The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered J Brinkmann, C Lissewski, V Pinna, Y Vial, F Pantaleoni, F Lepri, ... European Journal of Human Genetics 29 (3), 524-527, 2021 | 10 | 2021 |
Comparison between thrombophilic gene polymorphisms among high risk patients M Levkova, M Hachmeriyan, M Stoyanova, V Miteva, L Angelova Romanian Journal of Internal Medicine 58 (1), 20-26, 2020 | 8 | 2020 |
Maternal biochemical screening – an approach for genetic prevention. Part 2.Sequential approach with integrated risk assessment L Angelova, V Gadancheva, D Konstantinova, M Stoianova, ... Akusherstvo I Ginekologia (indexed in Medline) 52 (5), 14-18, 2013 | 6 | 2013 |
Standard karyotyping-a look through the European guidelines M Hachmeriyan, M Levkova, M Stoyanova, V Miteva, L Angelova Varna Medical Forum 8 (1), 90-96, 2019 | 4 | 2019 |
16p11. 2 Duplication Syndrome-a Case Report M Levkova, M Stoyanova, R Staneva, M Hachmeriyan, L Angelova Folia Medica 63 (1), 138-141, 2021 | 3 | 2021 |
Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour S Milena, H Mari, L Mariya, B Stoyan, G Miglena, M Vilhelm, L Angelova Folia Medica 64 (1), 27-32, 2022 | 2 | 2022 |
Women’s awareness towards prenatal Down syndrome tests in Bulgaria. LA Levkova M., M. Hachmeriyan, V. Miteva, M. Stoyanova, M. Tsvetkova, D ... Journal of Down Syndrome and Chromosome Abnormalities 4 (2), 2018 | 2 | 2018 |
Challenging Reproductive Genetic Counseling in Families at High Risk for Rare Genetic Syndromes – A Case Report with Possible Denys-Drash Syndrome AL Hachmeriyan M., Andonova S., Levkova M.,Stoyanova M., Kalchev K., Vasilev ... Journal of Genetic Disorders & Genetic Reports 7 (1), 2018 | 2* | 2018 |
Diagnosis of the socionic temperament of personality and creating a psychological portrait of the Western European SPA and wellness tourists in Bulgaria M Stoyanova Acta Scientifica Naturalis 4 (1), 84-88, 2017 | 2 | 2017 |
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, ... | 2 | |
Variants of uncertain significance in the era of next-generation sequencing M Levkova, M Stoyanova, M Benkova-Petrova, M Georgieva, L Angelova Journal of the American Association of Nurse Practitioners 34 (8), 1018-1021, 2022 | 1 | 2022 |
The application of the facial analysis program Face2Gene in a single genetic counseling center: a retrospective study D Yahya, M Stoyanova, M Hachmeriyan, M Levkova Egyptian Pediatric Association Gazette 73 (1), 1, 2025 | | 2025 |
NIPT Integration as a Patient-Paid Prenatal Screening Option—Observations and Challenges from a Bulgarian Genetic Counseling Center D Yahya, M Hachmeriyan, M Stoyanova, M Levkova Medical Sciences 13 (1), 3, 2024 | | 2024 |
A cost-efficient algorithm for diagnosing children with dysmorphic features M Levkova, M Stoyanova, M Hachmeriyan, L Angelova Egyptian Journal of Medical Human Genetics 25 (1), 76, 2024 | | 2024 |
The significance of follow-up in patients with dysmorphic features: a case from clinical practice M Levkova, M Stoyanova, M Hachmeriyan Romanian JouRnal of PediatRics 73 (2), 100, 2024 | | 2024 |
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 |
ACAN gene mutation in a patient born small for gestational age with familial short stature V Iotova, Y Deyanova, M Stoyanova, M Hachmeriyan HORMONE RESEARCH IN PAEDIATRICS 96, 338-338, 2023 | | 2023 |
Noonan syndrome patients with short stature at a single paediatric endocrinology centre Y Deyanova, V Iotova, M Stoyanova, I Halvadzhiyan, R Stoicheva, ... Scripta Scientifica Medica 54 (3), 21-26, 2022 | | 2022 |
Molecular genetic markers in acute myelogenous leukemia—the good, the bad, and the intermediate DA Yahya, M Hachmeriyan, M Stoyanova, L Angelova, I Micheva, ... Varna Medical Forum 11 (2), 7-19, 2022 | | 2022 |
Telegenetics: attitudes of genetic counselors and patients in Bulgaria M Levkova, M Hachmeriyan, M Stoyanova, V Miteva, L Angelova EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 570-570, 2022 | | 2022 |