Header Logo

Connection

Dharambir Sanghera to Humans

Back to Details
This is a "connection" page, showing publications Dharambir Sanghera has written about Humans.
Dharambir Sanghera
Connection Strength
1.295
Humans
  1. Corroborated evidence on change of metabolome after ischemic stroke due to large vessel occlusion. Metabolomics. 2025 Mar 23; 21(2):41.
    View in: PubMed
    Score: 0.055
  2. Contribution of circulating Mfge8 to human T2DM and cardiovascular disease. Gene. 2024 Nov 15; 927:148712.
    View in: PubMed
    Score: 0.053
  3. Discovery and validation of circulating stroke metabolites by NMR-based analyses using patients from the MISS and UK Biobank. Neurochem Int. 2023 Oct; 169:105588.
    View in: PubMed
    Score: 0.049
  4. Difference in acute and chronic stage ischemic stroke metabolic markers with controls. J Stroke Cerebrovasc Dis. 2023 Aug; 32(8):107211.
    View in: PubMed
    Score: 0.049
  5. Global Metabolomic Profiling Reveals Disrupted Lipid and Amino Acid Metabolism Between the Acute and Chronic Stages of Ischemic Stroke. J Stroke Cerebrovasc Dis. 2022 Apr; 31(4):106320.
    View in: PubMed
    Score: 0.045
  6. 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: 0.043
  7. A Bidirectional Mendelian Randomization Study to evaluate the causal role of reduced blood vitamin D levels with type 2 diabetes risk in South Asians and Europeans. Nutr J. 2021 07 27; 20(1):71.
    View in: PubMed
    Score: 0.043
  8. Genetic and Non-genetic Determinants of Cardiovascular Disease in South Asians. Curr Diabetes Rev. 2021; 17(9):e011721190373.
    View in: PubMed
    Score: 0.041
  9. Novel Metabolites as Potential Indicators of Ischemic Infarction Volume: a Pilot Study. Transl Stroke Res. 2021 10; 12(5):778-784.
    View in: PubMed
    Score: 0.041
  10. 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: 0.039
  11. 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: 0.039
  12. 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: 0.037
  13. Obesity genetics and cardiometabolic health: Potential for risk prediction. Diabetes Obes Metab. 2019 05; 21(5):1088-1100.
    View in: PubMed
    Score: 0.037
  14. Frequencies of poor metabolizer alleles of 12 pharmacogenomic actionable genes in Punjabi Sikhs of Indian Origin. Sci Rep. 2018 10 24; 8(1):15742.
    View in: PubMed
    Score: 0.036
  15. Vitamin D Status, Gender Differences, and Cardiometabolic Health Disparities. Ann Nutr Metab. 2017; 70(2):79-87.
    View in: PubMed
    Score: 0.032
  16. 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: 0.029
  17. Genetic and Cultural Reconstruction of the Migration of an Ancient Lineage. Biomed Res Int. 2015; 2015:651415.
    View in: PubMed
    Score: 0.029
  18. 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: 0.028
  19. 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: 0.026
  20. 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: 0.024
  21. Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Diabetes. 2013 May; 62(5):1746-55.
    View in: PubMed
    Score: 0.024
  22. A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. PLoS One. 2012; 7(5):e37056.
    View in: PubMed
    Score: 0.023
  23. Genetic determinants of cardiometabolic risk: a proposed model for phenotype association and interaction. J Clin Lipidol. 2013 Jan-Feb; 7(1):65-81.
    View in: PubMed
    Score: 0.023
  24. 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: 0.022
  25. Genome-wide linkage scan to identify loci associated with type 2 diabetes and blood lipid phenotypes in the Sikh Diabetes Study. PLoS One. 2011; 6(6):e21188.
    View in: PubMed
    Score: 0.021
  26. 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: 0.021
  27. 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: 0.021
  28. 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: 0.019
  29. 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: 0.019
  30. 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: 0.018
  31. 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: 0.017
  32. 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: 0.017
  33. 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: 0.016
  34. 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: 0.015
  35. 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: 0.013
  36. A saturated map of common genetic variants associated with human height. Nature. 2022 10; 610(7933):704-712.
