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Lista de obras de Heather Cordell

4th Pediatric Allergy and Asthma Meeting (PAAM)

artículo científico publicado en 2016

A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits

artículo científico publicado en 2015

A Bayesian network approach incorporating imputation of missing data enables exploratory analysis of complex causal biological relationships

artículo científico publicado en 2021

A case-control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE)

scientific article published on 16 December 2018

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

artículo científico publicado en 2012

A comparison of methods for inferring causal relationships between genotype and phenotype using additional biological measurements.

artículo científico

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

artículo científico publicado en 2016

A genome-wide scan for type 1 diabetes susceptibility genes in nuclear families with multiple affected siblings in Finland

artículo científico publicado en 2007

A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family.

artículo científico publicado en 2013

A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients

artículo científico publicado en 1998

A meta-analysis of genome-wide association studies identifies multiple longevity genes

scientific article published on 14 August 2019

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

artículo científico publicado en 2001

Accounting for relatedness in family-based association studies: application to Genetic Analysis Workshop 18 data

artículo científico publicado en 2014

Affected-sib-pair data can be used to distinguish two-locus heterogeneity from two-locus epistasis

artículo científico publicado en 2003

Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis

article

Analysis of Genetic Analysis Workshop 18 data with gene-based penalized regression

artículo científico publicado en 2014

Analysis of North American Rheumatoid Arthritis Consortium data using a penalized logistic regression approach

artículo científico publicado en 2009

Analysis of the role of DPB1-encoded amino acids in the genetic predisposition to type I diabetes mellitus

artículo científico publicado en 2002

Approaches to the analysis of QTL data in mice, using the nonobese diabetic mouse as an example

artículo científico publicado en 2002

Ascertainment bias in the estimation of sibling genetic risk parameters

artículo científico publicado en 2000

Association between Aldosterone Production and Variation in the 11β-Hydroxylase (CYP11B1) Gene

article

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Association between anti-tumour necrosis factor treatment response and genetic variants within the TLR and NF B signalling pathways

article

Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts

artículo científico publicado en 2014

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

artículo científico publicado en 2003

Bayesian network analysis incorporating genetic anchors complements conventional Mendelian randomization approaches for exploratory analysis of causal relationships in complex data

artículo científico publicado en 2020

Bias toward the null hypothesis in model-free linkage analysis is highly dependent on the test statistic used

artículo científico publicado en 2004

Bootstrap confidence intervals for relative risk parameters in affected-sib-pair data

artículo científico publicado en 2000

CD4+ and B Lymphocyte Expression Quantitative Traits at Rheumatoid Arthritis Risk Loci in Patients With Untreated Early Arthritis: Implications for Causal Gene Identification.

artículo científico publicado en 2017

Cardiac Imaging of Aortic Valve Area from 34,287 UK Biobank Participants Reveal Novel Genetic Associations and Shared Genetic Comorbidity with Multiple Disease Phenotypes

artículo científico publicado en 2020

Chromosome 11q13.5 variant associated with childhood eczema: an effect supplementary to filaggrin mutations

artículo científico publicado en 2010

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

scientific article published on 10 December 2021

Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS.

artículo científico publicado en 2011

Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans

artículo científico publicado en 2005

Compare and Contrast Meta Analysis (CCMA): A Method for Identification of Pleiotropic Loci in Genome-Wide Association Studies

artículo científico publicado en 2016

Comparison of methods to account for relatedness in genome-wide association studies with family-based data

artículo científico publicado en 2014

Confidence intervals for relative risk estimates from affected-sib-pair data ⬇️

artículo científico publicado el 1 de enero de 1997

Confirmation of the superior performance of the causal Graphical Analysis Using Genetics (cGAUGE) pipeline in comparison to various competing alternatives

artículo científico publicado en 2022

Congenital heart disease risk loci identified by genome-wide association study in European patients

scientific article published on 17 November 2020

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

artículo científico publicado en 2012

Correcting for ascertainment bias of relative-risk estimates obtained using affected-sib-pair linkage data

artículo científico publicado en 2000

Dealing with missing data in family-based association studies: a multiple imputation approach.

artículo científico publicado en 2007

Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis

artículo científico publicado en 2012

Determining the population frequency of the CFHR3/CFHR1 deletion at 1q32.

artículo científico publicado en 2013

Development of a methodology to describe udder conformation in sows.

artículo científico publicado en 2015

Dissection of the pathophysiology of type 1 diabetes by genetic analysis.

artículo científico publicado en 1993

Distinct genetic loci control development of benign and malignant skin tumours in mice ⬇️

artículo científico publicado el 1 de agosto de 1995

Evaluation of an on-farm method to assess colostrum IgG content in sows

artículo científico publicado en 2015

Examination of previously identified associations within the Genetic Analysis Workshop 19 data.

