Fabian Baertling

1.6k total citations
28 papers, 1.1k citations indexed

About

Fabian Baertling is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Fabian Baertling has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 14 papers in Clinical Biochemistry and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Fabian Baertling's work include Mitochondrial Function and Pathology (20 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (13 papers). Fabian Baertling is often cited by papers focused on Mitochondrial Function and Pathology (20 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (13 papers). Fabian Baertling collaborates with scholars based in Germany, Netherlands and Malaysia. Fabian Baertling's co-authors include Leo Nijtmans, Richard J. Rodenburg, Ertan Mayatepek, Sergio Guerrero‐Castillo, Ulrich Brandt, Felix Distelmaier, Hans J. C. T. Wessels, Susanne Arnold, Jan Smeıtınk and Jörg Schaper and has published in prestigious journals such as Brain, Neurology and Cell Metabolism.

In The Last Decade

Fabian Baertling

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabian Baertling Germany 17 882 356 86 70 65 28 1.1k
Monika Oláhová United Kingdom 16 690 0.8× 222 0.6× 49 0.6× 58 0.8× 75 1.2× 22 927
Markéta Tesařová Czechia 22 1.0k 1.2× 483 1.4× 31 0.4× 62 0.9× 63 1.0× 86 1.3k
Yuichi Matsushima Japan 21 1.1k 1.2× 353 1.0× 46 0.5× 77 1.1× 60 0.9× 52 1.3k
Eleonora Paradies Italy 11 702 0.8× 209 0.6× 59 0.7× 42 0.6× 97 1.5× 18 922
Susana Peralta United States 18 953 1.1× 329 0.9× 24 0.3× 70 1.0× 64 1.0× 29 1.1k
Luke E. Formosa Australia 16 941 1.1× 258 0.7× 29 0.3× 52 0.7× 72 1.1× 26 1.2k
Tamiko Nishimura Canada 16 890 1.0× 145 0.4× 31 0.4× 81 1.2× 105 1.6× 24 1.1k
Boris Reljić Australia 14 961 1.1× 206 0.6× 23 0.3× 49 0.7× 90 1.4× 20 1.2k
Reetta Hinttala Finland 16 455 0.5× 219 0.6× 31 0.4× 60 0.9× 37 0.6× 49 653
Atsuko Kasahara Japan 12 823 0.9× 223 0.6× 23 0.3× 65 0.9× 113 1.7× 18 1.0k

