Author

K. Messaoudi

2 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Sep 2026

Clinical utility of prenatal exome sequencing after normal chromosomal microarray in fetuses with structural anomalies.

Congenital anomalies detected by ultrasound occur in approximately 2-4% of pregnancies. Cytogenetic testing allows detection of chromosomal abnormalities, but the majority of fetuses remain without a diagnosis. It is in this context that exome sequencing was introduced into prenatal medicine. The objective of this stud...

M. Perrière, W. Darwiche, K. Messaoudi et al. · Morphologie : bulletin de l'... · 0 citations

Open access Aug 2026

Genetic Architecture of Pediatric Cardiomyopathies Assessed by Whole-Exome Sequencing: Insights Into Early-Onset and Syndromic Forms.

The findings support the use of WES as a first-line approach in pediatric CM and highlight the contribution of complex and syndromic genetic architectures to early-onset and severe diseases.

Luana Giovannangeli, Elise Daire, K. Messaoudi et al. · Clinical Genetics · 0 citations