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Connection

Habibul Ahsan to Genetic Predisposition to Disease

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This is a "connection" page, showing publications Habibul Ahsan has written about Genetic Predisposition to Disease.
Habibul Ahsan
Connection Strength
3.669
Genetic Predisposition to Disease
  1. Germline Variation and Breast Cancer Incidence: A Gene-Based Association Study and Whole-Genome Prediction of Early-Onset Breast Cancer. Cancer Epidemiol Biomarkers Prev. 2018 09; 27(9):1057-1064.
    View in: PubMed
    Score: 0.347
  2. Clinical assessment incorporating a personal genome. Lancet. 2010 Sep 11; 376(9744):869; author reply 869-70.
    View in: PubMed
    Score: 0.203
  3. Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk. Hum Hered. 2010; 69(3):193-201.
    View in: PubMed
    Score: 0.196
  4. Case-only genome-wide interaction study of disease risk, prognosis and treatment. Genet Epidemiol. 2010 Jan; 34(1):7-15.
    View in: PubMed
    Score: 0.193
  5. Arsenic metabolism, genetic susceptibility, and risk of premalignant skin lesions in Bangladesh. Cancer Epidemiol Biomarkers Prev. 2007 Jun; 16(6):1270-8.
    View in: PubMed
    Score: 0.162
  6. Variants in estrogen-biosynthesis genes CYP17 and CYP19 and breast cancer risk: a family-based genetic association study. Breast Cancer Res. 2005; 7(1):R71-81.
    View in: PubMed
    Score: 0.135
  7. Further development of the case-only design for assessing gene-environment interaction: evaluation of and adjustment for bias. Int J Epidemiol. 2004 Oct; 33(5):1014-24.
    View in: PubMed
    Score: 0.134
  8. A family-based genetic association study of variants in estrogen-metabolism genes COMT and CYP1B1 and breast cancer risk. Breast Cancer Res Treat. 2004 May; 85(2):121-31.
    View in: PubMed
    Score: 0.131
  9. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. 2024 Mar; 627(8003):347-357.
    View in: PubMed
    Score: 0.129
  10. Susceptibility to arsenic-induced hyperkeratosis and oxidative stress genes myeloperoxidase and catalase. Cancer Lett. 2003 Nov 10; 201(1):57-65.
    View in: PubMed
    Score: 0.126
  11. DNA repair gene XPD and susceptibility to arsenic-induced hyperkeratosis. Toxicol Lett. 2003 Jul 20; 143(2):123-31.
    View in: PubMed
    Score: 0.124
  12. Relative risk for genetic associations: the case-parent triad as a variant of case-cohort design. Int J Epidemiol. 2002 Jun; 31(3):669-78.
    View in: PubMed
    Score: 0.114
  13. Research Participants' Attitudes towards Receiving Information on Genetic Susceptibility to Arsenic Toxicity in Rural Bangladesh. Public Health Genomics. 2020; 23(1-2):69-76.
    View in: PubMed
    Score: 0.098
  14. Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. PLoS One. 2018; 13(4):e0196245.
    View in: PubMed
    Score: 0.086
  15. Screening for gene-environment (G×E) interaction using omics data from exposed individuals: an application to gene-arsenic interaction. Mamm Genome. 2018 02; 29(1-2):101-111.
    View in: PubMed
    Score: 0.085
  16. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Nat Genet. 2017 Dec; 49(12):1767-1778.
    View in: PubMed
    Score: 0.083
  17. Association analysis identifies 65 new breast cancer risk loci. Nature. 2017 11 02; 551(7678):92-94.
    View in: PubMed
    Score: 0.083
  18. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Nat Commun. 2016 04 27; 7:11375.
    View in: PubMed
    Score: 0.075
  19. Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study. Hum Mol Genet. 2015 Sep 15; 24(18):5356-66.
    View in: PubMed
    Score: 0.071
  20. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Nat Genet. 2015 Apr; 47(4):373-80.
    View in: PubMed
    Score: 0.069
  21. Interaction between arsenic exposure from drinking water and genetic susceptibility in carotid intima-media thickness in Bangladesh. Toxicol Appl Pharmacol. 2014 May 01; 276(3):195-203.
    View in: PubMed
    Score: 0.065
  22. A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Cancer Epidemiol Biomarkers Prev. 2014 Apr; 23(4):658-69.
    View in: PubMed
    Score: 0.064
  23. Arsenic metabolism efficiency has a causal role in arsenic toxicity: Mendelian randomization and gene-environment interaction. Int J Epidemiol. 2013 Dec; 42(6):1862-71.
    View in: PubMed
    Score: 0.063
  24. Unidentified genetic variants influence pancreatic cancer risk: an analysis of polygenic susceptibility in the PanScan study. Genet Epidemiol. 2012 Jul; 36(5):517-24.
