Fikret Erdogan

2.0k total citations
25 papers, 1.4k citations indexed

About

Fikret Erdogan is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Fikret Erdogan has authored 25 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 13 papers in Molecular Biology and 9 papers in Plant Science. Recurrent topics in Fikret Erdogan's work include Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (9 papers) and Congenital heart defects research (8 papers). Fikret Erdogan is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Chromosomal and Genetic Variations (9 papers) and Congenital heart defects research (8 papers). Fikret Erdogan collaborates with scholars based in Germany, Denmark and United Kingdom. Fikret Erdogan's co-authors include Reinhard Ullmann, Wei Chen, Hans‐Hilger Ropers, Andreas Tzschach, Vera M. Kalscheuer, H.-H. Ropers, George Kirov, Nadine Norton, Michael O’Donovan and L. Georgieva and has published in prestigious journals such as Nucleic Acids Research, Genome Research and Human Molecular Genetics.

In The Last Decade

Fikret Erdogan

24 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fikret Erdogan Germany 18 951 799 196 155 143 25 1.4k
Roberto Ciccone Italy 23 956 1.0× 681 0.9× 270 1.4× 283 1.8× 82 0.6× 51 1.4k
Peter M. Kroisel Austria 16 658 0.7× 935 1.2× 172 0.9× 148 1.0× 83 0.6× 38 1.5k
Marijke Bauters Belgium 17 911 1.0× 809 1.0× 138 0.7× 90 0.6× 199 1.4× 25 1.3k
Willy M. Nillesen Netherlands 23 1.3k 1.3× 1.3k 1.6× 247 1.3× 271 1.7× 156 1.1× 42 2.2k
Dorien Lugtenberg Netherlands 18 920 1.0× 1.0k 1.3× 97 0.5× 97 0.6× 209 1.5× 34 1.6k
Maria Antonietta Mencarelli Italy 26 1.2k 1.2× 982 1.2× 110 0.6× 105 0.7× 354 2.5× 65 1.9k
Katherine Lachlan United Kingdom 19 659 0.7× 869 1.1× 84 0.4× 82 0.5× 122 0.9× 45 1.4k
N R Dennis United Kingdom 20 793 0.8× 628 0.8× 157 0.8× 98 0.6× 152 1.1× 32 1.3k
Gotthold Barbi Germany 17 632 0.7× 560 0.7× 127 0.6× 188 1.2× 130 0.9× 59 1.1k
Marjorie Withers United States 17 1.1k 1.2× 925 1.2× 412 2.1× 150 1.0× 86 0.6× 23 1.6k

Countries citing papers authored by Fikret Erdogan

Since Specialization
Citations

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

Fields of papers citing papers by Fikret Erdogan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fikret Erdogan

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

All Works

20 of 20 papers shown
1.
Kariminejad, Roxana, Allan Lind-Thomsen, Zeynep Tümer, et al.. (2011). High frequency of rare copy number variants affecting functionally related genes in patients with structural brain malformations. Human Mutation. 32(12). 1427–1435. 24 indexed citations
2.
Schneider, Katja, Dimo Dietrich, Michael Fleischhacker, et al.. (2011). Correlation of SHOX2 Gene Amplification and DNA Methylation in Lung Cancer Tumors. BMC Cancer. 11(1). 102–102. 58 indexed citations
3.
Tzschach, Andreas, Corinna Menzel, Fikret Erdogan, et al.. (2010). Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement. American Journal of Medical Genetics Part A. 152A(4). 1008–1012. 16 indexed citations
4.
Chen, Wei, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2008). Mapping translocation breakpoints by next-generation sequencing. Genome Research. 18(7). 1143–1149. 102 indexed citations
5.
Shoichet, Sarah A., Stefan Waibel, Anne D. Sperfeld, et al.. (2008). Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization. Amyotrophic Lateral Sclerosis. 10(3). 162–167. 15 indexed citations
6.
Tzschach, Andreas, Christina Kelbova, Hartmut Peters, et al.. (2008). Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23). Ophthalmic Genetics. 29(1). 37–40. 6 indexed citations
7.
Erdogan, Fikret, Lars Allan Larsen, Litu Zhang, et al.. (2008). High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease. Journal of Medical Genetics. 45(11). 704–709. 86 indexed citations
8.
Walczak‐Sztulpa, Joanna, Marzena Wiśniewska, Anna Latos‐Bieleńska, et al.. (2008). Chromosome deletions in 13q33–34: Report of four patients and review of the literature. American Journal of Medical Genetics Part A. 146A(3). 337–342. 72 indexed citations
9.
Kirov, George, Wei Chen, Nadine Norton, et al.. (2007). Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics. 17(3). 458–465. 271 indexed citations
10.
Tzschach, Andreas, Wei Chen, Fikret Erdogan, et al.. (2007). Characterization of interstitial Xp duplications in two families by tiling path array CGH. American Journal of Medical Genetics Part A. 146A(2). 197–203. 29 indexed citations
11.
Ullmann, Reinhard, Gillian Turner, Maria Kirchhoff, et al.. (2007). Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation. Human Mutation. 28(7). 674–682. 204 indexed citations
12.
Tzschach, Andreas, Corinna Menzel, Fikret Erdogan, et al.. (2007). Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH. American Journal of Medical Genetics Part A. 143A(4). 333–337. 14 indexed citations
13.
Bartsch, Oliver, Fikret Erdogan, Reinhard Ullmann, et al.. (2007). Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 <i>(NF1)</i> microdeletion, in a girl with neurofibromatosis. Cytogenetic and Genome Research. 119(1-2). 158–164. 7 indexed citations
14.
Erdogan, Fikret, Reinhard Ullmann, Wei Chen, et al.. (2006). Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay. American Journal of Medical Genetics Part A. 143A(2). 172–178. 46 indexed citations
15.
Klopocki, Eva, Britta Fiebig, Peter N. Robinson, et al.. (2006). A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2. American Journal of Medical Genetics Part A. 140A(8). 873–877. 20 indexed citations
16.
Erdogan, Fikret, Wei Chen, Maria Kirchhoff, et al.. (2006). Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research. 115(3-4). 247–253. 58 indexed citations
17.
Chen, Wei, et al.. (2005). CGHPRO – A comprehensive data analysis tool for array CGH. BMC Bioinformatics. 6(1). 85–85. 86 indexed citations
18.
Garshasbi, Masoud, Mohammad Mahdi Motazacker, Kimia Kahrizi, et al.. (2005). SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Human Genetics. 118(6). 708–715. 60 indexed citations
19.
Erdogan, Fikret. (2001). Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarrays. Nucleic Acids Research. 29(7). 36e–36. 66 indexed citations
20.
Erdogan, Fikret, et al.. (2000). Analysis of theNF1 gene by temperature gradient gel electrophoresis reveals a high incidence of mutations in exon 4b. Electrophoresis. 21(3). 541–544. 25 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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