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Αβραμόπουλος Δ, Κίτσος Γ, Γρηγοριάδου Μ, Οικονόμου-Petersen Ε, Βασιλόπουλος Δ, Ψύλλας Κ, Petersen MB. Το πρωτογενές γλαύκωμα ανοικτής γωνίας ως παράδειγμα μιας αυτοσωματικής επικρατητικής νόσου. Κλινικά Χρονικά 1994;17:62-70.
Avramopoulos D, Kitsos G, Economou-Petersen E, Grigoriadou M, Vassilopoulos D, Papageorgiou C, Psilas K, Petersen MB. Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31. J Med Genet 1996;33:1043-1044.
Hertz JM, Juncker I, Persson U, Matthijs G, Schmidtke J, Petersen MB, Kjeldsen M, Gregersen N. Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome. Hum Mutat 2001;18:141-148.
Kitsos G, Eiberg H, Economou-Petersen E, Wirtz MK, Kramer PL, Aspiotis M, Tommerup N, Petersen MB, Psilas K. Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree. Eur J Hum Genet 2001;9:452-457.
Samples JR, Kitsos G, Economou-Petersen E, Steinkamp P, Sykes R, Rust K, Patzer C, Grigoriadou M, Aperis G, Psilas K, Petersen MB, Wirtz MK. Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis. Clin Genet 2004;65:40-44.
Nikas A, Kitsos G, Petersen MB, Papakostas V, Psylla M, Stefaniotou M. Stickler syndrome type II in a 10-year old boy. Ann Ophthalmol 2004;36:124-128.
Petersen MB, Kitsos G, Samples JR, Gaudette ND, Economou-Petersen E, Sykes R, Rust K, Grigoriadou M, Aperis G, Choi D, Psilas K, Craig JE, Kramer PL, Mackey DA, Wirtz MK. A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability. Invest Ophthalmol Vis Sci 2006;47:620-625.
Yang Z, Kitsos G, Tong Z, Payne M, Gorezis S, Psilas K, Grigoriadou M, Zhao Y, Kamaya S, Aperis G, Petersen MB, Zhang K. A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family. J Med Genet 2006;43:e57.
Hewitt AW, Samples JR, Allingham RR, Jarvela I, Kitsos G, Krishnadas SR, Richards JE, Lichter PR, Petersen MB, Sundaresan P, Wiggs JL, Mackey DA, Wirtz MK. Investigation of founder effects for the Thr377Met myocilin mutation in glaucoma families from differing ethnic backgrounds. Mol Vis 2007;13:487-492.
Πέτρου Ζ, Hewitt AW, Samples JR, Mackey DA, Wirtz MK, Petersen MB, Κίτσος Γ. Ιδρυτική μεταλλαγή Thr377Met της μυοσιλίνης σε εννέα οικογένειες με πρωτοπαθές γλαύκωμα ανοικτής γωνίας με διαφορετική μεταξύ τους εθνική καταγωγή. Οφθαλμολογικά Χρονικά 2007;17:289-294.
Wirtz MK, Konstas AGP, Samples JR, Kaltsos K, Economou A, Dimopoulos A, Georgiadou I, Petersen M. Myocilin variations and familial glaucoma in Taxiarchis, a small Greek village. Mol Vis 2008;14:774-781.
Bugiani M, Gyftodimou Y, Tsimpouka P, Lamantea E, Katzaki E, d’Adamo P, Nakou S, Georgoudi N, Grigoriadou M, Tsina E, Kabolis N, Milani D, Pandelia E, Kokotas H, Gasparini P, Giannoulia-Karantana A, Renieri A, Zeviani M, Petersen MB. Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population. Am J Med Genet (in press).
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