Éva Morava

16.5k citations

312 papers · 7.6k · h-index 47

Impact in

Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Molecular Biology top 1%
- Glycosylation and Glycoproteins Research
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research

Papers in

Molecular Biology 211
- Glycosylation and Glycoproteins Research 87
- Mitochondrial Function and Pathology 61
- ATP Synthase and ATPases Research 28
Genetics 85
- Connective tissue disorders research 22
- Genomics and Rare Diseases 22

Co-authors: Ron A. Wevers (71 shared papers)Dirk J. Lefeber (39 shared papers)Richard J. Rodenburg (37 shared papers)Tamás Kozicz (42 shared papers)Jan Smeıtınk (30 shared papers)Saskia B. Wortmann (21 shared papers)Suzan Wopereis (10 shared papers)Jaak Jaeken (18 shared papers)
Journals: Molecular Genetics and Metabolism (37 papers)Journal of Inherited Metabolic Disease (33 papers)European Journal of Human Genetics (8 papers)Clinical Chemistry (7 papers)Genetics in Medicine (7 papers)
Partner nations: United States Netherlands Germany

In The Last Decade

Éva Morava

293 papers receiving 7.5k citations

Peers

Countries citing papers authored by Éva Morava

Since Specialization

Citations

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

Fields of papers citing papers by Éva Morava

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 312 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy Nature Genetics ·Judith Fischer, Caroline Lefèvre, Éva Morava, Jean‐Marie Mussini, Pascal Laforêt, Anne Nègre‐Salvayre, Mark Lathrop, Robert Salvayre	2006	357
2	Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans Nature Genetics ·Stephen P. Robertson, Stephen R.F. Twigg, Andrew J. Sutherland‐Smith, Valérie Biancalana, Robert J. Gorlin, Denise Horn, Susan Kenwrick, Chong Ae Kim, Éva Morava, Ruth Newbury‐Ecob, Karen Helene Ørstavik, Oliver Quarrell, Charles E. Schwartz, Deborah Shears, Mohnish Suri, John Kendrick‐Jones, Andrew O.M. Wilkie	2003	297
3	Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2 Nature Genetics ·(unknown), Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou, Jeroen van Reeuwijk, Bjoern Fischer, Anna Rajab, Birgit Budde, Peter Nürnberg, François Foulquier, Dirk J. Lefeber, Zsolt Urbán, S Gruenewald, Wim Annaert, Han G. Brunner, Hans van Bokhoven, Ron A. Wevers, Éva Morava, Gert Matthijs, Lionel Van Maldergem, Stefan Mundlos	2007	259
4	Mitochondrial disease criteria Neurology ·Éva Morava, Lambertus P. van den Heuvel, Frans A. Hol, Maaike C. de Vries, Marije Hogeveen, Richard J. Rodenburg, Jan Smeıtınk	2006	202
5	Congenital disorders of glycosylation (CDG): Quo vadis? European Journal of Medical Genetics ·Romain Péanne, Pascale de Lonlay, François Foulquier, Uwe Kornak, Dirk J. Lefeber, Éva Morava, Belén Pérez, Nathalie Séta, Christian Thiel, Emile Van Schaftingen, Gert Matthijs, Jaak Jaeken	2017	181
6	A guide to diagnosis and treatment of Leigh syndrome Journal of Neurology Neurosurgery & Psychiatry ·Fabian Baertling, Richard J. Rodenburg, Jörg Schaper, Jan Smeıtınk, Werner J.H. Koopman, Ertan Mayatepek, Éva Morava, Felix Distelmaier	2013	170
7	SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness Brain ·Rosalba Carrozzo, Carlo Dionisi‐Vici, Ulrike Steuerwald, S. Lucioli, Federica Deodato, Silvia Di Giandomenico, Enrico Bertini, Barbara Franke, Leo A. J. Kluijtmans, Maria Chiara Meschini, Cristiano Rizzo, Fiorella Piemonte, Richard J. Rodenburg, René Santer, Filippo M. Santorelli, Arno van Rooij, Diana Vermunt‐de Koning, Éva Morava, Ron A. Wevers	2007	146
8	Mechanisms in Protein O-Glycan Biosynthesis and Clinical and Molecular Aspects of Protein O-Glycan Biosynthesis Defects: A Review Clinical Chemistry ·Suzan Wopereis, Dirk J. Lefeber, Éva Morava, Ron A. Wevers	2006	128
9	Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing Human Molecular Genetics ·Sharita Timal, Alexander Hoischen, Ludwig Lehle, Maciej Adamowicz, Karin Huijben, Jolanta Sykut‐Cegielska, Justyna Paprocka, Ewa Jamroz, Francjan J. van Spronsen, Christian Körner, Christian Gilissen, Richard J. Rodenburg, Ilse Eidhof, Lambert van den Heuvel, Christian Thiel, Ron A. Wevers, Éva Morava, Joris A. Veltman, Dirk J. Lefeber	2012	122
