G Manolov

1.5k total citations · 1 hit paper
31 papers, 943 citations indexed

About

G Manolov is a scholar working on Oncology, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, G Manolov has authored 31 papers receiving a total of 943 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Oncology, 9 papers in Pathology and Forensic Medicine and 8 papers in Molecular Biology. Recurrent topics in G Manolov's work include Viral-associated cancers and disorders (10 papers), Lymphoma Diagnosis and Treatment (8 papers) and Chronic Lymphocytic Leukemia Research (6 papers). G Manolov is often cited by papers focused on Viral-associated cancers and disorders (10 papers), Lymphoma Diagnosis and Treatment (8 papers) and Chronic Lymphocytic Leukemia Research (6 papers). G Manolov collaborates with scholars based in Sweden, Bulgaria and Austria. G Manolov's co-authors include Yanka Manolova, Peter Clifford, Eva Klein, Jayshree J. Nadkarni, Éva Mária Fenyõ, J. S. Nadkarni, E Tatsumi, George Klein, ALBERT LEVAN and Shizuko Harada and has published in prestigious journals such as Nature, The Lancet and Cancer.

In The Last Decade

G Manolov

27 papers receiving 833 citations

Hit Papers

Marker Band in One Chromosome 14 from Burkitt Lymphomas 1972 2026 1990 2008 1972 100 200 300 400
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Marker Band in One Chromosome 14 from Burkitt Lymphomas
    1972 454 citations G Manolov, Yanka Manolova profile →

Peers

G Manolov
Yanka Manolova Sweden
Amedea Donelli Italy
G. Reisbach Germany
Sarah H. Johnson United States
A Zander Germany
Sally M. Pittman Australia
I L Wolvers-Tettero Netherlands
J D Rowley United States
GP Schechter United States
Ludovica Riera Italy
Yanka Manolova Sweden
G Manolov
Citations per year, relative to G Manolov G Manolov (= 1×) peers Yanka Manolova

Countries citing papers authored by G Manolov

Since Specialization
Citations

This map shows the geographic impact of G Manolov'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 G Manolov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G Manolov more than expected).

Fields of papers citing papers by G Manolov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G Manolov. 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 G Manolov. The network helps show where G Manolov may publish in the future.

Co-authorship network of co-authors of G Manolov

This figure shows the co-authorship network connecting the top 25 collaborators of G Manolov. A scholar is included among the top collaborators of G Manolov 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 G Manolov. G Manolov 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.
Manolov, G, et al.. (2009). Genesis of the Philadelphia chromosome: Possible points of breakage in chromosome No. 22. Hereditas. 79(2). 301–303. 2 indexed citations
2.
Manolova, Yanka, et al.. (2009). The same marker chromosome, mar 17p+, in four consecutive cases of multiple myeloma Received November 22, 1978. Hereditas. 90(2). 307–310. 1 indexed citations
3.
Manolov, G, ALBERT LEVAN, J. S. Nadkarni, Jayshree J. Nadkarni, & Peter Clifford. (2009). Burkitt's lymphoma with female karyotype in an African male child. Hereditas. 66(1). 79–100. 2 indexed citations
4.
Manolov, G, Yanka Manolova, Geirid Fiskesjö, & ALBERT LEVAN. (2009). The complexity of the fluorescent pattern of the human Y chromosome. Hereditas. 68(2). 328–331. 3 indexed citations
5.
Manolov, G, et al.. (2009). Chromosome banding after treatment of living cells in vitro with histamine and thymidazol. Hereditas. 90(2). 304–307. 1 indexed citations
6.
Manolov, G, et al.. (2009). Cytogenetic study of foetal colon mouse tumour-AKATOL-1-71-cultivated in vitro. Hereditas. 90(2). 227–236.
7.
Manolov, G, Yanka Manolova, ALBERT LEVAN, & Georg Klein. (2009). Fluorescent pattern of apparently normal chromosomes in Burkitt lymphomas. Hereditas. 68(1). 160–163. 3 indexed citations
8.
Manolova, Yanka, G Manolov, J. Kieler, ALBERT LEVAN, & George Klein. (2009). Genesis of the 14q+ marker in Burkitt's lymphoma. Hereditas. 90(1). 5–10. 5 indexed citations
9.
Manolov, G, Yanka Manolova, ALBERT LEVAN, & Georg Klein. (2009). Experiments with fluorescent chromosome staining in Burkitt tumors. Hereditas. 68(2). 235–244. 4 indexed citations
10.
Manolov, G, Yanka Manolova, & ALBERT LEVAN. (2009). The fluorescence pattern of the human karyotype. Hereditas. 69(2). 273–286. 2 indexed citations
11.
Mitelman, Felix, Yanka Manolova, G Manolov, et al.. (2008). High resolution analysis of the 5q-marker chromosome in refractory anemia. Hereditas. 105(1). 49–54. 2 indexed citations
12.
Nacheva, Elisabeth P., Patricia Fischer, Oskar A. Haas, et al.. (2008). Acute myelogenous leukemia in a child with primary involvement of chromosomes 11 and X. Hereditas. 97(2). 273–288.
13.
Manolov, G, Yanka Manolova, & Tsvetan G. Gantchev. (2008). Specific patterns of differential condensation induced photochemically in human chromosomes. Hereditas. 111(2). 205–206.
14.
Manolov, G, et al.. (1991). Chromosomal alterations in lymphocytes of patients with Balkan endemic nephropathy and of healthy individuals after incubation in vitro with ochratoxin A.. PubMed. 267–72. 6 indexed citations
15.
Manolova, Yanka, et al.. (1990). Induction of characteristic chromosomal aberrations, particularly X-trisomy, in cultured human lymphocytes treated by ochratoxin A, A mycotoxin implicated in Balkan endemic nephropathy. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 231(2). 143–149. 26 indexed citations
16.
Dt, Purtilo, E Tatsumi, G Manolov, et al.. (1985). Epstein-Barr virus as an etiological agent in the pathogenesis of lymphoproliferative and aproliferative diseases in immune deficient patients.. PubMed. 27. 113–83. 61 indexed citations
17.
Petersen, John M., Raymond R. Tubbs, Richard A. Savage, et al.. (1985). Small noncleaved B cell burkitt-like lymphoma with chromosome t(8;14) translocation and epstein-barr virus nuclear-associated antigen in a homosexual man with acquired immune deficiency syndrome. The American Journal of Medicine. 78(1). 141–148. 76 indexed citations
18.
Purtilo, David T., et al.. (1984). Squamous-cell carcinoma, Kaposi's sarcoma and Burkitt's lymphoma are consequences of impaired immune surveillance of ubiquitous viruses in acquired immune deficiency syndrome, allograft recipients and tropical African patients.. PubMed. 749–70. 7 indexed citations
19.
20.
Nadkarni, J. S., Jayshree J. Nadkarni, Peter Clifford, et al.. (1969). Characteristics of new cell lines derived from Burkitt lymphomas. Cancer. 23(1). 64–79. 118 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Yanka Manolova Breakdown of academic impact, for papers by Amedea Donelli Breakdown of academic impact, for papers by G. Reisbach Breakdown of academic impact, for papers by Sarah H. Johnson Breakdown of academic impact, for papers by A Zander Breakdown of academic impact, for papers by Sally M. Pittman Breakdown of academic impact, for papers by I L Wolvers-Tettero Breakdown of academic impact, for papers by J D Rowley Breakdown of academic impact, for papers by GP Schechter Breakdown of academic impact, for papers by Ludovica Riera
Rankless by CCL
2026