Martin Zenker

19.2k total citations · 2 hit papers
227 papers, 6.3k citations indexed

About

Martin Zenker is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Martin Zenker has authored 227 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 154 papers in Molecular Biology, 63 papers in Genetics and 61 papers in Immunology. Recurrent topics in Martin Zenker's work include Protein Tyrosine Phosphatases (69 papers), Galectins and Cancer Biology (51 papers) and Peptidase Inhibition and Analysis (30 papers). Martin Zenker is often cited by papers focused on Protein Tyrosine Phosphatases (69 papers), Galectins and Cancer Biology (51 papers) and Peptidase Inhibition and Analysis (30 papers). Martin Zenker collaborates with scholars based in Germany, United States and United Kingdom. Martin Zenker's co-authors include Anita Rauch, Marco Tartaglia, Bruce D. Gelb, André Reis, Christian P. Kratz, Charlotte M. Niemeyer, Denny Schanze, Christian T. Thiel, Karen W. Gripp and Udo Trautmann and has published in prestigious journals such as Journal of Clinical Investigation, Nature Medicine and Nature Communications.

In The Last Decade

Martin Zenker

222 papers receiving 6.2k 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.

Germline KRAS mutations cause Noonan syndrome

2006 514 citations Martin Zenker, Anita Rauch et al. profile →
Identifying facial phenotypes of genetic disorders using deep learning

2018 411 citations Martin Zenker, Karen W. Gripp et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martin Zenker Germany	40	4.0k	1.9k	1.3k	1.1k	534	227	6.3k
Michael A. Patton United Kingdom	36	4.1k 1.0×	1.3k 0.7×	1.5k 1.1×	597 0.6×	381 0.7×	82	6.0k
Karen W. Gripp United States	40	3.4k 0.8×	1.8k 1.0×	904 0.7×	442 0.4×	390 0.7×	140	5.0k
Michael A. Simpson United Kingdom	44	2.7k 0.7×	1.2k 0.6×	859 0.6×	587 0.5×	626 1.2×	161	6.3k
John F. Tisdale United States	49	3.6k 0.9×	2.4k 1.3×	1.6k 1.2×	1.6k 1.5×	589 1.1×	267	10.0k
André Mégarbané Lebanon	43	4.1k 1.0×	2.1k 1.1×	806 0.6×	325 0.3×	440 0.8×	276	7.0k
Gerald de Haan Netherlands	45	3.9k 1.0×	1.0k 0.5×	1.6k 1.2×	982 0.9×	417 0.8×	159	7.8k
Lidia Larizza Italy	43	3.7k 0.9×	2.3k 1.3×	577 0.4×	530 0.5×	397 0.7×	271	6.3k
Lynn R. Goldin United States	54	2.7k 0.7×	2.4k 1.3×	1.3k 1.0×	1.2k 1.1×	305 0.6×	192	8.6k
Giuseppe Zampino Italy	30	3.1k 0.8×	1.1k 0.6×	1.4k 1.0×	657 0.6×	399 0.7×	184	4.7k
Murim Choi South Korea	35	3.2k 0.8×	1.5k 0.8×	548 0.4×	438 0.4×	1.1k 2.1×	112	5.9k

Countries citing papers authored by Martin Zenker

Since Specialization

Citations

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

Fields of papers citing papers by Martin Zenker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Zenker

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Zenker. A scholar is included among the top collaborators of Martin Zenker 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 Martin Zenker. Martin Zenker 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

Vilchez‐Vargas, Ramiro, Albrecht Hoffmeister, Jürgen Feisthammel, et al.. (2024). Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study. Scientific Reports. 14(1). 15335–15335. 4 indexed citations

Schanze, Denny, et al.. (2023). Happle‐Tinschert syndrome variable phenotype as part of the mosaic hedgehog spectrum: Report of three cases. Pediatric Dermatology. 40(4). 691–694. 2 indexed citations

Lingel, Holger, Denny Schanze, Martin Zenker, et al.. (2023). Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood. Nature Communications. 14(1). 5943–5943. 11 indexed citations

