40 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. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
12. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
13. Genome-wide tandem repeat expansions contribute to schizophrenia risk
14. Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies
15. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
16. Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes
17. 70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA
18. W61. IMPACT OF COMPOUND HETEROZYGOUS EVENTS INVOLVING DELETIONS AND SEQUENCE-LEVEL VARIANTS IN AUTISM
19. F57. INVESTIGATION OF THE SEX CHROMOSOMES IN AUTISM SPECTRUM DISORDER
20. W55. REGIONAL BURDEN ANALYSIS OF FUNCTIONAL VARIANTS REVEALS GENOMIC HOTSPOTS ENRICHED FOR REGULATORY ELEMENTS AND OVERLAPPING WITH RECURRENT PATHOGENIC CNVS
21. Polygenic risk for triglyceride levels in the presence of a high impact rare variant
22. Gene copy number variation and pediatric mental health/neurodevelopment in a general population
23. 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
24. Whole Genome Sequencing to Resolve the Genomic Architecture of Cerebral Palsy in a Canadian Cohort (P13-9.003)
25. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
26. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
27. 3. GENOMIC ARCHITECTURE OF AUTISM SPECTRUM DISORDER FROM COMPREHENSIVE WHOLE-GENOME SEQUENCE ANNOTATION
28. 34. A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS
29. Gene copy number variation in pediatric mental illness in a general population
30. T61. FUNCTIONAL VARIANTS AND HAPLOTYPES IN THE GABBR1 LOCUS SUGGEST POTENTIAL FOR AUTISM SUSCEPTIBILITY
31. 81. CHARACTERIZING THE GENETIC ARCHITECTURE OF AUTISM FROM A MULTI-ANCESTRY PERSPECTIVE
32. WHAT IS THE IMPACT OF COMPOUND HETEROZYGOUS EVENTS INVOLVING DELETIONS AND SEQUENCE-LEVEL VARIANTS IN AUTISM?
33. FUNCTIONAL-BASED ASSOCIATION STUDY OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IN EUROPEAN, AFRICAN, AND EAST ASIAN POPULATIONS
34. META-ANALYSIS OF RARE CNV GENOME-WIDE ASSOCIATION STUDIES ACROSS MAJOR PSYCHIATRIC DISORDERS IN EUR, AFR/AFAM, AND ASN/ASAM POPULATIONS
35. Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation
36. SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing
37. Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease relevant pathologies
38. 86. Low Frequency Genetic Variants Orchestrate Genetic Vulnerability for Autism Spectrum Disorders and Schizophrenia in Concert With Rare and Common Variants.
39. Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.
40. Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder.
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