Associated Papers
Missense and loss-of-function variants at GWAS loci in familial Alzheimer's disease.
Gunasekaran TI et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2024
Missense and Loss of Function Variants at GWAS Loci in Familial Alzheimer's Disease.
Gunasekaran TI et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Genetics of Alzheimer's Disease in the African American Population.
Logue MW et al.
Journal of Clinical Medicine, 2023
Challenge accepted: uncovering the role of rare genetic variants in Alzheimer's disease.
Khani M et al.
Molecular Neurodegeneration, 2022
35000612 (PubMed )
Supplement: 13024_2021_505_MOESM1_ESM.docx
Genomics of Alzheimer's disease implicates the innate and adaptive immune systems.
Li Y et al.
Cellular and Molecular Life Sciences : Cmls, 2021
How understudied populations have contributed to our understanding of Alzheimer's disease genetics.
Dehghani N et al.
Brain : a Journal of Neurology, 2021
Insight into the genetic etiology of Alzheimer's disease: A comprehensive review of the role of rare variants.
Hoogmartens J et al.
Alzheimer's & Dementia (amsterdam, Netherlands), 2021
Tau Phosphorylation is Impacted by Rare AKAP9 Mutations Associated with Alzheimer Disease in African Americans.
Ikezu T et al.
Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology, 2018
Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.
Vardarajan BN et al.
Annals of Clinical and Translational Neurology, 2018
Exome-wide somatic mutation characterization of small bowel adenocarcinoma.
Hänninen UA et al.
Plos Genetics, 2018
29522538 (PubMed )
Supplement: pgen.1007200.s003.xlsx › b
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