Adrian Wiestner

1.8k total citations · 1 hit paper
12 papers, 1.5k citations indexed

About

Adrian Wiestner is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Adrian Wiestner has authored 12 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 8 papers in Hematology and 6 papers in Molecular Biology. Recurrent topics in Adrian Wiestner's work include Platelet Disorders and Treatments (8 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (6 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers). Adrian Wiestner is often cited by papers focused on Platelet Disorders and Treatments (8 papers), Myeloproliferative Neoplasms: Diagnosis and Treatment (6 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers). Adrian Wiestner collaborates with scholars based in Switzerland, United Kingdom and Japan. Adrian Wiestner's co-authors include Radek C. Skoda, Nico Ghilardi, Markus H. Heim, Suzanne Ziegler, A. P. C. van der Maas, Ronald J. Schlemper, Akimichi Ohsaka, Masahiro Kikuchi, Claire Harrison and Rosemary E. Gale and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Adrian Wiestner

12 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Defective STAT signaling by the leptin receptor in diabetic mice.

1996 698 citations Nico Ghilardi, Suzanne Ziegler et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Adrian Wiestner Switzerland	10	580	539	425	395	368	12	1.5k
M C Postel-Vinay France	23	242 0.4×	53 0.1×	59 0.1×	153 0.4×	434 1.2×	40	1.5k
Ioanna Mosialou United States	12	76 0.1×	309 0.6×	136 0.3×	66 0.2×	552 1.5×	17	1.3k
Sara Bonissoni Italy	13	514 0.9×	73 0.1×	36 0.1×	327 0.8×	291 0.8×	17	1.3k
Maria Gueorguiev United Kingdom	22	415 0.7×	14 0.0×	129 0.3×	258 0.7×	295 0.8×	33	1.4k
Michael Hansen Denmark	8	31 0.1×	182 0.3×	178 0.4×	127 0.3×	189 0.5×	9	608
Ilya A. Vinnikov China	12	42 0.1×	184 0.3×	73 0.2×	38 0.1×	414 1.1×	20	986
Margaret Prechel United States	21	88 0.2×	221 0.4×	45 0.1×	26 0.1×	176 0.5×	58	1.4k
Moriko Ito United States	15	55 0.1×	49 0.1×	91 0.2×	25 0.1×	667 1.8×	16	1.2k
María‐Josefa Morán‐Jiménez Spain	11	51 0.1×	319 0.6×	241 0.6×	200 0.5×	224 0.6×	38	683

Countries citing papers authored by Adrian Wiestner

Since Specialization

Citations

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

Fields of papers citing papers by Adrian Wiestner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adrian Wiestner

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

All Works

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12 of 12 papers shown

1.

Tiedt, Ralph, Jörn Coers, Sandra Ziegler, et al.. (2008). Pronounced thrombocytosis in transgenic mice expressing reduced levels of Mpl in platelets and terminally differentiated megakaryocytes. Blood. 113(8). 1768–1777. 44 indexed citations

2.

Wiestner, Adrian, Stephan A. Padosch, Nico Ghilardi, et al.. (2000). Hereditary thrombocythaemia is a genetically heterogeneous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia. British Journal of Haematology. 110(1). 104–109. 29 indexed citations

3.

Ghilardi, Nico, Adrian Wiestner, Masahiro Kikuchi, Akimichi Ohsaka, & Radek C. Skoda. (1999). Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene. British Journal of Haematology. 107(2). 310–316. 97 indexed citations

4.

Smith, Monica, M. Lusher, Majlinda Lako, et al.. (1999). Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes. Human Genetics. 105(1-2). 104–111. 19 indexed citations

5.

Smith, Monica, M. Lusher, Majlinda Lako, et al.. (1999). Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes. Human Genetics. 105(1-2). 104–111. 7 indexed citations

6.

Wiestner, Adrian, Ronald J. Schlemper, A. P. C. van der Maas, & Radek C. Skoda. (1998). An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia. Nature Genetics. 18(1). 49–52. 227 indexed citations

7.

Harrison, Claire, Rosemary E. Gale, Adrian Wiestner, Radek C. Skoda, & David C. Linch. (1998). The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non-familial essential thrombocythaemia. British Journal of Haematology. 102(5). 0–0. 2 indexed citations

8.

Ghilardi, Nico, Adrian Wiestner, & Radek C. Skoda. (1998). Thrombopoietin Production Is Inhibited by a Translational Mechanism. Blood. 92(11). 4023–4030. 11 indexed citations

9.

Ghilardi, Nico, Adrian Wiestner, & Radek C. Skoda. (1998). Thrombopoietin Production Is Inhibited by a Translational Mechanism. Blood. 92(11). 4023–4030. 59 indexed citations

10.

Harrison, Claire, Rosemary E. Gale, Adrian Wiestner, Radek C. Skoda, & David C. Linch. (1998). The activating splice mutation in intron 3 of the thrombopoietin gene is not found in patients with non‐familial essential thrombocythaemia. British Journal of Haematology. 102(5). 1341–1343. 37 indexed citations

11.

Ghilardi, Nico, et al.. (1996). Defective STAT signaling by the leptin receptor in diabetic mice.. Proceedings of the National Academy of Sciences. 93(13). 6231–6235. 698 indexed citations breakdown →

12.

Wiestner, Adrian, et al.. (1996). Thrombopoietin in thrombocytopenic mice: evidence against regulation at the mRNA level and for a direct regulatory role of platelets. Blood. 87(2). 567–573. 224 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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