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DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.

Darki, Fahimeh (author)
Karolinska Institutet
Peyrard-Janvid, Myriam (author)
Karolinska Institutet
Matsson, Hans (author)
Karolinska Institutet
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Kere, Juha (author)
Karolinska Institutet
Klingberg, Torkel (author)
Karolinska Institutet
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 (creator_code:org_t)
2014
2014
English.
In: Journal of Neuroscience. - 0270-6474 .- 1529-2401. ; 34:43, s. 14455-62
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Three genes, DYX1C1, DCDC2, and KIAA0319, have been previously associated with dyslexia, neuronal migration, and ciliary function. Three polymorphisms within these genes, rs3743204 (DYX1C1), rs793842 (DCDC2), and rs6935076 (KIAA0319) have also been linked to normal variability of left temporoparietal white matter volume connecting the middle temporal cortex to the angular and supramarginal gyri. Here, we assessed whether these polymorphisms are also related to the cortical thickness of the associated regions during childhood development using a longitudinal dataset of 76 randomly selected children and young adults who were scanned up to three times each, 2 years apart. rs793842 in DCDC2 was significantly associated with the thickness of left angular and supramarginal gyri as well as the left lateral occipital cortex. The cortex was significantly thicker for T-allele carriers, who also had lower white matter volume and lower reading comprehension scores. There was a negative correlation between white matter volume and cortical thickness, but only white matter volume predicted reading comprehension 2 years after scanning. These results show how normal variability in reading comprehension is related to gene, white matter volume, and cortical thickness in the inferior parietal lobe. Possibly, the variability of gray and white matter structures could both be related to the role of DCDC2 in ciliary function, which affects both neuronal migration and axonal outgrowth.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

Keyword

SNP
ciliary function
developmental dyslexia
neuroimaging
reading ability
single nucleotide polymorphism
supramarginal and angular gyrus
Molekylär genetik
Molecular Genetics

Publication and Content Type

ref (subject category)
art (subject category)

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