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Polygenic Risk Score of Longevity Predicts Longer Survival Across an Age Continuum.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2021, v. 76, n. 5, p. 750, doi. 10.1093/gerona/glaa289
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- Article
Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Connecting dementia risk loci to the CSF proteome identifies pathophysiological leads for dementia.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 10, p. 3522, doi. 10.1093/brain/awae090
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- Article
Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease.
- Published in:
- 2017
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- Publication type:
- journal article
Rare missense variant (R251G) on APOE counterbalances the Alzheimer's disease risk associated with APOE‐ε4.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.060114
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- Publication type:
- Article
Protective association of HLA‐DRB1*04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 3, p. 1, doi. 10.1002/alz.060159
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- Publication type:
- Article
Pathway‐specific polygenic risk score of AD‐associated genetic variants associated with AD risk, resilience against AD, and progression to AD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.053500
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- Publication type:
- Article
BDNF‐Met polymorphism on top of amyloid pathology predisposes for faster cognitive decline in cognitively normal elderly: The SCIENCe Project: 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.042728
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- Publication type:
- Article
Immune response and endocytosis pathways are associated with the resilience against Alzheimer's disease: Genetics: Molecular genetics of AD and ADRD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042614
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- Publication type:
- Article
Polygenic risk score for Alzheimer's disease is related to amyloid positivity in subjective cognitive decline: The SCIENCe project: Neuroimaging: Imaging genetics.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.042116
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- Publication type:
- Article
Functional interpretation of genetic risk loci for dementia using a protein quantitative trait loci (pQTLs) approach in cerebrospinal fluid: Genetics: Molecular genetics of AD and ADRD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.040774
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- Publication type:
- Article
Novel genetic effects on amyloid and tau protein levels in cerebrospinal fluid: Towards a better knowledge of the genetics of Alzheimer's disease, the European Alzheimer Disease Biobank (EADB) Consortium.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.037973
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- Publication type:
- Article
P4‐525: ASSOCIATION OF CSF TAU WITH HYPERPLASTICITY IN ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1515, doi. 10.1016/j.jalz.2019.08.072
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- Publication type:
- Article
O5‐04‐01: A RARE GENETIC VARIANT IN THE PLCG2 GENE IS ASSOCIATED WITH A REDUCED RISK OF ALL MAJOR TYPES OF DEMENTIA AND AN INCREASED RISK TO REACH AN EXTREMELY OLD AGE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1648, doi. 10.1016/j.jalz.2018.06.3013
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- Publication type:
- Article
P2‐134: THE ADDED VALUE OF EXTREME PHENOTYPES IN ALZHEIMER'S DISEASE CASE‐CONTROL STUDIES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P719, doi. 10.1016/j.jalz.2018.06.820
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- Publication type:
- Article
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01577-3
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- Publication type:
- Article
Immune response and endocytosis pathways are associated with the resilience against Alzheimer's disease.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-01018-7
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- Publication type:
- Article
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-29108-8
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- Publication type:
- Article
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22491-8
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- Publication type:
- Article
ESTABLISHING THE EFFECT OF CODING VARIANTS ON ALZHEIMER’S DISEASE RELATED ENDOPHENOTYPES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1487, doi. 10.1016/j.jalz.2017.07.569
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- Publication type:
- Article
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia.
- Published in:
- Neurodegenerative Diseases, 2017, v. 17, n. 2/3, p. 83, doi. 10.1159/000448896
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- Publication type:
- Article
Intradermal lipopolysaccharide challenge as an acute in vivo inflammatory model in healthy volunteers.
- Published in:
- British Journal of Clinical Pharmacology, 2022, v. 88, n. 2, p. 680, doi. 10.1111/bcp.14999
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- Publication type:
- Article
Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.
- Published in:
- JAMA Neurology, 2017, v. 74, n. 7, p. 780, doi. 10.1001/jamaneurol.2017.0469
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- Publication type:
- Article
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's.
- Published in:
- 2016
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- Publication type:
- journal article
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 24, p. 5483, doi. 10.1093/hmg/ddw348
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- Publication type:
- Article
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 5, p. 821, doi. 10.1007/s00401-022-02454-z
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- Publication type:
- Article
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment.
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- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1025, doi. 10.1007/s00401-020-02138-6
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- Publication type:
- Article
Risk of dementia in APOE ε4 carriers is mitigated by a polygenic risk score.
- Published in:
- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12229
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- Publication type:
- Article
The Effect of Alzheimer's Disease-Associated Genetic Variants on Longevity.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.748781
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- Publication type:
- Article
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
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- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1147-9
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- Publication type:
- Article
Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping.
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- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-00962-4
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- Publication type:
- Article
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe.
- Published in:
- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0320-1
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- Publication type:
- Article
Disentangling Genetic Risks for Metabolic Syndrome.
- Published in:
- Diabetes, 2022, v. 71, n. 11, p. 2447, doi. 10.2337/db22-0478
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- Publication type:
- Article