Elsa Delaby
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
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- Autism Spectrum Disorder Research
Papers in
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Genomics and Rare Diseases 1
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- Congenital heart defects research 1
- Co-authors
- Joseph D. Buxbaum (1 shared paper)Catalina Betancur (2 shared papers)Alexander Kolevzon (1 shared paper)Elizabeth Berry‐Kravis (1 shared paper)Hubert Journel (1 shared paper)Martine Doco‐Fenzy (1 shared paper)Joris Andrieux (1 shared paper)Emilie Landais (1 shared paper)
- Journals
- American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)Molecular Autism (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- FranceCanadaUnited States
In The Last Decade
Elsa Delaby
3 papers receiving 71 citations
Peers
Comparison fields: 5 of 28
- Genetics 58
- Cognitive Neuroscience 30
- Developmental Neuroscience 3
- Molecular Biology 31
- Sensory Systems 2
Countries citing papers authored by Elsa Delaby
This map shows the geographic impact of Elsa Delaby'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 Elsa Delaby with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elsa Delaby more than expected).
Fields of papers citing papers by Elsa Delaby
This network shows the impact of papers produced by Elsa Delaby. 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 Elsa Delaby. The network helps show where Elsa Delaby may publish in the future.
Co-authors
The 25 scholars most cited alongside Elsa Delaby, 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 | 2019 | 45 | |
| 2 | 2009 | 27 | |
| 3 | 2016 | 1 |
About Elsa Delaby
Elsa Delaby is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cognitive Neuroscience and Infectious Diseases, having authored 3 papers that have together received 73 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (1 paper), Genomics and Rare Diseases (1 paper), Genetic factors in colorectal cancer (1 paper) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Genetics (58 citations), Cognitive Neuroscience (30 citations), Developmental Neuroscience (3 citations), Molecular Biology (31 citations) and Sensory Systems (2 citations). Elsa Delaby has collaborated with scholars based in France, Canada and United States. Frequent co-authors include Joseph D. Buxbaum, Catalina Betancur, Alexander Kolevzon, Elizabeth Berry‐Kravis, Hubert Journel, Martine Doco‐Fenzy, Joris Andrieux, Emilie Landais, Christèle Dubourg and Marlène Rio. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Molecular Autism and American Journal of Medical Genetics Part A.
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.