Search

Your search keyword '"Õunap, Katrin"' showing total 579 results

Search Constraints

Start Over You searched for: Author "Õunap, Katrin" Remove constraint Author: "Õunap, Katrin"
579 results on '"Õunap, Katrin"'

Search Results

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. RORA-neurodevelopmental disorder: A unique triad of developmental disability, cerebellar anomalies, and myoclonic seizures

5. Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets

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

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

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

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

11. Rare pathogenic variants in WNK3 cause X-linked intellectual disability

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

13. Genome Sequencing for Diagnosing Rare Diseases

14. Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders

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

16. A form of muscular dystrophy associated with pathogenic variants in JAG2

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

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

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

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

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

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

27. POLRMT mutations impair mitochondrial transcription causing neurological disease

28. CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum

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

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

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

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

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

40. Human skeletal myopathy myosin mutations disrupt myosin head sequestration

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

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

43. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

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

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

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

50. Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

Catalog

Books, media, physical & digital resources