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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

American journal of human genetics, 2003-05, Vol.72 (5), p.1251-1260

2003

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Hepatitis B vaccination strategies tailored to different endemicity levels: Some considerations

Vaccine, 2010-01, Vol.28 (4), p.893-900

2010

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Lack of association of MYO9B genetic variants with coeliac disease in a British cohort

Gut, 2006-07, Vol.55 (7), p.969-972

2006

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Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis

Gut, 2008-04, Vol.57 (4), p.463-467

2008

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Genetic Analysis of Innate Immunity in Crohn's Disease and Ulcerative Colitis Identifies Two Susceptibility Loci Harboring CARD9 and IL18RAP

American journal of human genetics, 2008-05, Vol.82 (5), p.1202-1210

2008

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Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort

Human Immunology, 2006-04, Vol.67 (4), p.341-345

2006

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Pneumococcal genetic variability in age-dependent bacterial carriage

eLife, 2022-07, Vol.11

2022

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Intradermal fractional booster dose of inactivated poliomyelitis vaccine with a jet injector in healthy adults

Vaccine, 2013-08, Vol.31 (36), p.3688-3694

2013

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Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

Nature genetics, 2005-12, Vol.37 (12), p.1341-1344

2005

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Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites

Gut, 2008-04, Vol.57 (4), p.463-467

2008

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Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis. Commentary

Gut, 2008, Vol.57 (4)

2008

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No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population

American journal of physiology: Gastrointestinal and liver physiology, 2005-09, Vol.289 (3), p.G495-G500

2005

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Fine-mapping of the coeliac disease linkage region on chromosome 19p13 reveals a new player in the field

European journal of gastroenterology & hepatology, 2006-01, Vol.18 (1), p.A34

2006

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FINE‐MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.616-616

2005

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FINE‐MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD: OP1‐01

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.616-616

2005

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FINE-MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD: OP1-01

Journal of pediatric gastroenterology and nutrition, 2005-05, Vol.40 (5), p.616

2005

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Erfelijke factoren bij coeliakie

Tijdschrift voor kindergeneeskunde, 2004-02, Vol.72 (1), p.13-19

2004

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Increased carriage of non-vaccine serotypes with low invasive disease potential four years after switching to the 10-valent pneumococcal conjugate vaccine in The Netherlands

PloS one, 2018-03, Vol.13 (3), p.e0194823-e0194823

2018

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Long-term effects of pneumococcal conjugate vaccine on nasopharyngeal carriage of S. pneumoniae, S. aureus, H. influenzae and M. catarrhalis

PloS one, 2012-06, Vol.7 (6), p.e39730-e39730

2012

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Persistence of Antibodies to Severe Acute Respiratory Syndrome Coronavirus 2 in Relation to Symptoms in a Nationwide Prospective Study

Clinical infectious diseases, 2021-12, Vol.73 (12), p.2155-2162

2021

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Detection of Neisseria meningitidis in saliva and oropharyngeal samples from college students

Scientific reports, 2021-11, Vol.11 (1), p.23138-23138, Article 23138

2021

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Extensive Characterization and Comparison of Endothelial Cells Derived from Dermis and Adipose Tissue: Potential Use in Tissue Engineering

PloS one, 2016-11, Vol.11 (11), p.e0167056-e0167056

2016

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Direct Comparison of Immunogenicity Induced by 10- or 13-Valent Pneumococcal Conjugate Vaccine around the 11-Month Booster in Dutch Infants

PloS one, 2015-12, Vol.10 (12), p.e0144739-e0144739

2015

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Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms

PloS one, 2008-05, Vol.3 (5), p.e2270-e2270

2008

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Reconstructed human skin shows epidermal invagination towards integrated neopapillae indicating early hair follicle formation in vitro

Journal of tissue engineering and regenerative medicine, 2020-06, Vol.14 (6), p.761-773

2020

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A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

Hepatitis B vaccination strategies tailored to different endemicity levels: Some considerations

Lack of association of MYO9B genetic variants with coeliac disease in a British cohort

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis

Genetic Analysis of Innate Immunity in Crohn's Disease and Ulcerative Colitis Identifies Two Susceptibility Loci Harboring CARD9 and IL18RAP

Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort

Pneumococcal genetic variability in age-dependent bacterial carriage

Intradermal fractional booster dose of inactivated poliomyelitis vaccine with a jet injector in healthy adults

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitisAn unusual case of ascites

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis. Commentary

No genetic association of the human prolyl endopeptidase gene in the Dutch celiac disease population

Fine-mapping of the coeliac disease linkage region on chromosome 19p13 reveals a new player in the field

FINE‐MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD

FINE‐MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD: OP1‐01

FINE-MAPPING OF THE COELIAC DISEASE LINKAGE REGION ON CHROMOSOME 19P13 REVEALS A NEW PLAYER IN THE FIELD: OP1-01

Erfelijke factoren bij coeliakie

Increased carriage of non-vaccine serotypes with low invasive disease potential four years after switching to the 10-valent pneumococcal conjugate vaccine in The Netherlands

Long-term effects of pneumococcal conjugate vaccine on nasopharyngeal carriage of S. pneumoniae, S. aureus, H. influenzae and M. catarrhalis

Persistence of Antibodies to Severe Acute Respiratory Syndrome Coronavirus 2 in Relation to Symptoms in a Nationwide Prospective Study

Detection of Neisseria meningitidis in saliva and oropharyngeal samples from college students

Extensive Characterization and Comparison of Endothelial Cells Derived from Dermis and Adipose Tissue: Potential Use in Tissue Engineering

Direct Comparison of Immunogenicity Induced by 10- or 13-Valent Pneumococcal Conjugate Vaccine around the 11-Month Booster in Dutch Infants

Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms

Reconstructed human skin shows epidermal invagination towards integrated neopapillae indicating early hair follicle formation in vitro

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