K. Agiannitopoulos

发表

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

C. Markopoulos, A. Apessos, G. Nasioulas, 2019, BMC Cancer.

Molecular predictive markers in tumors of the gastrointestinal tract

A. Apessos, G. Nasioulas, V. Metaxa-Mariatou, 2016, World journal of gastrointestinal oncology.

Characterization of the c.793-1G > A splicing variant in CHEK2 gene as pathogenic: a case report

M. Koçdor, S. Kampouri, G. Nasioulas, 2019, BMC Medical Genetics.

Clinical Utility of Functional RNA Analysis for the Reclassification of Splicing Gene Variants in Hereditary Cancer

C. Markopoulos, S. Kampouri, C. Christodoulou, 2021, Cancer Genomics & Proteomics.

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

K. Lamnissou, A. Manginas, K. Agiannitopoulos, 2014, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Genetic Variant in the CYP 17 Gene and Risk of Premature Coronary Artery Disease

K. Lamnissou, A. Manginas, K. Agiannitopoulos, 2014 .

Comprehensive BRCA mutation analysis in the Greek population. Experience from a single clinical diagnostic center.

C. Markopoulos, A. Apessos, G. Nasioulas, 2018, Cancer genetics.

Genetic variation in the HSD3B1 gene and recurrent spontaneous abortions

K. Lamnissou, K. Pantos, K. Agiannitopoulos, 2012, 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.

Genetic variation in the CYP17 gene and recurrent spontaneous abortions

K. Lamnissou, K. Pantos, K. Agiannitopoulos, 2011, Archives of Gynecology and Obstetrics.

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

C. Markopoulos, A. Apessos, S. Kampouri, 2019, BMC Cancer.

Revisiting the Implications of Positive Germline Testing Results Using Multi-gene Panels in Breast Cancer Patients

I. Boukovinas, C. Markopoulos, A. Psyrri, 2021, Cancer Genomics & Proteomics.

Revisiting the implications of positive germline testing results using multi-gene panels in a cohort of individuals with personal and/or family history of Breast cancer

Ioannis, Banu, C. Markopoulos, 2021 .

Report of a germline double heterozygote in MSH2 and PALB2

S. Kampouri, G. Nasioulas, G. Tsaousis, 2020, Molecular genetics & genomic medicine.

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

K. Lamnissou, P. Samara, K. Tsamis, 2018, In vivo.

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

Konstantinos Pantos, Georgios Tsaousis, K. Lamnissou, 2015, 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.

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

E. Marouli, K. Lamnissou, A. Manginas, 2016, Journal of clinical laboratory analysis.

Determination of EGFR and KRAS mutational status in Greek non-small-cell lung cancer patients

G. Aravantinos, M. Gaga, A. Apessos, 2015, Oncology letters.

A novel deletion of exon 4 in the Ectodysplasin A gene associated with X-linked hypohidrotic ectodermal dysplasia.

C. Yapijakis, G. Nasioulas, G. Tsaousis, 2023, Archives of oral biology.

miRNA polymorphisms and risk of premature coronary artery disease.

K. Lamnissou, P. Samara, G. Tsaousis, 2020, Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese.

Reclassification of Splicing Gene Variants in Hereditary Cancer: Cases Report and Literature Review

G. Nasioulas, G. Tsaousis, E. Papadopoulou, 2023, In Vivo.

CNV and RNA analysis reveal a germline pathogenic duplication of MSH2 exon 15 in a family with Lynch syndrome: A case report

K. Agiannitopoulos, 2023, Journal of Clinical Images and Medical Case Reports.

Genetic variant in the CYP19 gene and recurrent spontaneous abortions

K. Lamnissou, K. Agiannitopoulos, A. Hatzaki, 2017 .

Abstract P4-03-07: Analysis of hereditary cancer syndromes by using a panel of genes: Novel and multiple pathogenic mutations

C. Markopoulos, A. Apessos, G. Nasioulas, 2019, Poster Session Abstracts.