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AFRICAN RESEARCH NEXUS

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Vignal, Cédric

Author Metrics

Top Publications

Top Publications Authored or Co-Authored by "Vignal, Cédric"

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype
American Journal of Human Genetics, Volume 108, No. 11, Year 2021, Citations 33
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
Frontiers in Genetics, Volume 13, Article 883211, Year 2022, Citations 23
Novel variants causing megalencephalic leukodystrophy in Sudanese families
Journal of Human Genetics, Volume 67, No. 3, Year 2022, Citations 23
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
BMC Medical Genomics, Volume 15, No. 1, Article 236, Year 2022, Citations 16

Institutional Spectrum

Most Recent Affiliations

Institution	Country	Start Year	End Year	Affiliated Years
Hôpital Robert-Debré AP-HP	France	2016	2022	7
AP-HP Assistance Publique - Hopitaux de Paris	France	2016	2022	7

Disclaimer

All information and calculations provided are based on our current indexed publications and may change as more data is collected.

African Research Nexus

The African Research Nexus is a visionary initiative that seeks to increase the visibility of African Researchers and Institutions. We are a dynamic hub designed to transform the African research landscape and amplify the voices of our continent’s brightest minds.

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