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Gregory Papagregoriou | Researchclopedia

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Gregory Papagregoriou

University of Cyprus ORCID

50

Works

927

Citations

15

h-index

18

i10-index

Research Topics

Renal Diseases and Glomerulopathies Cell Adhesion Molecules Research Renal and related cancers

Affiliations

Broad Institute2018–2018

University of Cyprus2008–2025

Cyprus Institute of Neurology and Genetics2014–2017

Massachusetts Institute of Technology2018–2018

Top Works

Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy

Moran Dvela‐Levitt,Maria Kost‐Alimova,et al.

2019194 citations

Ion Transport and Channel Regulation

Genetic and Kidney Cyst Diseases

Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1

Eric Olinger,Patrick Hofmann,et al.

2020137 citations

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,et al.

201469 citations

Noninvasive Immunohistochemical Diagnosis and Novel MUC1 Mutations Causing Autosomal Dominant Tubulointerstitial Kidney Disease

Martina Živná,Kendrah Kidd,et al.

201853 citations

New miRNA Profiles Accurately Distinguish Renal Cell Carcinomas and Upper Tract Urothelial Carcinomas from the Normal Kidney

Apostolos Zaravinos,George Ι. Lambrou,et al.

201450 citations

A miR-1207-5p Binding Site Polymorphism Abolishes Regulation of HBEGF and Is Associated with Disease Severity in CFHR5 Nephropathy

Gregory Papagregoriou,Kamil Erguler,et al.

201248 citations

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

Konstantinos Voskarides,Gregory Papagregoriou,et al.

201842 citations

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Martina Živná,Kendrah Kidd,et al.

202040 citations

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,et al.

201739 citations