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Your search keyword '"Imielinski, Marcin"' showing total 185 results

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185 results on '"Imielinski, Marcin"'

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

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

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

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

5. Integrated mutational landscape analysis of uterine leiomyosarcomas

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

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

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

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

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

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

14. The evolutionary history of 2,658 cancers

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

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

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

20. Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2

21. Strong synaptic transmission impact by copy number variations in schizophrenia

22. Oncogenic and sorafenib-sensitive ARAF mutations in lung adenocarcinoma

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

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

25. Comprehensive molecular profiling of lung adenocarcinoma

26. Variants of DENND1B associated with asthma in children

27. Common genetic variants on 5p14.1 associate with autism spectrum disorders

28. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

29. High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations

30. Genomic footprints of activated telomere maintenance mechanisms in cancer

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

32. Mutational heterogeneity in cancer and the search for new cancer-associated genes

33. Comprehensive genomic characterization of squamous cell lung cancers

34. Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

36. Variants of DENND1B Associated with Asthma in Children

37. 17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

38. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

39. Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes

40. ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry

43. Portraits of genetic intra-tumour heterogeneity and subclonal selection across cancer types

45. High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications

46. Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

47. Common genetic variants on 5p14.1 associate with autism spectrum disorders

48. The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations.

49. 0ncogenic and sorafenib-sensitive ARAF mutations in lung adenocarcinoma.

50. A Pan-Cancer Analysis of Transcriptome Changes Associated with Somatic Mutations in U2AF1 Reveals Commonly Altered Splicing Events.

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