André Hanauer
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders 42
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 15
- Molecular Biology top 1%
- Chromatin Remodeling and Cancer 9
- Ubiquitin and proteasome pathways 9
- Genomics and Chromatin Dynamics 9
- Epigenetics and DNA Methylation 7
- Protein Degradation and Inhibitors 6
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- Genetic Neurodegenerative Diseases 7
- Cognitive Neuroscience top 5%
- Cell Biology top 2%
- Co-authors
- Jean‐Louis MandelSylvie JacquotPaolo Sassone‐CorsiI. OberléM. F. BertheasDidier DevysDominique HeitzF. Rousseau
- Journals
- Human Genetics (11 papers)European Journal of Human Genetics (6 papers)Journal of Medical Genetics (6 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
André Hanauer
86 papers receiving 5.4k citations
Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 2.5k
- Molecular Biology 4.0k
- Cellular and Molecular Neuroscience 771
- Cognitive Neuroscience 657
- Cell Biology 532
Countries citing papers authored by André Hanauer
This map shows the geographic impact of André Hanauer'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 André Hanauer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites André Hanauer more than expected).
Fields of papers citing papers by André Hanauer
This network shows the impact of papers produced by André Hanauer. 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 André Hanauer. The network helps show where André Hanauer may publish in the future.
Co-authorship network
The 25 scholars most cited alongside André Hanauer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 11 | |
| 2 | 2010 | 18 | |
| 3 | 2009 | 15 | |
| 4 | 2005 | 64 | |
| 5 | 2005 | 11 | |
| 6 | 2002 | 18 | |
| 7 | 2002 | 118 | |
| 8 | 1999 | 408 | |
| 9 | 1999 | 22 | |
| 10 | 1998 | 68 | |
| 11 | 1997 | 3 | |
| 12 | 1996 | 319 | |
| 13 | X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21. | 1995 | 20 |
| 14 | 1994 | 18 | |
| 15 | 1994 | 32 | |
| 16 | 1992 | 97 | |
| 17 | 1991 | 18 | |
| 18 | 1990 | 9 | |
| 19 | 1989 | 19 | |
| 20 | 1988 | 35 |
About André Hanauer
André Hanauer is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Genetics and Cell Biology, having authored 86 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (42 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers), Chromatin Remodeling and Cancer (9 papers), Ubiquitin and proteasome pathways (9 papers), Genomics and Chromatin Dynamics (9 papers), Genetic Neurodegenerative Diseases (7 papers), Epigenetics and DNA Methylation (7 papers) and Protein Degradation and Inhibitors (6 papers). The work is most often cited by research in Genetics (2.5k citations), Molecular Biology (4.0k citations), Cellular and Molecular Neuroscience (771 citations), Cognitive Neuroscience (657 citations) and Cell Biology (532 citations). André Hanauer has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Jean‐Louis Mandel, Sylvie Jacquot, Paolo Sassone‐Corsi, I. Oberlé, M. F. Bertheas, Didier Devys, Dominique Heitz, F. Rousseau, J Boué and Christine Kretz. Their work appears in journals such as Human Genetics, European Journal of Human Genetics, Journal of Medical Genetics, Genomics and Proceedings of the National Academy of Sciences.
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.