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1. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

2. Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network

4. Infobuttons for Genomic Medicine: Requirements and Barriers

5. Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing

6. Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

7. Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

8. Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores

10. Neptune: an environment for the delivery of genomic medicine

13. Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

14. A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

15. Participant choices for return of genomic results in the eMERGE Network

18. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

19. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

22. Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort

23. Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

24. Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention Pairs

26. The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth

27. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network

28. Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.

29. Trans-ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium study

30. Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium Study

34. Trans‐ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.

35. A Genome-Wide Association Study of Autism Incorporating Autism Diagnostic Interview-Revised, Autism Diagnostic Observation Schedule, and Social Responsiveness Scale

36. Trans-ethnic Genomic Informed Risk Assessment for Alzheimer’s disease: An International Hundred K+ Cohorts Consortium Study

38. Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research

39. Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results

40. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

42. Trans-ethnic polygenic risk scores for body mass index.

43. Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

45. Additional file 1 of Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach

47. Do Students Want Individualized Instruction?

48. New Careers: A Challenge to Adult Education.

49. An Analysis of Student Attitudes toward Divergent Modes of Instruction: Implications for Individualized Instruction.

50. Viewing Faculty Orientation as a Socialization Process.

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