J.G. Seidman

13.0k citations

117 papers · 9.8k indexed · 3 hit papers · h-index 49

Impact in

Immunology top 0.5%
- T-cell and B-cell Immunology
- Immune Cell Function and Interaction
Molecular Biology top 1%
- Congenital heart defects research
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
- dental development and anomalies

Papers in

Immunology 29
- T-cell and B-cell Immunology 22
- Immune Cell Function and Interaction 12
Cardiology and Cardiovascular Medicine 28
- Cardiomyopathy and Myosin Studies 19

Co-authors: Christine E. Seidman Philip Leder Edward E. Max Jack L. Strominger William H. McClain Heleni Vastardis Nadeem Y. Karimbux Deno P. Dialynas
Journals: Proceedings of the National Academy of Sciences (12 papers)Nature (7 papers)Science (7 papers)Journal of Molecular Biology (6 papers)Circulation Research (5 papers)
Partner nations: United States Japan United Kingdom

In The Last Decade

J.G. Seidman

116 papers receiving 9.2k citations

Hit Papers

align trajectories log scale

A human MSX1 homeodomain missense mutation causes selective tooth agenesis 1996 · 565 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

1996 Nature Genetics
1986 Nature
1979 Proceedings of the National Academy of Sciences

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-authors

The 25 scholars most cited alongside J.G. Seidman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with J.G. Seidman Line = papers co-authored together J.G. Seidman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot Frontiers in Cardiovascular Medicine ·Drayton C. Harvey, Riya Verma, Brandon Sedaghat, Brooke E. Hjelm, Sarah U. Morton, J.G. Seidman, S. Ram Kumar	2023	3
2	Dynamic Cellular Integration Drives Functional Assembly of the Heart’s Pacemaker Complex Cell Reports ·Michael Bressan, Trevor Henley, Jonathan D. Louie, Gary Liu, Danos C. Christodoulou, Xue Bai, Joan M. Taylor, Christine E. Seidman, J.G. Seidman, Takashi Mikawa	2018	18
3	Genome-wide identification of mouse congenital heart disease loci Human Molecular Genetics ·Anna Kamp, Michael Peterson, Karen L. Svenson, Bryan C. Bjork, Kathryn E. Hentges, Tharinda W. Rajapaksha, Jennifer L. Moran, Monica J. Justice, J.G. Seidman, Christine E. Seidman, Ivan P. Moskowitz, David R. Beier	2010	15
4	Sarcomere Gene Mutations in Hypertrophy and Heart Failure Journal of Cardiovascular Translational Research ·Hiroyuki Morita, Ryozo Nagai, J.G. Seidman, Christine E. Seidman	2010	23
5	Missense Mutations in theBCS1LGene as a Cause of the Björnstad Syndrome New England Journal of Medicine ·J. Travis Hinson, Valeria R. Fantin, Jost Schönberger, Noralv Breivik, Geir Siem, Barbara McDonough, Pankaj Sharma, Ivan Keogh, Ricardo Godinho, Felipe Santos, Alfonso Esparza, Yamileth Nicolau, Edgar Selvaag, Bruce H. Cohen, Charles L. Hoppel, Lisbeth Tranebjærg, Roland D. Eavey, J.G. Seidman, Christine E. Seidman	2007	140
6	A Molecular Pathway Including Id2, Tbx5, and Nkx2-5 Required for Cardiac Conduction System Development Cell ·Ivan P. Moskowitz, Jae Bum Kim, Meredith Moore, Cordula M. Wolf, Michael Peterson, Jay Shendure, Marcelo A. Nóbrega, Yoshifumi Yokota, Charles I. Berul, Seigo Izumo, J.G. Seidman, Christine E. Seidman	2007	202
7	Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis Developmental Biology ·Alessandro Mori, Yonghong Zhu, Ilyas Vahora, Brian J. Nieman, Kazuko Koshiba‐Takeuchi, Lorinda Davidson, Anne Pizard, J.G. Seidman, Christine E. Seidman, Xianhao Chen, R. Mark Henkelman, Benoit G. Bruneau	2006	130
8	A Mouse Model of Congenital Heart Disease: Cardiac Arrhythmias and Atrial Septal Defect Caused by Haploinsufficiency of the Cardiac Transcription Factor Csx/Nkx2.5 Cold Spring Harbor Symposia on Quantitative Biology ·Makoto Tanaka, Charles I. Berul, Masao Ishii, Patrick Y. Jay, Hiroko Wakimoto, Pamela S. Douglas, Naohito Yamasaki, T. Kawamoto, Josef Gehrmann, Colin T. Maguire, Martina Schinke, Christine E. Seidman, J.G. Seidman, Y Kurachi, Seigo Izumo	2002	45
9	Cardiomyopathy in Irx4-Deficient Mice Is Preceded by Abnormal Ventricular Gene Expression Molecular and Cellular Biology ·Benoit G. Bruneau, Zheng‐Zheng Bao, Diane Fatkin, José Xavier‐Neto, Dimitrios Georgakopoulos, Colin T. Maguire, Charles I. Berul, David A. Kass, Mercedes L. Kuroski de Bold, Joseph F. DeBold, David A. Conner, Nadia Rosenthal, Constance L. Cepko, Christine E. Seidman, J.G. Seidman	2001	121
10	Cardiac Expression of the Ventricle-Specific Homeobox Gene Irx4 Is Modulated by Nkx2-5 and dHand Developmental Biology ·Benoit G. Bruneau, Zheng‐Zheng Bao, Makoto Tanaka, Jean‐Jacques Schott, Seigo Izumo, Constance L. Cepko, J.G. Seidman, Christine E. Seidman	2000	149
11	Molecular genetic studies of familial hypertrophic cardiomyopathy Basic Research in Cardiology ·Christine E. Seidman, J.G. Seidman	1998	73
12	The Bjornstad Syndrome (Sensorineural Hearing Loss and Pili Torti) Disease Gene Maps to Chromosome 2q34-36 The American Journal of Human Genetics ·José Faibes Lubianca Neto, Leonard Lu, Roland D. Eavey, Marco Antonio Macias Flores, Raul Martinez Caldera, Somkiat Sangwatanaroj, Jean‐Jacques Schott, Barbara McDonough, Jose Ignatio Santos, Christine E. Seidman, J.G. Seidman	1998	16
13	The Cloning of Extracellular Ca2+-Sensing Receptors from Parathyroid and Kidney: Molecular Mechanisms of Extracellular Ca2+-Sensing Journal of Nutrition ·Edward M. Brown, Martin R. Pollak, Ya-Huei Wu Chou, Christine E. Seidman, J.G. Seidman, Steven Hébert	1995	13
14	A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1 Nature Genetics ·Susan Kass, Calum A. MacRae, Harry L. Graber, Elizabeth Sparks, Dennis McNamara, Harisios Boudoulas, Craig T. Basson, Peter B. Baker, Robert J. Cody, Mark C. Fishman, Nancy J. Cox, Augustine Kong, Charles F. Wooley, J.G. Seidman, Christine E. Seidman	1994	126
15	Isolation and restriction map of the V-J interval of the human T cell receptor γ chain locus Genomics ·Victor L. Fox, William M. Strauss, J.G. Seidman	1989	1
16	Characterization of a third form of the human T cell receptor gamma/delta. The Journal of Experimental Medicine ·Frans Hochstenbach, Christina M. Parker, Joanne McLean, Volkmar Gieselmann, Hamid Band, Ilan Bank, Leonard Chess, Hergen Spits, Jack L. Strominger, J.G. Seidman	1988	76
17	Nonlinkage of the t cell receptor α, β, and γ genes to systemic lupus erythematosus in multiplex families Arthritis & Rheumatism ·David W. S. Wong, Zvi Bentwich, Carlos Martinez‐Tarquino, J.G. Seidman, Allan D. Duby, Thomas Quertermous, Peter H. Schur	1988	19
18	Genetic conversion of G · C base-pairs to A · U base-pairs in a transfer RNA Journal of Molecular Biology ·William H. McClain, J.G. Seidman	1987	2
19	Genetic mapping of a human class II antigen beta-chain cDNA clone to the SB region of the HLA complex. Proceedings of the National Academy of Sciences ·Magali Roux-Dosseto, Cédric Auffray, James W. Lillie, Jeremy M. Boss, Daniel Cohen, Robert DeMars, Claude Mawas, J.G. Seidman, Jack L. Strominger	1983	93
20	Nucleic acid and protein sequences of phosphocholine-binding light chains. The Journal of Experimental Medicine ·Sau‐Ping Kwan, Stuart Rudikoff, J.G. Seidman, Philip Leder, Matthew D. Scharff	1981	42

