Janine Altmüller

32.0k total citations
213 papers, 6.5k citations indexed

About

Janine Altmüller is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Janine Altmüller has authored 213 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Molecular Biology, 59 papers in Genetics and 22 papers in Cell Biology. Recurrent topics in Janine Altmüller's work include RNA Research and Splicing (20 papers), Genomics and Rare Diseases (17 papers) and RNA and protein synthesis mechanisms (17 papers). Janine Altmüller is often cited by papers focused on RNA Research and Splicing (20 papers), Genomics and Rare Diseases (17 papers) and RNA and protein synthesis mechanisms (17 papers). Janine Altmüller collaborates with scholars based in Germany, United States and United Kingdom. Janine Altmüller's co-authors include Peter Nürnberg, Christian Becker, Hölger Thiele, Hanns Hatt, Günter Gisselmann, Hagen Scherb, Guido Fischer, Lyle J. Palmer, Matthias Wjst and Christoph Dieterich and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Janine Altmüller

210 papers receiving 6.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janine Altmüller Germany 48 3.4k 1.3k 773 664 640 213 6.5k
Takaya Abe Japan 45 3.9k 1.1× 730 0.5× 697 0.9× 561 0.8× 907 1.4× 170 7.3k
Suzanne M. Leal United States 47 5.0k 1.5× 4.7k 3.5× 692 0.9× 808 1.2× 460 0.7× 211 10.8k
Peter J. McKinnon United States 58 9.5k 2.8× 1.2k 0.9× 421 0.5× 1.7k 2.6× 1.1k 1.7× 136 12.0k
William J. Pavan United States 55 4.9k 1.4× 1.4k 1.0× 1.4k 1.8× 907 1.4× 2.7k 4.2× 177 10.0k
Dieter Riethmacher Germany 38 4.5k 1.3× 1.5k 1.1× 347 0.4× 663 1.0× 888 1.4× 60 8.6k
Edith Hümmler Switzerland 48 5.6k 1.6× 1.0k 0.8× 674 0.9× 278 0.4× 566 0.9× 133 8.9k
Mark Lathrop France 25 3.2k 0.9× 2.9k 2.2× 542 0.7× 509 0.8× 323 0.5× 48 7.2k
Stefano Gustincich Italy 44 4.9k 1.4× 564 0.4× 530 0.7× 1.4k 2.2× 442 0.7× 132 6.9k
Kazuhiro Ikenaka Japan 55 5.3k 1.6× 1.2k 0.9× 639 0.8× 937 1.4× 946 1.5× 251 10.4k
Linda C. Samuelson United States 48 3.0k 0.9× 1.3k 1.0× 425 0.5× 388 0.6× 374 0.6× 148 6.4k

Countries citing papers authored by Janine Altmüller

Since Specialization
Citations

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

Fields of papers citing papers by Janine Altmüller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janine Altmüller

