Marianne Schwartz

7.7k total citations
116 papers, 4.9k citations indexed

About

Marianne Schwartz is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Marianne Schwartz has authored 116 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 30 papers in Genetics and 22 papers in Clinical Biochemistry. Recurrent topics in Marianne Schwartz's work include Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (22 papers) and Cystic Fibrosis Research Advances (13 papers). Marianne Schwartz is often cited by papers focused on Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (22 papers) and Cystic Fibrosis Research Advances (13 papers). Marianne Schwartz collaborates with scholars based in Denmark, United States and Netherlands. Marianne Schwartz's co-authors include John Vissing, Morten Dunø, Flemming Skovby, Thomas Rosenberg, Christian Koch, Susanne Kjærgaard, Peter Garred, Karin Hammer‐Jespersen, Marie‐Louise Sveen and N. J. Brandt and has published in prestigious journals such as Science, New England Journal of Medicine and Journal of Biological Chemistry.

In The Last Decade

Marianne Schwartz

116 papers receiving 4.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marianne Schwartz Denmark 40 3.2k 1.2k 779 493 482 116 4.9k
Erik G. Puffenberger United States 38 2.8k 0.9× 2.9k 2.5× 971 1.2× 978 2.0× 266 0.6× 74 6.7k
André Mégarbané Lebanon 43 4.1k 1.3× 2.1k 1.8× 211 0.3× 370 0.8× 806 1.7× 276 7.0k
J Frézal France 31 4.7k 1.5× 1.4k 1.2× 365 0.5× 246 0.5× 193 0.4× 210 6.7k
A. Westerveld Netherlands 44 4.3k 1.3× 1.4k 1.2× 165 0.2× 321 0.7× 287 0.6× 153 6.1k
Anthony T. Moore United Kingdom 45 5.9k 1.8× 1.6k 1.4× 468 0.6× 317 0.6× 473 1.0× 107 8.0k
Michele D’Urso Italy 35 2.8k 0.9× 1.4k 1.2× 182 0.2× 227 0.5× 186 0.4× 100 4.2k
Brunella Franco Italy 44 4.5k 1.4× 3.4k 2.9× 265 0.3× 282 0.6× 332 0.7× 138 7.0k
Nathan Fischel‐Ghodsian United States 47 4.8k 1.5× 884 0.8× 877 1.1× 117 0.2× 697 1.4× 106 6.8k
Moshe Frydman Israel 37 2.4k 0.7× 1.4k 1.2× 142 0.2× 261 0.5× 363 0.8× 132 4.6k
Christian Gilissen Netherlands 47 4.6k 1.4× 4.4k 3.8× 253 0.3× 247 0.5× 703 1.5× 135 8.5k

Countries citing papers authored by Marianne Schwartz

Since Specialization
Citations

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

Fields of papers citing papers by Marianne Schwartz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marianne Schwartz

