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332 results on '"Kalaydjieva, L."'

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1. Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries.

2. Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.

3. Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

5. Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study

13. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

14. Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene

15. Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

16. UFM1 founder mutation in the Roma population causes severe variant of Hypomyelination with Atrophy of the Basal ganglia and Cerebellum (H-ABC)

17. Use of schizophrenia and bipolar disorder polygenic risk scores to identify psychotic disorders

18. Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains

22. Age at first birth in women is genetically associated with increased risk of schizophrenia

23. A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains.

24. Age at first birth in women is genetically associated with increased risk of schizophrenia

26. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

28. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

29. Angiopoietin-1 is required for Schlemm's canal development in mice and humans

30. BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain

31. Origins, admixture and founder lineages in European Roma

32. GNE myopathy in Roma patients homozygous for the p.I618T founder mutation

33. Mitochondrial lineages in the Roma

34. Genome-wide association analysis identifies 13 new risk loci for schizophrenia

35. The limb-girdle muscular dystrophy 2C in Gypsies

36. Biological insights from 108 schizophrenia-associated genetic loci

38. Analysis of published PKD1 gene sequence variants

39. Analysis of published PKD1 gene sequence variants [3]

40. Genetic Evidence for a Distinct Subtype of Schizophrenia Characterized by Pervasive Cognitive Deficit

41. The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time

43. Challenges of diagnostic exome sequencing in an inbred founder population

44. The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D.

45. Y-Chromosome Analysis in Individuals Bearing the Basarab Name of the First Dynasty of Wallachian Kings.

46. Y-chromosomal diversity within Europe is clinal and influenced primarily by geography rather than language

48. Dating the origin of the CCR5-Delta 32 AIDS-resistance allele by the coalescence of haplotypes

49. NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24

50. Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

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