about
Meta-analysis and imputation refines the association of 15q25 with smoking quantityThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataAlpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smokingLRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaA 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.Confirmatory evidence for linkage of relative hand skill to 2p12-q11Large recurrent microdeletions associated with schizophreniaPutative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UKInvestigating the effects of copy number variants on reading and language performance.Novel genetic loci underlying human intracranial volume identified through genome-wide associationThe chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationGenome-wide association and meta-analysis of bipolar disorder in individuals of European ancestryA genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide.A genome-wide investigation of SNPs and CNVs in schizophrenia.Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairmentA large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.Use of multivariate linkage analysis for dissection of a complex cognitive trait.A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetriesFine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.Genome-wide screening for DNA variants associated with reading and language traitsThe genetic basis of dyslexia.Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmentCommon genetic variants influence human subcortical brain structuresFailure to replicate effect of Kibra on human memory in two large cohorts of European origin.Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13.Understanding the genetics of behavioural and psychiatric traits will only be achieved through a realistic assessment of their complexity.Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment.A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.Copy number variations of chromosome 16p13.1 region associated with schizophrenia.Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers.Genes, cognition and dyslexia: learning to read the genome.Early developmental gene enhancers affect subcortical volumes in the adult human brain.Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.Novel genetic loci associated with hippocampal volume.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Clyde Francks
@ast
Clyde Francks
@en
Clyde Francks
@es
Clyde Francks
@nl
Clyde Francks
@sl
type
label
Clyde Francks
@ast
Clyde Francks
@en
Clyde Francks
@es
Clyde Francks
@nl
Clyde Francks
@sl
prefLabel
Clyde Francks
@ast
Clyde Francks
@en
Clyde Francks
@es
Clyde Francks
@nl
Clyde Francks
@sl
P106
P21
P2798
P31
P496
0000-0002-9098-890X
P569
2000-01-01T00:00:00Z