704 results on '"Liu, Ruby"'
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2. Influencing human–AI interaction by priming beliefs about AI can increase perceived trustworthiness, empathy and effectiveness
3. Focused Exome Sequencing Gives a High Diagnostic Yield in the Indian Subcontinent
4. Evidence from 2100 index cases supports genome sequencing as a first-tier genetic test
5. High diagnosis rate for nonimmune hydrops fetalis with prenatal clinical exome from the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study
6. An Interactive Mixed Reality Platform for Bedside Surgical Procedures
7. Prenatal Phenotype of Alkuraya‐Kučinskas Syndrome: A Novel Case and Systematic Literature Review.
8. Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional Microarray
9. Beyond Single Diagnosis: Exploring Multidiagnostic Realities in Pediatric Patients through Genome Sequencing
10. Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy in Patients Clinically Suspected of FSHD Using Optical Genome Mapping
11. An Interactive Mixed Reality Platform for Bedside Surgical Procedures
12. At-Risk Genomic Findings for Pediatric-Onset Disorders From Genome Sequencing vs Medically Actionable Gene Panel in Proactive Screening of Newborns and Children
13. P729: Identification of multiple diagnoses in pediatric patients through genome sequencing
14. P714: Genome screening of newborns: Sequencing is easy, assessing the clinical utility of genomic findings uncovered in asymptomatic children is challenging
15. P696: Case presentation: Co-segregation of a rare GLA variant of uncertain significance within 2 multiplex families facilitates variant reclassification to pathogenic
16. P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders
17. P643: Unveiling noncoding DMD variants: Synergizing RNA sequencing and DNA sequencing for enhanced molecular diagnosis
18. P638: Genomic breakpoint analysis facilitates identification of complex rearrangements and re-classification of non-tandem duplications in the DMD gene
19. P599: Beyond single nucleotide variants and copy number variations: Spinal muscular atrophy and repeat expansion disorders screening by whole genome sequencing
20. Influencing human–AI interaction by priming beliefs about AI can increase perceived trustworthiness, empathy and effectiveness
21. Molecular Diagnosis of Duchenne Muscular Dystrophy Using Single NGS‐Based Assay
22. P426: Recognizing the promise and potential pitfalls of genomic medicine through routine rapid whole genome sequencing
23. P519: Evidence of complex inheritance patterns in limb-girdle and other muscular dystrophies: Synergistic heterozygosity and multigenic inheritance
24. P389: Real-world evidence demonstrating why genome sequencing should be recommended as the first-tier genetic test*
25. P476: Identification and accurate sizing of D4Z4 repeat units in patients suspected of facioscapulohumeral muscular dystrophy (FSHD) using optical genome mapping*
26. P639: Prenatal diagnosis of Alkuraya-Kučinskas syndrome by exome sequencing
27. P425: Unparalleled power of genome sequencing in screening ostensibly healthy newborns and children: Findings from the first real-world dataset
28. P502: How does multiomics help variant reclassification?
29. COVCOG 1: Factors Predicting Physical, Neurological and Cognitive Symptoms in Long COVID in a Community Sample. A First Publication From the COVID and Cognition Study
30. COVCOG 2: Cognitive and Memory Deficits in Long COVID: A Second Publication From the COVID and Cognition Study
31. eP371: A diverse set of case presentation highlight the power of genome sequencing – What next?
32. eP355: Repeat expansion disorders screening by genome sequencing: Strategy and stumbling blocks
33. COVCOG 2: Cognitive and Memory Deficits in Long COVID: A Second Publication from the COVID and Cognition Study
34. COVCOG 1: Factors predicting Cognitive Symptoms in Long COVID. A First Publication from the COVID and Cognition Study
35. Fascioscapulohumeral muscular dystrophy genetic testing by optic mapping
36. Newborn screening second tier molecular testing is critical for identifying true positives in lysosomal storage diseases and X-linked adrenoleukodystrophy
37. Genetic basis of oculopharyngeal muscular dystrophy: detection of alanine repeats in PABPN1 gene by next generation sequencing
38. Towards implementation whole genome sequencing as a first tier test in genomic testing
39. 63 Hydrops-Yielding Diagnostic Results Of Prenatal Exome Sequencing (HYDROPS) Trial - Prenatal WES for NIHF
40. Interactive Navigation System in Mixed-Reality for Neurosurgery
41. eP429 - Genetic basis of oculopharyngeal muscular dystrophy: detection of alanine repeats in PABPN1 gene by next generation sequencing
42. eP419 - Newborn screening second tier molecular testing is critical for identifying true positives in lysosomal storage diseases and X-linked adrenoleukodystrophy
43. eP368 - Towards implementation whole genome sequencing as a first tier test in genomic testing
44. eP370 - Fascioscapulohumeral muscular dystrophy genetic testing by optic mapping
45. Characterizing DNA Nanotube Networks Assembled via Y-Junction DNA Origami Seeds
46. Chinese production data provides tailwind to SHFE base metals prices.
47. China's domestic alumina price stays flat amid thin trading.
48. SHFE base metals prices mixed; zinc the best performer.
49. Shanghai bonded base metals stocks mostly fall in Nov; zinc inventories surge.
50. Nickel posts largest gain among SHFE base metals prices.
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