Adolf Mühl

1.9k total citations
44 papers, 1.4k citations indexed

About

Adolf Mühl is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Adolf Mühl has authored 44 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Clinical Biochemistry, 13 papers in Molecular Biology and 13 papers in Physiology. Recurrent topics in Adolf Mühl's work include Metabolism and Genetic Disorders (23 papers), Folate and B Vitamins Research (8 papers) and Neonatal Health and Biochemistry (7 papers). Adolf Mühl is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Folate and B Vitamins Research (8 papers) and Neonatal Health and Biochemistry (7 papers). Adolf Mühl collaborates with scholars based in Austria, United States and Germany. Adolf Mühl's co-authors include Olaf A. Bodamer, Sylvia Stöckler‐Ipsiroglu, Chike Bellarmine Item, Carmen Stromberger, Joan Keutzer, Georg Heinze, Rene Ratschmann, Margareta Holub, Karin Tuschl and M. Alessandri and has published in prestigious journals such as Neurology, FEBS Letters and The American Journal of Human Genetics.

In The Last Decade

Adolf Mühl

44 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adolf Mühl Austria 20 503 446 399 382 256 44 1.4k
J. G. M. Huijmans Netherlands 26 555 1.1× 398 0.9× 207 0.5× 867 2.3× 190 0.7× 72 2.1k
David Cheillan France 25 489 1.0× 414 0.9× 387 1.0× 886 2.3× 133 0.5× 79 1.9k
A Sewell Germany 24 564 1.1× 527 1.2× 182 0.5× 756 2.0× 310 1.2× 89 1.7k
Mirjam Langeveld Netherlands 23 872 1.7× 156 0.3× 330 0.8× 612 1.6× 176 0.7× 78 1.5k
Joe T.R. Clarke Canada 32 1.5k 3.0× 537 1.2× 584 1.5× 1.1k 3.0× 431 1.7× 109 2.8k
Deborah Marsden United States 24 532 1.1× 1.2k 2.7× 175 0.4× 854 2.2× 283 1.1× 65 1.8k
Françoise Bontemps Belgium 24 266 0.5× 145 0.3× 142 0.4× 1.1k 3.0× 166 0.6× 71 2.0k
Alisa Gutman Israel 27 411 0.8× 746 1.7× 80 0.2× 916 2.4× 188 0.7× 84 1.8k
Misao Ōwada Japan 19 470 0.9× 126 0.3× 216 0.5× 343 0.9× 94 0.4× 70 1.3k
Georges Berghe Belgium 23 290 0.6× 358 0.8× 120 0.3× 1.4k 3.6× 225 0.9× 46 2.1k

Countries citing papers authored by Adolf Mühl

Since Specialization
Citations

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

Fields of papers citing papers by Adolf Mühl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adolf Mühl

