Thomas Müller

5.7k total citations
113 papers, 2.4k citations indexed

About

Thomas Müller is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Thomas Müller has authored 113 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 30 papers in Surgery and 29 papers in Genetics. Recurrent topics in Thomas Müller's work include Digestive system and related health (14 papers), Celiac Disease Research and Management (11 papers) and Trace Elements in Health (11 papers). Thomas Müller is often cited by papers focused on Digestive system and related health (14 papers), Celiac Disease Research and Management (11 papers) and Trace Elements in Health (11 papers). Thomas Müller collaborates with scholars based in Austria, Germany and United States. Thomas Müller's co-authors include Andreas Janecke, Wendt Müller, Hans G. Feichtinger, Peter Heinz‐Erian, Georg F. Vogel, Lukas A. Huber, Michael W. Hess, H Berger, Julia Vodopiutz and Michael J. Ausserlechner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Clinical Oncology.

In The Last Decade

Thomas Müller

105 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas Müller Austria 29 880 491 434 364 359 113 2.4k
Han‐Wook Yoo South Korea 33 1.8k 2.1× 971 2.0× 344 0.8× 266 0.7× 446 1.2× 300 4.0k
Rikke Nielsen Denmark 35 1.5k 1.7× 389 0.8× 257 0.6× 424 1.2× 386 1.1× 68 4.1k
Michel Sève France 23 876 1.0× 410 0.8× 830 1.9× 108 0.3× 286 0.8× 98 2.3k
Chiara Murgia Australia 21 487 0.6× 148 0.3× 842 1.9× 207 0.6× 107 0.3× 48 1.9k
Peter J. Malloy United States 28 1.1k 1.3× 970 2.0× 423 1.0× 574 1.6× 145 0.4× 52 3.5k
Meinrad Peterlik Austria 40 1.2k 1.4× 698 1.4× 950 2.2× 120 0.3× 310 0.9× 148 4.4k
Françis Frankenne Belgium 39 1.3k 1.4× 557 1.1× 142 0.3× 142 0.4× 397 1.1× 113 5.3k
Nathalie Charnaux France 33 836 0.9× 184 0.4× 156 0.4× 420 1.2× 195 0.5× 78 2.8k
Paula H. Stern United States 37 1.9k 2.2× 566 1.2× 296 0.7× 233 0.6× 358 1.0× 163 4.4k
Nalini Raghavachari United States 30 1.6k 1.9× 303 0.6× 102 0.2× 195 0.5× 191 0.5× 66 3.4k

Countries citing papers authored by Thomas Müller

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Müller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Müller

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Müller. A scholar is included among the top collaborators of Thomas Müller 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 Thomas Müller. Thomas Müller 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.
Åkeson, Pia Karlsland, et al.. (2024). PERCC1 ‐Related Congenital Enteropathy. Clinical Genetics. 107(1). 115–116.
2.
Kohlmaier, Benno, Kristijan Skok, Carolin Lackner, et al.. (2024). Steatotic liver disease associated with 2,4-dienoyl-CoA reductase 1 deficiency. International Journal of Obesity. 48(12). 1818–1821.
3.
Goßner, Liebwin, Dietmar Rieder, Thomas Müller, & Andreas Janecke. (2024). The Recurrent E-Cadherin (CDH1) Mutation c.760G>A Causes Orofacial Clefts but Does Not Predispose to Hereditary Cancer. Genes. 15(11). 1475–1475.
4.
Deeb, Asma, Abdelhadi Habeb, Anuradha Khadilkar, et al.. (2024). Natural history of Wolcott‐Rallison syndrome: A systematic review and follow‐up study. Liver International. 44(3). 811–822. 4 indexed citations
5.
Janecke, Andreas, Georg F. Vogel, Thomas Müller, et al.. (2023). SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption. Genes. 14(7). 1359–1359. 3 indexed citations
6.
Ploner, Christian, Débora C. Coraça‐Huber, Doris Wilflingseder, et al.. (2022). 3D bioprinted, vascularized neuroblastoma tumor environment in fluidic chip devices for precision medicine drug testing. Biofabrication. 14(3). 35002–35002. 55 indexed citations
7.
Liebscher, Gudrun, Taras Stasyk, Alexander Martin Heberle, et al.. (2021). The SZT2 Interactome Unravels New Functions of the KICSTOR Complex. Cells. 10(10). 2711–2711. 6 indexed citations
8.
Civan, Hasret Ayyıldız, Anna-Maria Schneider, Malte Cremer, et al.. (2021). Three Novel EPCAM Variants Causing Tufting Enteropathy in Three Families. Children. 8(6). 503–503. 4 indexed citations
9.
Crazzolara, Roman, Gabriele Kropshofer, Benjamin Hetzer, et al.. (2021). Omega-3 Fatty Acids and Their Role in Pediatric Cancer. Nutrients. 13(6). 1800–1800. 14 indexed citations
10.
Çakır, Murat, et al.. (2021). Early onset congenital diarrheas; single center experience. Pediatrics & Neonatology. 62(6). 612–619. 2 indexed citations
11.
Nair, Nitya, Ed Lemmens, Serena Chang, et al.. (2020). Single-Cell Immune Competency Signatures Associate with Survival in Phase II GVAX and CRS-207 Randomized Studies in Patients with Metastatic Pancreatic Cancer. Cancer Immunology Research. 8(5). 609–617. 17 indexed citations
12.
Vogel, Georg F., Andreas Janecke, Sally G. Mitton, et al.. (2017). Abnormal Rab11‐Rab8‐vesicles cluster in enterocytes of patients with microvillus inclusion disease. Traffic. 18(7). 453–464. 36 indexed citations
13.
Ellemunter, Helmut, et al.. (2016). Low sodium status in cystic fibrosis—as assessed by calculating fractional Na + excretion—is associated with decreased growth parameters. Journal of Cystic Fibrosis. 15(3). 400–405. 12 indexed citations
14.
Baumann, Matthias, Elisabeth Steichen‐Gersdorf, Birgit Krabichler, et al.. (2016). Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype–phenotype correlation. European Journal of Human Genetics. 25(2). 262–266. 30 indexed citations
15.
Müller, Thomas, Shuji Mizumoto, Julia Vodopiutz, et al.. (2013). Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers–Danlos syndrome. Human Molecular Genetics. 22(18). 3761–3772. 69 indexed citations
16.
Dündar, Munis, Thomas Müller, Qi Zhang, et al.. (2009). Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome. The American Journal of Human Genetics. 85(6). 873–882. 110 indexed citations
17.
Frühwirth, Martin, Andreas Janecke, Thomas Müller, et al.. (2003). Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome. The Journal of Pediatrics. 142(4). 441–447. 13 indexed citations
18.
Müller, Thomas, et al.. (2001). Seniors in Cyberspace. ACR Asia-Pacific Advances. 6 indexed citations
19.
Müller, Thomas, Cisca Wijmenga, Alan D. Phillips, et al.. (2000). Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes. Gastroenterology. 119(6). 1506–1513. 45 indexed citations
20.
Müller, Thomas, Wendt Müller, & Hans G. Feichtinger. (1998). Idiopathic copper toxicosis. American Journal of Clinical Nutrition. 67(5). 1082S–1086S. 84 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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