Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging

Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging

Identification of genes associated with brain aging should markedly improve our understanding of the biological processes that govern normal age-related decline. However, challenges to identifying genes that facilitate successful brain aging are considerable, including a lack of established phenotyp...

Cur síos iomlán

Sonraí bibleagrafaíochta
Príomhchruthaitheoirí:	Glahn, D, Kent, J, Sprooten, E, Diego, V, Winkler, A, Curran, J, McKay, DR, Knowles, E, Carless, M, Goring, H, Dyer, T, Olvera, R, Fox, P, Almasy, L, Charlesworth, J, Kochunov, P, Duggirala, R, Blangero, J
Formáid:	Journal article
Teanga:	English
Foilsithe / Cruthaithe:	National Academy of Sciences 2013
Ábhair:	Cognitive Neuroscience Neurogenetics Neuropsychology Neuroscience Genetics (medical sciences) Neurology

Míreanna comhchosúla

Influence of age, sex and genetic factors on the human brain
de réir: McKay, DR, et al.
Foilsithe / Cruthaithe: (2014)

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
de réir: Carless, M, et al.
Foilsithe / Cruthaithe: (2011)

Genetic influence on the working memory circuitry: Behavior, structure, function and extensions to illness
de réir: Karlsgodt, K, et al.
Foilsithe / Cruthaithe: (2011)

Reduced white matter integrity in sibling pairs discordant for bipolar disorder
de réir: Sprooten, E, et al.
Foilsithe / Cruthaithe: (2013)

Dissecting the functions of DISC1
de réir: Carless, M, et al.
Foilsithe / Cruthaithe: (2011)

Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2009)

Transcriptomics of cortical gray matter thickness decline during normal aging
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2013)

Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2010)

Genetic architecture of declarative memory: implications for complex illnesses
de réir: Bearden, C, et al.
Foilsithe / Cruthaithe: (2012)

Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies
de réir: Winkler, A, et al.
Foilsithe / Cruthaithe: (2010)

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2011)

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2011)

P-selectin expression tracks cerebral atrophy in Mexican-Americans
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2012)

The role of polycomb repressive complex 2 in postnatal subventricular zone neural stem/progenitor cell self-renewal and multipotency
de réir: Chang, EH
Foilsithe / Cruthaithe: (2012)

Identification of the transneuronal homeostatic machinery at a central synapse
de réir: Harrell, E, et al.
Foilsithe / Cruthaithe: (2014)

GPER1 Signaling Initiates Migration of Female V-SVZ-Derived Cells
de réir: Iris Haumann, et al.
Foilsithe / Cruthaithe: (2020-05-01)

Identification of epigenetic regulators of RNA editing mechanisms
de réir: Buss, G
Foilsithe / Cruthaithe: (2023)

Rate of tau propagation is a heritable disease trait in genetically diverse mouse strains
de réir: Lindsay A. Welikovitch, et al.
Foilsithe / Cruthaithe: (2023-02-01)

A KO mouse model for the lncRNA Lhx1os produces motor neuron alterations and locomotor impairment
de réir: Flaminia Pellegrini, et al.
Foilsithe / Cruthaithe: (2023-01-01)

The converging roles of Batten disease proteins in neurodegeneration and cancer
de réir: Shyong Quan Yap, et al.
Foilsithe / Cruthaithe: (2021-04-01)

Computational neuroscience : simulated demyelinating neuropathies and neuronopathies /
de réir: Stephanova, Diana Ivanova 545416, et al.
Foilsithe / Cruthaithe: (2013)

A novel mouse model of creatine transporter deficiency [v1; ref status: indexed, http://f1000r.es/4f8]
de réir: Laura Baroncelli, et al.
Foilsithe / Cruthaithe: (2014-09-01)

Social Isolation and Enrichment Induce Unique miRNA Signatures in the Prefrontal Cortex and Behavioral Changes in Mice
de réir: Natalia Popa, et al.
Foilsithe / Cruthaithe: (2020-12-01)

Optic Atrophy 1 Controls Human Neuronal Development by Preventing Aberrant Nuclear DNA Methylation
de réir: Safak Caglayan, et al.
Foilsithe / Cruthaithe: (2020-06-01)

Hyperactive mTORC1 disrupts habenula function and light preference in zebrafish model of Tuberous sclerosis complex
de réir: Olga Doszyn, et al.
Foilsithe / Cruthaithe: (2024-06-01)

Mate copying requires the coincidence detector Rutabaga in the mushroom bodies of Drosophila melanogaster
de réir: Sabine Nöbel, et al.
Foilsithe / Cruthaithe: (2023-09-01)

The Redox Activity of Protein Disulfide Isomerase Inhibits ALS Phenotypes in Cellular and Zebrafish Models
de réir: Sonam Parakh, et al.
Foilsithe / Cruthaithe: (2020-05-01)

Methods in genomic neuroscience /
de réir: Chin, Hemin R., et al.
Foilsithe / Cruthaithe: (2001)

Molecular and neural mechanisms of olfactory decision making in Drosophila melanogaster
de réir: Ferreira, C
Foilsithe / Cruthaithe: (2015)

Functional characterisation of synuclein-based novel genetic mouse models
de réir: Anwar, S
Foilsithe / Cruthaithe: (2011)

Neural tube patterning: From a minimal model for rostrocaudal patterning toward an integrated 3D model
de réir: Max Brambach, et al.
Foilsithe / Cruthaithe: (2021-06-01)

Computational neurogenetic modeling /
de réir: Benuskova, Lubica, 1958-, et al.
Foilsithe / Cruthaithe: (2007)

Functional investigation of microRNA pathways in human speech and language disorders
de réir: Ho, J
Foilsithe / Cruthaithe: (2014)

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration
de réir: Paracchini, S, et al.
Foilsithe / Cruthaithe: (2006)

Semantic clustering in verbal fluency: schizophrenic patients versus control participants
de réir: Elvevåg, B, et al.
Foilsithe / Cruthaithe: (2002)

Auditory discrimination in dyslexia - differences between university and non-university educated individuals
de réir: Pitt, A, et al.
Foilsithe / Cruthaithe: (2009)

Social neuroscience : brain, mind, and society /
de réir: Schutt, Russell K., editor, et al.
Foilsithe / Cruthaithe: (2015)

Testing the hypothesis of accelerated cerebral white matter aging in schizophrenia and major depression
de réir: Kochunov, P, et al.
Foilsithe / Cruthaithe: (2013)

Fetal sex-specific epigenetic associations with prenatal maternal depressive symptoms
de réir: Michelle Z.L. Kee, et al.
Foilsithe / Cruthaithe: (2022-09-01)

Identification of pleiotropic genetic effects on obesity and brain anatomy.
de réir: Curran, J, et al.
Foilsithe / Cruthaithe: (2013)