Countries citing papers authored by Fabian Baertling

Since Specialization
Citations

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

Fields of papers citing papers by Fabian Baertling

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabian Baertling

This figure shows the co-authorship network connecting the top 25 collaborators of Fabian Baertling. A scholar is included among the top collaborators of Fabian Baertling 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 Fabian Baertling. Fabian Baertling 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.
Lainka, Elke, Andrea Gangfuß, Alma Kuechler, et al.. (2024). Distinct neonatal hyperammonemia and liver synthesis dysfunction: case report of a severe MEGDHEL syndrome. Frontiers in Pediatrics. 12. 1278047–1278047. 1 indexed citations
2.
Welters, Alena, et al.. (2023). Delayed-Onset Transient Hyperinsulinism in Infants with Very Low and Extremely Low Birth Weights: A Cohort Study. The Journal of Pediatrics. 258. 113399–113399. 1 indexed citations
3.
Seibt, Annette, Ruchika Anand, Özer Degistirici, et al.. (2022). Mesenchymal stem cells improve redox homeostasis and mitochondrial respiration in fibroblast cell lines with pathogenic MT-ND3 and MT-ND6 variants. Stem Cell Research & Therapy. 13(1). 256–256. 2 indexed citations
4.
Sánchez‐Caballero, Laura, Dei M. Elurbe, Fabian Baertling, et al.. (2020). TMEM70 functions in the assembly of complexes I and V. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1861(8). 148202–148202. 34 indexed citations
5.
Baertling, Fabian, Laura Sánchez‐Caballero, Mariël A.M. van den Brand, et al.. (2018). A Heterozygous NDUFV1 Variant Aggravates Mitochondrial Complex I Deficiency in a Family with a Homoplasmic ND1 Variant. The Journal of Pediatrics. 196. 309–313.e3. 10 indexed citations
6.
Renkema, G. Herma, Gepke Visser, Fabian Baertling, et al.. (2017). Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions. Human Genetics. 136(6). 759–769. 27 indexed citations
7.
Baertling, Fabian, Laura Sánchez‐Caballero, Mariël A.M. van den Brand, et al.. (2017). NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect. European Journal of Human Genetics. 25(11). 1273–1277. 28 indexed citations
8.
Danhauser, Katharina, Annette Seibt, Özer Degistirici, et al.. (2017). Modulation of oxidative phosphorylation and redox homeostasis in mitochondrial NDUFS4 deficiency via mesenchymal stem cells. Stem Cell Research & Therapy. 8(1). 150–150. 34 indexed citations
9.
Baertling, Fabian, Laura Sánchez‐Caballero, Sharita Timal, et al.. (2016). Mutations in mitochondrial complex I assembly factor NDUFAF3 cause Leigh syndrome. Molecular Genetics and Metabolism. 120(3). 243–246. 21 indexed citations
10.
Baertling, Fabian, Bader Alhaddad, Annette Seibt, et al.. (2016). Neonatal encephalocardiomyopathy caused by mutations in VARS2. Metabolic Brain Disease. 32(1). 267–270. 21 indexed citations
11.
Guerrero‐Castillo, Sergio, Fabian Baertling, Hans J. C. T. Wessels, et al.. (2016). The Assembly Pathway of Mitochondrial Respiratory Chain Complex I. Cell Metabolism. 25(1). 128–139. 301 indexed citations
12.
Baertling, Fabian, Dirk Klee, Tobias B. Haack, et al.. (2016). The many faces of paediatric mitochondrial disease on neuroimaging. Child s Nervous System. 32(11). 2077–2083. 16 indexed citations
13.
Distelmaier, Felix, Tobias B. Haack, Claudia B. Catarino, et al.. (2015). MRPL44 mutations cause a slowly progressive multisystem disease with childhood-onset hypertrophic cardiomyopathy. Neurogenetics. 16(4). 319–323. 44 indexed citations
14.
Baertling, Fabian, Tobias B. Haack, Richard J. Rodenburg, et al.. (2015). MRPS22 mutation causes fatal neonatal lactic acidosis with brain and heart abnormalities. Neurogenetics. 16(3). 237–240. 26 indexed citations
15.
Baertling, Fabian, Ertan Mayatepek, Eva Thimm, et al.. (2014). Malonic aciduria: long-term follow-up of new patients detected by newborn screening. European Journal of Pediatrics. 173(12). 1719–1722. 12 indexed citations
16.
Mayer, Frank, et al.. (2013). Progesterone and estrogen prevent cisplatin-induced apoptosis of lung cancer cells.. PubMed. 33(3). 791–800. 19 indexed citations
17.
Baertling, Fabian, Richard J. Rodenburg, Jörg Schaper, et al.. (2013). A guide to diagnosis and treatment of Leigh syndrome. Journal of Neurology Neurosurgery & Psychiatry. 85(3). 257–265. 170 indexed citations
18.
Baertling, Fabian, Ertan Mayatepek, Patrick Gerner, et al.. (2013). Liver cirrhosis in glycogen storage disease Ib. Molecular Genetics and Metabolism. 108(3). 198–200. 5 indexed citations
19.
Baertling, Fabian, Maria Kokozidou, Thomas Pufe, et al.. (2010). ADAM12 is expressed by astrocytes during experimental demyelination. Brain Research. 1326. 1–14. 29 indexed citations
20.
Kramer, Martin, Jon Dang, Fabian Baertling, et al.. (2010). TTC staining of damaged brain areas after MCA occlusion in the rat does not constrict quantitative gene and protein analyses. Journal of Neuroscience Methods. 187(1). 84–89. 85 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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