249 results on '"Engchuan, Worrawat"'
Search Results
2. Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
3. Chromosome X-wide common variant association study in autism spectrum disorder
4. Rare copy number variation in posttraumatic stress disorder
5. Genomic architecture of autism from comprehensive whole-genome sequence annotation.
6. Three generation families: Analysis of de novo variants in autism
7. Genome-wide enhancer-associated tandem repeats are expanded in cardiomyopathy
8. Correction: Polygenic risk for triglyceride levels in the presence of a high impact rare variant
9. Polygenic risk for triglyceride levels in the presence of a high impact rare variant
10. Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study
11. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
12. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
13. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
14. Genome-wide tandem repeat expansions contribute to schizophrenia risk
15. Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies
16. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
17. FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instability
18. Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes
19. Genome-wide detection of tandem DNA repeats that are expanded in autism
20. 70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA
21. W61. IMPACT OF COMPOUND HETEROZYGOUS EVENTS INVOLVING DELETIONS AND SEQUENCE-LEVEL VARIANTS IN AUTISM
22. F57. INVESTIGATION OF THE SEX CHROMOSOMES IN AUTISM SPECTRUM DISORDER
23. W55. REGIONAL BURDEN ANALYSIS OF FUNCTIONAL VARIANTS REVEALS GENOMIC HOTSPOTS ENRICHED FOR REGULATORY ELEMENTS AND OVERLAPPING WITH RECURRENT PATHOGENIC CNVS
24. Polygenic risk for triglyceride levels in the presence of a high impact rare variant
25. Copy number variation in fetal alcohol spectrum disorder
26. Gene copy number variation and pediatric mental health/neurodevelopment in a general population
27. 51. An Emerging Landscape of Genomic Regions Where an Excess of Low Frequency Sequence Variants and Pathogenic CNVs are Associated With ASD and Schizophrenia Risk
28. Cross-Platform Pathway Activity Transformation and Classification of Microarray Data
29. Comparative Study of Web-Based Gene Expression Analysis Tools for Biomarkers Identification
30. TNorm: An Unsupervised Batch Effects Correction Method for Gene Expression Data Classification
31. A large data resource of genomic copy number variation across neurodevelopmental disorders
32. Whole Genome Sequencing to Resolve the Genomic Architecture of Cerebral Palsy in a Canadian Cohort (P13-9.003)
33. Pathway activity transformation for multi-class classification of lung cancer datasets
34. Pathway-Based Multi-class Classification of Lung Cancer
35. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
36. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
37. 3. GENOMIC ARCHITECTURE OF AUTISM SPECTRUM DISORDER FROM COMPREHENSIVE WHOLE-GENOME SEQUENCE ANNOTATION
38. 34. A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS
39. Gene copy number variation in pediatric mental illness in a general population
40. T61. FUNCTIONAL VARIANTS AND HAPLOTYPES IN THE GABBR1 LOCUS SUGGEST POTENTIAL FOR AUTISM SUSCEPTIBILITY
41. 81. CHARACTERIZING THE GENETIC ARCHITECTURE OF AUTISM FROM A MULTI-ANCESTRY PERSPECTIVE
42. WHAT IS THE IMPACT OF COMPOUND HETEROZYGOUS EVENTS INVOLVING DELETIONS AND SEQUENCE-LEVEL VARIANTS IN AUTISM?
43. FUNCTIONAL-BASED ASSOCIATION STUDY OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IN EUROPEAN, AFRICAN, AND EAST ASIAN POPULATIONS
44. META-ANALYSIS OF RARE CNV GENOME-WIDE ASSOCIATION STUDIES ACROSS MAJOR PSYCHIATRIC DISORDERS IN EUR, AFR/AFAM, AND ASN/ASAM POPULATIONS
45. Apriori Gene Set-based Microarray Analysis for Disease Classification Using Unlabeled Data
46. Classification of Real and Pseudo pre-miRNAs in Plant Species
47. Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation
48. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
49. Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease relevant pathologies
50. Genome-wide tandem repeat expansions contribute to schizophrenia risk
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