Jean‐Jacques Schott

16.2k total citations · 2 hit papers
132 papers, 7.6k citations indexed

About

Jean‐Jacques Schott is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Geophysics. According to data from OpenAlex, Jean‐Jacques Schott has authored 132 papers receiving a total of 7.6k indexed citations (citations by other indexed papers that have themselves been cited), including 78 papers in Molecular Biology, 75 papers in Cardiology and Cardiovascular Medicine and 18 papers in Geophysics. Recurrent topics in Jean‐Jacques Schott's work include Cardiac electrophysiology and arrhythmias (45 papers), Ion channel regulation and function (37 papers) and Cardiac Valve Diseases and Treatments (20 papers). Jean‐Jacques Schott is often cited by papers focused on Cardiac electrophysiology and arrhythmias (45 papers), Ion channel regulation and function (37 papers) and Cardiac Valve Diseases and Treatments (20 papers). Jean‐Jacques Schott collaborates with scholars based in France, United States and Netherlands. Jean‐Jacques Schott's co-authors include Vincent Probst, Hervé Le Marec, Denis Escande, Florence Kyndt, Christine E. Seidman, Arthur A.M. Wilde, D. Woodrow Benson, Craig T. Basson, G. Michael Silberbach and J. G. Seidman and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Jean‐Jacques Schott

128 papers receiving 7.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5

1998 944 citations Jean‐Jacques Schott, Christine E. Seidman et al. profile →
Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

2003 693 citations Peter J. Mohler, Jean‐Jacques Schott et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean‐Jacques Schott France	41	5.3k	4.8k	751	734	527	132	7.6k
Yutaka Hayashi Japan	48	2.7k 0.5×	802 0.2×	336 0.4×	655 0.9×	444 0.8×	348	7.7k
Yigang Wang United States	44	4.3k 0.8×	1.4k 0.3×	148 0.2×	323 0.4×	392 0.7×	197	7.6k
Yanhua Hu China	60	5.4k 1.0×	1.0k 0.2×	391 0.5×	708 1.0×	368 0.7×	196	10.6k
Thomas W. Gardner United States	65	5.6k 1.1×	606 0.1×	429 0.6×	850 1.2×	768 1.5×	242	18.6k
Yukio Ikeda Japan	43	1.8k 0.3×	291 0.1×	329 0.4×	649 0.9×	321 0.6×	242	6.5k
Ingrid Kockum Sweden	50	1.3k 0.2×	238 0.0×	2.2k 3.0×	499 0.7×	173 0.3×	248	8.1k
Pierre Moreau Canada	40	1.1k 0.2×	2.2k 0.5×	301 0.4×	145 0.2×	116 0.2×	152	5.2k
Anthony Lewis United States	34	1.4k 0.3×	515 0.1×	262 0.3×	326 0.4×	599 1.1×	122	4.5k
Satoru Tanaka Japan	38	578 0.1×	1.3k 0.3×	232 0.3×	76 0.1×	131 0.2×	270	5.8k
Frank Cuttitta United States	51	5.5k 1.0×	179 0.0×	482 0.6×	1.2k 1.7×	3.9k 7.4×	216	11.0k

Countries citing papers authored by Jean‐Jacques Schott

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Jacques Schott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Jacques Schott. 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 Jean‐Jacques Schott. The network helps show where Jean‐Jacques Schott may publish in the future.

Co-authorship network of co-authors of Jean‐Jacques Schott

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Jacques Schott. A scholar is included among the top collaborators of Jean‐Jacques Schott 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 Jean‐Jacques Schott. Jean‐Jacques Schott 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

Capoulade, Romain, Jean Mérot, Solena Le Scouarnec, et al.. (2023). Genetics and pathophysiology of mitral valve prolapse. Frontiers in Cardiovascular Medicine. 10. 1077788–1077788. 16 indexed citations

Yu, Mengyao, Sergiy Kyryachenko, Stéphanie Debette, et al.. (2021). Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse. Circulation Genomic and Precision Medicine. 14(5). e003148–e003148. 10 indexed citations

