High frequencies of de novo CNVs in bipolar disorder and schizophrenia (Q37578876)

21 August 2017

High frequencies of de novo CNVs in bipolar disorder and schizophrenia (English)

1 reference

21 August 2017

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11

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21 August 2017

21

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21 August 2017

24

Marcella Rietschel

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Vladimir Vacic

Vladimir Vacic

4

0 references

Jonathan Sebat

Jonathan Sebat

26

0 references

Aiden Corvin

Aiden Corvin

8

0 references

Sven Cichon

Sven Cichon

7

0 references

Markus M Nöthen

Markus M Nöthen

22

0 references

Jacob J Michaelson

Jacob J Michaelson

3

0 references

Katherine E Burdick

5

Katherine E Burdick

1 reference

21 August 2017

25

Thomas G Schulze

1 reference

21 August 2017

23

James B Potash

1 reference

21 August 2017

17

Deborah L Levy

1 reference

21 August 2017

13

John R Kelsoe

1 reference

21 August 2017

10

Elliot S Gershon

1 reference

21 August 2017

1

Dheeraj Malhotra

1 reference

21 August 2017

2

Shane McCarthy

1 reference

21 August 2017

14

Olga Krastoshevsky

1 reference

21 August 2017

15

Verena Krause

1 reference

21 August 2017

9

Sydney Gary

1 reference

21 August 2017

Seungtai Yoon

6

1 reference

21 August 2017

Maria Karayiorgou

12

1 reference

21 August 2017

Ellen Leibenluft

16

1 reference

21 August 2017

Vladimir Makarov

18

1 reference

21 August 2017

Abhishek Bhandari

19

1 reference

21 August 2017

Anil K Malhotra

20

1 reference

21 August 2017

language of work or name

English

0 references

publication date

1 December 2011

1 reference

21 August 2017

1 reference

21 August 2017

72

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21 August 2017

951-963

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21 August 2017

6

1 reference

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Exome sequencing supports a de novo mutational paradigm for schizophrenia.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

De novo rates and selection of large copy number variation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Microdeletions of 3q29 confer high risk for schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Functional impact of global rare copy number variation in autism spectrum disorders

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Microduplications of 16p11.2 are associated with schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Origins and functional impact of copy number variation in the human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Genome-wide association study of bipolar disorder in European American and African American individuals

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

The genetics of bipolar disorder

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Singleton deletions throughout the genome increase risk of bipolar disorder

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Large recurrent microdeletions associated with schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Rare chromosomal deletions and duplications increase risk of schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Strong association of de novo copy number mutations with sporadic schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Structural variation of chromosomes in autism spectrum disorder

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

The bipolar disorder phenome database: a resource for genetic studies

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Strong association of de novo copy number mutations with autism

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

High Concordance of Bipolar I Disorder in a Nationwide Sample of Twins

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

The Heritability of Bipolar Affective Disorder and the Genetic Relationship to Unipolar Depression

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Prospects for inferring pairwise relationships with single nucleotide polymorphisms

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Different familial transmission patterns in bipolar I disorder with onset before and after age 25.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

A pilot Swedish twin study of affective illness including hospital- and population-ascertained subsamples: results of model fitting

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3921625

Increased exonic de novo mutation rate in individuals with schizophrenia

1 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22196331

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22196331

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22196331

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NEURON.2011.11.007

1 reference

21 August 2017

1 reference

21 August 2017

1 reference