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4. Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

7. An Overview of Cancer in the First 315,000 All of Us Participants

12. Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

13. Comparison of oral collection methods for studies of microbiota

14. Reproducibility, stability, and accuracy of microbial profiles by fecal sample collection method in three distinct populations.

15. Association of KRAS Mutation and Gene Pathways in Colorectal Carcinoma: A Transcriptome- and Methylome-Wide Study and Potential Implications for Therapy.

18. Comparison of Fecal Collection Methods for Microbiota Studies in Bangladesh

19. Molecular Profiling and the Interaction of Somatic Mutations with Transcriptomic Profiles in Non-Melanoma Skin Cancer (NMSC) in a Population Exposed to Arsenic.

20. Air quality and cancer risk in the All of Us Research Program

21. Duration-sensitive association between air pollution exposure and changes in cardiometabolic biomarkers: Evidence from a predominantly African American cohort

26. The contribution of parent-to-offspring transmission of telomeres to the heritability of telomere length in humans

28. The Role of Health Insurance Type and Clinic Visit on Hypertension Status Among Multiethnic Chicago Residents

30. Erratum: 'Rare, protein-altering variants in AS3MT and arsenic metabolism efficiency: a multi-population association study'

31. Screening for gene–environment (G×E) interaction using omics data from exposed individuals: an application to gene-arsenic interaction

32. The impact of rare variation on gene expression across tissues

33. Dynamic landscape and regulation of RNA editing in mammals

34. Landscape of X chromosome inactivation across human tissues

35. Supplementary Table 1 from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

36. Data from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

37. Supplementary Methods, Tables 1 - 6 from 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

38. Supplementary Table 2 and Supplemental Figures from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

39. Supplementary Material: Funding, Acknowledgements, Consortia, and Bioinformatics Tools Funding sources from Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

40. Data from 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

43. Sequencing-based fine-mapping and in silico functional characterization of the 10q24.32 arsenic metabolism efficiency locus across multiple arsenic-exposed populations

44. Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications

45. Developing an algorithm across integrated healthcare systems to identify a history of cancer using electronic medical records

47. Somatic loss of the Y chromosome is associated with arsenic exposure among Bangladeshi men.

50. Interaction of Arsenic Exposure and Transcriptomic Profile in Basal Cell Carcinoma

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