Detalhe da pesquisa
1.
The selfish environment meets the selfish gene: Coevolution and inheritance of RNA and DNA pools: A model for organismal life incorporating coevolution, horizontal transfer, and inheritance of internal and external RNA and DNA pools.: A model for organismal life incorporating coevolution, horizontal transfer, and inheritance of internal and external RNA and DNA pools.
Bioessays
; 44(2): e2100239, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34985131
2.
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
3.
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts.
Hum Mol Genet
; 25(9): 1771-9, 2016 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26908617
4.
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on.
Eur J Neurosci
; 48(10): 3212-3233, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30218584
5.
Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing.
Cereb Cortex
; 27(12): 5831-5845, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29045729
6.
The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling.
Cereb Cortex
; 27(3): 1732-1747, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28334068
7.
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
PLoS Genet
; 10(9): e1004580, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25188300
8.
Changes in the expression of the type 2 diabetes-associated gene VPS13C in the ß-cell are associated with glucose intolerance in humans and mice.
Am J Physiol Endocrinol Metab
; 311(2): E488-507, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27329800
9.
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
PLoS Genet
; 9(9): e1003751, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24068947
10.
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
PLoS Genet
; 8(2): e1002521, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22346768
11.
PCSK6 is associated with handedness in individuals with dyslexia.
Hum Mol Genet
; 20(3): 608-14, 2011 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21051773
12.
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Nat Genet
; 30(1): 86-91, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11743577
13.
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12.
Am J Hum Genet
; 84(2): 279-85, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19200526
14.
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Am J Hum Genet
; 85(2): 264-72, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19646677
15.
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
J Med Genet
; 48(1): 48-54, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20972252
16.
A common variant associated with dyslexia reduces expression of the KIAA0319 gene.
PLoS Genet
; 5(3): e1000436, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19325871
17.
Rapid auditory processing and medial geniculate nucleus anomalies in Kiaa0319 knockout mice.
Genes Brain Behav
; 21(6): e12808, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35419947
18.
Discovery of 42 genome-wide significant loci associated with dyslexia.
Nat Genet
; 54(11): 1621-1629, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36266505
19.
The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.
J Biol Chem
; 285(51): 40148-62, 2010 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-20943657
20.
A functional genetic link between distinct developmental language disorders.
N Engl J Med
; 359(22): 2337-45, 2008 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-18987363