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Liana Fidani, MD PhD - Publications

Affiliations: 
Aristotle University of Thessaloniki, Thessaloniki, Greece 
Area:
http://www.biomedexperts.com/Profile.bme/398863/Liana_Fidani
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38 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Xiromerisiou G, Bourinaris T, Houlden H, Lewis PA, Senkevich K, Hammer M, Federoff M, Khan A, Spanaki C, Hadjigeorgiou GM, Bonstanjopoulou S, Fidani L, Ermolaev A, Gan-Or Z, Singleton A, et al. SORL1 mutation in a Greek family with Parkinson's disease and dementia. Annals of Clinical and Translational Neurology. PMID 34506082 DOI: 10.1002/acn3.51433  0.647
2020 Gogou M, Pavlou E, Kimiskidis V, Kouskouras K, Pavlidou E, Papadopoulos T, Haidopoulou K, Fidani L. Novel Mutations Involved in Charcot-Marie-Tooth 4C and Intrafamilial Variability: Let's Not Miss the Forest for the Trees Journal of Pediatric Genetics. DOI: 10.1055/S-0040-1709695  0.32
2016 Kalinderi K, Bostantjopoulou S, Fidani L. The genetic background of Parkinson's disease: Current progress and future prospects Acta Neurologica Scandinavica. DOI: 10.1111/Ane.12563  0.358
2015 Kalinderi K, Bostantjopoulou S, Katsarou Z, Dimikiotou M, Fidani L. D620N mutation in the VPS35 gene and R1205H mutation in the EIF4G1 gene are uncommon in the Greek population. Neuroscience Letters. 606: 113-6. PMID 26300542 DOI: 10.1016/J.Neulet.2015.08.020  0.473
2015 Dimitriadou M, Christoforidis A, Fidani L, Economou M, Vlachaki E, Athanassiou-Metaxa M, Katzos G. A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. PMID 26275438 DOI: 10.1007/S00198-015-3264-1  0.318
2015 Chatzikyriakidou A, Aidinidou L, Giannopoulos A, Papadopoulou-Legbelou K, Kalinderi K, Fidani L. Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients. Cardiology in the Young. 25: 681-3. PMID 24775607 DOI: 10.1017/S1047951114000626  0.413
2014 Gkampeta A, Fidani L, Clarimón J, Kalinderi K, Katopodi T, Zafeiriou D, Pavlou E. 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 Research. 108: 1734-9. PMID 25301525 DOI: 10.1016/J.Eplepsyres.2014.09.005  0.344
2014 Kara E, Xiromerisiou G, Spanaki C, Bozi M, Koutsis G, Panas M, Dardiotis E, Ralli S, Bras J, Letson C, Edsall C, Pliner H, Arepalli S, Kalinderi K, Fidani L, et al. Assessment of Parkinson's disease risk loci in Greece. Neurobiology of Aging. 35: 442.e9-442.e16. PMID 24080174 DOI: 10.1016/J.Neurobiolaging.2013.07.011  0.559
2014 Kalinderi K, Fragakis N, Koskinas K, Katritsis D, Letsas K, Efremidis M, Rossios K, Skeberis V, Vassilikos V, Fidani L. P378Variant rs2200733 on chromosome 4q25 independently confers increased risk of atrial fibrillation in a greek population Cardiovascular Research. 103: S69.3-S69. DOI: 10.1093/Cvr/Cvu091.61  0.314
2013 Kalinderi K, Bostantjopoulou S, Katsarou Z, Fidani L. Association study of rs6812193 polymorphism with Parkinson's disease in a Greek population. Neuroscience Letters. 541: 190-2. PMID 23473716 DOI: 10.1016/J.Neulet.2013.02.048  0.374
2013 Kalinderi K, Bostantjopoulou S, Katsarou Z, Fidani L. TLR9 -1237 T/C and TLR2 -194 to -174 del polymorphisms and the risk of Parkinson's disease in the Greek population: a pilot study. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 34: 679-82. PMID 22552867 DOI: 10.1007/S10072-012-1106-X  0.346
2012 Kalinderi K, Bostantjopoulou S, Katsarou Z, Clarimón J, Fidani L. Lack of association between CX3CR1 V249I and T280M polymorphisms and risk of Parkinson's disease in a Greek population. Genetic Testing and Molecular Biomarkers. 16: 974-7. PMID 22747084 DOI: 10.1089/Gtmb.2011.0330  0.36