This figure shows the co-authorship network connecting the top 25 collaborators of Adolf Mühl. A scholar is included among the top collaborators of Adolf Mühl 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 Adolf Mühl. Adolf Mühl 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.
Karg, Eszter, Sándor Túri, Gyula Wittmann, et al.. (2012). Newborn Screening for Lysosomal Storage Disorders in Hungary. JIMD Reports. 6. 117–125. 72 indexed citations
2.
Reuser, Arnold, Frans W. Verheijen, Deeksha Bali, et al.. (2011). The use of dried blood spot samples in the diagnosis of lysosomal storage disorders — Current status and perspectives. Molecular Genetics and Metabolism. 104(1-2). 144–148. 60 indexed citations
3.
Freilinger, Michael, Daniela Dunkler, Chike Bellarmine Item, et al.. (2011). Effects of Creatine Supplementation in Rett Syndrome: A Randomized, Placebo-Controlled Trial. Journal of Developmental & Behavioral Pediatrics. 32(6). 454–460. 18 indexed citations
4.
Huemer, Martina, Burkhard Simma, Adolf Mühl, et al.. (2010). Low Levels of Asymmetric Dimethylarginine in Children with Diabetes Mellitus Type I Compared with Healthy Children. The Journal of Pediatrics. 158(4). 602–606.e1. 17 indexed citations
5.
Dajnoki, Angéla, György Fekete, Joan Keutzer, et al.. (2010). Newborn screening for Fabry disease by measuring GLA activity using tandem mass spectrometry. Clinica Chimica Acta. 411(19-20). 1428–1431. 44 indexed citations
6.
Ratschmann, Rene, Milen Minkov, Christina Hung, et al.. (2009). Transcobalamin II deficiency at birth. Molecular Genetics and Metabolism. 98(3). 285–288. 20 indexed citations
7.
Huemer, Martina, Manuela Födinger, Olaf A. Bodamer, et al.. (2008). Total homocysteine, B-vitamins and genetic polymorphisms in patients with classical phenylketonuria. Molecular Genetics and Metabolism. 94(1). 46–51. 17 indexed citations
8.
Item, Chike Bellarmine, Ivana Mihalek, Anil Jalan, et al.. (2007). Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III. Molecular Genetics and Metabolism. 91(4). 379–383. 12 indexed citations
9.
Trittenwein, Gerhard, Gehan Ahmed Mostafa, Gudrun Burda, et al.. (2006). Bridging to transplantation in acute liver failure in a 7-month-old infant. Wiener klinische Wochenschrift. 118(9-10). 298–301. 4 indexed citations
10.
Votava, Felix, Jan Lebl, Adolf Mühl, et al.. (2006). Prevalence of congenital adrenal hyperplasia among sudden infant death in the Czech Republic and Austria. European Journal of Pediatrics. 166(1). 1–4. 26 indexed citations
11.
Holub, Margareta, et al.. (2005). Lack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome?. Acta Paediatrica. 94(1). 48–52. 9 indexed citations
12.
Item, Chike Bellarmine, et al.. (2005). Use of denaturing HPLC to provide efficient detection of mutations causing guanidinoacetate methyltransferase deficiency. Molecular Genetics and Metabolism. 86(1-2). 328–334. 4 indexed citations
13.
Tuschl, Karin, Olaf A. Bodamer, Wolfgang Erwa, & Adolf Mühl. (2004). Rapid analysis of total plasma homocysteine by tandem mass spectrometry. Clinica Chimica Acta. 351(1-2). 139–141. 31 indexed citations
14.
Item, Chike Bellarmine, Saadet Mercimek‐Mahmutoglu, Roberta Battini, et al.. (2004). Characterization of seven novel mutations in seven patients with GAMT deficiency. Human Mutation. 23(5). 524–524. 40 indexed citations
15.
Mühl, Adolf, et al.. (2001). Molecular characterisation of 34 patients with biotinidase deficiency ascertained by newborn screening and family investigation. European Journal of Human Genetics. 9(4). 237–243. 28 indexed citations
16.
Ipsiroglu, O., et al.. (2001). Changes of tissue creatine concentrations upon oral supplementation of creatine-monohydrate in various animal species. Life Sciences. 69(15). 1805–1815. 100 indexed citations
17.
Mühl, Adolf, et al.. (2000). Guanidinoacetate methyltransferase (GAMT) deficiency: non-invasive enzymatic diagnosis of a newly recognized inborn error of metabolism. Clinica Chimica Acta. 290(2). 179–188. 38 indexed citations
18.
Kapiotis, Stylianos, Marcela Hermann, Irmtraud Held, Adolf Mühl, & Bernhard Gmeiner. (1997). Tyrosine: an inhibitor of LDL oxidation and endothelial cell cytotoxicity initiated by superoxide/nitric oxide radicals1. FEBS Letters. 409(2). 223–226. 17 indexed citations
19.
Kapiotis, S., Gürkan Sengoelge, Wolfgang R. Sperr, et al.. (1996). Ibuprofen inhibits pyrogen-dependent expression of VCAM-1 and ICAM-1 on human endothelial cells. Life Sciences. 58(23). 2167–2181. 52 indexed citations
20.
Scheibenreiter, S, et al.. (1996). Austrian report on longitudinal outcome in phenylketonuria. European Journal of Pediatrics. 155(S1). S45–S49. 7 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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