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Profil bibliographique

Konstantinos Agiannitopoulos

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

56Publications signalées
435Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

BRCA gene mutations in cancerGenetic factors in colorectal cancerCancer Genomics and DiagnosticsGenomics and Rare DiseasesNutrition, Genetics, and Disease

Les publications récentes

Accès ouvert 2026 article OpenAlex

Investigation of IgM Monoclonal Paraprotein in Bone Marrow Aspiration: The Role of Immunophenotyping by Flow Cytometry in Selecting Cases for Molecular Testing for the p.MYD88 L265P Point Mutation

Georgios Boutsikas, Konstantinos Agiannitopoulos, Elisavet Kouvidi, Myrto Katraki et autres

BACKGROUND: Flow cytometry and real-time quantitative polymerase chain reaction (qRT-PCR) for MYD88 mutations (MYD88mt) are routinely performed on bone marrow aspirates during the diagnostic evaluation of IgM monoclonal paraproteinemia. The potential predictive value of immunophenotypic findings for molecular results, however, remains to …

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0 citations International Journal of Laboratory Hematology
Accès ouvert 2026 article OpenAlex

Flow Cytometry Immunophenotyping in Hematology Clinical Practice: Panacea or a Diagnostic Tool? Conclusions from a Case Report

Georgios Boutsikas, Konstantinos Agiannitopoulos, Ioannis Anagnostopoulos, Myrofora Vikentiou et autres

Flow cytometry is an essential diagnostic method in hematology, and one of its main applications is the assessment of the clonality of mature B cells. We present a case report of a patient referred for the investigation of absolute lymphocytosis. The flow …

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0 citations Hemato
Accès ouvert 2026 article OpenAlex

Pilot analysis of protein profile alterations in plasma and aortic tissue of spontaneously hypertensive rats

Anastasios Papageorgiou, Fragkiski-Ioanna Sofiou, ANASTASSIOS PHILIPPOU, Maria Gkrampovari et autres

The role of proteins in cellular activity has received close attention. Proteome analysis can detect early enough changes in the cell before the appearance of pathological changes. Due to the increasing number of cardiovascular complications, more specifically hypertension in modern life, this …

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0 citations Acta Biochimica Polonica
Accès ouvert 2026 article OpenAlex

The Role of Next-Generation Sequencing in Cardiovascular Disease: A New Era of Precision Cardiology

Konstantinos Agiannitopoulos, Anastasios Papageorgiou, Elisavet Kouvidi, Eleni Kalampoka et autres

Cardiovascular diseases (CVDs) are the foremost contributor to global mortality, with a significant inherited factor that has long been recognized but only recently become decipherable. Next-generation sequencing (NGS) has transformed the study of cardiovascular genetics, allowing researchers to move beyond single-gene analyses …

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1 citation Life
Accès ouvert 2025 article OpenAlex

The Application of Next-Generation Sequencing in Leukemia

Konstantinos Agiannitopoulos, Elisavet Kouvidi

Leukemia is a heterogeneous group of hematologic malignancies characterized by the dysfunctional proliferation of white blood cells in the bone marrow. Genetic alterations are important risk factors for the development and progression of leukemia, and their detection is crucial. Although many genetic …

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1 citation OBM Genetics
Accès ouvert 2024 article OpenAlex

The Clinical and Genetic Landscape of Hereditary Cancer: Experience from a Single Clinical Diagnostic Laboratory

Nikolaos Tsoulos, Konstantinos Agiannitopoulos, Kevisa Potska, Anastasia Katseli et autres

BACKGROUND/AIM: The application of next-generation sequencing (NGS) technology in the genetic investigation of hereditary cancer is important for clinical surveillance, therapeutic approach, and reducing the risk of developing new malignancies. The aim of the study was to explore genetic predisposition in individuals …

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7 citations Cancer Genomics & Proteomics
Accès ouvert 2024 article OpenAlex

Polygenic Risk Score (PRS) Combined with NGS Panel Testing Increases Accuracy in Hereditary Breast Cancer Risk Estimation

Nikolaos Tsoulos, Eirini Papadopoulou, Konstantinos Agiannitopoulos, Dimitrios Grigoriadis et autres

Breast cancer (BC) is the most prominent tumor type among women, accounting for 32% of newly diagnosed cancer cases. BC risk factors include inherited germline pathogenic gene variants and family history of disease. However, the etiology of the disease remains occult in …

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1 citation Diagnostics
Accès ouvert 2024 preprint OpenAlex

Uncovering Pathogenic Variants in Cancer Susceptibility Genes through Genetic Testing for Pancreatic Cancer Patients

Kevisa Potska, Anastasia Katseli, Konstantinos Agiannitopoulos, CHRISTINA NTOGKA et autres

Pancreatic cancer stands out as one of the most lethal forms of malignancies, representing 2% of all cancer cases and contributing to 5% of cancer-related fatalities. Therefore, early detection of pancreatic cancer is crucial for enhancing treatment outcomes. Various hereditary cancer syndromes …

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1 citation Preprints.org
Accès ouvert 2024 article OpenAlex

Microsatellite Instability Is Insufficiently Used as a Biomarker for Lynch Syndrome Testing in Clinical Practice

Eirini Papadopoulou, George Rigas, Elena Fountzilas, Anastasios L. Boutis et autres

PURPOSE The pan-cancer presence of microsatellite instability (MSI)–positive tumors demonstrates its clinical utility as an agnostic biomarker for identifying immunotherapy-eligible patients. Additionally, MSI is a hallmark of Lynch syndrome (LS), the most prevalent cancer susceptibility syndrome among patients with colorectal and endometrial …

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12 citations JCO Precision Oncology
Accès ouvert 2024 article OpenAlex

Neuroendocrine Breast Tumors: Could Multigene Assays Help in Guiding Treatment Decisions? Case Presentation

Christos J. Markopoulos, Nikolaos Tsoulos, Konstantinos Agiannitopoulos, Evangelia Karagianni

BACKGROUND/AIM: Breast cancer remains the most prevalent type of cancer among women worldwide, and it remains the primary cause of cancer-related deaths in this demographic. Neuroendocrine breast cancer (NBC), an uncommon subtype comprising less than 1% of cases, typically occurs in older …

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0 citations In Vivo
Accès ouvert 2024 article OpenAlex

Germline Co-deletion ofCDKN2AandCDKN2BGenes in Pleomorphic Xanthoastrocytoma: Case Report

Konstantinos Agiannitopoulos, Anastasia Katseli, Kevisa Potska, CHRISTINA NTOGKA et autres

BACKGROUND/AIM: Gliomas are highly heterogeneous malignancies originating from diverse cell types within the brain. Although their precise etiology is frequently unknown, risk factors, such as chemical exposure, radiation, and specific uncommon genetic disorders have been identified. Diagnosis typically entails imaging tests, such …

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1 citation In Vivo

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