Samira Lobo

785 total citations
5 papers, 520 citations indexed

About

Samira Lobo is a scholar working on Rheumatology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Samira Lobo has authored 5 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Rheumatology, 2 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Samira Lobo's work include Bone Tumor Diagnosis and Treatments (2 papers), Sarcoma Diagnosis and Treatment (2 papers) and Melanoma and MAPK Pathways (2 papers). Samira Lobo is often cited by papers focused on Bone Tumor Diagnosis and Treatments (2 papers), Sarcoma Diagnosis and Treatment (2 papers) and Melanoma and MAPK Pathways (2 papers). Samira Lobo collaborates with scholars based in United Kingdom, Netherlands and Australia. Samira Lobo's co-authors include Nadège Presneau, Dina Halai, Maria Fernanda Amary, Roberto Tirabosco, Adrienne M. Flanagan, Fitim Berisha, Malihe Eskandarpour, S. McCarthy, Valeria R. Fantin and P. Andrew Futreal and has published in prestigious journals such as Nature Genetics, Clinical Cancer Research and British Journal of Cancer.

In The Last Decade

Samira Lobo

5 papers receiving 514 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Samira Lobo United Kingdom	5	209	209	183	136	135	5	520
Lambert J. C. M. Van den Broek Netherlands	11	173 0.8×	229 1.1×	195 1.1×	126 0.9×	75 0.6×	14	543
W. Mellin Germany	13	152 0.7×	140 0.7×	342 1.9×	252 1.9×	152 1.1×	40	649
Kristin Andersen Norway	13	246 1.2×	104 0.5×	137 0.7×	98 0.7×	136 1.0×	55	499
Munir R. Tanas United States	20	261 1.2×	343 1.6×	670 3.7×	329 2.4×	114 0.8×	43	1.2k
Kari J. Kurppa Finland	13	486 2.3×	296 1.4×	100 0.5×	234 1.7×	80 0.6×	31	817
Kenneth J. Craddock Canada	12	162 0.8×	54 0.3×	250 1.4×	261 1.9×	163 1.2×	28	618
Joslyn Mills United States	9	279 1.3×	52 0.2×	355 1.9×	251 1.8×	75 0.6×	9	631
A. J. M. Balm Netherlands	11	279 1.3×	53 0.3×	175 1.0×	416 3.1×	79 0.6×	22	720
Lara Molendini Italy	13	295 1.4×	167 0.8×	353 1.9×	223 1.6×	173 1.3×	15	635
Nel J. Kuipers‐Dijkshoorn Netherlands	15	275 1.3×	88 0.4×	125 0.7×	217 1.6×	343 2.5×	23	731

Countries citing papers authored by Samira Lobo

Since Specialization

Citations

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

Fields of papers citing papers by Samira Lobo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samira Lobo

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

All Works

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5 of 5 papers shown

1.

Pillay, Nischalan, Vincent Plagnol, Patrick Tarpey, et al.. (2012). A common single-nucleotide variant in T is strongly associated with chordoma. Nature Genetics. 44(11). 1185–1187. 92 indexed citations

2.

Amary, Maria Fernanda, Stephen Damato, Dina Halai, et al.. (2011). Ollier disease and Maffucci syndrome are caused by somatic mosaic mutations of IDH1 and IDH2. Nature Genetics. 43(12). 1262–1265. 276 indexed citations

3.

Jewell, Rosalyn, Caroline Conway, Angana Mitra, et al.. (2010). Patterns of Expression of DNA Repair Genes and Relapse From Melanoma. Clinical Cancer Research. 16(21). 5211–5221. 42 indexed citations

4.

Mitra, Angana, Caroline Conway, Christy Walker, et al.. (2010). Melanoma sentinel node biopsy and prediction models for relapse and overall survival. British Journal of Cancer. 103(8). 1229–1236. 40 indexed citations

5.

Conway, Caroline, Angana Mitra, Rosalyn Jewell, et al.. (2009). Gene Expression Profiling of Paraffin-Embedded Primary Melanoma Using the DASL Assay Identifies Increased Osteopontin Expression as Predictive of Reduced Relapse-Free Survival. Clinical Cancer Research. 15(22). 6939–6946. 70 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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