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1. Causal machine learning for predicting treatment outcomes

2. Systematic Characterization of the Effectiveness of Alignment in Large Language Models for Categorical Decisions

3. Implications of mappings between ICD clinical diagnosis codes and Human Phenotype Ontology terms

6. Geoinference of author affiliations using NLP-based text classification

7. Event Stream GPT: A Data Pre-processing and Modeling Library for Generative, Pre-trained Transformers over Continuous-time Sequences of Complex Events

8. Construction of extra-large scale screening tools for risks of severe mental illnesses using real world healthcare data

9. Identifying Heterogeneous Treatment Effects in Multiple Outcomes using Joint Confidence Intervals

10. To do no harm — and the most good — with AI in health care

11. Polygenic risk scores for autoimmune related diseases are significantly different in cancer exceptional responders

12. Acute respiratory distress syndrome after SARS-CoV-2 infection on young adult population: International observational federated study based on electronic health records through the 4CE consortium

13. WINDOW OPENING STATUTES: Child Victims Act Claims and the Quest for Lost Policies

14. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

15. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

16. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

17. Disease progression strikingly differs in research and real-world Parkinson’s populations

19. The literacy barrier in clinical trial consents: a retrospective analysis

20. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

21. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

24. Aromatized liposomes for sustained drug delivery

25. Simulation of undiagnosed patients with novel genetic conditions

26. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

30. International comparisons of laboratory values from the 4CE collaborative to predict COVID-19 mortality

34. De novo variants in DENND5B cause a neurodevelopmental disorder

35. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

36. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

37. Potential pitfalls in the use of real-world data for studying long COVID

38. Copper chelation suppresses epithelial-mesenchymal transition by inhibition of canonical and non-canonical TGF-β signaling pathways in cancer

41. Copper chelation suppresses epithelial-mesenchymal transition by inhibition of canonical and non-canonical TGF-β signaling pathways in cancer

43. Validation of an internationally derived patient severity phenotype to support COVID-19 analytics from electronic health record data

44. BioN∅T: A searchable database of biomedical negated sentences

45. Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases.

46. An aptamer-based depot system for sustained release of small molecule therapeutics

47. Calculating the return on investment of mobile healthcare

48. Genomics Research with Undiagnosed Children: Ethical Challenges at the Boundaries of Research and Clinical Care

49. Clinical phenotypes and outcomes in children with multisystem inflammatory syndrome across SARS-CoV-2 variant eras: a multinational study from the 4CE consortium

50. Characterization of long COVID temporal sub-phenotypes by distributed representation learning from electronic health record data: a cohort study

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