Erwin Lankes

521 total citations
20 papers, 342 citations indexed

About

Erwin Lankes is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Epidemiology. According to data from OpenAlex, Erwin Lankes has authored 20 papers receiving a total of 342 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Epidemiology. Recurrent topics in Erwin Lankes's work include Neuroblastoma Research and Treatments (3 papers), Meningioma and schwannoma management (3 papers) and Thyroid Disorders and Treatments (3 papers). Erwin Lankes is often cited by papers focused on Neuroblastoma Research and Treatments (3 papers), Meningioma and schwannoma management (3 papers) and Thyroid Disorders and Treatments (3 papers). Erwin Lankes collaborates with scholars based in Germany, United States and Australia. Erwin Lankes's co-authors include Dirk Schnabel, M. Burdelski, Peter Freisinger, Bernhard Setzer, Klaus Gempel, René Santer, Ulrich A. Walker, Rita Horváth, Thomas M. Berger and Johannes Spalinger and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and European Journal of Endocrinology.

In The Last Decade

Erwin Lankes

18 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erwin Lankes Germany 11 158 74 72 65 49 20 342
Pamela Ghosh India 9 69 0.4× 54 0.7× 29 0.4× 42 0.6× 61 1.2× 13 325
Sahar Keshvari Australia 11 96 0.6× 33 0.4× 17 0.2× 35 0.5× 21 0.4× 28 344
Xiongze Zhang China 18 175 1.1× 25 0.3× 53 0.7× 17 0.3× 23 0.5× 77 1.0k
Stephen W. Anderson United States 10 96 0.6× 179 2.4× 20 0.3× 127 2.0× 117 2.4× 12 405
Esther Vamos Belgium 15 286 1.8× 179 2.4× 54 0.8× 17 0.3× 28 0.6× 21 533
Linda M. Randolph United States 13 176 1.1× 162 2.2× 156 2.2× 10 0.2× 63 1.3× 31 552
Frances Wu United States 9 252 1.6× 70 0.9× 18 0.3× 11 0.2× 28 0.6× 33 622
Nihal Demircan Türkiye 12 140 0.9× 39 0.5× 62 0.9× 19 0.3× 45 0.9× 30 622
Jiasun Su China 13 221 1.4× 202 2.7× 19 0.3× 211 3.2× 36 0.7× 38 477
Sara Bertok Slovenia 10 166 1.1× 122 1.6× 42 0.6× 27 0.4× 25 0.5× 35 354

Countries citing papers authored by Erwin Lankes

Since Specialization
Citations

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

Fields of papers citing papers by Erwin Lankes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erwin Lankes

