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

3. 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)

4. MYH9 Associated nephropathy

5. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1

6. Contribution of the TTC21B gene to glomerular and cystic kidney diseases

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

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

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

10. Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses.

11. ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization.

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

13. Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players.

14. Clinical and Genetic Features of Autosomal Dominant Alport Syndrome: A Cohort Study.

15. De Novo PORCN and ZIC2 Mutations in a Highly Consanguineous Family.

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

17. Autosomal Dominant Tubulointerstitial Kidney Disease: Clinical Presentation of Patients With ADTKD-UMOD and ADTKD-MUC1.

18. A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases.

19. Autosomal Dominant Polycystic Kidney Disease: Clinical Assessment of Rapid Progression.

20. Generation of integration-free induced pluripotent stem cell lines derived from two patients with X-linked Alport syndrome (XLAS).

21. Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport syndrome (ARAS).

22. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.

23. Insight into response to mTOR inhibition when PKD1 and TSC2 are mutated.

24. Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencing.

25. HLA-DQA1 and PLA2R1 polymorphisms and risk of idiopathic membranous nephropathy.

26. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.

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