L S Gray

738 total citations
17 papers, 632 citations indexed

About

L S Gray is a scholar working on Immunology, Radiology, Nuclear Medicine and Imaging and Molecular Biology. According to data from OpenAlex, L S Gray has authored 17 papers receiving a total of 632 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Immunology, 5 papers in Radiology, Nuclear Medicine and Imaging and 4 papers in Molecular Biology. Recurrent topics in L S Gray's work include Monoclonal and Polyclonal Antibodies Research (5 papers), Bacterial Infections and Vaccines (4 papers) and Ion channel regulation and function (3 papers). L S Gray is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (5 papers), Bacterial Infections and Vaccines (4 papers) and Ion channel regulation and function (3 papers). L S Gray collaborates with scholars based in United States. L S Gray's co-authors include Doris M. Haverstick, Erik L. Hewlett, Víctor H. Engelhard, Mary C. Gray, Ingrid Ehrmann, V M Gordon, Hikoichi Sakai, James R. Gnarra, John H. Russell and Margaretta Allietta and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and The Journal of Immunology.

In The Last Decade

L S Gray

17 papers receiving 617 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L S Gray United States 15 315 190 157 85 84 17 632
Verena Bachmann Germany 15 429 1.4× 69 0.4× 85 0.5× 29 0.3× 99 1.2× 17 686
Angeles Estellés United States 10 444 1.4× 105 0.6× 32 0.2× 28 0.3× 19 0.2× 13 638
Melanie Grove Germany 11 262 0.8× 287 1.5× 24 0.2× 57 0.7× 79 0.9× 15 582
E.D. Kuhlmann Netherlands 16 499 1.6× 150 0.8× 15 0.1× 36 0.4× 37 0.4× 27 842
S Moe United States 8 413 1.3× 250 1.3× 11 0.1× 25 0.3× 90 1.1× 8 805
Elisabeth Wende Germany 10 204 0.6× 301 1.6× 87 0.6× 31 0.4× 20 0.2× 10 528
Darinka Sakac Canada 16 259 0.8× 159 0.8× 20 0.1× 11 0.1× 46 0.5× 35 550
Dominique Semon Switzerland 8 408 1.3× 195 1.0× 33 0.2× 27 0.3× 170 2.0× 8 694
Hélène Defacque France 11 353 1.1× 115 0.6× 11 0.1× 56 0.7× 42 0.5× 15 613
Heinrich Horstmann Singapore 6 374 1.2× 147 0.8× 15 0.1× 15 0.2× 32 0.4× 6 629

Countries citing papers authored by L S Gray

Since Specialization
Citations

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

Fields of papers citing papers by L S Gray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L S Gray. 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 L S Gray. The network helps show where L S Gray may publish in the future.

Co-authorship network of co-authors of L S Gray

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

All Works

17 of 17 papers shown
1.
2.
Densmore, John, Doris M. Haverstick, Gábor Szabó, & L S Gray. (1996). A voltage-operable current is involved in Ca2+ entry in human lymphocytes whereas ICRAC has no apparent role. American Journal of Physiology-Cell Physiology. 271(5). C1494–C1503. 23 indexed citations
3.
Hewlett, Erik L., et al.. (1994). Pertussis toxin activates platelets through an interaction with platelet glycoprotein Ib. Infection and Immunity. 62(8). 3108–3114. 26 indexed citations
4.
Hewlett, Erik L., Mary C. Gray, Ingrid Ehrmann, et al.. (1993). Characterization of adenylate cyclase toxin from a mutant of Bordetella pertussis defective in the activator gene, cyaC.. Journal of Biological Chemistry. 268(11). 7842–7848. 25 indexed citations
5.
Haverstick, Doris M. & L S Gray. (1993). Increased intracellular Ca2+ induces Ca2+ influx in human T lymphocytes.. Molecular Biology of the Cell. 4(2). 173–184. 32 indexed citations
6.
Haverstick, Doris M. & L S Gray. (1992). Lymphocyte adhesion mediated by lymphocyte function-associated antigen-1. II. Interaction between phorbol ester- and cAMP-sensitive pathways. The Journal of Immunology. 149(2). 397–402. 22 indexed citations
7.
Haverstick, Doris M. & L S Gray. (1992). Lymphocyte adhesion mediated by lymphocyte function-associated antigen-1. I. Long term augmentation by transient increases in intracellular cAMP. The Journal of Immunology. 149(2). 389–396. 20 indexed citations
8.
Haverstick, Doris M., Hikoichi Sakai, & L S Gray. (1992). Lymphocyte adhesion can be regulated by cytoskeleton-associated, PMA-induced capping of surface receptors. American Journal of Physiology-Cell Physiology. 262(4). C916–C926. 88 indexed citations
9.
Ehrmann, Ingrid, Mary C. Gray, V M Gordon, L S Gray, & Erik L. Hewlett. (1991). Hemolytic activity of adenylate cyclase toxin fromBordetella pertussis. FEBS Letters. 278(1). 79–83. 86 indexed citations
10.
Haverstick, Doris M., Víctor H. Engelhard, & L S Gray. (1991). Three intracellular signals for cytotoxic T lymphocyte-mediated killing. Independent roles for protein kinase C, Ca2+ influx, and Ca2+ release from internal stores. The Journal of Immunology. 146(10). 3306–3313. 34 indexed citations
11.
Hewlett, Erik L., L S Gray, Margaretta Allietta, et al.. (1991). Adenylate cyclase toxin from Bordetella pertussis. Conformational change associated with toxin activity.. Journal of Biological Chemistry. 266(26). 17503–17508. 72 indexed citations
12.
Gray, L S, et al.. (1989). Pertussis toxin effects on T lymphocytes are mediated through CD3 and not by pertussis toxin catalyzed modification of a G protein.. The Journal of Immunology. 142(5). 1631–1638. 62 indexed citations
13.
Gray, L S, James R. Gnarra, Erik L. Hewlett, & Víctor H. Engelhard. (1988). Increased intracellular cyclic adenosine monophosphate inhibits T lymphocyte-mediated cytolysis by two distinct mechanisms.. The Journal of Experimental Medicine. 167(6). 1963–1968. 30 indexed citations
14.
Gray, L S, James R. Gnarra, J A Sullivan, Gerald L. Mandell, & Víctor H. Engelhard. (1988). Spatial and temporal characteristics of the increase in intracellular Ca2+ induced in cytotoxic T lymphocytes by cellular antigen.. The Journal of Immunology. 141(7). 2424–2430. 31 indexed citations
15.
Gray, L S, James R. Gnarra, & Víctor H. Engelhard. (1987). Demonstration of a calcium influx in cytolytic T lymphocytes in response to target cell binding.. The Journal of Immunology. 138(1). 63–69. 37 indexed citations
16.
Gray, L S & John H. Russell. (1986). Cytolytic T lymphocyte effector function requires plasma membrane chloride flux.. The Journal of Immunology. 136(8). 3032–3037. 29 indexed citations
17.
Gray, L S, Jeanine Kleeman, & S. P. Masouredis. (1983). Differential binding of IgG anti‐D and IgG autoantibodies to reticulocytes and red blood cells. British Journal of Haematology. 55(2). 335–345. 8 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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