Mehmet Tekman

2.8k total citations
14 papers, 168 citations indexed

About

Mehmet Tekman is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Mehmet Tekman has authored 14 papers receiving a total of 168 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Immunology. Recurrent topics in Mehmet Tekman's work include Genomics and Rare Diseases (3 papers), interferon and immune responses (2 papers) and Inflammasome and immune disorders (2 papers). Mehmet Tekman is often cited by papers focused on Genomics and Rare Diseases (3 papers), interferon and immune responses (2 papers) and Inflammasome and immune disorders (2 papers). Mehmet Tekman collaborates with scholars based in United Kingdom, Germany and United States. Mehmet Tekman's co-authors include Robert Kleta, Horia Stanescu, Daniela Iancu, Dorota Rowczenio, Hadija Trojer, Helen J. Lachmann, Chela James, Ashutosh Wechalekar, Polona Le Quesne Stabej and Thirusha Lane and has published in prestigious journals such as Bioinformatics, Developmental Cell and BMC Bioinformatics.

In The Last Decade

Mehmet Tekman

12 papers receiving 167 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mehmet Tekman United Kingdom 7 118 47 30 23 18 14 168
Dagmar Kruspe Germany 7 163 1.4× 65 1.4× 27 0.9× 43 1.9× 26 1.4× 8 225
Juan Francisco Quesada‐Espinosa Spain 6 67 0.6× 36 0.8× 81 2.7× 47 2.0× 5 0.3× 22 235
Patricia Bretones France 8 165 1.4× 128 2.7× 12 0.4× 16 0.7× 21 1.2× 14 301
Tossaporn Seeherunvong United States 7 131 1.1× 113 2.4× 6 0.2× 12 0.5× 18 1.0× 14 201
Alexandre Z. Daly United States 6 157 1.3× 86 1.8× 20 0.7× 12 0.5× 22 1.2× 9 282
Nadja Kokalj Vokač Slovenia 8 79 0.7× 62 1.3× 6 0.2× 20 0.9× 19 1.1× 27 179
Joanna J. Gell United States 9 194 1.6× 52 1.1× 28 0.9× 66 2.9× 34 1.9× 19 288
Valeh Hadavi Iran 11 97 0.8× 98 2.1× 43 1.4× 7 0.3× 19 1.1× 17 425
Myriam Châabouni Tunisia 9 113 1.0× 114 2.4× 20 0.7× 6 0.3× 32 1.8× 21 202

Countries citing papers authored by Mehmet Tekman

Since Specialization
Citations

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

Fields of papers citing papers by Mehmet Tekman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mehmet Tekman

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

All Works

14 of 14 papers shown
1.
Jakiela, Julia, Saskia Hiltemann, Jonathan Manning, et al.. (2025). Galaxy as a gateway to bioinformatics: Multi-Interface Galaxy Hands-on Training Suite (MIGHTS) for scRNA-seq. GigaScience. 14.
2.
Schwan, Carsten, Sheikh Nizamuddin, Andrea Prunotto, et al.. (2025). TAF2 condensation in nuclear speckles links basal transcription factor TFIID to RNA splicing factors. Cell Reports. 44(5). 115616–115616. 1 indexed citations
3.
Tekman, Mehmet, Simone Probst, Sebastian Preißl, et al.. (2024). EOMES establishes mesoderm and endoderm differentiation potential through SWI/SNF-mediated global enhancer remodeling. Developmental Cell. 60(5). 735–748.e5. 9 indexed citations
4.
Probst, Simone, et al.. (2023). Eomes restricts Brachyury functions at the onset of mouse gastrulation. Developmental Cell. 58(18). 1627–1642.e7. 17 indexed citations
5.
Tekman, Mehmet, Sarah E. Flanagan, Lisa M. Guay‐Woodford, et al.. (2021). Founder mutation in the PMM2 promotor causes hyperinsulinemic hypoglycaemia/polycystic kidney disease (HIPKD). Molecular Genetics & Genomic Medicine. 9(12). e1674–e1674. 2 indexed citations
6.
Downie, Mallory L., Sanjana Gupta, Mehmet Tekman, et al.. (2021). Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy. Kidney International Reports. 6(6). 1669–1676. 3 indexed citations
7.
Mozere, Monika, Mehmet Tekman, Jameela A. Kari, et al.. (2018). OVAS: an open-source variant analysis suite with inheritance modelling. BMC Bioinformatics. 19(1). 46–46.
8.
Stabej, Polona Le Quesne, Chela James, Louise Ocaka, et al.. (2017). An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes. Orphanet Journal of Rare Diseases. 12(1). 24–24. 14 indexed citations
9.
Tekman, Mehmet, Alan Medlar, Monika Mozere, Robert Kleta, & Horia Stanescu. (2017). HaploForge: a comprehensive pedigree drawing and haplotype visualization web application. Bioinformatics. 33(24). 3871–3877. 5 indexed citations
10.
Rowczenio, Dorota, Daniela Iancu, Hadija Trojer, et al.. (2016). Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue—a case series and genetic exploration. Lara D. Veeken. 56(2). 209–213. 43 indexed citations
11.
Iancu, Daniela, et al.. (2016). Founder mutation inKCNJ10in Pakistani patients with EAST syndrome. Molecular Genetics & Genomic Medicine. 4(5). 521–526. 10 indexed citations
12.
Stabej, Polona Le Quesne, Hywel Williams, Chela James, et al.. (2015). STAG3 truncating variant as the cause of primary ovarian insufficiency. European Journal of Human Genetics. 24(1). 135–138. 42 indexed citations
13.
14.
Drury, Suzanne, C. R. Boustred, Mehmet Tekman, et al.. (2014). A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis—Further evidence of genotype–phenotype correlation. American Journal of Medical Genetics Part A. 164(7). 1777–1783. 21 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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