I. Oberlé
Impact in
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 1%
- Autism Spectrum Disorder Research
Papers in
- Genetics 28
- Genetics and Neurodevelopmental Disorders 27
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Epigenetics and DNA Methylation 4
- Genomics and Chromatin Dynamics 3
- CRISPR and Genetic Engineering 3
- Co-authors
- Jean‐Louis Mandel (25 shared papers)Dominique Heitz (7 shared papers)Christine Kretz (5 shared papers)Didier Devys (3 shared papers)J Boué (4 shared papers)André Hanauer (3 shared papers)F. Rousseau (1 shared paper)M. F. Bertheas (1 shared paper)
- Journals
- Human Genetics (6 papers)Proceedings of the National Academy of Sciences (3 papers)Genomics (3 papers)Nucleic Acids Research (2 papers)Science (2 papers)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
I. Oberlé
36 papers receiving 3.4k citations
I. Oberlé's Hit Papers
Peers
Comparison fields: 5 of 81
- Genetics 2.7k
- Cognitive Neuroscience 1.2k
- Molecular Biology 2.1k
- Hematology 207
- Cellular and Molecular Neuroscience 291
Countries citing papers authored by I. Oberlé
This map shows the geographic impact of I. Oberlé'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 I. Oberlé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I. Oberlé more than expected).
Fields of papers citing papers by I. Oberlé
This network shows the impact of papers produced by I. Oberlé. 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 I. Oberlé. The network helps show where I. Oberlé may publish in the future.
Co-authors
The 25 scholars most cited alongside I. Oberlé, 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 37 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 | 1201 |
| 2 | Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation Hit paper breakdown → | 1991 | 539 |
| 3 | 1991 | 178 | |
| 4 | 1985 | 171 | |
| 5 | 1991 | 153 | |
| 6 | 1992 | 138 | |
| 7 | 1985 | 119 | |
| 8 | 1991 | 101 | |
| 9 | 1987 | 79 | |
| 10 | 1991 | 71 | |
| 11 | 1986 | 67 | |
| 12 | 1992 | 65 | |
| 13 | 1986 | 60 | |
| 14 | 1992 | 60 | |
| 15 | Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines. | 1990 | 55 |
| 16 | 1989 | 48 | |
| 17 | Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families. | 1988 | 48 |
| 18 | 1985 | 46 | |
| 19 | 1988 | 35 | |
| 20 | 1991 | 35 |
About I. Oberlé
I. Oberlé is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Genetics, having authored 37 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (27 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Autism Spectrum Disorder Research (4 papers), Epigenetics and DNA Methylation (4 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (3 papers) and CRISPR and Genetic Engineering (3 papers). The work is most often cited by research in Genetics (2.7k citations), Cognitive Neuroscience (1.2k citations), Molecular Biology (2.1k citations), Hematology (207 citations) and Cellular and Molecular Neuroscience (291 citations). I. Oberlé has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Jean‐Louis Mandel, Dominique Heitz, Christine Kretz, Didier Devys, J Boué, André Hanauer, F. Rousseau, M. F. Bertheas, Valérie Biancalana and Giovanna Camerino. Their work appears in journals such as Human Genetics, Proceedings of the National Academy of Sciences, Genomics, Nucleic Acids Research and Science.
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.