2012 Kalinderi K, Bostantjopoulou S, Katsarou Z, Clarimón J, Fidani L. Lack of association of the PICALM rs3851179 polymorphism with Parkinson's disease in the Greek population. The International Journal of Neuroscience. 122: 502-605. PMID 22715855 DOI: 10.3109/00207454.2012.697083  0.411
2011 Fidani L, Karagianni P, Tsakalidis C, Mitsiako G, Hatziioannidis I, Biancalana V, Nikolaidis N. Identification of a mutation in the MTM1 gene, associated with X-linked myotubular myopathy, in a Greek family. Hippokratia. 15: 278-9. PMID 22435031  0.342
2011 Karakasis C, Kalinderi K, Katsarou Z, Fidani L, Bostantjopoulou S. Association of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism with Parkinson's disease in a Greek population. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 18: 1744-5. PMID 22001244 DOI: 10.1016/J.Jocn.2011.03.015  0.357
2011 Dimitriadou M, Christoforidis A, Economou M, Teli A, Printza N, Tzimouli V, Tsatra I, Fidani L, Papachristou F, Athanassiou-Metaxa M. Fok-I polymorphism of vitamin D receptor gene and the presence of renal dysfunction in patients with β-thalassemia major. Pediatric Hematology and Oncology. 28: 509-16. PMID 21762013 DOI: 10.3109/08880018.2011.579231  0.322
2011 Kalinderi K, Fidani L, Katsarou Z, Clarimón J, Bostantjopoulou S, Kotsis A. GSK3β polymorphisms, MAPT H1 haplotype and Parkinson's disease in a Greek cohort. Neurobiology of Aging. 32: 546.e1-5. PMID 19573950 DOI: 10.1016/J.Neurobiolaging.2009.05.007  0.361
2009 Kalinderi K, Bostantjopoulou S, Paisan-Ruiz C, Katsarou Z, Hardy J, Fidani L. Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece. Neuroscience Letters. 452: 87-9. PMID 19383421 DOI: 10.1016/J.Neulet.2009.01.029  0.542
2009 Kalinderi K, Fidani L, Bostantjopoulou S. From 1997 to 2007: a decade journey through the H1 haplotype on 17q21 chromosome. Parkinsonism & Related Disorders. 15: 2-5. PMID 18424220 DOI: 10.1016/J.Parkreldis.2008.03.001  0.354
2008 Kalinderi K, Fidani L, Kourtesi G, Katsarou Z, Mioglou E, Bostantjopoulou S. No association of the Val158Met COMT polymorphism with Parkinson's disease in the Greek population. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 15: e83. PMID 18684304 DOI: 10.1111/J.1468-1331.2008.02186.X  0.385
2008 Goulas A, Kosmidou M, Hatzitolios AI, Molyva D, Fidani L, Giannopoulos S, Mirtsou V. Glutathione S-transferase null and cholesteryl ester transfer protein TaqI B polymorphisms and lipid response to atorvastatin in Greek dyslipidaemic patients. Basic & Clinical Pharmacology & Toxicology. 102: 559-62. PMID 18331394 DOI: 10.1111/J.1742-7843.2008.00220.X  0.304
2008 Fidani L, Karagianni P, Tsakalidis C, Mitsiakos G, Hatziioannidis I, Biancalana V, Nikolaidis N. Identification of a novel mutation in the MTM1 gene associated with X-linked myotubular myopathy, in a Greek family European Journal of Paediatric Neurology. 12. DOI: 10.1016/S1090-3798(08)70178-8  0.449
2007 Kalinderi K, Fidani L, Bostantjopoulou S, Katsarou Z, Kotsis A. The G2019S LRRK2 mutation is uncommon amongst Greek patients with sporadic Parkinson's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 14: 1088-90. PMID 17880562 DOI: 10.1111/J.1468-1331.2007.01867.X  0.423
2007 Fidani L, Clarimon J, Goulas A, Hatzitolios AI, Evans W, Tsirogianni E, Hardy J, Kotsis A. Association of phosphodiesterase 4D gene G0 haplotype and ischaemic stroke in a Greek population. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 14: 745-9. PMID 17594329 DOI: 10.1111/J.1468-1331.2007.01767.X  0.447
