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Grétel Oudesluijs | Researchclopedia

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Grétel Oudesluijs

11

Works

694

Citations

6

h-index

5

i10-index

Research Topics

Prenatal Screening and Diagnostics Genomic variations and chromosomal abnormalities Congenital Anomalies and Fetal Surgery

Affiliations

Erasmus MC2011–2016

Hendrix Genetics (Netherlands)2011–2011

National Center on Birth Defects and Developmental Disabilities2012–2012

Erasmus University Rotterdam2011–2013

Top Works

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

Marije Meuwissen,Rachel Schot,et al.

2016284 citations

RNA modifications and cancer

Congenital Ear and Nasal Anomalies

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

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

2013145 citations

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

Malgorzata I. Srebniak,Marjan Boter,et al.

2011107 citations

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities

Malgorzata I. Srebniak,Marjan Boter,et al.

201275 citations

Phenotypic variability of atypical 22q11.2 deletions not including<i>TBX1</i>

Judith M.A. Verhagen,Karin E. M. Diderich,et al.

201267 citations

Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect

Malgorzata I. Srebniak,Marjan Boter,et al.

20116 citations

Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics

Sam Riedijk,Grétel Oudesluijs,et al.

20126 citations

Omphalocele, radial ray defect and diaphragmatic hernia: another case of Gershoni-Baruch syndrome?

Grétel Oudesluijs

20142 citations

Pentalogy of Cantrell and supernumerary naris.

Grétel Oudesluijs

20112 citations