Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. (Q39922110)

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10 March 2020

title

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders (English)

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10 March 2020

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Steve A McCarroll

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32

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Himanshu Chheda

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Sebastian S Gerety

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Muhammad Ayub

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Trevor Cole

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Eve L Coomber

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Marta DiForti

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Alison Foster

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Shelagh Joss

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Jarmo Körkkö

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Minna Männikkö

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Carmel Moore

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David Roberts

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Jennifer Sambrook

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Swedish Schizophrenia Study

54

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INTERVAL Study

55

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DDD Study

56

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UK10 K Consortium

57

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Matthew E Hurles

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Jouko Lönnqvist

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publication date

14 March 2016

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10 March 2020

language of work or name

0 references

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volume

19

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issue

4

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page(s)

571-577

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Lifetime prevalence of psychotic and bipolar I disorders in a general population

10 March 2020

cites work

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De novo mutations in schizophrenia implicate synaptic networks

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Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene

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21 January 2018

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Wdr82 is a C-terminal domain-binding protein that recruits the Setd1A Histone H3-Lys4 methyltransferase complex to transcription start sites of transcribed human genes

21 January 2018

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Identifiers

DOI

10.1038/NN.4267

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26974950%20AND%20SRC:MED&resulttype=core&format=json

10 March 2020

1 reference

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10 March 2020

PubMed publication ID

26974950

1 reference