    View in: PubMed
    Score: 0.057
  25. Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. PLoS Genet. 2012; 8(2):e1002522.
    View in: PubMed
    Score: 0.056
  26. Genome-wide "pleiotropy scan" identifies HNF1A region as a novel pancreatic cancer susceptibility locus. Cancer Res. 2011 Jul 01; 71(13):4352-8.
    View in: PubMed
    Score: 0.053
  27. Association study of type 2 diabetes genetic susceptibility variants and risk of pancreatic cancer: an analysis of PanScan-I data. Cancer Causes Control. 2011 Jun; 22(6):877-83.
    View in: PubMed
    Score: 0.053
  28. Power and instrument strength requirements for Mendelian randomization studies using multiple genetic variants. Int J Epidemiol. 2011 Jun; 40(3):740-52.
    View in: PubMed
    Score: 0.051
  29. Methods for assessing familial aggregation: family history measures and confounding in the standard cohort, reconstructed cohort and case-control designs. Hum Hered. 2009; 68(3):201-8.
    View in: PubMed
    Score: 0.047
  30. Do placental genes affect maternal breast cancer? Association between offspring's CGB5 and CSH1 gene variants and maternal breast cancer risk. Cancer Res. 2008 Dec 01; 68(23):9729-34.
    View in: PubMed
    Score: 0.045
  31. A CYP19 (aromatase) polymorphism is associated with increased premenopausal breast cancer risk. Breast Cancer Res Treat. 2008 Oct; 111(3):481-7.
    View in: PubMed
    Score: 0.042
  32. TGFBR1*6A may contribute to hereditary colorectal cancer. J Clin Oncol. 2005 May 01; 23(13):3074-8.
    View in: PubMed
    Score: 0.035
  33. Covariate adjustment in family-based association studies. Genet Epidemiol. 2005 Apr; 28(3):244-55.
    View in: PubMed
    Score: 0.035
  34. Lung cancer etiology: independent and joint effects of genetics, tobacco, and arsenic. JAMA. 2004 Dec 22; 292(24):3026-9.
    View in: PubMed
    Score: 0.034
  35. No major association between TGFBR1*6A and prostate cancer. BMC Genet. 2004 Sep 22; 5:28.
    View in: PubMed
    Score: 0.034
  36. Measures of genotype versus gene products: promise and pitfalls in cancer prevention. Carcinogenesis. 2003 Sep; 24(9):1429-34.
    View in: PubMed
    Score: 0.031
  37. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Nat Genet. 2022 05; 54(5):560-572.
    View in: PubMed
    Score: 0.028
  38. Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. Commun Biol. 2022 04 07; 5(1):329.
    View in: PubMed
    Score: 0.028
  39. The effect of age on DNA methylation in whole blood among Bangladeshi men and women. BMC Genomics. 2019 Sep 10; 20(1):704.
    View in: PubMed
    Score: 0.024
  40. A meta-analysis approach with filtering for identifying gene-level gene-environment interactions. Genet Epidemiol. 2018 07; 42(5):434-446.
    View in: PubMed
    Score: 0.021
  41. Serum homocysteine, arsenic methylation, and arsenic-induced skin lesion incidence in Bangladesh: A one-carbon metabolism candidate gene study. Environ Int. 2018 04; 113:133-142.
    View in: PubMed
    Score: 0.021
  42. Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal. J Med Genet. 2018 01; 55(1):64-71.
    View in: PubMed
    Score: 0.021
  43. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent. PLoS Med. 2016 08; 13(8):e1002105.
    View in: PubMed
    Score: 0.019
  44. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry. Cancer Causes Control. 2016 May; 27(5):679-93.
    View in: PubMed
    Score: 0.019
  45. 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: 0.018
  46. Gene-arsenic interaction in longitudinal changes of blood pressure: Findings from the Health Effects of Arsenic Longitudinal Study (HEALS) in Bangladesh. Toxicol Appl Pharmacol. 2015 10 01; 288(1):95-105.
    View in: PubMed
    Score: 0.018
  47. A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh. Cancer. 2015 Jul 01; 121(13):2222-9.
    View in: PubMed
    Score: 0.017
  48. Variants of the adiponectin and adiponectin receptor 1 genes and breast cancer risk. Cancer Res. 2008 May 01; 68(9):3178-84.
    View in: PubMed
    Score: 0.011
  49. Combined genetic assessment of transforming growth factor-beta signaling pathway variants may predict breast cancer risk. Cancer Res. 2005 Apr 15; 65(8):3454-61.
    View in: PubMed
    Score: 0.009
  50. Polycyclic aromatic hydrocarbon-DNA adducts in liver tissues of hepatocellular carcinoma patients and controls. Int J Cancer. 2002 May 01; 99(1):14-21.
    View in: PubMed
    Score: 0.007
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.