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190 results on '"Sankaran VG"'

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1. A first update on mapping the human genetic architecture of COVID-19

2. Mapping the human genetic architecture of COVID-19

3. The Polygenic and Monogenic Basis of Blood Traits and Diseases

4. Rb and hematopoiesis: stem cells to anemia

5. Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas.

7. Transcription factor networks disproportionately enrich for heritability of blood cell phenotypes.

8. A guideline on the molecular ecosystem regulating ferroptosis.

9. Robustness and reliability of single-cell regulatory multi-omics with deep mitochondrial mutation profiling.

10. Genetic drivers and cellular selection of female mosaic X chromosome loss.

11. Genome Sequencing for Diagnosing Rare Diseases.

12. Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease.

13. Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood.

14. A noncoding regulatory variant in IKZF1 increases acute lymphoblastic leukemia risk in Hispanic/Latino children.

15. A torpor-like state (TLS) in mice slows blood epigenetic aging and prolongs healthspan.

16. Deciphering cell states and genealogies of human haematopoiesis.

17. Inherited blood cancer predisposition through altered transcription elongation.

18. What approaches are needed to understand human development and disease?

19. Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19.

20. RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation.

21. Systematic investigation of mitochondrial transfer between cancer cells and T cells at single-cell resolution.

22. Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease.

23. Getting an aMPLe grasp on hematopoiesis.

24. Shared and distinct genetic etiologies for different types of clonal hematopoiesis.

26. A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.

27. Unique Capabilities of Genome Sequencing for Rare Disease Diagnosis.

28. MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development.

29. Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells.

30. Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM-associated syndromes.

31. Massively parallel base editing to map variant effects in human hematopoiesis.

32. Perspectives of Rare Disease Experts on Newborn Genome Sequencing.

33. Mitochondrial single-cell ATAC-seq for high-throughput multi-omic detection of mitochondrial genotypes and chromatin accessibility.

34. Exploiting somatic mutations to decipher human blood production: a natural lineage-tracing strategy.

35. CD11c regulates neutrophil maturation.

36. Fetal Hemoglobin Regulation in Beta-Thalassemia.

38. Genetic regulation of fetal hemoglobin across global populations.

39. Hacking hematopoiesis - emerging tools for examining variant effects.

40. Development of a Thalassemia International Prognostic Scoring System (TIPSS).

41. Human hematopoietic stem cell vulnerability to ferroptosis.

42. Structural variation across 138,134 samples in the TOPMed consortium.

43. Population analyses of mosaic X chromosome loss identify genetic drivers and widespread signatures of cellular selection.

44. A genetic disorder reveals a hematopoietic stem cell regulatory network co-opted in leukemia.

45. Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.

46. Vade-MECOM: How to peel back the layers of hematopoiesis.

47. Variant to function mapping at single-cell resolution through network propagation.

48. Influences of rare copy-number variation on human complex traits.

49. Cellular barcoding to decipher clonal dynamics in disease.

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