This figure shows the co-authorship network connecting the top 25 collaborators of Erwin Lankes. A scholar is included among the top collaborators of Erwin Lankes 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 Erwin Lankes. Erwin Lankes 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.
Kühnen, Peter, K Rothe, Kathrin Hauptmann, et al.. (2025). [68Ga] labelled Exendin for radioguided surgery of intrapancreatic insulin producing lesions in patients with congenital hyperinsulinism. EJNMMI Research. 15(1). 107–107.
2.
Schaumann, Andreas, Matthias Schulz, Arne Grün, et al.. (2023). Neurosurgical treatment of pediatric brain tumors - results from a single center multidisciplinary setup. Child s Nervous System. 40(2). 381–393. 3 indexed citations
3.
Thee, Stephanie, V. Wahn, Nadine Unterwalder, et al.. (2023). Screening Newborns for Low T Cell Receptor Excision Circles (TRECs) Fails to Detect Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome. The Journal of Allergy and Clinical Immunology In Practice. 11(9). 2872–2883. 3 indexed citations
4.
Lodrini, Marco, Annika Sprüssel, Annette Künkele, et al.. (2022). Circulating Cell-Free DNA Assessment in Biofluids from Children with Neuroblastoma Demonstrates Feasibility and Potential for Minimally Invasive Molecular Diagnostics. Cancers. 14(9). 2080–2080. 16 indexed citations
5.
Meisel, Christian, Tim Meyer, Erwin Lankes, et al.. (2021). Mild COVID-19 despite autoantibodies against type I IFNs in autoimmune polyendocrine syndrome type 1. Journal of Clinical Investigation. 131(14). 55 indexed citations
6.
Tietze, Anna, et al.. (2021). First experience with augmented reality neuronavigation in endoscopic assisted midline skull base pathologies in children. Child s Nervous System. 37(5). 1525–1534. 18 indexed citations
7.
Becker, Marianne, Oliver Blankenstein, Erwin Lankes, Dirk Schnabel, & Heiko Krude. (2021). Severe Acquired Primary Hypothyroidism in Children and its Influence on Growth: A Retrospective Analysis of 43 Cases. Experimental and Clinical Endocrinology & Diabetes. 130(4). 217–222. 6 indexed citations
8.
Rohayem, Julia, Michael Zitzmann, Susanne Fricke‐Otto, et al.. (2021). Semen quality and testicular adrenal rest tumour development in 46,XY congenital adrenal hyperplasia: the importance of optimal hormonal replacement. European Journal of Endocrinology. 184(4). 487–501. 11 indexed citations
9.
Vetter, Céline, Till Roenneberg, Helene Werner, et al.. (2019). Sleep Timing in Patients with Precocious and Delayed Pubertal Development. Clocks & Sleep. 1(1). 140–150. 12 indexed citations
10.
Lankes, Erwin, Peter Kühnen, Dirk Schnabel, et al.. (2018). Mean High-Dose l-Thyroxine Treatment Is Efficient and Safe to Achieve a Normal IQ in Young Adult Patients With Congenital Hypothyroidism. The Journal of Clinical Endocrinology & Metabolism. 103(4). 1459–1469. 36 indexed citations
11.
Lankes, Erwin, Peter Kühnen, Dirk Schnabel, et al.. (2018). Mean high-dose L-thyroxine treatment is efficient and safe to achieve a normal IQ in young adult patients with congenital hypothyroidism. Yearbook of pediatric endocrinology.
12.
Grüters‐Kieslich, Annette, Amita Sharma, Erwin Lankes, et al.. (2018). Early-onset obesity: unrecognized first evidence for GNAS mutations and methylation changes. Yearbook of pediatric endocrinology. 2 indexed citations
13.
Grüters‐Kieslich, Annette, Monica Reyes, Amita Sharma, et al.. (2017). Early-Onset Obesity: Unrecognized First Evidence for GNAS Mutations and Methylation Changes. The Journal of Clinical Endocrinology & Metabolism. 102(8). 2670–2677. 21 indexed citations
14.
Quinkler, Marcus, U. Bogner, Ulf Elbelt, et al.. (2016). Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotype. European Journal of Endocrinology. 175(5). 421–431. 24 indexed citations
15.
Ottenhausen, Malte, Petra Bittigau, Arend Koch, et al.. (2015). Hamartoma of the optic nerve in a young child—case report and review of the literature. Child s Nervous System. 31(8). 1401–1406. 3 indexed citations
16.
Schnabel, Dirk, et al.. (2014). Severe but not neonatally lethal. A homozygous inactivating CaSR mutation in a 3 year old child. Experimental and Clinical Endocrinology & Diabetes. 122(3). 7 indexed citations
17.
Klopocki, Eva, Luitgard Graul‐Neumann, Sabine Uhrig, et al.. (2013). Novel mutations of the PRKAR1A gene in patients with acrodysostosis. Clinical Genetics. 84(6). 531–538. 21 indexed citations
18.
Lankes, Erwin, et al.. (2011). Unimpaired postnatal respiratory adaptation in a preterm human infant with a homozygous ENaC-α unit loss-of-function mutation. Journal of Perinatology. 31(12). 802–803. 11 indexed citations
19.
Freisinger, Peter, Erwin Lankes, Klaus Gempel, et al.. (2006). Hepatocerebral Mitochondrial DNA Depletion Syndrome Caused by Deoxyguanosine Kinase (DGUOK) Mutations. Archives of Neurology. 63(8). 1129–1129. 89 indexed citations
20.
Eichinger, Walter, N. Mendler, Erwin Lankes, et al.. (2002). In-vivo bacterial adherence to intracardiac prosthetic materials: a new experimental model.. PubMed. 11(3). 438–46. 4 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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