This figure shows the co-authorship network connecting the top 25 collaborators of Janine Altmüller. A scholar is included among the top collaborators of Janine Altmüller 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 Janine Altmüller. Janine Altmüller 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.
Kudin, Alexei P., Viktoriya Peeva, Janine Altmüller, et al.. (2023). The Fate of Oxidative Strand Breaks in Mitochondrial DNA. Antioxidants. 12(5). 1087–1087. 4 indexed citations
2.
Brauchitsch, Sophie von, Hölger Thiele, Felix Zahnert, et al.. (2023). The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing. Epilepsia Open. 8(2). 497–508. 6 indexed citations
3.
Chatzinikolaou, Georgia, Kalliopi Stratigi, Evi Goulielmaki, et al.. (2023). XPF interacts with TOP2B for R-loop processing and DNA looping on actively transcribed genes. Science Advances. 9(45). eadi2095–eadi2095. 6 indexed citations
4.
Andreotti, Sandro, Janine Altmüller, Claudia Quedenau, et al.. (2022). De Novo-Whole Genome Assembly of the Roborovski Dwarf Hamster ( Phodopus roborovskii ) Genome: An Animal Model for Severe/Critical COVID-19. Genome Biology and Evolution. 14(7). 3 indexed citations
5.
Silbern, Ivan, Janine Altmüller, Mario Keller, et al.. (2022). Npl3 functions in mRNP assembly by recruitment of mRNP components to the transcription site and their transfer onto the mRNA. Nucleic Acids Research. 51(2). 831–851. 8 indexed citations
6.
Averdunk, Luisa, Khalid Al‐Thihli, Harald Surowy, et al.. (2022). Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain. Clinical Genetics. 103(4). 484–491. 1 indexed citations
7.
Lackmann, Jan‐Wilm, et al.. (2022). Exon junction complex-associated multi-adapter RNPS1 nucleates splicing regulatory complexes to maintain transcriptome surveillance. Nucleic Acids Research. 50(10). 5899–5918. 10 indexed citations
8.
Elçioğlu, Nursel, Janine Altmüller, Silke Kaulfuß, et al.. (2022). Phenotypic spectrum of BLM ‐ and RMI1 ‐related Bloom syndrome. Clinical Genetics. 101(5-6). 559–564. 8 indexed citations
9.
Gizak, Agnieszka, Steffi Dreha‐Kulaczewski, Janusz Wiśniewski, et al.. (2021). A novel remitting leukodystrophy associated with a variant in FBP2. Brain Communications. 3(2). fcab036–fcab036. 2 indexed citations
10.
Budde, Birgit, Janine Altmüller, Susanne Motameny, et al.. (2020). Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics. 98(1). 32–42. 24 indexed citations
11.
Gerbracht, Jennifer V., Volker Boehm, Thiago Britto‐Borges, et al.. (2020). CASC3 promotes transcriptome-wide activation of nonsense-mediated decay by the exon junction complex. Nucleic Acids Research. 48(15). 8626–8644. 36 indexed citations
12.
Kubacki, Torsten, Assa Yeroslaviz, Martin R. Späth, et al.. (2020). The Integrated RNA Landscape of Renal Preconditioning against Ischemia-Reperfusion Injury. Journal of the American Society of Nephrology. 31(4). 716–730. 26 indexed citations
13.
Lanver, Daniel, Petra Happel, Gabriel Schweizer, et al.. (2018). The Biotrophic Development of Ustilago maydis Studied by RNA-Seq Analysis. The Plant Cell. 30(2). 300–323. 158 indexed citations
14.
Matei, Alexandra, Corinna Ernst, Markus Günl, et al.. (2018). How to make a tumour: cell type specific dissection of Ustilago maydis‐ induced tumour development in maize leaves. New Phytologist. 217(4). 1681–1695. 39 indexed citations
15.
Pankin, Artem, Janine Altmüller, Christian Becker, & Maria von Korff. (2018). Targeted resequencing reveals genomic signatures of barley domestication. New Phytologist. 218(3). 1247–1259. 67 indexed citations
16.
Broekaert, Ilse Julia, Kerstin Becker, Ingo Gottschalk, et al.. (2018). Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathy. Journal of Medical Genetics. 55(9). 637–640. 18 indexed citations
17.
Dennenmoser, Stefan, et al.. (2017). Copy number increases of transposable elements and protein‐coding genes in an invasive fish of hybrid origin. Molecular Ecology. 26(18). 4712–4724. 23 indexed citations
18.
Hatzold, Julia, Filippo Beleggia, Janine Altmüller, et al.. (2016). Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunit. eLife. 5. 22 indexed citations
19.
Bögershausen, Nina, Umut Altunoğlu, Filippo Beleggia, et al.. (2016). An unusual presentation of Kabuki syndrome with orbital cysts, microphthalmia, and cholestasis with bile duct paucity. American Journal of Medical Genetics Part A. 170(12). 3282–3288. 13 indexed citations
20.
Rosin, Nicole L., Nursel Elçioğlu, Filippo Beleggia, et al.. (2015). Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability. Human Molecular Genetics. 24(13). 3708–17. 25 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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