(Q91452698)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

title

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

main subject

autism spectrum disorder

1 reference

attention deficit hyperactivity disorder

inferred from title

0 references

author

F. Kyle Satterstrom

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Raymond K Walters

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Tarjinder Singh

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Emilie M Wigdor

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Ditte Demontis

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Jakob Grove

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Jonas Bybjerg-Grauholm

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Merete Nordentoft

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

David M Hougaard

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Thomas Werge

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Benjamin M. Neale

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Anders D. Børglum

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

Mark Joseph Daly

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

20

Preben Bo Mortensen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

12

Duncan S Palmer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

17

Elise B Robinson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

7

Jack A Kosmicki

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

11

Marie Bækvad-Hansen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

16

Ole Mors

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

13

Julian B Maller

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

9

Christine Stevens

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

5

Francesco Lescai

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

author name string

iPSYCH-Broad Consortium

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

publication date

25 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

22 April 2020

page(s)

1961-1965

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31768057%20AND%20SRC:MED&resulttype=core&format=json

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

22 April 2020

cites work

1 reference

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7 January 2021

Most genetic risk for autism resides with common variation

1 reference

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7 January 2021

The heritability of clinically diagnosed attention deficit hyperactivity disorder across the lifespan

1 reference

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7 January 2021

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

1 reference

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7 January 2021

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Identification of common genetic risk variants for autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Patterns and rates of exonic de novo mutations in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Synaptic, transcriptional and chromatin genes disrupted in autism

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

The contribution of de novo coding mutations to autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

A framework for the interpretation of de novo mutation in human disease

1 reference

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7 January 2021

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Analysis of protein-coding genetic variation in 60,706 humans

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

1 reference

https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders

1 reference

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7 January 2021

Quantifying the contribution of recessive coding variation to developmental disorders

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7 January 2021

Testing for an unusual distribution of rare variants

1 reference

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7 January 2021

A population genetic approach to mapping neurological disorder genes using deep resequencing

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https://api.crossref.org/works/10.1038%2FS41593-019-0527-8

7 January 2021

Prevalence and architecture of de novo mutations in developmental disorders

1 reference

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7 January 2021

Mutations in RAI1 associated with Smith-Magenis syndrome.

1 reference

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7 January 2021

Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants

1 reference

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7 January 2021

Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample

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7 January 2021

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7 January 2021

Phenylketonuria screening registry as a resource for population genetic studies

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7 January 2021

Whole Genome Amplification and Genetic Analysis after Extraction of Proteins from Dried Blood Spots

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7 January 2021

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA.

1 reference

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7 January 2021

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

1 reference

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7 January 2021

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

1 reference

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7 January 2021

The Ensembl Variant Effect Predictor

1 reference

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7 January 2021