Anuj Goel

• Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.

  Journal article

  Nüesch E. et al, (2016), Int J Epidemiol, 45, 1927 - 1937

• Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

  Journal article

  Huffman JE. et al, (2015), Blood, 126, e19 - e29

• Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis.

  Journal article

  Interleukin 1 Genetics Consortium None., (2015), Lancet Diabetes Endocrinol, 3, 243 - 253

• New genetic loci link adipose and insulin biology to body fat distribution.

  Journal article

  Shungin D. et al, (2015), Nature, 518, 187 - 196

• Genetic studies of body mass index yield new insights for obesity biology.

  Journal article

  Locke AE. et al, (2015), Nature, 518, 197 - 206

• Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.

  Journal article

  Do R. et al, (2015), Nature, 518, 102 - 106

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

  Journal article

  Wessel J. et al, (2015), Nat Commun, 6

• Modulation of genetic associations with serum urate levels by body-mass-index in humans.

  Journal article

  Huffman JE. et al, (2015), PLoS One, 10

• USE OF ENCODE DATA TO IDENTIFY PUTATIVE FUNCTIONAL VARIANTS IN CORONARY ARTERY DISEASE GWAS

  Conference paper

  Goel A. et al, (2014), ATHEROSCLEROSIS, 237, E8 - E8

• Defining the role of common variation in the genomic and biological architecture of adult human height.

  Journal article

  Wood AR. et al, (2014), Nat Genet, 46, 1173 - 1186

• Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.

  Journal article

  Hopewell JC. et al, (2014), J Intern Med, 276, 260 - 268

• A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.

  Journal article

  Kyriakou T. et al, (2014), Arterioscler Thromb Vasc Biol, 34, 2095 - 2099

• Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

  Journal article

  TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute None. et al, (2014), N Engl J Med, 371, 22 - 31

• Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.

  Journal article

  Simino J. et al, (2014), Am J Hum Genet, 95, 24 - 38

• Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.

  Journal article

  Tragante V. et al, (2014), Am J Hum Genet, 94, 349 - 360

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

  Journal article

  Peloso GM. et al, (2014), Am J Hum Genet, 94, 223 - 232

• Meta-analysis of gene-level tests for rare variant association.

  Journal article

  Liu DJ. et al, (2014), Nat Genet, 46, 200 - 204

• LPA NULL MUTATION GENOTYPING AND QPCR ANALYSIS REFINE KRINGLE ISOFORM ANALYSIS OF LP(A) LEVELS

  Conference paper

  Kyriakou T. et al, (2014), ATHEROSCLEROSIS, 232, E5 - E5

• No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.

  Journal article

  Baumert J. et al, (2014), PLoS One, 9

• Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia.

  Journal article

  Stitziel NO. et al, (2013), Arterioscler Thromb Vasc Biol, 33, 2909 - 2914

• Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study.

  Journal article

  Holmes MV. et al, (2013), J Am Coll Cardiol, 62, 1966 - 1976

• Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.

  Journal article

  Sabater-Lleal M. et al, (2013), Circulation, 128, 1310 - 1324

• Known SNPs in ADAMTS7, the 9p21 region and UBE2E interact with type 2 diabetes status to modify the risk of coronary artery disease in large populations

  Conference paper

  van Zuydam NR. et al, (2013), DIABETOLOGIA, 56, S76 - S77

• Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.

  Journal article

  van Meurs JB. et al, (2013), Am J Clin Nutr, 98, 668 - 676

• Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.

  Journal article

  Randall JC. et al, (2013), PLoS Genet, 9

• Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.

  Journal article

  Berndt SI. et al, (2013), Nat Genet, 45, 501 - 512

• CHROMOSOME 9P21 LOCUS AND ANGIOGRAPHIC CORONARY ARTERY DISEASE BURDEN: A COLLABORATIVE META-ANALYSIS

  Journal article

  Chan K. et al, (2013), HEART, 99, A75 - A75

• Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.

  Journal article

  Chan K. et al, (2013), J Am Coll Cardiol, 61, 957 - 970

• Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: A collaborative meta-analysis

  Journal article

  Chan K. et al, (2013), Journal of the American College of Cardiology, 61, 957 - 970

• Large-scale association analysis identifies new risk loci for coronary artery disease

  Journal article

  Deloukas P. et al, (2013), Nature Genetics, 45, 25 - 33

• Is urethral stricture only a circumferential disease? Reason for change in the plan of urethroplasty for bulbous urethral strictures shorter than 2 cm.

  Journal article

  Goel A. et al, (2013), Indian J Urol, 29, 27 - 30

• TILING ARRAY SHOWS LOW ANRIL, HIGH CDKN2B EXPRESSION ASSOCIATED WITH CHROMOSOME 9P21 CORONARY ARTERY DISEASE (CAD) RISK GENOTYPE

  Conference paper

  Beeton LD. et al, (2011), HEART, 97, 15 - 16

• A custom tiling expression microarray as a novel approach to study a coronary artery disease genetic risk locus

  Conference paper

  Green FR. et al, (2011), JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 9, 711 - 711

• COMMON GENETIC VARIANTS ASSOCIATED WITH LOW Lp(a) KRINGLE-IV COPY NUMBER, HIGH Lp(a) CONCENTRATION, AND INCREASED RISK OF CORONARY HEART DISEASE

  Conference paper

  Seedorf U. et al, (2010), ATHEROSCLEROSIS SUPPLEMENTS, 11, 13 - 13

• Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease

  Conference paper

  Clarke R. et al, (2009), CIRCULATION, 120, S589 - S589

• ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP

  Conference paper

  Goel A. et al, (2009), ATHEROSCLEROSIS, 207, E4 - E4

Recent Publications

• Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.

  Journal article

  Nüesch E. et al, (2016), Int J Epidemiol, 45, 1927 - 1937

• Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF.

  Journal article

  Huffman JE. et al, (2015), Blood, 126, e19 - e29

• Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis.

  Journal article

  Interleukin 1 Genetics Consortium None., (2015), Lancet Diabetes Endocrinol, 3, 243 - 253

• New genetic loci link adipose and insulin biology to body fat distribution.

  Journal article

  Shungin D. et al, (2015), Nature, 518, 187 - 196

• Genetic studies of body mass index yield new insights for obesity biology.

  Journal article

  Locke AE. et al, (2015), Nature, 518, 197 - 206