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1. Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

2. A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

3. Stratified analyses refine association between TLR7 rare variants and severe COVID-19

5. Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database

6. Mendelian Randomization with Incomplete Exposure Data: a Bayesian Approach

9. Long-term outcomes of early-onset myocardial infarction with non-obstructive coronary artery disease (MINOCA)

10. Comparing GBA1‐Parkinson's disease and idiopathic Parkinson's disease: α‐Synuclein oligomers and synaptic density as biomarkers in the skin biopsy.

11. Population Heterogeneity and Selection of Coronary Artery Disease Polygenic Scores.

13. Reply to: Hultström et al., Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19. Mannose-binding lectin genetics in COVID-19

14. Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules

15. Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty

16. Genetics of Autoimmune Liver Diseases

19. Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

20. Stratified analyses refine association between TLR7 rare variants and severe COVID-19

21. A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

22. Improving predictive accuracy in primary biliary cholangitis: A new genetic risk score.

26. Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease

27. Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

28. A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

29. 115 The mannose-binding lectin (MBL) in MIS-C: relationship between MBL genotype, levels, and functional activity against SARS-CoV-2

31. P32 Statistical colocalization identifies twenty-four novel risk loci associated with disease risk of primary biliary cholangitis

32. Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA‐repair genes

35. Prevalence of variant of unknown significance (VUS) in men with prostate cancer who serve as a benchmark for enhanced screening and for personalized therapy.

36. Assessing the mid-term impact of enhanced prostate cancer screening in Caucasian men with germline DNA repair pathogenic variants.

37. Regulation of inflammation and protection against invasive pneumococcal infection by the long pentraxin PTX3

38. Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer

39. Corrigendum to: “An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs” [J Hepatol 75 (2021) 572-581]

41. A second update on mapping the human genetic architecture of COVID-19

42. Mechanisms by which the cystic fibrosis transmembrane conductance regulator may influence SARS-CoV-2 infection and COVID-19 disease severity

44. Systematic rare variant analyses identify RAB32as a susceptibility gene for familial Parkinson’s disease

45. Awareness of genetic risk for prostate cancer (PCa) in men from families with germline mutations in DNA-repair genes.

46. In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear

48. The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile

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