Konstantin Strauch

50.5k total citations · 1 hit paper
127 papers, 4.3k citations indexed

About

Konstantin Strauch is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Konstantin Strauch has authored 127 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 48 papers in Molecular Biology and 15 papers in Surgery. Recurrent topics in Konstantin Strauch's work include Genetic Associations and Epidemiology (36 papers), Genetic Mapping and Diversity in Plants and Animals (15 papers) and Genetic Syndromes and Imprinting (13 papers). Konstantin Strauch is often cited by papers focused on Genetic Associations and Epidemiology (36 papers), Genetic Mapping and Diversity in Plants and Animals (15 papers) and Genetic Syndromes and Imprinting (13 papers). Konstantin Strauch collaborates with scholars based in Germany, Netherlands and United States. Konstantin Strauch's co-authors include Annette Peters, Christian Gieger, Mélanie Waldenberger, Jerzy Adamski, Max P. Baur, Thomas F. Wienker, Anne S. Quante, Thomas Illig, Sonja Zeilinger and Annette Becker and has published in prestigious journals such as Nature Communications, Blood and Bioinformatics.

In The Last Decade

Konstantin Strauch

122 papers receiving 4.2k 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.

Tobacco Smoking Leads to Extensive Genome-Wide Changes in DNA Methylation

2013 538 citations Sonja Zeilinger, Christian Gieger et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Konstantin Strauch Germany	35	1.6k	978	561	487	478	127	4.3k
Qiong Yang United States	40	1.8k 1.2×	1.3k 1.3×	504 0.9×	475 1.0×	537 1.1×	161	6.0k
Sarah J. Lewis United Kingdom	44	1.1k 0.7×	1.3k 1.4×	450 0.8×	1.0k 2.1×	984 2.1×	184	6.4k
Robert A. Wild United States	46	952 0.6×	739 0.8×	498 0.9×	627 1.3×	1.3k 2.6×	204	10.4k
Giuseppe Bellastella Italy	48	1.4k 0.9×	723 0.7×	608 1.1×	933 1.9×	1.2k 2.5×	208	7.2k
Henri Wallaschofski Germany	51	1.4k 0.9×	753 0.8×	361 0.6×	1.1k 2.2×	1.2k 2.4×	249	8.6k
Akira Hata Japan	41	1.5k 1.0×	1.5k 1.5×	398 0.7×	350 0.7×	908 1.9×	164	6.6k
Marianne Andersen Denmark	47	1.2k 0.8×	586 0.6×	254 0.5×	702 1.4×	890 1.9×	334	8.1k
Abbas Dehghan Netherlands	55	2.4k 1.5×	1.8k 1.8×	473 0.8×	1.1k 2.3×	1.0k 2.1×	201	9.3k
Dipender Gill United Kingdom	39	977 0.6×	1.6k 1.7×	329 0.6×	489 1.0×	708 1.5×	227	5.1k
Liesbeth Vandenput Sweden	38	1.5k 1.0×	1.1k 1.1×	736 1.3×	457 0.9×	510 1.1×	117	4.7k

Countries citing papers authored by Konstantin Strauch

Since Specialization

Citations

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

Fields of papers citing papers by Konstantin Strauch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konstantin Strauch

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

Sill, Martin, Rupert Öllinger, Enrique de Álava, et al.. (2025). Genomic and phenotypic stability of fusion-driven pediatric sarcoma cell lines. Nature Communications. 16(1). 380–380. 2 indexed citations

Böhm, Dieter, Thomas Ganslandt, Patrick Metzger, et al.. (2025). Empowering personalized oncology: evolution of digital support and visualization tools for molecular tumor boards. BMC Medical Informatics and Decision Making. 25(1). 29–29. 1 indexed citations

Huber, Yvonne, Jürgen H. Prochaska, Thomas Koeck, et al.. (2025). Incidence of Major Cardiovascular Events in Patients with Metabolic Dysfunction-Associated Steatotic Liver Disease in the General Population. European Journal of Heart Failure. 27(11). 2490–2500.

