(Q38030853)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

title

Whole-genome and whole-exome sequencing in neurological diseases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

main subject

whole genome sequencing

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

author name string

Jian-Jun Liu

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

Eng-King Tan

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

language of work or name

English

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publication date

31 July 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

published in

Nature Reviews Neurology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

page(s)

508-517

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22847385%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nrneurol.2012.148

9 February 2020

exact match

0 references

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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31 March 2020

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Statistical analysis strategies for association studies involving rare variants

31 March 2020

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Exome sequencing and the genetic basis of complex traits

31 March 2020

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Differential confounding of rare and common variants in spatially structured populations

31 March 2020

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Analysis of genetic inheritance in a family quartet by whole-genome sequencing

31 March 2020

1 reference

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

31 March 2020

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Increased exonic de novo mutation rate in individuals with schizophrenia

31 March 2020

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

31 March 2020

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

31 March 2020

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31 March 2020

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LRRK2 in Parkinson's disease: genetic and clinical studies from patients

31 March 2020

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Realizing genomic medicine

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRNEUROL.2012.148

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31 March 2020

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31 March 2020

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Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility

31 March 2020

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Personalized medicine: Bring clinical standards to human-genetics research

31 March 2020

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