E. Ferda Perçin

2.3k citations

80 papers · 1.3k indexed · h-index 17

Impact in

Developmental Biology top 5%
- Congenital limb and hand anomalies
Genetics top 5%
- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Genetics 43
- Genomic variations and chromosomal abnormalities 10
- Connective tissue disorders research 8
- Congenital Ear and Nasal Anomalies 7
- Genetics and Neurodevelopmental Disorders 6
Molecular Biology 32
- Congenital heart defects research 5

Co-authors: Nurten Akarsu (5 shared papers)Mehmet Ali Ergün (27 shared papers)Sevim Balcı (1 shared paper)Lynda S. Wright (2 shared papers)Jessica Martin (2 shared papers)Sarah Dickerson (2 shared papers)Han G. Brunner (1 shared paper)David M. Gamm (2 shared papers)
Journals: European Journal of Medical Genetics (4 papers)Nature Genetics (2 papers)Gene (2 papers)Clinical Genetics (2 papers)Journal of Intellectual Disability Research (1 paper)
Partner nations: Türkiye Germany United States

In The Last Decade

E. Ferda Perçin

74 papers receiving 1.3k citations

Peers

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-authors

The 25 scholars most cited alongside E. Ferda Perçin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E. Ferda Perçin Line = papers co-authored together E. Ferda Perçin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Human microphthalmia associated with mutations in the retinal homeobox gene CHX10 Nature Genetics ·E. Ferda Perçin, Ploder La, Yu Jj, Mustafa Kemal Arıcı, Horsford Dj, A.J. Rutherford, Bharati Bapat, Cox Dw, Duncan Am, Kalnins Vi, Ayse G. Koçak-Altintas, Jane C. Sowden, Elias I. Traboulsi, M. Sarfarazi, McInnes Rr	2000	222
2	Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome Nature Genetics ·Hans van Bokhoven, Jacopo Celli, Hülya Kayserili, Ellen van Beusekom, Sevim Balcı, Wim Brussel, F Skovby, Bronwyn Kerr, E. Ferda Perçin, Nurten Akarsu, Han G. Brunner	2000	195
3	Blood-Derived Human iPS Cells Generate Optic Vesicle–Like Structures with the Capacity to Form Retinal Laminae and Develop Synapses Investigative Ophthalmology & Visual Science ·M. Joseph Phillips, Kyle A. Wallace, Sarah Dickerson, Michael J. Miller, Amelia D. Verhoeven, Jessica Martin, Lynda S. Wright, Wei Shen, Elizabeth E. Capowski, E. Ferda Perçin, Enio T. Perez, Xiufeng Zhong, Marta Soler, David M. Gamm	2012	161
4	Modeling Human Retinal Development with Patient-Specific Induced Pluripotent Stem Cells Reveals Multiple Roles for Visual System Homeobox 2 Stem Cells ·M. Joseph Phillips, Enio T. Perez, Jessica Martin, Samantha T. Reshel, Kyle A. Wallace, Elizabeth E. Capowski, Ruchira Singh, Lynda S. Wright, Eric M. Clark, Patrick Barney, Ron Stewart, Sarah Dickerson, Michael J. Miller, E. Ferda Perçin, James A. Thomson, David M. Gamm	2014	98
5	Lrp4 Regulates Initiation of Ureteric Budding and Is Crucial for Kidney Formation – A Mouse Model for Cenani-Lenz Syndrome PLoS ONE ·Courtney M. Karner, Martin Dietrich, Eric B. Johnson, Kappesser Natalie, Tennert Christian, E. Ferda Perçin, Bernd Wollnik, Thomas J. Carroll, Joachim Herz	2010	49
6	Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis Clinical Genetics ·Sangamitra Boppudi, Nina Bögershausen, Hanne Hove, E. Ferda Perçin, Deniz Aslan, Radovan Dvorský, Gülsüm Kayhan, Y. Li, Claus Cursiefen, I. Tantcheva‐Poór, Peter Bjerre Toft, Oliver Bartsch, Christina Lißewski, Ilse Wieland, Sibylle Jakubiczka, Bernd Wollnik, Mohammad Reza Ahmadian, Ludwig M. Heindl, Martin Zenker	2016	45
7	ABCB1 C3435T polymorphism is associated with susceptibility to major depression, but not with a clinical response to citalopram in a Turkish population Pharmacological Reports ·Gül Özbey, Berna Yucel, Serap Erdoğan Taycan, Derya Kan, Nurdan Eren Bodur, Tayyibe Arslan, E. Ferda Perçin, Nevzat Yüksel, Cüneyt Güzey, Canan Uluoğlu	2014	36
8	Y chromosome azoospermia factor region microdeletions and recurrent pregnancy loss American Journal of Obstetrics and Gynecology ·Abdullah Karaer, Kadri Karaer, Gülnur Özakşit, Serdar Ceylaner, E. Ferda Perçin	2008	32
