(Q57239706)

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Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15768393%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15768393%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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based on heuristic

inferred from title

single-nucleotide polymorphism

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based on heuristic

inferred from title

5

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9 January 2020

Marie-Pierre Dubé

8

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9 January 2020

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Eric Shink

1

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9 January 2020

Mario Harvey

2

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9 January 2020

Monique Tremblay

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9 January 2020

Bernard Gagné

4

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9 January 2020

Catherine Raymond

6

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9 January 2020

Michel Labbé

7

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9 January 2020

Nicholas Barden

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9 January 2020

Ronald G Lafrenière

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9 January 2020

publication date

1 May 2005

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9 January 2020

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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9 January 2020

135B

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9 January 2020

1

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9 January 2020

50-58

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9 January 2020

The human DDX and DHX gene families of putative RNA helicases

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Genomewide scans of complex human diseases: true linkage is hard to find

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

No association between a neuronal nitric oxide synthase (NOS1) gene polymorphism on chromosome 12q24 and bipolar disorder.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Spb4p, an essential putative RNA helicase, is required for a late step in the assembly of 60S ribosomal subunits in Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

The future of genetic analysis of neurological disorders

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

CUX2, a potential regulator of NCAM expression: genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Molecular basis of lithium action: integration of lithium-responsive signaling and gene expression networks

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Homozygotes carrying an autosomal dominant TIGR mutation do not manifest glaucoma

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Replication of linkage studies of complex traits: an examination of variation in location estimates

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Power comparison of parametric and nonparametric linkage tests in small pedigrees

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Genetic heterogeneity in a very large bipolar affective disorder pedigree from Quebec

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Exclusion of non-synonymous SNPs and a polyglutamine tract in SMRT/N-CoR2 as common deleterious mutation for bipolar disorder in the Sagnenay-Lac-St-Jean population

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Candidate-gene approaches for studying complex genetic traits: practical considerations

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Polygenic disease: methods for mapping complex disease traits

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Molecular identification of high and low affinity receptors for nicotinic acid

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Association studies in psychiatric genetics

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30165

21 January 2018

Identifiers

10.1002/AJMG.B.30165

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15768393%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15768393%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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