Bernard Aral
Impact in
- Cancer Research top 2%
- Cancer, Hypoxia, and Metabolism
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- Medical Imaging Techniques and Applications
- Advanced MRI Techniques and Applications
- MRI in cancer diagnosis
Papers in
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- Biochemical and Molecular Research 4
- Molecular Biology Techniques and Applications 3
- Genetics 10
- Blood disorders and treatments 4
- Genomic variations and chromosomal abnormalities 4
- Myeloproliferative Neoplasms: Diagnosis and Treatment 3
- Co-authors
- Karlheinz Schlenger (1 shared paper)Uwe Schäffer (1 shared paper)M. Mitze (1 shared paper)Michael Höckel (1 shared paper)Peter Vaupel (1 shared paper)P. Kamoun (7 shared papers)Laurence Faivre (9 shared papers)Hyder A. Jinnah (2 shared papers)
- Journals
- European Journal of Human Genetics (2 papers)European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)Human Mutation (2 papers)Blood (2 papers)
- Partner nations
- FranceUnited StatesLebanon
In The Last Decade
Bernard Aral
31 papers receiving 1.8k citations
Bernard Aral's Hit Papers
Peers
Comparison fields: 5 of 99
- Cancer Research 925
- Radiology, Nuclear Medicine and Imaging 391
- Biotechnology 130
- Obstetrics and Gynecology 102
- Biophysics 74
Countries citing papers authored by Bernard Aral
This map shows the geographic impact of Bernard Aral'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 Bernard Aral with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernard Aral more than expected).
Fields of papers citing papers by Bernard Aral
This network shows the impact of papers produced by Bernard Aral. 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 Bernard Aral. The network helps show where Bernard Aral may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernard Aral, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Association between tumor hypoxia and malignant progression in advanced cancer of the uterine cervix. Hit paper breakdown → | 1996 | 1491 |
| 2 | 2001 | 55 | |
| 3 | 2014 | 37 | |
| 4 | 1997 | 25 | |
| 5 | 2020 | 23 | |
| 6 | 2012 | 22 | |
| 7 | 2009 | 22 | |
| 8 | Database cloning human delta 1-pyrroline-5-carboxylate synthetase (P5CS) cDNA: a bifunctional enzyme catalyzing the first 2 steps in proline biosynthesis. | 1996 | 21 |
| 9 | [A new inherited metabolic disease: delta1-pyrroline 5-carboxylate synthetase deficiency]. | 1998 | 20 |
| 10 | 2003 | 19 | |
| 11 | 2011 | 18 | |
| 12 | 2013 | 11 | |
| 13 | 2013 | 11 | |
| 14 | 1997 | 11 | |
| 15 | 2004 | 10 | |
| 16 | 2018 | 8 | |
| 17 | 2015 | 8 | |
| 18 | 2013 | 8 | |
| 19 | 1999 | 7 | |
| 20 | 2012 | 6 |
About Bernard Aral
Bernard Aral is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Genetics and Physiology, having authored 31 papers that have together received 1.9k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers), Blood disorders and treatments (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (3 papers), Prenatal Screening and Diagnostics (3 papers), Molecular Biology Techniques and Applications (3 papers) and Erythrocyte Function and Pathophysiology (3 papers). The work is most often cited by research in Cancer Research (925 citations), Radiology, Nuclear Medicine and Imaging (391 citations), Biotechnology (130 citations), Obstetrics and Gynecology (102 citations) and Biophysics (74 citations). Bernard Aral has collaborated with scholars based in France, United States and Lebanon. Frequent co-authors include Karlheinz Schlenger, Uwe Schäffer, M. Mitze, Michael Höckel, Peter Vaupel, P. Kamoun, Laurence Faivre, Hyder A. Jinnah, Chantal Benelli and Nadège Gigot. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Prenatal Diagnosis, Human Mutation and Blood.
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.