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1. Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease.

2. Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis

3. WNT signalling control by KDM5C during development affects cognition

4. The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant

5. Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature

6. Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

7. Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients.

9. Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia

10. Genome Sequencing for Diagnosing Rare Diseases

11. Biallelic mutations in SUPV3L1 cause an inherited neurodevelopmental disorder with variable leukodystrophy due to aberrant mitochondrial double stranded RNA processing

12. Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype

13. Monogenic variants in dystonia: an exome-wide sequencing study

15. Brain function in classic galactosemia, a galactosemia network (GalNet) members review

16. New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics

17. The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant

20. Hyperphenylalaninaemias in Estonia: Genotype–Phenotype Correlation and Comparative Overview of the Patient Cohort Before and After Nation-Wide Neonatal Screening

23. Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

24. POLRMT mutations impair mitochondrial transcription causing neurological disease

26. Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging

27. Refining the 9q34.3 microduplication syndrome reveals mild neurodevelopmental features associated with a distinct global DNA methylation profile.

28. Human skeletal myopathy myosin mutations disrupt myosin head sequestration

29. Biallelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome

30. Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

32. Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures

34. De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation

36. Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiency

37. Biallelic loss of function variants inWBP4, encoding a spliceosome protein, result in a variable neurodevelopmental delay syndrome

38. Impaired protein hydroxylase activity causes replication stress and developmental abnormalities in humans

39. Human skeletal myopathy myosin mutations disrupt myosin head sequestration

41. Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease

42. Untargeted metabolomics profiling in pediatric patients and adult populations indicates a connection between lipid imbalance and epilepsy

43. AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature

44. Alternative polyadenylation alters protein dosage by switching between intronic and 3′UTR sites

45. MOGS‐ CDG: Quantitative analysis of the diagnosticGlc 3 Mantetrasaccharide and clinical spectrum of six new cases

46. A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorder

48. A scoring system predicting the clinical course of CLPB defect based on the foetal and neonatal presentation of 31 patients

49. International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up

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