Nelle Lambert

3k citations
13 papers · 2.3k · 1 hit paper · h-index 10

Impact in

    • Neurogenesis and neuroplasticity mechanisms
  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities

Papers in

    • Neurogenesis and neuroplasticity mechanisms 5
    • Genetics and Neurodevelopmental Disorders 4
    • Genomic variations and chromosomal abnormalities 1

Nelle Lambert

13 papers receiving 2.2k citations

Nelle Lambert's Hit Papers

An RNA gene expressed during cortical development evolved rapidly in humans 2006 · 724 citations
7240+6+13Years since publication200400600

Peers

Nelle Lambert
Comparison fields: 5 of 89
  • Developmental Neuroscience 555
  • Genetics 581
  • Molecular Biology 877
  • Cancer Research 156
  • Cellular and Molecular Neuroscience 177
Replace Cotney Justin with:
Cotney Justin United States
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Albert E. Ayoub United States
Rui Luo United States
Kellen Diamond Winden United States
Marta Florio Germany
Amy Holt United States
Xander Nuttle United States
Lili C. Kudo United States
Andrew T.N. Tebbenkamp United States
Nelle Lambert relative to Cotney Justin United States Cotney Justin's profile →
Citations per field
00.5×1.5×2×2.3×
Cotney Justin · 1×
Citations per year

Countries citing papers authored by Nelle Lambert

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Nelle Lambert Line = papers co-authored together Nelle Lambert links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1
An RNA gene expressed during cortical development evolved rapidly in humans
Hit paper breakdown →
2006724
2 2013449
3 2012351
4 2018315
5 2013110
6 201296
7 201375
8 201161
9 200857
10 201818
11 20055
12 20142
13
Loss-of-function of the tRNA methyltransferase homolog gene TRMT10A causes young onset diabetes and primary microcephaly in humans
20131

About Nelle Lambert

Nelle Lambert is a scholar working on Developmental Neuroscience, Genetics, Pediatrics, Perinatology and Child Health, Cell Biology and Developmental Biology, having authored 13 papers that have together received 2.3k indexed citations. Recurring topics across this work include Neurogenesis and neuroplasticity mechanisms (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Microtubule and mitosis dynamics (2 papers), RNA modifications and cancer (2 papers), Pluripotent Stem Cells Research (1 paper), Epigenetics and DNA Methylation (1 paper), Birth, Development, and Health (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Developmental Neuroscience (555 citations), Genetics (581 citations), Molecular Biology (877 citations), Cancer Research (156 citations) and Cellular and Molecular Neuroscience (177 citations). Nelle Lambert has collaborated with scholars based in Belgium, United States and Switzerland. Frequent co-authors include Pierre Vanderhaeghen, Angéline Bilheu, Marie-Alexandra Lambot, Franck Polleux, Adèle Herpoel, Katherine S. Pollard, Sandra Coppens, David H. Haussler, Manuel Ares and Sol J. Katzman. Their work appears in journals such as Cell, Human Molecular Genetics, PLoS ONE, PLoS Genetics and Neuron.

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.

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