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135 results on '"Barron-Casella, Emily"'

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

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

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

4. De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

5. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

6. Hydroxyurea to prevent brain injury in children with sickle cell disease (HU Prevent)—A randomized, placebo‐controlled phase II feasibility/pilot study.

7. Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma

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

9. An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

12. Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function

13. Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

19. Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia

27. Whole Genome Sequencing Identifies CRISPLD2as a Lung Function Gene in Children With Asthma

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

30. An APOOPseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels

32. Magnetic Resonance Angiography-Defined Intracranial Vasculopathy Is Associated with Silent Cerebral Infarcts, and Glucose-6-Phosphate Dehydrogenase Mutation in Children with Sickle Cell Anemia (S29.001)

33. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans

34. A Genome-Wide Association Study of Total Bilirubin and Cholelithiasis Risk in Sickle Cell Anemia

37. Identification of Thrombospondin-1 and L-Selectin as Potential Plasma Biomarkers of Silent Cerebral Infarct In Children with Sickle Cell Disease Using a Proteomic-Based Approach

39. Glial Fibrillary Acidic Protein as a Plasma Biomarker of Brain Injury in Children with Sickle Cell Disease.

46. Meta-analysis of 2040 sickle cell anemia patients: BCL11Aand HBS1L-MYBare the major modifiers of HbF in African Americans

48. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.

49. Proteomic discovery in sickle cell disease: Elevated neurogranin levels in children with sickle cell disease.

50. Proteomic and biomarker studies and neurological complications of pediatric sickle cell disease.

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