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Extended genome‐wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5247, doi. 10.1002/alz.13880
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- Publication type:
- Article
A comparative study of structural variant calling in WGS from Alzheimer's disease families.
- Published in:
- Life Science Alliance, 2024, v. 7, n. 5, p. 1, doi. 10.26508/lsa.202302181
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- Publication type:
- Article
The APOE ε4 allele is associated with a reduction in FEV<sub>1</sub>/FVC in women: A cross-sectional analysis of the Long Life Family Study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0206873
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- Publication type:
- Article
Transposon DNA sequences facilitate the tissue-specific gene transfer of circulating tumor DNA between human cells.
- Published in:
- Nucleic Acids Research, 2024, v. 52, n. 13, p. 7539, doi. 10.1093/nar/gkae427
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- Publication type:
- Article
Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.
- Published in:
- Annals of Neurology, 2015, v. 78, n. 3, p. 487, doi. 10.1002/ana.24466
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- Publication type:
- Article
Coding mutations in SORL1 and Alzheimer disease.
- Published in:
- 2015
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- Publication type:
- journal article
Coding mutations in SORL 1 and Alzheimer disease.
- Published in:
- Annals of Neurology, 2015, v. 77, n. 2, p. 215, doi. 10.1002/ana.24305
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- Publication type:
- Article
Whole‐exome sequencing in 20,197 persons for rare variants in Alzheimer's disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 7, p. 832, doi. 10.1002/acn3.582
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- Publication type:
- Article
Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 4, p. 406, doi. 10.1002/acn3.537
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- Publication type:
- Article
F-box/ LRR-repeat protein 7 is genetically associated with Alzheimer's disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 8, p. 810, doi. 10.1002/acn3.223
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- Publication type:
- Article
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
- Published in:
- Nature Genetics, 2013, v. 45, n. 12, p. 1452, doi. 10.1038/ng.2802
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- Publication type:
- Article
Data‐Independent Acquisition and Label‐Free Quantification for Quantitative Proteomics Analysis of Human Cerebrospinal Fluid.
- Published in:
- Current Protocols, 2024, v. 4, n. 3, p. 1, doi. 10.1002/cpz1.1014
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- Publication type:
- Article
Analysis of individual families implicates noncoding DNA variation and multiple biological pathways in Alzheimer's disease risk: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.046456
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- Publication type:
- Article
The Alzheimer's disease sequencing project–follow up study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer's genetics research with addition of potential new cohorts: Genetics/genetic factors of non‐Alzheimer's tauopathies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.046400
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- Publication type:
- Article
High frequency of progranulin mutations in Caribbean Hispanic families with dementia: Neuropsychiatry and behavioral neurology/Assessment/Measurement of neuropsychiatric/Behavioral and psychological symptoms.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.046397
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- Publication type:
- Article
APOE‐stratified, genome‐wide, gene‐based analysis of episodic memory trajectories in a multi‐ethnic sample of 24,769 elderly: Genetics: Genetics of cognitive aging, other dementia, and endophenotypes.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.045997
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- Publication type:
- Article
Alzheimer's disease GWAS weighted by multi‐omics and endophenotypes identifies novel risk loci: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043977
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- Publication type:
- Article
Sex differences in genetic predictors of resilience to Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043259
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- Publication type:
- Article
P4‐097: RARE VARIANTS IN FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE IDENTIFIED FROM LARGE SCALE WHOLE GENOME SEQUENCING.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1312, doi. 10.1016/j.jalz.2019.06.3757
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- Publication type:
- Article
P4‐094: EXOME‐WIDE ANALYSIS IDENTIFIES NOVEL SEX‐SPECIFIC CANDIDATE GENES FOR ALZHEIMER DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1310, doi. 10.1016/j.jalz.2019.06.3754
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- Publication type:
- Article
O3‐13‐01: HIGHLY PENETRANT LATE‐ONSET ALZHEIMER DISEASE VARIANTS IN NOTCH3 IN ASHKENAZI JEWS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P918, doi. 10.1016/j.jalz.2019.06.4696
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- Publication type:
- Article
P2‐151: THE ALZHEIMER'S DISEASE SEQUENCING PROJECT – FOLLOW UP STUDY (ADSP‐FUS): INCREASING ETHNIC DIVERSITY IN ALZHEIMER'S GENETICS RESEARCH.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P634, doi. 10.1016/j.jalz.2019.06.4961
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- Publication type:
- Article
A rare missense variant of CASP7 is associated with familial late‐onset Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, n. 3, p. 441, doi. 10.1016/j.jalz.2018.10.005
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- Publication type:
- Article
P2‐140: GENOME‐WIDE ASSOCIATION STUDY FOR ALZHEIMER'S DISEASE IN A LARGE SAMPLE OF CARIBBEAN HISPANICS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P721, doi. 10.1016/j.jalz.2018.06.826
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- Publication type:
- Article
P2‐108: WHOLE‐GENOME SEQUENCING IN NON‐HISPANIC WHITE FAMILIES IMPLICATES RARE VARIATION IN LATE‐ONSET ALZHEIMER'S DISEASE RISK.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P710, doi. 10.1016/j.jalz.2018.06.794
