Despina Hadjipanagi

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

Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi et al. · BMC Nephrology · 2018 · 42 citations · Full text

Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlife

Aleksandra Żurowska, Olga Bielska, Patrycja Daca‐Roszak et al. · Kidney International · 2020 · 42 citations · Full text

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 et al. · Clinical Genetics · 2017 · 39 citations

Glomerular Disease, Genetics, Renal Pathology +22

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

Konstantinos Voskarides, Stéphane Mazières, Despina Hadjipanagi et al. · Investigative Genetics · 2016 · 31 citations · Full text

Evidence for Contribution of the Y Chromosome in Atherosclerotic Plaque Occurrence in Men

Konstantinos Voskarides, Despina Hadjipanagi, Louiza Papazachariou et al. · Genetic Testing and Molecular Biomarkers · 2014 · 17 citations

Greek Cypriot Men, Vascular Disease, Genetic Determinant +13