Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses

Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses

<p><strong>Background and Purpose—</strong> The volume of T2-hyperintense white matter (HWM) is an important neuroimaging marker of cerebral integrity with a demonstrated high heritability. Pathophysiology studies have shown that the regional, ependymal, and subcortical HWM lesions...

Podrobná bibliografie
Hlavní autoři:	Kochunov, P, Glahn, D, Lancaster, J, Winkler, A, Kent, J, Olvera, R, Cole, SA, Dyer, T, Almasy, L, Duggirala, R, Fox, P, Blangero, J
Médium:	Journal article
Jazyk:	English
Vydáno:	American Heart Association 2010
Témata:	Neurogenetics

Podobné jednotky

Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume
Autor: Kochunov, P, a další
Vydáno: (2009)

Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies
Autor: Winkler, A, a další
Vydáno: (2010)

Blood pressure and cerebral white matter share common genetic factors in Mexican Americans
Autor: Kochunov, P, a další
Vydáno: (2011)

Influence of age, sex and genetic factors on the human brain
Autor: McKay, DR, a další
Vydáno: (2014)

Transcriptomics of cortical gray matter thickness decline during normal aging
Autor: Kochunov, P, a další
Vydáno: (2013)

P-selectin expression tracks cerebral atrophy in Mexican-Americans
Autor: Kochunov, P, a další
Vydáno: (2012)

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain
Autor: Kochunov, P, a další
Vydáno: (2011)

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes
Autor: Carless, M, a další
Vydáno: (2011)

Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging
Autor: Glahn, D, a další
Vydáno: (2013)

Dissecting the functions of DISC1
Autor: Carless, M, a další
Vydáno: (2011)

Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; referees: 2 approved]
Autor: Desaraju Suresh Bhargav, a další
Vydáno: (2017-12-01)

Cou Cou, flying fish and a whole exome please... lessons learned from genetic testing in Barbados
Autor: Morris Scantlebury, a další
Vydáno: (2021-02-01)

Analysis of morphine responses in mice reveals a QTL on Chromosome 7 [version 2; referees: 2 approved]
Autor: Wim E. Crusio, a další
Vydáno: (2016-10-01)

Analysis of morphine responses in mice reveals a QTL on Chromosome 7 [version 1; referees: 2 approved]
Autor: Wim E. Crusio, a další
Vydáno: (2016-09-01)

Editorial: Each child with ADHD is unique: Treat the whole patient, not just their symptoms
Autor: Edmund J. S. Sonuga-Barke, a další
Vydáno: (2022-10-01)

Genetic influence on the working memory circuitry: Behavior, structure, function and extensions to illness
Autor: Karlsgodt, K, a další
Vydáno: (2011)

Reduced white matter integrity in sibling pairs discordant for bipolar disorder
Autor: Sprooten, E, a další
Vydáno: (2013)

Investigating rare genetic variants in common migraine
Autor: Weir, G
Vydáno: (2014)

Sensorimotor control of Drosophila copulation
Autor: Herbert, MR
Vydáno: (2020)

Genetics of microstructure of cerebral white matter using diffusion tensor imaging.
Autor: Kochunov, P, a další
Vydáno: (2010)

Genes to therapy: a comprehensive literature review of whole-exome sequencing in neurology and neurosurgery
Autor: Joecelyn Kirani Tan, a další
Vydáno: (2024-11-01)

Computational neurogenetic modeling /
Autor: Benuskova, Lubica, 1958-, a další
Vydáno: (2007)

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

Identification of the transneuronal homeostatic machinery at a central synapse
Autor: Harrell, E, a další
Vydáno: (2014)

The behavioural and molecular characterisation of a novel LRRK2 BAC transgenic rat model of Parkinson’s disease
Autor: Sloan, M, a další
Vydáno: (2014)

The regulation of enteric neuron connectivity by semaphorin 5A is affected by the autism-associated S956G missense mutation
Autor: Morgane E. Le Dréan, a další
Vydáno: (2024-05-01)

A proton-inhibited DEG/ENaC ion channel maintains neuronal ionstasis and promotes neuronal survival under stress
Autor: Dionysia Petratou, a další
Vydáno: (2023-07-01)

Leukocyte telomere length and hippocampus volume: a meta-analysis [version 1; referees: 2 approved]
Autor: Gustav Nilsonne, a další
Vydáno: (2015-10-01)

GPER1 Signaling Initiates Migration of Female V-SVZ-Derived Cells
Autor: Iris Haumann, a další
Vydáno: (2020-05-01)

Using computation to enhance diagnosis and therapy: a novel mutation operator for real-coded adaptive genetic algorithms [v1; ref status: indexed, http://f1000r.es/wf]
Autor: Maxinder S Kanwal, a další
Vydáno: (2013-06-01)

A novel pseudoderivative-based mutation operator for real-coded adaptive genetic algorithms [v2; ref status: indexed, http://f1000r.es/1td]
Autor: Maxinder S Kanwal, a další
Vydáno: (2013-11-01)

ANGDelMut – a web-based tool for predicting and analyzing functional loss mechanisms of amyotrophic lateral sclerosis-associated angiogenin mutations [v2; ref status: indexed, http://f1000r.es/2mc]
Autor: Aditya K Padhi, a další
Vydáno: (2013-12-01)

ANGDelMut – a web-based tool for predicting and analyzing functional loss mechanisms of amyotrophic lateral sclerosis-associated angiogenin mutations [v3; ref status: indexed, http://f1000r.es/2yt]
Autor: Aditya K Padhi, a další
Vydáno: (2014-02-01)

A multimodal assessment of the genetic control over working memory
Autor: Karlsgodt, K, a další
Vydáno: (2010)

Default mode network activity and white matter integrity in healthy middle-aged ApoE4 carriers
Autor: Patel, K, a další
Vydáno: (2013)

Genetic architecture of declarative memory: implications for complex illnesses
Autor: Bearden, C, a další
Vydáno: (2012)

Computational neuroscience : simulated demyelinating neuropathies and neuronopathies /
Autor: Stephanova, Diana Ivanova 545416, a další
Vydáno: (2013)

The intergenerational multiple deficit model and the case of dyslexia
Autor: van Bergen, E, a další
Vydáno: (2014)

A novel mouse model of creatine transporter deficiency [v1; ref status: indexed, http://f1000r.es/4f8]
Autor: Laura Baroncelli, a další
Vydáno: (2014-09-01)

Murine Cep290 phenotypes are modified by genetic backgrounds and provide an impetus for investigating disease modifier alleles [version 1; referees: 2 approved]
Autor: Simon Ramsbottom, a další
Vydáno: (2015-08-01)