Georgia Bardi

3.3k total citations
71 papers, 2.5k citations indexed

About

Georgia Bardi is a scholar working on Pathology and Forensic Medicine, Genetics and Cancer Research. According to data from OpenAlex, Georgia Bardi has authored 71 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Pathology and Forensic Medicine, 31 papers in Genetics and 27 papers in Cancer Research. Recurrent topics in Georgia Bardi's work include Genomic variations and chromosomal abnormalities (28 papers), Genetic factors in colorectal cancer (27 papers) and Cancer Genomics and Diagnostics (25 papers). Georgia Bardi is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Genetic factors in colorectal cancer (27 papers) and Cancer Genomics and Diagnostics (25 papers). Georgia Bardi collaborates with scholars based in Sweden, Denmark and Greece. Georgia Bardi's co-authors include Nikos Pandis, Felix Mitelman, Sverre Heim, Nils Mandahl, Sverre Heim, Claus Fenger, Johan A. Andersen, Ingrid Idvall, Manuel R. Teixeira and O Kronbörg and has published in prestigious journals such as Journal of Clinical Oncology, JNCI Journal of the National Cancer Institute and Cancer.

In The Last Decade

Georgia Bardi

71 papers receiving 2.5k citations

Peers

Georgia Bardi
B A Gusterson United Kingdom
Susan Shanley United Kingdom
Stephen Baylin United States
J Kassel United States
Georgia Bardi
Citations per year, relative to Georgia Bardi Georgia Bardi (= 1×) peers Nikos Pandis

Countries citing papers authored by Georgia Bardi

Since Specialization
Citations

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

Fields of papers citing papers by Georgia Bardi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Georgia Bardi

This figure shows the co-authorship network connecting the top 25 collaborators of Georgia Bardi. A scholar is included among the top collaborators of Georgia Bardi 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 Georgia Bardi. Georgia Bardi 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.
Papadopoulou, Anna, et al.. (2003). Cytogenetic Profile of Unknown Primary Tumors: Clues for Their Pathogenesis and Clinical Management. Neoplasia. 5(1). 23–31. 24 indexed citations
2.
Parada, Luis A., Magnus Hallén, K.‐G. Tranberg, et al.. (1999). Cytogenetic analyses of secondary liver tumors reveal significant differences in genomic imbalances between primary and metastatic colon carcinomas. Clinical & Experimental Metastasis. 17(6). 471–479. 29 indexed citations
3.
Pandis, Nikos, et al.. (1999). Karyotypic Evolution in Breast Carcinomas with i(1)(q10) and der(1;16)(q10;p10) as the Primary Chromosome Abnormality. Cancer Genetics and Cytogenetics. 113(2). 156–161. 23 indexed citations
4.
Teixeira, Manuel R., Nikos Pandis, Georgia Bardi, et al.. (1997). Discrimination between multicentric and multifocal breast carcinoma by cytogenetic investigation of macroscopically distinct ipsilateral lesions. Genes Chromosomes and Cancer. 18(3). 170–174. 30 indexed citations
5.
Adeyinka, Adewale, Nikos Pandis, Georgia Bardi, et al.. (1997). A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12. Cancer Genetics and Cytogenetics. 97(2). 119–121. 8 indexed citations
6.
Parada, Luis A., Georgia Bardi, Magnus Hallén, et al.. (1997). Cytogenetic Abnormalities and Clonal Evolution in an Adult Hepatoblastoma. The American Journal of Surgical Pathology. 21(11). 1381–1386. 27 indexed citations
7.
Bardi, Georgia, Luis A. Parada, Nikos Pandis, et al.. (1997). Cytogenetic findings in metastases from colorectal cancer. International Journal of Cancer. 72(4). 604–607. 16 indexed citations
8.
Gerdes, Anne‐Marie, Nikos Pandis, Claudia U. Dietrich, et al.. (1997). Fluorescence in situ hybridization of old G-banded and mounted chromosome preparations. Cancer Genetics and Cytogenetics. 98(1). 9–15. 5 indexed citations
9.
Bardi, Georgia, et al.. (1996). Chromosome abnormalities in colorectal adenomas: Two cytogenetic subgroups characterized by deletion of 1 p and numerical aberrations. Human Pathology. 27(11). 1192–1197. 21 indexed citations
10.
Teixeira, Manuel R., Nikos Pandis, Anne‐Marie Gerdes, et al.. (1996). Cytogenetic abnormalities in anin situ ductal carcinoma and five prophylactically removed breasts from members of a family with hereditary breast cancer. Breast Cancer Research and Treatment. 38(2). 177–182. 25 indexed citations
11.
Bardi, Georgia, Nikos Pandis, Karoline Schousboe, Berit Hølund, & Sverre Heim. (1995). Near-Diploid karyotypes with recurrent chromosome abnormalities characterize early-stage endometrial cancer. Cancer Genetics and Cytogenetics. 80(2). 110–114. 19 indexed citations
12.
Pandis, Nikos, Manuel R. Teixeira, Anne‐Marie Gerdes, et al.. (1995). Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors. Cancer. 76(2). 250–258. 63 indexed citations
13.
Pandis, Nikos, Yuesheng Jin, Ludmila Gorunova, et al.. (1995). Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups. Genes Chromosomes and Cancer. 12(3). 173–185. 179 indexed citations
14.
Johansson, Bertil, Georgia Bardi, Nikos Pandis, et al.. (1994). Karyotypic pattern of pancreatic adenocarcinomas correlates with survival and tumour grade. International Journal of Cancer. 58(1). 8–13. 26 indexed citations
15.
Bardi, Georgia, Pierre Åman, Bertil Johansson, et al.. (1994). Cytogenetic characterization of a periampullary adenocarcinoma of the pancreas, its liver metastasis, and a cell line established from the metastasis in a patient with Gardner's syndrome. Cancer Genetics and Cytogenetics. 76(1). 29–32. 9 indexed citations
16.
Pandis, Nikos, Yuesheng Jin, Janusz Limon, et al.. (1993). Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast. Genes Chromosomes and Cancer. 6(3). 151–155. 58 indexed citations
17.
Pandis, Nikos, Sverre Heim, Georgia Bardi, et al.. (1993). Chromosome analysis of 20 breast carcinomas: Cytogenetic multiclonality and karyotypic‐pathologic correlations. Genes Chromosomes and Cancer. 6(1). 51–57. 70 indexed citations
18.
Bardi, Georgia, Bertil Johansson, Nikos Pandis, et al.. (1992). Trisomy 7 in nonneoplastic focal steatosis of the liver. Cancer Genetics and Cytogenetics. 63(1). 22–24. 22 indexed citations
19.
Bardi, Georgia, B Johansson, Nikos Pandis, et al.. (1991). Trisomy 7 in Short‐Term Cultures of Colorectal Adenocarcinomas. Genes Chromosomes and Cancer. 3(2). 149–152. 40 indexed citations
20.
Bardi, Georgia, et al.. (1989). Mixed lineage leukemia with cytogenetically unrelated abnormal clones. Cancer Genetics and Cytogenetics. 40(1). 83–87. 4 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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