Clemens R. Müller

10.7k total citations · 2 hit papers
70 papers, 7.4k citations indexed

About

Clemens R. Müller is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Nutrition and Dietetics. According to data from OpenAlex, Clemens R. Müller has authored 70 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 13 papers in Cardiology and Cardiovascular Medicine and 12 papers in Nutrition and Dietetics. Recurrent topics in Clemens R. Müller's work include Ion channel regulation and function (13 papers), Vitamin K Research Studies (12 papers) and Muscle Physiology and Disorders (9 papers). Clemens R. Müller is often cited by papers focused on Ion channel regulation and function (13 papers), Vitamin K Research Studies (12 papers) and Muscle Physiology and Disorders (9 papers). Clemens R. Müller collaborates with scholars based in Germany, United Kingdom and Switzerland. Clemens R. Müller's co-authors include Benjamin D. Greenberg, Klaus‐Peter Lesch, Sue Z. Sabol, Jonathan Benjamin, Susanne Petri, Dean H. Hamer, Armin Heils, Dietmar Bengel, Dennis L. Murphy and Johannes Oldenburg and has published in prestigious journals such as Nature, Science and The Lancet.

In The Last Decade

Clemens R. Müller

69 papers receiving 7.2k citations

Hit Papers

align trajectories

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.

Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region

1996 4.0k citations Clemens R. Müller et al. profile →
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

2004 857 citations Simone Rost, Andreas Fregin et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Clemens R. Müller Germany	31	2.3k	1.9k	1.2k	1.1k	793	70	7.4k
Manfred Uhr Germany	57	1.7k 0.8×	1.1k 0.5×	354 0.3×	1.1k 0.9×	643 0.8×	199	10.2k
Synthia H. Mellon United States	57	3.3k 1.5×	2.3k 1.2×	349 0.3×	718 0.6×	219 0.3×	157	12.6k
Yedy Israel Canada	51	2.6k 1.2×	1.9k 1.0×	772 0.6×	253 0.2×	465 0.6×	236	10.0k
Anne Eckert Switzerland	66	5.4k 2.4×	3.3k 1.7×	161 0.1×	1.3k 1.2×	817 1.0×	253	14.7k
Marcus Ising Germany	53	1.2k 0.5×	1.1k 0.6×	233 0.2×	1.5k 1.3×	276 0.3×	185	10.3k
Robert H. Lipsky United States	44	2.6k 1.1×	2.5k 1.3×	158 0.1×	752 0.7×	267 0.3×	112	8.1k
Markus Schwarz Germany	64	2.7k 1.2×	1.3k 0.7×	319 0.3×	668 0.6×	171 0.2×	230	12.3k
Bernard Lerer Israel	58	2.8k 1.2×	2.9k 1.5×	408 0.3×	1.9k 1.7×	204 0.3×	339	12.6k
Fabìo Macciardi Italy	52	2.8k 1.3×	2.1k 1.1×	294 0.2×	741 0.7×	195 0.2×	206	7.8k
Christian P. Müller Germany	44	2.4k 1.1×	2.5k 1.3×	1.3k 1.1×	430 0.4×	199 0.3×	201	6.9k

Countries citing papers authored by Clemens R. Müller

Since Specialization

Citations

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

Fields of papers citing papers by Clemens R. Müller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Clemens R. Müller

This figure shows the co-authorship network connecting the top 25 collaborators of Clemens R. Müller. A scholar is included among the top collaborators of Clemens R. 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 Clemens R. Müller. Clemens R. Müller 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

Oldenburg, Johannes, et al.. (2015). Identification of deep intronic variants in 15 haemophilia A patients by next generation sequencing of the whole factor VIII gene. Thrombosis and Haemostasis. 114(10). 757–767. 25 indexed citations

Rost, Simone, Cordula Neuner, Indrajit Nanda, et al.. (2013). Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6. European Journal of Human Genetics. 22(2). 208–215. 50 indexed citations

Pelz, Hans‐Joachim, Simone Rost, Elisabeth Müller, et al.. (2011). Distribution and frequency of VKORC1 sequence variants conferring resistance to anticoagulants in Mus musculus. Pest Management Science. 68(2). 254–259. 45 indexed citations

