R. Mühlenberg

582 total citations
7 papers, 127 citations indexed

About

R. Mühlenberg is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics and Surgery. According to data from OpenAlex, R. Mühlenberg has authored 7 papers receiving a total of 127 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Endocrinology, Diabetes and Metabolism, 3 papers in Genetics and 1 paper in Surgery. Recurrent topics in R. Mühlenberg's work include Genetic Syndromes and Imprinting (2 papers), Pituitary Gland Disorders and Treatments (2 papers) and Growth Hormone and Insulin-like Growth Factors (2 papers). R. Mühlenberg is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Pituitary Gland Disorders and Treatments (2 papers) and Growth Hormone and Insulin-like Growth Factors (2 papers). R. Mühlenberg collaborates with scholars based in Germany, Switzerland and Estonia. R. Mühlenberg's co-authors include Susanne Fricke‐Otto, G. Heimann, Oliver Blankenstein, Stefan Wüller, Roland Pfäffle, Joachim Pohlenz, Nicole Pfarr, Matthias Begemann, Deniz Kanber and Michael Baudis and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Clinical Genetics and Hormone Research in Paediatrics.

In The Last Decade

R. Mühlenberg

6 papers receiving 124 citations

Peers

R. Mühlenberg

GENET

MB

EDM

PPCH

CR

Sinitdhorn Rujirabanjerd Thailand

Carlos Eduardo Seraphim Brazil

Lila Allou France

Anne‐Laure Mosca‐Boidron France

Pascal Arp Netherlands

Sobia Dil China

Deborah Osio United Kingdom

Aziz Mhanni Canada

Abdulrahman Swaid Saudi Arabia

Angela Hübner Germany

Sinitdhorn Rujirabanjerd Thailand

R. Mühlenberg

101 ×1.2

GENET

94 ×1.1

MB

12 ×0.3

EDM

23 ×0.5

PPCH

4 ×0.4

CR

Citations per year, relative to R. Mühlenberg R. Mühlenberg (= 1×) peers Sinitdhorn Rujirabanjerd

Countries citing papers authored by R. Mühlenberg

Since Specialization

Citations

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

Fields of papers citing papers by R. Mühlenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Mühlenberg

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

All Works

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7 of 7 papers shown

1.

Hermanns, Pia, et al.. (2013). Congenital Goitrous Primary Hypothyroidism in Two German Families Caused by Novel Thyroid Peroxidase (TPO) Gene Mutations. Experimental and Clinical Endocrinology & Diabetes. 121(6). 343–346. 7 indexed citations

2.

Begemann, Matthias, Sabrina Spengler, Deniz Kanber, et al.. (2010). Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. Clinical Genetics. 80(1). 83–88. 48 indexed citations

3.

Fricke‐Otto, Susanne, Nicole Pfarr, R. Mühlenberg, & Joachim Pohlenz. (2005). Mild Congenital Primary Hypothyroidism in a Turkish Family Caused by a Homozygous Missense Thyrotropin Receptor (TSHR) Gene Mutation (A593 V). Experimental and Clinical Endocrinology & Diabetes. 113(10). 582–585. 15 indexed citations

4.

Blankenstein, Oliver, et al.. (2001). A New C-Terminal Located Mutation (V272ter) in the <i>PIT-1 </i>Gene Manifesting with Severe Congenital Hypothyroidism. Hormone Research in Paediatrics. 56(3-4). 81–86. 28 indexed citations

5.

Haverkamp, F., Joachim Wölfle, Klaus Zerres, et al.. (1999). Growth Retardation in Turner Syndrome: Aneuploidy, Rather Than Specific Gene Loss, May Explain Growth Failure. The Journal of Clinical Endocrinology & Metabolism. 84(12). 4578–4582. 26 indexed citations

6.

Hauffa, B. P., Claudia Roll, R. Mühlenberg, & W. Havers. (1991). Growth in children with adrenocortical tumors. Klinische Pädiatrie. 203(2). 83–87. 3 indexed citations

7.

Mühlenberg, R., et al.. (1981). [Priapism in childhood (author's transl)].. PubMed. 129(10). 585–8.

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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