Gregory Papagregoriou

Author

University of Cyprus ORCID

Also Known As

G. Papagregoriou, GREGORY PAPAGREGORIOU, Gregory N. Papagregoriou, Gregory Papagregoriou

Publications

912

Citations

H-Index

Concepts

All Affiliations

University of Cyprus Cyprus Institute of Neurology and Genetics Hippocrateon Private Hospital Charles University Wake Forest University

About

Gregory Papagregoriou is an author at University of Cyprus specializing in medicine, glomerular disease, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	269
2	Nephrology	2	2	78
3	Natural Sciences	1	1	191
4	Immunology	1	1	191
5	Molecular Biology	1	1	191

Gregory Papagregoriou

Publications

790

Citations

H-Index

Page 1

	Year	Citations
Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy Moran Dvela‐Levitt, Maria Kost‐Alimova, Maheswarareddy Emani, Cell Protein FunctionAutoimmune DiseaseMedicineNatural SciencesT-regulatory Cell	2019	191
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1 Eric Olinger, Patrick Hofmann, Kendrah Kidd, Kidney International	2020	131
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
Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease Martina Živná, Kendrah Kidd, Anna Přistoupilová, Journal of the American Society of Nephrology	2018	52
New miRNA Profiles Accurately Distinguish Renal Cell Carcinomas and Upper Tract Urothelial Carcinomas from the Normal Kidney Apostolos Zaravinos, George Ι. Lambrou, Nikos Mourmouras, PLoS ONE	2014	49
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
Frequent <i><scp>COL4</scp></i> mutations in familial microhematuria accompanied by later‐onset Alport nephropathy due to focal segmental glomerulosclerosis L. Papazachariou, Gregory Papagregoriou, Despina Hadjipanagi, Clinical Genetics Glomerular DiseaseGeneticsRenal PathologyGenetic EpidemiologyPathology	2017	39
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes Martina Živná, Kendrah Kidd, Mohamad Zaidan, Kidney International Glomerular DiseaseGlomerulonephritisUrologyRenal DiseaseInternational Cohort Study	2020	39
Omega-3 fatty acids protect retinal neurons in the DBA/2J hereditary glaucoma mouse model Maria Kalogerou, Panagiotis Kolovos, Ekatherine Prokopiou, Experimental Eye Research	2017	36

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