J. David Lambert

2.6k total citations · 1 hit paper
47 papers, 2.1k citations indexed

About

J. David Lambert is a scholar working on Molecular Biology, Global and Planetary Change and Paleontology. According to data from OpenAlex, J. David Lambert has authored 47 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Global and Planetary Change and 11 papers in Paleontology. Recurrent topics in J. David Lambert's work include Developmental Biology and Gene Regulation (13 papers), Marine Ecology and Invasive Species (12 papers) and Marine Invertebrate Physiology and Ecology (11 papers). J. David Lambert is often cited by papers focused on Developmental Biology and Gene Regulation (13 papers), Marine Ecology and Invasive Species (12 papers) and Marine Invertebrate Physiology and Ecology (11 papers). J. David Lambert collaborates with scholars based in United States, France and Denmark. J. David Lambert's co-authors include István Módy, Uwe Heinemann, Lisa M. Nagy, Xin Yi Chan, Torben Nathan, Nancy A. Moran, Andreas Roepstorff, Jeremy S. Rabinowitz, R. Scott Jones and Yingli Duan and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

J. David Lambert

46 papers receiving 2.0k citations

Hit Papers

Low extracellular magnesium induces epileptiform activity... 1987 2026 2000 2013 1987 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. David Lambert United States 22 1.0k 755 464 327 249 47 2.1k
Hideo Mukai Japan 32 516 0.5× 1.1k 1.4× 489 1.1× 234 0.7× 51 0.2× 74 3.4k
Michael Schubert France 37 2.6k 2.4× 437 0.6× 523 1.1× 136 0.4× 29 0.1× 112 4.1k
Kaoru S. Imai Japan 27 2.2k 2.1× 297 0.4× 1.3k 2.9× 61 0.2× 389 1.6× 58 3.0k
William J. Moody United States 33 1.6k 1.5× 2.1k 2.8× 85 0.2× 669 2.0× 109 0.4× 63 3.1k
Daniela Vallone Germany 32 1.3k 1.2× 1.5k 1.9× 172 0.4× 342 1.0× 247 1.0× 64 4.0k
Yasushi Okamura Japan 38 4.0k 3.9× 2.6k 3.4× 498 1.1× 196 0.6× 16 0.1× 142 5.4k
Christine Morrow United Kingdom 20 830 0.8× 659 0.9× 178 0.4× 33 0.1× 29 0.1× 42 1.9k
Kunitaro Takahashi Japan 18 1.1k 1.0× 1.2k 1.6× 155 0.3× 329 1.0× 21 0.1× 24 1.9k
Philippe Vernier France 39 1.5k 1.5× 1.7k 2.2× 156 0.3× 270 0.8× 96 0.4× 63 3.9k
Jay A. Blundon United States 20 447 0.4× 495 0.7× 271 0.6× 437 1.3× 22 0.1× 31 1.4k

Countries citing papers authored by J. David Lambert

Since Specialization
Citations

This map shows the geographic impact of J. David 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 J. David Lambert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. David Lambert more than expected).

Fields of papers citing papers by J. David Lambert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. David 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 J. David Lambert. The network helps show where J. David Lambert may publish in the future.

Co-authorship network of co-authors of J. David Lambert

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

All Works

20 of 20 papers shown
1.
Lambert, J. David, et al.. (2024). A chitin-binding domain-containing gene is essential for shell development in the mollusc Tritia. Developmental Biology. 520. 1–12.
2.
Wu, Long‐Jun & J. David Lambert. (2020). A serpin is required for ectomesoderm, a hallmark of spiralian development. Developmental Biology. 469. 172–181. 1 indexed citations
3.
Wu, Long‐Jun, Laurel S. Hiebert, Yale J. Passamaneck, et al.. (2020). Genes with spiralian-specific protein motifs are expressed in spiralian ciliary bands. Nature Communications. 11(1). 4171–4171. 18 indexed citations
4.
Mazzoil, Marilyn, et al.. (2017). Effects of study area size on home range estimates of common bottlenose dolphins Tursiops truncatus. Current Zoology. 63(6). 693–701. 15 indexed citations
5.
Lambert, J. David, et al.. (2016). Mollusc models I. The snail Ilyanassa. Current Opinion in Genetics & Development. 39. 168–174. 13 indexed citations
6.
Lambert, J. David, et al.. (2016). Dpp/BMP2-4 Mediates Signaling from the D-Quadrant Organizer in a Spiralian Embryo. Current Biology. 26(15). 2003–2010. 35 indexed citations
7.
Chan, Xin Yi & J. David Lambert. (2014). Development of blastomere clones in the Ilyanassa embryo: transformation of the spiralian blastula into the larval body plan. Development Genes and Evolution. 224(3). 159–174. 26 indexed citations
8.
Chan, Xin Yi & J. David Lambert. (2010). Patterning a spiralian embryo: A segregated RNA for a Tis11 ortholog is required in the 3a and 3b cells of the Ilyanassa embryo. Developmental Biology. 349(1). 102–112. 21 indexed citations
9.
Lambert, J. David. (2010). Developmental Patterns in Spiralian Embryos. Current Biology. 20(2). R72–R77. 78 indexed citations
10.
Leise, Esther M., et al.. (2009). Obtaining Ilyanassa Snail Embryos. Cold Spring Harbor Protocols. 2009(4). pdb.prot5183–pdb.prot5183. 7 indexed citations
11.
Leise, Esther M., et al.. (2009). Pressure Injection of Ilyanassa Snail Embryos. Cold Spring Harbor Protocols. 2009(4). pdb.prot5185–pdb.prot5185. 2 indexed citations
12.
Lambert, J. David. (2009). Chapter 5 Patterning the Spiralian Embryo. Current topics in developmental biology. 86. 107–133. 12 indexed citations
13.
Leise, Esther M., et al.. (2009). Fixation of Ilyanassa Snail Embryos and Larvae: Figure 1.. Cold Spring Harbor Protocols. 2009(4). pdb.prot5186–pdb.prot5186. 3 indexed citations
14.
Leise, Esther M., et al.. (2009). Induction of Larval Metamorphosis in the Snail Ilyanassa: Figure 1.. Cold Spring Harbor Protocols. 2009(4). pdb.prot5184–pdb.prot5184. 3 indexed citations
15.
Rabinowitz, Jeremy S. & J. David Lambert. (2008). Asymmetric localization and functional role of the putative non-coding RNA IoLR5. Developmental Biology. 319(2). 576–576. 1 indexed citations
16.
Rabinowitz, Jeremy S., Xin Yi Chan, Evan P. Kingsley, Yingli Duan, & J. David Lambert. (2008). Nanos Is Required in Somatic Blast Cell Lineages in the Posterior of a Mollusk Embryo. Current Biology. 18(5). 331–336. 67 indexed citations
17.
Kingsley, Evan P., Xin Yi Chan, Yingli Duan, & J. David Lambert. (2007). Widespread RNA segregation in a spiralian embryo. Evolution & Development. 9(6). 527–539. 80 indexed citations
18.
Lambert, J. David. (2007). Mesoderm in spiralians: the organizer and the 4d cell. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 310B(1). 15–23. 65 indexed citations
19.
Zhou, Dan, Jin Xue, Jianming Chen, et al.. (2007). Experimental Selection for Drosophila Survival in Extremely Low O2 Environment. PLoS ONE. 2(5). e490–e490. 69 indexed citations
20.
Lambert, J. David & Lisa M. Nagy. (2002). Asymmetric inheritance of centrosomally localized mRNAs during embryonic cleavages. Nature. 420(6916). 682–686. 178 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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