(Q37506744)

20 August 2017

Identifying bipolar disorder susceptibility loci in a densely affected pedigree (English)

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20 August 2017

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F Mayoral

9

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Sven Cichon

object named as

S Cichon

10

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Marcella Rietschel

12

object named as

M Rietschel

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20 August 2017

11

M M Nöthen

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20 August 2017

13

P F Sullivan

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20 August 2017

A L Collins

1

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20 August 2017

Y Kim

2

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20 August 2017

J P Szatkiewicz

3

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20 August 2017

R J Bloom

4

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20 August 2017

C E Hilliard

5

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20 August 2017

C R Quackenbush

6

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20 August 2017

S Meier

7

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20 August 2017

F Rivas

8

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20 August 2017

language of work or name

English

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publication date

18 December 2012

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20 August 2017

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20 August 2017

18

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20 August 2017

12

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20 August 2017

1245-1246

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https://scigraph.springernature.com/pub.10.1038/mp.2012.176

20 August 2017

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cites work

Genetic architectures of psychiatric disorders: the emerging picture and its implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

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=3899577

Genomic analysis of mental illness: a changing landscape

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

Efficient identification of identical-by-descent status in pedigrees with many untyped 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=3899577

High-resolution detection of identity by descent in unrelated 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=3899577

Sporadic cases are the norm for complex disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

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=3899577

Whole population, genome-wide mapping of hidden relatedness

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3899577

23 August 2017

Identifiers

DOI

10.1038/MP.2012.176

1 reference

20 August 2017

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20 August 2017

PubMed publication ID

23247078

1 reference