Yiannis Athanasiou - Concepedia

Author

Yiannis Athanasiou

University of Cyprus

Also Known As

Y Athanasiou, Yiannis Athanasiou, Yiannis Athanasiou (333793)

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

University of Cyprus Nicosia General Hospital Hippocrateon Private Hospital Cyprus Institute of Neurology and Genetics Archbishop Makarios III Hospital

About

Yiannis Athanasiou is an author at University of Cyprus specializing in pathology, glomerulonephritis, and nephrology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	598
2	Nephrology	4	4	598
3	Cell Biology	1	1	210
4	Immunology	1	1	323
5	Molecular Genetics	1	1	11

Yiannis Athanasiou

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis Daniel P. Gale, Elena Goicoechea de Jorge, H. Terence Cook, The Lancet Glomerular DiseaseGlomerulonephritisComplement SystemAutoimmune DiseaseMedicine	2010	323
COL4A3/COL4A4 Mutations Producing Focal Segmental Glomerulosclerosis and Renal Failure in Thin Basement Membrane Nephropathy Konstantinos Voskarides, Loukas Damianou, Vassos Neocleous, Journal of the American Society of Nephrology Glomerular DiseaseGeneticsRenal PathologyPathologyCypriot Families	2007	210
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 Alkis Pierides, Konstantinos Voskarides, Yiannis Athanasiou, Nephrology Dialysis Transplantation	2009	157
Familial C3 Glomerulopathy Associated with CFHR5 Mutations Yiannis Athanasiou, Konstantinos Voskarides, Daniel P. Gale, Clinical Journal of the American Society of Nephrology	2011	139
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 Louiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri, PLoS ONE	2014	69
Evidence that NPHS2-R229Q predisposes to proteinuria and renal failure in familial hematuria Konstantinos Voskarides, Maria Arsali, Yiannis Athanasiou, Pediatric Nephrology GlomerulonephritisHemodialysisUrologyRenal FunctionNphs2-r229q Predisposes	2012	54
A miR-1207-5p Binding Site Polymorphism Abolishes Regulation of HBEGF and Is Associated with Disease Severity in CFHR5 Nephropathy Gregory Papagregoriou, Kamil Erguler, Harsh Dweep, PLoS ONE	2012	48
COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect? Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, BMC Nephrology	2018	42
Molecular investigation and long‐term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the <i>ATP6V1B1</i> gene Marianne L. Feldman, Marios Prikis, Yiannis Athanasiou, Clinical Genetics	2006	29
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 Konstantinos Voskarides, Charalambos Stefanou, Myrtani Pieri, PLoS ONE	2017	24

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