2006 Fidani L, Kalinderi K, Bostantjopoulou S, Clarimon J, Goulas A, Katsarou Z, Hardy J, Kotsis A. Association of the Tau haplotype with Parkinson's disease in the Greek population. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 1036-9. PMID 16552760 DOI: 10.1002/Mds.20864  0.495
2005 Fidani L, Hatzitolios AI, Goulas A, Savopoulos C, Basayannis C, Kotsis A. Cholesteryl ester transfer protein TaqI B and lipoprotein lipase Ser447Ter gene polymorphisms are not associated with ischaemic stroke in Greek patients. Neuroscience Letters. 384: 102-5. PMID 15896905 DOI: 10.1016/J.Neulet.2005.04.061  0.35
2004 Fidani L, Goulas A, Crook R, Petersen RC, Tangalos E, Kotsis A, Hardy J. An association study of the cholesteryl ester transfer protein TaqI B polymorphism with late onset Alzheimer's disease. Neuroscience Letters. 357: 152-4. PMID 15036597 DOI: 10.1016/J.Neulet.2003.11.071  0.499
2002 Goulas A, Fidani L, Kotsis A, Mirtsou V, Petersen RC, Tangalos E, Hardy J. An association study of a functional catalase gene polymorphism, -262C-->T, and patients with Alzheimer's disease. Neuroscience Letters. 330: 210-3. PMID 12231449 DOI: 10.1016/S0304-3940(02)00780-2  0.529
2002 Fidani L, Goulas A, Mirtsou V, Petersen RC, Tangalos E, Crook R, Hardy J. Interleukin-1A polymorphism is not associated with late onset Alzheimer's disease. Neuroscience Letters. 323: 81-3. PMID 11911995 DOI: 10.1016/S0304-3940(02)00114-3  0.483
2002 Fidani L, Compton D, Hardy J, Petersen RC, Tangalos E, Mirtsou V, Goulas A, De Vrieze FW. No association between the lipoprotein lipase S447X polymorphism and Alzheimer's disease. Neuroscience Letters. 322: 192-4. PMID 11897170 DOI: 10.1016/S0304-3940(02)00098-8  0.543
1993 Adroer R, Lopez-Acedo C, Oliva R, Hardy J, Fidani L. A novel silent variant at codon 711 and a variant at codon 708 of the APP sequence detected in Spanish Alzheimer and control cases. Neuroscience Letters. 150: 33-4. PMID 8469399 DOI: 10.1016/0304-3940(93)90101-P  0.621
1993 Brown J, Gydesen S, Sorensen SA, Brun A, Duff K, Houlden H, Fidani L, Kullkarni S, Cummings J, Goate A. Exclusion mapping in familial non-specific dementia. Dementia (Basel, Switzerland). 4: 163-6. PMID 8401786 DOI: 10.1159/000107317  0.655
1992 Fidani L, Goate A. Mutations in APP and their role in beta-amyloid deposition. Progress in Clinical and Biological Research. 379: 195-214. PMID 1409745  0.307
1992 Mullan M, Houlden H, Windelspecht M, Fidani L, Lombardi C, Diaz P, Rossor M, Crook R, Hardy J, Duff K. A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene. Nature Genetics. 2: 340-2. PMID 1303291 DOI: 10.1038/Ng1292-340  0.728
1992 Fidani L, Rooke K, Chartier-Harlin MC, Hughes D, Tanzi R, Mullan M, Roques P, Rossor M, Hardy J, Goate A. Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile. Human Molecular Genetics. 1: 165-8. PMID 1303172 DOI: 10.1093/Hmg/1.3.165  0.745
1991 Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J. Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene. Nature. 353: 844-6. PMID 1944558 DOI: 10.1038/353844A0  0.763
1991 Crawford F, Hardy J, Mullan M, Goate A, Hughes D, Fidani L, Roques P, Rossor M, Chartier-Harlin MC. Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequence. Neuroscience Letters. 133: 1-2. PMID 1791986 DOI: 10.1016/0304-3940(91)90042-R  0.749
1991 Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature. 349: 704-6. PMID 1671712 DOI: 10.1038/349704A0  0.752
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