Philippe Jonveaux
Impact in
- Hematology top 0.5%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Chronic Lymphocytic Leukemia Research
Papers in
- Genetics 62
- Genomic variations and chromosomal abnormalities 37
- Genetics and Neurodevelopmental Disorders 25
- Chronic Lymphocytic Leukemia Research 16
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- Congenital heart defects research 8
- Co-authors
- Roland Berger (23 shared papers)Christophe Philippe (30 shared papers)Olivier Bernard (6 shared papers)Maryvonne Le Coniat (8 shared papers)M Mauchauffé (3 shared papers)Violaine Bourdon (8 shared papers)Serge Romana (4 shared papers)Pierre Fenaux (6 shared papers)
In The Last Decade
Philippe Jonveaux
128 papers receiving 4.0k citations
Peers
Comparison fields: 5 of 100
- Hematology 1.1k
- Genetics 1.4k
- Genetics 501
- Molecular Biology 1.9k
- Aging 43
Countries citing papers authored by Philippe Jonveaux
This map shows the geographic impact of Philippe Jonveaux'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 Philippe Jonveaux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philippe Jonveaux more than expected).
Fields of papers citing papers by Philippe Jonveaux
This network shows the impact of papers produced by Philippe Jonveaux. 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 Philippe Jonveaux. The network helps show where Philippe Jonveaux may publish in the future.
Co-authors
The 25 scholars most cited alongside Philippe Jonveaux, 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 134 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1995 | 353 | |
| 2 | 2008 | 209 | |
| 3 | 1998 | 193 | |
| 4 | 1999 | 186 | |
| 5 | 1997 | 181 | |
| 6 | 1999 | 160 | |
| 7 | 1991 | 152 | |
| 8 | Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis. | 1992 | 121 |
| 9 | 1990 | 112 | |
| 10 | 1997 | 100 | |
| 11 | 1992 | 94 | |
| 12 | 2004 | 89 | |
| 13 | 2009 | 84 | |
| 14 | 2016 | 75 | |
| 15 | 2013 | 73 | |
| 16 | 1991 | 73 | |
| 17 | 2008 | 72 | |
| 18 | 2009 | 64 | |
| 19 | Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma. | 1996 | 64 |
| 20 | 2001 | 63 |
About Philippe Jonveaux
Philippe Jonveaux is a scholar working on Genetics, Molecular Biology, Hematology, Genetics and Pediatrics, Perinatology and Child Health, having authored 134 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Genetics and Neurodevelopmental Disorders (25 papers), Acute Myeloid Leukemia Research (25 papers), Chronic Lymphocytic Leukemia Research (16 papers), Prenatal Screening and Diagnostics (11 papers), Congenital heart defects research (8 papers), Chronic Myeloid Leukemia Treatments (8 papers) and Acute Lymphoblastic Leukemia research (8 papers). The work is most often cited by research in Hematology (1.1k citations), Genetics (1.4k citations), Genetics (501 citations), Molecular Biology (1.9k citations) and Aging (43 citations). Philippe Jonveaux has collaborated with scholars based in France, Belgium and Morocco. Frequent co-authors include Roland Berger, Christophe Philippe, Olivier Bernard, Maryvonne Le Coniat, M Mauchauffé, Violaine Bourdon, Serge Romana, Pierre Fenaux, Céline Bonnet and Josette Hillion. Their work appears in journals such as Blood, European Journal of Human Genetics, Genes Chromosomes and Cancer, European Journal of Medical Genetics and Prenatal Diagnosis.
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.