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1. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

2. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

3. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.

4. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

6. Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

7. Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest

8. Gene content evolution in the arthropods

9. Correction to: Genome-enabled insights into the biology of thrips as crop pests

10. Genome-enabled insights into the biology of thrips as crop pests

11. Sawfly genomes reveal evolutionary acquisitions that fostered the mega-radiation of parasitoid and eusocial Hymenoptera

12. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

13. Molecular evolutionary trends and feeding ecology diversification in the Hemiptera, anchored by the milkweed bug genome

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

16. Comparative genomics of the miniature wasp and pest control agent Trichogramma pretiosum.

17. Closing the gap: Solving complex medically relevant genes at scale

18. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

20. The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma

21. Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

22. INTRA- AND INTER-HOST EVOLUTION OF HUMAN NOROVIRUS IN HEALTHY ADULTS

23. Examining intra-host genetic variation of RSV by short read high-throughput sequencing

24. Functional Genomics of Gastrointestinal Escherichia coli Isolated from Patients with Cancer and Diarrhea

25. Modeling nonsegmented negative-strand RNA virus (NNSV) transcription with ejective polymerase collisions and biased diffusion

26. The genome of the water strider Gerris buenoi reveals expansions of gene repertoires associated with adaptations to life on the water

27. Long read sequencing and expression studies ofAHDC1deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism

28. Comparative genomics of the miniature wasp and pest control agent Trichogramma pretiosum

29. Identification of USP9Xas a leukemia susceptibility gene

30. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

31. Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

32. Fully resolved assembly of Cryptosporidium parvum

33. Germline Mutations in Shelterin Complex Genes Are Associated With Familial Glioma

34. Drivers of transcriptional variance in human intestinal epithelial organoids

35. Long read sequencing and expression studies of AHDC1 deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism.

36. A global reference for human genetic variation

37. Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals

38. Fully resolved assembly of Cryptosporidium parvum

39. Transmission event of SARS-CoV-2 Delta variant reveals multiple vaccine breakthrough infections

40. Additional file 2 of Transmission event of SARS-CoV-2 delta variant reveals multiple vaccine breakthrough infections

41. Multiethnic catalog of structural variants and their translational impact for disease phenotypes across 19,652 genomes

42. Oligonucleotide Capture Sequencing of the SARS-CoV-2 Genome and Subgenomic Fragments from COVID-19 Individuals

43. Comprehensive molecular characterization of clear cell renal cell carcinoma

46. Wolff–Parkinson–Whitesyndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation

47. The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

48. Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2

49. Reproductive Longevity Predicts Mutation Rates in Primates

50. Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

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