M. Alkan

440 total citations
13 papers, 317 citations indexed

About

M. Alkan is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, M. Alkan has authored 13 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cognitive Neuroscience. Recurrent topics in M. Alkan's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Cancer-related gene regulation (3 papers). M. Alkan is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Cancer-related gene regulation (3 papers). M. Alkan collaborates with scholars based in Switzerland, United States and Türkiye. M. Alkan's co-authors include D. Jasper G. Rees, Peter R. Winship, Gökçe Törüner, Celal Ülger, Joseph Rinaggio, Richard Wilk, Bin Tian, James Dermody, Marvin N. Schwalb and Meera Hameed and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Journal of Medical Genetics.

In The Last Decade

M. Alkan

13 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Alkan Switzerland 8 207 90 56 48 43 13 317
R. Tanner Hagelstrom United States 9 229 1.1× 75 0.8× 49 0.9× 38 0.8× 47 1.1× 16 325
Iskra Petković Croatia 11 179 0.9× 164 1.8× 53 0.9× 38 0.8× 20 0.5× 31 305
Molly C. Schroeder United States 9 203 1.0× 68 0.8× 26 0.5× 34 0.7× 45 1.0× 26 445
Detlef Trost France 10 224 1.1× 124 1.4× 39 0.7× 40 0.8× 51 1.2× 20 346
Caterina Barbieri Italy 9 228 1.1× 79 0.9× 18 0.3× 37 0.8× 40 0.9× 18 392
J.G. Dauwerse Netherlands 6 211 1.0× 129 1.4× 29 0.5× 16 0.3× 19 0.4× 7 307
Cinthya Zepeda‐Mendoza United States 9 122 0.6× 92 1.0× 32 0.6× 28 0.6× 11 0.3× 23 230
Kerry Baldwin Jedele Germany 9 123 0.6× 150 1.7× 28 0.5× 12 0.3× 11 0.3× 14 288
Ursula Giussani Italy 9 124 0.6× 90 1.0× 54 1.0× 17 0.4× 28 0.7× 16 226
Arvind Dev United States 12 521 2.5× 156 1.7× 69 1.2× 51 1.1× 37 0.9× 20 763

Countries citing papers authored by M. Alkan

Since Specialization
Citations

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

Fields of papers citing papers by M. Alkan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Alkan

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

All Works

13 of 13 papers shown
1.
Chetcuti, Albert, Safiye Aktaş, Celal Ülger, et al.. (2011). Expression profiling reveals MSX1 and EphB2 expression correlates with the invasion capacity of Wilms tumors. Pediatric Blood & Cancer. 57(6). 950–957. 23 indexed citations
2.
Törüner, Gökçe, Celal Ülger, M. Alkan, et al.. (2004). Association between gene expression profile and tumor invasion in oral squamous cell carcinoma. Cancer Genetics and Cytogenetics. 154(1). 27–35. 136 indexed citations
3.
Alkan, M., et al.. (2002). Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.. PubMed. 13(2). 151–6. 10 indexed citations
4.
Keser, İbrahim, Güven Lüleci, & M. Alkan. (2000). THE RESULTS OF MOLECULAR AND CYTOGENETIC ANALYSIS IN 6 FAMILIES WITH FRAGILE - X SYNDROME IN TURKEY. Marmara medical journal. 13(1). 7–10. 2 indexed citations
5.
Malik, Naseem, et al.. (1999). Rett syndrome and genetic drift. Brain and Development. 21(3). 175–178. 1 indexed citations
6.
Malik, N, et al.. (1993). Molecular genetic analysis of Turkish cystic fibrosis patients.. PubMed. 36(3). 144–9. 3 indexed citations
7.
Alkan, M., et al.. (1992). Arrangement of DYZ1 and DYZ2 repeats on the human Y-chromosome: a case with presence of DYZ1 and absence of DYZ2. Molecular and Cellular Probes. 6(3). 257–259. 9 indexed citations
8.
Tupler, Rossella, E. Bühler, M. Alkan, et al.. (1992). Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.. Journal of Medical Genetics. 29(1). 53–55. 26 indexed citations
9.
Liechti‐Gallati, Sabina, Naseem Malik, M. Alkan, et al.. (1991). Association between Haplotypes and Specific Mutations in Swiss Cystic Fibrosis Families. Pediatric Research. 30(4). 304–308. 8 indexed citations
10.
Liechti‐Gallati, Sabina, Volker Schneider, Marco Mächler, et al.. (1990). Haplotype analysis for CF‐linked DNA polymorphisms in Switzerland. Clinical Genetics. 37(6). 442–449. 3 indexed citations
11.
Malik, Naseem, et al.. (1990). Another model for the inheritance of Rett syndrome. American Journal of Medical Genetics. 36(1). 126–131. 28 indexed citations
12.
Winship, Peter R., D. Jasper G. Rees, & M. Alkan. (1989). DETECTION OF POLYMORPHISMS AT CYTOSINE PHOSPHOGUANADINE DINUCLEOTIDES AND DIAGNOSIS OF HAEMOPHILIA B CARRIERS. The Lancet. 333(8639). 631–634. 67 indexed citations
13.
Alkan, M., Stephen Wood, U. V. Borer, Sandra L. Hofmann, & E. Bühler. (1989). Physical mapping of D8S7 and D8S11 to the band 8p23.1 of the short arm of chromosome 8. Nucleic Acids Research. 17(20). 8395–8395. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by R. Tanner Hagelstrom Breakdown of academic impact, for papers by Iskra Petković Breakdown of academic impact, for papers by Molly C. Schroeder Breakdown of academic impact, for papers by Detlef Trost Breakdown of academic impact, for papers by Caterina Barbieri Breakdown of academic impact, for papers by J.G. Dauwerse Breakdown of academic impact, for papers by Cinthya Zepeda‐Mendoza Breakdown of academic impact, for papers by Kerry Baldwin Jedele Breakdown of academic impact, for papers by Ursula Giussani Breakdown of academic impact, for papers by Arvind Dev
Rankless by CCL
2026