This figure shows the co-authorship network connecting the top 25 collaborators of Marianne Schwartz. A scholar is included among the top collaborators of Marianne Schwartz 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 Marianne Schwartz. Marianne Schwartz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kamsteeg, Erik‐Jan, Wolfram Kreß, Claudio Catalli, et al.. (2012). Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2. European Journal of Human Genetics. 20(12). 1203–1208. 100 indexed citations
2.
Wibrand, Flemming, Tina D. Jeppesen, Anja Lisbeth Frederiksen, et al.. (2009). Limited diagnostic value of enzyme analysis in patients with mitochondrial tRNA mutations. Muscle & Nerve. 41(5). 607–613. 19 indexed citations
3.
Østergaard, Elsebet, Marianne Schwartz, Mustafa Batbayli, et al.. (2009). A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria. European Journal of Pediatrics. 169(2). 201–205. 39 indexed citations
4.
Jeppesen, Tina D., Marianne Schwartz, Eskild Colding‐Jørgensen, et al.. (2008). Phenotype and clinical course in a family with a new de novo Twinkle gene mutation. Neuromuscular Disorders. 18(4). 306–309. 11 indexed citations
5.
Rosenberg, Thomas, et al.. (2007). N965S is a common ABCA4 variant in Stargardt-related retinopathies in the Danish population.. PubMed. 13. 1962–9. 52 indexed citations
6.
Keller, Mette Kirstine, Nuno Vibe Hermann, Tron A. Darvann, et al.. (2007). Craniofacial Morphology in Muenke Syndrome. Journal of Craniofacial Surgery. 18(2). 374–386. 15 indexed citations
7.
Olsen, Birthe Susanne, Johanne M D Hahnemann, Marianne Schwartz, & Elsebet Østergaard. (2007). Thiamine-responsive megaloblastic anaemia: a cause of syndromic diabetes in childhood. Pediatric Diabetes. 8(4). 239–241. 20 indexed citations
8.
Schwartz, Marianne, et al.. (2005). dHPLC Screening of the NSD1 gene Identifies Nine Novel Mutations - Summary of the first 100 Sotos Syndrome Mutations. Annals of Human Genetics. 69(2). 222–226. 8 indexed citations
9.
Schwartz, Marianne & Morten Dunø. (2004). Improved Molecular Diagnosis of Dystrophin Gene Mutations Using the Multiplex Ligation-Dependent Probe Amplification Method. Genetic Testing. 8(4). 361–367. 75 indexed citations
10.
Colding‐Jørgensen, Eskild, Morten Dunø, Marianne Schwartz, & John Vissing. (2003). Decrement of compound muscle action potential is related to mutation type in myotonia congenita. Muscle & Nerve. 27(4). 449–455. 31 indexed citations
11.
Jeppesen, Tina D., Marianne Schwartz, David B. Olsen, & John Vissing. (2003). Oxidative capacity correlates with muscle mutation load in mitochondrial myopathy. Annals of Neurology. 54(1). 86–92. 65 indexed citations
12.
Schwartz, Marianne, et al.. (2003). A new mutation causing autosomal dominant periodic fever syndrome in a Danish family. The Journal of Pediatrics. 142(2). 191–193. 20 indexed citations
13.
Devriendt, Koenraad, Annette S. Kim, Suzanna G.M. Frints, et al.. (2001). Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia. Nature Genetics. 27(3). 313–317. 298 indexed citations
14.
Skakkeb�k, N. E., et al.. (1999). Steroid 21-hydroxylase deficiency: Mutational spectrum in Denmark, three novel mutations, and in vitro expression analysis. Human Mutation. 13(6). 482–486. 22 indexed citations
15.
Kjærgaard, Susanne, Flemming Skovby, & Marianne Schwartz. (1998). Absence of homozygosity for predominant mutations in PMM2 in Danish patients with carbohydrate-deficient glycoprotein syndrome type 1. European Journal of Human Genetics. 6(4). 331–336. 56 indexed citations
16.
Brandt, N. J., et al.. (1996). Psychological Impact of CarrierScreening for Cystic Fibrosisamong Pregnant Women. European Journal of Human Genetics. 4(2). 120–123. 13 indexed citations
17.
Bokhoven, Hans van, Cor W. R. J. Cremers, A. van Aarem, et al.. (1994). Mapping of the Choroideremia-like (CHML) Gene at 1q42-qter and Mutation Analysis in Patients with Usher Syndrome Type II. Genomics. 19(2). 385–387. 15 indexed citations
18.
Bokhoven, Hans van, Marianne Schwartz, Sten Andréasson, et al.. (1994). Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients. Human Molecular Genetics. 3(7). 1047–1051. 60 indexed citations
19.
Schwartz, Marianne. (1978). [59] Thymidine phosphorylase from Escherichia coli. Methods in enzymology on CD-ROM/Methods in enzymology. 51. 442–445. 43 indexed citations
20.
Schwartz, Marianne. (1971). Thymidine Phosphorylase from Escherichia coli. Properties and Kinetics. European Journal of Biochemistry. 21(2). 191–198. 73 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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