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L. Govaerts | Researchclopedia

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L. Govaerts

Hudson Institute

61

Works

1,205

Citations

19

h-index

27

i10-index

Research Topics

Prenatal Screening and Diagnostics Genomic variations and chromosomal abnormalities Peroxisome Proliferator-Activated Receptors

Affiliations

Hudson Institute2017–2020

Radboud University Nijmegen1982–1990

University of Liège2007–2012

University of Groningen1986–1987

Erasmus MC2003–2017

Top Works

Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature

M. C. de Wit,Malgorzata I. Srebniak,et al.

2013168 citations

Fetal and Pediatric Neurological Disorders

Metabolism and Genetic Disorders

Infantile Refsum disease: an inherited peroxisomal disorder

Bwee Tien Poll‐The,J. M. Saudubray,et al.

1987131 citations

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1‐5q31.3 in ten unbalanced carriers

Yvonne Arens,J.J.M. Engelen,et al.

200488 citations

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome

Johanna M. van Hagen,Jos N. van der Geest,et al.

200686 citations

Cerebro-hepato-renal syndrome of zellweger: Clinical symptoms and relevant laboratory findings in 16 patients

L. Govaerts,L.A.H. Monnens,et al.

198265 citations

A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus

Reinhard Oldenburg,M. F. van Dooren,et al.

200852 citations

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing

Sanne Steen,Karin E. M. Diderich,et al.

201450 citations

Phenotype–genotype correlation in a familial <i>IGF1R</i> microdeletion case

Danielle Veenma,H. J. Eussen,et al.

200949 citations

Omphalocele: comparison of outcome following prenatal or postnatal diagnosis

Titia E. Cohen‐Overbeek,Wing H. Tong,et al.

201046 citations