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Dharambir Sanghera to Risk Factors

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This is a "connection" page, showing publications Dharambir Sanghera has written about Risk Factors.
Dharambir Sanghera
Connection Strength
1.058
Risk Factors
  1. Genetic and Non-genetic Determinants of Cardiovascular Disease in South Asians. Curr Diabetes Rev. 2021; 17(9):e011721190373.
    View in: PubMed
    Score: 0.125
  2. Obesity genetics and cardiometabolic health: Potential for risk prediction. Diabetes Obes Metab. 2019 05; 21(5):1088-1100.
    View in: PubMed
    Score: 0.111
  3. Vitamin D Status, Gender Differences, and Cardiometabolic Health Disparities. Ann Nutr Metab. 2017; 70(2):79-87.
    View in: PubMed
    Score: 0.096
  4. Association of APOE polymorphisms with diabetes and cardiometabolic risk factors and the role of APOE genotypes in response to anti-diabetic therapy: results from the AIDHS/SDS on a South Asian population. J Diabetes Complications. 2015 Nov-Dec; 29(8):1191-7.
    View in: PubMed
    Score: 0.086
  5. Genetic variation in cholesterol ester transfer protein, serum CETP activity, and coronary artery disease risk in Asian Indian diabetic cohort. Pharmacogenet Genomics. 2012 Feb; 22(2):95-104.
    View in: PubMed
    Score: 0.067
  6. A low frequency variant within the GWAS locus of MTNR1B affects fasting glucose concentrations: genetic risk is modulated by obesity. Nutr Metab Cardiovasc Dis. 2012 Nov; 22(11):944-51.
    View in: PubMed
    Score: 0.064
  7. Replication of association between a common variant near melanocortin-4 receptor gene and obesity-related traits in Asian Sikhs. Obesity (Silver Spring). 2010 Feb; 18(2):425-9.
    View in: PubMed
    Score: 0.057
  8. Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk. BMC Med Genet. 2008 Jul 03; 9:59.
    View in: PubMed
    Score: 0.053
  9. TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels. Ann Hum Genet. 2008 Jul; 72(Pt 4):499-509.
    View in: PubMed
    Score: 0.052
  10. Genetic variation in the paraoxonase-3 (PON3) gene is associated with serum PON1 activity. Ann Hum Genet. 2008 Jan; 72(Pt 1):72-81.
    View in: PubMed
    Score: 0.050
  11. Role of an intronic polymorphism in the PDCD1 gene with the risk of sporadic systemic lupus erythematosus and the occurrence of antiphospholipid antibodies. Hum Genet. 2004 Oct; 115(5):393-8.
    View in: PubMed
    Score: 0.040
  12. Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat Genet. 2018 04; 50(4):524-537.
    View in: PubMed
    Score: 0.026
  13. The codon 55 polymorphism in the paraoxonase 1 gene is not associated with the risk of coronary heart disease in Asian Indians and Chinese. Atherosclerosis. 1998 Feb; 136(2):217-23.
    View in: PubMed
    Score: 0.026
  14. DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease. Am J Hum Genet. 1998 Jan; 62(1):36-44.
    View in: PubMed
    Score: 0.025
  15. Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. Nat Genet. 2017 Oct; 49(10):1450-1457.
    View in: PubMed
    Score: 0.025
  16. Genetic polymorphism of paraoxonase and the risk of coronary heart disease. Arterioscler Thromb Vasc Biol. 1997 Jun; 17(6):1067-73.
    View in: PubMed
    Score: 0.024
  17. Quantitative effects of the apolipoprotein E polymorphism in a biracial sample of 9-10-year-old girls. Atherosclerosis. 1996 Sep 27; 126(1):35-42.
    View in: PubMed
    Score: 0.023
  18. Investigation of Genetic Variation Underlying Central Obesity amongst South Asians. PLoS One. 2016; 11(5):e0155478.
    View in: PubMed
    Score: 0.023
  19. Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat Genet. 2015 11; 47(11):1282-1293.
    View in: PubMed
    Score: 0.022
  20. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet. 2014 Mar; 46(3):234-44.
    View in: PubMed
    Score: 0.019
  21. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet. 2013 Nov; 45(11):1345-52.
    View in: PubMed
    Score: 0.019
  22. The p22 phox polymorphism C242T is not associated with CHD risk in Asian Indians and Chinese. Eur J Clin Invest. 1999 Dec; 29(12):999-1002.
    View in: PubMed
    Score: 0.007
  23. Genetic variation in apolipoprotein H (beta2-glycoprotein I) affects the occurrence of antiphospholipid antibodies and apolipoprotein H concentrations in systemic lupus erythematosus. Lupus. 1999; 8(9):742-50.
    View in: PubMed
    Score: 0.007
  24. Gender-specific nonrandom association between the alpha 1-antichymotrypsin and apolipoprotein E polymorphisms in the general population and its implication for the risk of Alzheimer's disease. Genet Epidemiol. 1997; 14(2):169-80.
    View in: PubMed
    Score: 0.006
  25. APOE*4-associated Alzheimer's disease risk is modified by alpha 1-antichymotrypsin polymorphism. Nat Genet. 1995 Aug; 10(4):486-8.
    View in: PubMed
    Score: 0.005
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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.