Helmuth‐Günther Dörr

1.7k total citations
39 papers, 692 citations indexed

About

Helmuth‐Günther Dörr is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Helmuth‐Günther Dörr has authored 39 papers receiving a total of 692 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Endocrinology, Diabetes and Metabolism and 12 papers in Genetics. Recurrent topics in Helmuth‐Günther Dörr's work include Sexual Differentiation and Disorders (8 papers), Growth Hormone and Insulin-like Growth Factors (7 papers) and Childhood Cancer Survivors' Quality of Life (5 papers). Helmuth‐Günther Dörr is often cited by papers focused on Sexual Differentiation and Disorders (8 papers), Growth Hormone and Insulin-like Growth Factors (7 papers) and Childhood Cancer Survivors' Quality of Life (5 papers). Helmuth‐Günther Dörr collaborates with scholars based in Germany, Austria and United States. Helmuth‐Günther Dörr's co-authors include Manfred Rauh, Michael Gröschl, Dirk Schnabel, Anita Rauch, B Mayr, Christof Schöfl, André Reis, Christian T. Thiel, Walter Bonfig and Manfred Wildner and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and Endocrinology.

In The Last Decade

Helmuth‐Günther Dörr

36 papers receiving 662 citations

Peers

Helmuth‐Günther Dörr
Gabriela Guercio Argentina
Serpil Taheri Türkiye
Flavia Napoli Italy
Ulrike Kessler Germany
H. G. Doerr Germany
B. P. Hauffa Germany
Mark Stene United States
Carol A. Huseman United States
W. M. Teller Germany
Luiz de Lacerda Brazil
Gabriela Guercio Argentina
Helmuth‐Günther Dörr
Citations per year, relative to Helmuth‐Günther Dörr Helmuth‐Günther Dörr (= 1×) peers Gabriela Guercio

Countries citing papers authored by Helmuth‐Günther Dörr

Since Specialization
Citations

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

Fields of papers citing papers by Helmuth‐Günther Dörr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Helmuth‐Günther Dörr. 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 Helmuth‐Günther Dörr. The network helps show where Helmuth‐Günther Dörr may publish in the future.

Co-authorship network of co-authors of Helmuth‐Günther Dörr

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

All Works

20 of 20 papers shown
1.
Binder, Gerhard, Dirk Schnabel, Thomas Reinehr, et al.. (2020). Evolving pituitary hormone deficits in primarily isolated GHD: a review and experts’ consensus. PubMed. 7(1). 16–16. 11 indexed citations
2.
Dörr, Helmuth‐Günther, Markus Bettendorf, Gerhard Binder, et al.. (2020). Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. PubMed. 7(1). 8–8. 7 indexed citations
3.
Quitmann, Julia, Neuza Silva, Monika Bullinger, et al.. (2019). Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment. Frontiers in Pediatrics. 7. 164–164. 17 indexed citations
4.
Silva, Neuza, et al.. (2019). Psychometric properties of the quality of life in short statured youth (QoLISSY) questionnaire within the course of growth hormone treatment. Health and Quality of Life Outcomes. 17(1). 49–49. 9 indexed citations
5.
Sticht, Heinrich, Christian Büttner, Cornelia Kraus, et al.. (2017). Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature. Scientific Reports. 7(1). 12225–12225. 55 indexed citations
6.
Kessler, Kristin, Steffen Uebe, Nathalie Falk, et al.. (2015). DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects. Scientific Reports. 5(1). 11649–11649. 26 indexed citations
7.
Mayr, B, Dirk Schnabel, Helmuth‐Günther Dörr, & Christof Schöfl. (2015). GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment concepts. European Journal of Endocrinology. 174(5). R189–R208. 44 indexed citations
8.
Nennstiel, Uta, et al.. (2015). Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life. European Journal of Endocrinology. 174(2). 177–186. 44 indexed citations
9.
Trautmann, Udo, Arif B. Ekici, André Reis, et al.. (2011). Familial short stature due to a 5q22.1–q23.2 duplication refines the 5q duplication spectrum. European Journal of Medical Genetics. 54(5). e521–e524. 4 indexed citations
10.
Haag, Christine, Helmuth‐Günther Dörr, Dirk Schnabel, et al.. (2010). Novel Activating Mutations of the Calcium-Sensing Receptor: The Calcilytic NPS-2143 Mitigates Excessive Signal Transduction of Mutant Receptors. The Journal of Clinical Endocrinology & Metabolism. 95(10). E229–E233. 44 indexed citations
11.
Grünewald, Thomas G. P., Irene von Luettichau, Ulrich Welsch, et al.. (2010). First report of ectopic ACTH syndrome and PTHrP-induced hypercalcemia due to a hepatoblastoma in a child. European Journal of Endocrinology. 162(4). 813–818. 15 indexed citations
12.
Langer, Thor s ten, et al.. (2010). Erkennen, Vermeiden und Behandeln von Spätfolgen. Pädiatrie. 22(6). 428–433. 1 indexed citations
13.
Thiel, Christian T., Helmuth‐Günther Dörr, Udo Trautmann, et al.. (2008). A de novo 7.6 Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay. European Journal of Medical Genetics. 51(4). 362–367. 15 indexed citations
14.
Thiel, Christian T., Birgit Knebel, Ina Knerr, et al.. (2008). Two novel mutations in the insulin binding subunit of the insulin receptor gene without insulin binding impairment in a patient with Rabson–Mendenhall syndrome. Molecular Genetics and Metabolism. 94(3). 356–362. 22 indexed citations
15.
Arenz, S., Uta Nennstiel, Manfred Wildner, Helmuth‐Günther Dörr, & Rüdiger von Kries. (2008). Intellectual outcome, motor skills and BMI of children with congenital hypothyroidism: a population‐based study. Acta Paediatrica. 97(4). 447–450. 15 indexed citations
16.
Schroth, Michael, Christian Plank, Manfred Rauh, et al.. (2006). Pediatric renal allograft transplantation does not normalize the increased cortisol/cortisone ratios of chronic renal failure. European Journal of Endocrinology. 154(4). 555–561. 8 indexed citations
17.
Krone, Nils, Felix G. Riepe, Helmuth‐Günther Dörr, et al.. (2005). Thirteen novel mutations in theNR0B1(DAX1) gene as cause of adrenal hypoplasia congenita. Human Mutation. 25(5). 502–502. 16 indexed citations
18.
Gröschl, Michael, Manfred Rauh, & Helmuth‐Günther Dörr. (2003). Circadian Rhythm of Salivary Cortisol, 17α-Hydroxyprogesterone, and Progesterone in Healthy Children. Clinical Chemistry. 49(10). 1688–1691. 114 indexed citations
19.
Koch, A., Michael Hofbeck, G. Buheitel, et al.. (2002). Hypoparathyroidism in conotruncal heart defects. European Journal of Pediatrics. 161(4). 208–211. 3 indexed citations
20.
Beck, Jörn‐Dirk, Kurt Winkler, D. Niethammer, et al.. (1995). Die Nachsorge der von einer Krebserkrankung geheilten Kinder und jungen Erwachsenen. Erste Empfehlungen der Arbeitsgemeinschaft Spätfolgen. Klinische Pädiatrie. 207(4). 186–192. 17 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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