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1. The Prevalence of Post-Acute Sequelae of COVID-19 in Solid Organ Transplant Recipients: Evaluation of Risk in the National COVID Cohort Collaborative (N3C)

2. Predicting nutrition and environmental factors associated with female reproductive disorders using a knowledge graph and random forests

3. The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human disease

4. Outcomes of SARS-CoV-2 Infection Among Patients with Orthopaedic Fracture Surgery in the National COVID Cohort Collaborative (N3C)

5. Nonelective coronary artery bypass graft outcomes are adversely impacted by Coronavirus disease 2019 infection, but not altered processes of care: A National COVID Cohort Collaborative and National Surgery Quality Improvement Program analysis

6. Hormone Replacement Therapy and COVID-19 Outcomes in Solid Organ Transplant Recipients Compared with the General Population

7. Generalisable long COVID subtypes: findings from the NIH N3C and RECOVER programmes

8. Metformin is associated with reduced COVID-19 severity in patients with prediabetes

10. The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice

11. Identifying who has long COVID in the USA: a machine learning approach using N3C data

13. Long-term use of immunosuppressive medicines and in-hospital COVID-19 outcomes: a retrospective cohort study using data from the National COVID Cohort Collaborative

14. Characterizing Long COVID: Deep Phenotype of a Complex Condition

15. The Data Use Ontology to streamline responsible access to human biomedical datasets

16. Associations between HIV infection and clinical spectrum of COVID-19: a population level analysis based on US National COVID Cohort Collaborative (N3C) data

17. GA4GH: International policies and standards for data sharing across genomic research and healthcare

20. One is the loneliest number: genotypic matchmaking using the electronic health record

22. Response to Biesecker et al.

23. KG-COVID-19: A Framework to Produce Customized Knowledge Graphs for COVID-19 Response

24. Interpretable Clinical Genomics with a Likelihood Ratio Paradigm

25. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

26. FAIRshake: Toolkit to Evaluate the FAIRness of Research Digital Resources

27. Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy

29. De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Callosum, Axon, Cardiac, Ocular, and Genital Defects

30. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

31. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

32. Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification

33. The Pediatric Cell Atlas: Defining the Growth Phase of Human Development at Single-Cell Resolution

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

35. Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay

36. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative

37. IRF2BPL Is Associated with Neurological Phenotypes

38. IRF2BPL Is Associated with Neurological Phenotypes

39. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

40. Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder

41. MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome

42. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research

43. A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay

44. The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

45. A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3

46. A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease

47. Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency

48. Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease

49. Tools for exploring mouse models of human disease

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