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Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia

Translational psychiatry, 2018-11, Vol.8 (1), p.252-10, Article 252

2018

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Investigation of genetic base in the treatment of age-related macular degeneration

International ophthalmology, 2020-04, Vol.40 (4), p.985-997

2020

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miRNA polymorphisms and risk of premature coronary artery disease

Hellenic journal of cardiology, 2021-07, Vol.62 (4), p.278-284

2021

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Toll-like receptor signaling pathway in chronic lymphocytic leukemia: distinct gene expression profiles of potential pathogenic significance in specific subsets of patients

Haematologica (Roma), 2011-11, Vol.96 (11), p.1644-1652

2011

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Evaluating the glucose raising effect of established loci via a genetic risk score

PloS one, 2017-11, Vol.12 (11), p.e0186669-e0186669

2017

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Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study

BMC psychiatry, 2018-08, Vol.18 (1), p.249-249, Article 249

2018

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Genetic Variation of DKK3 May Modify Renal Disease Severity in ADPKD

Journal of the American Society of Nephrology, 2010-09, Vol.21 (9), p.1510-1520

2010

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Genetic Variant in the CYP19A1 Gene Associated with Coronary Artery Disease

Genetics Research International, 2015-01, Vol.2015, p.80-84

2015

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Evidence for association of the G1733A polymorphism of the androgen receptor gene with recurrent spontaneous abortions

Fertility and sterility, 2008-11, Vol.90 (5), p.2010.e9-2010.e12

2008

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Expression of miR-208b and miR-499 in Greek Patients with Acute Myocardial Infarction

In vivo (Athens), 2018-03, Vol.32 (2), p.313-318

2018

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Study on the admission levels of circulating cell-free DNA in patients with acute myocardial infarction using different quantification methods

Scandinavian journal of clinical and laboratory investigation, 2020-07, Vol.80 (4), p.348-350

2020

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Evidence for association of the rs605059 polymorphism of HSD17B1 gene with recurrent spontaneous abortions

The journal of maternal-fetal & neonatal medicine, 2015-12, Vol.28 (18), p.2250-2253

2015

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Sites of Differential DNA Methylation between Placenta and Peripheral Blood: Molecular Markers for Noninvasive Prenatal Diagnosis of Aneuploidies

The American journal of pathology, 2009-05, Vol.174 (5), p.1609-1618

2009

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Biomarkers in primary open angle glaucoma

Clinical chemistry and laboratory medicine, 2012-12, Vol.50 (12), p.2107-2119

2012

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MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21

Prenatal diagnosis, 2012-10, Vol.32 (10), p.996-1001

2012

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Gender Specificity of a Genetic Variant of Androgen Receptor and Risk of Coronary Artery Disease

Journal of clinical laboratory analysis, 2016-05, Vol.30 (3), p.204-207

2016

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Incompatibilities between Y chromosome and autosomes are responsible for male hybrid sterility in crosses between Drosophila virilis and Drosophila texana

Heredity, 1996-06, Vol.76 (6), p.603-609

1996

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Genetic variant in the CYP19 gene and recurrent spontaneous abortions

Gene reports, 2017-03, Vol.6, p.41-43

2017

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Genetic variant in the CYP17 gene and risk of premature coronary artery disease

Hellenic journal of cardiology, 2014-03, Vol.55 (2), p.126

2014

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Genetic variation in the HSD3B1 gene and recurrent spontaneous abortions

The journal of maternal-fetal & neonatal medicine, 2012-04, Vol.25 (4), p.408-410

2012

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Endothelial nitric oxide synthase gene polymorphisms in recurrent spontaneous abortions

Archives of gynecology and obstetrics, 2008-10, Vol.278 (4), p.349-352

2008

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Genetic variation in the CYP17 gene and recurrent spontaneous abortions

Archives of gynecology and obstetrics, 2011-02, Vol.283 (2), p.289-293

2011

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Screening for Familial Mediterranean Fever M694V and V726A mutations in the Greek population

Genetic testing and molecular biomarkers, 2009-06, Vol.13 (3), p.291-293

2009

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Lack of association between endothelial nitric oxide synthase gene polymorphisms and risk of premature coronary artery disease in the Greek population

Acta Cardiologica, 2008-10, Vol.63 (5), p.609-614

2008

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Sites of Differential DNA Methylation between Placenta and Peripheral Blood

The American journal of pathology, 2009, Vol.174 (5), p.1609-1618

2009

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Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia

Investigation of genetic base in the treatment of age-related macular degeneration

miRNA polymorphisms and risk of premature coronary artery disease

Toll-like receptor signaling pathway in chronic lymphocytic leukemia: distinct gene expression profiles of potential pathogenic significance in specific subsets of patients

Evaluating the glucose raising effect of established loci via a genetic risk score

Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study

Genetic Variation of DKK3 May Modify Renal Disease Severity in ADPKD

Genetic Variant in the CYP19A1 Gene Associated with Coronary Artery Disease

Evidence for association of the G1733A polymorphism of the androgen receptor gene with recurrent spontaneous abortions

Expression of miR-208b and miR-499 in Greek Patients with Acute Myocardial Infarction

Study on the admission levels of circulating cell-free DNA in patients with acute myocardial infarction using different quantification methods

Evidence for association of the rs605059 polymorphism of HSD17B1 gene with recurrent spontaneous abortions

Sites of Differential DNA Methylation between Placenta and Peripheral Blood: Molecular Markers for Noninvasive Prenatal Diagnosis of Aneuploidies

Biomarkers in primary open angle glaucoma

MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21

Gender Specificity of a Genetic Variant of Androgen Receptor and Risk of Coronary Artery Disease

Incompatibilities between Y chromosome and autosomes are responsible for male hybrid sterility in crosses between Drosophila virilis and Drosophila texana

Genetic variant in the CYP19 gene and recurrent spontaneous abortions

Genetic variant in the CYP17 gene and risk of premature coronary artery disease

Genetic variation in the HSD3B1 gene and recurrent spontaneous abortions

Endothelial nitric oxide synthase gene polymorphisms in recurrent spontaneous abortions

Genetic variation in the CYP17 gene and recurrent spontaneous abortions

Screening for Familial Mediterranean Fever M694V and V726A mutations in the Greek population

Lack of association between endothelial nitric oxide synthase gene polymorphisms and risk of premature coronary artery disease in the Greek population

Sites of Differential DNA Methylation between Placenta and Peripheral Blood

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