Malte Spielmann
Impact in
- Molecular Biology top 2%
- Single-cell and spatial transcriptomics
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
- CRISPR and Genetic Engineering
- Biophysics top 1%
Papers in
-
- Genomics and Chromatin Dynamics 12
- Single-cell and spatial transcriptomics 10
- Congenital heart defects research 8
- RNA Research and Splicing 7
- Genetics 40
- Genomic variations and chromosomal abnormalities 21
- Genomics and Rare Diseases 15
- Connective tissue disorders research 7
- Co-authors
- Stefan Mundlos (34 shared papers)Darío G. Lupiáñez (3 shared papers)Jay Shendure (4 shared papers)Cole Trapnell (4 shared papers)Junyue Cao (3 shared papers)Fan Zhang (2 shared papers)Frank J. Steemers (2 shared papers)Daniel M. Ibrahim (4 shared papers)
- Journals
- Journal of Medical Genetics (5 papers)European Journal of Human Genetics (4 papers)The American Journal of Human Genetics (4 papers)European Journal of Medical Genetics (4 papers)Clinical Genetics (3 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Malte Spielmann
83 papers receiving 5.7k citations
Malte Spielmann's Hit Papers
Peers
Comparison fields: 5 of 149
- Molecular Biology 3.9k
- Biophysics 277
- Cancer Research 678
- Neurology 361
- Genetics 1.2k
Countries citing papers authored by Malte Spielmann
This map shows the geographic impact of Malte Spielmann'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 Malte Spielmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Malte Spielmann more than expected).
Fields of papers citing papers by Malte Spielmann
This network shows the impact of papers produced by Malte Spielmann. 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 Malte Spielmann. The network helps show where Malte Spielmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Malte Spielmann, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 90 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The single-cell transcriptional landscape of mammalian organogenesis Hit paper breakdown → | 2019 | 2172 |
| 2 | Structural variation in the 3D genome Hit paper breakdown → | 2018 | 406 |
| 3 | A human cell atlas of fetal gene expression Hit paper breakdown → | 2020 | 383 |
| 4 | Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state Hit paper breakdown → | 2021 | 306 |
| 5 | 2016 | 270 | |
| 6 | 2021 | 170 | |
| 7 | 2016 | 156 | |
| 8 | 2015 | 151 | |
| 9 | 2008 | 129 | |
| 10 | 2008 | 126 | |
| 11 | 2015 | 121 | |
| 12 | 2015 | 103 | |
| 13 | 2014 | 90 | |
| 14 | 2016 | 89 | |
| 15 | 2022 | 85 | |
| 16 | 2012 | 83 | |
| 17 | 2017 | 66 | |
| 18 | 2014 | 48 | |
| 19 | 2005 | 44 | |
| 20 | 2013 | 43 |
About Malte Spielmann
Malte Spielmann is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Developmental Biology and Cancer Research, having authored 90 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (15 papers), Genomics and Chromatin Dynamics (12 papers), Single-cell and spatial transcriptomics (10 papers), Congenital heart defects research (8 papers), Congenital limb and hand anomalies (8 papers), RNA Research and Splicing (7 papers) and Connective tissue disorders research (7 papers). The work is most often cited by research in Molecular Biology (3.9k citations), Biophysics (277 citations), Cancer Research (678 citations), Neurology (361 citations) and Genetics (1.2k citations). Malte Spielmann has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Stefan Mundlos, Darío G. Lupiáñez, Jay Shendure, Cole Trapnell, Junyue Cao, Fan Zhang, Frank J. Steemers, Daniel M. Ibrahim, Xingfan Huang and Xiaojie Qiu. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics and Clinical Genetics.
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.