Elisabeth Steichen

1.1k total citations
13 papers, 447 citations indexed

About

Elisabeth Steichen is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Elisabeth Steichen has authored 13 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Elisabeth Steichen's work include Diabetes Management and Research (3 papers), Diabetes and associated disorders (3 papers) and Metabolism and Genetic Disorders (2 papers). Elisabeth Steichen is often cited by papers focused on Diabetes Management and Research (3 papers), Diabetes and associated disorders (3 papers) and Metabolism and Genetic Disorders (2 papers). Elisabeth Steichen collaborates with scholars based in Austria, United Kingdom and France. Elisabeth Steichen's co-authors include Françoise Clerget‐Darpoux, Anne‐Louise Leutenegger, Annick Toutain, Audrey Labalme, Patrick Edery, Elisabeth B. Binder, Sabine E. Hofer, Joëlle Chastang, Francis Rousseau and Renaud Touraine and has published in prestigious journals such as Science, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Elisabeth Steichen

12 papers receiving 436 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisabeth Steichen Austria	9	255	197	100	86	41	13	447
Yu Ding China	12	219 0.9×	170 0.9×	35 0.3×	55 0.6×	19 0.5×	38	359
C Lecointre France	10	336 1.3×	203 1.0×	55 0.6×	155 1.8×	36 0.9×	15	506
Stanisław Zajączek Poland	10	198 0.8×	129 0.7×	30 0.3×	29 0.3×	38 0.9×	36	354
Alice Goldenberg France	9	382 1.5×	87 0.4×	68 0.7×	24 0.3×	38 0.9×	12	527
Eva Maria Cutiongco Philippines	7	168 0.7×	180 0.9×	52 0.5×	28 0.3×	36 0.9×	7	327
Takaya Tohma Japan	11	203 0.8×	175 0.9×	31 0.3×	30 0.3×	21 0.5×	19	354
Laurence Michel‐Calemard France	9	325 1.3×	295 1.5×	57 0.6×	49 0.6×	48 1.2×	22	438
Masamichi Ogawa Japan	14	194 0.8×	238 1.2×	35 0.3×	282 3.3×	37 0.9×	29	425
Gabriele Krüger Germany	10	163 0.6×	146 0.7×	68 0.7×	15 0.2×	41 1.0×	19	389
Stacey E. Wirt United States	8	225 0.9×	128 0.6×	177 1.8×	68 0.8×	10 0.2×	9	406

Countries citing papers authored by Elisabeth Steichen

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth Steichen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Steichen

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

All Works

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13 of 13 papers shown

Smith, Chris, Adam Jackson, Andreas Janecke, et al.. (2025). Adrenal insufficiency associated with mutations in haem biosynthesis genes. Endocrine Abstracts. 1 indexed citations

Steichen, Elisabeth, et al.. (2023). Pituitary Stalk Interruption Syndrome – Clinical Presentation and Management of a Potentially Life-threatening Disease in Newborns. Journal of Clinical Research in Pediatric Endocrinology. 17(1). 0–0.

Smith, Chris, Adam Jackson, Andreas Janecke, et al.. (2023). SAT292 Adrenal Insufficiency Associated With Biallelic Mutations In Porphyria Genes. Journal of the Endocrine Society. 7(Supplement_1). 1 indexed citations

Warncke, Katharina, Sebastian Kummer, Klemens Raile, et al.. (2018). Frequency and Characteristics of MODY 1 (HNF4A Mutation) and MODY 5 (HNF1B Mutation): Analysis From the DPV Database. The Journal of Clinical Endocrinology & Metabolism. 104(3). 845–855. 28 indexed citations

Binder, Elisabeth B., A. Mühlbacher, Michael Edlinger, et al.. (2016). Genotyping of coeliac-specific human leucocyte antigen in children with type 1 diabetes: does this screening method make sense?. Archives of Disease in Childhood. 102(7). 603–606. 15 indexed citations

Ralser, Elisabeth, Ursula Kiechl‐Kohlendorfer, Sabine Scholl‐Bürgi, et al.. (2015). ALG8-CDG: novel patients and review of the literature. Orphanet Journal of Rare Diseases. 10(1). 73–73. 34 indexed citations

Möser, Christine V., et al.. (2015). Needle detachment in a slim and physically active child with insulin pump treatment. Pediatric Diabetes. 17(5). 385–388. 7 indexed citations

Binder, Elisabeth B., O. Lange, Michael Edlinger, et al.. (2015). Frequency of Dermatological Side Effects of Continuous Subcutaneous Insulin Infusion in Children and Adolescents with Type 1 Diabetes. Experimental and Clinical Endocrinology & Diabetes. 123(4). 260–264. 42 indexed citations

Kshirsagar, Sudhir, Elisabeth B. Binder, Magdalena Riedl, et al.. (2013). Enhanced Activity of Akt in Teff Cells From Children With Lupus Nephritis Is Associated With Reduced Induction of Tumor Necrosis Factor Receptor–Associated Factor 6 and Increased OX40 Expression. Arthritis & Rheumatism. 65(11). 2996–3006. 16 indexed citations

10.

Edery, Patrick, Charles Marcaillou, Mourad Sahbatou, et al.. (2011). Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA. Science. 332(6026). 240–243. 159 indexed citations

11.

Schober, Edith, Thomas Waldhoer, Sarah E. Flanagan, et al.. (2009). Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes Register. Pediatric Diabetes. 11(1). 18–23. 43 indexed citations

12.

Leutenegger, Anne‐Louise, Audrey Labalme, Emmanuelle Génin, et al.. (2006). Using Genomic Inbreeding Coefficient Estimates for Homozygosity Mapping of Rare Recessive Traits: Application to Taybi-Linder Syndrome. The American Journal of Human Genetics. 79(1). 62–66. 35 indexed citations

13.

Hatada, I., Akira Nabetani, Hiroko Morisaki, et al.. (1997). New p57 KIP2 mutations in Beckwith-Wiedemann syndrome. Human Genetics. 100(5-6). 681–683. 66 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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