M. Grigoriadou

发表

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.

D. Vassilopoulos, K. Brøndum‐Nielsen, G. Kitsos, 1997, American journal of medical genetics.

ZrO2 three-unit fixed partial dentures: comparison of failure load before and after exposure to a mastication simulator.

J. Strub, W. Att, M. Grigoriadou, 2007, Journal of oral rehabilitation.

Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population

M. Zeviani, P. Gasparini, E. Lamantea, 2008, American journal of medical genetics. Part A.

Sister-chromatid exchange in highly purified human CD4+ and CD8+ lymphocytes.

C. Baxevanis, M. Papamichail, C. Sarri, 1992, Mutation research.

Effectiveness of a Community-Based Crisis Resolution Team for Patients with Severe Mental Illness in Greece: A Prospective Observational Study

M. Grigoriadou, M. Margariti, Aikaterini Koureta, 2022, Community Mental Health Journal.

A female infant with Silver Russell Syndrome, mesocardia and enlargement of the clitoris

J. Kirkos, A. Galli-Tsinopoulou, M. Grigoriadou, 2008, Hormones.

Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece

J. Ioannidis, D. Mackey, A. Hewitt, 2010, Clinical ophthalmology.

Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia

H. Waterham, E. Patsouris, A. Konstantinidou, 2008, Prenatal diagnosis.

Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?

M. Petersen, I. del Castillo, M. Villamar, 2010, Genetic testing and molecular biomarkers.

Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population

J. Economides, A. Pampanos, G. Van Camp, 2008, American journal of medical genetics. Part A.

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism

E. Blennow, S. Kitsiou‐Tzeli, A. Tsezou, 1998, European Journal of Human Genetics.

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

Z. Tümer, N. Moschonas, S. Douzgou, 2011, American journal of medical genetics. Part A.

Clinical and hemorheological effects of buflomedil in diabetic subjects with intermittent claudication.

S. Raptis, G. Ifanti, E. Diamantopoulos, 2001, International angiology : a journal of the International Union of Angiology.

Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis

M. Petersen, V. Velissariou, E. Katsarou, 2002, European Journal of Human Genetics.

Prelingual Nonsyndromic Hearing Loss in Greece

D. Yannoukakos, J. Economides, A. Pampanos, 2002, ORL.

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

D. Yannoukakos, J. Economides, K. Brøndum‐Nielsen, 2002, International journal of pediatric otorhinolaryngology.

The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness.

M. Petersen, M. Grigoriadou, H. Kokotas, 2012, International journal of pediatric otorhinolaryngology.

A novel PIKFYVE mutation in fleck corneal dystrophy

D. Schorderet, M. Petersen, K. Droutsas, 2011, Molecular vision.

Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.

M. Petersen, M. Grigoriadou, T. Antoniadi, 2010, Genetic testing and molecular biomarkers.

35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome

K. Papanikolaou, Z. Tümer, K. Anagnostopoulou, 2015, Cytogenetic and Genome Research.

Monogenic nonsyndromic otosclerosis: audiological and linkage analysis in a large Greek pedigree.

J. Economides, E. Fransen, M. Petersen, 2006, International journal of pediatric otorhinolaryngology.

Effectiveness of a Community-Based Crisis Resolution Team for Patients with Severe Mental Illness in Greece: A Prospective Observational Study

M. Grigoriadou, M. Margariti, Aikaterini Koureta, 2022, Community Mental Health Journal.

Biomarkers in primary open angle glaucoma

K. Lamnissou, M. Petersen, G. Kitsos, 2012, Clinical chemistry and laboratory medicine.

Interleukin-1 as a genetic marker for periodontitis: review of the literature.

S. Koutayas, J. Strub, P. Madianos, 2010, Quintessence international.

Double supernumerary isodicentric chromosomes derived from 15 resulting in partial hexasomy

M. Qumsiyeh, S. K. Rafi, J. Gyftodimou, 2003, American journal of medical genetics. Part A.

Prenatal diagnosis of glycogen storage disease type IV

S. Dimauro, E. Patsouris, A. Konstantinidou, 2006, Prenatal diagnosis.

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face

K. Mrasek, Y. Gyftodimou, M. Petersen, 2006, Cytogenetic and Genome Research.

Antenatal diagnosis of duodenal atresia in dizygotic twins associated with congenital hearing impairment