About J.G. Seidman

J.G. Seidman is a scholar working on Immunology, Cardiology and Cardiovascular Medicine, Molecular Biology, Radiology, Nuclear Medicine and Imaging and Sensory Systems, having authored 117 papers that have together received 9.8k indexed citations. Recurring topics across this work include T-cell and B-cell Immunology (22 papers), Monoclonal and Polyclonal Antibodies Research (22 papers), Congenital heart defects research (20 papers), Cardiomyopathy and Myosin Studies (19 papers), RNA modifications and cancer (18 papers), RNA and protein synthesis mechanisms (18 papers), Bacteriophages and microbial interactions (12 papers) and Immune Cell Function and Interaction (12 papers). The work is most often cited by research in Immunology (2.6k citations), Molecular Biology (5.7k citations), Cardiology and Cardiovascular Medicine (1.7k citations), Radiology, Nuclear Medicine and Imaging (1.5k citations) and Genetics (1.6k citations). J.G. Seidman has collaborated with scholars based in United States, Japan and United Kingdom. Frequent co-authors include Christine E. Seidman, Philip Leder, Edward E. Max, Jack L. Strominger, William H. McClain, Heleni Vastardis, Nadeem Y. Karimbux, Deno P. Dialynas, Symon W. Guthua and Michael Arad. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature, Science, Journal of Molecular Biology and Circulation Research.

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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