158 results on '"Sabatti, Chiara"'
Search Results
2. Transfer Learning in Genome-Wide Association Studies with Knockoffs
3. False discovery rate control in genome-wide association studies with population structure
4. GhostKnockoff inference empowers identification of putative causal variants in genome-wide association studies
5. Causal inference in genetic trio studies
6. Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder
7. Distinct and shared contributions of diagnosis and symptom domains to cognitive performance in severe mental illness in the Paisa population: a case-control study
8. Progenitor identification and SARS-CoV-2 infection in human distal lung organoids
9. MULTILAYER KNOCKOFF FILTER : CONTROLLED VARIABLE SELECTION AT MULTIPLE RESOLUTIONS
10. Increased activation product of complement 4 protein in plasma of individuals with schizophrenia
11. Exome sequencing of Finnish isolates enhances rare-variant association power
12. Genetic analyses of diverse populations improves discovery for complex traits
13. Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates
14. Transcriptome-Based Determination of Multiple Transcription Regulator Activities in Escherichia coli by Using Network Component Analysis
15. Network Component Analysis: Reconstruction of Regulatory Signals in Biological Systems
16. Measuring Dependency with Volume Tests
17. Multi-resolution localization of causal variants across the genome
18. Genetic regulation of gene expression and splicing during a 10-year period of human aging
19. Generalised Gibbs Sampler and Multigrid Monte Carlo for Bayesian Computation
20. Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder
21. The impact of rare variation on gene expression across tissues
22. Dynamic landscape and regulation of RNA editing in mammals
23. Landscape of X chromosome inactivation across human tissues
24. SLOPE—ADAPTIVE VARIABLE SELECTION VIA CONVEX OPTIMIZATION
25. Genetic effects on gene expression across human tissues
26. Filtering the Rejection Set While Preserving False Discovery Rate Control.
27. Markov Models for Inferring Copy Number Variations from Genotype Data on Illumina Platforms
28. Bayesian Gaussian Mixture Models for High-Density Genotyping Arrays
29. Likelihood-Based Inference on Haplotype Effects in Genetic Association Studies [with Comment]
30. Linkage Disequilibrium and Haplotype Homozygosity in Population Samples Genotyped at a High Marker Density
31. Semilinear High-Dimensional Model for Normalization of Microarray Data: A Theoretical Analysis and Partial Consistency [with Comments, Rejoinder]
32. Increased paternal age and the influence on burden of genomic copy number variation in the general population
33. Original Investigation: Multisystem Component Phenotypes of Bipolar Disorder for Genetic Investigations of Extended Pedigrees
34. Robust discrimination between self and non-self neurites requires thousands of Dscam1 isoforms
35. Recurrent CNVs disrupt three candidate genes in schizophrenia patients
36. Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks
37. False discovery rate in linkage and association genome screens for complex disorders
38. Homozygosity and linkage disequilibrium
39. Phenotype mining in CNV carriers from a population cohort†
40. Biological, clinical and population relevance of 95 loci for blood lipids
41. Disruption of the neurexin 1 gene is associated with schizophrenia
42. Large recurrent microdeletions associated with schizophrenia
43. HUMAN GENETICS: Variants in common diseases
44. Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses
45. Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31–34
46. Bayesian sparse hidden components analysis for transcription regulation networks
47. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity
48. Guidelines for association studies in Human Molecular Genetics
49. Vocabulon: a dictionary model approach for reconstruction and localization of transcription factor binding sites
50. Hypotheses on a tree: new error rates and testing strategies.
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