(Q41967395)

14 October 2017

Detection of susceptibility genes as modifiers due to subgroup differences in complex disease (English)

1 reference

14 October 2017

1

1 reference

14 October 2017

4

Kenneth S Kendler

1 reference

14 October 2017

Brion S Maher

2

1 reference

14 October 2017

Ayman H Fanous

series ordinal

3

1 reference

14 October 2017

31 March 2010

1 reference

European Journal of Human Genetics

14 October 2017

1 reference

14 October 2017

18

1 reference

14 October 2017

8

1 reference

14 October 2017

960-964

1 reference

NOS1AP is a genetic modifier of the long-QT syndrome

14 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

An ordered subset approach to including covariates in the transmission disequilibrium test

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

New models of collaboration in genome-wide association studies: the Genetic Association Information Network

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Use of phenotypic covariates in association analysis by sequential addition of cases

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Susceptibility genes for age-related maculopathy on chromosome 10q26

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Predicting clinical severity in sickle cell anaemia.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population

5 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

5 June 2018

https://api.crossref.org/works/10.1038%2FEJHG.2010.39

Genetic heterogeneity, modifier genes, and quantitative phenotypes in psychiatric illness: searching for a framework

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Genotype-phenotype correlation in cystic fibrosis: the role of modifier genes.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Heterogeneity in the severity of cystic fibrosis and the role of CFTR gene mutations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Clinical spectrum of ataxia-telangiectasia in adulthood

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Catechol-O-methyltransferase and the clinical features of psychosis.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

COMT genotype and manic symptoms in schizophrenia

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Dysbindin genotype and negative symptoms in schizophrenia.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2896458

Disrupted in Schizophrenia 1 Genotype and Positive Symptoms in Schizophrenia

18 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2010.39

CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20354561

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Relationship between a high-risk haplotype in the DTNBP1 (dysbindin) gene and clinical features of schizophrenia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20354561

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage disequilibrium on the COMT gene in French schizophrenics and controls

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20354561

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2010.39

1 reference

Dimensions Publication ID

14 October 2017

0 references

1 reference

14 October 2017

PubMed publication ID

20354561

1 reference