Cihangir Özkınay

832 total citations
46 papers, 577 citations indexed

About

Cihangir Özkınay is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Cihangir Özkınay has authored 46 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 11 papers in Molecular Biology. Recurrent topics in Cihangir Özkınay's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (4 papers). Cihangir Özkınay is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (4 papers). Cihangir Özkınay collaborates with scholars based in Türkiye, United States and Sweden. Cihangir Özkınay's co-authors include Ferda Özkınay, Fadıl Vardar, Zafer Kurugöl, Özgür Çoğulu, Hüseyin Önay, Sacide Pehlıvan, Cumhur Gündüz, Güldane Koturoğlu, Felix Mitelman and Selda Erensoy and has published in prestigious journals such as Journal of Medical Genetics, Acta Paediatrica and Otolaryngology.

In The Last Decade

Cihangir Özkınay

44 papers receiving 550 citations

Peers

Countries citing papers authored by Cihangir Özkınay

Since Specialization

Citations

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

Fields of papers citing papers by Cihangir Özkınay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cihangir Özkınay

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Interferon-γ gene and interferon-γ receptor-1 gene polymorphisms in children with tuberculosis from Turkey 2010 ·Scandinavian Journal of Infectious Diseases ·Hüseyin Önay, (unknown), Burak Durmaz, (unknown), (unknown), Nuri Bayram, Demet Can, Haluk Akın, Cihangir Özkınay, Ferda Özkınay	12
2	Association between IL4 (–590), ACE (I)/(D), CCR5 (Δ32), CTLA4 (+49) and IL1-RN (VNTR in intron 2) gene polymorphisms and vitiligo 2009 ·European Journal of Dermatology ·Sacide Pehlıvan, Ferda Özkınay, Sibel Alper, Hüseyin Önay, (unknown), Mustafa Pehlıvan, Cihangir Özkınay	29
3	Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review 2009 ·Journal of Assisted Reproduction and Genetics ·(unknown), Ferda Özkınay, Derya Erçal, Özgür Çoğulu, (unknown), Barış Altay, Erol Tavmergen, Cumhur Gündüz, Cihangir Özkınay	36
4	Role of angiotensin‐converting enzyme gene polymorphisms in children with sepsis and septic shock 2008 ·Pediatrics International ·Özgür Çoğulu, Hüseyin Önay, (unknown), Cumhur Gündüz, Sacide Pehlıvan, Fadıl Vardar, (unknown), Cihangir Özkınay, Ferda Özkınay	16
5	THE EPIDEMIOLOGY OF HEPATITIS A INFECTION IN THE POPULATION OF BORNOVA, IZMIR, TURKEY 2007 ·DergiPark (Istanbul University) ·Ferda Özkınay, Zafer Kurugöl, Güldane Koturoğlu, Tijen Özacar, İmre Altuğlu, Fadıl Vardar, Cumhur Gündüz, Cihangir Özkınay	6
6	İZMİR'DE HEPATİT A ENFEKSİYONU EPİDEMİYOLOJİSİ 2007 ·Ege Tıp Dergisi ·Ferda Özkınay, Zafer Kurugöl, Güldane Koturoğlu, Tijen Özacar, İmre Altuğlu, Fadıl Vardar, Cumhur Gündüz, Cihangir Özkınay	1
7	Complications of varicella in healthy children in Izmir, Turkey 2005 ·Pediatrics International ·Güldane Koturoğlu, Zafer Kurugöl, (unknown), (unknown), Fadıl Vardar, Mehmet Rami Helvacı, (unknown), Ferda Özkınay, Cihangir Özkınay	33
8	Hair zinc level in Down syndrome 2004 ·Down Syndrome Research and Practice ·(unknown), Ferda Özkınay, Özgür Çoğulu, Canan Çöker, (unknown), (unknown), (unknown), Cihangir Özkınay	12
9	Evaluation of Telomerase mRNA (hTERT) in Childhood Acute Leukemia 2004 ·Leukemia & lymphoma ·Özgür Çoğulu, Buket Kosova, Emin Karaca, Cumhur Gündüz, Ferda Özkınay, Serap Aksoylar, (unknown), Mehmet Kantar, (unknown), Deniz Yılmaz Karapınar, (unknown), (unknown), Canan Vergin, Cihangir Özkınay	16
10	Evaluation of 80 children with prolonged fever 2003 ·Pediatrics International ·Özgür Çoğulu, Güldane Koturoğlu, Zafer Kurugöl, Ferda Özkınay, Fadıl Vardar, Cihangir Özkınay	27
11	Celiac disease in children with Down syndrome: Importance of follow‐up and serologic screening 2003 ·Pediatrics International ·Özgür Çoğulu, Ferda Özkınay, Cumhur Gündüz, Tufan Çankaya, Sema Aydoğdu, Funda Özgenç, Necil Kütükçüler, Cihangir Özkınay	21
12	New chromosome rearrangement in acute lymphoblastic leukemia 2002 ·Cancer Genetics and Cytogenetics ·Cumhur Gündüz, Özgür Çoğulu, (unknown), Mehmet Kantar, Tufan Çankaya, Cihangir Özkınay, Ferda Özkınay	4
13	Cerebro‐costo‐mandibular syndrome: A case report 2001 ·Pediatrics International ·Ferda Özkınay, Özgür Çoğulu, Cumhur Gündüz, Tufan Çankaya, Cihangir Özkınay	5
14	PROTEUS SENDROMU (OLGU SUNUMU) 2000 ·Ege Tıp Dergisi ·Ferda Özkınay, Özgür Çoğulu, Nuri Bayram, Cumhur Gündüz, Cihangir Özkınay	0
15	İDİYOPATİK MENTAL RETARDASYONLARDA FRAJİL-X SENDROMU ARAŞTIRILMASI 2000 ·Ege Tıp Dergisi ·Cumhur Gündüz, Özgür Çoğulu, Cihangir Özkınay, Sarenur Tütüncüoğlu, (unknown), (unknown), Ferda Özkınay	1
16	FISH analysis with locus‐specific probes in sperm from two translocation carrier men 1999 ·Clinical Genetics ·(unknown), (unknown), (unknown), Sevilhan Artan, (unknown), Seher Başaran, Cihangir Özkınay	4
17	Multiple pterygium syndrome 1997 ·The Indian Journal of Pediatrics ·Ferda Özkınay, Cihangir Özkınay, Haluk Akın, (unknown), Cumhur Gündüz	3
18	A case of Marden‐Walker syndrome with Dandy‐Walker malformation 1995 ·Clinical Genetics ·Ferda Özkınay, (unknown), Ali Rahmi Bakiler, (unknown), (unknown), Cihangir Özkınay, (unknown), (unknown)	3
19	Acromesomelic-spondyloepiphyseal dysplasia associated with congenital optic atrophy: Report of a family 1993 ·Pediatric Radiology ·R. N. Şener, (unknown), Cihangir Özkınay, Ayşenur Memiş, Orhan Oyar	2
20	Consanguineous marriages among parents of Down patients 1992 ·Clinical Genetics ·(unknown), Asım Cenani, Bekir Sıtkı Şaylı, Cihangir Özkınay, Sevilhan Artan, (unknown), (unknown), (unknown)	10

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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