artículo científico publicado en 2016

Factors determining penetrance in familial atypical haemolytic uraemic syndrome

artículo científico publicado en 2014

Fieller's theorem and linkage disequilibrium mapping

artículo científico publicado en 1999

Filaggrin null mutations and childhood atopic eczema: A population-based case-control study

article

Fine mapping and replication of genetic risk loci in primary sclerosing cholangitis

artículo científico publicado en 2012

Further investigations of the W-test for pairwise epistasis testing

artículo científico

Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans

artículo científico publicado en 2005

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci

artículo científico publicado en 2007

Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees

artículo científico publicado en 2014

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic and Functional Evidence Implicating DLL1 as the Gene That Influences Susceptibility to Visceral Leishmaniasis at Chromosome 6q27 ⬇️

artículo científico publicado el 1 de agosto de 2011

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

artículo científico publicado en 2008

Genetic association studies

artículo científico publicado en 2005

Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics Study

artículo científico publicado en 2009

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

artículo científico publicado en 2009

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.

artículo científico publicado en 2014

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

artículo científico publicado en 2011

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

scientific journal article

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

artículo científico publicado en 2013

Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms

artículo científico publicado en 2015

Genome-wide linkage analysis for human longevity: Genetics of Healthy Aging Study

artículo científico publicado en 2013

HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin

artículo científico publicado en 2009

Host genetic and epigenetic factors in toxoplasmosis

artículo científico publicado en 2009

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

artículo científico publicado en 2015

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

artículo científico publicado en 2016

Identification of Grouped Rare and Common Variants via Penalized Logistic Regression ⬇️

artículo científico publicado el 8 de julio de 2013

Imputation without doing imputation: a new method for the detection of non-genotyped causal variants

artículo científico publicado en 2014

Intercellular adhesion molecule-1 K469E polymorphism: study of association with multiple sclerosis

scientific article published on 01 March 2003

Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect

artículo científico publicado en 2011

Introduction to Genetic Analysis Workshop 15 summaries

artículo científico publicado en 2007

Investigating the prediction of CpG methylation levels from SNP genotype data to help elucidate relationships between methylation, gene expression and complex traits

artículo científico publicado en 2022

Investigation of genetically regulated gene expression and response to treatment in rheumatoid arthritis highlights an association between IL18RAP expression and treatment response

artículo científico publicado en 2020

Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring ⬇️

artículo científico publicado el 1 de enero de 2011

Joint linkage and association analysis for identification of potentially causal polymorphisms in GAW15 data

artículo científico publicado en 2007

Linkage analysis of GAW14 simulated data: comparison of multimarker, multipoint, and conditional approaches

artículo científico publicado en 2005

Linkage analysis of a derived glucose phenotype in the Genetic Analysis Workshop 13 simulated data using a variety of Haseman-Elston based regression methods

artículo científico publicado en 2003

Linkage analysis of candidate genes and gene-gene interactions in chinese hypertensive sib pairs

artículo científico publicado en 1999

Linkage and association analysis of GAW15 simulated data: fine-mapping of chromosome 6 region

artículo científico publicado en 2007

Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes

artículo científico publicado en 2003

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy.

artículo científico publicado en 2011

Mapping multiple linked quantitative trait loci in non-obese diabetic mice using a stepwise regression strategy

artículo científico publicado en 1998

Maternal-fetal interactions and birth order influence insulin variable number of tandem repeats allele class associations with head size at birth and childhood weight gain

artículo científico publicado en 2004

Meta-analysis of filaggrin polymorphisms in eczema and asthma: Robust risk factors in atopic disease

artículo científico publicado en 2009

Multifactorial inheritance in type 1 diabetes

artículo científico publicado en 1995

Multilocus linkage tests based on affected relative pairs.

artículo científico publicado en 2000

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling

artículo científico publicado en 2012

Parameters for reliable results in genetic association studies in common disease

article

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

artículo científico publicado en 2012

Polymorphisms spanning the TNFR2 and TACE genes do not contribute towards variable anti-TNF treatment response

artículo científico publicado en 2010

Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data ⬇️

article

Pretreatment prediction of response to ursodeoxycholic acid in primary biliary cholangitis: development and validation of the UDCA Response Score

artículo científico publicado en 2018

Prevalent and Low-Frequency Null Mutations in the Filaggrin Gene Are Associated with Early-Onset and Persistent Atopic Eczema

article

Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bank

artículo científico publicado en 2011

Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility

artículo científico publicado en 2009

Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility

artículo científico publicado en 2009

Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve

artículo científico publicado en 2017

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Regression mapping of association between the human leukocyte antigen region and Graves disease

artículo científico publicado en 2004

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

artículo científico publicado en 2004

Research capacity. Enabling the genomic revolution in Africa

artículo científico publicado en 2014

SNP Selection in genome‐wide and candidate gene studies via penalized logistic regression ⬇️

artículo científico publicado el 1 de diciembre de 2010

Speed-bumps ahead for the genetics of later-life diseases ⬇️

artículo científico publicado el 6 de agosto de 2011

The Plight of Muntaser Ibrahim

scientific article published on 25 March 2019

The heritability of G2 chromosomal radiosensitivity and its association with cancer in Danish cancer survivors and their offspring

artículo científico publicado en 2010

The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitis

artículo científico publicado en 2004

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

scientific journal article

Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis

scientific article published on 01 December 2020

Urinary tract effects of HPSE2 mutations

artículo científico publicado en 2014

Using gene expression data to identify causal pathways between genotype and phenotype in a complex disease: application to Genetic Analysis Workshop 19.

artículo científico publicado en 2016

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

artículo científico publicado en 2019

Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux

artículo científico publicado en 2009

Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan.

artículo científico publicado en 2007

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