Jean Weissenbach
Impact in
- Genetics top 0.1%
- Neurogenetic and Muscular Disorders Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 0.2%
- RNA modifications and cancer
- RNA Research and Splicing
- Genomics and Phylogenetic Studies
Papers in
-
- Genomics and Phylogenetic Studies 24
- RNA modifications and cancer 17
- RNA and protein synthesis mechanisms 16
- RNA Research and Splicing 12
- Genomics and Chromatin Dynamics 11
- Genetics 73
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
- Genomic variations and chromosomal abnormalities 16
- Co-authors
- Philippe Millasseau (3 shared papers)Corinne Cruaud (14 shared papers)Gàbor Gyapay (13 shared papers)Colette Dib (3 shared papers)Alain Vignal (3 shared papers)Jean Morissette (2 shared papers)Denis Le Paslier (11 shared papers)Delphine Samson (8 shared papers)
- Journals
- Genomics (27 papers)Nature Genetics (20 papers)Nature (11 papers)Genome Research (10 papers)Human Molecular Genetics (9 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Jean Weissenbach
183 papers receiving 23.8k citations
Jean Weissenbach's Hit Papers
Peers
Comparison fields: 5 of 176
- Genetics 3.3k
- Genetics 7.1k
- Molecular Biology 13.8k
- Neurology 2.6k
- Neurology 1.4k
Countries citing papers authored by Jean Weissenbach
This map shows the geographic impact of Jean Weissenbach'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 Jean Weissenbach with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jean Weissenbach more than expected).
Fields of papers citing papers by Jean Weissenbach
This network shows the impact of papers produced by Jean Weissenbach. 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 Jean Weissenbach. The network helps show where Jean Weissenbach may publish in the future.
Co-authors
The 25 scholars most cited alongside Jean Weissenbach, 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 183 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Identification and characterization of a spinal muscular atrophy-determining gene Hit paper breakdown → | 1995 | 3069 |
| 2 | A comprehensive genetic map of the human genome based on 5,264 microsatellites Hit paper breakdown → | 1996 | 2444 |
| 3 | Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia Hit paper breakdown → | 1996 | 1492 |
| 4 | A second-generation linkage map of the human genome Hit paper breakdown → | 1992 | 1436 |
| 5 | Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene Hit paper breakdown → | 1994 | 1237 |
| 6 | Mapping of a susceptibility locus for Crohn's disease on chromosome 16 Hit paper breakdown → | 1996 | 727 |
| 7 | Comparative Genomics of Multidrug Resistance in Acinetobacter baumannii Hit paper breakdown → | 2006 | 645 |
| 8 | Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy Hit paper breakdown → | 1995 | 506 |
| 9 | Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients Hit paper breakdown → | 1997 | 500 |
| 10 | A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family Hit paper breakdown → | 1997 | 467 |
| 11 | 1999 | 464 | |
| 12 | 1993 | 423 | |
| 13 | 2001 | 346 | |
| 14 | 1995 | 336 | |
| 15 | 2001 | 329 | |
| 16 | 1994 | 323 | |
| 17 | 2005 | 289 | |
| 18 | 2008 | 289 | |
| 19 | 1993 | 269 | |
| 20 | 2008 | 255 |
About Jean Weissenbach
Jean Weissenbach is a scholar working on Molecular Biology, Genetics, Plant Science, Cellular and Molecular Neuroscience and Cancer Research, having authored 183 papers that have together received 24.5k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (28 papers), Genomics and Phylogenetic Studies (24 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), RNA modifications and cancer (17 papers), RNA and protein synthesis mechanisms (16 papers), Genomic variations and chromosomal abnormalities (16 papers), RNA Research and Splicing (12 papers) and Genomics and Chromatin Dynamics (11 papers). The work is most often cited by research in Genetics (3.3k citations), Genetics (7.1k citations), Molecular Biology (13.8k citations), Neurology (2.6k citations) and Neurology (1.4k citations). Jean Weissenbach has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Philippe Millasseau, Corinne Cruaud, Gàbor Gyapay, Colette Dib, Alain Vignal, Jean Morissette, Denis Le Paslier, Delphine Samson, Judith Melki and Arnold Münnich. Their work appears in journals such as Genomics, Nature Genetics, Nature, Genome Research and Human Molecular 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.