Martina Müller‐Nurasyid

82.4k total citations
56 papers, 1.8k citations indexed

About

Martina Müller‐Nurasyid is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Martina Müller‐Nurasyid has authored 56 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Molecular Biology and 9 papers in Immunology. Recurrent topics in Martina Müller‐Nurasyid's work include Genetic Associations and Epidemiology (13 papers), Bioinformatics and Genomic Networks (6 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). Martina Müller‐Nurasyid is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Bioinformatics and Genomic Networks (6 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). Martina Müller‐Nurasyid collaborates with scholars based in Germany, United States and Austria. Martina Müller‐Nurasyid's co-authors include Thomas Illig, Iris M. Heid, Joachim Heinrich, Hans Demmelmair, Henning Gohlke, Lyle J. Palmer, Iris Kompauer, Berthold Koletzko, Moritz F. Sinner and Annette Peters and has published in prestigious journals such as Nature Communications, Bioinformatics and Journal of the American College of Cardiology.

In The Last Decade

Martina Müller‐Nurasyid

55 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martina Müller‐Nurasyid Germany 21 538 458 315 194 194 56 1.8k
Ivan Tancevski Austria 25 434 0.8× 177 0.4× 229 0.7× 205 1.1× 130 0.7× 81 1.9k
Zhen Yang China 24 471 0.9× 387 0.8× 187 0.6× 355 1.8× 126 0.6× 98 1.8k
György Balla Hungary 26 1.5k 2.7× 223 0.5× 359 1.1× 255 1.3× 103 0.5× 86 3.3k
Patricia L. Mitchell Canada 21 486 0.9× 146 0.3× 430 1.4× 235 1.2× 101 0.5× 62 1.5k
Anna V. Mathew United States 23 1.3k 2.4× 221 0.5× 142 0.5× 390 2.0× 110 0.6× 51 2.6k
Philippe Durand France 23 304 0.6× 194 0.4× 233 0.7× 177 0.9× 79 0.4× 60 1.8k
Lisa C. Hudgins United States 18 521 1.0× 312 0.7× 296 0.9× 568 2.9× 90 0.5× 36 2.0k
Dennis D. Black United States 24 523 1.0× 197 0.4× 382 1.2× 328 1.7× 126 0.6× 80 2.4k
Esther Granot Israel 23 388 0.7× 304 0.7× 268 0.9× 330 1.7× 110 0.6× 99 2.0k
Han Li China 22 257 0.5× 183 0.4× 99 0.3× 236 1.2× 73 0.4× 151 1.7k

Countries citing papers authored by Martina Müller‐Nurasyid

Since Specialization
Citations

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

Fields of papers citing papers by Martina Müller‐Nurasyid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martina Müller‐Nurasyid. 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 Martina Müller‐Nurasyid. The network helps show where Martina Müller‐Nurasyid may publish in the future.

Co-authorship network of co-authors of Martina Müller‐Nurasyid

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

All Works

20 of 20 papers shown
1.
Zimmermann, Katharina, Sören Weidemann, Stefan Lüth, et al.. (2025). Insights Into Hepatic Sarcoidosis: Analysis of Histological Patterns, Hepatic Complications and Therapeutic Approaches. Liver International. 45(3). e70037–e70037. 3 indexed citations
2.
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
3.
Fleischmann, Daniel F., Claudia Wolf, Arne Kandulski, et al.. (2025). Interprofessional approach to personalized medication management and therapy optimization in IBD care. Frontiers in Medicine. 12. 1446695–1446695. 1 indexed citations
4.
Ichim, Cristian, et al.. (2024). Assessing Key Factors Influencing Successful Resuscitation Outcomes in Out-of-Hospital Cardiac Arrest (OHCA). Journal of Clinical Medicine. 13(23). 7399–7399. 5 indexed citations
5.
Duijvestein, Marjolijn, Reena Sidhu, Emma V. Carrington, et al.. (2024). The United European Gastroenterology green paper—climate change and gastroenterology. United European Gastroenterology Journal. 12(9). 1292–1305. 7 indexed citations
6.
Zimmermann, Katharina, et al.. (2024). Increasing incidence of mycotoxicosis in South-Eastern Germany: a comprehensive analysis of mushroom poisonings at a University Medical Center. BMC Gastroenterology. 24(1). 450–450. 1 indexed citations
7.
Hartmann, Alica, Stephanie D. Grabitz, Felix Mathias Wagner, et al.. (2024). Bi-Gaussian analysis reveals distinct education-related alterations in spherical equivalent and axial length—results from the Gutenberg Health Study. Graefe s Archive for Clinical and Experimental Ophthalmology. 262(6). 1819–1828. 4 indexed citations
8.
Tilch, Erik, Barbara Schormair, Chen Zhao, et al.. (2022). ExomeChip-based rare variant association study in restless legs syndrome. Sleep Medicine. 94. 26–30. 1 indexed citations
9.
Hawe, Johann S., Ashis Saha, Mélanie Waldenberger, et al.. (2022). Network reconstruction for trans acting genetic loci using multi-omics data and prior information. Genome Medicine. 14(1). 125–125. 4 indexed citations
10.
Schweiger, Regev, Eyal Fisher, Omer Weissbrod, et al.. (2018). Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-tests. Nature Communications. 9(1). 4919–4919. 5 indexed citations
11.
Schweiger, Regev, Omer Weissbrod, Elior Rahmani, et al.. (2017). RL-SKAT: An Exact and Efficient Score Test for Heritability and Set Tests. Genetics. 207(4). 1275–1283. 13 indexed citations
12.
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
13.
Kunst, C, et al.. (2016). The p53 family in hepatocellular carcinoma. Translational Cancer Research. 5(6). 632–638. 8 indexed citations
14.
Standl, Marie, Falko Tesch, Hansjörg Baurecht, et al.. (2016). Association of Atopic Dermatitis with Cardiovascular Risk Factors and Diseases. Journal of Investigative Dermatology. 137(5). 1074–1081. 81 indexed citations
15.
Ott, Claudia, et al.. (2014). How fast up the ladder? Factors associated with immunosuppressive or anti-TNF therapies in IBD patients at early stages: results from a population-based cohort. International Journal of Colorectal Disease. 29(11). 1329–1338. 9 indexed citations
16.
Müller‐Nurasyid, Martina, Karl‐Peter Hopfner, & Gregor Witte. (2014). c‐di‐AMP recognition by Staphylococcus aureus PstA. FEBS Letters. 589(1). 45–51. 49 indexed citations
17.
Amin, Ahmad S., John R. Giudicessi, Anke J. Tijsen, et al.. (2011). Variants in the 3′ untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner. European Heart Journal. 33(6). 714–723. 94 indexed citations
18.
Herder, Christian, Thomas Illig, Jens Baumert, et al.. (2008). Macrophage migration inhibitory factor (MIF) and risk for coronary heart disease: Results from the MONICA/KORA Augsburg case-cohort study, 1984–2002. Atherosclerosis. 200(2). 380–388. 52 indexed citations
19.
Gohlke, Henning, Martina Müller‐Nurasyid, Iris M. Heid, et al.. (2006). Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. Human Molecular Genetics. 15(11). 1745–1756. 426 indexed citations
20.
Ott, Katja, H. Vogelsang, James Mueller, et al.. (2003). Chromosomal instability rather than p53 mutation is associated with response to neoadjuvant cisplatin-based chemotherapy in gastric carcinoma.. PubMed. 9(6). 2307–15. 64 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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