C R Müller

666 total citations
17 papers, 387 citations indexed

About

C R Müller is a scholar working on Molecular Biology, Clinical Biochemistry and Hematology. According to data from OpenAlex, C R Müller has authored 17 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 4 papers in Hematology. Recurrent topics in C R Müller's work include Muscle Physiology and Disorders (6 papers), Amino Acid Enzymes and Metabolism (4 papers) and Metabolism and Genetic Disorders (4 papers). C R Müller is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Amino Acid Enzymes and Metabolism (4 papers) and Metabolism and Genetic Disorders (4 papers). C R Müller collaborates with scholars based in Germany, United States and Slovakia. C R Müller's co-authors include T. Grimm, B. Müller, T. Bettecken, Sabina Liechti‐Gallati, Gerhard Meng, Jean‐Louis Guénet, Werner Wolz, Xavier Montagutelli, M. Janka and Andrea Gehrig and has published in prestigious journals such as Genomics, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

C R Müller

17 papers receiving 360 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C R Müller Germany	12	262	132	70	56	55	17	387
Dina Marek‐Yagel Israel	12	358 1.4×	63 0.5×	78 1.1×	50 0.9×	11 0.2×	26	507
Sara Scapolan Italy	10	271 1.0×	70 0.5×	49 0.7×	24 0.4×	34 0.6×	11	348
Matteo Granatiero Italy	6	420 1.6×	206 1.6×	46 0.7×	10 0.2×	32 0.6×	8	541
Silvio Ferraris Italy	12	262 1.0×	198 1.5×	42 0.6×	21 0.4×	16 0.3×	12	370
Daniel Beltrán Valero de Bernabé United States	6	469 1.8×	92 0.7×	77 1.1×	24 0.4×	45 0.8×	6	556
Michaela Brunner‐Krainz Austria	10	147 0.6×	129 1.0×	56 0.8×	12 0.2×	30 0.5×	22	393
Joan E. Pellegrino United States	11	256 1.0×	133 1.0×	215 3.1×	22 0.4×	16 0.3×	19	492
Charalampos Karadimas Greece	14	473 1.8×	245 1.9×	135 1.9×	11 0.2×	28 0.5×	17	627
Katarzyna Tońska Poland	14	400 1.5×	149 1.1×	44 0.6×	9 0.2×	13 0.2×	40	502

Countries citing papers authored by C R Müller

Since Specialization

Citations

This map shows the geographic impact of C 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 C 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 C R Müller more than expected).

Fields of papers citing papers by C R Müller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C R Müller

This figure shows the co-authorship network connecting the top 25 collaborators of C R Müller. A scholar is included among the top collaborators of C 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 C R Müller. C 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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17 of 17 papers shown

Maiers, Martin, Machteld Oudshoorn, Steven G. E. Marsh, et al.. (2010). World Marrow Donor Association framework for the implementation of HLA matching programs in hematopoietic stem cell donor registries and cord blood banks. Bone Marrow Transplantation. 46(3). 338–343. 20 indexed citations

Schessl, Joachim, Gudrun Schreiber, Ulrike Schara, et al.. (2008). Phenotypic variability in siblings with calpainopathy (LGMD2A).. PubMed. 27. 54–8. 12 indexed citations

Krüger, Rejko, Kay Seidel, Lüdger Schöls, et al.. (2007). Autosomal dominantly inherited Parkinson's disease: first investigation of the brain of a patient with the A30P mutation in the alpha-synuclein gene and initial insights into the degenerative process. Aktuelle Neurologie. 34(S 2). 1 indexed citations

Hanisch, F., C R Müller, Dirk Grimm, et al.. (2007). Frequency of calpain-3 c.550delA mutation in limb girdle muscular dystrophy type 2 and isolated hyperCKemia in German patients. Clinical Neuropathology. 26(7). 157–163. 19 indexed citations

Brummer, Dagmar, Maggie C. Walter, R Tomczak, et al.. (2005). Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutations.. PubMed. 24(1). 6–16. 16 indexed citations

Wiegand, Timothy J., C Raffoux, C K Hurley, et al.. (2004). A special report: suggested procedures for international unrelated donor search from the donor registries and quality assurance working groups of the World Marrow Donor Association (WMDA). Bone Marrow Transplantation. 34(2). 97–101. 13 indexed citations

Egeland, T, et al.. (2003). Donor and liability insurance of donor registries, donor centers, and collection centers – recommendations. Bone Marrow Transplantation. 33(5). 467–470. 11 indexed citations

Oldenburg, Johannes, Jörg Schröder, Jochen Graw, et al.. (2003). [Significance of mutation analysis in patients with haemophilia A].. PubMed. 23(1). 6–12. 4 indexed citations

Elçioğlu, Nursel, et al.. (2003). Alkaptonuria caused by compound heterozygote mutations.. PubMed. 14(2). 207–13. 5 indexed citations

10.

Müller, C R, et al.. (1999). Allelic heterogeneity of alkaptonuria in Central Europe. European Journal of Human Genetics. 7(6). 645–651. 24 indexed citations

11.

Gehrig, Andrea, et al.. (1997). Molecular defects in alkaptonuria. Cytogenetic and Genome Research. 76(1-2). 14–16. 39 indexed citations

12.

Grimm, T., Gerhard Meng, Sabina Liechti‐Gallati, et al.. (1994). On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.. Journal of Medical Genetics. 31(3). 183–186. 84 indexed citations

13.

Wolz, Werner, et al.. (1994). The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q. Genomics. 19(1). 5–8. 81 indexed citations

14.

Schwemmle, Sabine, K. Wolff, L. Palmucci, et al.. (1993). Multipoint Mapping of the Central Core Disease Locus. Genomics. 17(1). 205–207. 11 indexed citations

15.

Grimm, T., B. Müller, C R Müller, & M. Janka. (1990). Theoretical considerations on germline mosaicism in Duchenne muscular dystrophy.. Journal of Medical Genetics. 27(11). 683–687. 27 indexed citations

16.

Haaf, Thomas, W. Feichtinger, Martina Guttenbach, et al.. (1989). Berenil-induced undercondensation in human heterochromatin. Cytogenetic and Genome Research. 50(1). 27–33. 19 indexed citations

17.

Wolff, G., C R Müller, & T. Grimm. (1989). Benign muscular dystrophy: risk calculation in families with consanguinity.. Journal of Medical Genetics. 26(5). 299–304. 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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