J.G. Seidman

1.7k citations

35 papers · 1.3k indexed · h-index 20

Co-authors: Christine E. Seidman Allan D. Duby Philip Leder Edward G. D. Tuddenham Susumu Tonegawa Martin Weigert Claire L. Shovlin G. Matthyssens
Topics: CAR-T cell therapy research (5 papers)T-cell and Retrovirus Studies (4 papers)RNA modifications and cancer (4 papers)
Cited by: Developmental Biology Nephrology Genetics
Journals: Science Proceedings of the National Academy of Sciences Circulation
Partner nations: United States Canada United Kingdom

In The Last Decade

J.G. Seidman

33 papers receiving 1.3k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	THSD1(Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage 2016 ·Stroke ·Teresa Santiago‐Sim,Xiaoqian Fang,(unknown),(unknown),Steven R. DePalma,(unknown),Steven C. Greenway,Barbara McDonough,Georgene W. Hergenroeder,(unknown),(unknown),(unknown),John P. Hagan,Dianna M. Milewicz,Calum A. MacRae,Susan M. Dymecki,Christine E. Seidman,J.G. Seidman,Dong Kim	34
2	Ca ²⁺ dysregulation in Ryr1 ^I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods 2009 ·Proceedings of the National Academy of Sciences ·Elena Zvaritch,(unknown),Éric Bombardier,(unknown),Frederic Depreux,Douglas Holmyard,Alexander Kraev,Christine E. Seidman,J.G. Seidman,A. Russell Tupling,David H. MacLennan	52
3	Sequencing of TGF-β Pathway Genes in Familial Cases of Intracranial Aneurysm 2009 ·Stroke ·Teresa Santiago‐Sim,(unknown),Hariyadarshi Pannu,Dianna M. Milewicz,Christine E. Seidman,J.G. Seidman,Dong Kim	25
4	Adult Hallervorden–Spatz syndrome simulating amyotrophic lateral sclerosis 2003 ·Muscle & Nerve ·Olavo M. Vasconcelos,Donald H. Harter,C. Elise Duffy,Barbara McDonough,J.G. Seidman,Christine E. Seidman,W. W. Campbell	25
5	A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13 1998 ·Kidney International ·(unknown),Sung Hyun Kim,(unknown),Mark Haas,J.G. Seidman,Christine E. Seidman,Martin R. Pollak	77
6	Reduced Penetrance, Variable Expressivity, and Genetic Heterogeneity of Familial Atrial Septal Defects 1998 ·Circulation ·D. Woodrow Benson,(unknown),Diane Fatkin,Peter Lang,Craig T. Basson,Barbara McDonough,Arnold W. Strauss,J.G. Seidman,Christine E. Seidman	66
7	Genetic Heterogeneity Evidenced by Low Incidence of KAL-1 Gene Mutations in Sporadic Cases of Gonadotropin-Releasing Hormone Deficiency¹ 1997 ·The Journal of Clinical Endocrinology & Metabolism ·Neoklis A. Georgopoulos,François Pralong,Christine E. Seidman,J.G. Seidman,William F. Crowley,Mario Vallejo	82
8	Identification, Characterization, and Chromosomal Localization of the Human Homolog (hES) of ES/130 1996 ·Genomics ·Craig T. Basson,Calum A. MacRae,Marlena S. Fejzo,Cynthia C. Morton,Nancy B. Spinner,Anna Genin,Edward L. Krug,J.G. Seidman,Christine E. Seidman	4
9	A complex bilateral polysyndactyly disease locus maps to chromosome 7q36 1994 ·Nature Genetics ·Olga Tsukurov,Annemie L. M. Boehmer,Jack Flynn,Jean‐Philippe A. Nicolai,Ben C.J. Hamel,(unknown),David J. Zaleske,Henry J. Mankin,Howard B. Yeon,(unknown),Cliff Tabin,J.G. Seidman,Christine E. Seidman	74
10	A dinucleotide repeat polymorphism in the MYBPH gene 1994 ·Human Molecular Genetics ·Hugh Watkins,Calum A. MacRae,Donald A. Fischman,J.G. Seidman,Christine E. Seidman	1
11	A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3 1994 ·Nature Genetics ·Claire L. Shovlin,J. M. B. Hughes,Edward G. D. Tuddenham,(unknown),(unknown),James Scott,Christine E. Seidman,J.G. Seidman	153
12	T cell receptor (β chain) transgenic mice have selective deficits in γδ T cell subpopulations 1994 ·Transplant Immunology ·Ilonna J. Rimm,(unknown),Sunil Abhyankar,(unknown),Ian M. Orme,David S. Milstone,J.G. Seidman,James L.M. Ferrara	2
13	Regional localization of the human G protein αi2 (GNAI2) gene: Assignment to 3p21 and a related sequence (GNAI2L) to 12p12–p13 1992 ·Genomics ·(unknown),Siew‐Lan Ang,J.G. Seidman,(unknown),Eva J. Neer,(unknown)	11
14	The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families 1992 ·Nature Genetics ·Yah‐Huei Wu Chou,Edward M. Brown,(unknown),(unknown),Andrew Atkinson,Hans J. Arnqvist,(unknown),Ghada El‐Hajj Fuleihan,J.G. Seidman,Christine E. Seidman	114
15	Immunodominance is altered in T cell receptor (beta-chain) transgenic mice without the generation of a hole in the repertoire 1991 ·The Journal of Immunology ·David L. Perkins,(unknown),(unknown),J.G. Seidman,Ilonna J. Rimm	23
16	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. 1986 ·The Journal of Immunology ·Frances L. Owen,Benjamin A. Taylor,Alfred Zweidler,J.G. Seidman	26
17	Molecular linkage of the genes encoding adrenal steroid 21-hydroxylase to the S region of the murine major histocompatibility complex (MHC) 1985 ·Federation Proceedings ·David Chaplin,K L Parker,Peter S. White,J.G. Seidman	2
18	A Novel Mechanism of Somatic Rearrangement Predicted by a Human T-Cell Antigen Receptor β-Chain Complementary DNA 1985 ·Science ·Allan D. Duby,Karen A. Klein,Cornelis Murre,J.G. Seidman	35
19	Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool. 1985 ·Journal of Clinical Investigation ·Nancy Berliner,Allan D. Duby,Cynthia C. Morton,Philip Leder,J.G. Seidman	35
20	Detection of a Frequent Restriction Fragment Length Polymorphism in the Human T Cell Antigen Receptor Beta Chain Locus 1985 ·Nancy Berliner,Allan D. Duby,Cynthia C. Morton,Philip Leder,J.G. Seidman	7

About J.G. Seidman

J.G. Seidman is a scholar working on Sensory Systems, Immunology and Developmental Biology, having authored 35 papers that have together received 1.3k indexed citations. Recurring topics across this work include CAR-T cell therapy research (5 papers), T-cell and Retrovirus Studies (4 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Developmental Biology (59 citations), Nephrology (148 citations) and Genetics (215 citations). J.G. Seidman has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Christine E. Seidman, Allan D. Duby, Philip Leder, Edward G. D. Tuddenham, Susumu Tonegawa, Martin Weigert, Claire L. Shovlin, Christine E. Seidman, G. Matthyssens and Dawn E. Kelley. Their work appears in journals such as Science, Proceedings of the National Academy of Sciences and Circulation.

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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