Andrey Kirov

473 total citations
20 papers, 198 citations indexed

About

Andrey Kirov is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Andrey Kirov has authored 20 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in Andrey Kirov's work include Amyloidosis: Diagnosis, Treatment, Outcomes (10 papers), Pancreatitis Pathology and Treatment (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Andrey Kirov is often cited by papers focused on Amyloidosis: Diagnosis, Treatment, Outcomes (10 papers), Pancreatitis Pathology and Treatment (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Andrey Kirov collaborates with scholars based in Bulgaria, Germany and United States. Andrey Kirov's co-authors include Албена Тодорова, Tihomir Todorov, Vanio Mitev, Eiki Adachi, Ceco D. Dushkin, M. V. Abrashev, Alexandrе Loukanov, K. I. Papazova, Stayko Sarafov and Ivailo Tournev and has published in prestigious journals such as Gene, Clinica Chimica Acta and Colloids and Surfaces A Physicochemical and Engineering Aspects.

In The Last Decade

Andrey Kirov

18 papers receiving 193 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Andrey Kirov Bulgaria 8 83 68 56 37 23 20 198
Arnab B. Chowdry United States 7 122 1.5× 47 0.7× 33 0.6× 39 1.1× 4 0.2× 8 300
Shu Huang China 8 40 0.5× 43 0.6× 40 0.7× 22 0.6× 22 1.0× 45 222
Jiaxu Zhao China 6 133 1.6× 12 0.2× 83 1.5× 10 0.3× 18 0.8× 12 373
Xue‐Hui Shi China 13 139 1.7× 12 0.2× 82 1.5× 33 0.9× 10 0.4× 42 434
Susanne Weise Germany 6 181 2.2× 128 1.9× 21 0.4× 16 0.4× 12 0.5× 15 347
Ilaria Pezzini Italy 10 115 1.4× 26 0.4× 68 1.2× 11 0.3× 19 0.8× 15 316
Judy L. Chen United States 12 37 0.4× 34 0.5× 48 0.9× 6 0.2× 58 2.5× 30 445
Katarzyna Derwińska Poland 11 230 2.8× 222 3.3× 8 0.1× 37 1.0× 18 0.8× 19 412
Ahyoung Hong South Korea 7 145 1.7× 10 0.1× 47 0.8× 62 1.7× 16 0.7× 14 361

Countries citing papers authored by Andrey Kirov

Since Specialization
Citations

This map shows the geographic impact of Andrey Kirov's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrey Kirov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrey Kirov more than expected).

Fields of papers citing papers by Andrey Kirov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrey Kirov. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrey Kirov. The network helps show where Andrey Kirov may publish in the future.