Westhofen, Philipp, Matthias Watzka, Milka Marinova, et al.. (2011). Human Vitamin K 2,3-Epoxide Reductase Complex Subunit 1-like 1 (VKORC1L1) Mediates Vitamin K-dependent Intracellular Antioxidant Function. Journal of Biological Chemistry. 286(17). 15085–15094. 88 indexed citations

Broman, Marcus, Gunilla Islander, Frank Schuster, et al.. (2011). Screening of the Ryanodine 1 Gene for Malignant Hyperthermia Causative Mutations by High Resolution Melt Curve Analysis. Anesthesia & Analgesia. 113(5). 1120–1128. 11 indexed citations

Wehnert, Manfred, et al.. (2009). Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene. European Journal of Cell Biology. 88(10). 593–608. 29 indexed citations

Clemen, Christoph S., Dirk Fischer, Jens Reimann, et al.. (2008). How much mutant protein is needed to cause a protein aggregate myopathy in vivo? Lessons from an exceptional desminopathy. Human Mutation. 30(3). E490–E499. 23 indexed citations

Neumann, Sascha, Wenshu Lu, Martina Munck, et al.. (2007). Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells. Human Molecular Genetics. 16(23). 2944–2959. 58 indexed citations

Oldenburg, Johannes, Carville G. Bevans, Clemens R. Müller, & Matthias Watzka. (2006). Vitamin K Epoxide Reductase Complex Subunit 1 (VKORC1): The Key Protein of the Vitamin K Cycle. Antioxidants and Redox Signaling. 8(3-4). 347–353. 83 indexed citations

10.

Rost, Simone, et al.. (2004). Compound heterozygous mutations in the γ‐glutamyl carboxylase gene cause combined deficiency of all vitamin K‐dependent blood coagulation factors. British Journal of Haematology. 126(4). 546–549. 64 indexed citations

11.

Jungbluth, Heinz, Mark R. Davis, Clemens R. Müller, et al.. (2004). Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations. Neuromuscular Disorders. 14(12). 785–790. 102 indexed citations

12.

Oldenburg, Johannes, Vytautas Ivaškevičius, Simone Rost, et al.. (2001). Evaluation of DHPLC in the analysis of hemophilia A. Journal of Biochemical and Biophysical Methods. 47(1-2). 39–51. 66 indexed citations

13.

Oldenburg, Johannes, Simone Rost, Osman El‐Maarri, et al.. (2000). De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism. Blood. 96(8). 2905–2906. 30 indexed citations

14.

Schuster, Volker, Silvia Seidenspinner, Clemens R. Müller, & A. Rempen. (1999). Prenatal diagnosis in a family with severe type I plasminogen deficiency, ligneous conjunctivitis and congenital hydrocephalus. Prenatal Diagnosis. 19(5). 483–487. 18 indexed citations

15.

Ketelsen, Uwe‐Peter, et al.. (1997). Rare combination of Becker muscular dystrophy and Klinefelter's syndrome in one patient. Brain and Development. 19(5). 359–361. 7 indexed citations

16.

Oldenburg, Johannes, Andreas Fregin, Wolfram Kreß, et al.. (1997). Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy. British Journal of Haematology. 98(1). 240–244. 60 indexed citations

17.

Keating, Katherine E., Kathleen A. Quane, Bernadette M. Manning, et al.. (1994). Detection of a novel RYR1 mutation in four malignant hyperthermia pedigrees. Human Molecular Genetics. 3(10). 1855–1858. 63 indexed citations

18.

Saad, Fawzy A., et al.. (1994). Single base substitutions are detected by double strand conformation analysis. Nucleic Acids Research. 22(20). 4352–4353. 12 indexed citations

19.

Monaco, Anthony P., et al.. (1992). Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene. Human Mutation. 1(4). 280–287. 4 indexed citations

20.

Grimm, T., Gian Antonio Danieli, Clemens R. Müller, Giovanni Neri, & James F. Reynolds. (1988). Theoretical expectations for deletional mutations in duchenne muscular dystrophy. American Journal of Medical Genetics. 29(2). 445–451. 1 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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