I. Oberlé
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders 27
- Genomic variations and chromosomal abnormalities 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Cognitive Neuroscience top 1%
- Autism Spectrum Disorder Research 4
- Molecular Biology top 5%
- Epigenetics and DNA Methylation 4
- CRISPR and Genetic Engineering 3
- Genomics and Chromatin Dynamics 3
- Hematology top 5%
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- Chromosomal and Genetic Variations 5
I. Oberlé
36 papers receiving 3.4k citations
Hit Papers
Peers
Comparison fields: 5 of 82
- Genetics 2.8k
- Cognitive Neuroscience 1.3k
- Molecular Biology 2.2k
- Hematology 209
- Cellular and Molecular Neuroscience 294
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 139 | |
| 2 | 1992 | 60 | |
| 3 | 1992 | 29 | |
| 4 | 1992 | 16 | |
| 5 | 1992 | 65 | |
| 6 | 1992 | 21 | |
| 7 | 1992 | 2 | |
| 8 | 1991 | 71 | |
| 9 | 1991 | 14 | |
| 10 | 1991 | 12 | |
| 11 | 1991 | 179 | |
| 12 | 1991 | 35 | |
| 13 | Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardationbreakdown → | 1991 | 540 |
| 14 | Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome. | 1990 | 25 |
| 15 | 1990 | 16 | |
| 16 | 1989 | 19 | |
| 17 | 1989 | 49 | |
| 18 | 1989 | 25 | |
| 19 | 1988 | 35 | |
| 20 | From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm. | 1986 | 3 |
About I. Oberlé
I. Oberlé is a scholar working on Genetics, Genetics, Molecular Biology, Cognitive Neuroscience and Speech and Hearing, 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 (6 papers), Chromosomal and Genetic Variations (5 papers), Epigenetics and DNA Methylation (4 papers), Autism Spectrum Disorder Research (4 papers), CRISPR and Genetic Engineering (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Genetics (2.8k citations), Cognitive Neuroscience (1.3k citations), Molecular Biology (2.2k citations), Hematology (209 citations) and Cellular and Molecular Neuroscience (294 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, M. F. Bertheas, F. Rousseau, Valérie Biancalana and Giovanna Camerino. Their work appears in journals such as Human Genetics, Proceedings of the National Academy of Sciences, Genomics, Science and New England Journal of Medicine.
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.