Angela Apessos

543 total citations
16 papers, 294 citations indexed

About

Angela Apessos is a scholar working on Pathology and Forensic Medicine, Oncology and Genetics. According to data from OpenAlex, Angela Apessos has authored 16 papers receiving a total of 294 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pathology and Forensic Medicine, 7 papers in Oncology and 6 papers in Genetics. Recurrent topics in Angela Apessos's work include Genetic factors in colorectal cancer (6 papers), Cancer Genomics and Diagnostics (5 papers) and BRCA gene mutations in cancer (4 papers). Angela Apessos is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Cancer Genomics and Diagnostics (5 papers) and BRCA gene mutations in cancer (4 papers). Angela Apessos collaborates with scholars based in Greece, United Kingdom and United States. Angela Apessos's co-authors include Patrick M. Abou‐Sleiman, Joyce Harper, Joy Delhanty, George Nasioulas, Paul Serhal, Eirini Papadopoulou, Dagan Wells, Robert Winston, Wirawit Piyamongkol and Mary B. Davis and has published in prestigious journals such as Journal of Clinical Oncology, Cancer Research and British Journal of Cancer.

In The Last Decade

Angela Apessos

16 papers receiving 284 citations

Peers

Angela Apessos
Dagmar Tapon United Kingdom
Beike Leegte Netherlands
Myriam Goldstein Israel
Anna Abulí Spain
H. Tönnies Germany
Kristen L. Sund United States
Teresa Vendrell Spain
G. Del Porto Italy
Carole Goumy France
Maria Paola Recalcati Italy
Dagmar Tapon United Kingdom
Angela Apessos
Citations per year, relative to Angela Apessos Angela Apessos (= 1×) peers Dagmar Tapon

Countries citing papers authored by Angela Apessos

Since Specialization
Citations

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

Fields of papers citing papers by Angela Apessos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angela Apessos

This figure shows the co-authorship network connecting the top 25 collaborators of Angela Apessos. A scholar is included among the top collaborators of Angela Apessos 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 Angela Apessos. Angela Apessos is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Dawood, Shaheenah, et al.. (2018). Analysis of hereditary cancer syndromes in patients from the United Arab Emirates.. Journal of Clinical Oncology. 36(15_suppl). e13509–e13509. 2 indexed citations
2.
Apessos, Angela, Κωνσταντίνος Αγιαννιτόπουλος, Georgios Tsaousis, et al.. (2017). Comprehensive BRCA mutation analysis in the Greek population. Experience from a single clinical diagnostic center. Cancer Genetics. 220. 1–12. 9 indexed citations
3.
Papadopoulou, Eirini, et al.. (2016). Molecular predictive markers in tumors of the gastrointestinal tract. World Journal of Gastrointestinal Oncology. 8(11). 772–772. 6 indexed citations
4.
Papadopoulou, Eirini, Angela Apessos, Κωνσταντίνος Αγιαννιτόπουλος, et al.. (2015). Determination of EGFR and KRAS mutational status in Greek non-small-cell lung cancer patients. Oncology Letters. 10(4). 2176–2184. 20 indexed citations
5.
Apessos, Angela, Eirini Papadopoulou, Κωνσταντίνος Αγιαννιτόπουλος, et al.. (2015). Abstract P1-03-08: Different genomic rearrangements account for 17% of BRCA1/2 mutations in Greece. Cancer Research. 75(9_Supplement). P1–3. 1 indexed citations
6.
Negru, Șerban, Eirini Papadopoulou, Angela Apessos, et al.. (2014). KRAS,NRASandBRAFmutations in Greek and Romanian patients with colorectal cancer: a cohort study. BMJ Open. 4(5). e004652–e004652. 33 indexed citations
7.
Chalevelakis, G., et al.. (2008). Different Intrafamilial Clinical Presentation of FMF Mutation Carriers. Genetic Testing. 12(1). 125–127. 2 indexed citations
8.
Cattaneo, Francesca, Sara Molatore, Angela Apessos, et al.. (2007). Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis. Genetics in Medicine. 9(12). 836–841. 13 indexed citations
9.
Apessos, Angela, Hans G. Dauwerse, Voula Velissariou, et al.. (2005). Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients. BMC Cancer. 5(1). 40–40. 14 indexed citations
10.
Apessos, Angela, George Kallimanis, Niki J. Agnantis, et al.. (2005). hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients. British Journal of Cancer. 92(2). 396–404. 14 indexed citations
11.
Apessos, Angela, Stefanos Labropoulos, Antonios Keramopoulos, et al.. (2004). Characterization of a novel large deletion and single point mutations in the BRCA1gene in a Greek cohort of families with suspected hereditary breast cancer. BMC Cancer. 4(1). 61–61. 26 indexed citations
12.
Apessos, Angela, Eirini Papadopoulou, Niki J. Agnantis, et al.. (2003). Genetic alterations of the APC gene in familial adenomatous polyposis patients of the hellenic group for the study of colorectal cancer.. PubMed. 23(3A). 2191–3. 3 indexed citations
13.
Harper, Joyce, Dagan Wells, Wirawit Piyamongkol, et al.. (2002). Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders. Prenatal Diagnosis. 22(6). 525–533. 42 indexed citations
14.
Abou‐Sleiman, Patrick M., Angela Apessos, Joyce Harper, et al.. (2002). First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2). Prenatal Diagnosis. 22(6). 519–524. 21 indexed citations
15.
Apessos, Angela, et al.. (2002). Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR. Prenatal Diagnosis. 22(5). 360–365. 50 indexed citations
16.
Apessos, Angela, Patrick M. Abou‐Sleiman, Joyce Harper, & Joy Delhanty. (2001). Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers. Prenatal Diagnosis. 21(6). 504–511. 38 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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