Martin Lindner

7.7k total citations · 1 hit paper
76 papers, 3.4k citations indexed

About

Martin Lindner is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Martin Lindner has authored 76 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Clinical Biochemistry, 42 papers in Molecular Biology and 22 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Martin Lindner's work include Metabolism and Genetic Disorders (48 papers), Neonatal Health and Biochemistry (22 papers) and Mitochondrial Function and Pathology (21 papers). Martin Lindner is often cited by papers focused on Metabolism and Genetic Disorders (48 papers), Neonatal Health and Biochemistry (22 papers) and Mitochondrial Function and Pathology (21 papers). Martin Lindner collaborates with scholars based in Germany, United States and Italy. Martin Lindner's co-authors include Georg F. Hoffmann, Andreas Schulze, Ertan Mayatepek, Dirk Kohlmüller, Johannes Zschocke, Stefan Kölker, Peter Burgard, Bernhard Y. Renard, René Santer and Alberto Burlina and has published in prestigious journals such as Nucleic Acids Research, Nature Medicine and Bioinformatics.

In The Last Decade

Martin Lindner

75 papers receiving 3.3k citations

Hit Papers

Suggested guidelines for the diagnosis and management of ... 2019 2026 2021 2023 2019 50 100 150 200 250
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision
    2019 268 citations Johannes Häberle, Alberto Burlina et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Lindner Germany 30 2.5k 1.9k 909 597 506 76 3.4k
Adelbert A. Roscher Germany 37 1.2k 0.5× 2.4k 1.2× 404 0.4× 671 1.1× 244 0.5× 93 3.7k
Carol L. Greene United States 24 885 0.4× 1.3k 0.7× 329 0.4× 308 0.5× 262 0.5× 63 2.2k
Hiroki Morizono United States 32 1.0k 0.4× 2.0k 1.0× 298 0.3× 203 0.3× 153 0.3× 79 2.9k
L. I. Woolf United Kingdom 24 908 0.4× 841 0.4× 189 0.2× 466 0.8× 143 0.3× 72 1.9k
Enzo Ranieri Australia 23 328 0.1× 385 0.2× 370 0.4× 486 0.8× 233 0.5× 55 1.5k
Monique G.M. de Sain–van der Velden Netherlands 26 521 0.2× 698 0.4× 121 0.1× 284 0.5× 135 0.3× 74 1.7k
Markus Grube Germany 34 192 0.1× 785 0.4× 810 0.9× 292 0.5× 63 0.1× 71 3.3k
E.C. Abraham United States 24 547 0.2× 983 0.5× 253 0.3× 706 1.2× 37 0.1× 77 2.3k
Tomoji Maeda Japan 30 145 0.1× 799 0.4× 303 0.3× 257 0.4× 83 0.2× 77 2.1k
Edward Cotlier United States 29 334 0.1× 1.4k 0.7× 107 0.1× 529 0.9× 96 0.2× 112 2.6k

Countries citing papers authored by Martin Lindner

Since Specialization
Citations

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

Fields of papers citing papers by Martin Lindner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Lindner

