Martin Zenker

19.2k citations

227 papers · 6.3k indexed · 2 hit papers · h-index 40

Molecular Biology top 1%
Genetics top 0.5%
Immunology top 2%
Oncology top 2%
Surgery top 5%

Co-authors: Anita Rauch Marco Tartaglia Bruce D. Gelb André Reis Christian P. Kratz Charlotte M. Niemeyer Denny Schanze Christian T. Thiel
Topics: Protein Tyrosine Phosphatases (69 papers)Galectins and Cancer Biology (51 papers)Peptidase Inhibition and Analysis (30 papers)
Cited by: Genetics Immunology Molecular Biology
Journals: Journal of Clinical Investigation Nature Medicine Nature Communications
Partner nations: Germany United States United Kingdom

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, Kevin Shannon et al. profile →
Identifying facial phenotypes of genetic disorders using deep learning

2018 411 citations Martin Zenker et al. profile →

Peers

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

#	Work	Indexed citations
1	Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study 2024 ·Scientific Reports ·(unknown),(unknown),(unknown),Ramiro Vilchez‐Vargas,Albrecht Hoffmeister,Jürgen Feisthammel,(unknown),Denny Schanze,Martin Zenker,Ines Gockel,Alexander Link,Boris Jansen‐Winkeln	4
2	Cancer in Multilineage Mosaic RASopathies due to Pathogenic Variants in HRAS or KRAS : A Systematic Review and Meta-analysis 2024 ·Clinical Cancer Research ·(unknown),Gina M. Ney,Philip S. Rosenberg,Jung Kim,Martin Zenker,Douglas R. Stewart,Christian P. Kratz	1
3	Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood 2023 ·Nature Communications ·(unknown),(unknown),Holger Lingel,(unknown),(unknown),Denny Schanze,Martin Zenker,(unknown),Dunja Bruder,Robert Geffers,Thomas Hachenberg,Christoph Arens,Monika C. Brunner‐Weinzierl	11
4	Infantile epileptic spasms syndrome in children with cardiofaciocutanous syndrome: Clinical presentation and associations with genotype 2022 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Daniel Kenney‐Jung,(unknown),(unknown),(unknown),(unknown),Amy E. Roberts,Martin Zenker,Maria Luigia Gambardella,Ilaria Contaldo,Chiara Leoni,Roberta Onesimo,Giuseppe Zampino,Marco Tartaglia,Domenica Battaglia,Elizabeth I. Pierpont	4
5	Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome 2022 ·European Journal of Medical Genetics ·Luz Consuelo Zepeda‐Romero,Martin Zenker,Denny Schanze,Ina Schanze,(unknown),(unknown),(unknown),(unknown),(unknown),Lucina Bobadilla‐Morales,Alfredo Corona‐Rivera,Jorge Román Corona‐Rivera	4
6	Integration of genomic analysis and transcript expression of ABCC8 and KCNJ11 in focal form of congenital hyperinsulinism 2022 ·Frontiers in Endocrinology ·Ilse Wieland,Ina Schanze,(unknown),Winfried Barthlen,Silke Vogelgesang,Klaus Mohnike,Martin Zenker	6
7	MEK-Inhibition Treatment with Trametinib in a 7.7-Year-Old Girl with Noonan's Syndrome and Life-Threatening Lymphangiopathy 2021 ·The Thoracic and Cardiovascular Surgeon ·Michael Hofbeck,(unknown),G. Wiegand,Renate Kaulitz,Matthias Kumpf,Ludger Sieverding,Martin Zenker,Stephan Waldmüller,Grégor Andelfinger	2
8	Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformations 2021 ·American Journal of Medical Genetics Part A ·Vanessa F. Schmidt,Ilse Wieland,Walter A. Wohlgemuth,Jens Ricke,Moritz Wildgruber,Martin Zenker	11
9	KrasP34R and KrasT58I mutations induce distinct RASopathy phenotypes in mice 2020 ·JCI Insight ·Jasmine C. Wong,Pedro A. Pérez–Mancera,(unknown),(unknown),Joaquím Grego‐Bessa,(unknown),Scott C. Kogan,Amnon Sharir,(unknown),(unknown),Denny Schanze,Pau Castel,K. Hirose,Guo N. Huang,Martin Zenker,Dean Sheppard,Ophir D. Klein,David A. Tuveson,Benjamin S. Braun,Kevin Shannon	8
10	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 2020 ·Human Mutation ·Simone Martinelli,Luca Pannone,Christina Lißewski,Julia Brinkmann,Elisabetta Flex,Denny Schanze,Paolo Calligari,Massimiliano Anselmi,Francesca Pantaleoni,(unknown),Francesca Clementina Radio,Adonis S. Ioannides,Nils Rahner,Ina Schanze,Dragana Josifova,Gianfranco Bocchinfuso,Mina Ryten,Lorenzo Stella,Marco Tartaglia,Martin Zenker	1
