Martina Baethmann

2.0k total citations
25 papers, 1.2k citations indexed

About

Martina Baethmann is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology. According to data from OpenAlex, Martina Baethmann has authored 25 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 5 papers in Rheumatology. Recurrent topics in Martina Baethmann's work include Child Nutrition and Feeding Issues (4 papers), Metabolism and Genetic Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Martina Baethmann is often cited by papers focused on Child Nutrition and Feeding Issues (4 papers), Metabolism and Genetic Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Martina Baethmann collaborates with scholars based in Germany, Netherlands and Switzerland. Martina Baethmann's co-authors include Thomas Voït, Thomas Voit, Barbara Frühe, Kathrin Pietsch, Gerd Schulte‐Körne, Antje‐Kathrin Allgaier, Rudy Van Coster, D. Pongratz, Benedikt Schoser and C. Schwake and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Martina Baethmann

21 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martina Baethmann Germany 17 504 365 317 191 137 25 1.2k
Shu‐Chuan Chiang Taiwan 14 186 0.4× 428 1.2× 241 0.8× 92 0.5× 161 1.2× 22 913
Sandra Leistner‐Segal Brazil 22 276 0.5× 583 1.6× 249 0.8× 47 0.2× 133 1.0× 88 1.6k
Carolyn Ellaway Australia 29 959 1.9× 247 0.7× 187 0.6× 294 1.5× 268 2.0× 81 2.6k
Erika F. Augustine United States 16 209 0.4× 363 1.0× 133 0.4× 26 0.1× 63 0.5× 69 879
Justyna Paprocka Poland 15 341 0.7× 127 0.3× 60 0.2× 77 0.4× 139 1.0× 82 892
Semra Hız Kurul Türkiye 19 295 0.6× 123 0.3× 83 0.3× 94 0.5× 440 3.2× 104 1.2k
Paolo Ronchi Italy 23 329 0.7× 210 0.6× 26 0.1× 86 0.5× 154 1.1× 63 1.8k
Anne Tournay United States 13 141 0.3× 195 0.5× 75 0.2× 26 0.1× 560 4.1× 20 1.1k
Yung‐Ting Kuo Taiwan 17 189 0.4× 92 0.3× 46 0.1× 25 0.1× 199 1.5× 46 792
Karen E. Yates United States 20 377 0.7× 174 0.5× 229 0.7× 8 0.0× 158 1.2× 45 1.4k

Countries citing papers authored by Martina Baethmann

Since Specialization
Citations

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

Fields of papers citing papers by Martina Baethmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martina Baethmann

This figure shows the co-authorship network connecting the top 25 collaborators of Martina Baethmann. A scholar is included among the top collaborators of Martina Baethmann 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 Martina Baethmann. Martina Baethmann 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
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Bierhals, Tatjana, et al.. (2018). Novel DCC variants in congenital mirror movements and evaluation of disease-associated missense variants. European Journal of Medical Genetics. 61(6). 329–334. 7 indexed citations
5.
Capelle, Carine I. van, Jan C. van der Meijden, Johanna M. P. van den Hout, et al.. (2016). Childhood Pompe disease: clinical spectrum and genotype in 31 patients. Orphanet Journal of Rare Diseases. 11(1). 65–65. 47 indexed citations
6.
Hahn, Andreas, Nesrin Karabul, Dorle Schmidt, et al.. (2014). Outcome of Patients with Classical Infantile Pompe Disease Receiving Enzyme Replacement Therapy in Germany. JIMD Reports. 20. 65–75. 47 indexed citations
7.
Rosewich, Hendrik, Martina Baethmann, Andreas Ohlenbusch, Jutta Gärtner, & Knut Brockmann. (2014). A novel ATP1A3 mutation with unique clinical presentation. Journal of the Neurological Sciences. 341(1-2). 133–135. 20 indexed citations
8.
Allgaier, Antje‐Kathrin, et al.. (2012). Is the Children's Depression Inventory Short version a valid screening tool in pediatric care? A comparison to its full-length version. Journal of Psychosomatic Research. 73(5). 369–374. 147 indexed citations
9.
Frühe, Barbara, Antje‐Kathrin Allgaier, Kathrin Pietsch, et al.. (2011). Children’s Depression Screener (ChilD-S): Development and Validation of a Depression Screening Instrument for Children in Pediatric Care. Child Psychiatry & Human Development. 43(1). 137–151. 29 indexed citations
10.
Müller‐Felber, Wolfgang, Rita Horváth, Klaus Gempel, et al.. (2007). Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients. Neuromuscular Disorders. 17(9-10). 698–706. 193 indexed citations
11.
Assmann, Birgit, Martina Baethmann, Ron A. Wevers, et al.. (2006). Clinical Findings and a Therapeutic Trial in the First Patient with β-Ureidopropionase Deficiency. Neuropediatrics. 37(1). 20–25. 12 indexed citations
12.
Knaap, Marjo S. van der, Carola G.M. van Berkel, Jochen Herms, et al.. (2003). eIF2B-Related Disorders: Antenatal Onset and Involvement of Multiple Organs. The American Journal of Human Genetics. 73(5). 1199–1207. 114 indexed citations
13.
Voït, Thomas, Barbara Leube, Eva Neuen-Jacob, et al.. (2001). Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus. Neuromuscular Disorders. 11(1). 11–19. 39 indexed citations
14.
Heuvel, Lambert P.W.J. van den, A.J.M. Janssen, Roel Smeets, et al.. (2000). Combined Enzymatic Complex I and III Deficiency Associated with Mutations in the Nuclear Encoded NDUFS4 Gene. Biochemical and Biophysical Research Communications. 275(1). 63–68. 165 indexed citations
15.
Baethmann, Martina, et al.. (2000). Hydrocephalus Internus in Two Patients with 5,10-Methylenetetrahydrofolate Reductase Deficiency. Neuropediatrics. 31(6). 314–317. 24 indexed citations
16.
Klepper, Jörg, René Santer, Martina Baethmann, Darryl C. De Vivo, & Thomas Voit. (2000). Angeborene Störungen des Glukosetransports. Monatsschrift Kinderheilkunde. 148(1). 2–11. 4 indexed citations
17.
Baethmann, Martina, et al.. (1999). Localization of Laminin Isoforms in the Guinea Pig Cochlea. The Laryngoscope. 109(12). 2001–2004. 8 indexed citations
18.
Baethmann, Martina, et al.. (1998). HMSNL in a 13-year-old Bulgarian girl. Neuromuscular Disorders. 8(2). 90–94. 28 indexed citations
19.
Wallot, M., Martina Baethmann, Jörg Schaper, et al.. (1998). Acute cerebellitis with near-fatal cerebellar swelling and benign outcome under conservative treatment with high dose steroids. European Journal of Paediatric Neurology. 2(3). 157–162. 39 indexed citations
20.
Baethmann, Martina, et al.. (1996). Fetal CNS damage after exposure to maternal trauma during pregnancy. Acta Paediatrica. 85(11). 1331–1338. 48 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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