Articles in Scholarly Journals [Incomplete List]

1. A New Scientific Journal Linked to a Genetic Database: Towards a Novel Publication Modality
   Human Genomics and Proteomics, vol. 2009, Article ID 597478, 2 pages, 2009
2. Pharmacogenomics and Therapeutics of Hemoglobinopathies
   Hemoglobin, vol. 32, no. 1, pp. 229–236, 2008
3. Association Study of Human VN1R1 Pheromone Receptor Gene Alleles and Gender
   Genetic Testing, vol. 11, no. 2, pp. 128–132, 2007
4. FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide
   Nucleic Acids Research, vol. 35, no. Database, pp. D690–D695, 2007
5. Gene conversion: mechanisms, evolution and human disease
   Nature Reviews Genetics, vol. 8, no. 10, Article ID nrg2193, 13 pages, 2007
6. An Overview of Current Microarray-Based Human Globin Gene Mutation Detection Methods
   Hemoglobin, vol. 31, no. 3, pp. 289–311, 2007
7. A versatile denaturing HPLC approach for human β-globin gene mutation screening
   American Journal of Hematology, vol. 82, no. 2, pp. 168–170, 2007
8. Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in Central Greece compared to the rest of the country
   American Journal of Hematology, vol. 82, no. 7, pp. 634–636, 2007
9. Increased γ-globin gene expression in β-thalassemia intermedia patients correlates with a mutation in 3′HS1
   American Journal of Hematology, vol. 82, no. 11, pp. 1005–1009, 2007
10. PhenCode: connecting ENCODE data with mutations and phenotype
    Human Mutation, vol. 28, no. 6, pp. 554–562, 2007
11. Documentation of inherited disorders and mutation frequencies in the different religious communities in Israel in the Israeli National Genetic Database
    Human Mutation, vol. 28, no. 10, pp. 944–949, 2007
12. HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update
    Human Mutation, vol. 28, no. 2, pp. 206–206, 2007
13. The Cypriot and Iranian National Mutation Frequency Databases
    Human Mutation, vol. 27, no. 6, pp. 598–599, 2006
14. Mutation screening in the human ɛ-globin gene using single-strand conformation polymorphism analysis
    American Journal of Hematology, vol. 81, no. 2, pp. 136–138, 2006
15. National and ethnic mutation databases: recording populations' genography
    Human Mutation, vol. 27, no. 9, pp. 879–887, 2006
16. Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the βS/Benin haplotype
    American Journal of Hematology, vol. 80, no. 1, pp. 79–80, 2005
17. Hellenic National Mutation Database: a prototype database for mutations leading to inherited disorders in the Hellenic population
    Human Mutation, vol. 25, no. 4, pp. 327–333, 2005
18. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies
    Human Mutation, vol. 26, no. 5, pp. 399–412, 2005
19. DNA, diseases and databases: disastrously deficient
    Trends in Genetics, vol. 21, no. 6, pp. 333–338, 2005
20. Isolation and Characterization of Hematopoietic Transcription Factor Complexes by in Vivo Biotinylation Tagging and Mass Spectrometry
    Annals of the New York Academy of Sciences, vol. 1054, no. 1, pp. 55–67, 2005
21. Molecular Characterization and Diagnosis of Hb Crete [β129(H7)Ala→Pro]
    Hemoglobin, vol. 28, no. 4, pp. 339–342, 2004
22. Multiple interactions between regulatory regions are required to stabilize an active chromatin hub
    Genes & Development, vol. 18, no. 12, pp. 1495–1509, 2004
23. Glucose-6-phosphate dehydrogenase deficiency does not result from mutations in the promoter region of the G6PD gene
    Journal of Clinical Laboratory Analysis, vol. 17, no. 3, pp. 90–92, 2003
24. Biological variability of thyroid autoantibodies (anti-TPO and anti-Tg) in clinically and biochemically stable patients with autoimmune thyroid disease
    Journal of Clinical Laboratory Analysis, vol. 16, no. 1, pp. 37–39, 2002
25. Hypermethylation-associated transcriptional silencing of E-cadherin in primary sporadic colorectal carcinomas
    The Journal of Pathology, vol. 198, no. 4, pp. 442–449, 2002
26. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server
    Human Mutation, vol. 19, no. 3, pp. 225–233, 2002
27. A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes
    Journal of Molecular Medicine, vol. 80, no. 4, pp. 243–247, 2002
28. DNA hypermethylation: when tumour suppressor genes go silent
    Human Genetics, vol. 111, no. 2, pp. 115–127, 2002
29. A?-haplotypes: A new group of genetic markers for thalassemic mutations inside the 5? regulatory region of the human A?-globin gene
    American Journal of Hematology, vol. 66, no. 2, pp. 99–104, 2001
30. Molecular Heterogeneity of the Glucose-6-Phosphate Dehydrogenase Deficiency in the Hellenic Population
    Human Heredity, vol. 50, no. 4, pp. 237–241, 2000
31. A novel 23-bp deletion in exon 5 of the p53 tumor suppressor gene
    Journal of Molecular Medicine, vol. 77, no. 9, pp. 686–689, 1999
32. Contribution of gene conversion in the evolution of the human ?-like globin gene family
    Human Genetics, vol. 104, no. 2, pp. 117–125, 1999
33. The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A γ -158C→T] results from two independent gene conversion events
    Human Genetics, vol. 102, no. 6, pp. 629–634, 1998
34. HbF-Lesvos: An HbF variant due to a novel Gγ mutation (:Gγ 75 ATA→ACA) detected in a Greek family
    Human Genetics, vol. 97, no. 2, pp. 260–262, 1996
35. A Novel Dna Polymorphisf the Human Aγ-Globin Gene (Aγ -588, A
    Hemoglobin, vol. 19, no. 6, pp. 419–423, 1995