(Q57323060)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

attention deficit hyperactivity disorder

7 January 2020

main subject

0 references

1 reference

1 reference

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Clyde Francks

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Anthony Monaco

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

Gayán J

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Willcutt EG

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Cardon LR

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Olson RK

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Pennington BF

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Smith SD

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

DeFries JC

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

1 October 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Child Psychology and Psychiatry

7 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

46

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

1045-1056

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A major susceptibility locus for specific language impairment is located on 13q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Multiple regression analysis of twin data

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Meta-analysis of the association between the 7-repeat allele of the dopamine D(4) receptor gene and attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Developmental dyslexia: genetic dissection of a complex cognitive trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Continuing the search for dyslexia genes on 6p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Development of a structured psychiatric interview for children: agreement between child and parent on individual symptoms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Evidence for linkage and association with reading disability on 6p21.3-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Multiple regression analysis of twin data obtained from selected samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

DeFries-Fulker multiple regression analysis of sibship QTL data: a SAS macro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Genetic analysis of genome-wide variation in human gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A dominant gene for developmental dyslexia on chromosome 3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Two translocations of chromosome 15q associated with dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Evidence for linkage of spelling disability to chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Neuropsychological analyses of comorbidity between reading disability and attention deficit hyperactivity disorder: in search of the common deficit

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2005.01447.X

10.1111/J.1469-7610.2005.01447.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16178928%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference