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701 results on '"Mann, Graham"'

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1. The landscape of genomic structural variation in Indigenous Australians

2. Uncovering the complex relationship between balding, testosterone and skin cancers in men

3. The impact of coding germline variants on contralateral breast cancer risk and survival

4. The Recovery and Re-Calibration of a 13-Month Aerosol Extinction Profiles Dataset from Searchlight Observations from New Mexico, after the 1963 Agung Eruption

5. Analysis of the global atmospheric background sulfur budget in a multi-model framework

6. Whole-genome landscape of mucosal melanoma reveals diverse drivers and therapeutic targets.

7. Anatomic position determines oncogenic specificity in melanoma

9. A Natural Language Generation Technique for Automated Psychotherapy

11. Impact of personal genomic risk information on melanoma prevention behaviors and psychological outcomes: a randomized controlled trial

12. The Prognostic Significance of Low-Frequency Somatic Mutations in Metastatic Cutaneous Melanoma.

14. The 2019 Raikoke eruption as a testbed used by the Volcano Response group for rapid assessment of volcanic atmospheric impacts.

17. Acceptability and appropriateness of a risk-tailored organised melanoma screening program: Qualitative interviews with key informants

18. Evolution of late-stage metastatic melanoma is dominated by aneuploidy and whole genome doubling

19. Phylogenetic analyses of melanoma reveal complex patterns of metastatic dissemination

20. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

21. Molecular Genomic Profiling of Melanocytic Nevi

22. Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies

23. Antarctic Vortex Dehydration in 2023 as a Substantial Removal Pathway for Hunga Tonga‐Hunga Ha'apai Water Vapor.

25. ACEMID cohort study: protocol of a prospective cohort study using 3D total body photography for melanoma imaging and diagnosis

26. The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

27. Spatial Organization and Molecular Correlation of Tumor-Infiltrating Lymphocytes Using Deep Learning on Pathology Images

28. Molecular Characterization and Clinical Relevance of Metabolic Expression Subtypes in Human Cancers

29. Pan-Cancer Analysis of lncRNA Regulation Supports Their Targeting of Cancer Genes in Each Tumor Context

30. Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas

31. Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types

32. Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas

33. Systematic Analysis of Splice-Site-Creating Mutations in Cancer

34. Driver Fusions and Their Implications in the Development and Treatment of Human Cancers

35. Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas

36. Somatic Mutational Landscape of Splicing Factor Genes and Their Functional Consequences across 33 Cancer Types

37. Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families

39. Evaluation of Linkage of Breast Cancer to the Putative BRCA3 Locus on Chromosome 13q21 in 128 Multiple Case Families from the Breast Cancer Linkage Consortium

41. Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity

42. Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours

43. The 2019 Raikoke eruption as a testbed for rapid assessment of volcanic atmospheric impacts by the Volcano Response group

45. Cell death and barrier disruption by clinically used iodine concentrations

47. Interactive stratospheric aerosol models' response to different amounts and altitudes of SO2 injection during the 1991 Pinatubo eruption

48. Association of Germline Variants in Telomere Maintenance Genes (POT1, TERF2IP, ACD, TERT) with Spitzoid Morphology in Familial Melanoma: A Multi-Center Case Series

49. Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing

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