(Q41571023)

3 October 2017

title

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing (English)

1 reference

3 October 2017

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Zhongsheng Sun

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

author name string

Jinchen Li

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Yi Jiang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Tao Wang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Huiqian Chen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Qing Xie

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Qianzhi Shao

6

1 reference

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31 May 2020

Xia Ran

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Kun Xia

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Jinyu Wu

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

language of work or name

English

0 references

publication date

16 January 2015

1 reference

Journal of Medical Genetics

3 October 2017

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

volume

52

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

page(s)

275-281

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

A new paradigm emerges from the study of de novo mutations in the context of neurodevelopmental disease

31 May 2020

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Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

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21 January 2018

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21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json

release_uji2dx4swbba5kjuaus54hhmlq

31 May 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/uji2dx4swbba5kjuaus54hhmlq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25596308%20AND%20SRC:MED&resulttype=core&format=json