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- Publication type:
- Article
P1‐170: WHOLE‐EXOME SEQUENCING IN 20,197 INDIVIDUALS IDENTIFIES ULTRA‐RARE SORL1 LOSS‐OF‐FUNCTION VARIANTS IN LATE‐ONSET ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P344, doi. 10.1016/j.jalz.2018.06.174
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- Publication type:
- Article
P1‐161: RARE, SYNONYMOUS VARIANTS IN CDH23, SLC9A3R1, RHBDD2 AND ITIH2 ARE ASSOCIATED WITH ALZHEIMER'S DISEASE IN MULTIPLEX CARIBBEAN HISPANIC FAMILIES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P339, doi. 10.1016/j.jalz.2018.06.165
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- Publication type:
- Article
P1‐156: GENE‐BASED ANALYSES IN WHOLE GENOME SEQUENCING OF FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P336, doi. 10.1016/j.jalz.2018.06.160
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- Publication type:
- Article
S1‐02‐03: GENETICS OF SORL1 AND ITS ROLE AS AN APP NEURONAL SORTING RECEPTOR.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P198, doi. 10.1016/j.jalz.2018.06.2300
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- Publication type:
- Article
WHOLE-GENOME SEQUENCING IN FAMILIAL LATE-ONSET ALZHEIMER’S DISEASE IDENTIFIES RARE VARIATION IN AD CANDIDATE GENES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P571, doi. 10.1016/j.jalz.2017.07.188
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- Publication type:
- Article
WHOLE GENOME SEQUENCING IN HEALTHY ELDERLY APOE ε4 SUBJECTS IDENTIFIES PROTECTIVE GAIN OF FUNCTION MUTATIONS IN ALZHEIMER’S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P698, doi. 10.1016/j.jalz.2017.06.880
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- Publication type:
- Article
ABCA7 FRAMESHIFT DELETION ASSOCIATED WITH ALZHEIMER’S DISEASE IN AFRICAN AMERICANS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P177, doi. 10.1016/j.jalz.2016.06.305
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- Publication type:
- Article
PATHOGENIC SORL1 MUTATIONS AND PARKINSONIAN FEATURES IN ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P451, doi. 10.1016/j.jalz.2016.06.874
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- Publication type:
- Article
WHOLE GENOME SEQUENCING IN FAMILIAL LATE-ONSET ALZHEIMER’S DISEASE IDENTIFIES VARIATIONS IN TTC3 AND FSIP2.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P197, doi. 10.1016/j.jalz.2016.06.343
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- Publication type:
- Article
IDENTIFICATION OF NOVEL CANDIDATE GENES FOR EARLY-ONSET ALZHEIMER'S DISEASE THROUGH INTEGRATED WHOLE-EXOME SEQUENCING AND EXOME CHIP ARRAY ASSOCIATION ANALYSIS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P177, doi. 10.1016/j.jalz.2016.06.306
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- Publication type:
- Article
WHOLE EXOME SEQUENCING IN HEALTHY ELDERLY APOE E44 SUBJECTS TO IDENTIFY PROTECTIVE VARIANTS IN ALZHEIMER’S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P178, doi. 10.1016/j.jalz.2016.06.307
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- Publication type:
- Article
MAPT haplotypes modify the association between head injury and risk of Alzheimer’s disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P361, doi. 10.1016/j.jalz.2015.06.256
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- Publication type:
- Article
ABCA7 deletion associated with Alzheimer's disease in african americans.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P485, doi. 10.1016/j.jalz.2015.06.549
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- Publication type:
- Article
Rare coding mutations identified by targeted sequencing of Alzheimer’s disease loci detected in genome-wide association studies.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P252, doi. 10.1016/j.jalz.2015.07.313
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- Publication type:
- Article
Admixture analysis of Alzheimer’s disease in caribbean hispanics.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P229, doi. 10.1016/j.jalz.2015.07.264
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- Publication type:
- Article
Genome wide analyses of runs of homozygosity among african americans revealed further evidence of recessive inheritance for Alzheimer’s disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P228, doi. 10.1016/j.jalz.2015.07.262
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- Publication type:
- Article
Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, n. 6, p. 609, doi. 10.1016/j.jalz.2014.06.010
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- Publication type:
- Article
Candidate gene study in the endosome-to-Golgi retrieval pathway reveals association of retromer genes with Alzheimer's disease
- Published in:
- 2010
- By:
- Publication type:
- Abstract
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
- Published in:
- JAMA Network Open, 2019, v. 2, n. 3, p. e191350, doi. 10.1001/jamanetworkopen.2019.1350
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- Publication type:
- Article
Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 5, p. 744, doi. 10.1002/acn3.51757
- By:
- Publication type:
- Article
Nerve growth factor receptor (Ngfr) induces neurogenic plasticity by suppressing reactive astroglial Lcn2/Slc22a17 signaling in Alzheimer's disease.
- Published in:
- NPJ Regenerative Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41536-023-00311-5
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- Publication type:
- Article
ZCCHC17 Modulates Neuronal RNA Splicing and Supports Cognitive Resilience in Alzheimer's Disease.
- Published in:
- Journal of Neuroscience, 2024, v. 44, n. 3, p. 1, doi. 10.1523/JNEUROSCI.2324-22.2023
- By:
- Publication type:
- Article
Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00239
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- Publication type:
- Article
Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.
- Published in:
- Genetic Epidemiology, 2018, v. 42, n. 6, p. 500, doi. 10.1002/gepi.22133
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- Publication type:
- Article
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.
- Published in:
- JAMA Neurology, 2017, v. 74, n. 9, p. 1113, doi. 10.1001/jamaneurol.2017.1518
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- Publication type:
- Article