Nelle Lambert

3.0k total citations · 1 hit paper
14 papers, 2.0k citations indexed

About

Nelle Lambert is a scholar working on Molecular Biology, Genetics and Social Psychology. According to data from OpenAlex, Nelle Lambert has authored 14 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Social Psychology. Recurrent topics in Nelle Lambert's work include Genomics and Chromatin Dynamics (4 papers), RNA modifications and cancer (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Nelle Lambert is often cited by papers focused on Genomics and Chromatin Dynamics (4 papers), RNA modifications and cancer (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Nelle Lambert collaborates with scholars based in Belgium, United States and France. Nelle Lambert's co-authors include Pierre Vanderhaeghen, Marie-Alexandra Lambot, Angéline Bilheu, Franck Polleux, Katherine S. Pollard, Adèle Herpoel, David Haussler, Adam Siepel, Sofie R. Salama and Sol Katzman and has published in prestigious journals such as Nature, Cell and Neuron.

In The Last Decade

Nelle Lambert

14 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An RNA gene expressed during cortical development evolved rapidly in humans

2006 672 citations Katherine S. Pollard, Sofie R. Salama et al. Nature profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Nelle Lambert Belgium	11	1.5k	504	328	319	250	14	2.0k
Jennifer L. Fish United States	23	1.6k 1.1×	627 1.2×	616 1.9×	285 0.9×	245 1.0×	49	2.5k
Albert E. Ayoub United States	15	1.1k 0.7×	435 0.9×	562 1.7×	450 1.4×	193 0.8×	16	1.8k
Matthew F. Rose United States	13	1.1k 0.7×	430 0.9×	324 1.0×	307 1.0×	152 0.6×	15	1.7k
Mareike Albert Germany	18	1.5k 1.0×	338 0.7×	338 1.0×	191 0.6×	192 0.8×	24	2.1k
Paul Q. Thomas Australia	31	2.4k 1.5×	1.4k 2.8×	170 0.5×	303 0.9×	242 1.0×	90	3.5k
Christiane Haffner Germany	16	1.5k 1.0×	355 0.7×	800 2.4×	301 0.9×	423 1.7×	20	2.0k
Marta Florio Germany	16	1.9k 1.2×	441 0.9×	833 2.5×	417 1.3×	253 1.0×	17	2.5k
Harrison W. Gabel United States	23	2.2k 1.4×	1.1k 2.1×	139 0.4×	397 1.2×	237 0.9×	36	2.9k
Ben Martynoga United Kingdom	19	2.1k 1.3×	428 0.8×	901 2.7×	434 1.4×	348 1.4×	21	2.6k
Fernando Giráldez Spain	34	2.1k 1.4×	201 0.4×	210 0.6×	684 2.1×	284 1.1×	81	3.4k

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-authorship network of co-authors of Nelle Lambert

This figure shows the co-authorship network connecting the top 25 collaborators of Nelle Lambert. A scholar is included among the top collaborators of Nelle Lambert 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 Nelle Lambert. Nelle Lambert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Suzuki, Ikuo, David Gacquer, Roxane Van Heurck, et al.. (2018). Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch Regulation. Cell. 173(6). 1370–1384.e16. 255 indexed citations

Lambert, Nelle, Emmanuelle Ranza, Periklis Makrythanasis, et al.. (2018). Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother. Journal of Human Genetics. 63(7). 847–850. 17 indexed citations

Lambert, Nelle. (2014). Génétique et transmission transgénérationnelle. Cahiers de psychologie clinique. n° 43(2). 11–28. 2 indexed citations

Lambert, Nelle, Vanessa Wermenbol, Bruno Pichon, et al.. (2014). A Familial Heterozygous Null Mutation of MET in Autism Spectrum Disorder. Autism Research. 7(5). 617–622. 11 indexed citations

Igoillo‐Esteve, Mariana, Nelle Lambert, Julie Désir, et al.. (2013). tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans. PLoS Genetics. 9(10). e1003888–e1003888. 95 indexed citations

Espuny-Camacho, Ira, Kimmo A. Michelsen, David Gall, et al.. (2013). Pyramidal Neurons Derived from Human Pluripotent Stem Cells Integrate Efficiently into Mouse Brain Circuits In Vivo. Neuron. 77(3). 440–456. 411 indexed citations

Simonis, Nicolas, Isabelle Migeotte, Nelle Lambert, et al.. (2013). FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. Journal of Medical Genetics. 50(9). 585–592. 61 indexed citations

Igoillo‐Esteve, Mariana, Nelle Lambert, Isabelle Pirson, et al.. (2013). Loss-of-function of the tRNA methyltransferase homolog gene TRMT10A causes young onset diabetes and primary microcephaly in humans. 1 indexed citations

Genin, Anna, Julie Désir, Nelle Lambert, et al.. (2012). Kinetochore KMN network gene CASC5 mutated in primary microcephaly. Human Molecular Genetics. 21(24). 5306–5317. 80 indexed citations

10.

Charrier, Cécile, Kaumudi Joshi, Jaeda Coutinho‐Budd, et al.. (2012). Inhibition of SRGAP2 Function by Its Human-Specific Paralogs Induces Neoteny during Spine Maturation. Cell. 149(4). 923–935. 297 indexed citations

11.

Lambert, Nelle, Marie-Alexandra Lambot, Angéline Bilheu, et al.. (2011). Genes Expressed in Specific Areas of the Human Fetal Cerebral Cortex Display Distinct Patterns of Evolution. PLoS ONE. 6(3). e17753–e17753. 56 indexed citations

12.

Marques, Ana Claudia, Manuela Weier, Nelle Lambert, et al.. (2008). Birth and Rapid Subcellular Adaptation of a Hominoid-Specific CDC14 Protein. PLoS Biology. 6(6). e140–e140. 59 indexed citations

13.

Pollard, Katherine S., Sofie R. Salama, Nelle Lambert, et al.. (2006). An RNA gene expressed during cortical development evolved rapidly in humans. Nature. 443(7108). 167–172. 672 indexed citations breakdown →

14.

Lambert, Nelle & Françoise Lotstra. (2005). L'attachement. De Konrad Lorenz à Larry Young : de l'éthologie à la neurobiologie. Cahiers critiques de thérapie familiale et de pratiques de réseaux. n o 35(2). 83–97. 5 indexed citations

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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