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List of works by 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

scientific article

A genome-wide investigation of SNPs and CNVs in schizophrenia

scientific article

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

scientific article

A genomewide linkage screen for relative hand skill in sibling pairs

scientific article published on 3 January 2002

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

scientific article

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

scientific article published on 28 March 2002

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

scientific article

A schizophrenia-associated HLA locus affects thalamus volume and asymmetry

scientific article

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

scientific article published on 20 February 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

scientific article

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

scientific article published on 10 March 2020

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

scientific article published on July 2014

Association analysis of dyslexia candidate genes in a Dutch longitudinal sample

scientific article published on 11 January 2017

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

scientific article published on 7 August 2014

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

scientific article

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

scientific article published on 01 October 2005

Common genetic variants influence human subcortical brain structures

scientific article

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

scientific article

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

scientific article published on 29 September 2009

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

scientific article published on 26 June 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

scientific article

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

scientific article published on 4 December 2015

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

scientific article published on 18 February 2016

Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries

scientific article

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

scientific article published on 20 May 2016

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

scientific article

Exploring human brain lateralization with molecular genetics and genomics

scientific article published on 06 May 2015

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

scientific article

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

scientific article

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.

scientific article

Genes, cognition and dyslexia: learning to read the genome

scientific article

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

scientific article published on 29 November 2019

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

scientific article published on 14 August 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.

scientific article

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

scientific article

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

scientific article published on 11 February 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

scientific article published on 14 October 2020

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

scientific article published on May 2004

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

scientific article

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

scientific article

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

scientific article published on 13 October 2016

Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophrenia

scientific article published on 11 August 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

scientific article

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

scientific article published on 17 December 2001

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

scientific article

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

scientific article

Large recurrent microdeletions associated with schizophrenia

scientific article

Lateralization of gene expression in human language cortex

scientific article published on 18 March 2015

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

scientific article

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

article published in the Proceedings of the National Academy of Sciences of the United States of America

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

scientific article

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

scientific article

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

scientific article published on 27 July 2016

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

scientific article published on 14 March 2017

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

scientific article

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

scientific article published on 21 August 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

scientific article (publication date: 3 October 2016)

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

scientific article published on 12 February 2014

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

scientific article

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

scientific article published on 16 January 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.

scientific article

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

scientific article

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

scientific article published in 2021

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

scientific article

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

scientific article published on 26 August 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

scientific article published in April 2022

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

scientific article

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

scientific article

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

scientific article

The genetic basis of dyslexia

scientific article

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

scientific article published on 04 September 2018

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

scientific article

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

scientific article

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

scientific article published on 12 November 2015

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