| Comparison between thrombophilic gene polymorphisms among high risk patients LA Mariya Levkova, Mari Hachmeriyan, Milena Stoyanova, Valentina Miteva Romanian Journal of Internal Medicine 58 (1), 20-26, 2020 | 7 | 2020 |
| Standard karyotyping - a look through the European guidelines LA Mari Hachmeriyan, Maria Levkova, Milena Stoyanova, Valentina Miteva Varna Medical Forum 8 (1), 90 - 96, 2019 | 4 | 2019 |
| Women’s awareness towards prenatal down syndrome tests in Bulgaria AL Levkova Mariya, Hachmeriyan Mari, Miteva Valentina, Stoyanova Milena ... Journal of Down Syndrome & Chromosome Abnormalities 4 (129), 1-4, 2018 | 2* | 2018 |
| Tendencies of cytogenetic analysis of patients with acute myeloid leukemia–an 11-year single-centre experience report D Yahya, T Ruseva, M Tsvetkova, M Stoyanova, M Levkova, V Miteva, ... 13th EUROPEAN CYTOGENOMICS CONFERENCE 48 (73), 2021 | 1* | 2021 |
| HEREDITARY BREAST AND OVARIAN CANCER–GENETIC COUNSELING EXPERIENCE REPORT D Yahya, M Hachmeriyan, V MITEVA, M STOYANOVA, M Levkova, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 339-339, 2024 | | 2024 |
| Cytogenetic analysis of patients with hematological malignancies D Yahya, V Miteva, I Micheva, T Ruseva, L Angelova Cytology and Genetics 57 (3), 272-281, 2023 | | 2023 |
| Cytogenetic findings in 126 patients with multiple myeloma A retrospective single-centre study V Miteva, C Ruseva, Т Chervenkov, I Micheva Archives of Hellenic medicine 40 (3), 349-355, 2023 | | 2023 |
| Prenatal screening – Evolution of pregnant women’s choice AL Yahya D., Hachmeriyan M., Stoyanova M., Miteva V., Levkova M Prenatal Diagnosis 43 (Suppl 1), 93, 2023 | | 2023 |
| Telegenetics: attidutes of genetic counselors and patients in Bulgaria LA Mariya Levkova, Mari Hachmeriyan, Milena Stoyanova, Valentina Miteva EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPP 1), 570-570, 2022 | | 2022 |
| COVID-19 effect on post-test genetic counselling LA Mari Hachmeriyan, Maria Levkova, Dinnar Yahya, Milena Stoyanova ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 561-561, 2022 | | 2022 |
| Incidental findings in cytogenetics - the old new LA Valentina Miteva, Tsanka Ruseva, Dinnar Yahya, Marya Levkova, Milena ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 560-561, 2022 | | 2022 |
| Evaluation of the diagnostic rate in children with dysmorphic features-one genetic center experience LA Milena Stoyanova, Mari Hachmeriyan, Mariya Levkova, Valentina Miteva EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 338-338, 2022 | | 2022 |
| Chromosomal abnormalities and their prognostic significance in patients with multiple myeloma. V Miteva, C Ruseva, T Chervenkov, I Micheva | | 2022 |
| ХРОМОЗОМНИ НАРУШЕНИЯ И ТЯХНОТО ПРЕДИКТИВНО ЗНАЧЕНИЕ ПРИ ПАЦИЕНТИ С МНОЖЕСТВЕН МИЕЛОМ. В Митева, Ц Русева, Т Червенков, И Мичева Medical Review/Meditsinski Pregled 58 (1), 2022 | | 2022 |
| ЦИТОГЕНЕТИЧНИ АБЕРАЦИИ ПРИ ПАЦИЕНТИ С МНОЖЕСТВЕН МИЕЛОМ В Митева, М Хачмериян, Т Червенков, И Мичева Medical Review/Meditsinski Pregled 57 (5), 2021 | | 2021 |
| Cytogenetic aberrations in patients with multiple myeloma. V Miteva, M Hachmeriyan, T Chervenkov, I Micheva | | 2021 |
| Цитогенетични изследвания при деца - опитът на Лаборатория по медицинска генетика - Варна за период от 10 години ЛА М. Стоянова, М. Цветкова, М. Левкова, В. Митева, Д. Яхя, В. Йотова, М ... Педиатрия 61 (2), 31-34, 2021 | | 2021 |
| A retrospective study of patients with Multiple Myeloma tested in Laboratory of Medical genetics, Varna, Bulgaria LA V. Miteva, T. Ruseva, M. Hachmeriyan, M. Levkova EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 940-941, 2020 | | 2020 |
| Single - gene pathology in pediatric patients referred for genetic counseling for a period of five years VM Milena Stoyanova, Lyudmila Angelova, Mary Hachmeriyan, Mariya Levkova EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 782-782, 2020 | | 2020 |
| Patients' understanding of routine genetic testing LA Mariya Levkova, Mary Hachmeriyan, Valentina Miteva, Milena Stoyanova EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 783-783, 2020 | | 2020 |
