|
| 38050142 | ZCCHC17 Modulates Neuronal RNA Splicing and Supports Cognitive Resilience in Alzheimer's Disease. | J Neurosci | 2024 |
| 36539198 | Admixture mapping identifies novel Alzheimer's disease risk regions in African Americans. | Alzheimers Dement | 2023 |
| 37662203 | Lysophosphatidylcholines are associated with P-tau181 levels in early stages of Alzheimer's Disease. | medRxiv | 2023 |
| 37483004 | Reliability and Validity of Self-Reported Vascular Risk Factors: Hypertension, Diabetes, and Heart Disease, in a Multi-Ethnic Community Based Study of Aging and Dementia. | J Alzheimers Dis | 2023 |
| 37745545 | Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. | medRxiv | 2023 |
| 37645764 | Risk of Alzheimer's Disease is Associated with Longitudinal Changes in Plasma Biomarkers in the Multiethnic Washington Heights, Inwood Columbia Aging Project Cohort. | medRxiv | 2023 |
| 37927256 | Linking Air Pollution Exposure to Blood-Based Metabolic Features in a Community-Based Aging Cohort with and without Dementia. | J Alzheimers Dis | 2023 |
| 36993746 | ZCCHC17 modulates neuronal RNA splicing and supports cognitive resilience in Alzheimer's disease. | bioRxiv | 2023 |
| 37051669 | A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease. | Alzheimers Dement | 2023 |
| 36946865 | Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease. | Ann Clin Transl Neurol | 2023 |
| 37245481 | Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease. | EBioMedicine | 2023 |
| 37169873 | CARMA is a new Bayesian model for fine-mapping in genome-wide association meta-analyses. | Nat Genet | 2023 |
| 37131736 | Reliability and Validity of self-reported Vascular Risk Factors in a Multi-Ethnic Community Based Study of Aging and Dementia. | medRxiv | 2023 |
| 37429840 | Nerve growth factor receptor (Ngfr) induces neurogenic plasticity by suppressing reactive astroglial Lcn2/Slc22a17 signaling in Alzheimer's disease. | NPJ Regen Med | 2023 |
| 35210353 | An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns. | Genome Res | 2022 |
| 35379992 | New insights into the genetic etiology of Alzheimer's disease and related dementias. | Nat Genet | 2022 |
| 35608697 | FMNL2 regulates gliovascular interactions and is associated with vascular risk factors and cerebrovascular pathology in Alzheimer's disease. | Acta Neuropathol | 2022 |
| 35640154 | Genotype-phenotype correlation of T-cell subtypes reveals senescent and cytotoxic genes in Alzheimer's disease. | Hum Mol Genet | 2022 |
| 35365809 | Admixture Mapping of Alzheimer's disease in Caribbean Hispanics identifies a new locus on 22q13.1. | Mol Psychiatry | 2022 |
| 35552371 | Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease. | Brain | 2022 |
| 35258170 | Progranulin mutations in clinical and neuropathological Alzheimer's disease. | Alzheimers Dement | 2022 |
| 34978149 | The National Institute on Aging Late-Onset Alzheimer's Disease Family Based Study: A resource for genetic discovery. | Alzheimers Dement | 2022 |
| 34038570 | Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics. | Ann Neurol | 2021 |
| 33902942 | Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus. | Neurobiol Aging | 2021 |
| 34473944 | Stem cell-derived neurons reflect features of protein networks, neuropathology, and cognitive outcome of their aged human donors. | Neuron | 2021 |
| 34756330 | Embryonic lethal genetic variants and chromosomally normal pregnancy loss. | Fertil Steril | 2021 |
| 34547244 | Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene. | Am J Hum Genet | 2021 |
| 29988083 | A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. | Mol Psychiatry | 2020 |
| 32637632 | Synonymous variants associated with Alzheimer disease in multiplex families. | Neurol Genet | 2020 |
| 32740652 | A quantitative trait rare variant nonparametric linkage method with application to age-at-onset of Alzheimer's disease. | Eur J Hum Genet | 2020 |
| 32844198 | Genetic variants and functional pathways associated with resilience to Alzheimer's disease. | Brain | 2020 |
| 32377558 | Differences in plasma metabolites related to Alzheimer's disease, <i>APOE</i> ε4 status, and ethnicity. | Alzheimers Dement (N Y) | 2020 |
| 32568366 | Association Between Common Variants in RBFOX1, an RNA-Binding Protein, and Brain Amyloidosis in Early and Preclinical Alzheimer Disease. | JAMA Neurol | 2020 |
| 30503768 | A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease. | Alzheimers Dement | 2019 |
| 29857119 | Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project. | Genomics | 2019 |
| 31585107 | A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data. | Am J Hum Genet | 2019 |
| 31348909 | Somatic mosaicism of sex chromosomes in the blood and brain. | Brain Res | 2019 |
| 30924900 | Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry. | JAMA Netw Open | 2019 |
| 30863791 | Genomic variation in educational attainment modifies Alzheimer disease risk. | Neurol Genet | 2019 |
| 31058951 | Association of Variants in PINX1 and TREM2 With Late-Onset Alzheimer Disease. | JAMA Neurol | 2019 |
| 31001313 | Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools. | Front Genet | 2019 |
| 30820047 | Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. | Nat Genet | 2019 |
| 29486463 | Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. | Dement Geriatr Cogn Disord | 2018 |
| 29862559 | Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP. | Genet Epidemiol | 2018 |
| 30040223 | Pedigree Selection and Information Content. | Curr Protoc Hum Genet | 2018 |
| 29930110 | Analysis of shared heritability in common disorders of the brain. | Science | 2018 |
| 30037983 | An Alzheimer's Disease-Linked Loss-of-Function CLN5 Variant Impairs Cathepsin D Maturation, Consistent with a Retromer Trafficking Defect. | Mol Cell Biol | 2018 |
| 30009200 | Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease. | Ann Clin Transl Neurol | 2018 |
| 30084846 | A multi-omic atlas of the human frontal cortex for aging and Alzheimer's disease research. | Sci Data | 2018 |
| 30462667 | Episodic memory performance in a multi-ethnic longitudinal study of 13,037 elderly. | PLoS One | 2018 |