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Publications by Pamela St. Jean

Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

Multidisciplinary

English

Mapping Loci for Pentylenetetrazol-Induced Seizure Susceptibility in Mice

Journal of Neuroscience

English

Related publications

Genetic Influences on Atrophy Patterns in Familial Alzheimer's Disease: A Comparison of APP and PSEN1 Mutations

Journal of Alzheimer's Disease

Clinical Psychology

English

Common Variants in Alzheimer's Disease: Novel Association of Six Genetic Variants With AD and Risk Stratification by Polygenic Risk Scores

English

A Rare Mutation in UNC5C Predisposes to Late-Onset Alzheimer's Disease and Increases Neuronal Cell Death

Nature Medicine

Molecular Biology

English

Whole-Exome Sequencing in 20,197 Persons for Rare Variants in Alzheimer's Disease

Annals of Clinical and Translational Neurology

English

Evidence for Defective Retinoid Transport and Function in Late Onset Alzheimer's Disease

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Early and Late Onset Types of Alzheimer's Disease

English

PLD3 Rare Variants Identified in Late-Onset Alzheimer’s Disease Affect Amyloid-Β Levels in Cellular Model

Frontiers in Neuroscience

English

Role of Common and Rare APP DNA Sequence Variants in Alzheimer Disease

English

Early-Onset Alzheimer's Disease: Nonamnestic Subtypes and Type 2 AD

Archives of Medical Research

English