10	Apolipoprotein C-III Isofocusing in the Diagnosis of Genetic Defects in O-Glycan Biosynthesis Clinical Chemistry ·Suzan Wopereis, Stephanie Grünewald, Éva Morava, Johannes Penzien, Paz Briones, M.T. García‐Silva, Pierre N.M. Demacker, Karin Huijben, Ron A. Wevers	2003	108
11	Contractions of D4Z4 on 4qB Subtelomeres Do Not Cause Facioscapulohumeral Muscular Dystrophy The American Journal of Human Genetics ·Richard J F L Lemmers, Mariëlle Wohlgemuth, Rune R. Frants, George W. Padberg, Éva Morava, Silvère M. van der Maarel	2004	92
12	Mitochondria and the economy of stress (mal)adaptation Neuroscience & Biobehavioral Reviews ·Éva Morava, Tamás Kozicz	2013	87
13	Congenital disorders of glycosylation: new defects and still counting Journal of Inherited Metabolic Disease ·Kyle Scott, Therese Gadomski, Tamás Kozicz, Éva Morava	2014	85
14	The challenge of CDG diagnosis Molecular Genetics and Metabolism ·Rita Francisco, Dorinda Marques‐da‐Silva, Sandra Brasil, Carlota Pascoal, Vanessa dos Reis Ferreira, Éva Morava, Jaak Jaeken	2018	81
15	A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia European Journal of Human Genetics ·Éva Morava, Renate Zeevaert, Eckhard Korsch, Karin Huijben, Suzan Wopereis, Gert Matthijs, Kathelijn Keymolen, Dirk J. Lefeber, Linda De Meırleır, Ron A. Wevers	2007	81
16	Autosomal recessive cutis laxa syndrome revisited European Journal of Human Genetics ·Éva Morava, Maïlys Guillard, Dirk J. Lefeber, Ron A. Wevers	2009	80
17	Measurement of the Energy-Generating Capacity of Human Muscle Mitochondria: Diagnostic Procedure and Application to Human Pathology Clinical Chemistry ·A.J.M. Janssen, Frans J.M. Trijbels, R. C. A. Sengers, Liesbeth T. Wintjes, W. Ruitenbeek, Jan Smeıtınk, Éva Morava, Baziel G.M. van Engelen, Lambert P. van den Heuvel, Richard J. Rodenburg	2006	80
18	Null mutations causing depletion of the type 1 ryanodine receptor (RYR1) are commonly associated with recessive structural congenital myopathies with cores Human Mutation ·Nicole Monnier, Isabelle Marty, Julien Fauré, Claudia Castiglioni, Claude Desnuelle, Sabrina Sacconi, B. Estournet, Ana Ferreiro, Norma B. Romero, Annie Laquerrière, Leïla Lazaro, Jean‐Jacques Martin, Éva Morava, Annick Rossi, Anneke J. van der Kooi, Marianne de Visser, Corien Verschuuren, Joël Lunardi	2008	75
19	Galactose supplementation in phosphoglucomutase-1 deficiency; review and outlook for a novel treatable CDG Molecular Genetics and Metabolism ·Éva Morava	2014	74
20	The 3‐methylglutaconic acidurias: what's new? Journal of Inherited Metabolic Disease ·Saskia B. Wortmann, Leo A. J. Kluijtmans, Udo F. H. Engelke, Ron A. Wevers, Éva Morava	2010	71

About Éva Morava

Éva Morava is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Physiology and Rheumatology, having authored 312 papers that have together received 7.6k indexed citations. Recurring topics across this work include Glycosylation and Glycoproteins Research (87 papers), Metabolism and Genetic Disorders (73 papers), Mitochondrial Function and Pathology (61 papers), Lysosomal Storage Disorders Research (40 papers), ATP Synthase and ATPases Research (28 papers), Carbohydrate Chemistry and Synthesis (27 papers), Connective tissue disorders research (22 papers) and Genomics and Rare Diseases (22 papers). The work is most often cited by research in Clinical Biochemistry (1.7k citations), Molecular Biology (5.3k citations), Biochemistry (519 citations), Biological Psychiatry (167 citations) and Genetics (1.6k citations). Éva Morava has collaborated with scholars based in United States, Netherlands and Germany. Frequent co-authors include Ron A. Wevers, Dirk J. Lefeber, Richard J. Rodenburg, Tamás Kozicz, Jan Smeıtınk, Saskia B. Wortmann, Suzan Wopereis, Jaak Jaeken, Peter Witters and Leo A. J. Kluijtmans. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, European Journal of Human Genetics, Clinical Chemistry and Genetics in Medicine.

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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