Perrot, Nicolas, Sébastien Thériault, Sidwell Rigade, et al.. (2020). Lipoprotein-associated phospholipase A2 activity, genetics and calcific aortic valve stenosis in humans. Heart. 106(18). 1407–1412. 15 indexed citations

Labbé, Pauline, Emilie Faure, Simon Lecointe, et al.. (2017). The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1864(7). 1142–1152. 14 indexed citations

Liu, Hui, Stéphanie Chatel, Christophe Simard, et al.. (2013). Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel. PLoS ONE. 8(1). e54131–e54131. 112 indexed citations

Maugenre, Svetlana, Nathalie Neyroud, Elise Balse, et al.. (2011). MOG1. Circulation Cardiovascular Genetics. 4(3). 261–268. 114 indexed citations

Léoni, Anne‐Laure, Bruno Gavillet, Jean‐Sébastien Rougier, et al.. (2010). Variable Nav1.5 Protein Expression from the Wild-Type Allele Correlates with the Penetrance of Cardiac Conduction Disease in the Scn5a+/− Mouse Model. PLoS ONE. 5(2). e9298–e9298. 57 indexed citations

Probst, Vincent, Arthur A.M. Wilde, Julien Barc, et al.. (2009). SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome. Circulation Cardiovascular Genetics. 2(6). 552–557. 211 indexed citations

Barc, Julien, Vincent Probst, Arthur A.M. Wilde, et al.. (2009). G023 SCN5A mutations and the role of genetic background in the pathophysiology of brugada syndrome. Archives of cardiovascular diseases. 102. S70–S70. 1 indexed citations

10.

Scouarnec, Solena Le, Naina Bhasin, Thomas J. Hund, et al.. (2008). Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease. Proceedings of the National Academy of Sciences. 105(40). 15617–15622. 109 indexed citations

11.

Kyndt, Florence, Solena Le Scouarnec, Antoine Legendre, et al.. (2007). [Genetic aspects of valvulopathies].. PubMed. 100(12). 1013–20. 8 indexed citations

12.

Probst, Vincent, Solena Le Scouarnec, Pierre Boisseau, et al.. (2006). P4-2. Heart Rhythm. 3(5). S219–S219. 1 indexed citations

13.

Probst, Vincent, et al.. (2005). Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation. The American Journal of Cardiology. 95(5). 700–702. 22 indexed citations

14.

Thébault, Erwan, Jean‐Jacques Schott, & Mioara Mandéa. (2003). A new proposal for Spherical Cap Harmonic Analysis. EAEJA. 5953. 6 indexed citations

15.

Bruneau, Benoit G., Zheng‐Zheng Bao, Makoto Tanaka, et al.. (2000). Cardiac Expression of the Ventricle-Specific Homeobox Gene Irx4 Is Modulated by Nkx2-5 and dHand. Developmental Biology. 217(2). 266–277. 149 indexed citations

16.

Trochu, Jean‐Noël, Florence Kyndt, Jean‐Jacques Schott, et al.. (2000). Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28. Journal of the American College of Cardiology. 35(7). 1890–1897. 33 indexed citations

17.

Schott, Jean‐Jacques. (1999). Partial common principal component subspaces. Biometrika. 86(4). 899–908. 18 indexed citations

18.

Pravenec, Michal, Dominique Gauguier, Jean‐Jacques Schott, et al.. (1995). Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.. Journal of Clinical Investigation. 96(4). 1973–1978. 143 indexed citations

19.

Schott, Jean‐Jacques. (1988). Lower Permian to Miocene apparent polar wander path for Iberia and its bearings on kinematic evolution.. Journal of iberian geology: an international publication of earth sciences. 12(12). 21–38. 3 indexed citations

20.

Schott, Jean‐Jacques, et al.. (1957). Incapacité d'une autogreffe hypophysaire fonctionnelle à maintenir l'intégrité de la fonction sexuelle lorsqúelle est implantée hors de la région infundibulaire. I. Etude chez Rana temporaria L.. Comptes rendus des séances de la Société de biologie et de ses filiales. 151(1). 3 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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