Ketty Schwartz

17.0k citations

92 papers · 10.7k indexed · 7 hit papers · h-index 44

Impact in

Cardiology and Cardiovascular Medicine top 0.2%
- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Cardiac electrophysiology and arrhythmias
Molecular Biology top 0.5%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- Nuclear Structure and Function
- Ion channel regulation and function

Papers in

Cardiology and Cardiovascular Medicine 65
- Cardiomyopathy and Myosin Studies 51
- Cardiac electrophysiology and arrhythmias 18
- Cardiovascular Effects of Exercise 16
- Viral Infections and Immunology Research 14
Molecular Biology 55
- Ion channel regulation and function 16
- Muscle Physiology and Disorders 16
- RNA Research and Splicing 13
- Congenital heart defects research 10

Co-authors: Gisèle Bonne Lucie Carrier Pascale Richard Bernard Hainque Michel Desnos Michel Komajda Albert Hagège Pascale Guicheney
Journals: Circulation (15 papers)Journal of Molecular and Cellular Cardiology (8 papers)Circulation Research (6 papers)Neuromuscular Disorders (5 papers)Journal of the American College of Cardiology (5 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Ketty Schwartz

92 papers receiving 10.4k citations

Hit Papers

7 papers align trajectories log scale

Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction 2003 · 793 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.

2003 Journal of the American College of Cardiology
2003 Circulation
1999 Nature Genetics
1997 Nature Genetics
1995 Nature Genetics
1981 Nature
1979 Nature

Peers

Countries citing papers authored by Ketty Schwartz

Since Specialization

Citations

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

Fields of papers citing papers by Ketty Schwartz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ketty Schwartz. 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 Ketty Schwartz. The network helps show where Ketty Schwartz may publish in the future.

