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Zornitsa Kamburova

Observed names: Z Kamburova, Z. Kamburova, Zornica B. Kamburova, Zornica Bogomilova Kamburova, Zornica Kamburova, Zornitsa B. KAMBUROVA, Zornitsa B. Kamburova, Zornitsa Bogomilova Kamburova, Зорница Камбурова
ORCID: 0000-0002-9377-9775
Observed ORCID: 0000-0002-9377-9775
OpenAlex ID: A5075401192
Genetic Basis of Dual Diagnosis: A Review of Genome-Wide Association Studies (GWAS) Focusing on Patients with Mood or Anxiety Disorders and Co-Occurring Alcohol-Use Disorders
2021 · Kaloyan Stoychev, Dancho Dilkov, et al. · Diagnostics · 16
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Chromosomal Abnormalities and Y Chromosome Microdeletions in Bulgarian Male With Azoospermia or Severe Oligospermia
2018 · Katya Kovacheva, Rumen Kotsev, et al. · Journal of IMAB - Annual Proceeding (Scientific Papers) · 6
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Genetic predisposition in female patients with triple‑negative breast cancer
2023 · Zornitsa Kamburova, Savelina Popovska, et al. · World Academy of Sciences Journal · 4
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Familial Lynch syndrome with early age of onset and confirmed splice site mutation in MSH2: A case report
2022 · Zornitsa Kamburova, Savelina Popovska, et al. · Biomedical Reports · 4
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Lynch-like syndrome with germline WRN mutation in Bulgarian patient with synchronous endometrial and ovarian cancer
2023 · Zornitsa Bogomilova Kamburova, Polina Damyanova Dimitrova, et al. · Hereditary Cancer in Clinical Practice · 3
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Molecular Landscape of Metastatic Lung Adenocarcinoma in Bulgarian Patients—A Prospective Study
2025 · George Dimitrov, Vladislav Nankov, et al. · International Journal of Molecular Sciences · 2
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[Morphologically qnd immunohistochemically based screening criteria for selection of patients with possible mutation of BRCA1 gene in primary ovarian cancer].
2014 · S Popovska, I Ivanov, et al. · PubMed · 2
Study of the Carrier State for Five BRCA1/BRCA2 Deleterious Mutations in Bulgarian Women with Breast Cancer
2013 · Katia S. Kovacheva, Zornica B. Kamburova, et al. · Journal of Biomedical and Clinical Research · 2
Precision oncology in Bulgaria: a prospective study of metastatic colorectal cancer patients
2026 · George Dimitrov, Zornitsa Kamburova, et al. · Cancer Treatment and Research Communications · 1
Colorectal Cancer: A Brief and Simplified Analysis of a Complex Disease
2024 · Krasimir Todorov Petrov, Ivan Nedkov Ivanov, et al. · Medicina · 1
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Autosomal recessive type of dystrophic epidermolysis bullosa with a novel variant in the COL7A1 gene
2024 · Slavena Nikolova, Zornitsa Kamburova, et al. · Biomedical Reports · 1
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Prevalence of Five BRCA1/2 Mutations in Bulgarian Breast Cancer Patients
2018 · Katia S. Kovacheva, Zornitsa B. Kamburova, et al. · Journal of Biomedical and Clinical Research · 1
163P: Prevalence of epidermal growth factor receptor (EGFR) gene mutations in non small cell lung cancer (NSCLC) in Bulgarian population
2016 · S. Popovska, N. Chilingirova, et al. · Journal of Thoracic Oncology · 1
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Genomic profiling in Bulgarian women with ovarian cancer: a dual-sample NGS approach
2026 · Zornitsa Kamburova, Savelina Popovska, et al. · Hereditary Cancer in Clinical Practice
Mucinous borderline ovarian tumour with concurrent germline WRN and somatic KRAS mutations: a case report
2026 · Zornitsa Kamburova, Savelina Popovska, et al. · Journal of Biomedical and Clinical Research
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Personalized surveillance in giant congenital melanocytic nevus, including the role of AI, histopathology and MC1R genotyping: A case report
2026 · Preslav Vasilev, Ivelina Yordanova, et al. · Biomedical Reports
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Cutaneous Metastasis as a Debut of Colorectal Cancer – Case Report
2025 · Radoslav G. TRIFONOV, Tatyana M. BETOVA, et al. · Archives of the Balkan Medical Union
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Carrier Screening for Single-Gene Disorders – A Brief Review
2021 · Katya S. Kovacheva, Slavena E. Nikolova, et al. · Journal of Biomedical and Clinical Research
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Pfeiffer syndrome type 2 – two cases from the Pleven Registry of Congenital Anomalies
2018 · Katya Kovacheva, Zornica Kamburova, et al. · Paediatria Croatica
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Клиничен случай на новородено момиче с Ichthyosis congenita, резултат от мутация в ALOX12B гена
2017 · Катя Ковачева, Зорница Камбурова, et al. · Редки болести и лекарства сираци
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Preliminary Data from a Study on Polymorphism RS4244285 of P4502c19 Cytochrome Gene in Patients with Acute Coronary Syndrome, Undergoing Treatment with Dual Antiplatelet Therapy With Clopidogrel and Aspirin
2016 · Katya S. Kovacheva, Petya A. Nikolova, et al. · Journal of Biomedical and Clinical Research
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Works count: 21
Citation count: 44
H-index: 4
I10-index: 1
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