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Maria Grigoriadou

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Mustafa Tekin; Suna Tokgoz-Yilmaz; Xia-Juan Xia; Juan I Young; Jun Aruga; F Basak Cengiz; Barry A Chioza; Harold E Cross; Oscar Diaz-Horta; Duygu Duman; Joseph Foster; Maria Grigoriadou; Kay Gurtz; Haris Kokotas; Yoshifumi Matsumoto; Heather L Moore-Barton; Yuri S Odaka; Maya Ota; Arti Pandya; Michael A Patton; Michael B Petersen; Kazuto Sakoori; Ajith Sreekantan-Nair; Oya Tekeli; Andrew H Crosby
SLITRK6 mutations cause myopia and deafness in humans and mice.
Dimitrios Chiras; Kleanthi Dima; Maria Grigoriadou; Anastasia Kastania; Haris Kokotas; Christos Kroupis; Samantha C Oliveira; Michael B Petersen; Maria Stefaniotou; Konstantina Tzika; Miltiadis Aspiotis; Georgios Kitsos
Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek population.
Haris Kokotas; Christos Kroupis; Klea Lamnissou; Michael B Petersen; Dimitrios Chiras; Maria Grigoriadou; Georgios Kitsos
Biomarkers in primary open angle glaucoma.

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2013: Mustafa Tekin; Suna Tokgoz-Yilmaz; Xia-Juan Xia; Juan I Young; Jun Aruga; F Basak Cengiz; Barry A Chioza; Harold E Cross; Oscar Diaz-Horta; Duygu Duman; Joseph Foster; Maria Grigoriadou; Kay Gurtz; Haris Kokotas; Yoshifumi Matsumoto; Heather L Moore-Barton; Yuri S Odaka; Maya Ota; Arti Pandya; Michael A Patton; Michael B Petersen; Kazuto Sakoori; Ajith Sreekantan-Nair; Oya Tekeli; Andrew H Crosby
SLITRK6 mutations cause myopia and deafness in humans and mice.
The Journal of clinical investigation 2013;123(5):2094-102.
2013: Dimitrios Chiras; Kleanthi Dima; Maria Grigoriadou; Anastasia Kastania; Haris Kokotas; Christos Kroupis; Samantha C Oliveira; Michael B Petersen; Maria Stefaniotou; Konstantina Tzika; Miltiadis Aspiotis; Georgios Kitsos
Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek population.
Molecular vision 2013;19():1006-16.
2012: Haris Kokotas; Christos Kroupis; Klea Lamnissou; Michael B Petersen; Dimitrios Chiras; Maria Grigoriadou; Georgios Kitsos
Biomarkers in primary open angle glaucoma.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2012;50(12):2107-19.
2012: Michael B Petersen; Maria Koutroumpe; Maria Grigoriadou; Haris Kokotas
The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness.
International journal of pediatric otorhinolaryngology 2012;76(7):969-71.
2012: Michael B Petersen; John Economides; Maria Grigoriadou; Haris Kokotas
Compound heterozygosity of the novel c.292C>T (p.R98W) and the c.35delG GJB2 mutations in postlingual, non-syndromic, sensorineural deafness.
International journal of pediatric otorhinolaryngology 2012;76(4):549-51.
2012: Haris Kokotas; Konstantina Papagiannaki; Michael B Petersen; Maria Grigoriadou; A Katsarou
Erythrokeratodermia variabilis: report of two cases and a novel missense variant in GJB4 encoding connexin 30.3.
European journal of dermatology : EJD 2012;22(2):182-6.
2011: Catherine Sarri; Virginia Theodorou; Zeynep Tümer; Kirstine Ravn; Theologia Sarafidou; Sofia Douzgou; Maria Grigoriadou; Yolanda Gyftodimou; GEORGIA KARADIMA; Haris Kokotas; Harry Kontos; Nicholas K Moschonas; Effie Pandelia; A Pasparaki; Michael B Petersen
Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
American journal of medical genetics. Part A 2011;155A(11):2841-54.
