177 results on '"Zhao, Guihu"'
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2. Risk factors associated with age at onset of Parkinson’s disease in the UK Biobank
3. Severity of Autism Spectrum Disorder Symptoms Associated with de novo Variants and Pregnancy-Induced Hypertension
4. A comprehensive analysis of the health effects associated with smoking in the largest population using UK Biobank genotypic and phenotypic data
5. Establishment of machine learning-based tool for early detection of pulmonary embolism
6. Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders
7. Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders
8. Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-coding Variants
9. A comprehensive perspective of Huntington’s disease and mitochondrial dysfunction
10. Revealing a novel contributing landscape of ferroptosis-related genes in Parkinson’s disease
11. GPCards: An integrated database of genotype–phenotype correlations in human genetic diseases
12. De novo mutations in folate-related genes associated with common developmental disorders
13. Casual associations between brain structure and sarcopenia: A large‐scale genetic correlation and mendelian randomization study.
14. Genetic correlation and causality between smoking and 42 neuropsychiatric and gastrointestinal diseases
15. Glycated haemoglobin: a biomarker of the life expectancy of Parkinson’s disease patients with type 2 diabetes
16. De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders
17. Verbal--Spatial IQ Discrepancies Impact Brain Activation Associated with the Resolution of Cognitive Conflict in Children and Adolescents
18. Establishment of machine learning-based tool for early detection of pulmonary embolism
19. VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome
20. Association between ovarian reserve and spontaneous miscarriage and their shared genetic architecture
21. Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder
22. ATP10B variants in Parkinson’s disease: a large cohort study in Chinese mainland population
23. Polarimetric synthetic aperture radar image segmentation by convolutional neural network using graphical processing units
24. Smart pathological brain detection by synthetic minority oversampling technique, extreme learning machine, and Jaya algorithm
25. Cat Swarm Optimization applied to alcohol use disorder identification
26. Exploring a smart pathological brain detection method on pseudo Zernike moment
27. Combined Associations of Genetic and Environmental Risk Factors in Age of Parkinson’s Disease Onset
28. Reward-Based Spatial Learning in Teens With Bulimia Nervosa
29. VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome.
30. Interactions of genetic risks for autism and the broad autism phenotypes
31. Bidirectional Association between Ovarian Reserve and Spontaneous Miscarriage and Their Shared Genetic Architecture
32. Severity of Autism Spectrum Disorder Symptoms Associated with de novo Variants and Pregnancy-Induced Hypertension
33. Performance evaluation of differential splicing analysis methods and splicing analytics platform construction
34. Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing
35. Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-Coding Variants
36. The Contribution of Non-Canonical Splice Sites Variants in Parkinson's Disease-Associated Genes to RNA Splicing
37. Genetic landscape of human mitochondrial genome using whole-genome sequencing
38. The Association Between Lysosomal Storage Disorder Genes and Parkinson’s Disease: A Large Cohort Study in Chinese Mainland Population
39. Gene4HL: An Integrated Genetic Database for Hearing Loss
40. Performance Comparison of Computational Prediction Methods for the Function and Pathogenicity of Non-coding Variants
41. Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders
42. Gene4PD: A Comprehensive Genetic Database of Parkinson’s Disease
43. Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease
44. Characterizing the Expression Patterns of Parkinson’s Disease Associated Genes
45. Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes
46. Genetic landscape of human mitochondrial genome using whole-genome sequencing.
47. PSAP variants in Parkinson’s disease: a large cohort study in Chinese mainland population
48. AsCRISPR: A Web Server for Allele-Specific Single Guide RNA Design in Precision Medicine
49. Gene4PD: a comprehensive genetic database of Parkinson's disease
50. The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population
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