Heinrich Schmidt

3.5k total citations
79 papers, 1.2k citations indexed

About

Heinrich Schmidt is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Heinrich Schmidt has authored 79 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 28 papers in Endocrinology, Diabetes and Metabolism and 23 papers in Genetics. Recurrent topics in Heinrich Schmidt's work include Sexual Differentiation and Disorders (21 papers), Hormonal and reproductive studies (11 papers) and Growth Hormone and Insulin-like Growth Factors (11 papers). Heinrich Schmidt is often cited by papers focused on Sexual Differentiation and Disorders (21 papers), Hormonal and reproductive studies (11 papers) and Growth Hormone and Insulin-like Growth Factors (11 papers). Heinrich Schmidt collaborates with scholars based in Germany, United Kingdom and United States. Heinrich Schmidt's co-authors include Walter Bonfig, Hans Peter Schwarz, Susanne Bechtold, Dietrich Knorr, Nicole Reisch, Philipp Pagel, Martin Bidlingmaier, Matthias K. Auer, Laurence Legeai‐Mallet and J. Weissenbach and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and Journal of Allergy and Clinical Immunology.

In The Last Decade

Heinrich Schmidt

73 papers receiving 1.2k citations

Peers

Heinrich Schmidt
E A Werder Switzerland
Christine Trivin France
C Bergadá Argentina
Luisa De Sanctis Italy
Emily L. Germain‐Lee United States
I. Christopher Lloyd United Kingdom
Laurie H. Seaver United States
Todor Arsov Australia
M Karp Israel
Muriel Houang France
E A Werder Switzerland
Heinrich Schmidt
Citations per year, relative to Heinrich Schmidt Heinrich Schmidt (= 1×) peers E A Werder

Countries citing papers authored by Heinrich Schmidt

Since Specialization
Citations

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

Fields of papers citing papers by Heinrich Schmidt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heinrich Schmidt

This figure shows the co-authorship network connecting the top 25 collaborators of Heinrich Schmidt. A scholar is included among the top collaborators of Heinrich Schmidt 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 Heinrich Schmidt. Heinrich Schmidt 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.
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Nowotny, H., Matthias K. Auer, Christian Lottspeich, et al.. (2021). Salivary Profiles of 11-oxygenated Androgens Follow a Diurnal Rhythm in Patients With Congenital Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 106(11). e4509–e4519. 17 indexed citations
3.
Auer, Matthias K., Lorenz C. Hofbauer, Martina Rauner, et al.. (2020). Effects of androgen excess and glucocorticoid exposure on bone health in adult patients with 21-hydroxylase deficiency. The Journal of Steroid Biochemistry and Molecular Biology. 204. 105734–105734. 22 indexed citations
4.
Dürr, H. R., et al.. (2020). Hypercalcaemia after treatment with denosumab in children: bisphosphonates as an option for therapy and prevention?. World Journal of Pediatrics. 16(5). 520–527. 23 indexed citations
5.
Niculescu, Liviu, Matias Wagner, Dominik S. Westphal, et al.. (2018). A Case of Ankyloblepharon-ectodermal Defects-cleft Lip/palate-syndrome with Choanal Atresia and Skin Erosions: Phenotypic Variability of TP63-related Disorders. Acta Dermato Venereologica. 99(1). 0–0. 1 indexed citations
6.
Dörr, Helmuth G., Markus Bettendorf, Gerhard Binder, et al.. (2015). Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial. Hormone Research in Paediatrics. 84(4). 266–274. 15 indexed citations
7.
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
8.
9.
Bechtold, Susanne, et al.. (2012). Effect of Antiandrogen Treatment on Bone Density and Bone Geometry in Adolescents with Polycystic Ovary Syndrome. Journal of Pediatric and Adolescent Gynecology. 25(3). 175–180. 9 indexed citations
10.
Schwarzer, A., et al.. (2010). Delayed Gastric Emptying in Patients with Prader Willi Syndrome. Journal of Pediatric Endocrinology and Metabolism. 23(9). 867–71. 17 indexed citations
11.
Schmidt, Heinrich, et al.. (2008). Intranasal insulin to improve developmental delay in children with 22q13 deletion syndrome: an exploratory clinical trial. Journal of Medical Genetics. 46(4). 217–222. 40 indexed citations
12.
Bonfig, Walter, Susanne Bechtold, Heinrich Schmidt, Dietrich Knorr, & Hans Peter Schwarz. (2007). Reduced Final Height Outcome in Congenital Adrenal Hyperplasia under Prednisone Treatment: Deceleration of Growth Velocity during Puberty. The Journal of Clinical Endocrinology & Metabolism. 92(5). 1635–1639. 111 indexed citations
13.
Novosel, Astrid, et al.. (2004). Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutation. European Journal of Pediatrics. 163(12). 701–703. 10 indexed citations
14.
Bechtold, Susanne, et al.. (2004). Musculoskeletal and functional muscle-bone analysis in children with rheumatic disease using peripheral quantitative computed tomography. Osteoporosis International. 16(7). 757–763. 29 indexed citations
15.
Rudolph, Günther, Thomas Bettecken, Peter Lichtner, et al.. (2003). Spondylo-ocular syndrome: a new entity with crystalline lens malformation, cataract, retinal detachment, osteoporosis, and platyspondyly. American Journal of Ophthalmology. 135(5). 681–687. 11 indexed citations
16.
Schmidt, Heinrich & Gerd Geißlinger. (2002). Pharmakologie der COX-2-Hemmer. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 45(9). 692–698. 1 indexed citations
17.
Heinz‐Erian, Peter, et al.. (1999). Congenital Microvillus Atrophy in a Girl with Autosomal Dominant Hypochondroplasia. Journal of Pediatric Gastroenterology and Nutrition. 28(2). 203–205. 11 indexed citations
18.
Schuffenhauer, Simone, Tina Buchholz, S. Stengel‐Rutkowski, et al.. (1996). A familial deletion in the Prader-Willi syndrome region including the imprinting control region. Human Mutation. 8(3). 288–292. 6 indexed citations
19.
Driever, Pablo Hernáiz, et al.. (1996). Congenital microgastria, growth hormone deficiency and diabetes insipidus. European Journal of Pediatrics. 156(1). 37–40. 7 indexed citations
20.
Schmidt, Heinrich, et al.. (1981). Aussagewert anamnestischer Angaben, klinischer und urodynamischer Untersuchungsbefunde für das postoperative Ergebnis einer Inkontinenzoperation. Archives of Gynecology and Obstetrics. 232(1-4). 700–702.

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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