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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

Export 25 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Haplotypes  [Clear All Filters]
2018
Fountoulakis, K. N., & Gonda X. (2018).  Ancestry and different rates of suicide and homicide in European countries: A study with population-level data.. J Affect Disord. 232, 152-162.
Olalde, I., Brace S., Allentoft M. E., Armit I., Kristiansen K., Booth T., et al. (2018).  The Beaker phenomenon and the genomic transformation of northwest Europe.. Nature. 555(7695), 190-196.
2017
Aung, T., Ozaki M., Lee M. Chin, Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., et al. (2017).  Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.. Nat Genet. 49(7), 993-1004.
2016
Tsitoura, M-E. I., Stavrou E. F., Maraziotis I. A., Sarafidis K., Athanassiadou A., & Dimitriou G. (2016).  Surfactant Protein A and B Gene Polymorphisms and Risk of Respiratory Distress Syndrome in Late-Preterm Neonates.. PLoS One. 11(11), e0166516.
2015
Founti, P., Haidich A-B., Chatzikyriakidou A., Salonikiou A., Anastasopoulos E., Pappas T., et al. (2015).  Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-Analysis.. Ann Hum Genet. 79(6), 431-50.
2014
Dardiotis, E., Paterakis K., Tsivgoulis G., Tsintou M., Hadjigeorgiou G. F., Dardioti M., et al. (2014).  AQP4 tag single nucleotide polymorphisms in patients with traumatic brain injury.. J Neurotrauma. 31(23), 1920-6.
Gkampeta, A., Fidani L., Clarimón J., Kalinderi K., Katopodi T., Zafeiriou D., et al. (2014).  Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population.. Epilepsy Res. 108(10), 1734-9.
Panoutsopoulou, K., Hatzikotoulas K., Xifara D. Kiara, Colonna V., Farmaki A-E., Ritchie G. R. S., et al. (2014).  Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.. Nat Commun. 5, 5345.
Kontakioti, E., Domvri K., Papakosta D., & Daniilidis M. (2014).  HLA and asthma phenotypes/endotypes: a review.. Hum Immunol. 75(8), 930-9.
Pana, Z. Dorothea, Samarah F., Papi R., Antachopoulos C., Papageorgiou T., Farmaki E., et al. (2014).  Mannose binding lectin and ficolin-2 polymorphisms are associated with increased risk for bacterial infections in children with B acute lymphoblastic leukemia.. Pediatr Blood Cancer. 61(6), 1017-22.
Giantsis, I. A., Abatzopoulos T. J., Angelidis P., & Apostolidis A. P. (2014).  Mitochondrial control region variability in Mytilus galloprovincialis populations from the central-Eastern Mediterranean Sea.. Int J Mol Sci. 15(7), 11614-25.
Pancoska, P., Kirkwood J. M., Bouros S., Spyropoulou-Vlachou M., Pectasides E., Tsoutsos D., et al. (2014).  A new mathematical model for the interpretation of translational research evaluating six CTLA-4 polymorphisms in high-risk melanoma patients receiving adjuvant interferon.. PLoS One. 9(1), e86375.
Ballantyne, K. N., Ralf A., Aboukhalid R., Achakzai N. M., Anjos M. J., Ayub Q., et al. (2014).  Toward male individualization with rapidly mutating y-chromosomal short tandem repeats.. Hum Mutat. 35(8), 1021-32.
2012
Kalinderi, K., Bostantjopoulou S., Katsarou Z., Clarimón J., & Fidani L. (2012).  Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population.. Genet Test Mol Biomarkers. 16(8), 974-7.
2011
Vasilopoulos, Y., Bagiatis V., Stamatopoulou D., Zisopoulos D., Alexiou I., Sarafidou T., et al. (2011).  Association of anti-CCP positivity and carriage of TNFRII susceptibility variant with anti-TNF-α response in rheumatoid arthritis.. Clin Exp Rheumatol. 29(4), 701-4.
McKay, G. J., Patterson C. C., Chakravarthy U., Dasari S., Klaver C. C., Vingerling J. R., et al. (2011).  Evidence of association of APOE with age-related macular degeneration: a pooled analysis of 15 studies.. Hum Mutat. 32(12), 1407-16.
Kalinderi, K., Fidani L., Katsarou Z., Clarimón J., Bostantjopoulou S., & Kotsis A. (2011).  GSK3β polymorphisms, MAPT H1 haplotype and Parkinson's disease in a Greek cohort.. Neurobiol Aging. 32(3), 546.e1-5.
Antoniades, D., Katopodi T., Pappa S., Lampropoulos A., Konsta V., Frydas E., et al. (2011).  The role of reelin gene polymorphisms in the pathogenesis of Alzheimer's disease in a Greek population.. J Biol Regul Homeost Agents. 25(3), 351-8.
2010
Kalifatidis, A., Albanidou-Farmaki E., Daniilidis M., Markopoulos A. K., Karyotis N., & Antoniades D. Z. (2010).  HLA alleles and fissured tongue.. Int J Immunogenet. 37(6), 509-11.
2009
Panagopoulou, P., Stamna E., Tsolkas G., Galli-Tsinopoulou A., Pavlitou-Tsiontsi E., Nousia-Arvanitakis S., et al. (2009).  Adiponectin gene polymorphisms in obese Greek youth.. J Pediatr Endocrinol Metab. 22(10), 955-9.
Kalinderi, K., Fidani L., & Bostantjopoulou S. (2009).  From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome.. Parkinsonism Relat Disord. 15(1), 2-5.
Kovatsi, L., Saunier J. L., & Irwin J. A. (2009).  Population genetics of Y-chromosome STRs in a population of Northern Greeks.. Forensic Sci Int Genet. 4(1), e21-2.
2007
Fidani, L., Clarimon J., Goulas A., Hatzitolios A. I., Evans W., Tsirogianni E., et al. (2007).  Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population.. Eur J Neurol. 14(7), 745-9.
2006
Fidani, L., Kalinderi K., Bostantjopoulou S., Clarimón J., Goulas A., Katsarou Z., et al. (2006).  Association of the Tau haplotype with Parkinson's disease in the Greek population.. Mov Disord. 21(7), 1036-9.
Vierimaa, O., Georgitsi M., Lehtonen R., Vahteristo P., Kokko A., Raitila A., et al. (2006).  Pituitary adenoma predisposition caused by germline mutations in the AIP gene.. Science. 312(5777), 1228-30.

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