Alexander Laemmle

816 total citations
19 papers, 412 citations indexed

About

Alexander Laemmle is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Alexander Laemmle has authored 19 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 4 papers in Biochemistry. Recurrent topics in Alexander Laemmle's work include Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (6 papers) and Amino Acid Enzymes and Metabolism (4 papers). Alexander Laemmle is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (6 papers) and Amino Acid Enzymes and Metabolism (4 papers). Alexander Laemmle collaborates with scholars based in Switzerland, United States and Germany. Alexander Laemmle's co-authors include Adrian Keogh, Daniel Candinas, Deborah Stroka, Mario P. Tschan, Stephan A. Vorburger, Vincent Roh, Johannes Häberle, René Fahrner, Jean‐Marc Nuoffer and Matteo Montani and has published in prestigious journals such as PLoS ONE, Hepatology and Journal of Hepatology.

In The Last Decade

Alexander Laemmle

16 papers receiving 406 citations

Peers

Alexander Laemmle
Radha Uppala United States
Boquan Wu China
Saien Lu China
In Hyuk Bang South Korea
Logan P. Poole United States
Radha Uppala United States
Alexander Laemmle
Citations per year, relative to Alexander Laemmle Alexander Laemmle (= 1×) peers Radha Uppala

Countries citing papers authored by Alexander Laemmle

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Laemmle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Laemmle

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

All Works

19 of 19 papers shown
2.
Underhaug, Jarl, Déborah Mathis, Shirou Matsumoto, et al.. (2025). Novel Treatment Strategy for Patients With Urea Cycle Disorders: Pharmacological Chaperones Enhance Enzyme Stability and Activity in Patient‐Derived Liver Disease Models. Journal of Inherited Metabolic Disease. 48(3). e70043–e70043.
3.
Lämmle, Bernhard & Alexander Laemmle. (2024). Vitamin B12 deficiency misdiagnosed as TTP: What can we learn from it?. British Journal of Haematology. 205(4). 1255–1256.
4.
Gautschi, Matthias, et al.. (2024). Inborn errors of the malate aspartate shuttle – Update on patients and cellular models. Molecular Genetics and Metabolism. 142(4). 108520–108520. 5 indexed citations
5.
Mathis, Déborah, Christa E. Flück, Anne‐Christine Uldry, et al.. (2024). Induced pluripotent stem cell-derived hepatocytes reveal TCA cycle disruption and the potential basis for triheptanoin treatment for malate dehydrogenase 2 deficiency. Molecular Genetics and Metabolism Reports. 39. 101066–101066. 2 indexed citations
6.
Brachet, Cécile, Alexander Laemmle, Martine Cools, et al.. (2024). Insight into the role of TXNRD2 in steroidogenesis through a novel homozygous TXNRD2 splice variant. European Journal of Endocrinology. 191(2). 144–155. 1 indexed citations
7.
Schaller, André, et al.. (2023). Induced pluripotent stem cell technology as diagnostic tool in patients with suspected ornithine transcarbamylase deficiency lacking genetic confirmation. Molecular Genetics and Metabolism Reports. 37. 101007–101007. 1 indexed citations
8.
Laemmle, Alexander, André Schaller, Andrea Felser, et al.. (2021). Triheptanoin – Novel therapeutic approach for the ultra-rare disease mitochondrial malate dehydrogenase deficiency. Molecular Genetics and Metabolism Reports. 29. 100814–100814. 12 indexed citations
9.
Laemmle, Alexander, Véronique Rüfenacht, Joshua F. Robinson, et al.. (2021). Aquaporin 9 induction in human iPSC‐derived hepatocytes facilitates modeling of ornithine transcarbamylase deficiency. Hepatology. 76(3). 646–659. 16 indexed citations
10.
Lee-Montiel, Felipe T., Alexander Laemmle, Verena Charwat, et al.. (2021). Integrated Isogenic Human Induced Pluripotent Stem Cell–Based Liver and Heart Microphysiological Systems Predict Unsafe Drug–Drug Interaction. Frontiers in Pharmacology. 12. 667010–667010. 45 indexed citations
11.
Laemmle, Alexander, Tamar Stricker, & Johannes Häberle. (2016). Switch from Sodium Phenylbutyrate to Glycerol Phenylbutyrate Improved Metabolic Stability in an Adolescent with Ornithine Transcarbamylase Deficiency. JIMD Reports. 31. 11–14. 5 indexed citations
12.
Laemmle, Alexander, Renata C. Gallagher, Adrian Keogh, et al.. (2016). Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD). PLoS ONE. 11(4). e0153358–e0153358. 37 indexed citations
13.
Laemmle, Alexander, Dagmar Hahn, Liyan Hu, et al.. (2015). Fatal hyperammonemia and carbamoyl phosphate synthetase 1 (CPS1) deficiency following high-dose chemotherapy and autologous hematopoietic stem cell transplantation. Molecular Genetics and Metabolism. 114(3). 438–444. 13 indexed citations
14.
Laemmle, Alexander, et al.. (2014). Propionic acidemia in a previously healthy adolescent with acute onset of dilated cardiomyopathy. European Journal of Pediatrics. 173(7). 971–974. 19 indexed citations
15.
Fahrner, René, Adrian Keogh, Alexander Laemmle, et al.. (2013). Antitumor Effect of SIRT1 Inhibition in Human HCC Tumor Models In Vitro and In Vivo. Molecular Cancer Therapeutics. 12(4). 499–508. 101 indexed citations
16.
Laemmle, Alexander, Vincent Roh, Adrian Keogh, et al.. (2012). Inhibition of SIRT1 Impairs the Accumulation and Transcriptional Activity of HIF-1α Protein under Hypoxic Conditions. PLoS ONE. 7(3). e33433–e33433. 125 indexed citations
17.
Wagner, Markus, Vincent Roh, Alexander Laemmle, et al.. (2009). Effective Treatment of Advanced Colorectal Cancer by Rapamycin and 5-FU/Oxaliplatin Monitored by TIMP-1. Journal of Gastrointestinal Surgery. 13(10). 1781–1790. 17 indexed citations
18.
Roh, Vincent, Alexander Laemmle, Urs von Holzen, et al.. (2008). Dual induction of PKR with E2F-1 and IFN-α to enhance gene therapy against hepatocellular carcinoma. Cancer Gene Therapy. 15(10). 636–644. 11 indexed citations
19.
Laemmle, Alexander, et al.. (2008). 339 TARGETING THE HISTONE DEACETYLASE-SIRT1 FOR ANTI-TUMOR THERAPY: INHIBITION OF SIRT1 DOWN-REGULATES HIF-1. Journal of Hepatology. 48. S133–S134. 2 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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