Rachel Golub

3.0k total citations
52 papers, 1.7k citations indexed

About

Rachel Golub is a scholar working on Immunology, Molecular Biology and Surgery. According to data from OpenAlex, Rachel Golub has authored 52 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Immunology, 12 papers in Molecular Biology and 9 papers in Surgery. Recurrent topics in Rachel Golub's work include Immune Cell Function and Interaction (28 papers), IL-33, ST2, and ILC Pathways (23 papers) and T-cell and B-cell Immunology (14 papers). Rachel Golub is often cited by papers focused on Immune Cell Function and Interaction (28 papers), IL-33, ST2, and ILC Pathways (23 papers) and T-cell and B-cell Immunology (14 papers). Rachel Golub collaborates with scholars based in France, United States and Canada. Rachel Golub's co-authors include Ana Cumano, Sylvestre Chea, Laurent Boucontet, Maxime Petit, Thibaut Perchet, Julien Bertrand, Sandrine Schmutz, Anne Louise, Gillian E. Wu and Abdelali Jalil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Rachel Golub

51 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rachel Golub France 24 1.3k 477 373 233 209 52 1.7k
Bethany Tesar United States 16 995 0.8× 280 0.6× 274 0.7× 67 0.3× 70 0.3× 32 1.5k
Manabu Musashi Japan 14 517 0.4× 429 0.9× 400 1.1× 54 0.2× 320 1.5× 45 1.3k
Chang Kyu Oh United States 15 870 0.7× 119 0.2× 392 1.1× 126 0.5× 205 1.0× 25 1.5k
C A Parkos United States 7 405 0.3× 167 0.4× 319 0.9× 137 0.6× 86 0.4× 8 949
Richard J. Fish Switzerland 21 348 0.3× 162 0.3× 586 1.6× 144 0.6× 230 1.1× 51 1.5k
Hiroaki Takatori Japan 23 1.5k 1.2× 315 0.7× 489 1.3× 65 0.3× 99 0.5× 44 2.3k
Odile Burlen‐Defranoux France 19 1.1k 0.9× 94 0.2× 289 0.8× 117 0.5× 122 0.6× 23 1.5k
Jean Leif United States 23 919 0.7× 374 0.8× 367 1.0× 29 0.1× 333 1.6× 44 1.7k
Zane Orinska Germany 19 1.1k 0.8× 72 0.2× 299 0.8× 135 0.6× 110 0.5× 39 1.5k
D Grail Australia 11 1.2k 1.0× 270 0.6× 606 1.6× 58 0.2× 277 1.3× 15 2.2k

Countries citing papers authored by Rachel Golub

Since Specialization
Citations

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

Fields of papers citing papers by Rachel Golub

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rachel Golub. 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 Rachel Golub. The network helps show where Rachel Golub may publish in the future.

