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1. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

2. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

3. Rare coding variants in ten genes confer substantial risk for schizophrenia.

4. Characterisation of age and polarity at onset in bipolar disorder.

5. Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

6. The Degree of Cardiovascular Autonomic Dysfunction is not Different in GBA-Related and Idiopathic Parkinson’s Disease Patients: A Case-Control Instrumental Evaluation

7. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

8. Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

9. New challenges call for new skills: providing quality education for sustainable destination managers with the WeNaTour project.

11. A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder.

12. The Genetic Puzzle of a SOD1-Patient with Ocular Ptosis and a Motor Neuron Disease: How Many Variants Contribute to the Phenotype?

13. Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene

16. Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia

17. Rare coding variants in 10 genes confer substantial risk for schizophrenia

18. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

19. Characterisation of age and polarity at onset in bipolar disorder

21. Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa

22. Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa

24. Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

25. GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel Therapies

26. Genetic variation in the miR‐708 gene and its binding targets in bipolar disorder

27. Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen

31. Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data

34. Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies

36. Phenopolis: an open platform for harmonization and analysis of sequencing and phenotype data

39. Exome sequence analysis and follow up genotyping implicates rare <italic>ULK1</italic> variants to be involved in susceptibility to schizophrenia.

40. Genetic association and functional characterization of MCPH1gene variation in bipolar disorder and schizophrenia

43. The functional GRM3 Kozak sequence variant rs148754219 affects the risk of schizophrenia and alcohol dependence as well as bipolar disorder

47. Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia.

48. Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data.

49. Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

50. The functional GRM3 Kozak sequence variant rs148754219 affects the risk of schizophrenia and alcohol dependence as well as bipolar disorder.

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