Detalhe da pesquisa
1.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
; 26(7): 3004-3017, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057169
2.
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
Am J Hum Genet
; 94(1): 23-32, 2014 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24360809
3.
DCDC2 polymorphism is associated with left temporoparietal gray and white matter structures during development.
J Neurosci
; 34(43): 14455-62, 2014 Oct 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-25339756
4.
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.
Hum Genet
; 134(11-12): 1239-48, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26400686
5.
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
J Hum Genet
; 60(7): 399-401, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25877001
6.
Polymorphisms in the dopamine receptor 2 gene region influence improvements during working memory training in children and adolescents.
J Cogn Neurosci
; 26(1): 54-62, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24001007
7.
The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.
Behav Genet
; 42(4): 509-27, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22426781
8.
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Behav Genet
; 41(1): 134-40, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21203819
9.
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.
Am J Med Genet A
; 155A(6): 1314-21, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21574244
10.
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
Transl Psychiatry
; 9(1): 77, 2019 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30741946
11.
AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjects.
J Appl Physiol (1985)
; 103(1): 315-22, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17463303
12.
Human ROBO1 regulates white matter structure in corpus callosum.
Brain Struct Funct
; 222(2): 707-716, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27240594
13.
Identification of NCAN as a candidate gene for developmental dyslexia.
Sci Rep
; 7(1): 9294, 2017 08 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-28839234
14.
Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophy.
FASEB J
; 19(7): 750-60, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15857889
15.
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
Eur J Hum Genet
; 13(12): 1261-7, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16160700
16.
Family-based association study of DYX1C1 variants in autism.
Eur J Hum Genet
; 13(1): 127-30, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15470369
17.
Nonword repetition--a clinical marker for specific language impairment in Swedish associated with parents' language-related problems.
PLoS One
; 9(2): e89544, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24586859
18.
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Eur J Hum Genet
; 22(5): 675-80, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24022301
19.
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.
Biol Psychiatry
; 72(8): 671-6, 2012 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22683091
20.
Dopamine, working memory, and training induced plasticity: implications for developmental research.
Dev Psychol
; 48(3): 836-43, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22103304