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Items: 1 to 20 of 50

1.

Correction to: Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.

Voskarides K, Dweep H, Chrysostomou C.

Hum Genomics. 2019 Jul 2;13(1):29. doi: 10.1186/s40246-019-0214-6.

2.

Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.

Voskarides K, Dweep H, Chrysostomou C.

Hum Genomics. 2019 Jun 7;13(1):26. doi: 10.1186/s40246-019-0210-x. Erratum in: Hum Genomics. 2019 Jul 2;13(1):29.

3.

The "cancer-cold" hypothesis and possible extensions for the Nordic populations.

Voskarides K.

Scand J Public Health. 2019 Jul;47(5):477-481. doi: 10.1177/1403494819831905. Epub 2019 Feb 28.

PMID:
30813844
4.

Genes that improved fitness also cost modern humans: evidence for genes with antagonistic effects on longevity and disease.

Byars SG, Voskarides K.

Evol Med Public Health. 2019 Jan 23;2019(1):4-6. doi: 10.1093/emph/eoz002. eCollection 2019. No abstract available.

5.

Influenza Virus-Host Co-evolution. A Predator-Prey Relationship?

Voskarides K, Christaki E, Nikolopoulos GK.

Front Immunol. 2018 Sep 7;9:2017. doi: 10.3389/fimmu.2018.02017. eCollection 2018. Review.

6.

COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?

Voskarides K, Papagregoriou G, Hadjipanagi D, Petrou I, Savva I, Elia A, Athanasiou Y, Pastelli A, Kkolou M, Hadjigavriel M, Stavrou C, Pierides A, Deltas C.

BMC Nephrol. 2018 May 16;19(1):114. doi: 10.1186/s12882-018-0906-5.

7.

Group Selection May Explain Cancer Predisposition and Other Human Traits' Evolution.

Voskarides K.

J Mol Evol. 2018 Apr;86(3-4):184-186. doi: 10.1007/s00239-018-9841-0. Epub 2018 Apr 5.

PMID:
29623350
8.
9.

Distal renal tubular acidosis in a Libyan patient: Evidence for digenic inheritance.

Nagara M, Papagregoriou G, Ben Abdallah R, Landoulsi Z, Bouyacoub Y, Elouej S, Kefi R, Pippucci T, Voskarides K, Bashamboo A, McElreavey K, Hachicha M, Romeo G, Seri M, Deltas C, Abdelhak S.

Eur J Med Genet. 2018 Jan;61(1):1-7. doi: 10.1016/j.ejmg.2017.10.002. Epub 2017 Oct 9.

PMID:
29024829
10.

Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.

Papazachariou L, Papagregoriou G, Hadjipanagi D, Demosthenous P, Voskarides K, Koutsofti C, Stylianou K, Ioannou P, Xydakis D, Tzanakis I, Papadaki A, Kallivretakis N, Nikolakakis N, Perysinaki G, Gale DP, Diamantopoulos A, Goudas P, Goumenos D, Soloukides A, Boletis I, Melexopoulou C, Georgaki E, Frysira E, Komianou F, Grekas D, Paliouras C, Alivanis P, Vergoulas G, Pierides A, Daphnis E, Deltas C.

Clin Genet. 2017 Nov;92(5):517-527. doi: 10.1111/cge.13077. Epub 2017 Sep 25.

PMID:
28632965
11.

A functional variant in NEPH3 gene confers high risk of renal failure in primary hematuric glomerulopathies. Evidence for predisposition to microalbuminuria in the general population.

Voskarides K, Stefanou C, Pieri M, Demosthenous P, Felekkis K, Arsali M, Athanasiou Y, Xydakis D, Stylianou K, Daphnis E, Goulielmos G, Loizou P, Savige J, Höhne M, Völker LA, Benzing T, Maxwell PH, Gale DP, Gorski M, Böger C, Kollerits B, Kronenberg F, Paulweber B, Zavros M, Pierides A, Deltas C.

PLoS One. 2017 Mar 23;12(3):e0174274. doi: 10.1371/journal.pone.0174274. eCollection 2017.

12.

Y chromosome and cardiovascular risk: What are we missing?

Voskarides K.

Atherosclerosis. 2017 Apr;259:97-98. doi: 10.1016/j.atherosclerosis.2017.02.026. Epub 2017 Mar 1. No abstract available.

