André Hanauer
Impact in
- Nephrology top 1%
- Parathyroid Disorders and Treatments
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 61
- Genetics and Neurodevelopmental Disorders 41
- Genetic Associations and Epidemiology 9
- Genomic variations and chromosomal abnormalities 6
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- Genetic Neurodegenerative Diseases 8
- Hereditary Neurological Disorders 7
- Co-authors
- Jean‐Louis Mandel (26 shared papers)Sylvie Jacquot (16 shared papers)Paolo Sassone‐Corsi (7 shared papers)Isabelle Oberlé (3 shared papers)Solange Pannetier (20 shared papers)Didier Devys (1 shared paper)François Rousseau (1 shared paper)J G Boué (1 shared paper)
- Journals
- Human Genetics (13 papers)Journal of Medical Genetics (6 papers)European Journal of Human Genetics (6 papers)Genomics (5 papers)Human Molecular Genetics (4 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
André Hanauer
100 papers receiving 6.9k citations
André Hanauer's Hit Papers
Peers
Comparison fields: 5 of 99
- Nephrology 934
- Genetics 2.6k
- Cellular and Molecular Neuroscience 708
- Molecular Biology 2.3k
- Developmental Neuroscience 63
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-authors
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
Showing the 20 most-cited of 100 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome Hit paper breakdown → | 1991 | 1299 |
| 2 | A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets Hit paper breakdown → | 1995 | 944 |
| 3 | 2004 | 702 | |
| 4 | 1999 | 412 | |
| 5 | 1996 | 342 | |
| 6 | 1998 | 268 | |
| 7 | 1984 | 164 | |
| 8 | 1999 | 127 | |
| 9 | 2002 | 125 | |
| 10 | 1992 | 112 | |
| 11 | 2009 | 110 | |
| 12 | 1992 | 104 | |
| 13 | 1983 | 85 | |
| 14 | 2001 | 77 | |
| 15 | 1998 | 71 | |
| 16 | 2006 | 70 | |
| 17 | 2005 | 66 | |
| 18 | 1999 | 64 | |
| 19 | 1989 | 61 | |
| 20 | 1988 | 60 |
About André Hanauer
André Hanauer is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Nephrology and Clinical Biochemistry, having authored 100 papers that have together received 7.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (41 papers), Genetic Associations and Epidemiology (9 papers), Genetic Neurodegenerative Diseases (8 papers), Hereditary Neurological Disorders (7 papers), Protein Kinase Regulation and GTPase Signaling (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Parathyroid Disorders and Treatments (6 papers) and Muscle Physiology and Disorders (5 papers). The work is most often cited by research in Nephrology (934 citations), Genetics (2.6k citations), Cellular and Molecular Neuroscience (708 citations), Molecular Biology (2.3k citations) and Developmental Neuroscience (63 citations). André Hanauer has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Jean‐Louis Mandel, Sylvie Jacquot, Paolo Sassone‐Corsi, Isabelle Oberlé, Solange Pannetier, Didier Devys, François Rousseau, J G Boué, Christine Kretz and M. F. Bertheas. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, European Journal of Human Genetics, Genomics 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.