Alexander von Werder

1.5k total citations
33 papers, 1.1k citations indexed

About

Alexander von Werder is a scholar working on Oncology, Epidemiology and Molecular Biology. According to data from OpenAlex, Alexander von Werder has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Oncology, 9 papers in Epidemiology and 8 papers in Molecular Biology. Recurrent topics in Alexander von Werder's work include Neuroendocrine Tumor Research Advances (7 papers), Pituitary Gland Disorders and Treatments (6 papers) and Cancer Research and Treatments (5 papers). Alexander von Werder is often cited by papers focused on Neuroendocrine Tumor Research Advances (7 papers), Pituitary Gland Disorders and Treatments (6 papers) and Cancer Research and Treatments (5 papers). Alexander von Werder collaborates with scholars based in Germany, United States and Japan. Alexander von Werder's co-authors include Roland M. Schmid, Günter Schneider, Dieter Saur, Barbara Seidler, Oliver G. Opitz, Marlena Messer, Stefan Eser, Philipp Pagel, Hiroshi Nakagawa and Johannes von Burstin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gastroenterology and Oncogene.

In The Last Decade

Alexander von Werder

31 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexander von Werder Germany	14	540	364	178	171	143	33	1.1k
Silvia Giunco Italy	17	332 0.6×	307 0.8×	111 0.6×	113 0.7×	88 0.6×	37	880
María Dirlei Begnami Brazil	19	390 0.7×	323 0.9×	172 1.0×	158 0.9×	47 0.3×	51	961
Miranda Buitenhuis Netherlands	19	506 0.9×	431 1.2×	77 0.4×	143 0.8×	125 0.9×	30	1.3k
Shu Sun Denmark	17	324 0.6×	176 0.5×	140 0.8×	171 1.0×	233 1.6×	45	1.2k
Koichiro Minami Japan	19	396 0.7×	153 0.4×	221 1.2×	287 1.7×	59 0.4×	46	980
Elvis Terci Valera Brazil	18	725 1.3×	275 0.8×	141 0.8×	186 1.1×	69 0.5×	108	1.4k
Toshifumi Fujiwara Japan	19	522 1.0×	293 0.8×	139 0.8×	239 1.4×	116 0.8×	74	1.2k
Stephen J. Elliman Ireland	14	416 0.8×	364 1.0×	225 1.3×	129 0.8×	32 0.2×	26	1.1k
Matthias Herrmann Germany	9	464 0.9×	184 0.5×	116 0.7×	135 0.8×	96 0.7×	20	1.0k

Countries citing papers authored by Alexander von Werder

Since Specialization

Citations

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

Fields of papers citing papers by Alexander von Werder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander von Werder. 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 Alexander von Werder. The network helps show where Alexander von Werder may publish in the future.

Co-authorship network of co-authors of Alexander von Werder

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

All Works

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20 of 20 papers shown

Kasajima, Atsuko, Nicole Pfarr, Alexander von Werder, et al.. (2024). Rapid Evolution of Metastases in Patients with Treated G3 Neuroendocrine Tumors Associated with NEC-Like Transformation and TP53 Mutation. Endocrine Pathology. 35(4). 313–324. 14 indexed citations

Steiger, Katja, Carolin Mogler, Bruno Märkl, et al.. (2024). ARX, PDX1, ISL1, and CDX2 Expression Distinguishes 5 Subgroups of Pancreatic Neuroendocrine Tumors With Correlations to Histology, Hormone Expression, and Outcome. Modern Pathology. 37(11). 100595–100595. 10 indexed citations

Agaimy, Abbas, Atsuko Kasajima, Robert Stoehr, et al.. (2023). Gene fusions are frequent in ACTH-secreting neuroendocrine neoplasms of the pancreas, but not in their non-pancreatic counterparts. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 482(3). 507–516. 13 indexed citations

Kasajima, Atsuko, Nicole Pfarr, Alexander von Werder, et al.. (2023). Renal neuroendocrine tumors: clinical and molecular pathology with an emphasis on frequent association with ectopic Cushing syndrome. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 483(4). 465–476. 8 indexed citations

Lange, Nicole, A. Podtschaske, Jan Martin, et al.. (2022). Anterior Pituitary Hormones in Blood and Cerebrospinal Fluid of Patients in Neurocritical Care. PubMed. 18(1). 71–71. 1 indexed citations