Schulz, Andreas, et al.. (2024). Interpretability of bi‐level variable selection methods. Biometrical Journal. 66(2). e2300063–e2300063. 1 indexed citations

Schmidtmann, Irene, et al.. (2024). Sparse Group Penalties for bi‐level variable selection. Biometrical Journal. 66(4). e2200334–e2200334. 2 indexed citations

Cate, Vincent ten, Marina Panova‐Noeva, Steffen Rapp, et al.. (2024). Cardiovascular and genetic determinants of platelet high responsiveness: results from the Gutenberg Health Study. Blood Advances. 8(15). 3870–3874. 1 indexed citations

Michal, Matthias, Andreas Schulz, Philipp S. Wild, et al.. (2023). Tryptophan catabolites and depression in the general population: results from the Gutenberg Health Study. BMC Psychiatry. 23(1). 27–27. 2 indexed citations

Rathmann, Wolfgang, et al.. (2021). Prediction of type 2 diabetes mellitus based on nutrition data. Journal of Nutritional Science. 10. e46–e46. 5 indexed citations

Gaonkar, Krutika S., Fédérico Marini, Komal S. Rathi, et al.. (2020). annoFuse: an R Package to annotate, prioritize, and interactively explore putative oncogenic RNA fusions. BMC Bioinformatics. 21(1). 577–577. 7 indexed citations

10.

Schmidt, Melissa, Donna P. Ankerst, Yiyao Chen, et al.. (2020). Epidemiologic Risk Factors in a Comparison of a Barrett Esophagus Registry (BarrettNET) and a Case–Control Population in Germany. Cancer Prevention Research. 13(4). 377–384. 11 indexed citations

11.

Barco, Stefano, Alice Trinchero, Dagmar Laubert‐Reh, et al.. (2020). c.451dupT in KLKB1 is common in Nigerians, confirming a higher prevalence of severe prekallikrein deficiency in Africans compared to Europeans. Journal of Thrombosis and Haemostasis. 19(1). 147–152.

12.

Erhart, Gertraud, Claudia Lamina, Terho Lehtimäki, et al.. (2018). Genetic Factors Explain a Major Fraction of the 50% Lower Lipoprotein(a) Concentrations in Finns. Arteriosclerosis Thrombosis and Vascular Biology. 38(5). 1230–1241. 32 indexed citations

13.

Bartsch, Detlef K., Konstantin Strauch, Elvira Matthäi, et al.. (2018). The Combination of MiRNA-196b, LCN2, and TIMP1 is a Potential Set of Circulating Biomarkers for Screening Individuals at Risk for Familial Pancreatic Cancer. Journal of Clinical Medicine. 7(10). 295–295. 29 indexed citations

14.

Thorand, Barbara, Cornelia Huth, Katja Berger, et al.. (2018). The Association between Serum 25-Hydroxyvitamin D and Cancer Risk: Results from the Prospective KORA F4 Study. Oncology Research and Treatment. 41(3). 117–121. 15 indexed citations

15.

Jäger, Susanne, Simone Wahl, Janine Kröger, et al.. (2017). Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes. Scientific Reports. 7(1). 6037–6037. 11 indexed citations

16.

Jegan, Nikita, Markus Brugger, Annika Viniol, et al.. (2017). Psychological risk and protective factors for disability in chronic low back pain – a longitudinal analysis in primary care. BMC Musculoskeletal Disorders. 18(1). 114–114. 44 indexed citations

17.

Quante, Anne S., Susanne Rospleszcz, Moritz Tobiasch, et al.. (2016). Goblet Cell Ratio in Combination with Differentiation and Stem Cell Markers in Barrett Esophagus Allow Distinction of Patients with and without Esophageal Adenocarcinoma. Cancer Prevention Research. 10(1). 55–66. 18 indexed citations

18.

Petersen, Ann-Kristin, Sonja Zeilinger, Gabi Kastenmüller, et al.. (2013). Epigenetics meets metabolomics: an epigenome-wide association study with blood serum metabolic traits. Human Molecular Genetics. 23(2). 534–545. 123 indexed citations

19.

Becker, Annette, Marcus Redaèlli, Jean‐François Chenot, et al.. (2011). Implementation of a Guideline for Low Back Pain Management in Primary Care. Spine. 37(8). 701–710. 47 indexed citations

20.

Kurz, Thorsten, Konstantin Strauch, Sandra Braun, et al.. (2004). Multilocus haplotype analyses reveal association between 5 novel IL-15 polymorphisms and asthma. Journal of Allergy and Clinical Immunology. 113(5). 896–901. 22 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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