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Brigitte H. W. Faas | Researchclopedia

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Brigitte H. W. Faas

Radboud University Nijmegen ORCID

75

Works

3,871

Citations

29

h-index

43

i10-index

Research Topics

Prenatal Screening and Diagnostics Fetal and Pediatric Neurological Disorders Genomic variations and chromosomal abnormalities

Affiliations

Radboud University Nijmegen2006–2025

University Medical Center2025–2025

Radboud University Medical Center2006–2025

Weatherford College2012–2012

Radboud Institute for Molecular Life Sciences2019–2022

Top Works

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Sébastien Jacquemont,Alexandre Reymond,et al.

2011476 citations

Parvovirus B19 Infection Studies

Congenital Anomalies and Fetal Surgery

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands

Karuna R. M. van der Meij,Erik A. Sistermans,et al.

2019369 citations

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Joseph I. Friedman,Terry Vrijenhoek,et al.

2007298 citations

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

Peter Benn,A. Borrell,et al.

2015289 citations

Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

Peter Benn,Antoni Borell,et al.

2013215 citations

Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype

Mariëlle E.M. Swinkels,Annet Simons,et al.

2008169 citations

Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part I—clinical impact

Dick Oepkes,Godelieve C.M.L. Page‐Christiaens,et al.

2016153 citations

Prenatal diagnostic testing of the Noonan syndrome genes in fetuses with abnormal ultrasound findings

Ellen A. Croonen,Willy M. Nillesen,et al.

2013145 citations

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

Brigitte H. W. Faas,I. van der Bürgt,et al.

2010144 citations