Nelle Lambert
Impact in
- Developmental Neuroscience top 1%
- Neurogenesis and neuroplasticity mechanisms
- Molecular Biology top 5%
- Pluripotent Stem Cells Research
- RNA Research and Splicing
- RNA modifications and cancer
- CRISPR and Genetic Engineering
- RNA and protein synthesis mechanisms
- Genomics and Chromatin Dynamics
Papers in
-
- Genomics and Chromatin Dynamics 4
- Epigenetics and DNA Methylation 3
- RNA modifications and cancer 3
- RNA Research and Splicing 3
- Congenital heart defects research 2
- Genetics 4
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Pierre Vanderhaeghen (8 shared papers)Marie-Alexandra Lambot (3 shared papers)Angéline Bilheu (3 shared papers)Franck Polleux (2 shared papers)Katherine S. Pollard (2 shared papers)Adèle Herpoel (2 shared papers)Courtney Onodera (1 shared paper)David Haussler (1 shared paper)
- Journals
- Cell (2 papers)PLoS ONE (1 paper)Human Molecular Genetics (1 paper)Neuron (1 paper)Nature (1 paper)
- Partner nations
- BelgiumUnited StatesFrance
In The Last Decade
Nelle Lambert
13 papers receiving 2.1k citations
Nelle Lambert's Hit Papers
Peers
Comparison fields: 5 of 101
- Developmental Neuroscience 348
- Molecular Biology 1.5k
- Aging 36
- Genetics 499
- Cellular and Molecular Neuroscience 319
Countries citing papers authored by Nelle Lambert
This map shows the geographic impact of Nelle Lambert'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 Nelle Lambert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nelle Lambert more than expected).
Fields of papers citing papers by Nelle Lambert
This network shows the impact of papers produced by Nelle Lambert. 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 Nelle Lambert. The network helps show where Nelle Lambert may publish in the future.
Co-authors
The 25 scholars most cited alongside Nelle Lambert, 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 | An RNA gene expressed during cortical development evolved rapidly in humans Hit paper breakdown → | 2006 | 714 |
| 2 | 2013 | 430 | |
| 3 | 2012 | 326 | |
| 4 | 2018 | 273 | |
| 5 | 2013 | 99 | |
| 6 | 2012 | 87 | |
| 7 | 2013 | 65 | |
| 8 | 2008 | 61 | |
| 9 | 2011 | 58 | |
| 10 | 2018 | 17 | |
| 11 | 2005 | 5 | |
| 12 | 2014 | 2 | |
| 13 | Loss-of-function of the tRNA methyltransferase homolog gene TRMT10A causes young onset diabetes and primary microcephaly in humans | 2013 | 1 |
About Nelle Lambert
Nelle Lambert is a scholar working on Molecular Biology, Genetics, Social Psychology, Cell Biology and Cellular and Molecular Neuroscience, having authored 13 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), Epigenetics and DNA Methylation (3 papers), RNA modifications and cancer (3 papers), RNA Research and Splicing (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Autism Spectrum Disorder Research (1 paper). The work is most often cited by research in Developmental Neuroscience (348 citations), Molecular Biology (1.5k citations), Aging (36 citations), Genetics (499 citations) and Cellular and Molecular Neuroscience (319 citations). Nelle Lambert has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Pierre Vanderhaeghen, Marie-Alexandra Lambot, Angéline Bilheu, Franck Polleux, Katherine S. Pollard, Adèle Herpoel, Courtney Onodera, David Haussler, Colette Dehay and Adam Siepel. Their work appears in journals such as Cell, PLoS ONE, Human Molecular Genetics, Neuron and Nature.
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.