Bivariate linkage analyses for reading difficulties and rapid naming

Bivariate linkage analyses for reading difficulties and rapid naming

Bibliographic Details
Main Authors:	Davis, C, Fisher, S, Francks, C, MacPhie, I, Gayan, J, Smith, S, Cardon, L, Pennington, B, Olson, R, Monaco, A, DeFries, J
Format:	Journal article
Published:	2002

Similar Items

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder
by: Gayan, J, et al.
Published: (2004)

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.
by: Gayán, J, et al.
Published: (2005)

Association mapping of the 6p23-21.3 QTL for reading disability
by: Francks, C, et al.
Published: (2004)

Use of multivariate linkage analysis for dissection of a complex cognitive trait.
by: Marlow, A, et al.
Published: (2003)

A genomewide linkage screen for relative hand skill in sibling pairs.
by: Francks, C, et al.
Published: (2002)

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
by: Francks, C, et al.
Published: (2004)

Quantitative trait analysis of the entire genome in large samples of dyslexic sib-pairs from the UK and US.
by: Fisher, S, et al.
Published: (2002)

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
by: Fisher, S, et al.
Published: (2002)

The genetic basis of dyslexia.
by: Francks, C, et al.
Published: (2002)

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
by: Francks, C, et al.
Published: (2002)

Familial and genetic effects on motor coordination, laterality, and reading-related cognition.
by: Francks, C, et al.
Published: (2003)

Characterisation of a major locus for developmental dyslexia on 18p11.2.
by: MacPhie, I, et al.
Published: (2001)

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
by: Scerri, T, et al.
Published: (2004)

Molecular genetic analysis of a quantitative measure of relative hand skill
by: Francks, C, et al.
Published: (2002)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
by: Scerri, T, et al.
Published: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
by: Richardson, A, et al.
Published: (2010)

Genome-wide scan of reading ability in affected sibling pairs with Attention-Deficit/Hyperactivity Disorder: Unique and shared genetic effects.
by: Loo, S, et al.
Published: (2003)

Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
by: Loo, S, et al.
Published: (2004)

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.
by: Smalley, S, et al.
Published: (2002)

Multivariate multipoint linkage analysis of QTL in dyslexia
by: Marlow, A, et al.
Published: (2002)

Genome-wide screening for DNA variants associated with reading and language traits.
by: Gialluisi, A, et al.
Published: (2014)

Genetic linkage of attention deficit hyperactivity disorder to a region on chromosome 16p13.
by: Kustanovich, V, et al.
Published: (2002)

Familial correlations between reading measures in a UK sib-pair cohort
by: Marlow, A, et al.
Published: (2000)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
by: Thomas S Scerri, et al.
Published: (2010-10-01)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
by: Thomas S. Scerri, et al.
Published: (2010-01-01)

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.
by: Ogdie, M, et al.
Published: (2003)

Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK.
by: Marlow, A, et al.
Published: (2001)

Genome-wide scan in attention deficit hyperactivity disorder (ADHD).
by: Smalley, S, et al.
Published: (2001)

Understanding Reading and Reading Difficulties Through Naming Speed Tasks
by: Noor Z. Al Dahhan, et al.
Published: (2016-11-01)

Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
by: Francks, C, et al.
Published: (2003)

Genes, cognition and dyslexia: learning to read the genome.
by: Fisher, S, et al.
Published: (2006)

The impact of COVID-19 on care of early inflammatory arthritis in the UK
by: MacPhie, E, et al.
Published: (2022)

I know the name well, but cannot read it correctly: difficulties in reading recent Japanese names
by: Yuji Ogihara
Published: (2021-06-01)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
by: Scerri, T, et al.
Published: (2010)

Developmental dyslexia: genetic dissection of a complex cognitive trait.
by: Fisher, S, et al.
Published: (2002)

A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
by: Francks, C, et al.
Published: (2000)

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.
by: Fisher, S, et al.
Published: (2002)

The Role of Phonological Awareness and Rapid Automatized Naming in the Prediction of Reading Difficulties in Portuguese
by: Mirelle F. Michalick-Triginelli, et al.
Published: (2015-12-01)

The neurobiology of reading difficulties.
by: Stein, J
Published: (2000)

The neurobiology of reading difficulties
by: Stein, J
Published: (2002)