Found: 40
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Multi-modality machine learning predicting Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00288-w
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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
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
Bioinformatic approach for the discovery of cis-eQTL signals during fruit ripening of a woody species as grape (Vitis vinifera L.).
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-11689-5
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- Publication type:
- Article
CoExp: A Web Tool for the Exploitation of Co-expression Networks.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.630187
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- Publication type:
- Article
The non-specific lethal complex regulates genes and pathways genetically linked to Parkinson's disease.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. 4974, doi. 10.1093/brain/awad246
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- Publication type:
- Article
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 7, p. 2869, doi. 10.1093/brain/awad009
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- Publication type:
- Article
A genetic link between risk for Alzheimer's disease and severe COVID-19 outcomes via the OAS1 gene.
- Published in:
- 2021
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- Publication type:
- Journal Article
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders.
- Published in:
- 2020
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- Publication type:
- journal article
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination.
- Published in:
- 2019
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- Publication type:
- journal article
Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsy.
- Published in:
- 2019
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- Publication type:
- journal article
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.
- Published in:
- 2018
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- Publication type:
- journal article
The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Artificial intelligence for dementia genetics and omics.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 12, p. 5905, doi. 10.1002/alz.13427
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- Publication type:
- Article
Preclinical Alzheimer's Disease accurate prediction using plasma cell‐free RNA sequences.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.060825
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- Publication type:
- Article
ASL expression in ALDH1A1<sup>+</sup> neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype.
- Published in:
- Human Genetics, 2021, v. 140, n. 10, p. 1471, doi. 10.1007/s00439-021-02345-5
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- Publication type:
- Article
A predictive model for hospitalization and survival to COVID-19 in a retrospective population-based study.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-22547-9
- By:
- Publication type:
- Article
Leveraging omic features with F3UTER enables identification of unannotated 3'UTRs for synaptic genes.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30017-z
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- Publication type:
- Article
CREATING CONTEXT-AWARE COLLABORATIVE WORKING ENVIRONMENTS.
- Published in:
- International Journal on Artificial Intelligence Tools, 2011, v. 20, n. 1, p. 195
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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
An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks.
- Published in:
- BMC Systems Biology, 2017, v. 11, p. 1, doi. 10.1186/s12918-017-0420-6
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- Publication type:
- Article
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets.
- Published in:
- JAMA Neurology, 2021, v. 78, n. 4, p. 464, doi. 10.1001/jamaneurol.2020.5257
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- Publication type:
- Article
A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies.
- Published in:
- Neuropathology & Applied Neurobiology, 2022, v. 48, n. 1, p. 1, doi. 10.1111/nan.12758
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- Publication type:
- Article
An Approach for Representing Sensor Data to Validate Alerts in Ambient Assisted Living.
- Published in:
- Sensors (14248220), 2012, v. 12, n. 5, p. 6282, doi. 10.3390/s120506282
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- Publication type:
- Article
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation.
- Published in:
- 2019
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- Publication type:
- journal article
Trem2 promotes anti-inflammatory responses in microglia and is suppressed under pro-inflammatory conditions.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 19, p. 3224, doi. 10.1093/hmg/ddaa209
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- Publication type:
- Article
Design and evaluation of an ambient assisted living system based on an argumentative multi-agent system.
- Published in:
- Personal & Ubiquitous Computing, 2011, v. 15, n. 4, p. 377, doi. 10.1007/s00779-010-0361-1
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- Publication type:
- Article
White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 1, p. 135, doi. 10.1007/s00401-019-02074-0
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- Publication type:
- Article
Correction to: Picomolar concentrations of oligomeric alpha-synuclein sensitizes TLR4 to play an initiating role in Parkinson's disease pathogenesis.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Picomolar concentrations of oligomeric alpha-synuclein sensitizes TLR4 to play an initiating role in Parkinson's disease pathogenesis.
- Published in:
- Acta Neuropathologica, 2019, v. 137, n. 1, p. 103, doi. 10.1007/s00401-018-1907-y
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- Publication type:
- Article
IntroVerse: a comprehensive database of introns across human tissues.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. D1, p. D167, doi. 10.1093/nar/gkac1056
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- Publication type:
- Article
Toward a framework for the specification of hybrid fuzzy modeling.
- Published in:
- International Journal of Intelligent Systems, 2005, v. 20, n. 2, p. 225, doi. 10.1002/int.20064
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- Publication type:
- Article
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
- Published in:
- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1147-9
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- Publication type:
- Article
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis.
- Published in:
- Molecular Neurodegeneration, 2016, v. 11, p. 1, doi. 10.1186/s13024-016-0085-4
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- Publication type:
- Article
Towards an approach for debugging multi-agent systems through the analysis of agent messages.
- Published in:
- Computer Systems Science & Engineering, 2005, v. 20, n. 4, p. 237
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- Publication type:
- Article
Combining the real world with simulations for a robust testing of Ambient Intelligence services.
- Published in:
- Artificial Intelligence Review, 2014, v. 42, n. 4, p. 723, doi. 10.1007/s10462-012-9340-4
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- Publication type:
- Article
A loss‐of‐function homozygous mutation in <italic>DDX59</italic> implicates a conserved DEAD‐box RNA helicase in nervous system development and function.
- Published in:
- Human Mutation, 2018, v. 39, n. 2, p. 187, doi. 10.1002/humu.23368
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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
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- Publication type:
- Article
Analysis of subcellular RNA fractions demonstrates significant genetic regulation of gene expression in human brain post-transcriptionally.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-40324-0
- 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