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1. Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

2. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

3. Rare coding variants in ten genes confer substantial risk for schizophrenia.

4. Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

5. Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

6. Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

7. Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants

8. Genetic mechanisms of immune evasion in colorectal cancer

9. Integrated Molecular Characterization of Testicular Germ Cell Tumors

10. The Integrated Genomic Landscape of Thymic Epithelial Tumors

12. Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas

13. Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma

14. Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma

15. Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing

16. Integrative Genomic Analysis of Cholangiocarcinoma Identifies Distinct IDH-Mutant Molecular Profiles

17. Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

18. Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

19. Analysis of protein-coding genetic variation in 60,706 humans.

20. Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma

21. Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction

22. The Molecular Taxonomy of Primary Prostate Cancer

23. Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer

24. A global reference for human genetic variation

25. Paired exome analysis of Barrett's esophagus and adenocarcinoma

26. A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination

27. Genomic Classification of Cutaneous Melanoma

28. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction

29. Comprehensive genomic characterization of head and neck squamous cell carcinomas

30. Highly evolvable malaria vectors: The genomes of 16 Anopheles mosquitoes

31. Mosquito genomics. Highly evolvable malaria vectors: the genomes of 16 Anopheles mosquitoes.

32. Comprehensive molecular characterization of gastric adenocarcinoma

33. Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes

34. The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma

35. Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

36. Comprehensive molecular profiling of lung adenocarcinoma

37. Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

38. Author Correction: Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants

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

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

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

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

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

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

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

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

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

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

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

50. The Cancer Genome Atlas Pan-Cancer analysis project

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