The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease

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Publication Details

Journal
Molecular Neurodegeneration Advances
Published
2025-10-20
DOI
https://doi.org/10.1186/s44477-025-00004-x
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease

Harry V. Vinters, Wim Annaert, Mihaela Campan, Bart De Strooper et al.
Molecular Neurodegeneration Advances
Alzheimer's disease research and treatments
article

The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease

Harry V. Vinters, Wim Annaert, Mihaela Campan, Bart De Strooper, Lutgarde Serneels, Lucía Chávez‐Gutiérrez, Shino Magaki, Inmaculada Sanjuan-Ruiz, Joanna C. Jen, David W. Craig, Katleen Craessaerts, John M. Ringman, Nasim Sheikh‐Bahaei, Alison Goate, Yonggang Shi, Eliana Marisa Ramos, Pamela Ward, Kelly Bartlone
article en

Abstract

No abstract available for this paper.
Molecular Neurodegeneration AdvancesVol. 1(1)
University of Southern California (US), City Of Hope National Medical Center (US), University of California, Los Angeles (US), Keck Hospital of USC (US), Vlaams Instituut voor Biotechnologie (BE), Alzheimer’s Disease Neuroimaging Initiative (US), UK Dementia Research Institute (GB), VIB-KU Leuven Center for Brain & Disease Research (BE), University College London (GB), Icahn School of Medicine at Mount Sinai (US)
Eisai, KU Leuven, Genentech
Openalex Percentile: Top 63%
Alzheimer's disease research and treatments
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The curious case of a heterozygous loss-of-function PSEN1 variant associated with early-onset Alzheimer’s disease — Harry V. Vinters, Wim Annaert, et al. · Molecular Neurodegeneration Advances (2025) | TGRS Research Map | TGRS