Réda Garidi

2.5k citations
16 papers · 240 · h-index 8

Impact in

  • Genetics top 10%
    • Glioma Diagnosis and Treatment
    • Chronic Lymphocytic Leukemia Research
  • Neurology top 10%
    • CNS Lymphoma Diagnosis and Treatment
    • Peripheral Neuropathies and Disorders

Papers in

Réda Garidi

14 papers receiving 234 citations

Peers

Réda Garidi
Comparison fields: 5 of 46
  • Genetics 80
  • Neurology 93
  • Pathology and Forensic Medicine 76
  • Hematology 46
  • Oncology 49
Replace Maaike de Bie with:
Maaike de Bie Netherlands
Sergio Fava Italy
Yuki Arakawa Japan
Masahiro Sekimizu Japan
Shankaranarayana Paneesha United Kingdom
Rocco Pastano Italy
Michele Pizzuti Italy
Sharon Bergeron United States
Kathryn Fife United Kingdom
Katerina Bakunina Netherlands
Réda Garidi relative to Maaike de Bie Netherlands Maaike de Bie's profile →
Citations per field
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Maaike de Bie · 1×
Citations per year

Countries citing papers authored by Réda Garidi

Since Specialization
Citations

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

Fields of papers citing papers by Réda Garidi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Réda Garidi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Réda Garidi Line = papers co-authored together Réda Garidi links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1 200545
2 201133
3 201133
4 201428
5 201027
6 201524
7 200019
8 20079
9 20097
10 20097
11 20163
12 20092
13 20142
14 20181
15 20250
16 20110

About Réda Garidi

Réda Garidi is a scholar working on Pathology and Forensic Medicine, Genetics, Neurology, Oncology and Hematology, having authored 16 papers that have together received 240 indexed citations. Recurring topics across this work include Lymphoma Diagnosis and Treatment (5 papers), Chronic Lymphocytic Leukemia Research (3 papers), CNS Lymphoma Diagnosis and Treatment (3 papers), Multiple Myeloma Research and Treatments (2 papers), Cancer Treatment and Pharmacology (2 papers), Peripheral Neuropathies and Disorders (2 papers), Vascular Tumors and Angiosarcomas (2 papers) and Eosinophilic Disorders and Syndromes (2 papers). The work is most often cited by research in Genetics (80 citations), Neurology (93 citations), Pathology and Forensic Medicine (76 citations), Hematology (46 citations) and Oncology (49 citations). Réda Garidi has collaborated with scholars based in France and Canada. Frequent co-authors include Bruno Royer, Gandhi Damaj, Bérengère Gruson, Marie Brevet, Lavinia Merlusca, B Desablens, Carol Alliot, Jean Pierre Marolleau, Kamel Ghomari and P. Merle. Their work appears in journals such as Journal of the Peripheral Nervous System, Annals of Pharmacotherapy, Haematologica, Annals of Oncology and Clinical Oncology.

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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