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Lindner. A scholar is included among the top collaborators of Martin Lindner 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 Martin Lindner. Martin Lindner 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.
Giarraputo, Alessia, Leela Morená, Rodrigo Benedetti Gassen, et al.. (2026). Immune profiling in a living human recipient of a gene-edited pig kidney. Nature Medicine. 32(1). 270–280.
2.
Park, Sarah Y., Martin Lindner, Kevin Brick, et al.. (2023). Detection of Mpox Virus Using Microbial Cell-Free DNA: The Potential of Pathogen-Agnostic Sequencing for Rapid Identification of Emerging Pathogens. The Journal of Infectious Diseases. 229(Supplement_2). S144–S155. 2 indexed citations
3.
Blankenstein, Oliver, Inken Brockow, Regina Ensenauer, et al.. (2021). Neonatal Screening for Congenital Metabolic and Endocrine Disorders. Deutsches Ärzteblatt international. 118(7). 101–108. 21 indexed citations
4.
Rand, Kenneth H., Martin Lindner, David K. Hong, et al.. (2020). Rapid, Noninvasive Diagnosis of Balamuthia mandrillaris Encephalitis by a Plasma-Based Next-Generation Sequencing Test. Open Forum Infectious Diseases. 7(7). ofaa189–ofaa189. 21 indexed citations
5.
Piro, Vitor C., Martin Lindner, & Bernhard Y. Renard. (2016). DUDes: a top-down taxonomic profiler for metagenomics. Bioinformatics. 32(15). 2272–2280. 31 indexed citations
6.
Cornel, Martina C., Tessel Rigter, Stephanie S. Weinreich, et al.. (2013). A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document. European Journal of Human Genetics. 22(1). 12–17. 45 indexed citations
7.
Häberle, Johannes, Nathalie Boddaert, Alberto Burlina, et al.. (2012). Suggested guidelines for the diagnosis and management of urea cycle disorders. Orphanet Journal of Rare Diseases. 7(1). 32–32. 399 indexed citations
8.
Gramer, Gwendolyn, C. Springer, Gisela Haege, et al.. (2012). Visual functions in phenylketonuria—evaluating the dopamine and long-chain polyunsaturated fatty acids depletion hypotheses. Molecular Genetics and Metabolism. 108(1). 1–7. 12 indexed citations
9.
Grünert, Sarah C., U. Wendel, Martin Lindner, et al.. (2012). Clinical and neurocognitive outcome in symptomatic isovaleric acidemia. Orphanet Journal of Rare Diseases. 7(1). 9–9. 60 indexed citations
10.
Walter, Melanie, et al.. (2010). Two inborn errors of metabolism in a newborn: Glutaric aciduria type I combined with isobutyrylglycinuria. Clinica Chimica Acta. 411(23-24). 2087–2091. 13 indexed citations
11.
Lindner, Martin. (2007). Rom und seine Kaiser im Historienfilm. 4 indexed citations
12.
Zschocke, Johannes, Martin Lindner, François Feillet, et al.. (2007). Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency. Human Mutation. 29(1). 167–175. 144 indexed citations
13.
Lindner, Martin. (2006). Drehbuch Geschichte : die antike Welt im Film. Lit eBooks. 1 indexed citations
14.
Freisinger, Peter, Erwin Lankes, Klaus Gempel, et al.. (2006). Hepatocerebral Mitochondrial DNA Depletion Syndrome Caused by Deoxyguanosine Kinase (DGUOK) Mutations. Archives of Neurology. 63(8). 1129–1129. 89 indexed citations
15.
Hoffmann, Georg F., Martin Lindner, Andreas Schulze, et al.. (2004). Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany. European Journal of Pediatrics. 163(2). 76–80. 44 indexed citations
16.
Lindner, Martin, Robert Steinfeld, Peter Burgard, et al.. (2003). Tetrahydrobiopterin sensitivity in German patients with mild phenylalanine hydroxylase deficiency. Human Mutation. 21(4). 400–400. 33 indexed citations
17.
Lindner, Martin, et al.. (2001). Tetrahydrobiopterin Responsiveness in Phenylketonuria Differs between Patients with the Same Genotype. Molecular Genetics and Metabolism. 73(1). 104–106. 56 indexed citations
18.
Zschocke, Johannes, Andreas Schulze, Martin Lindner, et al.. (2001). Molecular and functional characterisation of mild MCAD deficiency. Human Genetics. 108(5). 404–408. 52 indexed citations
19.
Brinkhaus, Benno, et al.. (2000). Phytobalneotherapy with Flores graminis (hay bath) - an alternative with few side effects to "hot" bath.. Perfusion. 13(11). 476–485. 2 indexed citations
20.
Zschocke, Johannes, Jos P.N. Ruiter, Martin Lindner, et al.. (2000). Progressive Infantile Neurodegeneration Caused by 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency: A Novel Inborn Error of Branched-Chain Fatty Acid and Isoleucine Metabolism. Pediatric Research. 48(6). 852–855. 88 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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