Lista de obras -

A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

artículo científico publicado en 2020

A Stepwise Procedure to Define a Data Collection Framework for a Clinical Biobank

artículo científico publicado en 2018

A within-subjects comparison of learning and memory performance before and after cardiac catheterization.

artículo científico publicado en 2007

AGORA, a data- and biobank for birth defects and childhood cancer.

artículo científico publicado en 2016

Availability, content and quality of local guidelines for the assessment of suicide attempters in university and general hospitals in the Netherlands

artículo científico publicado en 2006

Bias in patient series with VACTERL association

artículo científico publicado en 2011

Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy.

artículo científico publicado en 2018

Common variants in DGKK are strongly associated with risk of hypospadias

scientific journal article

Complications after Hypospadias Correction: Prognostic Factors and Impact on Final Clinical Outcome

artículo científico publicado en 2017

Computational Resource Demands of a Predictive Bayesian Brain

scholarly article

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association

artículo científico publicado en 2013

Deep Analogical Inference as the Origin of Hypotheses

artículo científico publicado en 2019

Deletions and loss-of-function variants in TP63 associated with orofacial clefting

artículo científico publicado en 2019

Differences in risk factors for second and third degree hypospadias in the national birth defects prevention study

artículo científico publicado en 2014

Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?

artículo científico publicado en 2003

Erratum: Corrigendum: Common variants in DGKK are strongly associated with risk of hypospadias

scholarly article published in Nature Genetics

Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.

artículo científico publicado en 2019

Exploration of gene-environment interactions, maternal effects and parent of origin effects in the etiology of hypospadias

artículo científico publicado en 2012

Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias

artículo científico publicado en 2014

First results of a European multi-center registry of patients with anorectal malformations.

artículo científico publicado en 2013

Genetic and nongenetic etiology of nonsyndromic anorectal malformations: a systematic review

artículo científico publicado en 2014

Genetics of Hypospadias: Are Single-Nucleotide Polymorphisms inSRD5A2,ESR1,ESR2, andATF3Really Associated with the Malformation?

article

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

artículo científico publicado en 2014

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

artículo científico publicado en 2014

Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts.

artículo científico publicado en 2012

Inter- and Intraobserver Variation in the Assessment of Preoperative Colostograms in Male Anorectal Malformations: An ARM-Net Consortium Survey

artículo científico publicado en 2020

Interaction between MTHFR 677C>T and periconceptional folic acid supplementation in the risk of Hypospadias

artículo científico publicado en 2016

Is the Rehbein procedure obsolete in the treatment of Hirschsprung’s disease? ⬇️

artículo científico publicado el 1 de noviembre de 2010

Long-term follow-up of functional outcome in patients with a cloacal malformation: a systematic review

artículo científico publicado en 2013

Low maternal dietary intakes of iron, magnesium, and niacin are associated with spina bifida in the offspring

artículo científico publicado en 2004

Marginal maternal vitamin B12 status increases the risk of offspring with spina bifida

artículo científico publicado en 2004

Maternal and paternal risk factors for anorectal malformations: a Dutch case-control study

artículo científico publicado en 2010

Maternal dietary B vitamin intake, other than folate, and the association with orofacial cleft in the offspring

artículo científico publicado en 2004

Maternal hypertensive disorders and subtypes of hypospadias: A Dutch case-control study

scientific article published on 13 July 2020

Maternal nutritional status and the risk for orofacial cleft offspring in humans

artículo científico publicado en 2004

Maternal recall of prescription medication use during pregnancy using a paper-based questionnaire: a validation study in the Netherlands.

artículo científico publicado en 2013

Maternal risk associated with the VACTERL association: A case-control study

artículo científico publicado en 2020

Maternal risk factors for the VACTERL association: A EUROCAT case-control study

scientific article published on 22 April 2020

Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract: A case-control study.

artículo científico publicado en 2016

More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation.

artículo científico publicado en 2016

Naturalism, tractability and the adaptive toolbox ⬇️

artículo científico publicado en 2019

No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformations

artículo científico publicado en 2014

Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene

scientific article published on 07 December 2019

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

artículo científico publicado en 2016

Orofacial clefts and spina bifida: N-acetyltransferase phenotype, maternal smoking, and medication use.

artículo científico publicado en 2002

Parental subfertility, fertility treatment, and the risk of congenital anorectal malformations

artículo científico publicado en 2015

Periconceptional folate intake by supplement and food reduces the risk of nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2004

Perioperative Nutritional Management in Congenital Perineal and Vestibular Fistulas: A Systematic Review

artículo científico publicado en 2015

Preoperative Illnesses in Children Do Not Increase the Risk of Complications After Hypospadias Repair

artículo científico publicado en 2019

Previous miscarriages and GLI2 are associated with anorectal malformations in offspring

artículo científico publicado en 2017

Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT.

