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Connection

Muhammad G. Kibriya to Genetic Predisposition to Disease

This is a "connection" page, showing publications Muhammad G. Kibriya has written about Genetic Predisposition to Disease.
  1. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. 2024 Mar; 627(8003):347-357.
    View in: PubMed
    Score: 0.129
  2. 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: 0.087
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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: 0.040
  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: 0.033
  9. 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: 0.032
  10. 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: 0.029
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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: 0.016
  21. 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: 0.014
  22. 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: 0.011
  23. 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: 0.010
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.