9	An unexpected finding in a child with neurological problems: mosaic ring chromosome 18 European Journal of Pediatrics ·Altuğ Koç, Derya Kan, Kadri Karaer, Mehmet Ali Ergün, Meral Yirmibeş Karaoğuz, Kıvılcım Gücüyener, Sophie Hinreiner, Thomas Liehr, E. Ferda Perçin	2007	26
10	TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia American Journal of Medical Genetics Part A ·Yasemin Alanay, Bekir Ergüner, Eda Ütine, Orçun Haçarız, Pelin Özlem Şimşek‐Kiper, Ekim Z. Taşkıran, E. Ferda Perçin, Elif Uz, Mahmut Şamil Sağıroğlu, Bayram Yüksel, Koray Boduroğlu, Nurten Akarsu	2013	23
11	Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type The American Journal of Human Genetics ·Sajid Malik, E. Ferda Perçin, Dorothea Bornholdt, Beate Albrecht, Antonio Percesepe, Manuela C. Koch, Antonio Landi, Bárbara Fritz, Rizwan Khan, Sara Mumtaz, Nurten Akarsu, Karl‐Heinz Grzeschik	2014	22
12	A Turkish family with Nance-Horan syndrome due to a novel mutation Gene ·Esra Tuğ, Nihal F. Dilek, Shahrbanou Javadiyan, Kathryn P. Burdon, E. Ferda Perçin	2013	22
13	Influence of Folate-Related Gene Polymorphisms on High-Dose Methotrexate-Related Toxicity and Prognosis in Turkish Children with Acute Lymphoblastic Leukemia Turkish Journal of Hematology ·Burcu Yazıcıoğlu, Zühre Kaya, Sezen Güntekin Ergün, E. Ferda Perçin, Ülker Koçak, İdil Yenicesu, Türkiz Gursel	2016	21
14	MEFV gene mutations and its impact on the clinical course in ulcerative colitis patients Rheumatology International ·Beytullah Yıldırım, Candan Tunçer, Derya Kan, Bilge Tunç, Mehmet Derya Demirağ, E. Ferda Perçin, Şeminur Haznedaroğlu, Hakan Alagözlü	2010	19
15	Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3 American Journal of Medical Genetics Part A ·Sajid Malik, E. Ferda Perçin, Wasim Ahmad, Sıtkı Perçin, Nurten Akarsu, Manuela C. Koch, Karl‐Heinz Grzeschik	2005	17
16	Association of microsomal epoxide hydrolase gene polymorphism and pre‐eclampsia in Turkish women Journal of obstetrics and gynaecology research ·Ergün Pınarbaşı, E. Ferda Perçin, Meral Yılmaz, Egemen Akgün, Meral Çetin, Ali Çetin	2007	17
17	First-Trimester Diagnosis of Robinow Syndrome Fetal Diagnosis and Therapy ·E. Ferda Perçin, Tevfik Güvenal, Ali Çetin, Sıtkı Perçin, Fahrettin Göze, Sema Arıcı	2001	16
18	Thiopurine methyltransferase polymorphisms and mercaptopurine tolerance in Turkish children with acute lymphoblastic leukemia Cancer Chemotherapy and Pharmacology ·Meryem Albayrak, Uljan Konyssova, Zühre Kaya, Türkiz Gursel, Sezen Güntekin, E. Ferda Perçin, Ülker Koçak	2011	16
19	Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I? Journal of Medical Genetics ·E. Ferda Perçin, Sıtkı Perçin, Hatice Reyhan Eğilmez, I Sezgin, F Ozbas, Nurten Akarsu	1998	14
20	Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population Journal of Pediatric Hematology/Oncology ·Hülya Kayılıoğlu, Ülker Koçak, Derya Karaer, E. Ferda Perçin, Ertan Sal, Funda Tekkeşin, Melek Işık, Nergiz Öner, Fatma Burcu Belen, Ebru Yılmaz Keskin, Arzu Okur, Meryem Albayrak, Zühre Kaya, Faruk Güçlü Pınarlı, İdil Yenicesu, Ceyda Karadeniz, Aynur Oğuz, Türkiz Gursel	2017	14

About E. Ferda Perçin

E. Ferda Perçin is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 80 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (8 papers), Congenital limb and hand anomalies (8 papers), Congenital Ear and Nasal Anomalies (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Congenital heart defects research (5 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Developmental Biology (85 citations), Genetics (454 citations), Molecular Biology (853 citations), Genetics (99 citations) and Cellular and Molecular Neuroscience (156 citations). E. Ferda Perçin has collaborated with scholars based in Türkiye, Germany and United States. Frequent co-authors include Nurten Akarsu, Mehmet Ali Ergün, Sevim Balcı, Lynda S. Wright, Jessica Martin, Sarah Dickerson, Han G. Brunner, David M. Gamm, Enio T. Perez and Ellen van Beusekom. Their work appears in journals such as European Journal of Medical Genetics, Nature Genetics, Gene, Clinical Genetics and Journal of Intellectual Disability Research.

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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