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Your search keyword '"Piscia D"' showing total 35 results

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35 results on '"Piscia D"'

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1. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

2. Wnt genes in colonic polyposis predisposition.

3. Treatabolome DB: linking gene and variants with treatments for rare diseases

6. Treatabolome database: current state and new developments towards enhancing rare disease treatment visibility

7. Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases

8. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

9. Treatabolome database: towards enhancing Rare Diseases’ treatment visibility

10. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

11. Treatabolome: a rare diseases treatment awareness project

12. RD-Connect: data sharing and analysis for rare disease research within the integrated platform and through GA4GH Beacon and Matchmaker Exchange

13. RD-Connect: Data sharing and analysis for rare disease research within the integrated platform and through GA4GH beacon and matchmaker exchange

14. Shading screens for the improvement of the night time climate of unheated greenhouses

15. Shading screens for the improvement of the night time climate of unheated greenhouses

20. The Treatabolome flags treatable genes and variants: an emerging concept

21. A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome

22. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

23. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

24. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

25. Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report.

26. An interconnected data infrastructure to support large-scale rare disease research.

27. Remote visualization of large-scale genomic alignments for collaborative clinical research and diagnosis of rare diseases.

28. Wnt genes in colonic polyposis predisposition.

29. The GA4GH Phenopacket schema defines a computable representation of clinical data.

30. The RD-Connect Genome-Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases.

32. Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome.

33. From research to rapid response: mass COVID-19 testing by volunteers at the Centre for Genomic Regulation.

34. Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity.

35. A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome.

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