Co-authorship network of co-authors of Rachel Golub

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Golub. A scholar is included among the top collaborators of Rachel Golub 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 Rachel Golub. Rachel Golub 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.
Darbois, Aurélie, Virginie Prémel, Ludovic Colombeau, et al.. (2023). Role of MR1-driven signals and amphiregulin on the recruitment and repair function of MAIT cells during skin wound healing. Immunity. 56(1). 78–92.e6. 56 indexed citations
2.
Cacialli, Pietro, Marie-Pierre Mailhé, Ingrid Wagner, et al.. (2022). Synergistic prostaglandin E synthesis by myeloid and endothelial cells promotes fetal hematopoietic stem cell expansion in vertebrates. The EMBO Journal. 41(19). e108536–e108536. 7 indexed citations
3.
Perchet, Thibaut, et al.. (2020). Tbet promotes CXCR6 expression in immature natural killer cells and natural killer cell egress from the bone marrow. Immunology. 161(1). 28–38. 9 indexed citations
4.
Burlen‐Defranoux, Odile, Thibaut Perchet, Lorea Iturri, et al.. (2020). A wave of bipotent T/ILC-restricted progenitors shapes the embryonic thymus microenvironment in a time-dependent manner. Blood. 137(8). 1024–1036. 32 indexed citations
5.
Golub, Rachel. (2020). The Notch signaling pathway involvement in innate lymphoid cell biology. Biomedical Journal. 44(2). 133–143. 21 indexed citations
6.
Simic, Milesa, Lionel Spinelli, Rebecca Gentek, et al.. (2020). Distinct Waves from the Hemogenic Endothelium Give Rise to Layered Lymphoid Tissue Inducer Cell Ontogeny. Cell Reports. 32(6). 108004–108004. 40 indexed citations
7.
Xu, Wei, Sylvestre Chea, Christian A. J. Vosshenrich, et al.. (2019). An Id2RFP-Reporter Mouse Redefines Innate Lymphoid Cell Precursor Potentials. Immunity. 50(4). 1054–1068.e3. 120 indexed citations
8.
Luci, Carmelo, et al.. (2019). Natural Killer Cells and Type 1 Innate Lymphoid Cells Are New Actors in Non-alcoholic Fatty Liver Disease. Frontiers in Immunology. 10. 1192–1192. 48 indexed citations
9.
Lombardi, Vincent, Sonia Luce, S. Horiot, et al.. (2018). CCR10+ILC2s with ILC1‐like properties exhibit a protective function in severe allergic asthma. Allergy. 74(5). 933–943. 21 indexed citations
10.
Berthault, Claire, Cyrille Ramond, Odile Burlen‐Defranoux, et al.. (2017). Asynchronous lineage priming determines commitment to T cell and B cell lineages in fetal liver. Nature Immunology. 18(10). 1139–1149. 20 indexed citations
11.
Perchet, Thibaut, Sylvestre Chea, Milena Hasan, Ana Cumano, & Rachel Golub. (2017). Single-cell Gene Expression Using Multiplex RT-qPCR to Characterize Heterogeneity of Rare Lymphoid Populations. Journal of Visualized Experiments. 5 indexed citations
12.
Perchet, Thibaut, et al.. (2017). Single-cell Gene Expression Using Multiplex RT-qPCR to Characterize Heterogeneity of Rare Lymphoid Populations. Journal of Visualized Experiments. 1 indexed citations
13.
Chea, Sylvestre, Sandrine Schmutz, Claire Berthault, et al.. (2016). Single-Cell Gene Expression Analyses Reveal Heterogeneous Responsiveness of Fetal Innate Lymphoid Progenitors to Notch Signaling. Cell Reports. 14(6). 1500–1516. 66 indexed citations
14.
Chea, Sylvestre, et al.. (2015). CXCR6 Expression Is Important for Retention and Circulation of ILC Precursors. Mediators of Inflammation. 2015(1). 368427–368427. 43 indexed citations
15.
Golub, Rachel & Ana Cumano. (2013). Embryonic hematopoiesis. Blood Cells Molecules and Diseases. 51(4). 226–231. 78 indexed citations
16.
Desanti, Guillaume E., Julien Bertrand, & Rachel Golub. (2007). Fetal spleen development, the ride toward multiple functions. HAL (Le Centre pour la Communication Scientifique Directe). 78–90. 4 indexed citations
17.
Huang, Ching‐Yu, Rachel Golub, Gillian E. Wu, & Osami Kanagawa. (2002). Superantigen-Induced TCR α Locus Secondary Rearrangement: Role in Tolerance Induction. The Journal of Immunology. 168(7). 3259–3265. 25 indexed citations
18.
Golub, Rachel, Denise A. Martin, Fred E. Bertrand, et al.. (2001). VH Gene Replacement in Thymocytes. The Journal of Immunology. 166(2). 855–860. 7 indexed citations
19.
Golub, Rachel, Julien S. Fellah, & Jacques Charlemagne. (1997). Structure and diversity of the heavy chain VDJ junctions in the developing Mexican axolotl. Immunogenetics. 46(5). 402–409. 23 indexed citations
20.
Descamps‐Latscha, Béatrice, Rachel Golub, & Anh Nguyen. (1989). Role of oxygen-dependent mechanisms in monoclonal-antibody-induced lysis of normal T cells by phagocytes. Research in Immunology. 140(1). 33–54. 1 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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