artículo científico publicado en 2016

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

scientific article published on 01 May 2019

Reproductive disorders among male and female greenhouse workers

artículo científico publicado en 2007

Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populations

artículo científico publicado en 2010

Risk factors for different phenotypes of hypospadias: results from a Dutch case-control study

artículo científico publicado en 2013

SLC20A1 Is Involved in Urinary Tract and Urorectal Development

artículo científico publicado en 2020

Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias

artículo científico publicado en 2014

Social Categorization in Connectionist Models: A Conceptual Integration

artículo científico publicado en 2018

Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

scientific article published on 09 September 2019

Structure Learning in Predictive Processing Needs Revision

artículo científico publicado en 2022

Surgical Complications in Children with CDH: A Multivariate Analysis

artículo científico publicado en 2020

Teratogenic mechanisms associated with prenatal medication exposure

artículo científico

Teratogenic mechanisms of medical drugs

artículo científico publicado en 2010

The Challenges of the European Anorectal Malformations-Net Registry

artículo científico publicado en 2015

The Tractable Cognition Thesis ⬇️

artículo científico publicado el 1 de septiembre de 2008

The clinical efficacy and cost effectiveness of the vacuum-assisted closure technique in the management of acute and chronic wounds: a randomized controlled trial

artículo científico publicado en 2006

Uncontrolled maternal chronic respiratory diseases in pregnancy: A new potential risk factor suggested to be associated with anorectal malformations in offspring

scientific article published on 19 December 2018

Vitamin and homocysteine status of mothers and infants and the risk of nonsyndromic orofacial clefts

artículo científico publicado en 2003

What do pediatric surgeons think about sexual issues in dealing with patients with anorectal malformations? The ARM-Net consortium members' opinion

scientific article published on 05 July 2019

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

artículo científico publicado en 2013

Lista de obras de

A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies

A Stepwise Procedure to Define a Data Collection Framework for a Clinical Biobank

A within-subjects comparison of learning and memory performance before and after cardiac catheterization.

AGORA, a data- and biobank for birth defects and childhood cancer.

Availability, content and quality of local guidelines for the assessment of suicide attempters in university and general hospitals in the Netherlands

Bias in patient series with VACTERL association

Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy.

Common variants in DGKK are strongly associated with risk of hypospadias

Complications after Hypospadias Correction: Prognostic Factors and Impact on Final Clinical Outcome

Computational Resource Demands of a Predictive Bayesian Brain

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association

Deep Analogical Inference as the Origin of Hypotheses

Deletions and loss-of-function variants in TP63 associated with orofacial clefting

Differences in risk factors for second and third degree hypospadias in the national birth defects prevention study

Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?

Erratum: Corrigendum: Common variants in DGKK are strongly associated with risk of hypospadias

Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.

Exploration of gene-environment interactions, maternal effects and parent of origin effects in the etiology of hypospadias

Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias

First results of a European multi-center registry of patients with anorectal malformations.

Genetic and nongenetic etiology of nonsyndromic anorectal malformations: a systematic review

Genetics of Hypospadias: Are Single-Nucleotide Polymorphisms inSRD5A2,ESR1,ESR2, andATF3Really Associated with the Malformation?

Genome-wide association analyses identify variants in developmental genes associated with hypospadias

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts.

Inter- and Intraobserver Variation in the Assessment of Preoperative Colostograms in Male Anorectal Malformations: An ARM-Net Consortium Survey

Interaction between MTHFR 677C>T and periconceptional folic acid supplementation in the risk of Hypospadias

Is the Rehbein procedure obsolete in the treatment of Hirschsprung’s disease? ⬇️

Long-term follow-up of functional outcome in patients with a cloacal malformation: a systematic review

Low maternal dietary intakes of iron, magnesium, and niacin are associated with spina bifida in the offspring

Marginal maternal vitamin B12 status increases the risk of offspring with spina bifida

Maternal and paternal risk factors for anorectal malformations: a Dutch case-control study

Maternal dietary B vitamin intake, other than folate, and the association with orofacial cleft in the offspring

Maternal hypertensive disorders and subtypes of hypospadias: A Dutch case-control study

Maternal nutritional status and the risk for orofacial cleft offspring in humans

Maternal recall of prescription medication use during pregnancy using a paper-based questionnaire: a validation study in the Netherlands.

Maternal risk associated with the VACTERL association: A case-control study

Maternal risk factors for the VACTERL association: A EUROCAT case-control study

Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract: A case-control study.

More than fetal urine: enteral uptake of amniotic fluid as a major predictor for fetal growth during late gestation.

Naturalism, tractability and the adaptive toolbox ⬇️

No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformations

Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene

Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesis

Orofacial clefts and spina bifida: N-acetyltransferase phenotype, maternal smoking, and medication use.

Parental subfertility, fertility treatment, and the risk of congenital anorectal malformations

Periconceptional folate intake by supplement and food reduces the risk of nonsyndromic cleft lip with or without cleft palate

Perioperative Nutritional Management in Congenital Perineal and Vestibular Fistulas: A Systematic Review

Preoperative Illnesses in Children Do Not Increase the Risk of Complications After Hypospadias Repair

Previous miscarriages and GLI2 are associated with anorectal malformations in offspring

Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT.

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

Reproductive disorders among male and female greenhouse workers

Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populations

Risk factors for different phenotypes of hypospadias: results from a Dutch case-control study

SLC20A1 Is Involved in Urinary Tract and Urorectal Development

Sequencing of the DKK1 gene in patients with anorectal malformations and hypospadias

Social Categorization in Connectionist Models: A Conceptual Integration

Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

Structure Learning in Predictive Processing Needs Revision

Surgical Complications in Children with CDH: A Multivariate Analysis

Teratogenic mechanisms associated with prenatal medication exposure

Teratogenic mechanisms of medical drugs

The Challenges of the European Anorectal Malformations-Net Registry

The Tractable Cognition Thesis ⬇️

The clinical efficacy and cost effectiveness of the vacuum-assisted closure technique in the management of acute and chronic wounds: a randomized controlled trial

Uncontrolled maternal chronic respiratory diseases in pregnancy: A new potential risk factor suggested to be associated with anorectal malformations in offspring

Vitamin and homocysteine status of mothers and infants and the risk of nonsyndromic orofacial clefts

What do pediatric surgeons think about sexual issues in dealing with patients with anorectal malformations? The ARM-Net consortium members' opinion

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association