Martin Oti

2.5k total citations
28 papers, 1.1k citations indexed

About

Martin Oti is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Martin Oti has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Oncology. Recurrent topics in Martin Oti's work include Bioinformatics and Genomic Networks (8 papers), Genomics and Chromatin Dynamics (5 papers) and Genomics and Rare Diseases (4 papers). Martin Oti is often cited by papers focused on Bioinformatics and Genomic Networks (8 papers), Genomics and Chromatin Dynamics (5 papers) and Genomics and Rare Diseases (4 papers). Martin Oti collaborates with scholars based in Netherlands, Australia and Germany. Martin Oti's co-authors include HG Brunner, Martijn A. Huynen, Huiqing Zhou, Han G. Brunner, Evelyn N. Kouwenhoven, Hans van Bokhoven, Hendrik G. Stunnenberg, Joost Schalkwijk, Hanna Niehues and Simon J. van Heeringen and has published in prestigious journals such as Molecular Cell, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Martin Oti

25 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Martin Oti Netherlands	16	890	344	106	78	71	28	1.1k
Tamsin E. M. Jones United Kingdom	11	624 0.7×	179 0.5×	63 0.6×	150 1.9×	52 0.7×	14	912
Naoki Nariai Japan	18	661 0.7×	225 0.7×	53 0.5×	120 1.5×	40 0.6×	29	938
Haiming Chen United States	16	754 0.8×	311 0.9×	125 1.2×	216 2.8×	21 0.3×	28	1.2k
Laura Riva Italy	14	789 0.9×	108 0.3×	95 0.9×	188 2.4×	23 0.3×	33	1.0k
Ramu Elango Saudi Arabia	19	447 0.5×	263 0.8×	60 0.6×	104 1.3×	26 0.4×	76	1.0k
Ruslan Sharipov Russia	11	909 1.0×	171 0.5×	80 0.8×	196 2.5×	17 0.2×	36	1.2k
M Orlic-Milacic Canada	11	535 0.6×	132 0.4×	254 2.4×	111 1.4×	28 0.4×	24	878
Kathryn E. Hentges United Kingdom	17	895 1.0×	457 1.3×	42 0.4×	52 0.7×	13 0.2×	41	1.2k
Gene Cutler United States	13	598 0.7×	129 0.4×	167 1.6×	86 1.1×	22 0.3×	18	1.1k
Jorge Urresti United States	8	459 0.5×	240 0.7×	50 0.5×	48 0.6×	15 0.2×	12	659

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-authorship network of co-authors of Martin Oti

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Oti. A scholar is included among the top collaborators of Martin Oti 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 Martin Oti. Martin Oti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Alanis‐Lobato, Gregorio, Martin Oti, Werner Rust, et al.. (2025). Mapping administration route-dependent transduction profiles of commonly used AAV variants in mice by barcode amplicon sequencing. Molecular Therapy — Methods & Clinical Development. 33(2). 101468–101468.

Oti, Martin, et al.. (2025). AAV yield, bioactivity, and particle heterogeneity are impacted by genome size and non-coding DNA elements. Molecular Therapy — Methods & Clinical Development. 33(3). 101499–101499.

Kroeze, Yvet, Martin Oti, Ellen van Beusekom, et al.. (2025). Genetic Inactivation of the Serotonin Transporter Dysregulates Expression of Neurotransmission Genes and Genome‐Wide DNA Methylation Levels in the Medial Prefrontal Cortex of Male Rats During Postnatal Development. Developmental Neurobiology. 85(3). e22973–e22973.

Kienle, Eike, Martin Oti, María Méndez-Lago, et al.. (2023). An unbiased AAV-STARR-seq screen revealing the enhancer activity map of genomic regions in the mouse brain in vivo. Scientific Reports. 13(1). 6745–6745. 10 indexed citations

Seruggia, Davide, Martin Oti, Pratibha Tripathi, et al.. (2019). TAF5L and TAF6L Maintain Self-Renewal of Embryonic Stem Cells via the MYC Regulatory Network. Molecular Cell. 74(6). 1148–1163.e7. 29 indexed citations

Oti, Martin, Rob ter Horst, Christopher J. Neufeldt, et al.. (2018). Establishing normal metabolism and differentiation in hepatocellular carcinoma cells by culturing in adult human serum. Scientific Reports. 8(1). 11685–11685. 20 indexed citations

Qu, Jieqiong, Sabine E.J. Tanis, Jos P.H. Smits, et al.. (2018). Mutant p63 Affects Epidermal Cell Identity through Rewiring the Enhancer Landscape. Cell Reports. 25(12). 3490–3503.e4. 42 indexed citations

Oti, Martin & Michael Sammeth. (2017). Comparative Genomics in Homo sapiens. Methods in molecular biology. 1704. 451–472. 2 indexed citations

Oti, Martin, Attilio Pane, & Michael Sammeth. (2017). Comparative Genomics in Drosophila. Methods in molecular biology. 1704. 433–450. 2 indexed citations

10.

Oti, Martin, et al.. (2016). CTCF-mediated chromatin loops enclose inducible gene regulatory domains. BMC Genomics. 17(1). 252–252. 32 indexed citations

11.

Kouwenhoven, Evelyn N., Martin Oti, Hanna Niehues, et al.. (2015). Transcription factor p63 bookmarks and regulates dynamic enhancers during epidermal differentiation. EMBO Reports. 16(7). 863–878. 124 indexed citations

12.

Gregor, Anne, Martin Oti, Evelyn N. Kouwenhoven, et al.. (2013). De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability. The American Journal of Human Genetics. 93(1). 124–131. 112 indexed citations

13.

Oortveld, Merel A.W., Shivakumar Keerthikumar, Martin Oti, et al.. (2013). Human Intellectual Disability Genes Form Conserved Functional Modules in Drosophila. PLoS Genetics. 9(10). e1003911–e1003911. 28 indexed citations

14.

Ballouz, Sara, Jason Y. Liu, Richard A. George, et al.. (2013). GentrepidV2.0: a web server for candidate disease gene prediction. BMC Bioinformatics. 14(1). 249–249. 4 indexed citations

15.

Ballouz, Sara, Jason Y. Liu, Martin Oti, et al.. (2011). Analysis of genome-wide association study data using the protein knowledge base. BMC Genetics. 12(1). 98–98. 8 indexed citations

16.

Oti, Martin, Martijn A. Huynen, & Han G. Brunner. (2009). The Biological Coherence of Human Phenome Databases. The American Journal of Human Genetics. 85(6). 801–808. 32 indexed citations

17.

Ala, Ugo, Rosario M. Piro, Elena Grassi, et al.. (2008). Prediction of Human Disease Genes by Human-Mouse Conserved Coexpression Analysis. PLoS Computational Biology. 4(3). e1000043–e1000043. 103 indexed citations

18.

Oti, Martin, Martijn A. Huynen, & Han G. Brunner. (2008). Phenome connections. Trends in Genetics. 24(3). 103–106. 84 indexed citations

19.

Kensche, Philip, Martin Oti, Bas E. Dutilh, & Martijn A. Huynen. (2008). Conservation of divergent transcription in fungi. Trends in Genetics. 24(5). 207–211. 30 indexed citations

20.

Oti, Martin & HG Brunner. (2006). The modular nature of genetic diseases. Clinical Genetics. 71(1). 1–11. 308 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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