(Q48133294)

http://europepmc.org/abstract/MED/27479843

9 February 2018

meta-analysis

0 references

review article

1 reference

title

Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability. (English)

1 reference

http://europepmc.org/abstract/MED/27479843

9 February 2018

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22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479843%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

Reijnders MRF

2

1 reference

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11 June 2020

Servi Jc Stevens

12

1 reference

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11 June 2020

Alexander P Stegmann

15

1 reference

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11 June 2020

Patrick Rump

16

1 reference

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11 June 2020

Joris A Veltman

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479843%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

21

Han G Brunner

1 reference

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11 June 2020

Marjolein H Willemsen

8

object named as

Marjolein H Willemsen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479843%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

4

Helger G Yntema

1 reference

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11 June 2020

3

Rolph Pfundt

1 reference

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11 June 2020

9

Tjitske Kleefstra

1 reference

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11 June 2020

1

Stefan H Lelieveld

1 reference

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11 June 2020

20

Lisenka E L M Vissers

1 reference

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11 June 2020

18

Marcel R Nelen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479843%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

5

Erik-Jan Kamsteeg

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479843%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

11

Maaike Vreeburg

1 reference

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11 June 2020

13

Ineke van der Burgt

1 reference

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11 June 2020

17

Tuula Rinne

1 reference

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11 June 2020

7

Bert B A de Vries

1 reference

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11 June 2020

14

Ernie M H F Bongers

1 reference

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11 June 2020

author name string

Petra de Vries

6

1 reference

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11 June 2020

Katharina Löhner

10

1 reference

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11 June 2020

language of work or name

English

0 references

publication date

1 August 2016

1 reference

http://europepmc.org/abstract/MED/27479843

9 February 2018

published in

Nature Neuroscience

1 reference

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11 June 2020

volume

19

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11 June 2020

issue

9

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11 June 2020

page(s)

1194-1196

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https://scigraph.springernature.com/pub.10.1038/nn.4352

11 June 2020

exact match

0 references

cites work

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network

1 reference

The contribution of de novo coding mutations to autism spectrum disorder

21 January 2018

1 reference

Genome sequencing identifies major causes of severe intellectual disability

21 January 2018

1 reference

Recurrent de novo mutations implicate novel genes underlying simplex autism risk

21 January 2018

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

21 January 2018

1 reference

Mutations in SETD2 cause a novel overgrowth condition.

21 January 2018

1 reference

Brief Report: SETD2 Mutation in a Child with Autism, Intellectual Disabilities and Epilepsy.

21 January 2018

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A de novo convergence of autism genetics and molecular neuroscience

21 January 2018

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Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

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Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory.

21 January 2018

1 reference

Rate of de novo mutations and the importance of father's age to disease risk

21 January 2018

1 reference

Multiple hypothesis testing in genomics.

21 January 2018

1 reference

A systematic survey of loss-of-function variants in human protein-coding genes

21 January 2018

1 reference

How many human genes can be defined as housekeeping with current expression data?

21 January 2018

1 reference

Genic intolerance to functional variation and the interpretation of personal genomes

21 January 2018

1 reference

A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

21 January 2018

1 reference

Large-scale discovery of novel genetic causes of developmental disorders

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27479843

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NN.4352

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27479843%20AND%20SRC:MED&resulttype=core&format=json

11 June 2020

1 reference