Host genetic and epigenetic factors in toxoplasmosis (Q37326304)

19 August 2017

Host genetic and epigenetic factors in toxoplasmosis (English)

1 reference

19 August 2017

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3

Eskild Petersen

1 reference

19 August 2017

Heather Cordell

2

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ORCID Public Data File 2021

Jenefer Blackwell

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6

object named as

Jenefer M Blackwell

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19 August 2017

Sarra E Jamieson

1

1 reference

PMCID

2735098

19 August 2017

Rima McLeod

series ordinal

4

1 reference

PMCID

2735098

19 August 2017

Ruth E Gilbert

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5

1 reference

19 August 2017

1 March 2009

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19 August 2017

8

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Memórias do Instituto Oswaldo Cruz

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published in

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19 August 2017

104

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19 August 2017

162-169

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19 August 2017

2

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Assessing genuine parents-offspring trios for genetic association studies

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Strengthening causal inference in cardiovascular epidemiology through Mendelian randomization

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Common statistical issues in genome-wide association studies: a review on power, data quality control, genotype calling and population structure

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Haplotypic analysis of Wellcome Trust Case Control Consortium data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Two-stage candidate gene study of chromosome 3p demonstrates an association between nonsynonymous variants in the MST1R gene and Crohn's disease.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Rheumatoid arthritis association at 6q23.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genetic determinants of hair, eye and skin pigmentation in Europeans

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Identifying genes for coronary artery disease: An idea whose time has come

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genomewide association analysis of coronary artery disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

A new multipoint method for genome-wide association studies by imputation of genotypes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genome-wide association study identifies novel breast cancer susceptibility loci

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

A genome-wide association study identifies novel risk loci for type 2 diabetes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genetic susceptibility to infectious diseases: big is beautiful, but will bigger be even better?

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Shaking the tree: mapping complex disease genes with linkage disequilibrium

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genetic association studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Genomic screening and replication using the same data set in family-based association testing

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-review

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Power consequences of linkage disequilibrium variation between populations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Perturbation analysis: a simple method for filtering SNPs with erroneous genotyping in genome-wide association studies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Whole genome-amplified DNA: insights and imputation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Examining the statistical properties of fine-scale mapping in large-scale association studies

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease

26 June 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

A genome-wide association study of sporadic ALS in a homogenous Irish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

The ABCA4 gene in autosomal recessive cone-rod dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Association between prenatal treatment and clinical manifestations of congenital toxoplasmosis in infancy: a cohort study in 13 European centres

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

The v-MFG test: investigating maternal, offspring and maternal-fetal genetic incompatibility effects on disease and viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

HLA-class II genes modify outcome of Toxoplasma gondii infection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Outcome of treatment for congenital toxoplasmosis, 1981-2004: the National Collaborative Chicago-Based, Congenital Toxoplasmosis Study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Effect of timing and type of treatment on the risk of mother to child transmission of Toxoplasma gondii

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2735098

Maternal genotype effects can alias case genotype effects in case–control studies

2 September 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0074-02762009000200006

Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP

21 January 2018

1 reference

12 December 2020

Genome studies: genetics by numbers

1 reference

12 December 2020

Improved correction for population stratification in genome-wide association studies by identifying hidden population structures

1 reference

12 December 2020

Mother-to-child transmission of toxoplasmosis: risk estimates for clinical counselling

1 reference

12 December 2020

Detection of a novel parasite kinase activity at the Toxoplasma gondii parasitophorous vacuole membrane capable of phosphorylating host IkappaBalpha

1 reference

12 December 2020

Stickler syndrome: clinical characteristics and diagnostic criteria

1 reference

12 December 2020

Host and parasite-derived IKK activities direct distinct temporal phases of NF-kappaB activation and target gene expression following Toxoplasma gondii infection

1 reference

12 December 2020

10.1590/S0074-02762009000200006

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

1 reference

PMCID

2735098