DNA, diseases and databases: disastrously deficientPATRINOS, George P; BROOKES, Anthony J.Trends in genetics (Regular ed.). 2005, Vol 21, Num 6, pp 333-338, issn 0168-9525, 6 p.Article

Mutation screening in the human ε-globin gene using single-strand conformation polymorphism analysisPAPACHATZOPOULOU, Adamantia; MENOUNOS, Panagiotis G; KOLONELOU, Christina et al.American journal of hematology. 2006, Vol 81, Num 2, pp 136-138, issn 0361-8609, 3 p.Article

Molecular diagnosis of neurogenetic disordersPATRINOS, George P; GARINIS, George A.Recent research developments in neuroscience (Vol. 1 (2004)). Recent research developments in neuroscience. 2003, pp 43-60, isbn 81-7736-207-0, 18 p.Book Chapter

A versatile denaturing HPLC approach for human β-globin gene mutation screeningBOURNAZOS, Stavros N; TSERGA, Aggeliki; PATRINOS, George P et al.American journal of hematology. 2007, Vol 82, Num 2, pp 168-170, issn 0361-8609, 3 p.Article

Gene conversion : mechanisms, evolution and human diseaseCHEN, Jian-Min; COOPER, David N; CHUZHANOVA, Nadia et al.Nature reviews. Genetics (Print). 2007, Vol 8, Num 10, pp 762-775, issn 1471-0056, 14 p.Article

DNA hypermethylation: when tumour suppressor genes go silentGARINIS, George A; PATRINOS, George P; SPANAKIS, Nick E et al.Human genetics. 2002, Vol 111, Num 2, pp 115-127, issn 0340-6717Article

A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotesPAPADAKIS, Manoussos N; PATRINOS, George P; TSAFTARIDIS, Panayotis et al.Journal of molecular medicine (Berlin. Print). 2002, Vol 80, Num 4, pp 243-247, issn 0946-2716Article

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachGIARDINE, Belinda; BORG, Joseph; COSTA, Flavia C et al.Nature genetics. 2011, Vol 43, Num 4, pp 295-301, issn 1061-4036, 7 p.Article

RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease ResearchTHOMPSON, Rachel; JOHNSTON, Louise; ENSINI, Monica et al.Journal of general internal medicine. 2014, Vol 29, issn 0884-8734, S780-S787, SUP3Article

Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central greece compared to the rest of the countrySAMARA, Maria; CHIOTOGLOU, Ioanna; KOLLIA, Panagoula et al.American journal of hematology. 2007, Vol 82, Num 7, pp 634-636, issn 0361-8609, 3 p.Article

Haploinsufficiency for the erythroid transcription factor KLF 1 causes hereditary persistence of fetal hemoglobinBORG, Joseph; PAPADOPOULOS, Petros; CASSAR, Wilhelmina et al.Nature genetics. 2010, Vol 42, Num 9, pp 801-805, issn 1061-4036, 5 p.Article

Increased γ-globin gene expression in β-thalassemia intermedia patients correlates with a mutation in 3'HS1PAPACHATZOPOULOU, Adamantia; KAIMAKIS, Polynikis; POURFARZAD, Farzin et al.American journal of hematology. 2007, Vol 82, Num 11, pp 1005-1009, issn 0361-8609, 5 p.Article

Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the β^s/benin haplotypePATRINOS, George P; SAMPERI, Piera; LO NIGRO, Luca et al.American journal of hematology. 2005, Vol 80, Num 1, pp 79-80, issn 0361-8609, 2 p.Article

Hypermethylation-associated transcriptional silencing of E-cadherin in primary sporadic colorectal carcinomasGARINIS, George A; MENOUNOS, Panayiotis G; SPANAKIS, Nick E et al.Journal of pathology. 2002, Vol 198, Num 4, pp 442-449, issn 0022-3417, 8 p.Article

Population-ethnic group specific genome variation allele frequency data: A querying and visualization journeyVIENNAS, Emmanouil; GKANTOUNA, Vassiliki; IOANNOU, Marina et al.Genomics (San Diego, Calif.). 2012, Vol 100, Num 2, pp 93-101, issn 0888-7543, 9 p.Article

High frequency of concomitant nm23-H1 and E-cadherin transcriptional inactivation in primary non-inheriting colorectal carcinomasGARINIS, George A; MANOLIS, Evangelos N; SPANAKIS, Nick E et al.Journal of molecular medicine (Berlin. Print). 2003, Vol 81, Num 4, pp 256-263, issn 0946-2716, 8 p.Article

Aγ-haplotypes : A new group of genetic markers for thalassemic mutations inside the 5' regulatory region of the human Aγ-globin genePATRINOS, George P; KOLLIA, Panagoula; PAPAPANAGIOTOU, Elisavet et al.American journal of hematology. 2001, Vol 66, Num 2, pp 99-104, issn 0361-8609Article