Get started
Author

Aline Zaréa

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
2022 · Henne Holstege, Marc Hulsman, et al. · Nature Genetics · 225
PDF
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
2017 · Céline Bellenguez, Camille Charbonnier, et al. · Neurobiology of Aging · 167
PDF
Seizures in dominantly inherited Alzheimer disease
2016 · Aline Zarea, Camille Charbonnier, et al. · Neurology · 110
Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic features
2017 · Juliette Svahn, Philippe Petiot, et al. · Journal of Neurology Neurosurgery & Psychiatry · 107
Added value of 18 F‐florbetaben amyloid PET in the diagnostic workup of most complex patients with dementia in France: A naturalistic study
2017 · Mathieu Ceccaldi, Mathieu Ceccaldi, et al. · Alzheimer s & Dementia · 56
PDF
Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer’s Disease Before 51 Years
2019 · Morgane Lacour, Olivier Quenez, et al. · Journal of Alzheimer s Disease · 54
Cerebrospinal Fluid Profile of Tau, Phosphorylated Tau, Aβ42, and Aβ40 in Probable Cerebral Amyloid Angiopathy
2022 · Lou Grangeon, Claire Paquet, et al. · Journal of Alzheimer s Disease · 28
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes
2022 · Catherine Schramm, Camille Charbonnier, et al. · Genome Medicine · 26
PDF
Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening
2024 · Gaël Nicolas, Aline Zaréa, et al. · Genetics in Medicine · 25
Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers
2021 · David Wallon, Susana Boluda, et al. · Acta Neuropathologica · 20
Phenotype and imaging features associated with APP duplications
2023 · Lou Grangeon, Camille Charbonnier, et al. · Alzheimer s Research & Therapy · 19
PDF
Domain mapping of disease mutations supports genetic testing of specific SORL1 variants in familial Alzheimer’s Disease
2023 · Henne Holstege, Matthijs W. J. de Waal, et al. · medRxiv · 10
PDF
Molecular characteristics of multifocal brain histiocytic sarcoma
2018 · F. Marguet, N. Piton, et al. · Neuropathology and Applied Neurobiology · 10
Ageing stereotypes and prodromal Alzheimer’s disease (AGING): study protocol for an ongoing randomised clinical study
2019 · Kim Gauthier, Alexandrine Morand, et al. · BMJ Open · 8
PDF
Publisher Correction: Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes
2022 · Catherine Schramm, Camille Charbonnier, et al. · Genome Medicine · 5
PDF
Domain mapping of disease mutations reveals pathogenic SORL1 variants in Alzheimer’s disease
2025 · Olav M. Andersen, Matthijs W. J. de Waal, et al. · Molecular Neurodegeneration · 4
PDF
Input of exome sequencing in early‐onset cerebral amyloid angiopathy
2024 · Lou Grangeon, Camille Charbonnier, et al. · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · 4
PDF
Ipilimumab-induced severe meningoradiculitis
2018 · Morgane Lacour, Lou Grangeon, et al. · Journal of Clinical Neuroscience · 3
PDF
Soluble SorLA in CSF, a novel biomarker to explore disrupted trafficking of SorLA protein in Alzheimer disease
2025 · Romain Castelot, Aline Zarea, et al. · Alzheimer s Research & Therapy · 2
PDF
Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk
2026 · Olivier Quenez, Catherine Schramm, et al. · The American Journal of Human Genetics · 1
APOE and genetic risk variants influence Alzheimer's disease onset in carriers of an extra copy of APP , with and without Down syndrome
2026 · Joan Groeneveld, Danna Perlaza, et al. · Alzheimer s & Dementia · 1
The genetic landscape of frontotemporal lobar degeneration: investigation of a diagnostic cohort of 2747 probands
2025 · Guillaume Cogan, Marion Houot, et al. · Brain · 1
Summary statistics for "Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's Disease"
2022 · Henne Holstege, Hulsman, Marc, et al. · ePrints Soton (University of Southampton) · 1
Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer's disease
2021 · Holstege, Henne, Hulsman, Marc, et al. · EUR Research Repository (Erasmus University Rotterdam) · 1
Penetrance estimation of SORL1 loss-of-function variants using a family-based strategy adjusted on APOE genotypes suggest a non-monogenic inheritance
2021 · Catherine Schramm, Camille Charbonnier, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1
PDF
Works count: 43
Citation count: 890
H-index: 11
I10-index: 12
Year
Topic
Type