List of works - Nancy J Cox

The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans

scientific article published on 26 January 2011

Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals

scientific journal article

Identification of common genetic variants that account for transcript isoform variation between human populations.

scientific article published on 04 December 2008

Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas

scientific article published on 15 May 2011

A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose

scientific article

Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior

scientific article

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

scientific article

Genome-wide association studies in pharmacogenomics: successes and lessons

scientific article

Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia

scientific journal article

Genetic architecture of microRNA expression: implications for the transcriptome and complex traits

scientific article

Genome-wide meta-analysis for severe diabetic retinopathy

scientific article

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

scientific article

Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus

scientific article

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

scientific article

Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33

scientific article published on 01 January 2004

The importance of genealogy in determining genetic associations with complex traits

scientific article published on November 2001

Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues

scientific article

Genome-wide identification of microRNA expression quantitative trait loci

scientific article

A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303

scientific journal article

Exprtarget: an integrative approach to predicting human microRNA targets

scientific article

Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families

scientific article

Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research

scientific article

Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry

scientific article published on 22 February 2012

The neutrophil alloantigen HNA-3a (5b) is located on choline transporter-like protein 2 and appears to be encoded by an R>Q154 amino acid substitution

scientific article

Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.

scientific article published in October 2004

Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients

scientific article

Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from

scientific article

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

scientific article

Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines

scientific article published on November 2007

Re: CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 trial.

scientific article published on 31 July 2012

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

scientific article

A genome-wide association study of breast cancer in women of African ancestry

scientific article published on 25 August 2012

Genomewide significant linkage to stuttering on chromosome 12.

scientific article

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

scientific article

Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait

scientific article

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci

scientific article

Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas

scientific article

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study

scientific article

New complexities in the genetics of stuttering: significant sex-specific linkage signals

scientific article

Variation in the calpain-10 gene affects blood glucose levels in the British population

scientific article published in January 2002

On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy

scientific article

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

scientific article

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

scientific article

Variants affecting exon skipping contribute to complex traits.

scientific article

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

scientific article published in July 2004

Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects

scientific article

A statistical method for identification of polymorphisms that explain a linkage result

scientific article published on 08 January 2002

Genetic studies of stuttering in a founder population

scientific article

Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome

scientific article

Disease associations. Chance, artifact, or susceptibility genes?

scientific article

List of works by Nancy J Cox

The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans

Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals

Identification of common genetic variants that account for transcript isoform variation between human populations.

Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas

A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose

Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

Genome-wide association studies in pharmacogenomics: successes and lessons

Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia

Genetic architecture of microRNA expression: implications for the transcriptome and complex traits

Genome-wide meta-analysis for severe diabetic retinopathy

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33

The importance of genealogy in determining genetic associations with complex traits

Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues

Genome-wide identification of microRNA expression quantitative trait loci

A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303

Exprtarget: an integrative approach to predicting human microRNA targets

Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families

Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research

Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry

The neutrophil alloantigen HNA-3a (5b) is located on choline transporter-like protein 2 and appears to be encoded by an R>Q154 amino acid substitution

Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.

Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients

Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines

Re: CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 trial.

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

A genome-wide association study of breast cancer in women of African ancestry

Genomewide significant linkage to stuttering on chromosome 12.

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait

A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci

Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study

New complexities in the genetics of stuttering: significant sex-specific linkage signals

Variation in the calpain-10 gene affects blood glucose levels in the British population

On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

Variants affecting exon skipping contribute to complex traits.

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects

A statistical method for identification of polymorphisms that explain a linkage result

Genetic studies of stuttering in a founder population

Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome

Disease associations. Chance, artifact, or susceptibility genes?