Max Schubach
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- Genomics and Chromatin Dynamics
- Retinal Development and Disorders
- RNA and protein synthesis mechanisms
- Genomics and Phylogenetic Studies
- RNA Research and Splicing
Papers in
-
- Genomics and Chromatin Dynamics 8
- RNA and protein synthesis mechanisms 6
- Genomics and Phylogenetic Studies 5
- CRISPR and Genetic Engineering 2
- RNA Research and Splicing 2
- Genetics 10
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 3
- Genetic and Kidney Cyst Diseases 2
- Co-authors
- Martin Kircher (10 shared papers)Jay Shendure (4 shared papers)Philipp Rentzsch (1 shared paper)Peter N. Robinson (7 shared papers)Marten Jäger (4 shared papers)Tomasz Żemojtel (4 shared papers)Giorgio Valentini (6 shared papers)Lusiné Nazaretyan (2 shared papers)
- Journals
- BMC Bioinformatics (4 papers)European Journal of Human Genetics (3 papers)Nature Communications (2 papers)GigaScience (2 papers)Genome Medicine (2 papers)
- Partner nations
- GermanyUnited StatesItaly
In The Last Decade
Max Schubach
25 papers receiving 1.6k citations
Max Schubach's Hit Papers
Peers
Comparison fields: 5 of 104
- Genetics 683
- Molecular Biology 906
- Cancer Research 140
- Ophthalmology 72
- Genetics 47
Countries citing papers authored by Max Schubach
This map shows the geographic impact of Max Schubach'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 Max Schubach with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Max Schubach more than expected).
Fields of papers citing papers by Max Schubach
This network shows the impact of papers produced by Max Schubach. 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 Max Schubach. The network helps show where Max Schubach may publish in the future.
Co-authors
The 25 scholars most cited alongside Max Schubach, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | CADD-Splice—improving genome-wide variant effect prediction using deep learning-derived splice scores Hit paper breakdown → | 2021 | 335 |
| 2 | 2015 | 237 | |
| 3 | 2013 | 207 | |
| 4 | 2016 | 160 | |
| 5 | 2019 | 135 | |
| 6 | CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions Hit paper breakdown → | 2024 | 133 |
| 7 | 2020 | 75 | |
| 8 | 2013 | 69 | |
| 9 | 2017 | 58 | |
| 10 | 2018 | 28 | |
| 11 | 2016 | 28 | |
| 12 | 2015 | 27 | |
| 13 | 2018 | 22 | |
| 14 | 2017 | 21 | |
| 15 | 2025 | 21 | |
| 16 | 2022 | 18 | |
| 17 | 2010 | 16 | |
| 18 | 2016 | 15 | |
| 19 | 2020 | 11 | |
| 20 | 2014 | 11 |
About Max Schubach
Max Schubach is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Pathology and Forensic Medicine, having authored 27 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (8 papers), RNA and protein synthesis mechanisms (6 papers), Genomics and Rare Diseases (6 papers), Genomics and Phylogenetic Studies (5 papers), Genomic variations and chromosomal abnormalities (3 papers), CRISPR and Genetic Engineering (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Genetics (683 citations), Molecular Biology (906 citations), Cancer Research (140 citations), Ophthalmology (72 citations) and Genetics (47 citations). Max Schubach has collaborated with scholars based in Germany, United States and Italy. Frequent co-authors include Martin Kircher, Jay Shendure, Philipp Rentzsch, Peter N. Robinson, Marten Jäger, Tomasz Żemojtel, Giorgio Valentini, Lusiné Nazaretyan, Damian Smedley and Nicole Washington. Their work appears in journals such as BMC Bioinformatics, European Journal of Human Genetics, Nature Communications, GigaScience and Genome Medicine.
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.