Search

Your search keyword '"Levy Shawn"' showing total 1,046 results

Search Constraints

Start Over You searched for: Author "Levy Shawn" Remove constraint Author: "Levy Shawn"
1,046 results on '"Levy Shawn"'

Search Results

1. The Space Omics and Medical Atlas (SOMA) and international astronaut biobank

2. Longitudinal multi-omics analysis of host microbiome architecture and immune responses during short-term spaceflight

3. Metagenomic Methods for Addressing NASA's Planetary Protection Policy Requirements on Future Missions: A Workshop Report.

4. Sequencing by avidity enables high accuracy with low reagent consumption

5. The genetic landscape of immune-competent and HIV lymphoma

7. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.

8. Novel human genetic variants associated with extrapulmonary tuberculosis: a pilot genome wide association study

9. Polymorphisms in IL-1β, vitamin D receptor Fok1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis

10. Complementary RNA amplification methods enhance microarray identification of transcripts expressed in the C. elegans nervous system

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

12. TGF-β1 induction of the adenine nucleotide translocator 1 in astrocytes occurs through Smads and Sp1 transcription factors

14. Correction to: Comprehensive benchmarking and ensemble approaches for metagenomic classifiers

15. The Extracellular RNA Communication Consortium: Establishing Foundational Knowledge and Technologies for Extracellular RNA Research

16. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

17. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

18. A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease

19. Comprehensive benchmarking and ensemble approaches for metagenomic classifiers

20. Enteropathy-associated T cell lymphoma subtypes are characterized by loss of function of SETD2

21. Genomic Methods and Microbiological Technologies for Profiling Novel and Extreme Environments for the Extreme Microbiome Project (XMP).

22. Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study

23. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

25. The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls

26. ArCH: improving the performance of clonal hematopoiesis variant calling and interpretation

28. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

29. The COVID-19 XPRIZE and the need for scalable, fast, and widespread testing

31. Sept8/SEPTIN8 involvement in cellular structure and kidney damage is identified by genetic mapping and a novel human tubule hypoxic model

32. Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

33. The whole-genome landscape of Burkitt lymphoma subtypes

34. Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification

35. The Extracellular RNA Communication Consortium: Establishing Foundational Knowledge and Technologies for Extracellular RNA Research

36. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

37. Ectonucleoside Triphosphate Diphosphohydrolase-3 Antibody Targets Adult Human Pancreatic β Cells for In Vitro and In Vivo Analysis

38. Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individuals

40. The Airplane Cabin Microbiome

41. Diversity and genomic insights into the uncultured Chloroflexi from the human microbiota

42. Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome

43. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative

46. IRF2BPL Is Associated with Neurological Phenotypes

48. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

49. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

50. α Cell Function and Gene Expression Are Compromised in Type 1 Diabetes

Catalog

Books, media, physical & digital resources