List of works - Kent D Taylor

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

scientific article

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

scientific article

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

scientific article

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

scientific article

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

scientific article

Genome-wide association study of blood pressure and hypertension

scientific journal article

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

scientific journal article

Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis

scientific article

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

scientific article published on September 2008

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

scientific article

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

scientific article

Common variants at five new loci associated with early-onset inflammatory bowel disease

scientific article

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

scientific article published on 18 April 2016

Association of antibody responses to microbial antigens and complications of small bowel Crohn's disease

scientific article published in February 2004

Genomewide association studies of stroke

scientific article published on 15 April 2009

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

scientific article

New gene functions in megakaryopoiesis and platelet formation

scientific article published on 30 November 2011

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scientific article

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

scientific article published in September 2002

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

scientific article

Epigenetic Signatures of Cigarette Smoking

scientific article

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

scientific article

Rare and low-frequency coding variants alter human adult height

scientific article (publication date: February 2017)

Long-range LD can confound genome scans in admixed populations

scientific article published on July 2008

Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

scientific article

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

scientific article

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

scientific article published on 12 September 2016

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

scientific article published on 08 October 2018

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

scientific article

Serum immune responses predict rapid disease progression among children with Crohn's disease: immune responses predict disease progression

scientific article

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

scientific article published on 06 January 2013

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

scientific article

Exome-wide association study of plasma lipids in >300,000 individuals

scientific article published on 30 October 2017

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

scientific article published on 11 September 2011

Increased immune reactivity predicts aggressive complicating Crohn's disease in children

scientific article published on 10 July 2008

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

scientific article published on 12 March 2018

Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium

scientific article

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

scientific article published in November 2015

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans

scientific article

ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease

scientific article

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

scientific article published on 12 September 2016

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

scientific article

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

scientific article

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

scientific article

A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

scientific article

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

scientific article

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

scientific article published in October 2010

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

scientific article

Variation in the 3-hydroxyl-3-methylglutaryl coenzyme a reductase gene is associated with racial differences in low-density lipoprotein cholesterol response to simvastatin treatment

scientific article published on 10 March 2008

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

scientific article

List of works by Kent D Taylor

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

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

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

Genome-wide association study of blood pressure and hypertension

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

Common variants at five new loci associated with early-onset inflammatory bowel disease

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Association of antibody responses to microbial antigens and complications of small bowel Crohn's disease

Genomewide association studies of stroke

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

New gene functions in megakaryopoiesis and platelet formation

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

Epigenetic Signatures of Cigarette Smoking

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

Rare and low-frequency coding variants alter human adult height

Long-range LD can confound genome scans in admixed populations

Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Serum immune responses predict rapid disease progression among children with Crohn's disease: immune responses predict disease progression

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

Exome-wide association study of plasma lipids in >300,000 individuals

Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

Increased immune reactivity predicts aggressive complicating Crohn's disease in children

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans

ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

Variation in the 3-hydroxyl-3-methylglutaryl coenzyme a reductase gene is associated with racial differences in low-density lipoprotein cholesterol response to simvastatin treatment

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins