E. Ferda Perçin

2.3k total citations
80 papers, 1.3k citations indexed

About

E. Ferda Perçin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, E. Ferda Perçin has authored 80 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Genetics, 32 papers in Molecular Biology and 17 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in E. Ferda Perçin's work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Connective tissue disorders research (8 papers). E. Ferda Perçin is often cited by papers focused on Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Connective tissue disorders research (8 papers). E. Ferda Perçin collaborates with scholars based in Türkiye, Germany and United States. E. Ferda Perçin's co-authors include Nurten Akarsu, Mehmet Ali Ergün, F Skovby, Han G. Brunner, Elizabeth E. Capowski, Jessica Martin, Wim Brussel, Sarah Dickerson, M. Joseph Phillips and Kyle A. Wallace and has published in prestigious journals such as Nature Genetics, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

E. Ferda Perçin

74 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Ferda Perçin Türkiye 17 853 454 156 143 123 80 1.3k
Louise Brueton United Kingdom 24 908 1.1× 604 1.3× 126 0.8× 205 1.4× 154 1.3× 34 1.5k
Palma Finelli Italy 29 1.2k 1.5× 1.0k 2.3× 98 0.6× 211 1.5× 139 1.1× 95 2.2k
Pierre Bitoun France 17 1.4k 1.6× 818 1.8× 113 0.7× 144 1.0× 137 1.1× 39 1.9k
Bertrand Isidor France 26 1.3k 1.5× 908 2.0× 144 0.9× 107 0.7× 157 1.3× 112 2.1k
Luitgard M. Neumann Germany 20 708 0.8× 1.0k 2.2× 68 0.4× 110 0.8× 207 1.7× 46 1.7k
Roberto Mendoza‐Londono Canada 26 1.0k 1.2× 1.2k 2.6× 54 0.3× 151 1.1× 174 1.4× 85 2.1k
Anna Rajab Oman 23 1.2k 1.4× 628 1.4× 110 0.7× 180 1.3× 132 1.1× 58 1.9k
Alice Goldenberg France 20 678 0.8× 565 1.2× 124 0.8× 91 0.6× 100 0.8× 49 1.1k
Ariana Kariminejad Iran 21 756 0.9× 715 1.6× 80 0.5× 75 0.5× 207 1.7× 100 1.5k
Armand Bottani Switzerland 24 1.2k 1.5× 1.3k 2.9× 147 0.9× 302 2.1× 178 1.4× 62 2.2k

Countries citing papers authored by E. Ferda Perçin

Since Specialization
Citations

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

Fields of papers citing papers by E. Ferda Perçin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Ferda Perçin. 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 E. Ferda Perçin. The network helps show where E. Ferda Perçin may publish in the future.

Co-authorship network of co-authors of E. Ferda Perçin

This figure shows the co-authorship network connecting the top 25 collaborators of E. Ferda Perçin. A scholar is included among the top collaborators of E. Ferda Perçin 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 E. Ferda Perçin. E. Ferda Perçin 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.
Özaslan, Ahmet, et al.. (2021). Identification of copy number variants in children and adolescents with autism spectrum disorder: a study from Turkey. Molecular Biology Reports. 48(11). 7371–7378. 3 indexed citations
2.
Yurtçu, Erkan, Deniz Karçaaltıncaba, Hasan Hüseyin Kazan, et al.. (2020). Is cervical swab an efficient method for developing a new noninvasive prenatal diagnostic test for numerical and structural chromosome anomalies?. TURKISH JOURNAL OF MEDICAL SCIENCES. 51(3). 1043–1048. 2 indexed citations
3.
Koç, Altuğ, et al.. (2020). Warburg Micro Syndrome 1 due to Segmental Paternal Uniparental Isodisomy of Chromosome 2 Detected by Whole-Exome Sequencing and Homozygosity Mapping. Cytogenetic and Genome Research. 160(6). 309–315. 2 indexed citations
4.
Ergün, Mehmet Ali, et al.. (2020). Intelligent Ratio: A New Method for Carrier and Newborn Screening in Spinal Muscular Atrophy. Genetic Testing and Molecular Biomarkers. 24(9). 569–577. 4 indexed citations
5.
6.
Perçin, E. Ferda, et al.. (2018). THE 3rd W522X MUTATION IN EIF2AK3 GENE FROM TURKEY: A NEW PATIENT WITH WOLCOTT-RALLISON SYNDROME.. PubMed. 27(3). 411–418. 2 indexed citations
7.
Ergün, Mehmet Ali, et al.. (2018). Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome. Genetic Testing and Molecular Biomarkers. 22(8). 474–480. 8 indexed citations
8.
Korkmaz, Murat, et al.. (2017). Polymorphisms in the Growth Differentiation Factor 5 (GDF 5) Gene in Knee Osteoarthritis.. PubMed. 27(10). 602–605. 13 indexed citations
9.
Gümüş‐Akay, Güvem, et al.. (2017). LRP5-linked osteoporosis-pseudoglioma syndrome mimicking isolated microphthalmia. European Journal of Medical Genetics. 60(3). 200–204. 6 indexed citations
10.
11.
12.
Kurt, Gökhan, et al.. (2011). Spondylocostal dysostosis associated with type i split cord malformation and double nipple on one side: a case report. Turkish Neurosurgery. 23(2). 256–9. 11 indexed citations
13.
Karner, Courtney M., Martin Dietrich, Eric B. Johnson, et al.. (2010). Lrp4 Regulates Initiation of Ureteric Budding and Is Crucial for Kidney Formation – A Mouse Model for Cenani-Lenz Syndrome. PLoS ONE. 5(4). e10418–e10418. 49 indexed citations
14.
Koç, Altuğ, et al.. (2010). The importance of systematic genetic approach to familial schizophrenia cases and discussion of cryptic mosaic X chromosome aneuploidies in schizophrenia pathogenesis. International Journal of Psychiatry in Clinical Practice. 14(3). 204–211. 4 indexed citations
15.
Pınarbaşı, Ergün, et al.. (2007). Association of microsomal epoxide hydrolase gene polymorphism and pre‐eclampsia in Turkish women. Journal of obstetrics and gynaecology research. 33(1). 32–37. 17 indexed citations
16.
Çetin, Meral, et al.. (2005). No association of polymorphisms in the glutathione S‐transferase genes with pre‐eclampsia, eclampsia and HELLP syndrome in a Turkish population. Journal of obstetrics and gynaecology research. 31(3). 236–241. 12 indexed citations
17.
Malik, Sajid, E. Ferda Perçin, Wasim Ahmad, et al.. (2005). Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3. American Journal of Medical Genetics Part A. 134A(4). 404–408. 17 indexed citations
18.
Perçin, E. Ferda, et al.. (2003). A case with Pyle type metaphyseal dysplasia: clinical, radiological and histological evaluation.. PubMed. 14(4). 387–93. 3 indexed citations
19.
Bokhoven, Hans van, Jacopo Celli, Hülya Kayserili, et al.. (2000). Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome. Nature Genetics. 25(4). 423–426. 195 indexed citations
20.
Perçin, E. Ferda, et al.. (1999). Esterase D and ABO Polymorphisms in Turkish Population. DergiPark (Istanbul University). 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 Louise Brueton Breakdown of academic impact, for papers by Palma Finelli Breakdown of academic impact, for papers by Pierre Bitoun Breakdown of academic impact, for papers by Bertrand Isidor Breakdown of academic impact, for papers by Luitgard M. Neumann Breakdown of academic impact, for papers by Roberto Mendoza‐Londono Breakdown of academic impact, for papers by Anna Rajab Breakdown of academic impact, for papers by Alice Goldenberg Breakdown of academic impact, for papers by Ariana Kariminejad Breakdown of academic impact, for papers by Armand Bottani
Rankless by CCL
2026