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6. Who Goes First? Influences of Human-AI Workflow on Decision Making in Clinical Imaging

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

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

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

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

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

13. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder

14. A New Perspective on Adoption: Delivering Water Conservation Extension Programming to Nursery and Greenhouse Growers

15. RapidRead: Global Deployment of State-of-the-art Radiology AI for a Large Veterinary Teleradiology Practice

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

18. 'It's Working Together with What You've Got': Healthcare Professionals' Experiences of Working with People with Combined Intellectual Disability and Personality Disorder Diagnoses

20. De novo variants in DENND5B cause a neurodevelopmental disorder

22. Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples

23. Single photon frequency conversion for frequency multiplexed quantum networks in the telecom band

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

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

29. Pharmacological inhibition of MDA-9/Syntenin blocks breast cancer metastasis through suppression of IL-1β

30. Relevance of Molecular Groups in Children with Newly Diagnosed Atypical Teratoid Rhabdoid Tumor: Results from Prospective St. Jude Multi-institutional Trials.

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

32. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

33. Cellular Bioenergetics and AMPK and TORC1 Signalling in Blood Lymphoblasts Are Biomarkers of Clinical Status in FMR1 Premutation Carriers

34. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

35. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

37. An integrated optical device for frequency conversion across the full telecom C-band spectrum

38. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

39. Lumefantrine, an antimalarial drug, reverses radiation and temozolomide resistance in glioblastoma

40. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

42. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

46. Preface

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50. Enhancing Extension Programs by Discussing Water Conservation Technology Adoption with Growers

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