Lista de obras - Clyde Francks - Dominio Público Uruguay

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

artículo científico publicado en 2004

A genome-wide investigation of SNPs and CNVs in schizophrenia

artículo científico publicado en 2009

A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.

artículo científico publicado en 2014

A genomewide linkage screen for relative hand skill in sibling pairs

artículo científico publicado en 2002

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

artículo científico publicado en 2003

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

artículo científico publicado en 2002

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

A schizophrenia-associated HLA locus affects thalamus volume and asymmetry

artículo científico publicado en 2015

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.

artículo científico publicado en 2018

ADAMTSL3 as a candidate gene for schizophrenia: gene sequencing and ultra-high density association analysis by imputation

scientific article published on 15 January 2011

Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking

artículo científico publicado en 2008

Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets

scientific article published on 31 October 2019

Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium

An overview of the first 5 years of the ENIGMA obsessive-compulsive disorder working group: The power of worldwide collaboration

artículo científico publicado en 2020

Assessing the effects of common variation in the FOXP2 gene on human brain structure

artículo científico publicado en 2014

Association analysis of dyslexia candidate genes in a Dutch longitudinal sample

artículo científico publicado en 2017

Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity

artículo científico publicado en 2014

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

artículo científico publicado en 2004

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci

artículo científico publicado en 2005

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Confirmatory evidence for linkage of relative hand skill to 2p12-q11 ⬇️

artículo científico publicado en 2003

Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure

scientific article published on 18 May 2020

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

artículo científico publicado en 2009

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

artículo científico publicado en 2015

Differences in cerebral cortical anatomy of left- and right-handers

scientific article published on 28 March 2014

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

artículo científico publicado en 2013

ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide

artículo científico publicado en 2015

Early developmental gene enhancers affect subcortical volumes in the adult human brain

artículo científico publicado en 2016

Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries

artículo científico publicado en 2017

Evaluation of results from genome-wide studies of language and reading in a novel independent dataset.

artículo científico publicado en 2016

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment

artículo científico publicado en 2015

Exploring human brain lateralization with molecular genetics and genomics

artículo científico

Failure to replicate effect of Kibra on human memory in two large cohorts of European origin

artículo científico publicado en 2008

Familial and genetic effects on motor coordination, laterality, and reading-related cognition

artículo científico publicado en 2003

Finding functional disease-associated non-coding variation using next-generation sequencing

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

artículo científico publicado en 2002

Genes, cognition and dyslexia: learning to read the genome

artículo científico publicado en 2006

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment

artículo científico publicado en 2019

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

artículo científico publicado en 2002

Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

artículo científico publicado en 2014

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

artículo científico publicado en 2011

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

scientific journal article

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

artículo científico publicado en 2019

Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts

scholarly article by P Muglia et al published 23 December 2008 in Molecular Psychiatry

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

artículo científico publicado en 2020

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects

artículo científico publicado en 2004

Genome-wide screening for DNA variants associated with reading and language traits

artículo científico publicado en 2014

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment

artículo científico publicado en 2014

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.

artículo científico publicado en 2016

Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia

artículo científico publicado en 2014

In search of the biological roots of typical and atypical human brain asymmetry: Comment on "Phenotypes in hemispheric functional segregation? Perspectives and challenges" by Guy Vingerhoets

scientific article published on 16 July 2019

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

artículo científico publicado en 2001

Investigating the effects of copy number variants on reading and language performance

artículo científico publicado en 2016

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

artículo científico publicado en 2007

Large recurrent microdeletions associated with schizophrenia

artículo científico publicado en 2008

Lateralization of gene expression in human language cortex

artículo científico

Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development.

artículo científico publicado en 2017

Leucine-Rich Repeat Genes and the Fine-Tuning of Synapses

article

Mapping Cortical Brain Asymmetry in 17,141 Healthy Individuals Worldwide via the ENIGMA Consortium

Mapping brain asymmetry in health and disease through the ENIGMA consortium

scientific article published on 18 May 2020

Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium

artículo científico publicado en 2018

Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets

artículo científico publicado en 2013

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

artículo científico publicado en 2010

Neuroimaging genetic analyses of novel candidate genes associated with reading and language

artículo científico publicado en 2016

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

artículo científico publicado en 2017

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

artículo científico publicado en 2017

No association between NRG1 and ErbB4 genes and psychopathological symptoms of schizophrenia

artículo científico publicado en 2014

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

On the other hand: including left-handers in cognitive neuroscience and neurogenetics.

