C. Wijers

发表

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

I. V. van Rooij, D. Tibboel, V. Tasic, 2013, Kidney international.

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

I. V. van Rooij, H. Brunner, M. Clementi, 2010, Pediatric Surgery International.

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

L. Kiemeney, P. Tam, I. V. van Rooij, 2019, PloS one.

Lymph node staging with fluorine-18 prostate specific membrane antigen 1007-positron emission tomography/computed tomography in newly diagnosed intermediate- to high-risk prostate cancer using histopathological evaluation of extended pelvic node dissection as reference

D. Somford, C. Wijers, H. Küsters-Vandevelde, 2022, European Journal of Nuclear Medicine and Molecular Imaging.

Bias in patient series with VACTERL association

I. V. van Rooij, N. Zwink, E. Jenetzky, 2011, American journal of medical genetics. Part A.

VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis

M. Nöthen, I. V. van Rooij, M. Mattheisen, 2012, Clinical dysmorphology.

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

B. Franke, I. V. van Rooij, A. Kuijpers-Jagtman, 2016, Birth defects research. Part A, Clinical and molecular teratology.

Parental Subfertility, Fertility Treatment, and the Risk of Congenital Anorectal Malformations

I. V. van Rooij, H. Brunner, N. Roeleveld, 2015, Epidemiology.

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

I. V. van Rooij, H. Brunner, N. Roeleveld, 2014, Birth defects research. Part C, Embryo today : reviews.

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

I. V. van Rooij, E. Jenetzky, H. Reutter, 2013, Journal of pediatric surgery.

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

I. V. van Rooij, N. Knoers, N. Roeleveld, 2010, Birth defects research. Part A, Clinical and molecular teratology.

D. Somford, C. Wijers, H. Küsters-Vandevelde, 2022, European Journal of Nuclear Medicine and Molecular Imaging.

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

D. Tibboel, M. Lacher, N. Roeleveld, 2016, European Journal of Pediatrics.

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

M. Nöthen, B. Herrmann, L. Wittler, 2013, European Journal of Human Genetics.

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

I. V. van Rooij, N. Roeleveld, W. Feitz, 2016, Birth defects research. Part A, Clinical and molecular teratology.

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.

M. Nöthen, I. V. van Rooij, T. Becker, 2014, Human molecular genetics.

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

H. Brunner, M. Hakobjan, N. Roeleveld, 2015, European Journal of Pediatrics.

Patients with anorectal malformation and upper limb anomalies: genetic evaluation is warranted

A. de Klein, I. de Blaauw, C. Wijers, 2015, European Journal of Pediatrics.

Previous miscarriages and GLI2 are associated with anorectal malformations in offspring

I. V. van Rooij, N. Roeleveld, I. de Blaauw, 2017, Human reproduction.

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

I. V. van Rooij, H. Brunner, R. Hofstra, 2014, Birth defects research. Part A, Clinical and molecular teratology.

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

I. V. van Rooij, E. Bongers, N. Knoers, 2016, Birth defects research. Part A, Clinical and molecular teratology.

Haemorrhagic stroke related to the use of 4-fluoroamphetamine

M. Visser, R. Niesink, C. Wijers, 2018, Journal of Neurology.

Preoperative PSMA-PET/CT as a predictor of biochemical persistence and early recurrence following radical prostatectomy with lymph node dissection

D. Somford, M. Gotthardt, C. Wijers, 2021, Prostate cancer and prostatic diseases.

Etiology of congenital anorectal malformations : genetic and non-genetic risk factors

C. Wijers, 2016 .

Diagnostic accuracy of three prevailing rapid antigen tests for detection of SARS-CoV-2 infection in the general population: cross sectional study

J. H. van de Wijgert, K. Moons, Z. Iglói, 2021, medRxiv.

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

I. V. van Rooij, D. Tibboel, V. Tasic, 2013, Kidney international.

Acute toxic effects related to 4-fluoroamphetamine

R. Niesink, C. Wijers, E. Croes, 2017, The Lancet.

Effect of different quilting techniques on seroma formation after breast surgery: retrospective study

L. Strobbe, C. Wijers, J. D. de Wilt, 2023, BJS open.