PMID:
28279402
13.

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics.

Mizzi C, Dalabira E, Kumuthini J, Dzimiri N, Balogh I, Başak N, Böhm R, Borg J, Borgiani P, Bozina N, Bruckmueller H, Burzynska B, Carracedo A, Cascorbi I, Deltas C, Dolzan V, Fenech A, Grech G, Kasiulevicius V, Kádaši Ľ, Kučinskas V, Khusnutdinova E, Loukas YL, Macek M Jr, Makukh H, Mathijssen R, Mitropoulos K, Mitropoulou C, Novelli G, Papantoni I, Pavlovic S, Saglio G, Sertić J, Stojiljkovic M, Stubbs AP, Squassina A, Torres M, Turnovec M, van Schaik RH, Voskarides K, Wakil SM, Werk A, Del Zompo M, Zukic B, Katsila T, Lee MT, Motsinger-Rief A, Mc Leod HL, van der Spek PJ, Patrinos GP.

PLoS One. 2017 Feb 16;12(2):e0172595. doi: 10.1371/journal.pone.0172595. eCollection 2017.

14.

Plasticity vs Mutation. The role of microRNAs in human adaptation.

Voskarides K.

Mech Ageing Dev. 2017 Apr;163:36-39. doi: 10.1016/j.mad.2016.12.014. Epub 2017 Jan 3. Review.

PMID:
28057445
15.

'Plasticity-First' Evolution and the Role of miRNAs: A Comment on Levis and Pfennig.

Voskarides K.

Trends Ecol Evol. 2016 Nov;31(11):816-817. doi: 10.1016/j.tree.2016.08.006. Epub 2016 Sep 14. No abstract available.

PMID:
27637167
16.

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics.

Mizzi C, Dalabira E, Kumuthini J, Dzimiri N, Balogh I, Başak N, Böhm R, Borg J, Borgiani P, Bozina N, Bruckmueller H, Burzynska B, Carracedo A, Cascorbi I, Deltas C, Dolzan V, Fenech A, Grech G, Kasiulevicius V, Kádaši Ľ, Kučinskas V, Khusnutdinova E, Loukas YL, Macek M Jr, Makukh H, Mathijssen R, Mitropoulos K, Mitropoulou C, Novelli G, Papantoni I, Pavlovic S, Saglio G, Setric J, Stojiljkovic M, Stubbs AP, Squassina A, Torres M, Turnovec M, van Schaik RH, Voskarides K, Wakil SM, Werk A, Del Zompo M, Zukic B, Katsila T, Lee MT, Motsinger-Rief A, Mc Leod HL, van der Spek PJ, Patrinos GP.

PLoS One. 2016 Sep 16;11(9):e0162866. doi: 10.1371/journal.pone.0162866. eCollection 2016. Erratum in: PLoS One. 2017 Feb 16;12 (2):e0172595.

17.

Y-chromosome phylogeographic analysis of the Greek-Cypriot population reveals elements consistent with Neolithic and Bronze Age settlements.

Voskarides K, Mazières S, Hadjipanagi D, Di Cristofaro J, Ignatiou A, Stefanou C, King RJ, Underhill PA, Chiaroni J, Deltas C.

Investig Genet. 2016 Feb 11;7:1. doi: 10.1186/s13323-016-0032-8. eCollection 2016.

18.

Molecular and Clinical Investigation of Cystinuria in the Greek-Cypriot Population.

Athanasiou Y, Voskarides K, Chatzikyriakidou A, Ignatiou A, Demosthenous P, Elia A, Zavros M, Georgiou I, Pierides A, Deltas C.

Genet Test Mol Biomarkers. 2015 Nov;19(11):641-5. doi: 10.1089/gtmb.2015.0144. Epub 2015 Nov 5.

PMID:
26540609
19.

Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life.

Deltas C, Savva I, Voskarides K, Papazachariou L, Pierides A.

Nephron. 2015;130(4):271-80. doi: 10.1159/000435789. Epub 2015 Jul 17. Review.

PMID:
26201269
20.

Homo sapiens exhibit a distinct pattern of CNV genes regulation: an important role of miRNAs and SNPs in expression plasticity.

Dweep H, Kubikova N, Gretz N, Voskarides K, Felekkis K.

Sci Rep. 2015 Jul 16;5:12163. doi: 10.1038/srep12163.

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