Olivier Alibeu

Paris, France

Last Updated: 09/26/2026

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Found 18 publications

Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect.

Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect.

Journal: Nature communications
Published: June 22, 2022

Somatic genetic rescue of a germline ribosome assembly defect.

Somatic genetic rescue of a germline ribosome assembly defect.

Journal: Nature communications
Published: October 20, 2020

Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study.

Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study.

Journal: Journal of Crohn's & colitis
Published: September 08, 2020

Early Acute Microvascular Kidney Transplant Rejection in the Absence of Anti-HLA Antibodies Is Associated with Preformed IgG Antibodies against Diverse Glomerular Endothelial Cell Antigens.

Early Acute Microvascular Kidney Transplant Rejection in the Absence of Anti-HLA Antibodies Is Associated with Preformed IgG Antibodies against Diverse Glomerular Endothelial Cell Antigens.

Journal: Journal of the American Society of Nephrology : JASN
Published: August 25, 2018

Optimization of CRISPR/Cas9 Delivery to Human Hematopoietic Stem and Progenitor Cells for Therapeutic Genomic Rearrangements.

Optimization of CRISPR/Cas9 Delivery to Human Hematopoietic Stem and Progenitor Cells for Therapeutic Genomic Rearrangements.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: April 18, 2018

Loss of ARHGEF1 causes a human primary antibody deficiency.

Loss of ARHGEF1 causes a human primary antibody deficiency.

Journal: The Journal of clinical investigation
Published: February 15, 2018

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

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

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: January 19, 2018

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

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

Journal: Molecular autism
Published: January 04, 2018

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

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

Journal: Journal of Crohn's & colitis
Published: December 13, 2017

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

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

Journal: Clinical immunology (Orlando, Fla.)
Published: August 18, 2017

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

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

Journal: Birth defects research
Published: July 11, 2017

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

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

Journal: American journal of medical genetics. Part A
Published: June 08, 2017
Showing 1-12 of 18

Last Updated: 09/26/2026