Co-authorship network of co-authors of Andrey Kirov

This figure shows the co-authorship network connecting the top 25 collaborators of Andrey Kirov. A scholar is included among the top collaborators of Andrey Kirov based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrey Kirov. Andrey Kirov is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Chamova, Teodora, Мариана Господинова, Tihomir Todorov, et al.. (2022). Seven Years of Selective Genetic Screening Program and Follow-Up of Asymptomatic Carriers With Hereditary Transthyretin Amyloidosis in Bulgaria. Frontiers in Neurology. 13. 844595–844595. 3 indexed citations
2.
Sarafov, Stayko, Tihomir Todorov, Andrey Kirov, et al.. (2021). Characterization of population genetic structure of hereditary transthyretin amyloidosis in Bulgaria. Amyloid. 28(4). 219–225. 4 indexed citations
3.
Господинова, Мариана, Stayko Sarafov, Teodora Chamova, et al.. (2020). Cardiac involvement, morbidity and mortality in hereditary transthyretin amyloidosis because of p.Glu89Gln mutation. Journal of Cardiovascular Medicine. 21(9). 688–695. 8 indexed citations
4.
Nakov, Radislav, Stayko Sarafov, Мариана Господинова, et al.. (2020). Transthyretin amyloidosis: Testing strategies and model for center of excellence support. Clinica Chimica Acta. 509. 228–234. 9 indexed citations
5.
Yordanova, Iglika, Andrey Kirov, Tihomir Todorov, et al.. (2019). Monoallelic expression of the TTR gene as a contributor to the age at onset and penetrance of TTR-related amyloidosis. Gene. 705. 16–21. 5 indexed citations
6.
Nakov, Radislav, Stayko Sarafov, Мариана Господинова, et al.. (2019). Transthyretin Amyloidosis with Gastrointestinal Manifestation: a Case Report. Journal of Gastrointestinal and Liver Diseases. 28(3). 359–361. 7 indexed citations
7.
Kirov, Andrey, Stayko Sarafov, Tihomir Todorov, et al.. (2019). Founder effect of the Glu89Gln TTR mutation in the Bulgarian population. Amyloid. 26(4). 181–185. 18 indexed citations
8.
Nakov, Radislav, Stayko Sarafov, Мариана Господинова, et al.. (2019). Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis associated with Glu89Gln Mutation. Journal of Gastrointestinal and Liver Diseases. 28(4). 421–426. 7 indexed citations
9.
Chamova, Teodora, Andrey Kirov, Velina Guergueltcheva, et al.. (2016). Clinical Spectrum and Genetic Variability in Bulgarian Patients with Niemann-Pick Disease Type C. European Neurology. 75(3-4). 113–123. 7 indexed citations
10.
Господинова, Мариана, Stayko Sarafov, Velina Guergueltcheva, et al.. (2015). Cardiac involvement and clinical follow up of patients with hereditary transthyretin related amyloidosis associated with Glu89Gln mutation. Orphanet Journal of Rare Diseases. 10(Suppl 1). P54–P54.
11.
Господинова, Мариана, Stayko Sarafov, Velina Guergueltcheva, et al.. (2015). Cardiomyopathy and peripheral polyneuropathy severity in patients with Glu89Gln mutation at the time of diagnosis. Orphanet Journal of Rare Diseases. 10(S1). 1 indexed citations
12.
13.
Kirov, Andrey, Petia Dimova, Албена Тодорова, et al.. (2013). 15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in Bulgaria. Epilepsy Research. 104(3). 241–245. 7 indexed citations
14.
Litvinenko, Ivan, et al.. (2013). One Novel and One Recurrent Mutation in IGHMBP2 Gene, Causing Severe Spinal Muscular Atrophy Respiratory Distress 1 With Onset Soon After Birth. Journal of Child Neurology. 29(6). 799–802. 6 indexed citations
15.
Dimova, Petia, Andrey Kirov, Албена Тодорова, Tihomir Todorov, & Vanio Mitev. (2012). A Novel PCDH19 Mutation Inherited From an Unaffected Mother. Pediatric Neurology. 46(6). 397–400. 21 indexed citations
16.
Kirov, Andrey, et al.. (2012). Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism.. PubMed. 23(4). 505–11. 14 indexed citations
17.
Kirov, Andrey, et al.. (2010). Toll-Like Receptor (TLR2 and TLR4) Polymorphisms: Markers of Innate Immunity in Oral Infection in Children. Oral Health and Dental Management. 2010(3). 0–0. 2 indexed citations
18.
Тодоров, Т., et al.. (2009). Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPA. BMJ Case Reports. 2009. bcr0620080139–bcr0620080139. 12 indexed citations
19.
Loukanov, Alexandrе, Ceco D. Dushkin, K. I. Papazova, et al.. (2004). Photoluminescence depending on the ZnS shell thickness of CdS/ZnS core-shell semiconductor nanoparticles. Colloids and Surfaces A Physicochemical and Engineering Aspects. 245(1-3). 9–14. 66 indexed citations
20.
Kirov, Andrey, et al.. (1979). Therapeutic effects of Corynebacterium parvum in experimental burn disease of mice. Burns. 6(1). 45–47. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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