Butenschöen, Vicki M., et al.. (2021). Transsphenoidal pituitary adenoma resection: do early post-operative cortisol levels predict permanent long-term hypocortisolism?. Neurosurgical Review. 45(2). 1353–1362. 7 indexed citations

Kessler, Lukas, Anna Melissa Schlitter, Martin Krönke, et al.. (2020). First Experience Using ¹⁸F-Flubrobenguane PET Imaging in Patients with Suspected Pheochromocytoma or Paraganglioma. Journal of Nuclear Medicine. 62(4). 479–485. 5 indexed citations

Butenschöen, Vicki M., et al.. (2020). Visual acuity and its postoperative outcome after transsphenoidal adenoma resection. Neurosurgical Review. 44(4). 2245–2251. 12 indexed citations

Bette, Stefanie, Benedikt Wiestler, Alexander von Werder, et al.. (2018). MRI criteria of subtypes of adenomas and epithelial cysts of the pituitary gland. Neurosurgical Review. 43(1). 265–272. 6 indexed citations

10.

Queisser, Angela, et al.. (2013). Inhibition of telomerase induces alternative lengthening of telomeres during human esophageal carcinogenesis. Cancer Genetics. 206(11). 374–386. 28 indexed citations

11.

Schlag, Christoph, Knut Brockow, Bernhard Haller, et al.. (2013). Serum Eosinophil Cationic Protein is Superior to Mast Cell Tryptase as Marker for Response to Topical Corticosteroid Therapy in Eosinophilic Esophagitis. Journal of Clinical Gastroenterology. 48(7). 600–606. 19 indexed citations

12.

Werder, Alexander von, Barbara Seidler, Roland M. Schmid, Günter Schneider, & Dieter Saur. (2012). Production of avian retroviruses and tissue-specific somatic retroviral gene transfer in vivo using the RCAS/TVA system. Nature Protocols. 7(6). 1167–1183. 39 indexed citations

13.

Eser, Stefan, Marlena Messer, Philipp Eser, et al.. (2011). In vivo diagnosis of murine pancreatic intraepithelial neoplasia and early-stage pancreatic cancer by molecular imaging. Proceedings of the National Academy of Sciences. 108(24). 9945–9950. 67 indexed citations

14.

Werder, Alexander von, Martina Mayr, Günter Schneider, et al.. (2011). Truncated IRAG variants modulate cGMP-mediated inhibition of human colonic smooth muscle cell contraction. American Journal of Physiology-Cell Physiology. 301(6). C1445–C1457. 6 indexed citations

15.

Lahmer, Tobias, Matthias Treiber, Alexander von Werder, et al.. (2010). Relapsing polychondritis: An autoimmune disease with many faces. Autoimmunity Reviews. 9(8). 540–546. 107 indexed citations

16.

Heeg, Steffen, Angela Queisser, Hannah Schmieg, et al.. (2010). EGFR overexpression induces activation of telomerase via PI3K/AKT‐mediated phosphorylation and transcriptional regulation through Hif1‐alpha in a cellular model of oral–esophageal carcinogenesis. Cancer Science. 102(2). 351–360. 40 indexed citations

17.

Burstin, Johannes von, Stefan Eser, Mariel C. Paul, et al.. (2009). E-Cadherin Regulates Metastasis of Pancreatic Cancer In Vivo and Is Suppressed by a SNAIL/HDAC1/HDAC2 Repressor Complex. Gastroenterology. 137(1). 361–371.e5. 287 indexed citations

18.

Mayr, Ulrich, Alexander von Werder, Barbara Seidler, et al.. (2008). RCAS-Mediated Retroviral Gene Delivery: A Versatile Tool for the Study of Gene Function in a Mouse Model of Pancreatic Cancer. Human Gene Therapy. 19(9). 896–906. 7 indexed citations

19.

Quante, Michael, William C. Hahn, Hideki Harada, et al.. (2005). Creating oral squamous cancer cells: A cellular model of oral–esophageal carcinogenesis. Proceedings of the National Academy of Sciences. 102(43). 15599–15604. 43 indexed citations

20.

Quante, Michael, Steffen Heeg, Alexander von Werder, et al.. (2005). Differential transcriptional regulation of human telomerase in a cellular model representing important genetic alterations in esophageal squamous carcinogenesis. Carcinogenesis. 26(11). 1879–1889. 14 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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