S. Sifakis, M. Petersen, O. Koukoura, 2011, 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.

Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek population

M. Petersen, G. Kitsos, A. Kastania, 2013, Molecular vision.

A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13–16.1

C. Cremers, M. Petersen, Richard J. H. Smith, 2007, European Journal of Human Genetics.

Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing

H. Kremer, J. Economides, J. Gómez-Skarmeta, 2010, Human Genetics.

FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population

P. Patsalis, I. Georgiou, M. Petersen, 1998, Genetic epidemiology.

M. Petersen, M. Grigoriadou, H. Kokotas, 2011, Clinical chemistry and laboratory medicine.

Meiotic Nondisjunction—The Major Cause of Trisomy 21

M. Petersen, M. Grigoriadou, H. Kokotas, 2007 .

Investigating the Impact of the Down Syndrome Related Common MTHFR 677C>T Polymorphism in the Danish Population

M. Petersen, M. Mikkelsen, M. Grigoriadou, 2010, Disease Markers.

A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family

Z. Tong, G. Kitsos, K. Psilas, 2006, Journal of Medical Genetics.

A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.

M. King, M. Tekin, X. Liu, 2010, American journal of human genetics.

with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

M. Tekin, S. Züchner, X. Liu, 2010 .

A common mutation in the methylenetetrahydrofolate reductase gene is not a risk factor for Down syndrome in a population-based study

M. Petersen, M. Mikkelsen, M. Grigoriadou, 2000 .

Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31.

D. Vassilopoulos, G. Kitsos, K. Psilas, 1996, Journal of medical genetics.

Perinuclear antineutrophil cytoplasmic antibody myeloperoxidase-positive vasculitis in association with ulcerative colitis

C. Roussos, S. Raptis, A. Panani, 2006, Clinical Rheumatology.

Apolipoprotein E allele distribution in parents of Down's syndrome children

D. Avramopoulos, D. Vassilopoulos, M. Petersen, 1996, The Lancet.

The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.

G. Korres, M. Petersen, D. Kandiloros, 2009, Biochemical and biophysical research communications.

Management and outcome of severe diabetic foot infections.

S. Raptis, E. Diamantopoulos, M. Grigoriadou, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Detection of Deafness-Causing Mutations in the Greek Mitochondrial Genome

G. Korres, M. Petersen, D. Kandiloros, 2011, Disease markers.

Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation

N. Apostolopoulos, A. Pampanos, M. Petersen, 2000, Clinical genetics.

Screening of a Greek deafness population for the A7445G mitochondrial DNA mutation.

G. Korres, M. Petersen, D. Kandiloros, 2010, Molecular genetics and metabolism.

Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?

G. Korres, M. Petersen, D. Kandiloros, 2010, Journal of Human Genetics.

Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss.

G. Korres, Y. Gyftodimou, M. Petersen, 2011, International journal of pediatric otorhinolaryngology.

Sudden hearing loss in a family with GJB2 related progressive deafness.

G. Korres, M. Petersen, M. Grigoriadou, 2008, International journal of pediatric otorhinolaryngology.

Erythrokeratodermia variabilis: report of two cases and a novel missense variant in GJB4 encoding connexin 30.3.

M. Petersen, A. Katsarou, M. Grigoriadou, 2012, European journal of dermatology : EJD.

SLITRK6 mutations cause myopia and deafness in humans and mice.

Juan I. Young, M. Tekin, A. Pandya, 2013, The Journal of clinical investigation.

SLITRK 6 mutations cause myopia and deafness in humans and mice

Juan I. Young, M. Tekin, A. Pandya, 2013 .

Refining the primary open‐angle glaucoma GLC1C region on chromosome 3 by haplotype analysis

M. K. Wirtz, G. Kitsos, K. Psilas, 2003, Clinical genetics.

Impaired erythrocyte deformability precedes vascular changes in experimental diabetes mellitus.

C. Kittas, S. Raptis, G. Ifanti, 2004, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece

A. Pampanos, M. Petersen, V. Iliadou, 2004, European Archives of Oto-Rhino-Laryngology and Head & Neck.

Depressive symptomatology, attachment style, job insecurity and burnout of civil servants in the Greek economic crisis

G. Kleftaras, M. Grigoriadou, 2017 .

Compound heterozygosity of the novel c.292C>T (p.R98W) and the c.35delG GJB2 mutations in postlingual, non-syndromic, sensorineural deafness.

J. Economides, M. Petersen, M. Grigoriadou, 2012, International Journal of Pediatric Otorhinolaryngology.

Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.

H. Kremer, J. Economides, J. Gómez-Skarmeta, 2010, Human genetics.