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Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5740, doi. 10.1002/alz.13873
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- Publication type:
- Article
A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease.
- Published in:
- 2019
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- Publication type:
- letter
Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus.
- Published in:
- 2018
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- Publication type:
- letter
No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization study.
- Published in:
- 2017
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- Publication type:
- journal article
ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies.
- Published in:
- 2017
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- Publication type:
- letter
Mendelian Randomization - the Key to Understanding Aspects of Parkinson's Disease Causation?
- Published in:
- 2016
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- Publication type:
- journal article
Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI).
- Published in:
- 2016
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- Publication type:
- journal article
Genetic risk and age in Parkinson's disease: Continuum not stratum.
- Published in:
- Movement Disorders, 2015, v. 30, n. 6, p. 850, doi. 10.1002/mds.26192
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- Publication type:
- Article
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset.
- Published in:
- NPJ Parkinson's Disease, 2019, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41531-019-0080-x
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- Publication type:
- Article
The Parkinson's phenome—traits associated with Parkinson's disease in a broadly phenotyped cohort.
- Published in:
- NPJ Parkinson's Disease, 2019, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41531-019-0077-5
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- Publication type:
- Article
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability.
- Published in:
- NPJ Parkinson's Disease, 2019, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41531-019-0076-6
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- Publication type:
- Article
Anticholinergic Drug Induced Cognitive and Physical Impairment: Results from the InCHIANTI Study.
- Published in:
- 2020
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- Publication type:
- journal article
Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study.
- Published in:
- 2016
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- Publication type:
- journal article
Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.
- Published in:
- 2016
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- Publication type:
- Other
Meta‐analysis of genome‐wide association studies for circulating phylloquinone (818.9).
- Published in:
- FASEB Journal, 2014, v. 28, p. N.PAG, doi. 10.1096/fasebj.28.1_supplement.818.9
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- Publication type:
- Article
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 5, p. 1504, doi. 10.1093/hmg/ddu560
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- Publication type:
- Article
Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 2, p. 572, doi. 10.1093/hmg/ddu454
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- Publication type:
- Article
Genetic comorbidities in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 831
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- Publication type:
- Article
Plasma 24-metabolite Panel Predicts Preclinical Transition to Clinical Stages of Alzheimer's Disease.
- Published in:
- Frontiers in Neurology, 2015, v. 6, p. 1, doi. 10.3389/fneur.2015.00237
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- Publication type:
- Article
Genetic risk factor clustering within and across neurodegenerative diseases.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 11, p. 4486, doi. 10.1093/brain/awad161
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- Publication type:
- Article
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease.
- Published in:
- 2018
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- Publication type:
- journal article
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
- Published in:
- 2018
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- Publication type:
- journal article
Genetic variation at 16q24.2 is associated with small vessel stroke.
- Published in:
- 2017
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- Publication type:
- journal article
Is the MC1R variant p.R160W associated with Parkinson's?
- Published in:
- 2016
- By:
- Publication type:
- letter
Polygenic risk of Parkinson disease is correlated with disease age at onset.
- Published in:
- Annals of Neurology, 2015, v. 77, n. 4, p. 582, doi. 10.1002/ana.24335
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- Publication type:
- Article
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity.
- Published in:
- Diabetes, 2020, v. 69, n. 12, p. 2806, doi. 10.2337/db20-0070
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- Publication type:
- Article
Genome-wide association study of neocortical Lewy-related pathology.
- Published in:
- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 9, p. 920, doi. 10.1002/acn3.231
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- Publication type:
- Article
Genetic variability at the PARK16 locus.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 12, p. 1356, doi. 10.1038/ejhg.2010.125
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- Publication type:
- Article
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
- Published in:
- Nature Genetics, 2014, v. 46, n. 9, p. 989, doi. 10.1038/ng.3043
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- Publication type:
- Article
A Novel <i>MMP12</i> Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 7, p. 1, doi. 10.1371/journal.pgen.1004469
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- Publication type:
- Article
Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study.
- Published in:
- 2017
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- Publication type:
- journal article
Shared mechanisms for cognitive impairment and physical frailty: Amodel for complex systems.
- Published in:
- Alzheimer's & Dementia: Translational Research & Clinical Interventions, 2020, v. 6, n. 1, p. 1, doi. 10.1002/trc2.12027
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- Publication type:
- Article
Genome‐Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent.
- Published in:
- Molecular Nutrition & Food Research, 2018, v. 62, n. 3, p. 1, doi. 10.1002/mnfr.201700347
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- Publication type:
- Article
Modeling multifunctionality of genes with secondary gene co-expression networks in human brain provides novel disease insights.
- Published in:
- Bioinformatics, 2021, v. 37, n. 18, p. 2905, doi. 10.1093/bioinformatics/btab175
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- Publication type:
- Article
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
- Published in:
- NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00526-9
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- Publication type:
- Article
Identification and prediction of Parkinson's disease subtypes and progression using machine learning in two cohorts.
- Published in:
- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00439-z
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- Publication type:
- Article
Comparison Between Southern Blots and qPCR Analysis of Leukocyte Telomere Length in the Health ABC Study.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2014, v. 69, n. 5, p. 527, doi. 10.1093/gerona/glt121
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- Publication type:
- Article
Evaluating the harmonisation potential of diverse cohort datasets.
- Published in:
- European Journal of Epidemiology, 2023, v. 38, n. 6, p. 605, doi. 10.1007/s10654-023-00997-3
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- Publication type:
- Article
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-55479-y
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- Publication type:
- Article
Prospective Associations of Coronary Heart Disease Loci in African Americans Using the MetaboChip: The PAGE Study.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113203
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- Publication type:
- Article
Another explanation for apparent epistasis.
- Published in:
- Nature, 2014, v. 514, n. 7520, p. E3, doi. 10.1038/nature13691
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- Publication type:
- Article
Proteomics and Epidemiological Models of Human Aging.
- Published in:
- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.674013
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- Publication type:
- Article
Novel age-associated DNA methylation changes and epigenetic age acceleration in middle-aged African Americans and whites.
- Published in:
- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0722-1
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- Publication type:
- Article
Analysis of Y chromosome haplogroups in Parkinson's disease.
- Published in:
- Brain Communications, 2022, v. 4, n. 6, p. 1, doi. 10.1093/braincomms/fcac277
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- Publication type:
- Article
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
- Published in:
- JAMA Neurology, 2020, v. 77, n. 6, p. 746, doi. 10.1001/jamaneurol.2020.0428
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- Publication type:
- Article
Multiple modality biomarker prediction of cognitive impairment in prospectively followed de novo Parkinson disease.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0175674
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- Publication type:
- Article
PhenoExam: gene set analyses through integration of different phenotype databases.
- Published in:
- BMC Bioinformatics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12859-022-05122-x
- By:
- Publication type:
- Article
Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-14483-x
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- Publication type:
- Article
Mis-spliced transcripts generate de novo proteins in TDP-43–related ALS/FTD.
- Published in:
- Science Translational Medicine, 2024, v. 16, n. 734, p. 1, doi. 10.1126/scitranslmed.adg7162
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- Publication type:
- Article
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.
- Published in:
- Brain: A Journal of Neurology, 2014, v. 137, n. 12, p. e311, doi. 10.1093/brain/awu265
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- Publication type:
- Article