Sami Belhadj

587 total citations
8 papers, 157 citations indexed

About

Sami Belhadj is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Sami Belhadj has authored 8 papers receiving a total of 157 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 4 papers in Genetics. Recurrent topics in Sami Belhadj's work include Cancer Genomics and Diagnostics (4 papers), Genetic factors in colorectal cancer (4 papers) and DNA Repair Mechanisms (3 papers). Sami Belhadj is often cited by papers focused on Cancer Genomics and Diagnostics (4 papers), Genetic factors in colorectal cancer (4 papers) and DNA Repair Mechanisms (3 papers). Sami Belhadj collaborates with scholars based in Spain, Australia and Poland. Sami Belhadj's co-authors include Gabriel Capellá, Laura Valle, Matilde Navarro, Mariona Terradas, Joan Brunet, Gemma Aiza, Marta Pineda, Conxi Lázaro, Olga Campos and Xavier Muñoz and has published in prestigious journals such as Journal of Clinical Oncology, Gut and Scientific Reports.

In The Last Decade

Sami Belhadj

8 papers receiving 156 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sami Belhadj Spain 8 79 70 53 51 46 8 157
Lily Hoang United States 6 82 1.0× 32 0.5× 79 1.5× 72 1.4× 73 1.6× 12 197
Munemasa Nagao Japan 7 143 1.8× 37 0.5× 66 1.2× 79 1.5× 37 0.8× 13 211
Sophia Peters Germany 8 66 0.8× 67 1.0× 42 0.8× 46 0.9× 35 0.8× 12 178
Brandon M. Wenz United States 3 61 0.8× 28 0.4× 72 1.4× 50 1.0× 55 1.2× 9 145
Monica Marabelli Italy 7 87 1.1× 81 1.2× 90 1.7× 57 1.1× 65 1.4× 17 185
Oscar Pellón-Cárdenas United States 9 78 1.0× 32 0.5× 26 0.5× 41 0.8× 39 0.8× 9 139
Stacey E. P. Joosten Netherlands 7 91 1.2× 16 0.2× 58 1.1× 65 1.3× 54 1.2× 9 184
Jessada Thutkawkorapin Sweden 7 65 0.8× 58 0.8× 62 1.2× 42 0.8× 36 0.8× 18 164
Lenka Stolařová Czechia 4 65 0.8× 47 0.7× 72 1.4× 39 0.8× 38 0.8× 6 156
Olga Campos Spain 9 138 1.7× 100 1.4× 129 2.4× 67 1.3× 96 2.1× 18 270

Countries citing papers authored by Sami Belhadj

Since Specialization
Citations

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

Fields of papers citing papers by Sami Belhadj

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sami Belhadj

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

All Works

8 of 8 papers shown
1.
Offit, Kenneth, Catherine M. Sharkey, Magan Trottier, et al.. (2022). Regulation of Laboratory-Developed Tests in Preventive Oncology: Emerging Needs and Opportunities. Journal of Clinical Oncology. 41(1). 11–21. 9 indexed citations
2.
Evans, Tiffany‐Jane, Sami Belhadj, Dagmara Dymerska, et al.. (2021). A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants. Scientific Reports. 11(1). 11401–11401. 7 indexed citations
3.
Terradas, Mariona, Pilar Mur, Sami Belhadj, et al.. (2020). TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut. 70(6). 1139–1146. 11 indexed citations
4.
Belhadj, Sami, Mariona Terradas, Gemma Aiza, et al.. (2020). Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human Mutation. 41(9). 1563–1576. 30 indexed citations
5.
Valle, Jesús Del, Paula Rofes, Adriana López‐Doriga, et al.. (2020). Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients. Cancers. 12(4). 829–829. 51 indexed citations
6.
Belhadj, Sami, Pilar Mur, M. Henar Alonso, et al.. (2019). NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas. Scientific Reports. 9(1). 9020–9020. 18 indexed citations
7.
Belhadj, Sami, Cátia Moutinho, Pilar Mur, et al.. (2019). Germline variation in O6-methylguanine-DNA methyltransferase (MGMT) as cause of hereditary colorectal cancer. Cancer Letters. 447. 86–92. 13 indexed citations
8.
Terradas, Mariona, Sami Belhadj, Gemma Aiza, et al.. (2019). Contribution to colonic polyposis of recently proposed predisposing genes and assessment of the prevalence of NTHL1 ‐ and MSH3 ‐associated polyposes. Human Mutation. 40(11). 1910–1923. 18 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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