Detalles de la búsqueda
1.
Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways.
Hum Mol Genet;
32(11): 1932-1942, 2023 05 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-37010288
2.
Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech.
Cell Mol Life Sci;
81(1): 129, 2024 Mar 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-38472514
3.
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.
Hum Mol Genet;
30(12): 1160-1171, 2021 06 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33864365
4.
Evaluation of elements in hair samples of children with developmental language disorder (DLD).
Nutr Neurosci;
26(2): 138-147, 2023 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-35034571
5.
Language and reading impairments are associated with increased prevalence of non-right-handedness.
Child Dev;
94(4): 970-984, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36780127
6.
Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.
Am J Med Genet C Semin Med Genet;
184(2): 256-266, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32452638
7.
Play and prosociality are associated with fewer externalizing problems in children with developmental language disorder: The role of early language and communication environment.
Int J Lang Commun Disord;
55(4): 583-602, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32497383
8.
Candidate gene variant effects on language disorders in Robinson Crusoe Island.
Ann Hum Biol;
46(2): 109-119, 2019 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-31132892
9.
Logical and Methodological Issues Affecting Genetic Studies of Humans Reported in Top Neuroscience Journals.
J Cogn Neurosci;
30(1): 25-41, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-28949821
10.
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.
Hum Mol Genet;
25(9): 1771-9, 2016 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-26908617
11.
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.
PLoS Genet;
11(3): e1004925, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25781923
12.
Family aggregation of language impairment in an isolated Chilean population from Robinson Crusoe Island.
Int J Lang Commun Disord;
53(3): 643-655, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29575355
13.
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Dev Med Child Neurol;
56(4): 346-53, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24117048
14.
Corrigendum: Genome-wide association study of motor coordination.
Front Hum Neurosci;
18: 1360116, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38322780
15.
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.
PLoS Genet;
11(6): e1005336, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26114769
16.
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Nat Genet;
30(1): 86-91, 2002 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-11743577
17.
The Development of Mental Health Difficulties in Young People With and Without Developmental Language Disorder: A Gene-Environment Interplay Study Using Polygenic Scores.
J Speech Lang Hear Res;
66(5): 1639-1657, 2023 05 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37040695
18.
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Am J Hum Genet;
85(2): 264-72, 2009 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-19646677
19.
The Genetic and Molecular Basis of Developmental Language Disorder: A Review.
Children (Basel);
9(5)2022 Apr 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-35626763
20.
A functional genetic link between distinct developmental language disorders.
N Engl J Med;
359(22): 2337-45, 2008 Nov 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-18987363