Author

Richelle Senden

Observed names: Richelle E M Senden, Richelle E.M. Senden

Institution: Erasmus MC

Observed institutions: Utrecht University, Erasmus MC, University Medical Center Utrecht

OpenAlex ID: A5085534500

The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations

2022 · Geeske M. van Woerden, Richelle Senden, et al. · Human Mutation · 18

Mild cerebellar injury does not significantly affect cerebral white matter microstructural organization and neurodevelopmental outcome in a contemporary cohort of preterm infants

2018 · Richelle E M Senden, Kristin Keunen, et al. · Pediatric Research · 9

A patient with chromosome 18p deletion and congenital hypoglossia

2017 · Sanne Klaphake, Marieke F. van Dooren, et al. · Clinical Dysmorphology · 2

Involvement of MAP3K7 in FMD2 and CSCF, delineation of genotype/phenotype correlations.

2021 · Geeske van Woerden, Richelle Senden, et al.

Works count: 4

Citation count: 28

H-index: 2

I10-index: 1