Dietmar Müller

1.6k total citations
16 papers, 906 citations indexed

About

Dietmar Müller is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Dietmar Müller has authored 16 papers receiving a total of 906 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Surgery. Recurrent topics in Dietmar Müller's work include Connective tissue disorders research (4 papers), Head and Neck Anomalies (3 papers) and Congenital limb and hand anomalies (2 papers). Dietmar Müller is often cited by papers focused on Connective tissue disorders research (4 papers), Head and Neck Anomalies (3 papers) and Congenital limb and hand anomalies (2 papers). Dietmar Müller collaborates with scholars based in Germany, United States and Belgium. Dietmar Müller's co-authors include André Reis, Peter Nürnberg, Karl Sperling, Russell E. Ware, Ada L. Olins, Katrin Hoffmann, Amparo Vayá, Justo Aznar, Norberto Sotelo Cruz and Harald Herrmann and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Dietmar Müller

16 papers receiving 887 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dietmar Müller Germany	12	622	271	135	103	82	16	906
Lana N. Pho United States	8	241 0.4×	121 0.4×	67 0.5×	71 0.7×	48 0.6×	11	581
Haiyan I. Li Canada	2	728 1.2×	166 0.6×	83 0.6×	58 0.6×	81 1.0×	2	1.2k
R. M. Scarborough United States	7	340 0.5×	198 0.7×	74 0.5×	96 0.9×	103 1.3×	8	1.1k
Louise Aagaard Austria	6	921 1.5×	104 0.4×	174 1.3×	85 0.8×	54 0.7×	7	1.2k
Peter Lichter Germany	15	536 0.9×	210 0.8×	41 0.3×	57 0.6×	61 0.7×	17	781
R. A. Furlong United Kingdom	11	456 0.7×	179 0.7×	67 0.5×	139 1.3×	45 0.5×	22	924
Susan V. Outram United Kingdom	20	761 1.2×	145 0.5×	28 0.2×	125 1.2×	283 3.5×	26	1.0k
Kai-Ping Yan France	7	798 1.3×	115 0.4×	37 0.3×	48 0.5×	142 1.7×	7	973
Kenneth Nakahara United States	12	798 1.3×	251 0.9×	125 0.9×	100 1.0×	316 3.9×	15	1.6k
Amanda J. Atherton United Kingdom	10	277 0.4×	91 0.3×	54 0.4×	76 0.7×	50 0.6×	17	603

Countries citing papers authored by Dietmar Müller

Since Specialization

Citations

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

Fields of papers citing papers by Dietmar Müller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dietmar Müller

This figure shows the co-authorship network connecting the top 25 collaborators of Dietmar Müller. A scholar is included among the top collaborators of Dietmar 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 Dietmar Müller. Dietmar 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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16 of 16 papers shown

Müller, Dietmar, et al.. (2019). Phantom Borders in Eastern Europe: A New Concept for Regional Research. Slavic Review. 78(2). 368–389. 23 indexed citations

Sukalo, Maja, Hülya Kayserili, Dietmar Müller, et al.. (2015). DOCK6Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies. Human Mutation. 36(6). 593–598. 35 indexed citations

Eckl, Katja‐Martina, Rotem Tidhar, Holger Thiele, et al.. (2013). Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length. Journal of Investigative Dermatology. 133(9). 2202–2211. 130 indexed citations

Sznajer, Yves, et al.. (2010). Additional clinical and molecular analyses of TFAP2A in patients with the branchio‐oculo‐facial syndrome. American Journal of Medical Genetics Part A. 152A(4). 994–999. 17 indexed citations

Koenig, Rainer, Peter Meinecke, Alma Kuechler, Dieter Schäfer, & Dietmar Müller. (2010). Wiedemann–Steiner syndrome: Three further cases. American Journal of Medical Genetics Part A. 152A(9). 2372–2375. 26 indexed citations

Azzarello‐Burri, Silvia, Gabriele Gillessen‐Kaesbach, Peter Meinecke, et al.. (2009). Goltz–Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. European Journal of Human Genetics. 17(10). 1207–1215. 28 indexed citations

Kornak, Uwe, Hans Christian Hennies, Johannes Egerer, et al.. (2009). Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a novel RAB-6 interacting golgin. Bone. 44. S232–S232. 1 indexed citations

Müller, Dietmar, et al.. (2007). Exclusion of genes from the EYA‐DACH‐SIX‐PAX pathway as candidates for Branchio–Oculo–Facial syndrome (BOFS). American Journal of Medical Genetics Part A. 143A(18). 2185–2188. 10 indexed citations

Thiel, Christian T., Denise Horn, Bernhard Zabel, et al.. (2005). Severely Incapacitating Mutations in Patients with Extreme Short Stature Identify RNA-Processing Endoribonuclease RMRP as an Essential Cell Growth Regulator. The American Journal of Human Genetics. 77(5). 795–806. 101 indexed citations

10.

Robinson, Peter N., Luitgard M. Neumann, Stephanie Demuth, et al.. (2005). Shprintzen–Goldberg syndrome: Fourteen new patients and a clinical analysis. American Journal of Medical Genetics Part A. 135A(3). 251–262. 54 indexed citations

11.

Lehmann, Katarina, Petra Seemann, Sigmar Stricker, et al.. (2003). Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2. Proceedings of the National Academy of Sciences. 100(21). 12277–12282. 124 indexed citations

12.

Hoffmann, Katrin, Ada L. Olins, Donald E. Olins, et al.. (2002). Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly). Nature Genetics. 31(4). 410–414. 261 indexed citations

13.

Hummel, Susanne, Bernd Herrmann, Dietmar Müller, et al.. (1999). Proving the Authenticity of Ancient DNA by Comparative Genomic Hybridization. Die Naturwissenschaften. 86(10). 500–503. 5 indexed citations

14.

Lin, Angela E., Robert J. Gorlin, Iosif W. Lurie, et al.. (1995). Further delineation of the branchio‐oculo‐facial syndrome. American Journal of Medical Genetics. 56(1). 42–59. 60 indexed citations

15.

Traupe, Heiko, Dietmar Müller, David J. Atherton, et al.. (1992). Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation. Human Genetics. 89(6). 659–665. 29 indexed citations

16.

Künzel, W., et al.. (1982). [Type III shortrib-polydactyly syndrome (Verma-Naumoff) in concomitance with ectodermal dysplasia (author's transl)].. PubMed. 104(9). 568–75. 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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