Wallid Deb
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
-
- Pluripotent Stem Cells Research
- Ubiquitin and proteasome pathways
- RNA modifications and cancer
- Inflammasome and immune disorders
Papers in
- Genetics 28
- Genetics and Neurodevelopmental Disorders 22
- Genomics and Rare Diseases 12
-
- Ubiquitin and proteasome pathways 6
- Pluripotent Stem Cells Research 1
- RNA Research and Splicing 1
- Co-authors
- Virginie Vignard (1 shared paper)Stéphane Bezieau (2 shared papers)Sandra Mercier (1 shared paper)Sébastien Küry (1 shared paper)Frédéric Ebstein (1 shared paper)Bertrand Isidor (2 shared papers)Achille Iolascon (1 shared paper)Brunella Franco (1 shared paper)
- Journals
- The American Journal of Human Genetics (9 papers)Genetics in Medicine (6 papers)Nature Communications (3 papers)European Journal of Human Genetics (2 papers)Clinical Genetics (2 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Wallid Deb
27 papers receiving 730 citations
Peers
Comparison fields: 5 of 64
- Genetics 290
- Molecular Biology 302
- Developmental Neuroscience 12
- Clinical Biochemistry 16
- Cellular and Molecular Neuroscience 38
Countries citing papers authored by Wallid Deb
This map shows the geographic impact of Wallid Deb'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 Wallid Deb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wallid Deb more than expected).
Fields of papers citing papers by Wallid Deb
This network shows the impact of papers produced by Wallid Deb. 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 Wallid Deb. The network helps show where Wallid Deb may publish in the future.
Co-authors
The 19 scholars most cited alongside Wallid Deb, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 140 | |
| 2 | 2018 | 103 | |
| 3 | 2017 | 90 | |
| 4 | 2019 | 48 | |
| 5 | 2022 | 42 | |
| 6 | 2019 | 41 | |
| 7 | 2018 | 33 | |
| 8 | 2022 | 33 | |
| 9 | 2022 | 29 | |
| 10 | 2023 | 24 | |
| 11 | 2021 | 21 | |
| 12 | 2023 | 20 | |
| 13 | 2023 | 19 | |
| 14 | 2022 | 17 | |
| 15 | 2021 | 16 | |
| 16 | 2017 | 15 | |
| 17 | 2024 | 11 | |
| 18 | 2024 | 8 | |
| 19 | 2022 | 6 | |
| 20 | 2023 | 6 |
About Wallid Deb
Wallid Deb is a scholar working on Genetics, Molecular Biology, Developmental Neuroscience, Clinical Biochemistry and Urology, having authored 33 papers that have together received 736 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (22 papers), Genomics and Rare Diseases (12 papers), Ubiquitin and proteasome pathways (6 papers), Pluripotent Stem Cells Research (1 paper), Lysosomal Storage Disorders Research (1 paper), Metabolism and Genetic Disorders (1 paper), RNA Research and Splicing (1 paper) and Vascular Malformations Diagnosis and Treatment (1 paper). The work is most often cited by research in Genetics (290 citations), Molecular Biology (302 citations), Developmental Neuroscience (12 citations), Clinical Biochemistry (16 citations) and Cellular and Molecular Neuroscience (38 citations). Wallid Deb has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Virginie Vignard, Stéphane Bezieau, Sandra Mercier, Sébastien Küry, Frédéric Ebstein, Bertrand Isidor, Achille Iolascon, Brunella Franco, Manuela Morleo and Valeria Tiranti. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Nature Communications, European Journal of Human Genetics and Clinical Genetics.
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.