Adrian M. Stütz

58.8k total citations · 1 hit paper
44 papers, 3.3k citations indexed

About

Adrian M. Stütz is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Adrian M. Stütz has authored 44 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Plant Science. Recurrent topics in Adrian M. Stütz's work include Genomics and Phylogenetic Studies (10 papers), Chromosomal and Genetic Variations (9 papers) and Genomic variations and chromosomal abnormalities (6 papers). Adrian M. Stütz is often cited by papers focused on Genomics and Phylogenetic Studies (10 papers), Chromosomal and Genetic Variations (9 papers) and Genomic variations and chromosomal abnormalities (6 papers). Adrian M. Stütz collaborates with scholars based in Germany, United States and United Kingdom. Adrian M. Stütz's co-authors include Jan O. Korbel, Tobias Rausch, Thomas Zichner, Andreas Schlattl, Vladimı́r Beneš, Maximilian Woisetschläger, George Argyropoulos, Hugo Y. K. Lam, Nicolas Delhomme and Raeka S. Aiyar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Adrian M. Stütz

44 papers receiving 3.3k 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.

DELLY: structural variant discovery by integrated paired-end and split-read analysis

2012 1.3k citations Tobias Rausch, Thomas Zichner et al. profile →

Peers

Countries citing papers authored by Adrian M. Stütz

Since Specialization

Citations

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

Fields of papers citing papers by Adrian M. Stütz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adrian M. Stütz

