Found: 22
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Apolipoprotein E Genotype is Associated with Temporal and Hippocampal Atrophy Rates in Healthy Elderly Adults: A Tensor-Based Morphometry Study.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 23, n. 3, p. 433, doi. 10.3233/JAD-2010-101398
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- Publication type:
- Article
Apolipoprotein E genotype is associated with temporal and hippocampal atrophy rates in healthy elderly adults: a tensor-based morphometry study.
- Published in:
- 2011
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- Publication type:
- journal article
Accelerated cognitive decline and hippocampal volume loss in mild cognitive impaired carriers of Apolipoprotein‐E ε4.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 6, p. 1, doi. 10.1002/alz.065115
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- Publication type:
- Article
Brain structure and obesity.
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- Human Brain Mapping, 2010, v. 31, n. 3, p. 353, doi. 10.1002/hbm.20870
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- Publication type:
- Article
Measurement of cortical thickness from MRI by minimum line integrals on soft-classified tissue.
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- Human Brain Mapping, 2009, v. 30, n. 10, p. 3188, doi. 10.1002/hbm.20740
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- Publication type:
- Article
Automated 3D mapping of hippocampal atrophy and its clinical correlates in 400 subjects with Alzheimer's disease, mild cognitive impairment, and elderly controls.
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- Human Brain Mapping, 2009, v. 30, n. 9, p. 2766, doi. 10.1002/hbm.20708
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- Publication type:
- Article
Protein co-expression network analysis in Alzheimer’s disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P299, doi. 10.1016/j.jalz.2015.07.414
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- Publication type:
- Article
O1-02-05: Automated longitudinal 3D mapping of hippocampal ADAS-cog delayed recall effects in 293 normal elderly, MCI and Alzheimer's disease subjects
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- 2008
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- Publication type:
- Abstract
IC-P3-223: Automated longitudinal 3D mapping of hippocampal ADASCPG delayed recall effects in 293 normal elderly, MCI and AD subjects
- Published in:
- 2008
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- Publication type:
- Abstract
A large meta-analysis identifies genes associated with anterior uveitis.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43036-1
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- Publication type:
- Article
A large meta-analysis identifies genes associated with anterior uveitis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43036-1
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- Publication type:
- Article
Case Report: A False Negative Case of Anti-Yo Paraneoplastic Myelopathy.
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- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.728700
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- Publication type:
- Article
Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders.
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- Nature Reviews Genetics, 2015, v. 16, n. 8, p. 441, doi. 10.1038/nrg3934
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- Publication type:
- Article
Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex.
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- Journal of Neurodevelopmental Disorders, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s11689-018-9237-x
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- Publication type:
- Article
Transcriptional profiling in microglia across physiological and pathological states identifies a transcriptional module associated with neurodegeneration.
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- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06684-7
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- Publication type:
- Article
Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders.
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- Nature Communications, 2016, v. 7, n. 2, p. 10717, doi. 10.1038/ncomms10717
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- Publication type:
- Article
Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.
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- Human Molecular Genetics, 2019, v. 28, n. 13, p. 2201, doi. 10.1093/hmg/ddz052
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- Publication type:
- Article
Spatiotemporal dynamics of the postnatal developing primate brain transcriptome.
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- Human Molecular Genetics, 2015, v. 24, n. 15, p. 4327, doi. 10.1093/hmg/ddv166
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- Publication type:
- Article
RBFOX1 regulates both splicing and transcriptional networks in human neuronal development.
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- Human Molecular Genetics, 2012, v. 21, n. 19, p. 4171, doi. 10.1093/hmg/dds240
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- Publication type:
- Article
De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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- Nature, 2012, v. 485, n. 7397, p. 237, doi. 10.1038/nature10945
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- Publication type:
- Article
Integrative network analysis reveals biological pathways associated with Williams syndrome.
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- Journal of Child Psychology, 2019, v. 60, n. 5, p. 585, doi. 10.1111/jcpp.12999
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- Publication type:
- Article
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51819-3
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- Publication type:
- Article