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Dharambir Sanghera to Middle Aged

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This is a "connection" page, showing publications Dharambir Sanghera has written about Middle Aged.
Dharambir Sanghera
Connection Strength
1.258
Middle Aged
  1. Contribution of circulating Mfge8 to human T2DM and cardiovascular disease. Gene. 2024 Nov 15; 927:148712.
    View in: PubMed
    Score: 0.106
  2. APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups. Lipids Health Dis. 2021 Sep 21; 20(1):113.
    View in: PubMed
    Score: 0.087
  3. A rare missense variant in the milk fat globule-EGF factor 8 (MFGE8) increases T2DM susceptibility and cardiovascular disease risk with population-specific effects. Acta Diabetol. 2020 Jun; 57(6):733-741.
    View in: PubMed
    Score: 0.078
  4. Potential Metabolite Biomarkers for Acute Versus Chronic Stage of Ischemic Stroke: A Pilot Study. J Stroke Cerebrovasc Dis. 2020 Apr; 29(4):104618.
    View in: PubMed
    Score: 0.078
  5. Targeted sequencing of candidate genes of dyslipidemia in Punjabi Sikhs: Population-specific rare variants in GCKR promote ectopic fat deposition. PLoS One. 2019; 14(8):e0211661.
    View in: PubMed
    Score: 0.075
  6. Vitamin D Status, Gender Differences, and Cardiometabolic Health Disparities. Ann Nutr Metab. 2017; 70(2):79-87.
    View in: PubMed
    Score: 0.064
  7. Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study. J Steroid Biochem Mol Biol. 2016 Apr; 158:149-156.
    View in: PubMed
    Score: 0.059
  8. 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: 0.057
  9. Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort. Circ Cardiovasc Genet. 2014 Jun; 7(3):287-95.
    View in: PubMed
    Score: 0.052
  10. Carriers of a novel frame-shift insertion in WNT16a possess elevated pancreatic expression of TCF7L2. BMC Genet. 2013 Apr 23; 14:28.
    View in: PubMed
    Score: 0.049
  11. 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: 0.045
  12. 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: 0.043
  13. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. BMC Med Genet. 2011 Jan 24; 12:18.
    View in: PubMed
    Score: 0.042
  14. PPARG and ADIPOQ gene polymorphisms increase type 2 diabetes mellitus risk in Asian Indian Sikhs: Pro12Ala still remains as the strongest predictor. Metabolism. 2010 Apr; 59(4):492-501.
    View in: PubMed
    Score: 0.038
  15. 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: 0.038
  16. Testing the association of novel meta-analysis-derived diabetes risk genes with type II diabetes and related metabolic traits in Asian Indian Sikhs. J Hum Genet. 2009 Mar; 54(3):162-8.
    View in: PubMed
    Score: 0.037
  17. 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: 0.035
  18. 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: 0.034
  19. 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: 0.033
  20. The Khatri Sikh Diabetes Study (SDS): study design, methodology, sample collection, and initial results. Hum Biol. 2006 Feb; 78(1):43-63.
    View in: PubMed
    Score: 0.030
  21. Burden of Type 2 Diabetes and Associated Cardiometabolic Traits and Their Heritability Estimates in Endogamous Ethnic Groups of India: Findings From the INDIGENIUS Consortium. Front Endocrinol (Lausanne). 2022; 13:847692.
    View in: PubMed
    Score: 0.023
  22. Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations. J Clin Endocrinol Metab. 2018 04 01; 103(4):1380-1392.
    View in: PubMed
    Score: 0.017
  23. 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: 0.017
  24. 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: 0.017
  25. 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: 0.016
  26. Investigation of Genetic Variation Underlying Central Obesity amongst South Asians. PLoS One. 2016; 11(5):e0155478.
    View in: PubMed
    Score: 0.015
  27. 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: 0.014
  28. PhenX RISING: real world implementation and sharing of PhenX measures. BMC Med Genomics. 2014 Mar 20; 7:16.
    View in: PubMed
    Score: 0.013
  29. An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumference. Diabet Med. 2011 Jun; 28(6):673-80.
    View in: PubMed
    Score: 0.011
  30. Apolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes. J Rheumatol. 2009 Feb; 36(2):315-22.
    View in: PubMed
    Score: 0.009
  31. 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: 0.005
  32. Genetic variation in the apolipoprotein H (beta2-glycoprotein I) gene affects plasma apolipoprotein H concentrations. Hum Genet. 1999 Jul-Aug; 105(1-2):63-71.
    View in: PubMed
    Score: 0.005
  33. 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: 0.005
  34. Racial differences in the distribution of a low density lipoprotein receptor-related protein (LRP) polymorphism and its association with serum lipoprotein, lipid and apolipoprotein levels. Atherosclerosis. 1998 Mar; 137(1):187-95.
    View in: PubMed
    Score: 0.004
  35. 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: 0.004
  36. 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: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.