Alexandra Afenjar
- Genetics top 5%
- Molecular Biology
- Psychiatry and Mental health top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Cellular and Molecular Neuroscience
- Co-authors
- Delphine HéronThierry BienvenuNadia Bahi‐BuissonNathalie BoddaertMarlène RioChristophe PhilippeMathieu MilhBenôıt Girard
- Topics
- Genetics and Neurodevelopmental Disorders (14 papers)Genomic variations and chromosomal abnormalities (9 papers)Genomics and Rare Diseases (7 papers)
- Journals
- Nature GeneticsBrainNeurology
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
Alexandra Afenjar
39 papers receiving 991 citations
Peers
Comparison fields: 5 of 70
- Genetics 621
- Molecular Biology 521
- Psychiatry and Mental health 127
- Pediatrics, Perinatology and Child Health 113
- Cellular and Molecular Neuroscience 106
Countries citing papers authored by Alexandra Afenjar
This map shows the geographic impact of Alexandra Afenjar'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 Alexandra Afenjar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandra Afenjar more than expected).
Fields of papers citing papers by Alexandra Afenjar
This network shows the impact of papers produced by Alexandra Afenjar. 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 Alexandra Afenjar. The network helps show where Alexandra Afenjar may publish in the future.
Co-authorship network of co-authors of Alexandra Afenjar
This figure shows the co-authorship network connecting the top 25 collaborators of Alexandra Afenjar. A scholar is included among the top collaborators of Alexandra Afenjar based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Alexandra Afenjar. Alexandra Afenjar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 10 | |
| 4 | 26 | |
| 5 | 2 | |
| 6 | 25 | |
| 7 | 3 | |
| 8 | 38 | |
| 9 | 28 | |
| 10 | 6 | |
| 11 | 117 | |
| 12 | 9 | |
| 13 | 8 | |
| 14 | 3 | |
| 15 | 139 | |
| 16 | 53 | |
| 17 | 26 | |
| 18 | 0 | |
| 19 | 43 | |
| 20 | 15 |
About Alexandra Afenjar
Alexandra Afenjar is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 42 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (621 citations), Clinical Biochemistry (63 citations) and Psychiatry and Mental health (127 citations). Alexandra Afenjar has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Delphine Héron, Thierry Bienvenu, Nadia Bahi‐Buisson, Nathalie Boddaert, Marlène Rio, Christophe Philippe, Mathieu Milh, Benôıt Girard, Juliette Nectoux and Jamel Chelly. Their work appears in journals such as Nature Genetics, Brain and Neurology.
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.