2011: Stavros Sifakis; Ourania Koukoura; N Mantas; Eleftheria Papadopoulou; Maria Grigoriadou; Jiannis Hajiioannou; George Vlahakis; Michael B Petersen
Antenatal diagnosis of duodenal atresia in dizygotic twins associated with congenital hearing impairment.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2011;24(6):871-2.
2011: Haris Kokotas; Maria Grigoriadou; Michael B Petersen
Age-related macular degeneration: genetic and clinical findings.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2011;49(4):601-16.
2011: Andreas Kotoulas; Daniel F Schorderet; Hasret Bajrami; Konstantinos Droutsas; Maria Grigoriadou; Haris Kokotas; Konstantinos Kopsidas; Michael B Petersen
A novel PIKFYVE mutation in fleck corneal dystrophy.
Molecular vision 2011;17():2776-81.
2011: Haris Kokotas; George S Korres; Stavros Korres; Elisa Ferekidou; Maria Grigoriadou; Dimitrios Kandiloros; Michael B Petersen
Detection of deafness-causing mutations in the Greek mitochondrial genome.
Disease markers 2011;30(6):283-9.
2011: Haris Kokotas; Maria Grigoriadou; Li Yang; Marianne Lodahl; Nanna Dahl Rendtorff; Yolanda Gyftodimou; George S Korres; Elisabeth Ferekidou; Dimitrios Kandiloros; Stavros Korres; Lisbeth Tranebjaerg; Min-Xin Guan; Michael B Petersen
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss.
International journal of pediatric otorhinolaryngology 2011;75(1):89-94.
2010: Silvia Naranjo; Krysta Voesenek; Elisa de la Calle-Mustienes; Alex Robert-Moreno; Haris Kokotas; Maria Grigoriadou; John Economides; Guy Van Camp; Nele Hilgert; Felipe Moreno; Berta Alsina; Michael B Petersen; Hannie Kremer; José Luis Gómez-Skarmeta
Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.
Human genetics 2010;128(4):411-9.
2010: Haris Kokotas; Maria Grigoriadou; George S Korres; Elisabeth Ferekidou; Dimitrios Kandiloros; Stavros Korres; Michael B Petersen
Screening of a Greek deafness population for the A7445G mitochondrial DNA mutation.
Molecular genetics and metabolism 2010;100(3):300-1.
2010: Asli Sirmaci; Seyra Erbek; Justin Price; Mingqian Huang; Duygu Duman; Filiz Basak Cengiz; Güney Bademci; Suna Tokgöz-Yilmaz; Burcu Hişmi; Hilal Ozdağ; Banu Oztürk; Sevsen Kulaksizoğlu; Erkan Yildirim; Haris Kokotas; Maria Grigoriadou; Michael B Petersen; Hashem Shahin; Moien Kanaan; Mary-Claire King; Zheng-Yi Chen; S Blanton; Xue Zhong Liu; Stephan Zuchner; Nejat Akar; Mustafa Tekin
A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.
American journal of human genetics 2010;86(5):797-804.
2010: Haris Kokotas; Maria Grigoriadou; George S Korres; Elisabeth Ferekidou; Aglaia Giannoulia-Karantana; Dimitrios Kandiloros; Stavros Korres; Michael B Petersen
Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?
Journal of human genetics 2010;55(5):265-9.
2010: Haris Kokotas; Maria Grigoriadou; Manuela Villamar; Aglaia Giannoulia-Karantana; Ignacio del Castillo; Michael B Petersen
Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?
Genetic testing and molecular biomarkers 2010;14(2):183-7.
2010: Haris Kokotas; Maria Grigoriadou; Angeliki Hatzaki; Thalia Antoniadi; Aglaia Giannoulia-Karantana; Michael B Petersen
Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.
Genetic testing and molecular biomarkers 2010;14(2):189-92.
