(Q59667688)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21743468%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Increased exonic de novo mutation rate in individuals with schizophrenia (English)

1 reference

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7 February 2020

1 reference

1

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7 February 2020

Marie-Odile Krebs

21

1 reference

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7 February 2020

22

Guy A Rouleau

1 reference

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7 February 2020

3

Anne Noreau

1 reference

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7 February 2020

19

Patrick A Dion

1 reference

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7 February 2020

5

Sirui Zhou

1 reference

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7 February 2020

Alexandre Dionne-Laporte

7

Alexandre Dionne-Laporte

1 reference

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7 February 2020

11

Pascale Thibodeau

1 reference

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7 February 2020

17

Nematollah Jaafari

1 reference

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7 February 2020

Loubna Jouan

6

Loubna Jouan

1 reference

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7 February 2020

Dan Spiegelman

8

Dan Spiegelman

1 reference

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7 February 2020

Isabelle Bachand

12

Isabelle Bachand

1 reference

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7 February 2020

Bruno Millet

16

Bruno Millet

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7 February 2020

author name string

Lan Xiong

4

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7 February 2020

Edouard Henrion

9

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7 February 2020

Ousmane Diallo

10

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7 February 2020

Jessie Y J Bao

13

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7 February 2020

Amy Hin Yan Tong

14

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7 February 2020

Chi-Ho Lin

15

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7 February 2020

Ridha Joober

18

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7 February 2020

Si Lok

20

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7 February 2020

Julie Gauthier

2

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7 February 2020

language of work or name

English

0 references

publication date

10 July 2011

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7 February 2020

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7 February 2020

volume

43

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7 February 2020

page(s)

860-863

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7 February 2020

issue

9

1 reference

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https://scigraph.springernature.com/pub.10.1038/ng.886

7 February 2020

exact match

0 references

cites work

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

12 December 2020

Large recurrent microdeletions associated with schizophrenia

1 reference

12 December 2020

Common variants on chromosome 6p22.1 are associated with schizophrenia

1 reference

12 December 2020

Developmental regulation of V(D)J recombination and lymphocyte differentiation

1 reference

12 December 2020

Confirmation of an association between a polymorphism in exon 3 of the low-density lipoprotein receptor-related protein gene and Alzheimer's disease.

1 reference

12 December 2020

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

1 reference

12 December 2020

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

1 reference

12 December 2020

Nonrandomness of point mutation as reflected in nucleotide substitutions in pseudogenes and its evolutionary implications

1 reference

12 December 2020

VarScan: variant detection in massively parallel sequencing of individual and pooled samples

1 reference

12 December 2020

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

1 reference

12 December 2020

Rate, molecular spectrum, and consequences of human mutation

1 reference

12 December 2020

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

1 reference

12 December 2020

The roles of the RAG1 and RAG2 "non-core" regions in V(D)J recombination and lymphocyte development

1 reference

12 December 2020

The Sequence Alignment/Map format and SAMtools

1 reference

12 December 2020

A de novo paradigm for mental retardation.

1 reference

12 December 2020

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

1 reference

12 December 2020

A method and server for predicting damaging missense mutations

1 reference

12 December 2020

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment

1 reference

12 December 2020

Common variants conferring risk of schizophrenia

1 reference

12 December 2020

Amyloid precursor protein regulates brain apolipoprotein E and cholesterol metabolism through lipoprotein receptor LRP1

1 reference

12 December 2020

Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics

1 reference

12 December 2020

Predicting deleterious amino acid substitutions

1 reference

12 December 2020

Detection of nonneutral substitution rates on mammalian phylogenies

1 reference

12 December 2020

A map of human genome variation from population-scale sequencing

1 reference

12 December 2020

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

12 December 2020

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

12 December 2020

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

1 reference

12 December 2020

Amino acid difference formula to help explain protein evolution

1 reference

12 December 2020

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

1 reference

12 December 2020

Identifiers

DOI

10.1038/NG.886

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21743468%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

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