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1. Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption

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

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

4. Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.

5. Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

6. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

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

8. A second generation human haplotype map of over 3.1 million SNPs

9. The Molecular Taxonomy of Primary Prostate Cancer

10. Integrated genomic characterization of oesophageal carcinoma

11. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

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

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

14. Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences

15. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

16. Integrated genomic characterization of endometrial carcinoma

17. An integrated map of genetic variation from 1,092 human genomes

18. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

19. A single human ciliopathy locus highlights the evolutionary dynamics of non-duplicated but adjacent genes

20. Genome-wide detection and characterization of positive selection in human populations

21. Defining the role of common variation in the genomic and biological architecture of adult human height.

22. Comprehensive molecular characterization of gastric adenocarcinoma

23. Genome-Wide association study of coronary heart disease and its risk factors in 8,090 african americans: The nhlbi CARe project

24. Biological, clinical and population relevance of 95 loci for blood lipids

25. High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

26. The International HapMap Project

28. Defining the role of common variation in the genomic and biological architecture of adult human height

29. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

30. Genetic studies of body mass index yield new insights for obesity biology

31. RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies

32. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

33. Somatic mutations affect key pathways in lung adenocarcinoma

34. Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

35. Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan.

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

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

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

39. Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.

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

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

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

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

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

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

46. Pooling for SARS-CoV2 Surveillance: Validation and Strategy for Implementation in K-12 Schools.

47. Cross-Sectional Assessment of SARS-CoV-2 Viral Load by Symptom Status in Massachusetts Congregate Living Facilities.

48. Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, Massachusetts.

49. Cross-Site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms for the CIMAC-CIDC Network.

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

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