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Mariya Levkova
Mariya Levkova
在 mu-varna.bg 的电子邮件经过验证 - 首页
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引用次数
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Single nucleotide polymorphisms in microrna genes and colorectal cancer risk and prognosis
M Radanova, M Levkova, G Mihaylova, R Manev, M Maneva, R Hadgiev, ...
Biomedicines 10 (1), 156, 2022
142022
Potential role of dynein‐related genes in the etiology of male infertility: A systematic review and a meta‐analysis
M Levkova, M Radanova, L Angelova
Andrology 10 (8), 1484-1499, 2022
72022
Oncogenic functions and clinical significance of circular rnas in colorectal cancer
M Radanova, G Mihaylova, N Nazifova-Tasinova, M Levkova, O Tasinov, ...
Cancers 13 (14), 3395, 2021
62021
Association between polymorphic markers human leucocyte antigen-G and tumour necrosis factor alpha and susceptibility to recurrent miscarriages among Bulgarian women
M Levkova, T Chervenkov, M Hachmeriyan, L Angelova
Turkish Journal of Obstetrics and Gynecology 17 (1), 34, 2020
62020
Factor V Leiden, Factor II, Protein C, Protein S, and antithrombin and ischemic strokes in young adults: a meta-analysis
M Tsalta-Mladenov, M Levkova, S Andonova
Genes 13 (11), 2081, 2022
52022
CFTR gene variants as a reason for impaired spermatogenesis: a pilot study and a Meta-analysis of published data
M Levkova, T Chervenkov, M Hachmeriyan, L Angelova
Human Fertility 25 (4), 728-737, 2022
52022
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
52020
Double aneuploidy 48, ХХХ,+ 21 of a Bulgarian newborn with Down phenotype: a case report
M Tsvetkova, M Levkova, S Tsvetkova, M Hachmeriyan, E Kovachev, ...
Egyptian Journal of Medical Human Genetics 21, 1-5, 2020
42020
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
42019
Preauricular sinus: Incidence and inheritance
GS Stoyanov, A Renjilian, B Matev, M Bliznakova, V Gaydardzhiev, ...
Scripta Scientifica Medica 50 (4), 27-32, 2018
42018
Genus-level analysis of gut microbiota in children with autism spectrum disorder: a mini review
M Levkova, T Chervenkov, R Pancheva
Children 10 (7), 1103, 2023
32023
The association of gr/gr deletion in the Y chromosome and impaired spermatogenesis in Bulgarian males: a pilot study
M Levkova, T Chervenkov, L Angelova
Middle East Fertility Society Journal 25, 1-5, 2020
32020
Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour
M Stoyanova, M Hachmeriyan, M Levkova, S Bichev, M Georgieva, ...
Folia Medica 64 (1), 27-32, 2022
22022
Chromosomal polymorphism in Bulgarian patients with reproductive problems—One genetic center experience
L Angelova, M Tsvetkova, M Levkova
J. IMAB 27, 4133-4138, 2021
22021
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 (2), 1-4, 2018
2*2018
Challenging Reproductive Genetic Counseling in Families at High Risk for Rare Genetic Syndromes – A Case Report with Possible Denys-Drash Syndrome
BIAL Hachmeriyan M, Andonova S, Levkova M, Stoyanova M, Kalchev K, Vasilev P ...
Journal of Genetic Disorders & Genetic Reports 7 (2), 1-4, 2018
2*2018
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
12022
16p11.2 Duplication Syndrome – a Case Report
M Levkova, M Stoyanova, R Staneva, M Hachmeriyan, L Angelova
Folia Medica 63 (1), 138-141, 2021
12021
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, ...
1
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
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