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1. Cancer phylogenetic tree inference at scale from 1000s of single cell genomes

2. Transformer-based segmentation of adnexal lesions and ovarian implants in CT images

4. Luminal breast epithelial cells of BRCA1 or BRCA2 mutation carriers and noncarriers harbor common breast cancer copy number alterations

5. Automated real-world data integration improves cancer outcome prediction

6. DNA liquid biopsy-based prediction of cancer-associated venous thromboembolism

8. Author Correction: Proteogenomic analysis of enriched HGSOC tumor epithelium identifies prognostic signatures and therapeutic vulnerabilities

10. Proteogenomic analysis of enriched HGSOC tumor epithelium identifies prognostic signatures and therapeutic vulnerabilities

12. Single-cell mtDNA dynamics in tumors is driven by coregulation of nuclear and mitochondrial genomes

13. Epigenetic dysregulation from chromosomal transit in micronuclei.

17. Non-coding somatic mutations converge on the PAX8 pathway in ovarian cancer.

18. Ovarian cancer mutational processes drive site-specific immune evasion

19. Single-cell genomic variation induced by mutational processes in cancer

20. Overall survival with circulating tumor DNA-guided therapy in advanced non-small-cell lung cancer

21. Multimodal integration of radiology, pathology and genomics for prediction of response to PD-(L)1 blockade in patients with non-small cell lung cancer

22. Fundamental immune–oncogenicity trade-offs define driver mutation fitness

23. Multimodal data integration using machine learning improves risk stratification of high-grade serous ovarian cancer

25. Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer

26. Accurate determination of CRISPR-mediated gene fitness in transplantable tumours

27. Single-cell profiling reveals a memory B cell-like subtype of follicular lymphoma with increased transformation risk

28. The driver landscape of sporadic chordoma.

29. Kronos: a workflow assembler for genome analytics and informatics

30. Enhancing Knowledge Discovery from Cancer Genomics Data with Galaxy

31. Joint Inference of Genome Structure and Content in Heterogeneous Tumour Samples

33. Multimodal histopathologic models stratify hormone receptor-positive early breast cancer

34. FIGURE 4 from Weakly Supervised Deep Learning Predicts Immunotherapy Response in Solid Tumors Based on PD-L1 Expression

35. Divergent clonal selection dominates medulloblastoma at recurrence

36. TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma

37. Multifocal endometriotic lesions associated with cancer are clonal and carry a high mutation burden

38. Regulation of pH by Carbonic Anhydrase 9 Mediates Survival of Pancreatic Cancer Cells With Activated KRAS in Response to Hypoxia

40. Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4

41. Weakly supervised deep learning predicts immunotherapy response in solid tumors based on PD-L1 expression

42. Tumor-associated antigen PRAME exhibits dualistic functions that are targetable in diffuse large B cell lymphoma

43. TERT promoter mutation in adult granulosa cell tumor of the ovary

44. Author Correction: Fundamental immune–oncogenicity trade-offs define driver mutation fitness

45. Probabilistic cell-type assignment of single-cell RNA-seq for tumor microenvironment profiling

46. The clonal and mutational evolution spectrum of primary triple-negative breast cancers

48. Genetic profiling of MYC and BCL2 in diffuse large B-cell lymphoma determines cell-of-origin–specific clinical impact

49. Eleven grand challenges in single-cell data science

50. Chemogenomic profiling of breast cancer patient-derived xenografts reveals targetable vulnerabilities for difficult-to-treat tumors

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