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| 36658389 | Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia. | Leukemia | 2023 |
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| 29930474 | Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in <i>PAX6</i> in a South African family. | Mol Vis | 2018 |
| 27161491 | The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes. | Nat Commun | 2016 |
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| 25811787 | Modulation of genetic associations with serum urate levels by body-mass-index in humans. | PLoS One | 2015 |
| 25673413 | Genetic studies of body mass index yield new insights for obesity biology. | Nature | 2015 |
| 25916844 | TP53 mutations, tetraploidy and homologous recombination repair defects in early stage high-grade serous ovarian cancer. | Nucleic Acids Res | 2015 |
| 25732040 | Glioblastoma adaptation traced through decline of an IDH1 clonal driver and macro-evolution of a double-minute chromosome. | Ann Oncol | 2015 |
| 23202125 | Large-scale association analysis identifies new risk loci for coronary artery disease. | Nat Genet | 2013 |
| 24154874 | APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma. | Cancer Res | 2013 |
| 23563607 | Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. | Nat Genet | 2013 |
| 23263486 | Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. | Nat Genet | 2013 |
| 22238593 | A genome-wide association search for type 2 diabetes genes in African Americans. | PLoS One | 2012 |
| 22479202 | Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. | PLoS Genet | 2012 |
| 22885924 | Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. | Nat Genet | 2012 |
| 22581228 | A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. | Nat Genet | 2012 |
| 22607825 | Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study. | Lancet | 2012 |
| 22990020 | Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. | Blood | 2012 |
| 22898070 | Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. | J Am Coll Cardiol | 2012 |
| 22100073 | Blood pressure loci identified with a gene-centric array. | Am J Hum Genet | 2011 |
| 22001757 | Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. | Nat Genet | 2011 |
| 21875899 | Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour. | Human Molecular Genetics | 2011 |
| 21909115 | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. | Nature | 2011 |
| 21909110 | Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. | Nat Genet | 2011 |
| 21873549 | Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. | Diabetes | 2011 |
| 20231535 | Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. | Circulation | 2010 |
| 20881960 | Hundreds of variants clustered in genomic loci and biological pathways affect human height. | Nature | 2010 |
| 20935629 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. | Nat Genet | 2010 |
| 20858683 | Common variants at 10 genomic loci influence hemoglobin Aâ¿(C) levels via glycemic and nonglycemic pathways. | Diabetes | 2010 |
| 20081858 | New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. | Nat Genet | 2010 |
| 20595679 | HLA has strongest association with IgA nephropathy in genome-wide analysis. | J Am Soc Nephrol | 2010 |
| 20032323 | Genetic variants associated with Lp(a) lipoprotein level and coronary disease. | N Engl J Med | 2009 |
| 19430483 | Genome-wide association study identifies eight loci associated with blood pressure. | Nat Genet | 2009 |
| 19525478 | Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study. | Blood | 2009 |
| 19567438 | Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. | JAMA | 2009 |
| 19557161 | Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. | PLoS Genet | 2009 |
| 19503597 | Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. | PLoS Genet | 2009 |
| 19888323 | Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants. | PLoS ONE | 2009 |
| 18223314 | Quantitative trait genetic linkage analysis of body mass index in familial coronary artery disease. | Human Heredity | 2008 |
| 18048406 | Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. | Human Molecular Genetics | 2008 |
| 17133260 | Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study. | European Journal of Human Genetics | 2007 |
| 16710446 | Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17. | PLoS Genetics | 2006 |
| 15676066 | Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori. | BMC Genomics | 2005 |
| 15728743 | Variation in the strength of selected codon usage bias among bacteria. | Nucleic Acids Res | 2005 |
| 14594720 | SNP cherry picker: maximizing the chance of finding an association with a disease SNP. | Bioinformatics | 2003 |
| 11313762 | Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects. | European Journal of Human Genetics | 2001 |
| 11157800 | Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster. | Hum Mol Genet | 2001 |
| 11157797 | Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16. | Hum Mol Genet | 2001 |
| 10710307 | Complete genome sequence of Neisseria meningitidis serogroup B strain MC58. | Science | 2000 |