All Stories

  1. Neurocognitive and Psychiatric Markers for Addiction: Common vs. Specific Endophenotypes for Heroin and Amphetamine Dependence
  2. Validation of an NGS Approach for Diagnostic BRCA1/BRCA2 Mutation Testing
  3. Relative quantitative expression of hypoxia-inducible factor-1α, -2α and -3α, and vascular endothelial growth factor A in laryngeal carcinoma
  4. Combinations of Serum Prostate-Specific Antigen and Plasma Expression Levels of let-7c, miR-30c, miR-141, and miR-375 as Potential Better Diagnostic Biomarkers for Prostate Cancer
  5. Dominance of Multidrug-Resistant Denmark 14 -32 (ST230) Clone Among Streptococcus pneumoniae Serotype 19A Isolates Causing Pneumococcal Disease in Bulgaria from 1992 to 2013
  6. Auditory Outcome After Cochlear Implantation in Patients With Congenital Nonsyndromic Hearing Loss
  7. Mutational Status of CDKN2A and TP53 Genes in Laryngeal Squamous Cell Carcinoma
  8. Clinical presentation of a Roma family with autosomal recessive Usher Syndrome
  9. Association between estrogen receptor-α gene polymorphisms and dermatomyositis in Bulgarian patients
  10. Fine-Mapping the HOXB Region Detects Common Variants Tagging a Rare Coding Allele: Evidence for Synthetic Association in Prostate Cancer
  11. IDH1/IDH2but NotTP53Mutations Predict Prognosis in Bulgarian Glioblastoma Patients
  12. IL-1RN SNP in SLE and DM patients
  13. Transmission disequilibrium of DISC1 haplotypes in Bulgarian families with affective disorder
  14. Promoter hypermethylation ofCDKN2A,MGMT,MLH1, andDAPKgenes in laryngeal squamous cell carcinoma and their associations with clinical profiles of the patients
  15. The rs266729 single-nucleotide polymorphism in the adiponectin gene shows association with gestational diabetes
  16. Clinical findings in a Roma family with autosomal dominant cone-rod dystrophy
  17. Genetic screening for mild cognitive impairment in people with cardiovascular risk factors
  18. Evidence of an association between bipolar disorder and rs16917237 in the BDNF gene in a Bulgarian sample
  19. Exome sequencing in roma families identifies tandem GRM1 mutations in a novel form of congenital cerebellar ataxia
  20. Role of the Promoter Polymorphism IL-6 −174G/C in Dermatomyositis and Systemic Lupus Erythematosus
  21. Reconstructing the Population History of European Romani from Genome-wide Data
  22. Autosomal-Recessive Congenital Cerebellar Ataxia Is Caused by Mutations in Metabotropic Glutamate Receptor 1
  23. A novel locus for autosomal dominant cone-rod dystrophy maps to chromosome 10q
  24. TNF-Alpha SNPs in SLE and DM patients
  25. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
  26. IL-10 Single Nucleotide Polymorphisms and Lupus-Nephritis
  27. A novel GEFS+ locus on 12p13.33 in a large Roma family
  28. Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population
  29. ANO10 c.1150_1151del is a founder mutation causing autosomal recessive cerebellar ataxia in Roma/Gypsies
  30. Focal epilepsy of probable temporal lobe origin in a Gypsy family showing linkage to a novel locus on 7p21.3
  31. No evidence of association between 118A>G OPRM1 polymorphism and heroin dependence in a large Bulgarian case–control sample
  32. LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population
  33. Rare Mutations in the PIK3CA Gene Contribute to Aggressive Endometrial Cancer
  34. Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
  35. Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32
  36. A mutation in an alternative untranslated exon of hexokinase 1 associated with Hereditary Motor and Sensory Neuropathy – Russe (HMSNR)
  37. Bipolar disorder in the Bulgarian Gypsies: Genetic heterogeneity in a young founder population
  38. CHEK2 I157T and Endometrial Cancer
  39. The First Genomewide Interaction and Locus-Heterogeneity Linkage Scan in Bipolar Affective Disorder: Strong Evidence of Epistatic Effects between Loci on Chromosomes 2q and 6q
  40. Lack of genetic association between the phospholipase A2 gene and bipolar mood disorder in a European multicentre case???control study
  41. Vitamin D and estrogen receptor gene polymorphisms and the risk of colorectal cancer in Bulgaria
  42. Molecular screening for hereditary nonpolyposis colorectal cancer in Bulgaria
  43. Genomewide Scan and Fine-Mapping Linkage Studies in Four European Samples with Bipolar Affective Disorder Suggest a New Susceptibility Locus on Chromosome 1p35-p36 and Provides Further Evidence of Loci on Chromosome 4q31 and 6q24
  44. Linkage analysis in bipolar pedigrees adds support for a susceptibility locus on 21q22
  45. Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study
  46. Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case???control study
  47. Lack of association between the 5HT2A receptor polymorphism (T102C) and unipolar affective disorder in a multicentric European study
  48. Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European multicenter association study of affective disorders
  49. Positive association of dopamine D2 receptor polymorphism with bipolar affective disorder in a European multicenter association study of affective disorders
  50. Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder
  51. Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: a multicenter association study
  52. A European multicenter association study of HTR2A receptor polymorphism in bipolar affective disorder
  53. A European multicenter association study ofHTR2A receptor polymorphism in bipolar affective disorder
  54. Nuclear matrix protein mitotin messenger RNA is expressed at constant levels during the cell cycle
  55. Expression of the nuclear protein mitotin in differentiating in vitro HL 60 cells