2010: Georgios Kitsos; Zacharias Petrou; Maria Grigoriadou; John R Samples; Alex W Hewitt; Haris Kokotas; Aglaia Giannoulia-Karantana; David A Mackey; Mary K Wirtz; Marilita Moschou; John Ioannidis; Michael B Petersen
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece.
Clinical ophthalmology (Auckland, N.Z.) 2010;4():171-8.
2009: Haris Kokotas; Maria Grigoriadou; George S Korres; Elisabeth Ferekidou; Eleftheria Papadopoulou; Polyxene Neou; Aglaia Giannoulia-Karantana; Dimitrios Kandiloros; Stavros Korres; Michael B Petersen
The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
Biochemical and biophysical research communications 2009;390(3):755-7.
2009: Haris Kokotas; Maria Grigoriadou; M Mikkelsen; Aglaia Giannoulia-Karantana; Michael B Petersen
Investigating the impact of the Down syndrome related common MTHFR 677C>T polymorphism in the Danish population.
Disease markers 2009;27(6):279-85.
2008: Haris Kokotas; Lut Van Laer; Maria Grigoriadou; Vasiliki iliadou; John Economides; Stella Pomoni; Andreas Pampanos; Nikolaos Eleftheriades; Elisabeth Ferekidou; Stavros Korres; Aglaia Giannoulia-Karantana; Guy Van Camp; Michael B Petersen
Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population.
American journal of medical genetics. Part A 2008;146A(22):2879-84.
2008: Haris Kokotas; Maria Theodosiou; George Korres; Maria Grigoriadou; Elisabeth Ferekidou; Aglaia Giannoulia-Karantana; Michael B Petersen; Stavros Korres
Sudden hearing loss in a family with GJB2 related progressive deafness.
International journal of pediatric otorhinolaryngology 2008;72(11):1735-40.
2008: Marianna Bugiani; Yolanda Gyftodimou; Paraskevi Tsimpouka; Eleonora Lamantea; Eleni Katzaki; Pio d'Adamo; Sheena Nakou; Nelli Georgoudi; Maria Grigoriadou; Efthymia Tsina; Nikolaos Kabolis; Donatella Milani; Efthimia Pandelia; Haris Kokotas; Paolo Gasparini; Aglaia Giannoulia-Karantana; Alessandra Renieri; Massimo Zeviani; Michael B Petersen
Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population.
American journal of medical genetics. Part A 2008;146A(17):2221-6.
2008: Anastasia E Konstantinidou; Charalampos Karadimas; Hans R Waterham; andrea superti-furga; Petros Kaminopetros; Maria Grigoriadou; Haris Kokotas; George Agrogiannis; Aglaia Giannoulia-Karantana; Efstratios Patsouris; Michael B Petersen
Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia.
Prenatal diagnosis 2008;28(4):309-12.
2008: Assimina Galli-Tsinopoulou; Eleftheria Emmanouilidou; Paraskevi Karagianni; Maria Grigoriadou; John Kirkos; George S Varlamis
A female infant with Silver Russell Syndrome, mesocardia and enlargement of the clitoris.
Hormones (Athens, Greece) 2008;7(1):77-81.
2007: Melissa Thys; Kris Van Den Bogaert; Vasiliki iliadou; Kathleen Vanderstraeten; Nele Dieltjens; Isabelle Schrauwen; Wenjie Chen; Nikolaos Eleftheriades; Maria Grigoriadou; Robert J Pauw; Cor R W J Cremers; Richard J H Smith; Michael B Petersen; Guy Van Camp
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1.
European journal of human genetics : EJHG 2007;15(3):362-8.
2006: Z Yang; Georgios Kitsos; Z Tong; M Payne; Spiridon Gorezis; Konstantinos Psilas; Maria Grigoriadou; Y Zhao; S Kamaya; George Aperis; Michael B Petersen; K Zhang
A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family.
