Dirk Kohlmüller

1.4k total citations
22 papers, 1.0k citations indexed

About

Dirk Kohlmüller is a scholar working on Molecular Biology, Clinical Biochemistry and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Dirk Kohlmüller has authored 22 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Dirk Kohlmüller's work include Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (6 papers) and Diet and metabolism studies (4 papers). Dirk Kohlmüller is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (6 papers) and Diet and metabolism studies (4 papers). Dirk Kohlmüller collaborates with scholars based in Germany, United States and Poland. Dirk Kohlmüller's co-authors include Andreas Schulze, Ertan Mayatepek, Georg F. Hoffmann, Martin Lindner, W. Kochen, Christian Opherk, Günther Schütz, Wolfgang Schmid, Christoph Kellendonk and François Tronche and has published in prestigious journals such as PEDIATRICS, Analytical Biochemistry and Molecular Endocrinology.

In The Last Decade

Dirk Kohlmüller

22 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dirk Kohlmüller Germany	13	540	515	217	206	132	22	1.0k
Naoto Terada Japan	10	459 0.8×	555 1.1×	233 1.1×	185 0.9×	75 0.6×	23	789
Toshiyo Sonta Japan	11	345 0.6×	263 0.5×	69 0.3×	396 1.9×	60 0.5×	13	1.2k
L. Bruinvis Netherlands	17	707 1.3×	746 1.4×	76 0.4×	214 1.0×	36 0.3×	33	1.0k
Maria João Pinho Portugal	18	569 1.1×	73 0.1×	81 0.4×	132 0.6×	32 0.2×	44	946
M. F. B. Silva Portugal	18	383 0.7×	290 0.6×	470 2.2×	75 0.4×	28 0.2×	31	970
Y. Urata Japan	12	348 0.6×	158 0.3×	77 0.4×	92 0.4×	39 0.3×	20	802
Alan Cahill United States	16	556 1.0×	111 0.2×	72 0.3×	120 0.6×	43 0.3×	23	1.3k
Hans‐Christoph Curtius Switzerland	14	349 0.6×	344 0.7×	92 0.4×	128 0.6×	66 0.5×	28	697
Srinivas M. Tipparaju United States	18	629 1.2×	35 0.1×	116 0.5×	208 1.0×	49 0.4×	50	1.3k
Christopher M. Loughrey United Kingdom	20	711 1.3×	121 0.2×	24 0.1×	78 0.4×	62 0.5×	43	1.5k

Countries citing papers authored by Dirk Kohlmüller

Since Specialization

Citations

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

Fields of papers citing papers by Dirk Kohlmüller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dirk Kohlmüller

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

All Works

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20 of 20 papers shown

Gramer, Gwendolyn, Saskia B. Wortmann, Junmin Fang‐Hoffmann, et al.. (2024). New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening Center. International Journal of Neonatal Screening. 10(1). 17–17. 2 indexed citations

Hämmerling, Susanne, Dirk Kohlmüller, Patrik Feyh, et al.. (2024). Influence of Season, Storage Temperature and Time of Sample Collection in Pancreatitis-Associated Protein-Based Algorithms for Newborn Screening for Cystic Fibrosis. International Journal of Neonatal Screening. 10(1). 5–5. 2 indexed citations

Okun, Jürgen G., Dirk Kohlmüller, Georgi Manukjan, et al.. (2024). Newborn screening for aromatic l-amino acid decarboxylase deficiency – Strategies, results, and implication for prevalence calculations. Molecular Genetics and Metabolism. 141(3). 108148–108148. 3 indexed citations

Monostori, Péter, Markus Godejohann, Joachim Janda, et al.. (2022). Identification of potential interferents of methylmalonic acid: A previously unrecognized pitfall in clinical diagnostics and newborn screening. Clinical Biochemistry. 111. 72–80. 5 indexed citations

Sommerburg, Olaf, Mirjam Stahl, Susanne Hämmerling, et al.. (2021). Final results of the southwest German pilot study on cystic fibrosis newborn screening – Evaluation of an IRT/PAP protocol with IRT-dependent safety net. Journal of Cystic Fibrosis. 21(3). 422–433. 9 indexed citations

