Moritz Mall

2.7k total citations
23 papers, 1.8k citations indexed

About

Moritz Mall is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Moritz Mall has authored 23 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Moritz Mall's work include Pluripotent Stem Cells Research (11 papers), CRISPR and Genetic Engineering (8 papers) and Nuclear Structure and Function (4 papers). Moritz Mall is often cited by papers focused on Pluripotent Stem Cells Research (11 papers), CRISPR and Genetic Engineering (8 papers) and Nuclear Structure and Function (4 papers). Moritz Mall collaborates with scholars based in United States, Germany and United Kingdom. Moritz Mall's co-authors include Marius Wernig, Qian Yi Lee, Cheen Euong Ang, Soham Chanda, Henrik Ahlenius, Iain W. Mattaj, Jonathan Davila, Winston Koh, Norma Neff and S. Ali M. Shariati and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Moritz Mall

21 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
Moritz Mall United States 17 1.6k 294 218 180 149 23 1.8k
Roger Pedersen United Kingdom 15 1.2k 0.8× 366 1.2× 343 1.6× 277 1.5× 155 1.0× 21 1.8k
Teresa Rayón United Kingdom 15 1.5k 1.0× 121 0.4× 140 0.6× 162 0.9× 230 1.5× 21 1.8k
Debbie L. C. van den Berg United Kingdom 16 1.5k 1.0× 125 0.4× 283 1.3× 210 1.2× 118 0.8× 20 1.7k
Daniel Fuentes United States 7 1.6k 1.0× 381 1.3× 355 1.6× 196 1.1× 58 0.4× 7 1.8k
Pierre J. Fabre Switzerland 14 1.1k 0.7× 295 1.0× 196 0.9× 160 0.9× 123 0.8× 17 1.6k
Fausto Ulloa Spain 18 1.4k 0.9× 344 1.2× 296 1.4× 282 1.6× 275 1.8× 32 1.8k
E. Hilary Gustafson Germany 11 1.4k 0.9× 191 0.6× 126 0.6× 194 1.1× 65 0.4× 12 1.7k
Lijian Shen United States 8 1.1k 0.7× 164 0.6× 260 1.2× 228 1.3× 79 0.5× 8 1.5k
Daniel Gyllborg Sweden 13 1.0k 0.7× 231 0.8× 163 0.7× 120 0.7× 90 0.6× 15 1.3k
Jennie Close United States 15 1.2k 0.8× 328 1.1× 330 1.5× 183 1.0× 190 1.3× 18 1.6k