Journal of medical genetics 2006;43(12):e57.
2006: Hasan O Akman; Charalampos Karadimas; Yolanda Gyftodimou; Maria Grigoriadou; Haris Kokotas; Anastasia E Konstantinidou; Hector Anninos; Efstratios Patsouris; Harshwardhan M Thaker; Jeffrey B Kaplan; Isaam Besharat; Konstantina Hatzikonstantinou; Spyridon Fotopoulos; Salvatore DiMauro; Michael B Petersen
Prenatal diagnosis of glycogen storage disease type IV.
Prenatal diagnosis 2006;26(10):951-5.
2006: Vasiliki iliadou; Kris Van Den Bogaert; Nikolaos Eleftheriades; George Aperis; Kathleen Vanderstraeten; Erik Fransen; Melissa Thys; Maria Grigoriadou; Andreas Pampanos; John Economides; Theophilos Iliades; Guy Van Camp; Michael B Petersen
Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree.
International journal of pediatric otorhinolaryngology 2006;70(4):631-7.
2006: Michael B Petersen; Georgios Kitsos; John R Samples; N Donna Gaudette; Effrosini Economou-Petersen; Renée Sykes; Kristal Rust; Maria Grigoriadou; George Aperis; Dongseok Choi; Konstantinos Psilas; Jamie E Craig; Patricia L Kramer; David A Mackey; Mary K Wirtz
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variability.
Investigative ophthalmology & visual science 2006;47(2):620-5.
2006: Anna D Panani; Maria Grigoriadou; Eleni E Magira; Charis Roussos; Sotirios A Raptis
Perinuclear antineutrophil cytoplasmic antibody myeloperoxidase-positive vasculitis in association with ulcerative colitis.
Clinical rheumatology 2006;25(1):35-7.
2006: Catherine Sarri; Yolanda Gyftodimou; Maria Grigoriadou; Effie Pandelia; S Kalogirou; Haris Kokotas; Kristin Mrasek; Anja Weise; Michael B Petersen
Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face.
Cytogenetic and genome research 2006;114(3-4):330-7.
2004: Vasiliki iliadou; Nikolaos Eleftheriades; Aristomenis Metaxas; Antonios Skevas; Trifon Kiratzidis; Andreas Pampanos; Nikolaos Voyiatzis; Maria Grigoriadou; Michael B Petersen; Theophilos Iliades
Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2004;261(5):259-61.
2004: John R Samples; Georgios Kitsos; Effrosini Economou-Petersen; P Steinkamp; Renée Sykes; Kristal Rust; C Patzer; Maria Grigoriadou; George Aperis; Konstantinos Psilas; Michael B Petersen; Mary K Wirtz
Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis.
Clinical genetics 2004;65(1):40-4.
2003: Mazin B Qumsiyeh; Syed K Rafi; Catherine Sarri; Maria Grigoriadou; Jolanda Gyftodimou; Effie Pandelia; Hara Laskari; Michael B Petersen
Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy.
American journal of medical genetics. Part A 2003;116A(4):356-9.
2002: Voula Velissariou; Thalia Antoniadi; Jolanda Gyftodimou; Katerina Bakou; Maria Grigoriadou; Stavroula Christopoulou; Athina Hatzipouliou; Jackie Donoghue; Panagiotis Karatzis; Efstathia Katsarou; Michael B Petersen
Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis.
European journal of human genetics : EJHG 2002;10(11):694-8.
2002: Andreas Pampanos; John Economides; Vasiliki iliadou; Polyxeni Neou; Paulos Leotsakos; Nikolaos Voyiatzis; Nikolaos Eleftheriades; Michael Tsakanikos; Thalia Antoniadi; Angeliki Hatzaki; Irene Konstantopoulou; Drakoulis Yannoukakos; Karen Gronskov; karen brondum-nielsen; Maria Grigoriadou; Jolanda Gyftodimou; Theophilos Iliades; Antonios Skevas; Michael B Petersen
Prevalence of GJB2 mutations in prelingual deafness in the Greek population.
