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PubPharm (97)
31
GRIN2B predicts attention problems among disadvantaged children
enthalten in:
European child & adolescent psychiatry
| 2015
von
Riva, V.
|
Battaglia, M.
|
Nobile, M.
| +8
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32
The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability
enthalten in:
Cerebral cortex (New York, N.Y. : 1991)
| 2015
von
Gori, S.
|
Mascheretti, S.
|
Giora, E.
| +5
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33
Strong motion deficits in dyslexia associated with DCDC2 gene alteration
enthalten in:
The Journal of neuroscience : the official journal of the Society for Neuroscience
| 2015
von
Cicchini, G.
|
Marino, C.
|
Mascheretti, S.
| +2
CommentIn: Cortex. 2016 Jun;79:155-8. - PMID 27085512
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34
Putative risk factors in developmental dyslexia : a case-control study of Italian children
enthalten in:
Journal of learning disabilities
| 2015
von
Mascheretti, S.
|
Marino, C.
|
Simone, D.
| +6
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35
The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems
enthalten in:
European child & adolescent psychiatry
| 2015
von
Riva, V.
|
Marino, C.
|
Giorda, R.
| +2
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36
GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia
enthalten in:
Psychiatric genetics
| 2015
von
Mascheretti, S.
|
Facoetti, A.
|
Giorda, R.
| +5
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37
GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexia
enthalten in:
Psychiatric genetics
| 2015
von
Mascheretti, S.
|
Facoetti, A.
|
Giorda, R.
| +5
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38
Phenotypic and genetic associations between reading comprehension, decoding skills, and ADHD dimensions: evidence from two population‐based studies
enthalten in:
The journal of child psychology and psychiatry
| 2015
von
Plourde, V.
|
Boivin, M.
|
Forget‐Dubois, N.
| +5
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39
Putative Risk Factors in Developmental Dyslexia: A Case-Control Study of Italian Children
enthalten in:
Journal of learning disabilities
| 2015
von
Mascheretti, S.
|
Marino, C.
|
Simone, D.
| +6
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40
Strong motion deficits in dyslexia associated with DCDC2 gene alteration
enthalten in:
The journal of neuroscience
| 2015
von
Cicchini, G.
|
Marino, C.
|
Mascheretti, S.
| +2
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31
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Dyslexia
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DCDC2 protein, human
9
Microtubule-Associated Proteins
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Nerve Tissue Proteins
6
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6
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developmental dyslexia
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DCDC2 gene
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Motion perception
4
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SLC6A4 protein, human
4
Serotonin Plasma Membrane Transport Proteins
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White matter
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