Max Schubach

4.8k citations
40 papers · 3.1k · 3 hit papers · h-index 23

Impact in

  • Genetics top 2%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Retinal Development and Disorders
    • Genomics and Chromatin Dynamics
    • Genomics and Phylogenetic Studies
    • RNA and protein synthesis mechanisms

Papers in

    • Genomics and Rare Diseases 12
    • Genomic variations and chromosomal abnormalities 5
    • Genetics and Neurodevelopmental Disorders 3
    • Genomics and Chromatin Dynamics 11
    • RNA and protein synthesis mechanisms 9
    • Genomics and Phylogenetic Studies 5
    • Machine Learning in Bioinformatics 3
    • Bioinformatics and Genomic Networks 3

Max Schubach

40 papers receiving 3.1k citations

Max Schubach's Hit Papers

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions 2023 · 189 citations
1890+4+8Years since publication100200300400

Peers

Max Schubach
Comparison fields: 5 of 134
  • Genetics 1.2k
  • Molecular Biology 1.6k
  • Cancer Research 267
  • Ophthalmology 100
  • Health Informatics 13
Replace Eugene Bragin with:
Eugene Bragin United Kingdom
Zafer Yüksel Türkiye
J. Bradley Holmes United States
Juan David Arbelaez Velez United States
Michele Pinelli Italy
Andrea Ciolfi Italy
Namiko Abe United States
Wenwu Cui United States
J. Scott Newberry United States
Žiga Avsec Germany
Max Schubach relative to Eugene Bragin United Kingdom Eugene Bragin's profile →
Citations per field
00.5×2×4×5.9×
Eugene Bragin · 1×
Citations per year

Countries citing papers authored by Max Schubach

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Max Schubach Line = papers co-authored together Max Schubach links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 40 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 →
2021457
2
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Hit paper breakdown →
2014406
3 2015296
4 2012280
5 2013225
6 2016193
7
CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions
Hit paper breakdown →
2023189
8 2019153
9 201690
10 201381
11 202076
12 201873
13 201765
14 201965
15 201949
16 202446
17 201939
18 202431
19 201829
20 201629

About Max Schubach

Max Schubach is a scholar working on Genetics, Molecular Biology, Ophthalmology, Radiology, Nuclear Medicine and Imaging and Genetics, having authored 40 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Genomics and Chromatin Dynamics (11 papers), RNA and protein synthesis mechanisms (9 papers), Genomics and Phylogenetic Studies (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Machine Learning in Bioinformatics (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Bioinformatics and Genomic Networks (3 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (1.6k citations), Cancer Research (267 citations), Ophthalmology (100 citations) and Health Informatics (13 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, Lusiné Nazaretyan, Tomasz Żemojtel, Marten Jäger, Thorben Maaß, Sebastian Röner and Giorgio Valentini. Their work appears in journals such as BMC Bioinformatics, Human Mutation, Genome Medicine, European Journal of Human Genetics and GigaScience.

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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