Countries citing papers authored by Moritz Mall

Since Specialization
Citations

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

Fields of papers citing papers by Moritz Mall

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moritz Mall

This figure shows the co-authorship network connecting the top 25 collaborators of Moritz Mall. A scholar is included among the top collaborators of Moritz Mall 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 Moritz Mall. Moritz Mall 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.
Liu, Ke, Yuxin Zhang, Daniel Novak, et al.. (2025). Direct transdifferentiation of tumorigenic melanoma cells induces tumor cell reversion. Cell Death and Disease. 16(1). 563–563.
2.
Ang, Cheen Euong, Qian Yi Lee, Rahul Sinha, et al.. (2024). Generation of human excitatory forebrain neurons by cooperative binding of proneural NGN2 and homeobox factor EMX1. Proceedings of the National Academy of Sciences. 121(11). e2308401121–e2308401121. 10 indexed citations
3.
Mall, Moritz, et al.. (2024). Canalizing cell fate by transcriptional repression. Molecular Systems Biology. 20(3). 144–161. 3 indexed citations
4.
Wang, Changwen, Meng Sun, Chunxuan Shao, et al.. (2024). A multidimensional atlas of human glioblastoma-like organoids reveals highly coordinated molecular networks and effective drugs. npj Precision Oncology. 8(1). 19–19. 14 indexed citations
5.
Wöhr, Markus, Justyna A. Janas, Moritz Mall, et al.. (2022). Myt1l haploinsufficiency leads to obesity and multifaceted behavioral alterations in mice. Molecular Autism. 13(1). 19–19. 17 indexed citations
6.
Narayanan, Ashwin, Damir Krunic, Marion Bähr, et al.. (2022). MEOX2 homeobox gene promotes growth of malignant gliomas. Neuro-Oncology. 24(11). 1911–1924. 17 indexed citations
7.
Janas, Justyna A., Lichao Zhang, János Demeter, et al.. (2022). Tip60-mediated H2A.Z acetylation promotes neuronal fate specification and bivalent gene activation. Molecular Cell. 82(24). 4627–4646.e14. 26 indexed citations
8.
Adrian-Segarra, Juan M., et al.. (2021). Combining Cell Fate Reprogramming and Protein Engineering to Study Transcription Factor Functions. Methods in molecular biology. 2352. 227–236.
9.
Lee, Qian Yi, Moritz Mall, Soham Chanda, et al.. (2020). Pro-neuronal activity of Myod1 due to promiscuous binding to neuronal genes. Nature Cell Biology. 22(4). 401–411. 37 indexed citations
10.
Luo, Chongyuan, Qian Yi Lee, Orly L. Wapinski, et al.. (2019). Global DNA methylation remodeling during direct reprogramming of fibroblasts to neurons. eLife. 8. 57 indexed citations
11.
Yang, Nan, Soham Chanda, Samuele Marro, et al.. (2017). Generation of pure GABAergic neurons by transcription factor programming. Nature Methods. 14(6). 621–628. 229 indexed citations
12.
Mall, Moritz, Michael S. Kareta, Soham Chanda, et al.. (2017). Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates. Nature. 544(7649). 245–249. 149 indexed citations
13.
Chuang, Wen‐Po, Arun Sharma, Praveen Shukla, et al.. (2017). Partial Reprogramming of Pluripotent Stem Cell-Derived Cardiomyocytes into Neurons. Scientific Reports. 7(1). 44840–44840. 17 indexed citations
14.
Mall, Moritz & Marius Wernig. (2017). The novel tool of cell reprogramming for applications in molecular medicine. Journal of Molecular Medicine. 95(7). 695–703. 16 indexed citations
15.
Treutlein, Barbara, Qian Yi Lee, J. Gray Camp, et al.. (2016). Dissecting direct reprogramming from fibroblast to neuron using single-cell RNA-seq. Nature. 534(7607). 391–395. 321 indexed citations
16.
Durruthy-Durruthy, Jens, Vittorio Sebastiano, Mark Wossidlo, et al.. (2015). The primate-specific noncoding RNA HPAT5 regulates pluripotency during human preimplantation development and nuclear reprogramming. Nature Genetics. 48(1). 44–52. 135 indexed citations
17.
Chanda, Soham, Cheen Euong Ang, Jonathan Davila, et al.. (2014). Generation of Induced Neuronal Cells by the Single Reprogramming Factor ASCL1. Stem Cell Reports. 3(2). 282–296. 278 indexed citations
18.
Asencio, Claudio, Iain F. Davidson, Rachel Santarella‐Mellwig, et al.. (2012). Coordination of Kinase and Phosphatase Activities by Lem4 Enables Nuclear Envelope Reassembly during Mitosis. Cell. 150(1). 122–135. 132 indexed citations
19.
Mansfeld, Jörg, Stephan Güttinger, Nelly Panté, et al.. (2006). The Conserved Transmembrane Nucleoporin NDC1 Is Required for Nuclear Pore Complex Assembly in Vertebrate Cells. Molecular Cell. 22(1). 93–103. 181 indexed citations
20.
Unger, Kristian, Axel Walch, Moritz Mall, et al.. (2006). RET rearrangements in post-Chernobyl papillary thyroid carcinomas with a short latency analysed by interphase FISH. British Journal of Cancer. 94(10). 1472–1477. 29 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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