Brennenstuhl, Heiko, Dirk Kohlmüller, Gwendolyn Gramer, et al.. (2019). High throughput newborn screening for aromatic ʟ‐amino‐acid decarboxylase deficiency by analysis of concentrations of 3‐O‐methyldopa from dried blood spots. Journal of Inherited Metabolic Disease. 43(3). 602–610. 25 indexed citations

Stopsack, Konrad H., J. Hammermann, Olaf Sommerburg, et al.. (2016). A product of immunoreactive trypsinogen and pancreatitis-associated protein as second-tier strategy in cystic fibrosis newborn screening. Journal of Cystic Fibrosis. 15(6). 752–758. 15 indexed citations

Gan‐Schreier, Hongying, Dorothea Haas, Sven W. Sauer, et al.. (2013). Bile Acid Precursors Compete with very Long Chain Fatty Acids for Translocation into Peroxisomes. Journal of Gastroenterology and Hepatology Research. 2(1). 362–366. 1 indexed citations

Binder, Gerhard, et al.. (2011). Analysis of the GH content within archived dried blood spots of newborn screening cards from children diagnosed with growth hormone deficiency after the neonatal period. Growth Hormone & IGF Research. 21(6). 314–317. 8 indexed citations

10.

Okun, Jürgen G., Ute Spiekerkötter, Martin Lindner, et al.. (2005). Quantitative Acylcarnitine Profiling in Peripheral Blood Mononuclear Cells Using In Vitro Loading With Palmitic and 2-Oxoadipic Acids: Biochemical Confirmation of Fatty Acid Oxidation and Organic Acid Disorders. Pediatric Research. 58(5). 873–880. 10 indexed citations

11.

Opherk, Christian, François Tronche, Christoph Kellendonk, et al.. (2004). Inactivation of the Glucocorticoid Receptor in Hepatocytes Leads to Fasting Hypoglycemia and Ameliorates Hyperglycemia in Streptozotocin-Induced Diabetes Mellitus. Molecular Endocrinology. 18(6). 1346–1353. 166 indexed citations

12.

Schulze, Andreas, et al.. (2003). Accurate measurement of free carnitine in dried blood spots by isotope-dilution electrospray tandem mass spectrometry without butylation. Clinica Chimica Acta. 335(1-2). 137–145. 22 indexed citations

13.

Kochen, W., et al.. (2003). The Endogeneous Formation of Highly Chlorinated Tetrahydro-ß-Carbolines as a Possible Causative Mechanism in Idiopathic Parkinson’s Disease. Advances in experimental medicine and biology. 527. 253–263. 34 indexed citations

14.

Kölker, Stefan, Jürgen G. Okun, Barbara Ahlemeyer, et al.. (2002). Chronic treatment with glutaric acid induces partial tolerance to excitotoxicity in neuronal cultures from chick embryo telencephalons. Journal of Neuroscience Research. 68(4). 424–431. 54 indexed citations

15.

Okun, Jürgen G., Stefan Kölker, Andreas Schulze, et al.. (2002). A method for quantitative acylcarnitine profiling in human skin fibroblasts using unlabelled palmitic acid: diagnosis of fatty acid oxidation disorders and differentiation between biochemical phenotypes of MCAD deficiency. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1584(2-3). 91–98. 60 indexed citations

16.

Kölker, Stefan, Jürgen G. Okun, Friederike Hörster, et al.. (2001). 3‐Ureidopropionate contributes to the neuropathology of 3‐ureidopropionase deficiency and severe propionic aciduria: A hypothesis. Journal of Neuroscience Research. 66(4). 666–673. 35 indexed citations

17.

Meyburg, Jochen, et al.. (1999). Postnatal changes in human acylcarnitine profile. Pediatric Research. 45(6). 922–922. 1 indexed citations

18.

Kohlmüller, Dirk, et al.. (1998). Transient trimethylaminuria in childhood. Acta Paediatrica. 87(11). 1205–1207. 30 indexed citations

19.

Mayatepek, Ertan, et al.. (1997). Continuous mannose infusion in carbohydrate‐deficient glycoprotein syndrome type I. Acta Paediatrica. 86(10). 1138–1140. 53 indexed citations

20.

Kohlmüller, Dirk & W. Kochen. (1993). Is n-Pentane Really an Index of Lipid Peroxidation in Humans and Animals? A Methodological Reevaluation. Analytical Biochemistry. 210(2). 268–276. 100 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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