Kenney‐Jung, Daniel, Amy E. Roberts, Martin Zenker, et al.. (2022). Infantile epileptic spasms syndrome in children with cardiofaciocutanous syndrome: Clinical presentation and associations with genotype. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 190(4). 501–509. 4 indexed citations

Elbracht, Miriam, Julia Carlens, Felix Zeppernick, et al.. (2021). Unusual phenotypes in patients with a pathogenic germline variant in DICER1. Familial Cancer. 22(4). 475–480. 6 indexed citations

Schmidt, Vanessa F., Ilse Wieland, Walter A. Wohlgemuth, et al.. (2021). Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformations. American Journal of Medical Genetics Part A. 185(10). 3122–3128. 11 indexed citations

Hofbeck, Michael, G. Wiegand, Renate Kaulitz, et al.. (2021). MEK-Inhibition Treatment with Trametinib in a 7.7-Year-Old Girl with Noonan's Syndrome and Life-Threatening Lymphangiopathy. The Thoracic and Cardiovascular Surgeon. 69. 2 indexed citations

Kunz, Felix, Hülya Kayserili, Alina T. Midro, et al.. (2020). Characteristic dental pattern with hypodontia and short roots in Fraser syndrome. American Journal of Medical Genetics Part A. 182(7). 1681–1689. 7 indexed citations

Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation. Human Mutation. 41(6). 1171–1182. 1 indexed citations

10.

Martin, Kenneth W., K. Nicole Weaver, Khalid Alhasan, et al.. (2020). MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome. American Journal of Neuroradiology. 41(10). 1943–1948. 21 indexed citations

11.

Wong, Jasmine C., Pedro A. Pérez–Mancera, Joaquím Grego‐Bessa, et al.. (2020). KrasP34R and KrasT58I mutations induce distinct RASopathy phenotypes in mice. JCI Insight. 5(21). 8 indexed citations

12.

Jamra, Rami Abou, Arndt Borkhardt, Triantafyllia Brozou, et al.. (2020). QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum. Clinical Genetics. 99(1). 199–207. 6 indexed citations

13.

Gelb, Bruce D., Hélène Cavé, Mitchell W. Dillon, et al.. (2018). ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation. Genetics in Medicine. 20(11). 1334–1345. 90 indexed citations

14.

Pothula, Santosh, Saeideh Nakhaei‐Rad, Carolina Montenegro‐Venegas, et al.. (2017). Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy. PLoS Genetics. 13(3). e1006684–e1006684. 20 indexed citations

15.

Lingel, Holger, Josef Wissing, Denny Schanze, et al.. (2017). CTLA-4-mediated posttranslational modifications direct cytotoxic T-lymphocyte differentiation. Cell Death and Differentiation. 24(10). 1739–1749. 35 indexed citations

16.

Ivanova, Daniela, Carolina Montenegro‐Venegas, Cornelia Schöne, et al.. (2015). Synaptic activity controls localization and function of Ct BP 1 via binding to B assoon and P iccolo. The EMBO Journal. 34(8). 1056–1077. 46 indexed citations

17.

Lißewski, Christina, Sarina G. Kant, Zornitza Stark, Ina Schanze, & Martin Zenker. (2015). Copy number variants including RAS pathway genes—How much RASopathy is in the phenotype?. American Journal of Medical Genetics Part A. 167(11). 2685–2690. 12 indexed citations

18.

Mainberger, F, Martin Zenker, Nikolai H. Jung, et al.. (2013). Impaired motor cortex plasticity in patients with Noonan syndrome. Clinical Neurophysiology. 124(12). 2439–2444. 8 indexed citations

19.

Sukalo, Maja, Marie-Claude Addor, Han G. Brunner, et al.. (2011). Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome. PLoS ONE. 6(9). e24925–e24925. 39 indexed citations

20.

Rauch, Anita, Juliane Hoyer, Sabine Guth, et al.. (2006). Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. American Journal of Medical Genetics Part A. 140A(19). 2063–2074. 288 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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