Anne Lecrux-Rovelet

Rouen, 76000, France

Last Updated: 09/26/2026

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Found 54 publications

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.

Journal: American journal of human genetics

Published: April 20, 2026

Assessing the de novo paradigm in sporadic early-onset Alzheimer disease trios.

Assessing the de novo paradigm in sporadic early-onset Alzheimer disease trios.

Journal: Molecular psychiatry

Published: October 02, 2025

Generation of two isogenic-corrected control cell lines (IRMBi001-A-1; IRMBi001-A-2) from Autosomal dominant Alzheimer's disease patient-derived iPSCs carrying a G217D mutation in presenilin 1 gene.

Generation of two isogenic-corrected control cell lines (IRMBi001-A-1; IRMBi001-A-2) from Autosomal dominant Alzheimer's disease patient-derived iPSCs carrying a G217D mutation in presenilin 1 gene.

Journal: Stem cell research

Published: February 17, 2025

Soluble SorLA in CSF, a novel biomarker to explore disrupted trafficking of SorLA protein in Alzheimer disease.

Soluble SorLA in CSF, a novel biomarker to explore disrupted trafficking of SorLA protein in Alzheimer disease.

Journal: Alzheimer's research & therapy

Published: November 18, 2024

Prognostic value of HPV circulating tumor DNA detection and quantification in locally advanced cervical cancer.

Prognostic value of HPV circulating tumor DNA detection and quantification in locally advanced cervical cancer.

Journal: Frontiers in oncology

Published: February 04, 2024

Assessment of the transcriptomic consequences and MAU2 protein levels in edited induced pluripotent stem cells with NIPBL pathogenic variants.

Assessment of the transcriptomic consequences and MAU2 protein levels in edited induced pluripotent stem cells with NIPBL pathogenic variants.

Journal: Genes & diseases

Published: January 23, 2024

Upstream open reading frame-introducing variants in patients with primary familial brain calcification.

Upstream open reading frame-introducing variants in patients with primary familial brain calcification.

Journal: European journal of human genetics : EJHG

Published: December 13, 2023

Generation of induced pluripotent stem cell lines IRMBi003-A and IRMBi003-B from a healthy donor to model Alzheimer's disease.

Generation of induced pluripotent stem cell lines IRMBi003-A and IRMBi003-B from a healthy donor to model Alzheimer's disease.

Journal: Stem cell research

Published: August 05, 2023

Establishment of induced pluripotent stem cells IRMBi005-A from a patient with sporadic Alzheimer's disease.

Establishment of induced pluripotent stem cells IRMBi005-A from a patient with sporadic Alzheimer's disease.

Journal: Stem cell research

Published: August 05, 2023

Phenotype and imaging features associated with APP duplications.

Phenotype and imaging features associated with APP duplications.

Journal: Alzheimer's research & therapy

Published: August 19, 2022

uORF-introducing variants in the 5'UTR of the NIPBL gene as a cause of Cornelia de Lange syndrome.

uORF-introducing variants in the 5'UTR of the NIPBL gene as a cause of Cornelia de Lange syndrome.

Journal: Human mutation

Published: December 02, 2021

Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease.

Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease.

Journal: Acta neuropathologica communications

Published: November 10, 2021

Showing 1-12 of 54

Last Updated: 09/26/2026