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440 results on '"Gabriel, Stacey B."'

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

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

7. Outbreak of SARS-CoV-2 Infections, Including COVID-19 Vaccine Breakthrough Infections, Associated with Large Public Gatherings — Barnstable County, Massachusetts, July 2021

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

9. Genetic mechanisms of immune evasion in colorectal cancer

10. Integrated Molecular Characterization of Testicular Germ Cell Tumors

11. Transmission from vaccinated individuals in a large SARS-CoV-2 Delta variant outbreak

12. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

13. The Integrated Genomic Landscape of Thymic Epithelial Tumors

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

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

16. Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma

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

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

19. Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma

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

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

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

24. Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction

25. The Molecular Taxonomy of Primary Prostate Cancer

26. Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer

27. A global reference for human genetic variation

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

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

30. Genomic Classification of Cutaneous Melanoma

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

32. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

33. Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia

34. The Genetic Landscape of Diamond-Blackfan Anemia

35. Comprehensive Molecular Characterization of the Hippo Signaling Pathway in Cancer

36. A Pan-Cancer Analysis Reveals High-Frequency Genetic Alterations in Mediators of Signaling by the TGF-β Superfamily

37. Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

38. Integrated Molecular Characterization of Testicular Germ Cell Tumors

39. The Immune Landscape of Cancer

40. Comprehensive Characterization of Cancer Driver Genes and Mutations

41. Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics

42. Pathogenic Germline Variants in 10,389 Adult Cancers

43. Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation

44. A Pan-Cancer Analysis of Enhancer Expression in Nearly 9000 Patient Samples

45. An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics

46. Oncogenic Signaling Pathways in The Cancer Genome Atlas

47. Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer

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

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

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

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