(Q37523180)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

Genome-wide association study of shared components of reading disability and language impairment (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

genome-wide association study

20 February 2020

main subject

0 references

0 references

1 reference

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

George Davey Smith

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Natalie R Powers

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Hauke Bartsch

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Trevor Brown

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

25

A M Dale

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

author name string

J D Eicher

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

L L Miller

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

N Akshoomoff

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

D G Amaral

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

C S Bloss

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

O Libiger

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

N J Schork

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

B F Darst

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

B J Casey

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

L Chang

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

T Ernst

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

J Frazier

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

W E Kaufmann

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

B Keating

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

T Kenet

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

D Kennedy

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

S Mostofsky

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

S S Murray

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

E R Sowell

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

J M Kuperman

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

D J Hagler

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

T L Jernigan

26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

S M Ring

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

J R Gruen

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Pediatric Imaging, Neurocognition, and Genetics Study

31

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

language of work or name

English

0 references

publication date

9 October 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

Genes, Brain and Behavior

20 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

volume

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

page(s)

792-801

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

20 February 2020

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

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1 reference

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Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments

23 August 2017

1 reference

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Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment

23 August 2017

1 reference

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A genome-wide association study for reading and language abilities in two population cohorts.

23 August 2017

1 reference

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DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilities

23 August 2017

1 reference

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Cognition assessment using the NIH Toolbox.

23 August 2017

1 reference

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BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies

23 August 2017

1 reference

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The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure

23 August 2017

1 reference

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Long-term influence of normal variation in neonatal characteristics on human brain development

23 August 2017

1 reference

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Multimodal imaging of the self-regulating developing brain

23 August 2017

1 reference

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Neuroanatomical assessment of biological maturity

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

23 August 2017

Developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Cohort profile: the 'children of the 90s'—the index offspring of the Avon Longitudinal Study of Parents and Children

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

COL4A2 mutation associated with familial porencephaly and small-vessel disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

De novo and inherited mutations in COL4A2, encoding the type IV collagen α2 chain cause porencephaly

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Imaging genetics of FOXP2 in dyslexia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

DCDC2, KIAA0319 and CMIP are associated with reading-related traits

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

A dyslexia-associated variant in DCDC2 changes gene expression

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

A versatile gene-based test for genome-wide association studies

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Genetics of developmental dyslexia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Fast model-based estimation of ancestry in unrelated individuals

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

CMIP and ATP2C2 modulate phonological short-term memory in language impairment

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Language pathway abnormalities in schizophrenia: a review of fMRI and other imaging studies

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Paying attention to reading: the neurobiology of reading and dyslexia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Automated white-matter tractography using a probabilistic diffusion tensor atlas: Application to temporal lobe epilepsy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Relations among speech, language, and reading disorders

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

PLINK: a tool set for whole-genome association and population-based linkage analyses

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Human thioesterase superfamily member 2 (hTHEM2) is co-localized with beta-tubulin onto the microtubule

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

From single to multiple deficit models of developmental disorders

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Are specific language impairment and dyslexia distinct disorders?

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Reliability in multi-site structural MRI studies: effects of gradient non-linearity correction on phantom and human data

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Language fMRI abnormalities associated with FOXP2 gene mutation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

A genomewide scan identifies two novel loci involved in specific language impairment

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Multi-modal volume registration by maximization of mutual information

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Diffusion tensor MR imaging of the human brain

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

MR diffusion tensor spectroscopy and imaging

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Decoding the genetics of speech and language

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

The relationship among receptive and expressive vocabulary, listening comprehension, pre-reading skills, word identification skills, and reading comprehension by children with reading disabilities

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Efficient correction of inhomogeneous static magnetic field-induced distortion in Echo Planar Imaging

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

A twin study of the etiology of comorbidity: attention-deficit hyperactivity disorder and dyslexia

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Correction of eddy-current distortions in diffusion tensor images using the known directions and strengths of diffusion gradients

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3904347

Multivariate Linkage Analysis of Specific Language Impairment (SLI)

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FGBB.12085

The Children's Test of Nonword Repetition: a test of phonological working memory

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24024963

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Very early language deficits in dyslexic children

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24024963

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/GBB.12085

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

PubMed publication ID

24024963

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24024963%20AND%20SRC:MED&resulttype=core&format=json