Wenke Seifert

1.5k total citations
16 papers, 716 citations indexed

About

Wenke Seifert is a scholar working on Genetics, Immunology and Cell Biology. According to data from OpenAlex, Wenke Seifert has authored 16 papers receiving a total of 716 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 6 papers in Immunology and 4 papers in Cell Biology. Recurrent topics in Wenke Seifert's work include Blood disorders and treatments (6 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Cellular transport and secretion (4 papers). Wenke Seifert is often cited by papers focused on Blood disorders and treatments (6 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Cellular transport and secretion (4 papers). Wenke Seifert collaborates with scholars based in Germany, Netherlands and Poland. Wenke Seifert's co-authors include Hans Christian Hennies, Denise Horn, Jirko Kühnisch, Volker Haucke, Tanja Maritzen, Andrea Maul‐Pavicic, Julia Strauß, Gillian M. Griffiths, Karin Beutel and Gudrun Nürnberg and has published in prestigious journals such as Journal of Biological Chemistry, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Wenke Seifert

15 papers receiving 703 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wenke Seifert Germany 11 313 256 254 184 121 16 716
Valentina Cetica Italy 20 384 1.2× 137 0.5× 427 1.7× 217 1.2× 247 2.0× 33 917
Andrew R. Cullinane United States 16 157 0.5× 401 1.6× 97 0.4× 390 2.1× 17 0.1× 20 824
Stuart Ellison United Kingdom 14 112 0.4× 109 0.4× 116 0.5× 250 1.4× 21 0.2× 27 552
Pierangela Castorina Italy 19 115 0.4× 185 0.7× 70 0.3× 494 2.7× 33 0.3× 35 894
Lidia Karabon Poland 22 646 2.1× 216 0.8× 170 0.7× 198 1.1× 27 0.2× 68 1.2k
H. Link Germany 17 373 1.2× 56 0.2× 146 0.6× 118 0.6× 72 0.6× 41 862
Jonathan J. Waters United Kingdom 17 111 0.4× 439 1.7× 127 0.5× 362 2.0× 88 0.7× 32 1.0k
Damián Heine‐Suñer Spain 18 153 0.5× 311 1.2× 89 0.4× 447 2.4× 13 0.1× 50 879
Rachel Dickinson United Kingdom 11 191 0.6× 107 0.4× 88 0.3× 236 1.3× 26 0.2× 16 622
Myrna Medlej‐Hashim Lebanon 16 432 1.4× 59 0.2× 76 0.3× 693 3.8× 25 0.2× 32 924

Countries citing papers authored by Wenke Seifert

Since Specialization
Citations

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

Fields of papers citing papers by Wenke Seifert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wenke Seifert

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

All Works

16 of 16 papers shown
1.
Schottmann, Gudrun, Jürgen Kohlhase, Nastassja Himmelreich, et al.. (2024). Impact of genetic test interpretation on a VPS13B missense variant in Cohen syndrome. Frontiers in Neuroscience. 18. 1488133–1488133.
2.
Kühnisch, Jirko, et al.. (2022). Disease relevance of rare VPS13B missense variants for neurodevelopmental Cohen syndrome. Scientific Reports. 12(1). 9686–9686. 13 indexed citations
3.
Torğutalp, Murat, et al.. (2019). Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Idiopathic Arthritis: A Novel <b><i>SLCO2A1</i></b> Mutation and Imaging Findings. Cytogenetic and Genome Research. 158(3). 126–132. 2 indexed citations
4.
Seifert, Wenke, York Posor, Peter Schu, et al.. (2016). The progressive ankylosis protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface. Human Molecular Genetics. 25(17). 3836–3848. 10 indexed citations
5.
Seifert, Wenke, Vera Jankowski, Ralf Mrowka, et al.. (2014). Annexin A2 Mediates Apical Trafficking of Renal Na+-K+-2Cl− Cotransporter. Journal of Biological Chemistry. 289(14). 9983–9997. 22 indexed citations
6.
Seifert, Wenke, Peter Meinecke, Gabriele Krüger, et al.. (2014). Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome. BMC Medical Genetics. 15(1). 127–127. 23 indexed citations
7.
Seifert, Wenke, Peter Meinecke, Gabriele Krüger, et al.. (2014). Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome. BMC Medical Genetics. 15(1). 127–127. 1 indexed citations
8.
Seifert, Wenke, Jirko Kühnisch, Tanja Maritzen, et al.. (2014). Cohen Syndrome-associated Protein COH1 Physically and Functionally Interacts with the Small GTPase RAB6 at the Golgi Complex and Directs Neurite Outgrowth. Journal of Biological Chemistry. 290(6). 3349–3358. 71 indexed citations
9.
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
10.
11.
Seifert, Wenke, Jirko Kühnisch, Tanja Maritzen, et al.. (2011). Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity. Journal of Biological Chemistry. 286(43). 37665–37675. 101 indexed citations
12.
Seifert, Wenke, Katrin Hoffmann, Tom H. Lindner, et al.. (2009). HPGD mutations cause cranioosteoarthropathy but not autosomal dominant digital clubbing. European Journal of Human Genetics. 17(12). 1570–1576. 22 indexed citations
13.
Stadt, Udo zur, Jan Rohr, Wenke Seifert, et al.. (2009). Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11. The American Journal of Human Genetics. 85(4). 482–492. 284 indexed citations
14.
Kornak, Uwe, Hans Christian Hennies, Johannes Egerer, et al.. (2009). Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a novel RAB-6 interacting golgin. Bone. 44. S232–S232. 1 indexed citations
15.
Seifert, Wenke, Muriel Holder‐Espinasse, Jirko Kühnisch, et al.. (2008). Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants ofCOH1. Human Mutation. 30(2). E404–E420. 38 indexed citations
16.
Hennies, Hans Christian, Anita Rauch, Wenke Seifert, et al.. (2004). Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome. The American Journal of Human Genetics. 75(1). 138–145. 55 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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