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Connection

Habibul Ahsan to Genome-Wide Association Study

This is a "connection" page, showing publications Habibul Ahsan has written about Genome-Wide Association Study.
Connection Strength

3.439
  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: 0.376
  2. Mediation analysis demonstrates that trans-eQTLs are often explained by cis-mediation: a genome-wide analysis among 1,800 South Asians. PLoS Genet. 2014 Dec; 10(12):e1004818.
    View in: PubMed
    Score: 0.294
  3. Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. PLoS One. 2014; 9(8):e105062.
    View in: PubMed
    Score: 0.288
  4. 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: 0.247
  5. 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: 0.243
  6. Case-only genome-wide interaction study of disease risk, prognosis and treatment. Genet Epidemiol. 2010 Jan; 34(1):7-15.
    View in: PubMed
    Score: 0.209
  7. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. 2024 Mar; 627(8003):347-357.
    View in: PubMed
    Score: 0.139
  8. 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: 0.123
  9. 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: 0.122
  10. Co-occurring expression and methylation QTLs allow detection of common causal variants and shared biological mechanisms. Nat Commun. 2018 02 23; 9(1):804.
    View in: PubMed
    Score: 0.092
  11. 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: 0.090
  12. Association analysis identifies 65 new breast cancer risk loci. Nature. 2017 11 02; 551(7678):92-94.
    View in: PubMed
    Score: 0.090
  13. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Nat Commun. 2016 04 27; 7:11375.
    View in: PubMed
    Score: 0.081
  14. Epigenetic Alterations and Canonical Pathway Disruption in Papillary Thyroid Cancer: A Genome-wide Methylation Analysis. Ann Surg Oncol. 2016 07; 23(7):2302-9.
    View in: PubMed
    Score: 0.080
  15. 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: 0.078
  16. Genome-wide association study of parity in Bangladeshi women. PLoS One. 2015; 10(3):e0118488.
    View in: PubMed
    Score: 0.075
  17. Genome-wide association study of smoking behaviours among Bangladeshi adults. J Med Genet. 2014 May; 51(5):327-33.
    View in: PubMed
    Score: 0.070
  18. 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: 0.069
  19. A genome-wide study of cytogenetic changes in colorectal cancer using SNP microarrays: opportunities for future personalized treatment. PLoS One. 2012; 7(2):e31968.
    View in: PubMed
    Score: 0.061
  20. 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: 0.057
  21. 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: 0.057
  22. Clinical assessment incorporating a personal genome. Lancet. 2010 Sep 11; 376(9744):869; author reply 869-70.
    View in: PubMed
    Score: 0.055
  23. 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: 0.055
  24. Genetic susceptibility to type 2 diabetes is associated with reduced prostate cancer risk. Hum Hered. 2010; 69(3):193-201.
    View in: PubMed
    Score: 0.053
  25. Whole-genome amplification enables accurate genotyping for microarray-based high-density single nucleotide polymorphism array. Cancer Epidemiol Biomarkers Prev. 2008 Dec; 17(12):3499-508.
    View in: PubMed
    Score: 0.049
  26. A pilot genome-wide association study of early-onset breast cancer. Breast Cancer Res Treat. 2009 Apr; 114(3):463-77.
    View in: PubMed
    Score: 0.047
  27. DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits. Nat Genet. 2023 01; 55(1):112-122.
    View in: PubMed
    Score: 0.032
  28. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nat Genet. 2021 09; 53(9):1300-1310.
    View in: PubMed
    Score: 0.029
  29. Genetic Determinants of Reduced Arsenic Metabolism Efficiency in the 10q24.32 Region Are Associated With Reduced AS3MT Expression in Multiple Human Tissue Types. Toxicol Sci. 2020 08 01; 176(2):382-395.
    View in: PubMed
    Score: 0.027
  30. PBMC gene expression profiles of female Bangladeshi adults chronically exposed to arsenic-contaminated drinking water. Environ Pollut. 2020 Apr; 259:113672.
    View in: PubMed
    Score: 0.026
  31. 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: 0.023
  32. 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: 0.023
  33. 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: 0.022
  34. Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. Cancer Res. 2016 09 01; 76(17):5103-14.
    View in: PubMed
    Score: 0.020
  35. 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: 0.019
  36. Interpretation of genome-wide infinium methylation data from ligated DNA in formalin-fixed, paraffin-embedded paired tumor and normal tissue. BMC Res Notes. 2012 Feb 22; 5:117.
    View in: PubMed
    Score: 0.015
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.