    View in: PubMed
    Score: 0.012
  37. 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: 0.011
  38. Chimpanzee apolipoprotein H (beta2-glycoprotein I): report on the gene structure, a common polymorphism, and a high prevalence of antiphospholipid antibodies. Hum Genet. 2001 Jul; 109(1):63-72.
    View in: PubMed
    Score: 0.011
  39. Associations of autozygosity with a broad range of human phenotypes. Nat Commun. 2019 10 31; 10(1):4957.
    View in: PubMed
    Score: 0.010
  40. 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: 0.009
  41. 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: 0.009
  42. 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: 0.008
  43. 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: 0.008
  44. 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: 0.008
  45. Molecular basis of the apolipoprotein H (beta 2-glycoprotein I) protein polymorphism. Hum Genet. 1997 Jul; 100(1):57-62.
    View in: PubMed
    Score: 0.008
  46. 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: 0.008
  47. Identification of structural mutations in the fifth domain of apolipoprotein H (beta 2-glycoprotein I) which affect phospholipid binding. Hum Mol Genet. 1997 Feb; 6(2):311-6.
    View in: PubMed
    Score: 0.008
  48. No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. Sci Rep. 2016 10 12; 6:35278.
    View in: PubMed
    Score: 0.008
  49. 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: 0.008
  50. Investigation of Genetic Variation Underlying Central Obesity amongst South Asians. PLoS One. 2016; 11(5):e0155478.
    View in: PubMed
    Score: 0.008
  51. Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes. Nat Commun. 2016 Jan 28; 7:10531.
    View in: PubMed
    Score: 0.007
  52. 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: 0.007
  53. A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Nat Genet. 2015 Oct; 47(10):1121-1130.
    View in: PubMed
    Score: 0.007
  54. Directional dominance on stature and cognition in diverse human populations. Nature. 2015 Jul 23; 523(7561):459-462.
    View in: PubMed
    Score: 0.007
  55. PhenX RISING: real world implementation and sharing of PhenX measures. BMC Med Genomics. 2014 Mar 20; 7:16.
    View in: PubMed
    Score: 0.006
  56. 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: 0.006
  57. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet. 2013 Nov; 45(11):1345-52.
    View in: PubMed
    Score: 0.006
  58. Discovery and refinement of loci associated with lipid levels. Nat Genet. 2013 Nov; 45(11):1274-1283.
    View in: PubMed
    Score: 0.006
  59. Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians. Diabetologia. 2012 Apr; 55(4):981-95.
    View in: PubMed
    Score: 0.006
  60. Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet. 2011 Aug 28; 43(10):984-9.
    View in: PubMed
    Score: 0.005
  61. 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: 0.005
  62. Apolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes. J Rheumatol. 2009 Feb; 36(2):315-22.
    View in: PubMed
    Score: 0.005
  63. Single nucleotide polymorphisms in the coding region of the apolipoprotein H (beta2-glycoprotein I) gene and their correlation with the protein polymorphism, anti-beta2glycoprotein I antibodies and cardiolipin binding: description of novel haplotypes and their evolution. Ann Hum Genet. 2004 Jul; 68(Pt 4):285-99.
    View in: PubMed
    Score: 0.003
  64. 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: 0.002
  65. 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: 0.002
  66. Apolipoprotein J polymorphisms and serum HDL cholesterol levels in African blacks. Hum Biol. 1999 Apr; 71(2):197-218.
    View in: PubMed
    Score: 0.002
  67. Structure of the human beta2-glycoprotein I (apolipoprotein H) gene. Eur J Biochem. 1999 Jan; 259(1-2):435-40.
    View in: PubMed
    Score: 0.002
  68. 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: 0.002
  69. 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: 0.002
  70. 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: 0.002
  71. Short report on DNA marker at candidate locus. Two new alleles in the tetranucleotide repeat polymorphism in the LDL-receptor-related protein (LRP) gene. Clin Genet. 1996 Jul; 50(1):54-5.
    View in: PubMed
    Score: 0.002
  72. 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: 0.002
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.