52 results on '"Sebat, Jonathan"'
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2. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
3. The Relationship of Attention-Deficit/Hyperactivity Disorder With Posttraumatic Stress Disorder: A Two-Sample Mendelian Randomization and Population-Based Sibling Comparison Study
4. Genomic architecture of autism from comprehensive whole-genome sequence annotation
5. Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
6. SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrains
7. Developmental and temporal characteristics of clonal sperm mosaicism
8. Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene
9. Getting to the Cores of Autism
10. Modeling the Interplay Between Neurons and Astrocytes in Autism Using Human Induced Pluripotent Stem Cells
11. Frequency and Complexity of De Novo Structural Mutation in Autism
12. Spatiotemporal 16p11.2 Protein Network Implicates Cortical Late Mid-Fetal Brain Development and KCTD13-Cul3-RhoA Pathway in Psychiatric Diseases
13. Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia
14. Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia
15. COLLABORATIVE STUDY OF THE COMBINED EFFECTS OF RARE CNVS AND POLYGENIC RISK ON PSYCHIATRIC TRAITS
16. FUNCTIONAL-BASED ASSOCIATION STUDY OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IN EUROPEAN, AFRICAN, AND EAST ASIAN POPULATIONS
17. META-ANALYSIS OF RARE CNV GENOME-WIDE ASSOCIATION STUDIES ACROSS MAJOR PSYCHIATRIC DISORDERS IN EUR, AFR/AFAM, AND ASN/ASAM POPULATIONS
18. Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation
19. Differential Relationship of DNA Replication Timing to Different Forms of Human Mutation and Variation
20. CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
21. High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
22. Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders
23. Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
24. W56. UNRAVELING THE IMPACT OF GENOMIC VARIATIONS ON COGNITIVE ABILITY ACROSS THE HUMAN CORTEX: INSIGHTS FROM GENE EXPRESSION AND COPY NUMBER VARIANTS
25. 69. GENOME-WIDE ASSOCIATION OF COPY NUMBER VARIANTS ACROSS SIX MAJOR PSYCHIATRIC DISORDERS REVEALS GENOTYPE-PHENOTYPE RELATIONSHIPS OF RARE VARIANTS
26. 70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA
27. Chapter 23 - Current progress and future direction in the genetics of PTSD: Focus on the development and contributions of the PGC-PTSD working group
28. Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development
29. Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements
30. CHARACTERIZATION OF THE COMBINED EFFECTS OF RARE VARIANTS AND POLYGENIC RISK BY WHOLE GENOME ANALYSIS OF PSYCHIATRIC DISORDERS AND QUANTITATIVE TRAITS
31. INTERACTIONS OF RARE CNVS WITH POLYGENIC RISK SCORES IN PSYCHIATRIC DISORDERS AND QUANTITATIVE TRAITS
32. 34. A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS
33. STATISTICAL AND FUNCTIONAL CONVERGENCE OF COMMON AND RARE VARIANT RISK FOR AUTISM SPECTRUM DISORDERS AT CHROMOSOME 16P
34. Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis
35. 48. A PHENOTYPIC SPECTRUM OF AUTISM IS ATTRIBUTABLE TO THE COMBINED EFFECTS OF RARE VARIANTS, POLYGENIC RISK AND SEX
36. 6. CONTRIBUTION OF COPY NUMBER VARIANTS TO SCHIZOPHRENIA IN EAST ASIAN POPULATIONS
37. 11. ANALYSIS OF GENOMIC COPY NUMBER VARIATION AND THEIR INTERACTION WITH POLYGENIC RISK SCORES ACROSS PSYCHIATRIC DISORDERS
38. ANALYSIS OF COPY NUMBER VARIATION ACROSS THE MAJOR PSYCHIATRIC DISORDERS: BIPOLAR DISORDER, SCHIZOPHRENIA, AND AUTISM SPECTRUM DISORDER
39. ADVANCES IN AUTISM GENETICS: FROM GENE DISCOVERY TO ASPECTS OF HETEROGENEITY
40. Analysis of Genomic Copy Number Variation Across Psychiatric Disorders
41. Chapter 4 - Genome Tools and Methods: Rare Genetic Variation
42. Partial Pharmacological “Rescue” and MRS spectroscopy in Two Carriers of a Rare Marker Chromosome Containing Extra Copies of the GLDC Gene Encoding a Glycine-Degrading Enzyme Implicate NMDA Receptor Hypofunction in Psychosis
43. Contributors
44. 84 16P11.2 PATIENT-DERIVED CEREBRAL ORGANOIDS SHOW MIGRATION AND SYNAPTIC DEFECTS
45. RARE COPY NUMBER VARIATION AND COMMON POLYGENIC RISK IN BIPOLAR DISORDER SUBTYPES
46. 20EVALUATING GENETIC CAUSATION AND PERSONALIZED PHARMACOLOGICAL TREATMENT OF AN ULTRA-RARE DISEASE ASSOCIATED WITH DELETION OF CACNG2
47. A CONTRIBUTION OF RARE COPY NUMBER VARIATIONS TO THE DEVELOPMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER: GENOME-WIDE META-ANALYSES IN 12548 INDIVIDUALS
48. NEW FINDINGS FROM YOUNG INVESTIGATORS IN THE PSYCHIATRIC GENOMICS CONSORTIUM
49. Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51
50. Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects
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