artículo científico publicado en 2014

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

artículo científico publicado en 2003

Persistence and transmission of recessive deafness and sign language: new insights from village sign languages

artículo científico publicado en 2013

Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

scientific article published on 01 January 2006

Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13.

artículo científico publicado en 2008

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

artículo científico publicado en 2004

Relations between hemispheric asymmetries of grey matter and auditory processing of spoken syllables in 281 healthy adults

artículo científico publicado en 2021

Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

artículo científico publicado en 2014

Reproducibility in the absence of selective reporting: An illustration from large-scale brain asymmetry research

scientific article published on 25 August 2020

Structural asymmetries of the human cerebellum in relation to cerebral cortical asymmetries and handedness

artículo científico publicado en 2016

Subtle left-right asymmetry of gene expression profiles in embryonic and foetal human brains

scientific article published in Scientific Reports

Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium

artículo científico publicado en 2022

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

artículo científico publicado en 2006

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The genetic basis of dyslexia

artículo científico publicado en 2002

Transcriptomic analysis of left-right differences in human embryonic forebrain and midbrain

artículo científico publicado en 2018

Understanding the genetics of behavioural and psychiatric traits will only be achieved through a realistic assessment of their complexity

artículo científico publicado en 2009

Use of multivariate linkage analysis for dissection of a complex cognitive trait

artículo científico publicado en 2003

Whole exome sequencing for handedness in a large and highly consanguineous family

artículo científico publicado en 2015

Lista de obras de Clyde Francks

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

A genome-wide investigation of SNPs and CNVs in schizophrenia

A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.

A genomewide linkage screen for relative hand skill in sibling pairs

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

A schizophrenia-associated HLA locus affects thalamus volume and asymmetry

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.

ADAMTSL3 as a candidate gene for schizophrenia: gene sequencing and ultra-high density association analysis by imputation

Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking

Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets

Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium

An overview of the first 5 years of the ENIGMA obsessive-compulsive disorder working group: The power of worldwide collaboration

Assessing the effects of common variation in the FOXP2 gene on human brain structure

Association analysis of dyslexia candidate genes in a Dutch longitudinal sample

Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci

Common genetic variants influence human subcortical brain structures

Confirmatory evidence for linkage of relative hand skill to 2p12-q11 ⬇️

Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

Differences in cerebral cortical anatomy of left- and right-handers

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

ENIGMA and the individual: Predicting factors that affect the brain in 35 countries worldwide

Early developmental gene enhancers affect subcortical volumes in the adult human brain

Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries

Evaluation of results from genome-wide studies of language and reading in a novel independent dataset.

Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment

Exploring human brain lateralization with molecular genetics and genomics

Failure to replicate effect of Kibra on human memory in two large cohorts of European origin

Familial and genetic effects on motor coordination, laterality, and reading-related cognition

Finding functional disease-associated non-coding variation using next-generation sequencing

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

Genes, cognition and dyslexia: learning to read the genome

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Genetic architecture of subcortical brain structures in 38,851 individuals

Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects

Genome-wide screening for DNA variants associated with reading and language traits

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.

Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia

In search of the biological roots of typical and atypical human brain asymmetry: Comment on "Phenotypes in hemispheric functional segregation? Perspectives and challenges" by Guy Vingerhoets

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

Investigating the effects of copy number variants on reading and language performance

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Large recurrent microdeletions associated with schizophrenia

Lateralization of gene expression in human language cortex

Left-Right Asymmetry of Maturation Rates in Human Embryonic Neural Development.

Leucine-Rich Repeat Genes and the Fine-Tuning of Synapses

Mapping Cortical Brain Asymmetry in 17,141 Healthy Individuals Worldwide via the ENIGMA Consortium

Mapping brain asymmetry in health and disease through the ENIGMA consortium

Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium

Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

Neuroimaging genetic analyses of novel candidate genes associated with reading and language

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

No association between NRG1 and ErbB4 genes and psychopathological symptoms of schizophrenia

Novel genetic loci associated with hippocampal volume

Novel genetic loci underlying human intracranial volume identified through genome-wide association

On the other hand: including left-handers in cognitive neuroscience and neurogenetics.

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

Persistence and transmission of recessive deafness and sign language: new insights from village sign languages

Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13.

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK