(Q35900760)

11 August 2017

Copy number variations of chromosome 16p13.1 region associated with schizophrenia (English)

1 reference

11 August 2017

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29

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37

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11 August 2017

C Francks

9

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Engilbert Sigurdsson

E Sigurdsson

4

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Hreinn Stefansson

H Stefansson

45

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Elvira Bramon

E Bramon

27

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Sven Cichon

S Cichon

3

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Srdjan Djurovic

S Djurovic

36

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Thomas Werge

39

T Werge

1 reference

11 August 2017

42

M Rietschel

1 reference

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48

K Stefansson

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49

D M St Clair

1 reference

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43

M M Nöthen

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11 August 2017

15

T Hansen

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25

J Suvisaari

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28

L A Kiemeney

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11 August 2017

30

R Murray

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11 August 2017

19

H-J Möller

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Annamari Tuulio-Henriksson

11 August 2017

26

A Tuulio-Henriksson

1 reference

Jacobine E Buizer-Voskamp

11 August 2017

7

J E Buizer-Voskamp

1 reference

11 August 2017

A Ingason

1

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11 August 2017

D Rujescu

2

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11 August 2017

T Sigmundsson

5

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11 August 2017

O P H Pietiläinen

6

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11 August 2017

E Strengman

8

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11 August 2017

P Muglia

10

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11 August 2017

A Gylfason

11

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11 August 2017

O Gustafsson

12

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11 August 2017

P I Olason

13

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11 August 2017

S Steinberg

14

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11 August 2017

K D Jakobsen

16

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11 August 2017

H B Rasmussen

17

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11 August 2017

I Giegling

18

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11 August 2017

A Hartmann

20

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11 August 2017

C Crombie

21

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G Fraser

22

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11 August 2017

N Walker

23

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11 August 2017

J Lonnqvist

24

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11 August 2017

E Vassos

31

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11 August 2017

T Toulopoulou

32

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11 August 2017

T W Mühleisen

33

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11 August 2017

S Tosato

34

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11 August 2017

M Ruggeri

35

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11 August 2017

Z Zhang

38

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11 August 2017

R A Ophoff

40

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11 August 2017

GROUP Investigators

41

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H Petursson

44

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11 August 2017

L Peltonen

46

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11 August 2017

D Collier

47

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11 August 2017

language of work or name

English

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publication date

29 September 2009

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11 August 2017

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16

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11 August 2017

17-25

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11 August 2017

1

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https://scigraph.springernature.com/pub.10.1038/mp.2009.101

11 August 2017

0 references

cites work

A genome-wide investigation of SNPs and CNVs in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Copy number variation and schizophrenia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Large recurrent microdeletions associated with schizophrenia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Rare chromosomal deletions and duplications increase risk of schizophrenia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Strong association of de novo copy number mutations with sporadic schizophrenia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Association between microdeletion and microduplication at 16p11.2 and autism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

A unified genetic theory for sporadic and inherited autism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Strong association of de novo copy number mutations with autism

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Attentional and neurocognitive characteristics of high-risk offspring of parents with schizophrenia compared with DSM-IV attention deficit hyperactivity disorder children

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Fine-scale structural variation of the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Genomic imbalances in mental retardation

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Psychosis proneness and ADHD in young relatives of schizophrenia patients

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Anterior cingulate cortex pathology in schizophrenia and bipolar disorder.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Varying intertrial interval reveals temporally defined memory deficits and enhancements in NTAN1-deficient mice

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Altered activity, social behavior, and spatial memory in mice lacking the NTAN1p amidase and the asparagine branch of the N-end rule pathway

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Serotonin depletion during synaptogenesis leads to decreased synaptic density and learning deficits in the adult rat: a possible model of neurodevelopmental disorders with cognitive deficits.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Association within a family of a balanced autosomal translocation with major mental illness

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Schizophrenia: genome, interrupted.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Replication of 1q42 linkage in Finnish schizophrenia pedigrees.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Cytokine effects on cortical neuron MAP-2 immunoreactivity: implications for schizophrenia.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

A hot spot of genetic instability in autism.

24 September 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.101

Phenotypic variations on the theme of CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.101

Familiality of Polarity at Illness Onset in Bipolar Affective Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.101

Genetics of Recurrent Early-Onset Major Depression (GenRED): Final Genome Scan Report

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.101

Familiality of Polarity at Illness Onset in Bipolar Affective Disorder

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3330746

Serotonin depletion in the adult rat causes loss of the dendritic marker MAP-2. A new animal model of schizophrenia?

14 November 2018

1 reference

12 December 2020

Relationship between childhood behavioral disturbance and later schizophrenia in the New York High-Risk Project

1 reference

12 December 2020

No association between the NDE1 gene and schizophrenia in the Japanese population

1 reference

12 December 2020

A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22–21, 4p16, 6q14–22, 10q26 and 16p13.3

1 reference

12 December 2020

Genetics of recurrent early-onset major depression (GenRED): final genome scan report

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.101

7 January 2021

inferred from DOI database lookup

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FMP.2009.101

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/MP.2009.101

1 reference

Dimensions Publication ID

11 August 2017

0 references

1 reference

11 August 2017

1 reference