G. Dedoussis

Wilson Disease: High Prevalence in a Mountaineous Area of Crete

E. Tsafantakis, J. Genschel, B. Bochow, 2005 .

Liver transplantation in a subject with familial hypercholesterolemia carrying the homozygous p.W577R LDL‐receptor gene mutation

H. Schlitt, K. Oldhafer, U. Tietge, 2007, Clinical transplantation.

Fetal hemoglobin expression in the compound heterozygous state for−117 (G→A) Aγ HPFH and IVS‐1 nt 110 (G→A) β+ thalassemia: a case study

K. Sinopoulou, G. Dedoussis, M. Gyparaki, 2000, European journal of haematology.

Genetic mechanisms of 184 neuro-related proteins in human plasma

R. Marioni, A. Reiner, I. Deary, 2023, medRxiv.

Development of a high-resolution melting method for mutation detection in familial hypercholesterolaemia patients

S. Humphries, G. Dedoussis, C. Hubbart, 2010, Annals of clinical biochemistry.

FH clinical phenotype in Greek patients with LDL‐R defective vs. negative mutations

G. Dedoussis, C. Stefanadis, C. Pitsavos, 2004, European journal of clinical investigation.

Co‐inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney disease

H. Cantiello, G. Dedoussis, P. Harris, 2008, European journal of clinical investigation.

Liver transplantation in a subject with familial hypercholesterolemia carrying the homozygous p.W577R LDL‐receptor gene mutation

H. Schlitt, K. Oldhafer, U. Tietge, 2007, Clinical transplantation.