| human | Q5 |
| P106 | occupation | researcher | Q1650915 |
| Q28267020 | A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease |
| Q36522200 | A novel haplotype in ABCA1 gene effects plasma HDL-C concentration |
| Q40254292 | ANGPTL3 Deficiency and Protection Against Coronary Artery Disease |
| Q33831563 | Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysis |
| Q30420031 | Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke? |
| Q37731775 | Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans |
| Q33887961 | Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study |
| Q34558126 | Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular Disease. |
| Q36232030 | Effects of apolipoprotein E polymorphism on the development of stroke. |
| Q64108431 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls |
| Q45071322 | Exome-wide association study of plasma lipids in >300,000 individuals |
| Q33278264 | Factors associated with adherence to anti-hypertensive treatment in Pakistan |
| Q40191164 | Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms |
| Q36536523 | Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes |
| Q29417002 | Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India |
| Q29417126 | Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci |
| Q29417007 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility |
| Q40244307 | Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity |
| Q40059063 | Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease |
| Q39192859 | Junctional epidermolysis bullosa in the Middle East: clinical and genetic studies in a series of consanguineous families |
| Q37241867 | Lack of association of methylenetetrahydrofolate reductase 677C>T mutation with coronary artery disease in a Pakistani population |
| Q34165010 | Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates |
| Q33382363 | Molecular analysis of the XLRS1 gene in 4 females affected with X-linked juvenile retinoschisis |
| Q35873193 | Physical activity, smoking, and genetic predisposition to obesity in people from Pakistan: the PROMIS study |
| Q29615729 | Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study |
| Q57303741 | Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes |
| Q52327404 | Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes |
| Q36494736 | Stroke radiology and distinguishing characteristics of intracranial atherosclerotic disease in native South Asian Pakistanis |
| Q33482477 | The Karachi intracranial stenosis study (KISS) Protocol: an urban multicenter case-control investigation reporting the clinical, radiologic and biochemical associations of intracranial stenosis in Pakistan |
| Q37229051 | The Pakistan Risk of Myocardial Infarction Study: a resource for the study of genetic, lifestyle and other determinants of myocardial infarction in South Asia |
| Q37649785 | The cradle of the deltaF508 mutation. |
| Q37324554 | Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension |
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