253 results on '"Magri, Chiara"'
Search Results
2. A miR-137–Related Biological Pathway of Risk for Schizophrenia Is Associated With Human Brain Emotion Processing
3. Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy
4. Near-Complete Response to Osimertinib for Advanced Non-Small-Cell Lung Cancer in a Pretreated Patient Bearing Rare Compound Exon 20 Mutation (S768I + V774M): A Case Report.
5. Investigating an in silico approach for prioritizing antidepressant drug prescription based on drug-induced expression profiles and predicted gene expression
6. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium
7. Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial)
8. Alterations observed in the interferon α and β signaling pathway in MDD patients are marginally influenced by cis-acting alleles
9. Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder
10. Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.
11. A miR-137-related biological pathway of risk for Schizophrenia is associated with human brain emotion processing
12. The effect of childhood trauma on blood transcriptome expression in major depressive disorder
13. Assessment of haptoglobin alleles in autism spectrum disorders
14. Immune Checkpoint Inhibitors in “Special” NSCLC Populations: A Viable Approach?
15. Genome‐wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA‐A*03:01 allele
16. Author Correction: A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme
17. Transcriptional Profiling of Rat Prefrontal Cortex after Acute Inescapable Footshock Stress
18. LRRK2 Kinase Inhibition Attenuates Astrocytic Activation in Response to Amyloid β1-42 Fibrils
19. Genome-wide analysis of consistently RNA edited sites in human blood reveals interactions with mRNA processing genes and suggests correlations with cell types and biological variables
20. Investigation on the high recurrence of the ATTRv-causing transthyretin variant Val142Ile in central Italy
21. A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzyme
22. Clinical and Histological Prognostic Factors of Recurrence and Malignant Transformation in a Large Series of Oral Potentially Malignant Disorders
23. LRRK2 Kinase Inhibition Attenuates Astrocytic Activation in Response to Amyloid β 1-42 Fibrils.
24. Whole Blood Transcriptome Characterization of 3xTg-AD Mouse and Its Modulation by Transcranial Direct Current Stimulation (tDCS)
25. Additional file 1 of Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial)
26. Whole Blood Transcriptome Characterization of 3xTg-AD Mouse and Its Modulation by Transcranial Direct Current Stimulation (tDCS)
27. ROLE OF ALLELIC VARIANTS OF FK506-BINDING PROTEIN 51 (FKBP5) GENE IN THE DEVELOPMENT OF ANXIETY DISORDERS
28. Evidence of an interaction between FXR1 and GSK3β polymorphisms on levels of Negative Symptoms of Schizophrenia and their response to antipsychotics
29. Saami and Berbers--an unexpected mitochondrial DNA link
30. The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool
31. Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in Europe
32. Origin, diffusion, and differentiation of Y-chromosome haplogroups E and J: inferences on the neolithization of Europe and later migratory events in the Mediterranean area
33. Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation. (Report)
34. Investigating an in silico approach for prioritizing antidepressant drug prescription based on drug-induced expression profiles and predicted gene expression
35. RNA Editing and Modifications in Mood Disorders
36. Association study betweenHTR2Ars6313 polymorphism and early response to risperidone and olanzapine in schizophrenia patients
37. Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response
38. ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency
39. Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients
40. Genomic restricted maximum likelihood (GREML) analysis to estimate the heritability of response/resistance in major depressive disorder (MDD)
41. Combined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections
42. An imputation approach to determine the Haptoglobin allele frequency in autism spectrum disorder
43. SA43ANALYSIS OF GENETIC AND ENVIRONMENTAL CONTRIBUTION TO ALTERED GENE EXPRESSION PROFILES OBSERVED IN MAJOR DEPRESSIVE DISORDER
44. SA49THE EFFECT OF CHILDHOOD TRAUMA ON BLOOD EXPRESSION OF MED22 IN PATIENTS WITH MAJOR DEPRESSIVE DISORDER IS MEDIATED BY CIS-ACTING SNPS
45. F49GENETIC DETERMINANTS OF CIRCULATING VEGF LEVELS IN MAJOR DEPRESSIVE DISORDER
46. 'GenotypeColour™': colour visualisation of SNPs and CNVs
47. Genome-wide analysis of consistently RNA edited sites in human blood reveals interactions with mRNA processing genes and suggests correlations with cell types and biological variables
48. The 49a,f haplotype 11 is a new marker of the EU19 lineage that traces migrations from northern regions of the black sea
49. The impairment of GABAergic pathway as one of the driver forces in the etiopathogenesis of schizophrenia: evidence from functional studies and gene-set enrichment analyses
50. Functional study of a novel homozygous mutation in the GAD1 gene, detected in a patient with schizophrenia
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