Varaico: Literature-Extracted Genetic Variants

Gene:PSEN1
Variant:p.I437V
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PSEN1

NM_000021.4:p.I437V

Associated Papers

Biobank-scale genetic characterization of Alzheimer's disease and related dementias across diverse ancestries.

Khani M et al.

Nature Communications, 2025

The landscape of autosomal-dominant Alzheimer's disease: global distribution and age of onset.

Liu H et al.

Brain : a Journal of Neurology, 2025

39903689 (PubMed )
Supplement: awaf038_supplementary_data.zip › 2-Supplemental_Table1_AR_20250121_JLliF.pdf

Huntington's disease phenocopy syndromes revisited: a clinical comparison and next-generation sequencing exploration.

Koriath CAM et al.

Journal of Neurology, Neurosurgery, and Psychiatry, 2025

Evaluating pathogenicity of variants of unknown significance in APP, PSEN1, and PSEN2.

Marsh JA et al.

Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics, 2025

Identification and characterization of variants in PSEN1, PSEN2, and APP genes in Chinese patients with early-onset Alzheimer's disease.

Nan H et al.

Alzheimer's Research & Therapy, 2025

Leveraging large-scale multi-omics evidences to identify therapeutic targets from genome-wide association studies.

Lessard S et al.

Bmc Genomics, 2024

Biobank-scale characterization of Alzheimer's disease and related dementias identifies potential disease-causing variants, risk factors, and genetic modifiers across diverse ancestries.

Khani M et al.

Medrxiv : the Preprint Server for Health Sciences, 2024

Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening.

Nicolas G et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2024

Aβ42/Aβ40 Ratios of Presenilin 1 Mutations Correlate with Clinical Onset of Alzheimer's Disease.

Tang N et al.

Journal of Alzheimer's Disease : Jad, 2018

APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.

Lanoiselée HM et al.

Plos Medicine, 2017

28350801 (PubMed )
Supplement: pmed.1002270.s001.xlsx › PSEN1_mutations

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons.

Nicolas G et al.

European Journal of Human Genetics : Ejhg, 2016

Loss of gamma-secretase function impairs endocytosis of lipoprotein particles and membrane cholesterol homeostasis.

Tamboli IY et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2008

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."