510-515

2013

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Serum CA-125 in Relation to Adnexal Dysplasia and Cancer in Women at Hereditary High Risk of Ovarian Cancer

Journal of clinical oncology, 2007-04, Vol.25 (11), p.1383-1389

2007

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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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CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening

Genetic testing, 2008-03, Vol.12 (1), p.25-35

2008

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Relative frequency and morphology of cancers in STK11 mutation carriers

Gastroenterology (New York, N.Y. 1943), 2004-06, Vol.126 (7), p.1788-1794

2004

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Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

Cancer research (Chicago, Ill.), 2010-12, Vol.70 (23), p.9742-9754

2010

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Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium

Cancer epidemiology, biomarkers & prevention, 2020-02, Vol.29 (2), p.368-378

2020

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Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

PLoS genetics, 2010-10, Vol.6 (10), p.e1001183-e1001183

2010

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Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers

JNCI : Journal of the National Cancer Institute, 2011-01, Vol.103 (2), p.105-116

2011

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Histopathological characteristics of BRCA1- and BRCA2-associated intraperitoneal cancer: a clinic-based study

Familial cancer, 2003, Vol.2 (2), p.73-78

2003

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Calprotectin as an early biomarker of bacterial infections in critically ill patients: An exploratory cohort assessment

Critical care and resuscitation, 2017-09, Vol.19 (3), p.205-213

2017

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On-demand pre-exposure prophylaxis with tenofovir disoproxil fumarate plus emtricitabine among men who have sex with men with less frequent sexual intercourse: a post-hoc analysis of the ANRS IPERGAY trial

The lancet HIV, 2020-02, Vol.7 (2), p.e113-e120

2020

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Molecular Evidence Linking Primary Cancer of the Fallopian Tube to BRCA1 Germline Mutations

Gynecologic oncology, 2000-01, Vol.76 (1), p.45-50

2000

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Effectiveness of methotrexate and bridging glucocorticoids with or without early introduction of a 6-month course of etanercept in early RA: results of the 2-year, pragmatic, randomised CareRA2020 trial

Rheumatic & musculoskeletal diseases open, 2024-08, Vol.10 (3), p.e004535

2024

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Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer

Investigation of the Birt–Hogg–Dubé tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer

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

Birt-Hogg-Dubé Syndrome: Clinical and Genetic Studies of 20 Families

Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and Fallopian tube in women at hereditary high risk of breast and ovarian cancer

Familial multiple discoid fibromas: A look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus

Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study

A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

An Autosomal Dominant High Bone Mass Phenotype in Association With Craniosynostosis in an Extended Family Is Caused by an LRP5 Missense Mutation

Multifocal and microscopic chromophobe renal cell carcinomatous lesions associated with ‘capsulomas’ without FCLN gene abnormality

Serum CA-125 in Relation to Adnexal Dysplasia and Cancer in Women at Hereditary High Risk of Ovarian Cancer

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

CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening

Cohort profile: a nationwide study in Dutch CHEK2 c.1100delC families using the infrastructure of the HEreditary Breast and Ovarian cancer study Netherlands – Hebon-CHEK2

Relative frequency and morphology of cancers in STK11 mutation carriers

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium

Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers

Histopathological characteristics of BRCA1- and BRCA2-associated intraperitoneal cancer: a clinic-based study

Calprotectin as an early biomarker of bacterial infections in critically ill patients: An exploratory cohort assessment

On-demand pre-exposure prophylaxis with tenofovir disoproxil fumarate plus emtricitabine among men who have sex with men with less frequent sexual intercourse: a post-hoc analysis of the ANRS IPERGAY trial

Molecular Evidence Linking Primary Cancer of the Fallopian Tube to BRCA1 Germline Mutations

Effectiveness of methotrexate and bridging glucocorticoids with or without early introduction of a 6-month course of etanercept in early RA: results of the 2-year, pragmatic, randomised CareRA2020 trial

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