Michael Hadjigavriel

Author

Cyprus Institute of Neurology and Genetics

Also Known As

Hadjigavriel, Michael, M Hadjigavriel, Michael Hadjigavriel, Michael Hadjigavriel (675499)

Publications

636

Citations

H-Index

Concepts

All Affiliations

Cyprus Institute of Neurology and Genetics Limassol General Hospital Larnaca College Archbishop Makarios III Hospital Paphos General Hospital

About

Michael Hadjigavriel is an author at Cyprus Institute of Neurology and Genetics specializing in medicine, genetics, and immunohematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	133
2	Public Health	2	2	61
3	Health Sciences	1	1	15
4	Cell Biology	1	1	15
5	Epidemiology	1	1	14

Michael Hadjigavriel

Publications

477

Citations

H-Index

Page 1

	Year	Citations
Survival of medically treated thalassemia patients in Cyprus. Trends and risk factors over the period 1980-2004. Paul Telfer, Pietro G. Coen, Soteroula Christou, PubMed	2006	192
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
Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1 Michael Koptides, Rolandos Constantinides, George Kyriakides, Human Genetics UrologyRenal DiseaseMendelian DisorderGenetic DisorderMedicine	1998	57
Update on fertility in thalassaemia major. Nicos Skordis, Loizos Petrikkos, Meropi Toumba, PubMed FertilityGeneticsReproductive HealthGynecologyFemale Reproductive System	2004	47
The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study Petros Kountouris, Ioanna Kousiappa, Thessalia Papasavva, Scientific Reports	2016	46
Restless legs syndrome is contributing to fatigue and low quality of life levels in hemodialysis patients Christoforos D. Giannaki, Michael Hadjigavriel, Akis Lazarou, World Journal of Nephrology	2017	37
A novel mutation in the erythroid transcription factor KLF1 is likely responsible for ameliorating β‐thalassemia major Pavlos Fanis, Ioanna Kousiappa, Marios Phylactides, Human Mutation ImmunohematologyIron MetabolismGeneticsBlood CellMolecular Genetics	2019	15
Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus Petros Kountouris, Kyriaki Michailidou, Soteroula Christou, Haematologica ImmunohematologyGenetic EpidemiologyRegular TransfusionPopulation Health SciencesTransfusion-dependent Thalassemia Patients	2020	14

Page 1