Martin Oti

2.5k citations
28 papers · 1.1k · h-index 16

Impact in

    • Bioinformatics and Genomic Networks
    • Genomics and Chromatin Dynamics
    • Gene expression and cancer classification
    • Epigenetics and DNA Methylation
  • Genetics top 10%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genetic Associations and Epidemiology

Papers in

    • Bioinformatics and Genomic Networks 5
    • Genomics and Chromatin Dynamics 4
    • Epigenetics and DNA Methylation 3
    • CRISPR and Genetic Engineering 3
    • Genetic Associations and Epidemiology 3
    • Virus-based gene therapy research 3
    • Genetics and Neurodevelopmental Disorders 2

Martin Oti

26 papers receiving 1.1k citations

Peers

Martin Oti
Comparison fields: 5 of 100
  • Molecular Biology 797
  • Genetics 305
  • Aging 10
  • Cancer Research 73
  • Oncology 104
Replace Gene Cutler with:
Gene Cutler United States
Arnaud Stigliani Denmark
Tokuyuki Shinohara Japan
Ulrich Göpfert Germany
Solenne Correard Canada
Annelien Verfaillie Belgium
Sayeeda B. Zain United States
Terrence F. Meehan United States
Jeffrey B. Stavenhagen United States
Jorge Urresti United States
Martin Oti relative to Gene Cutler United States Gene Cutler's profile →
Citations per field
00.5×3.9×
Gene Cutler · 1×
Citations per year

Countries citing papers authored by Martin Oti

Since Specialization
Citations

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

Fields of papers citing papers by Martin Oti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Martin Oti, 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 Martin Oti Line = papers co-authored together Martin Oti links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2006308
2 2015124
3 2013114
4 2008103
5 200884
6 201842
7 201538
8 200932
9 201632
10 200831
11 200830
12 201930
13 201328
14 201821
15 201115
16 201715
17 201915
18 201514
19 202311
20 20138

About Martin Oti

Martin Oti is a scholar working on Molecular Biology, Genetics, Oncology, Cancer Research and Cellular and Molecular Neuroscience, having authored 28 papers that have together received 1.1k indexed citations. Recurring topics across this work include Bioinformatics and Genomic Networks (5 papers), Cancer-related Molecular Pathways (4 papers), Genomics and Chromatin Dynamics (4 papers), Epigenetics and DNA Methylation (3 papers), Genetic Associations and Epidemiology (3 papers), CRISPR and Genetic Engineering (3 papers), Virus-based gene therapy research (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Molecular Biology (797 citations), Genetics (305 citations), Aging (10 citations), Cancer Research (73 citations) and Oncology (104 citations). Martin Oti has collaborated with scholars based in Netherlands, Australia and Germany. Frequent co-authors include HG Brunner, Martijn A. Huynen, Huiqing Zhou, Han G. Brunner, Evelyn N. Kouwenhoven, Hans van Bokhoven, Hendrik G. Stunnenberg, Hanna Niehues, Joost Schalkwijk and Simon J. van Heeringen. Their work appears in journals such as Cell Reports, BMC Bioinformatics, Molecular Therapy — Methods & Clinical Development, Trends in Genetics and The American Journal of Human 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.

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