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A comprehensive gene mutation screen in men with asthenozoospermia

Fertility and sterility, 2011-03, Vol.95 (3), p.1020-1024.e9

2011

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Mortality Risk of Untreated Myosin-Binding Protein C-Related Hypertrophic Cardiomyopathy: Insight Into the Natural History

Journal of the American College of Cardiology, 2011-11, Vol.58 (23), p.2406-2414

2011

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Mortality Risk of Untreated Myosin-Binding Protein C–Related Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, , Vol.58 (23), p.2406-2414

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Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study

Circulation. Cardiovascular genetics, 2009-10, Vol.2 (5), p.418

2009

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Chromosomal region 11p15 is associated with male factor subfertility

Molecular human reproduction, 2003-10, Vol.9 (10), p.587-592

2003

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WT1 Deletion Leading to Severe 46,XY Gonadal Dysgenesis, Wilms Tumor and Gonadoblastoma: Case Report

Hormone research in paediatrics, 2015-01, Vol.83 (3), p.211-216

2015

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Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding

Human reproduction update, 2004-11, Vol.10 (6), p.533-539

2004

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Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern

Human reproduction (Oxford), 2004-01, Vol.19 (1), p.71-76

2004

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Additional risk factors influence excess mortality in heterozygous familial hypercholesterolaemia

Atherosclerosis, 2000-04, Vol.149 (2), p.421-425

2000

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Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis

Fertility and sterility, 2005-02, Vol.83 (2), p.513-515

2005

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Absence of mutations in the PCI gene in subfertile men

Molecular human reproduction, 2004-11, Vol.10 (11), p.807-813

2004

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Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in the Netherlands

Clinical genetics, 2000-02, Vol.57 (2), p.116-124

2000

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Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations

Atherosclerosis, 1998-02, Vol.136 (2), p.247-254

1998

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Expression analysis of subtractively enriched libraries (EASEL): a widely applicable approach to the identification of differentially expressed genes

Journal of biochemical and biophysical methods, 2003-07, Vol.57 (1), p.17-33

2003

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Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics

Human genetics, 1997-08, Vol.100 (2), p.266-270

1997

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CDNA arrays: the ups and downs

Cardiovascular drugs and therapy, 2001-03, Vol.15 (2), p.99-101

2001

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Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rate

Genetic testing, 2006-06, Vol.10 (2), p.77

2006

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First independent evaluation of QuantiFERON-TB Plus performance

The European respiratory journal, 2016-05, Vol.47 (5), p.1587-1590

2016

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High expression of miR-17-5p in tumor epithelium is a predictor for poor prognosis for prostate cancer patients

Scientific reports, 2021-07, Vol.11 (1), p.13864-13864, Article 13864

2021

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Estrogen Receptor Signaling Pathways Involved in Invasion and Colony Formation of Androgen-Independent Prostate Cancer Cells PC-3

International journal of molecular sciences, 2021-01, Vol.22 (3), p.1153

2021

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Clinical validation of Xpert MTB/RIF for the diagnosis of extrapulmonary tuberculosis

The European respiratory journal, 2012-08, Vol.40 (2), p.442-447

2012

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Molecular targets and oxidative stress biomarkers in hepatocellular carcinoma: an overview

Journal of translational medicine, 2011-10, Vol.9 (1), p.171-171, Article 171

2011

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Estrogen Receptors Promote Migration, Invasion and Colony Formation of the Androgen-Independent Prostate Cancer Cells PC-3 Through β-Catenin Pathway

Frontiers in endocrinology (Lausanne), 2020-04, Vol.11, p.184-184

2020

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Long-Term Prognostic Value of Cardiac Magnetic Resonance in Left Ventricle Noncompaction

Journal of the American College of Cardiology, 2016-11, Vol.68 (20), p.2166-2181

2016

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Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience

Circulation (New York, N.Y.), 2013-10, Vol.128 (14), p.1513-1521

2013

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A comprehensive gene mutation screen in men with asthenozoospermia

Mortality Risk of Untreated Myosin-Binding Protein C-Related Hypertrophic Cardiomyopathy: Insight Into the Natural History

Mortality Risk of Untreated Myosin-Binding Protein C–Related Hypertrophic Cardiomyopathy

Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study

Chromosomal region 11p15 is associated with male factor subfertility

WT1 Deletion Leading to Severe 46,XY Gonadal Dysgenesis, Wilms Tumor and Gonadoblastoma: Case Report

Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding

Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern

Additional risk factors influence excess mortality in heterozygous familial hypercholesterolaemia

Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis

Absence of mutations in the PCI gene in subfertile men

Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in the Netherlands

Similar response to simvastatin in patients heterozygous for familial hypercholesterolemia with mRNA negative and mRNA positive mutations

Expression analysis of subtractively enriched libraries (EASEL): a widely applicable approach to the identification of differentially expressed genes

Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics

CDNA arrays: the ups and downs

Molecular genetic testing for familial hypercholesterolemia in the Netherlands: a stepwise screening strategy enhances the mutation detection rate

First independent evaluation of QuantiFERON-TB Plus performance

High expression of miR-17-5p in tumor epithelium is a predictor for poor prognosis for prostate cancer patients

Estrogen Receptor Signaling Pathways Involved in Invasion and Colony Formation of Androgen-Independent Prostate Cancer Cells PC-3

Clinical validation of Xpert MTB/RIF for the diagnosis of extrapulmonary tuberculosis

Molecular targets and oxidative stress biomarkers in hepatocellular carcinoma: an overview

Estrogen Receptors Promote Migration, Invasion and Colony Formation of the Androgen-Independent Prostate Cancer Cells PC-3 Through β-Catenin Pathway

Long-Term Prognostic Value of Cardiac Magnetic Resonance in Left Ventricle Noncompaction

Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience

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