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List of works by Olivier Alibeu

APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries

scientific article published on 01 November 2019

CE-SSCP and CE-FLA, simple and high-throughput alternatives for fungal diversity studies

scientific article

Diagnostic Yield of Next-generation Sequencing in Very Early-onset Inflammatory Bowel Diseases: A Multicentre Study

scientific article published on 01 August 2018

Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome

scientific article published on 14 July 2016

MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence

scientific article published on 21 November 2017

Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects

scientific article

Mutations in SNRPB, encoding components of the core splicing machinery, cause cerebro-costo-mandibular syndrome

scientific article published on 11 December 2014

Mutations of CEP83 cause infantile nephronophthisis and intellectual disability

scientific article

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

scientific article published on 9 January 2018

Phylogenetic analysis of the Aspergillus niger aggregate in relation to feruloyl esterase activity.

scientific article published on 07 April 2007

Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome.

scientific article published on 12 January 2018

Role of miR-146a in neural stem cell differentiation and neural lineage determination: relevance for neurodevelopmental disorders.

scientific article published on 19 June 2018

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

scientific article published on 31 May 2017

Whole exome sequencing diagnoses the first fetal case of Bainbridge-Ropers syndrome presenting as pontocerebellar hypoplasia type 1

scientific article published on 08 January 2018

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