(Q42753493)

6 November 2017

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'. (English)

1 reference

6 November 2017

autism spectrum disorder

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3

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5

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8

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9

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12

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13

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16

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6 November 2017

G Breen

11

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Mark Joseph Daly

15

object named as

M J Daly

1 reference

6 November 2017

4

S Ripke

1 reference

6 November 2017

E B Robinson

1

1 reference

6 November 2017

D Howrigan

2

1 reference

6 November 2017

L E Duncan

6

1 reference

6 November 2017

L Jostins

7

1 reference

6 November 2017

D G MacArthur

10

1 reference

6 November 2017

B Devlin

14

1 reference

6 November 2017

P F Sullivan

17

1 reference

6 November 2017

B M Neale

18

1 reference

6 November 2017

language of work or name

English

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publication date

22 October 2013

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6 November 2017

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19

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8

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6 November 2017

859-861

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Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported

6 November 2017

start time

22 October 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/mp.2013.125

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cites work

Individual common variants exert weak effects on the risk for autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

INRICH: interval-based enrichment analysis for genome-wide association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

Hundreds of variants clustered in genomic loci and biological pathways affect human height

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

The genetic interpretation of area under the ROC curve in genomic profiling

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

Common genetic variants and gene-expression changes associated with bipolar disorder are over-represented in brain signaling pathway genes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4113933

Midbrain presynaptic dopamine tone predicts sustained and transient neural response to emotional salience in humans: fMRI, MEG and FDOPA PET

16 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2013.125

inferred from DOI database lookup

7 January 2021

based on heuristic

Loss of dopaminergic nigrostriatal neurons accounts for the motivational and affective deficits in Parkinson's disease

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FMP.2013.125

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/MP.2013.125

1 reference

6 November 2017

1 reference

6 November 2017

PubMed publication ID

24145379

1 reference