J.G. Seidman

1.7k total citations
35 papers, 1.3k citations indexed

About

J.G. Seidman is a scholar working on Molecular Biology, Immunology and Oncology. According to data from OpenAlex, J.G. Seidman has authored 35 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Immunology and 8 papers in Oncology. Recurrent topics in J.G. Seidman's work include CAR-T cell therapy research (5 papers), T-cell and Retrovirus Studies (4 papers) and RNA modifications and cancer (4 papers). J.G. Seidman is often cited by papers focused on CAR-T cell therapy research (5 papers), T-cell and Retrovirus Studies (4 papers) and RNA modifications and cancer (4 papers). J.G. Seidman collaborates with scholars based in United States, Canada and United Kingdom. J.G. Seidman's co-authors include Christine E. Seidman, Allan D. Duby, Philip Leder, Martin Weigert, Edward G. D. Tuddenham, Susumu Tonegawa, Christine E. Seidman, Claire L. Shovlin, James Scott and G. Matthyssens and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

J.G. Seidman

33 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.G. Seidman United States 20 634 297 244 215 169 35 1.3k
Andrew Goodearl United States 16 725 1.1× 338 1.1× 138 0.6× 58 0.3× 115 0.7× 26 1.6k
James O’Sullivan United Kingdom 22 1.4k 2.2× 169 0.6× 510 2.1× 136 0.6× 111 0.7× 40 2.0k
A Wohlwend Switzerland 21 913 1.4× 230 0.8× 170 0.7× 132 0.6× 161 1.0× 29 2.2k
Geneviève Piétu France 26 839 1.3× 274 0.9× 323 1.3× 219 1.0× 174 1.0× 69 2.0k
David J. Pennisi Australia 19 1.1k 1.8× 218 0.7× 296 1.2× 40 0.2× 177 1.0× 35 1.6k
David J. Bunyan United Kingdom 23 991 1.6× 73 0.2× 979 4.0× 216 1.0× 153 0.9× 60 2.0k
Branka Dabovic United States 23 1.1k 1.7× 168 0.6× 693 2.8× 67 0.3× 375 2.2× 32 2.0k
Judith Mühlhauser Italy 13 616 1.0× 183 0.6× 185 0.8× 119 0.6× 97 0.6× 20 1.3k
Luitgard M. Neumann Germany 20 708 1.1× 53 0.2× 1.0k 4.2× 110 0.5× 208 1.2× 46 1.7k
Naotoshi Kanda Japan 19 1.0k 1.6× 100 0.3× 380 1.6× 78 0.4× 91 0.5× 40 1.7k

Countries citing papers authored by J.G. Seidman

Since Specialization
Citations

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

Fields of papers citing papers by J.G. Seidman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.G. Seidman

