Alinoë Lavillaureix
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- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 2
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- Autism Spectrum Disorder Research 2
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- Organ and Tissue Transplantation Research 2
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- RNA modifications and cancer 2
- Congenital heart defects research 2
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- Neurological diseases and metabolism 1
- Co-authors
- Michela TragliaLauren A. WeissIleena MitraErika YehMichael C. OldhamChristine Ladd‐AcostaDavid G. AmaralKimberly A. Aldinger
- Cited by
- GeneticsCognitive NeuroscienceAging
- Journals
- PLoS Genetics (2 papers)Frontiers in Endocrinology (1 paper)Acta Obstetricia Et Gynecologica Scandinavica (1 paper)
- Partner nations
- FranceUnited StatesCanada
In The Last Decade
Alinoë Lavillaureix
11 papers receiving 156 citations
Peers
Comparison fields: 5 of 54
- Genetics 90
- Cognitive Neuroscience 48
- Aging 4
- Transplantation 4
- Developmental Neuroscience 5
Countries citing papers authored by Alinoë Lavillaureix
This map shows the geographic impact of Alinoë Lavillaureix'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 Alinoë Lavillaureix with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alinoë Lavillaureix more than expected).
Fields of papers citing papers by Alinoë Lavillaureix
This network shows the impact of papers produced by Alinoë Lavillaureix. 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 Alinoë Lavillaureix. The network helps show where Alinoë Lavillaureix may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Alinoë Lavillaureix, 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 | 2024 | 0 | |
| 2 | 2023 | 5 | |
| 3 | 2022 | 7 | |
| 4 | 2021 | 4 | |
| 5 | 2021 | 15 | |
| 6 | 2020 | 8 | |
| 7 | 2020 | 3 | |
| 8 | 2017 | 34 | |
| 9 | 2017 | 2 | |
| 10 | 2016 | 56 | |
| 11 | 2015 | 28 | |
| 12 | 2014 | 7 |
About Alinoë Lavillaureix
Alinoë Lavillaureix is a scholar working on Transplantation, Genetics and Nephrology, having authored 12 papers that have together received 169 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA modifications and cancer (2 papers), Genomics and Rare Diseases (2 papers), Congenital heart defects research (2 papers), Autism Spectrum Disorder Research (2 papers), Organ and Tissue Transplantation Research (2 papers) and Neurological diseases and metabolism (1 paper). The work is most often cited by research in Genetics (90 citations), Cognitive Neuroscience (48 citations) and Aging (4 citations). Alinoë Lavillaureix has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Michela Traglia, Lauren A. Weiss, Ileena Mitra, Erika Yeh, Michael C. Oldham, Christine Ladd‐Acosta, David G. Amaral, Kimberly A. Aldinger, Solveig Heide and Stanley F. Nelson. Their work appears in journals such as PLoS Genetics, Frontiers in Endocrinology and Acta Obstetricia Et Gynecologica Scandinavica.
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.