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Konstantinos Voskarides

Observed names: K Voskarides, K. Voskarides, KONSTANTINOS VOSKARIDES, Voskarides, Konstantinos, Voskarides, Konstantinos A.
ORCID: 0000-0002-3705-3451
Observed ORCID: 0000-0002-3705-3451
OpenAlex ID: A5048901221
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
2010 · Daniel P Gale, Elena Goicoechea de Jorge, et al. · The Lancet · 337
COL4A3/COL4A4 Mutations Producing Focal Segmental Glomerulosclerosis and Renal Failure in Thin Basement Membrane Nephropathy
2007 · Konstantinos Voskarides, Loukas Damianou, et al. · Journal of the American Society of Nephrology · 214
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis
2009 · Alkis Pierides, Konstantinos Voskarides, et al. · Nephrology Dialysis Transplantation · 162
A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics
2016 · Clint Mizzi, Eleni Dalabira, et al. · PLoS ONE · 156
Familial C3 Glomerulopathy Associated with CFHR5 Mutations
2011 · Yiannis Athanasiou, Konstantinos Voskarides, et al. · Clinical Journal of the American Society of Nephrology · 156
The Role of TP53 in Adaptation and Evolution
2023 · Konstantinos Voskarides, Nefeli Giannopoulou · Cells · 147
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Antagonistic Pleiotropy in Human Disease
2019 · Sean G. Byars, Konstantinos Voskarides · Journal of Molecular Evolution · 101
Evidence for Activation of the Unfolded Protein Response in Collagen IV Nephropathies
2013 · Myrtani Pieri, Charalambos Stefanou, et al. · Journal of the American Society of Nephrology · 96
Molecular genetics of familial hematuric diseases
2013 · C. Deltas, A. Pierides, et al. · Nephrology Dialysis Transplantation · 81
Carriers of Autosomal Recessive Alport Syndrome with Thin Basement Membrane Nephropathy Presenting as Focal Segmental Glomerulosclerosis in Later Life
2015 · Constantinos Deltas, Isavella Savva, et al. · The Nephron journals/Nephron journals · 77
Frequency of COL4A3/COL4A4 Mutations amongst Families Segregating Glomerular Microscopic Hematuria and Evidence for Activation of the Unfolded Protein Response. Focal and Segmental Glomerulosclerosis Is a Frequent Development during Ageing
2014 · Louiza Papazachariou, Panayiota Demosthenous, et al. · PLoS ONE · 75
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Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria
2012 · Konstantinos Voskarides, Maria Arsali, et al. · Pediatric Nephrology · 55
Ischemic but not mechanical preconditioning attenuates ischemia/reperfusion induced myocardial apoptosis in anaesthetized rabbits: The role of Bcl-2 family proteins and ERK1/2
2006 · Antigone Lazou, E. K. Iliodromitis, et al. · APOPTOSIS · 55
Combination of 247 Genome-Wide Association Studies Reveals High Cancer Risk as a Result of Evolutionary Adaptation
2017 · Konstantinos Voskarides · Molecular Biology and Evolution · 50
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Large expert-curated database for benchmarking document similarity detection in biomedical literature search
2019 · Peter Brown, Aik-Choon Tan, et al. · Database · 49
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A miR-1207-5p Binding Site Polymorphism Abolishes Regulation of HBEGF and Is Associated with Disease Severity in CFHR5 Nephropathy
2012 · Gregory Papagregoriou, Kamil Erguler, et al. · PLoS ONE · 47
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The role of molecular genetics in diagnosing familial hematuria(s)
2011 · Constantinos Deltas, Alkis Pierides, et al. · Pediatric Nephrology · 46
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Frequent COL4 mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis
2017 · L. Papazachariou, G. Papagregoriou, et al. · Clinical Genetics · 42
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
2018 · Konstantinos Voskarides, Gregory Papagregoriou, et al. · BMC Nephrology · 41
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X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure.
2013 · A Pierides, K Voskarides, et al. · Europe PMC (PubMed Central) · 41
X‐linked Alport syndrome in Hellenic families: Phenotypic heterogeneity and mutations near interruptions of the collagen domain in COL4A5
2011 · P Demosthenous, K Voskarides, et al. · Clinical Genetics · 41
SARS-CoV-2: tracing the origin, tracking the evolution
2022 · Konstantinos Voskarides · BMC Medical Genomics · 37
Y-chromosome phylogeographic analysis of the Greek-Cypriot population reveals elements consistent with Neolithic and Bronze Age settlements
2016 · Konstantinos Voskarides, Stéphane Mazières, et al. · Investigative Genetics · 33
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C3 Glomerulonephritis/CFHR5 Nephropathy Is an Endemic Disease in Cyprus: Clinical and Molecular Findings in 21 Families
2012 · Constantinos Deltas, Daniel Gale, et al. · Advances in experimental medicine and biology · 32
Increased Number of MicroRNA Target Sites in Genes Encoded in CNV Regions. Evidence for an Evolutionary Genomic Interaction
2011 · K. Felekkis, K. Voskarides, et al. · Molecular Biology and Evolution · 31
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Works count: 97
Citation count: 2,719
H-index: 26
I10-index: 47
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