This figure shows the co-authorship network connecting the top 25 collaborators of J.G. Seidman. A scholar is included among the top collaborators of J.G. Seidman 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.G. Seidman. J.G. Seidman 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.
Santiago‐Sim, Teresa, Xiaoqian Fang, Steven R. DePalma, et al.. (2016). THSD1(Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage. Stroke. 47(12). 3005–3013. 34 indexed citations
2.
Zvaritch, Elena, Éric Bombardier, Frederic Depreux, et al.. (2009). Ca 2+ dysregulation in Ryr1 I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods. Proceedings of the National Academy of Sciences. 106(51). 21813–21818. 52 indexed citations
3.
Santiago‐Sim, Teresa, Hariyadarshi Pannu, Dianna M. Milewicz, et al.. (2009). Sequencing of TGF-β Pathway Genes in Familial Cases of Intracranial Aneurysm. Stroke. 40(5). 1604–1611. 25 indexed citations
4.
Vasconcelos, Olavo M., Donald H. Harter, C. Elise Duffy, et al.. (2003). Adult Hallervorden–Spatz syndrome simulating amyotrophic lateral sclerosis. Muscle & Nerve. 28(1). 118–122. 25 indexed citations
5.
Benson, D. Woodrow, Diane Fatkin, Peter Lang, et al.. (1998). Reduced Penetrance, Variable Expressivity, and Genetic Heterogeneity of Familial Atrial Septal Defects. Circulation. 97(20). 2043–2048. 66 indexed citations
6.
Kim, Sung Hyun, et al.. (1998). A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13. Kidney International. 53(2). 282–286. 77 indexed citations
7.
Georgopoulos, Neoklis A., François Pralong, Christine E. Seidman, et al.. (1997). Genetic Heterogeneity Evidenced by Low Incidence of KAL-1 Gene Mutations in Sporadic Cases of Gonadotropin-Releasing Hormone Deficiency1. The Journal of Clinical Endocrinology & Metabolism. 82(1). 213–217. 82 indexed citations
8.
Basson, Craig T., Calum A. MacRae, Marlena S. Fejzo, et al.. (1996). Identification, Characterization, and Chromosomal Localization of the Human Homolog (hES) of ES/130. Genomics. 35(3). 628–631. 4 indexed citations
9.
Tsukurov, Olga, Annemie L. M. Boehmer, Jack Flynn, et al.. (1994). A complex bilateral polysyndactyly disease locus maps to chromosome 7q36. Nature Genetics. 6(3). 282–286. 74 indexed citations
10.
Shovlin, Claire L., J. M. B. Hughes, Edward G. D. Tuddenham, et al.. (1994). A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3. Nature Genetics. 6(2). 205–209. 153 indexed citations
11.
Watkins, Hugh, Calum A. MacRae, Donald A. Fischman, J.G. Seidman, & Christine E. Seidman. (1994). A dinucleotide repeat polymorphism in the MYBPH gene. Human Molecular Genetics. 3(12). 2267–2267. 1 indexed citations
12.
Rimm, Ilonna J., Sunil Abhyankar, Ian M. Orme, et al.. (1994). T cell receptor (β chain) transgenic mice have selective deficits in γδ T cell subpopulations. Transplant Immunology. 2(3). 218–224. 2 indexed citations
13.
14.
Chou, Yah‐Huei Wu, Edward M. Brown, Andrew Atkinson, et al.. (1992). The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families. Nature Genetics. 1(4). 295–300. 114 indexed citations
15.
Perkins, David L., et al.. (1991). Immunodominance is altered in T cell receptor (beta-chain) transgenic mice without the generation of a hole in the repertoire. The Journal of Immunology. 146(9). 2960–2964. 23 indexed citations
16.
Owen, Frances L., Benjamin A. Taylor, Alfred Zweidler, & J.G. Seidman. (1986). The murine gamma-chain of the T cell receptor is closely linked to a spermatocyte specific histone gene and the beige coat color locus on chromosome 13.. The Journal of Immunology. 137(3). 1044–1046. 26 indexed citations
17.
Chaplin, David, K L Parker, Peter S. White, & J.G. Seidman. (1985). Molecular linkage of the genes encoding adrenal steroid 21-hydroxylase to the S region of the murine major histocompatibility complex (MHC). Federation Proceedings. 44(3). 2 indexed citations
18.
Duby, Allan D., Karen A. Klein, Cornelis Murre, & J.G. Seidman. (1985). A Novel Mechanism of Somatic Rearrangement Predicted by a Human T-Cell Antigen Receptor β-Chain Complementary DNA. Science. 228(4704). 1204–1206. 35 indexed citations
19.
Berliner, Nancy, Allan D. Duby, Cynthia C. Morton, Philip Leder, & J.G. Seidman. (1985). Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool.. Journal of Clinical Investigation. 76(3). 1283–1285. 35 indexed citations
20.
Seidman, J.G., Edward E. Max, B. Norman, Marion M. Nau, & Philip Leder. (1980). The sources of kappa light chain diversity: a review.. 35–49. 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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