International journal of pediatric otorhinolaryngology 2002;65(2):101-8.
2002: Theophilos Iliades; Nikolaos Eleftheriades; Vasiliki iliadou; Andreas Pampanos; Nikolaos Voyiatzis; John Economides; P Leotsakos; Polyxeni Neou; Michael Tsakanikos; Thalia Antoniadi; Irene Konstantopoulou; Drakoulis Yannoukakos; Maria Grigoriadou; Antonios Skevas; Michael B Petersen
Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.
ORL; journal for oto-rhino-laryngology and its related specialties 2002;64(5):321-3.
2000: Andreas Pampanos; Polyxeni Neou; Theophilos Iliades; Nikolaos Apostolopoulos; Nikolaos Voyiatzis; Maria Grigoriadou; L Katsichti; Antonios Skevas; Michael B Petersen
Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation.
Clinical genetics 2000;57(3):232-4.
1998: GEORGIA KARADIMA; Merete Bugge; P Nicolaidis; Dimitrios Vassilopoulos; Dimitrios Avramopoulos; Maria Grigoriadou; Beate Albrecht; Eberhard Passarge; Göran Annerén; Elisabeth Blennow; Niels Clausen; Angeliki Galla-Voumvouraki; Aspasia Tsezou; Sophia Kitsiou-Tzeli; Johanne M D Hahnemann; Jens Michael Hertz; Gunnar Houge; M Kuklík; Milan Macek Jr.; D Lacombe; K Miller; A Moncla; I López Pajares; Philippos C Patsalis; Michael B Petersen
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
European journal of human genetics : EJHG 1998;6(5):432-8.
1998: Maria Syrrou; Ioannis Georgiou; Maria Grigoriadou; Michael B Petersen; Sophia Kitsiou-Tzeli; Gerassimos N Pagoulatos; Philippos C Patsalis
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
Genetic epidemiology 1998;15(1):103-9.
1997: Catherine Sarri; Jolanda Gyftodimou; Dimitrios Avramopoulos; Maria Grigoriadou; W Pedersen; Effie Pandelia; Constantinos Pangalos; Danae Abazis; Georgios Kitsos; Dimitrios Vassilopoulos; Karen Brøndum-Nielsen; Michael B Petersen
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter.
American journal of medical genetics 1997;70(1):87-94.
1996: Dimitrios Avramopoulos; G Kitsos; Effrosini Economou-Petersen; Maria Grigoriadou; Dimitrios Vassilopoulos; C Papageorgiou; Konstantinos Psilas; Michael B Petersen
Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31.
Journal of medical genetics 1996;33(12):1043-4.
1996: Dimitrios Avramopoulos; M Mikkelsen; Dimitrios Vassilopoulos; Maria Grigoriadou; Michael B Petersen
Apolipoprotein E allele distribution in parents of Down's syndrome children.
Lancet 1996;347(9005):862-5.
1994: Euterpe Bazopoulou-Kyrkanidou; I Vrotsos; S Kyrkanides; K Tsichlakis; Konstantinos I Tosios; K Mandalenaki-Lambrou; A Kondyli; H Nassi; Catherine Sarri; Maria Grigoriadou
Hyperbrachycephaly, short face, midface hypoplasia, fusion of cervical vertebrae, radiolucent bone defects, and severe destruction of periodontium--a new syndrome: craniofaciocervical osteoglyphic dysplasia.
Genetic counseling (Geneva, Switzerland) 1994;5(3):257-67.
1992: Catherine Sarri; Constantin N Baxevanis; Gilbert B. Côté; G J Reclos; E Sarafidou; T Spanos; M Papanastasiou; Maria Grigoriadou; Michael Papamichail
Sister-chromatid exchange in highly purified human CD4+ and CD8+ lymphocytes.
Mutation research 1992;270(2):125-33.