This figure shows the co-authorship network connecting the top 25 collaborators of Adrian M. Stütz. A scholar is included among the top collaborators of Adrian M. Stütz 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 M. Stütz. Adrian M. Stütz 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	Quantification of Translocation-Specific ctDNA Provides an Integrating Parameter for Early Assessment of Treatment Response and Risk Stratification in Ewing Sarcoma 2021 ·Clinical Cancer Research ·Manuela Krumbholz, (unknown), Andreas Ranft, Jakob Zierk, Christian Schmidkonz, Adrian M. Stütz, (unknown), Eleni M. Tomazou, Abbas Agaimy, Tobias Bäuerle, Wolfgang Hartmann, Uta Dirksen, Markus Metzler	23
2	A scalable CRISPR/Cas9-based fluorescent reporter assay to study DNA double-strand break repair choice 2020 ·Nature Communications ·(unknown), Stéphanie Sungalee, Salvatore Benfatto, Özdemirhan Serçin, Adrian M. Stütz, Amir Abdollahi, Jan Mauer, Frank T. Zenke, Jan O. Korbel, Balca R. Mardin	30
3	Genome-wide Screens Implicate Loss of Cullin Ring Ligase 3 in Persistent Proliferation and Genome Instability in TP53-Deficient Cells 2020 ·Cell Reports ·Alexandros P. Drainas, (unknown), (unknown), Özdemirhan Serçin, Ioannis Sarropoulos, Mike L. Smith, (unknown), Benjamin Raeder, Adrian M. Stütz, Sebastian M. Waszak, Balca R. Mardin, Jan O. Korbel	20
4	Systematic Identification of Determinants for Single-Strand Annealing-Mediated Deletion Formation inSaccharomyces cerevisiae 2017 ·G3 Genes Genomes Genetics ·Maia Segura‐Wang, Megumi Onishi‐Seebacher, Adrian M. Stütz, Balca R. Mardin, Jan O. Korbel	2
5	Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms 2015 ·Nature Communications ·Alexej Abyzov, Shantao Li, (unknown), Marghoob Mohiyuddin, Adrian M. Stütz, Nicholas F. Parrish, Xinmeng Jasmine Mu, Wyatt T. Clark, Ken Chen, Matthew E. Hurles, Jan O. Korbel, Hugo Y. K. Lam, Charles Lee, Mark Gerstein	63
6	A cell‐based model system links chromothripsis with hyperploidy 2015 ·Molecular Systems Biology ·Balca R. Mardin, Alexandros P. Drainas, Sebastian M. Waszak, Joachim Weischenfeldt, Mayumi Isokane, Adrian M. Stütz, Benjamin Raeder, (unknown), Christopher Buccitelli, Maia Segura‐Wang, Paul A. Northcott, Stefan M. Pfister, Peter Lichter, Jan Ellenberg, Jan O. Korbel	92
7	SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome 2014 ·Genes and Immunity ·Susanne Bens, Thomas Zichner, Adrian M. Stütz, Amke Caliebe, Rabea Wagener, Kirstin Hoff, Jan O. Korbel, Philipp von Bismarck, Reiner Siebert	17
8	Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads 2014 ·Nature Biotechnology ·(unknown), Santiago González, Sı́lvia Beà, Lise O. Andrieux, Itziar Salaverría, Cristina Royo, Laura Martínez Gómez, Montserrat Puiggròs, Maia Segura‐Wang, Adrian M. Stütz, Alba Navarro, Romina Royo, Josep Lluís Gelpí, Marta Gut, Carlos López-Otı́n, Modesto Orozco, Jan O. Korbel, Elı́as Campo, Xosé S. Puente, David Torrents	48
9	Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype 2013 ·Matrix Biology ·(unknown), Barbara M. Grüner, Stephanie Spranger, Adrian M. Stütz, Tobias Rausch, Jan O. Korbel, Dominik Seelow, Peter Nürnberg, Heinrich Sticht, Ekkehart Lausch, Bernhard Zabel, Andreas Winterpacht, Andreas Tagariello	17
10	An Improved Protocol for Sequencing of Repetitive Genomic Regions and Structural Variations Using Mutagenesis and Next Generation Sequencing 2012 ·PLoS ONE ·Botond Sipos, Tim Massingham, Adrian M. Stütz, Nick Goldman	6
11	Fine mapping of a QTL on chromosome 13 for submaximal exercise capacity training response: the HERITAGE Family Study 2011 ·European Journal of Applied Physiology ·Treva Rice, Mark A. Sarzynski, Yan V. Sun, George Argyropoulos, Adrian M. Stütz, Margarita Terán‐García, D. C. Rao, Claude Bouchard, Tuomo Rankinen	14
12	Case–control association study of TGOLN2 in attempted suicide 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Pamela B. Mahon, Adrian M. Stütz, Fayaz Seifuddin, Yuqing Huo, Fernando S. Goes, Dubravka Jancic, Jennifer Judy, J. Raymond DePaulo, Elliot S. Gershon, Francis J. McMahon, Peter P. Zandi, James B. Potash, Virginia L. Willour	7
13	Systematic Inference of Copy-Number Genotypes from Personal Genome Sequencing Data Reveals Extensive Olfactory Receptor Gene Content Diversity 2010 ·PLoS Computational Biology ·Sebastian M. Waszak, Yehudit Hasin-Brumshtein, Thomas Zichner, Tsviya Olender, Ifat Keydar, Miriam Khen, Adrian M. Stütz, Andreas Schlattl, Doron Lancet, Jan O. Korbel	47
14	Circadian Expression of Genes Regulating Food Intake 2007 ·Obesity ·Adrian M. Stütz, Jarosław Staszkiewicz, Andrey Ptitsyn, George Argyropoulos	64
15	CD45 isoform expression is associated with different susceptibilities of human naive and effector CD4⁺ T cells to respond to IL‐4 2005 ·European Journal of Immunology ·Adrian M. Stütz, Philipp Graf, (unknown), (unknown), Christine Neumann, Maximilian Woisetschläger, Thomas Jung	3
16	The Th2 Cell Cytokines IL-4 and IL-13 Regulate Found in Inflammatory Zone 1/Resistin-Like Molecule α Gene Expression by a STAT6 and CCAAT/Enhancer-Binding Protein-Dependent Mechanism 2003 ·The Journal of Immunology ·Adrian M. Stütz, (unknown), Alexandre Trifilieff, Thomas Baumruker, (unknown), Maximilian Woisetschläger	108
17	Assembly, Annotation, and Integration of UNIGENE Clusters into the Human Genome Draft 2001 ·Genome Research ·Degen Zhuo, Wenyuan Zhao, Fred A. Wright, Haiyan Yang, Jipeng Wang, Rosalie C. Sears, (unknown), Do‐Hoon Kwon, David Gordon, Summer L. Gibbs, Dongjuan Dai, Qingyong Yang, Jeffrey R. Spitzner, Ralf Krahe, D Stredney, Adrian M. Stütz, Bo Yuan	48
18	Inhibition of Interleukin-4- and CD40-induced IgE Germline Gene Promoter Activity by 2′-Aminoethoxy-modified Triplex-forming Oligonucleotides 2001 ·Journal of Biological Chemistry ·Adrian M. Stütz, Jutta Horejs‐Hoeck, François Natt, Bernard Cuenoud, Maximilian Woisetschläger	22
19	Functional synergism of STAT6 with either NF-kappa B or PU.1 to mediate IL-4-induced activation of IgE germline gene transcription. 1999 ·PubMed ·Adrian M. Stütz, Maximilian Woisetschläger	76
20	Immune Response to the 23-Valent Pneumococcal Polysaccharide Vaccine in Lymphoma Patients and Patients with Chronic Renal Diseases 1997 ·Advances in experimental medicine and biology ·O Kühnemund, Adrian M. Stütz, Arno Fuchshuber, Uwe Querfeld, S. Petrasch, Ralf René Reinert, Rudolf Lütticken	1

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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