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Muhammad G. Kibriya to Polymorphism, Single Nucleotide

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This is a "connection" page, showing publications Muhammad G. Kibriya has written about Polymorphism, Single Nucleotide.
Muhammad G. Kibriya
Connection Strength
1.809
Polymorphism, Single Nucleotide
  1. 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: 0.231
  2. 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: 0.230
  3. 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: 0.184
  4. The contribution of parent-to-offspring transmission of telomeres to the heritability of telomere length in humans. Hum Genet. 2019 Jan; 138(1):49-60.
    View in: PubMed
    Score: 0.092
  5. 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: 0.089
  6. 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: 0.073
  7. The Genetic Architecture of Arsenic Metabolism Efficiency:A SNP-Based Heritability Study of Bangladeshi Adults. Environ Health Perspect. 2015 10; 123(10):985-92.
    View in: PubMed
    Score: 0.071
  8. Genome-wide association study of parity in Bangladeshi women. PLoS One. 2015; 10(3):e0118488.
    View in: PubMed
    Score: 0.071
  9. Genome-wide association study of smoking behaviours among Bangladeshi adults. J Med Genet. 2014 May; 51(5):327-33.
    View in: PubMed
    Score: 0.067
  10. 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: 0.066
  11. 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: 0.058
  12. 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: 0.044
  13. Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays. Cancer Genet Cytogenet. 2008 Apr 15; 182(2):69-74.
    View in: PubMed
    Score: 0.044
  14. 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: 0.043
  15. Sequencing-based fine-mapping and in silico functional characterization of the 10q24.32 arsenic metabolism efficiency locus across multiple arsenic-exposed populations. PLoS Genet. 2023 01; 19(1):e1010588.
    View in: PubMed
    Score: 0.031
  16. 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
  17. 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: 0.029
  18. Rare, Protein-Altering Variants in AS3MT and Arsenic Metabolism Efficiency: A Multi-Population Association Study. Environ Health Perspect. 2021 04; 129(4):47007.
    View in: PubMed
    Score: 0.027
  19. A missense variant in FTCD is associated with arsenic metabolism and toxicity phenotypes in Bangladesh. PLoS Genet. 2019 03; 15(3):e1007984.
    View in: PubMed
    Score: 0.024
  20. Lack of Association between Opioid-Receptor Genotypes and Smoking Cessation Outcomes in a Randomized, Controlled Naltrexone Trial. Alcohol Alcohol. 2019 Jan 09; 54(5):559-565.
    View in: PubMed
    Score: 0.023
  21. 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: 0.022
  22. 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: 0.022
  23. 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: 0.022
  24. 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
  25. 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: 0.020
  26. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Nat Commun. 2016 04 27; 7:11375.
    View in: PubMed
    Score: 0.019
  27. 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
  28. 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: 0.019
  29. 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
  30. 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: 0.018
  31. 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: 0.018
  32. Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study. Environ Health Perspect. 2015 May; 123(5):451-7.
    View in: PubMed
    Score: 0.018
  33. 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
  34. 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: 0.012
  35. 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: 0.010
  36. 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: 0.008
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