11	QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum 2020 ·Clinical Genetics ·(unknown),Rami Abou Jamra,Arndt Borkhardt,Triantafyllia Brozou,Petra Muschke,Bernt Popp,(unknown),Jörg Schaper,Harald Surowy,Martin Zenker,Christiane Zweier,Dagmar Wieczorek,Silke Redler	6
12	MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome 2020 ·American Journal of Neuroradiology ·Kenneth W. Martin,K. Nicole Weaver,Khalid Alhasan,(unknown),Bonnie Sullivan,Martin Zenker,Friedhelm Hildebrandt,Julie D. Saba	21
13	Characteristic dental pattern with hypodontia and short roots in Fraser syndrome 2020 ·American Journal of Medical Genetics Part A ·Felix Kunz,Hülya Kayserili,Alina T. Midro,(unknown),(unknown),Yeliz Güven,Jan Borys,Denny Schanze,Angelika Stellzig‐Eisenhauer,Agnès Bloch‐Zupan,Martin Zenker	7
14	Genetic basis of hypertrophic cardiomyopathy in children 2018 ·Clinical Research in Cardiology ·Stefan Rupp,(unknown),Anne Schänzer,Dietmar Schranz,(unknown),Martin Zenker,(unknown),(unknown),Josef Thul,Christian Jux,Andreas Hahn	20
15	CTLA-4-mediated posttranslational modifications direct cytotoxic T-lymphocyte differentiation 2017 ·Cell Death and Differentiation ·Holger Lingel,Josef Wissing,(unknown),Denny Schanze,Stefan Lienenklaus,Frank Klawonn,Mandy Pierau,Martin Zenker,Lothar Jänsch,Monika C. Brunner‐Weinzierl	35
16	Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy 2017 ·PLoS Genetics ·(unknown),Santosh Pothula,(unknown),Saeideh Nakhaei‐Rad,Carolina Montenegro‐Venegas,(unknown),Claudia Marini,Mònica Santos,Denny Schanze,Dirk Montag,Mohammad Reza Ahmadian,Oliver Stork,Martin Zenker,Anna Fejtová	20
17	Surgery in Focal Congenital Hyperinsulinism (CHI) - The "Hyperinsulinism Germany International" Experience in 30 Children. 2016 ·PubMed ·Winfried Barthlen,(unknown),(unknown),Ilse Wieland,Martin Zenker,Wolfgang Mohnike,Silke Vogelgesang,Klaus Mohnike	16
18	Copy number variants including RAS pathway genes—How much RASopathy is in the phenotype? 2015 ·American Journal of Medical Genetics Part A ·Christina Lißewski,Sarina G. Kant,Zornitza Stark,Ina Schanze,Martin Zenker	12
19	Loss-of-function variants in HIVEP2 are a cause of intellectual disability 2015 ·European Journal of Human Genetics ·Siddharth Srivastava,Hartmut Engels,Ina Schanze,Kirsten Cremer,Thomas Wieland,Moritz Menzel,Max Schubach,Saskia Biskup,Martina Kreiß,Sabine Endele,Tim M. Strom,Dagmar Wieczorek,Martin Zenker,Siddharth Gupta,Julie S. Cohen,Alexander M. Zink,Sakkubai Naidu	31
20	Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair 2008 ·Genome Research ·Marijke Bauters,Hilde Van Esch,Michael J. Friez,Odile Boespflug‐Tanguy,Martin Zenker,Angela Maria Vianna‐Morgante,Carla Rosenberg,Jaakko Ignatius,Martine Raynaud,Karen Hollanders,Karen Govaerts,(unknown),Florence Niel,Pierre Blanc,Roger E. Stevenson,Jean‐Pierre Fryns,Peter Marynen,Charles E. Schwartz,Guy Froyen	92

About Martin Zenker

Martin Zenker is a scholar working on Immunology, Genetics and Nephrology, having authored 227 papers that have together received 6.3k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (69 papers), Galectins and Cancer Biology (51 papers) and Peptidase Inhibition and Analysis (30 papers). The work is most often cited by research in Genetics (1.9k citations), Immunology (1.3k citations) and Molecular Biology (4.0k citations). Martin Zenker has collaborated with scholars based in Germany, United States and United Kingdom. Frequent 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. Their work appears in journals such as Journal of Clinical Investigation, Nature Medicine and Nature Communications.

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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