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Your search keyword '"Imielinski, Marcin"' showing total 466 results

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1. Ultrasensitive plasma-based monitoring of tumor burden using machine-learning-guided signal enrichment

2. Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes.

3. Whole-genome characterization of lung adenocarcinomas lacking the RTK/RAS/RAF pathway.

4. HLA-DP on Epithelial Cells Enables Tissue Damage by NKp44+ Natural Killer Cells in Ulcerative Colitis

5. Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions

6. Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer

7. Patterns of somatic structural variation in human cancer genomes

8. The evolutionary history of 2,658 cancers

9. Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.

10. Next-generation characterization of the Cancer Cell Line Encyclopedia

11. Somatic whole genome dynamics of precancer in Barrett’s esophagus reveals features associated with disease progression

12. Integrated mutational landscape analysis of uterine leiomyosarcomas

13. System-wide transcriptome damage and tissue identity loss in COVID-19 patients

14. Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

15. Author Correction: The evolutionary history of 2,658 cancers

18. Histone H1 loss drives lymphoma by disrupting 3D chromatin architecture

19. High-throughput Phenotyping of Lung Cancer Somatic Mutations

20. Comprehensive molecular profiling of lung adenocarcinoma

21. A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events.

22. Detecting significantly recurrent genomic connections from simple and complex rearrangements in the cancer genome

24. The importance of escalating molecular diagnostics in patients with low-grade pediatric brain cancer

26. Comprehensive genomic characterization of squamous cell lung cancers

27. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

28. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.

29. Supplementary Figures from Molecular Evolution of Classic Hodgkin Lymphoma Revealed Through Whole-Genome Sequencing of Hodgkin and Reed Sternberg Cells

30. Supplementary Data 2 from Molecular Evolution of Classic Hodgkin Lymphoma Revealed Through Whole-Genome Sequencing of Hodgkin and Reed Sternberg Cells

31. Data from Molecular Evolution of Classic Hodgkin Lymphoma Revealed Through Whole-Genome Sequencing of Hodgkin and Reed Sternberg Cells

32. Supplementary Tables from Molecular Evolution of Classic Hodgkin Lymphoma Revealed Through Whole-Genome Sequencing of Hodgkin and Reed Sternberg Cells

33. Supplementary Data 1 from Molecular Evolution of Classic Hodgkin Lymphoma Revealed Through Whole-Genome Sequencing of Hodgkin and Reed Sternberg Cells

35. Supplementary Figure from SETD2 Haploinsufficiency Enhances Germinal Center–Associated AICDA Somatic Hypermutation to Drive B-cell Lymphomagenesis

36. Data from SETD2 Haploinsufficiency Enhances Germinal Center–Associated AICDA Somatic Hypermutation to Drive B-cell Lymphomagenesis

37. Supplementary Table S3 from Discovery of Candidate DNA Methylation Cancer Driver Genes

38. Data from Discovery of Candidate DNA Methylation Cancer Driver Genes

39. Supplementary Data from Discovery of Candidate DNA Methylation Cancer Driver Genes

40. Molecular Evolution of Classic Hodgkin Lymphoma Revealed Through Whole-Genome Sequencing of Hodgkin and Reed Sternberg Cells

41. Whole-genome characterization of myoepithelial carcinomas of the soft tissue

42. A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns

43. Combined burden and functional impact tests for cancer driver discovery using DriverPower

44. Integrative pathway enrichment analysis of multivariate omics data

45. Pathway and network analysis of more than 2500 whole cancer genomes

46. Divergent mutational processes distinguish hypoxic and normoxic tumours

47. Genomic footprints of activated telomere maintenance mechanisms in cancer

48. Genetic modifiers of EGFR dependence in non-small cell lung cancer

50. Abstract 6196: Fanconi anemia pathway deficiency drives copy number variation in squamous cell carcinoma

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