Co-authors

The 25 scholars most cited alongside Ketty Schwartz, 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 Ketty Schwartz Line = papers co-authored together Ketty Schwartz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Distinction Between Two Populations of Islet-1-Positive Cells in Hearts of Different Murine Strains Stem Cells and Development ·Patricia Khattar, Felix W. Friedrich, Gisèle Bonne, Lucie Carrier, Thomas Eschenhagen, Sylvia Μ. Evans, Ketty Schwartz, Marc Fiszman, Jean‐Thomas Vilquin	2010	27
2	Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy European Journal of Human Genetics ·Odette Poirier, Viviane Nicaud, Theresa A. McDonagh, Henry J. Dargie, Michel Desnos, Richard Dorent, Gérard Roizès, Ketty Schwartz, Laurence Tiret, Michel Komajda, François Cambien	2003	22
3	The coronary sinus: A safe and effective route for percutaneous myoblast transplantation Journal of the American College of Cardiology ·Camille Brasselet, C Carrión, Patrick Bruneval, Didier Heudes, Ketty Schwartz, Albert Hagège, Jean‐Thomas Vilquin, Emmanuel Messas, Michel Desnos, Antoine Lafont, Philippe Menasché	2003	2
4	Building the translational highway: toward new partnerships between academia and the private sector Nature Medicine ·Ketty Schwartz, Jean‐Thomas Vilquin	2003	13
5	Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction Journal of the American College of Cardiology ·Philippe Menasché, Albert Hagège, Jean‐Thomas Vilquin, Michel Desnos, Éric Abergel, Bruno Pouzet, Alain Bel, Sorin Sarateanu, Marcio Scorsin, Ketty Schwartz, Patrick Bruneval, M Benbunan, Jean‐Pierre Marolleau, Denis Duboc Hit paper breakdown →	2003	793
6	82nd ENMC international workshop, 5th international Emery–Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15–16 September 2000, Naarden, The Netherlands Neuromuscular Disorders ·Gisèle Bonne, Jaqueline Capeau, Marianne de Visser, Denis Duboc, Luciano Merlini, Glenn E. Morris, Francesco Muntoni, Dominique Récan, Caroline A. Sewry, Stefano Squarzoni, Colin L. Stewart, Beril Talim, Anneke J. van der Kooi, Howard J. Worman, Ketty Schwartz	2002	21
7	A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block Neuromuscular Disorders ·T. Kitaguchi, Shiro Matsubara, Masaru Sato, Kazuhito Miyamoto, Shunsaku Hirai, Ketty Schwartz, Gisèle Bonne	2001	38
8	Comparison of the effects of fetal cardiomyocyte and skeletal myoblast transplantation on postinfarction left ventricular function Journal of Thoracic and Cardiovascular Surgery ·Marcio Scorsin, Albert Hagège, Jean‐Thomas Vilquin, Marc Fiszman, Françoise Marotte, Jane‐Lise Samuel, L. Rappaport, Ketty Schwartz, Philippe Menasché	2000	224
9	Homozygotes for a R869G Mutation in the β -myosin Heavy Chain Gene have a Severe Form of Familial Hypertrophic Cardiomyopathy Journal of Molecular and Cellular Cardiology ·Pascale Richard, Philippe Charron, Christophe Leclercq, C. Ledeuil, Lucie Carrier, Olivier Dubourg, Michel Desnos, Jean-Brieuc Bouhour, Ketty Schwartz, Jean Claude Daubert, Michel Komajda, Bernard Hainque	2000	39
10	Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy Journal of the American College of Cardiology ·Laurence Tiret, Christine Mallet, Odette Poirier, Viviane Nicaud, A Millaire, Jean-Brieuc Bouhour, Gérard Roizès, Michel Desnos, Richard Dorent, Ketty Schwartz, François Cambien, Michel Komajda	2000	80
11	Deletion in the Cardiac Troponin I Gene in a Family From Northern Sweden with Hypertrophic Cardiomyopathy Journal of Molecular and Cellular Cardiology ·Stellan Mörner, Pascale Richard, Elsadig Kazzam, Bernard Hainque, Ketty Schwartz, Anders Waldenström	2000	30
12	Identification of homozygous and heterozygous dy mice by PCR Neuromuscular Disorders ·Jean‐Thomas Vilquin, Nicolas Vignier, Jacques P. Tremblay, Eva Engvall, Ketty Schwartz, Marc Fiszman	2000	13
13	Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy Nature Genetics ·Gisèle Bonne, Marina Raffaele di Barletta, Shaïda Varnous, Henri-Marc Bécane, E. Hammouda, Luciano Merlini, Francesco Muntoni, Cheryl R. Greenberg, Françoise Gary, J.A. Urtizberea, Denis Duboc, Michel Fardeau, Daniela Toniolo, Ketty Schwartz Hit paper breakdown →	1999	1032
14	Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome European Journal of Human Genetics ·Nathalie Neyroud, Isabelle Denjoy, Claire Donger, Françoise Gary, E Villain, Antoine Leenhardt, Karim Bénali, Ketty Schwartz, P Coumel, Pascale Guicheney	1998	35
15	The sarco(endo)plasmic reticulum Ca2+-ATPase gene is regulated at the transcriptional level during compensated left ventricular hypertrophy in the rat Comptes Rendus de l Académie des Sciences - Series III - Sciences de la Vie ·Antoine Ribadeau Dumas, C Wisnewsky, Kenneth R. Boheler, Henk ter Keurs, Marc Fiszman, Ketty Schwartz	1997	19
16	The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy Human Genetics ·Isam Naom, Mariella D’Alessandro, Caroline A. Sewry, Alessandra Ferlini, Haluk Topaloğlu, A. Leclerc, Pascale Guicheney, Ketty Schwartz, Zühal Akçören, Victor Dubowitz, Francesco Muntoni	1997	11
17	Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy Nature Genetics ·Gisèle Bonne, Lucie Carrier, J. Bercovici, Corinne Cruaud, Pascale Richard, Bernard Hainque, Mathias Gautel, Siegfried Labeit, Michael R. James, J. Beckmann, Jean Weissenbach, Hans-Peter Vosberg, Marc Fiszman, Michel Komajda, Ketty Schwartz	1995	336
18	Molecular Genetics of Familial Hypertrophic Cardiomyopathy Journal of Molecular and Cellular Cardiology ·Christian Hengstenberg, Ketty Schwartz	1994	18
19	Genetics of familial hypertrophic cardiomyopathy Trends in Cardiovascular Medicine ·Christian Hengstenberg, Michel Komajda, Ketty Schwartz	1993	6
20	Description of an in vitro transcription assay in nuclei isolated from control and hemodynamically overloaded rat cardiac myocytes SPIRE - Sciences Po Institutional REpository ·Catherine Chassagne, Kenneth R. Boheler, Ketty Schwartz	1991	3

About Ketty Schwartz

Ketty Schwartz is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology, Developmental Neuroscience, Aging and Developmental Biology, having authored 92 papers that have together received 10.7k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (51 papers), Cardiac electrophysiology and arrhythmias (18 papers), Cardiovascular Effects of Exercise (16 papers), Ion channel regulation and function (16 papers), Muscle Physiology and Disorders (16 papers), Viral Infections and Immunology Research (14 papers), RNA Research and Splicing (13 papers) and Congenital heart defects research (10 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (5.9k citations), Molecular Biology (7.3k citations), Genetics (1.1k citations), Biomaterials (635 citations) and Cell Biology (755 citations). Ketty Schwartz has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Gisèle Bonne, Lucie Carrier, Pascale Richard, Bernard Hainque, Michel Desnos, Michel Komajda, Albert Hagège, Pascale Guicheney, Jean‐Thomas Vilquin and Denis Duboc. Their work appears in journals such as Circulation, Journal of Molecular and Cellular Cardiology, Circulation Research, Neuromuscular Disorders and Journal of the American College of Cardiology.

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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