(Q35642209)

9 August 2017

title

Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD. (English)

1 reference

9 August 2017

12

Carol A Mathews

1 reference

9 August 2017

Jessica Ross

1

1 reference

9 August 2017

Judith Badner

2

1 reference

9 August 2017

Helena Garrido

3

1 reference

9 August 2017

Brooke Sheppard

4

1 reference

9 August 2017

Denise A Chavira

5

1 reference

9 August 2017

Marco Grados

6

1 reference

9 August 2017

Jonathan M Woo

7

1 reference

9 August 2017

Pamela Doo

8

1 reference

9 August 2017

Paula Umaña

9

1 reference

9 August 2017

Eduardo Fournier

10

1 reference

9 August 2017

Sarah Shaw Murray

11

1 reference

9 August 2017

publication date

21 June 2011

1 reference

9 August 2017

1 reference

9 August 2017

volume

130

1 reference

9 August 2017

issue

6

1 reference

9 August 2017

page(s)

795-805

1 reference

Genome partitioning of genetic variation for complex traits using common SNPs

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Involvement of ryanodine receptors in neurotrophin-induced hippocampal synaptic plasticity and spatial memory formation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Uncovering the roles of rare variants in common disease through whole-genome sequencing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Finding the missing heritability of complex diseases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Comprehensive behavioral phenotyping of ryanodine receptor type 3 (RyR3) knockout mice: decreased social contact duration in two social interaction tests.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

The genetics of obsessive compulsive disorder: a review of the evidence

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Integrating evidence from neuroimaging and neuropsychological studies of obsessive-compulsive disorder: the orbitofronto-striatal model revisited.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

F-SNP: computationally predicted functional SNPs for disease association studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

The role of clinical phenotypes in understanding the genetics of obsessive-compulsive disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Molecular biology and genetics of Alzheimer's disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

SIFT: Predicting amino acid changes that affect protein function

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Probing striato-thalamic function in obsessive-compulsive disorder and Tourette syndrome using neuroimaging methods

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Predicting deleterious amino acid substitutions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Complex segregation analysis provides compelling evidence for a major gene underlying obsessive-compulsive disorder and for heterogeneity by sex.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Molecular cloning and characterization of a human brain ryanodine receptor

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Sublocalization of an ataxia-telangiectasia gene distal to D11S384 by ancestral haplotyping in Costa Rican families

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

The gene for an inherited form of deafness maps to chromosome 5q31

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder.

12 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Robust estimation of critical values for genome scans to detect linkage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Further evidence for co-segregation between pediatric obsessive compulsive disorder and attention deficit hyperactivity disorder: a familial risk analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

The power to detect linkage in complex disease by means of simple LOD-score analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Best estimate of lifetime psychiatric diagnosis: a methodological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Genetic studies of neuropsychiatric disorders in Costa Rica: a model for the use of isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Biased distribution of inverted and direct Alus in the human genome: implications for insertion, exclusion, and genome stability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Generation and characterization of mutant mice lacking ryanodine receptor type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Gender differences in genetic linkage and association on 11p15 in obsessive-compulsive disorder families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Differential regulation of CaMKII inhibitor beta protein expression after exposure to a novel context and during contextual fear memory formation

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

A comparative study of obsessive-compulsive disorder in Costa Rica and the United States

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Mutant mice lacking ryanodine receptor type 3 exhibit deficits of contextual fear conditioning and activation of calcium/calmodulin-dependent protein kinase II in the hippocampus.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4442699

Association Testing of the Positional and Functional Candidate Gene SLC1A1/EAAC1 in Early-Onset Obsessive-compulsive Disorder

25 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1033-6

Complex segregation analysis for obsessive compulsive disorder and related disorders

21 January 2018

1 reference

12 December 2020

Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q and 6q

1 reference

12 December 2020

Ca2+ entry via AMPA-type glutamate receptors triggers Ca2+-induced Ca2+ release from ryanodine receptors in rat spiral ganglion neurons

1 reference

12 December 2020

Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands

1 reference

12 December 2020

HaploPainter: a tool for drawing pedigrees with complex haplotypes

1 reference

12 December 2020

Compulsivity in mouse strains homologous with chromosomes 7p and 15q linked to obsessive-compulsive disorder

1 reference

12 December 2020

Complex segregation analysis of obsessive-compulsive disorder in families with pediatric probands

1 reference

12 December 2020

10.1007/S00439-011-1033-6

Identifiers

DOI

1 reference

release_hz4c4lmzwjd43ghjqwbtfe34ai

9 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hz4c4lmzwjd43ghjqwbtfe34ai

24 November 2022

mapped directly with Wikidata item

PMC publication ID

4442699

1 reference

9 August 2017

1 reference