Volkan Okur

796 total citations
15 papers, 205 citations indexed

About

Volkan Okur is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Volkan Okur has authored 15 papers receiving a total of 205 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Volkan Okur's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and RNA modifications and cancer (3 papers). Volkan Okur is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and RNA modifications and cancer (3 papers). Volkan Okur collaborates with scholars based in United States, Türkiye and United Kingdom. Volkan Okur's co-authors include Wendy K. Chung, Usha Krishnan, Shannon N. Nees, Dmitriy Niyazov, Jonathan Picker, Roy N. Alcalay, Ashley Wilson, Lindsay B. Henderson, Carolyn Applegate and Cem Yıldırım and has published in prestigious journals such as Annals of Neurology, Movement Disorders and British Journal of Ophthalmology.

In The Last Decade

Volkan Okur

15 papers receiving 204 citations

Peers

Countries citing papers authored by Volkan Okur

Since Specialization

Citations

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

Fields of papers citing papers by Volkan Okur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Volkan Okur

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease 2023 ·Circulation Genomic and Precision Medicine ·Thomas Hays, Rebecca Hernan, (unknown), (unknown), (unknown), (unknown), Ganga Krishnamurthy, (unknown), Atteeq U. Rehman, Amanda Thomas‐Wilson, Saurav Guha, (unknown), Volkan Okur, (unknown), Vanessa Felice, Avinash Abhyankar, Vaidehi Jobanputra, Wendy K. Chung	11
2	Predictive functional, statistical and structural analysis of CSNK2A1 and CSNK2B variants linked to neurodevelopmental diseases 2022 ·Frontiers in Molecular Biosciences ·(unknown), (unknown), Janice Weinberg, Volkan Okur, (unknown), Isabel Domínguez	9
3	Clinical and genomic characterization of 8p cytogenomic disorders 2021 ·Genetics in Medicine ·Volkan Okur, (unknown), (unknown), Caroline M. Mebane, Scott Robinson, Brynn Levy, Wendy K. Chung	3
4	Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1 2021 ·Movement Disorders ·Sarah A. O’Shea, Richard A. Hickman, Etty Cortés, Jean Paul Vonsattel, Stanley Fahn, Volkan Okur, Roy N. Alcalay, Wendy K. Chung	6
5	Early‐Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation 2020 ·Annals of Neurology ·Christine Kim, Thomas Wirth, Cécile Hubsch, Andrea H. Németh, Volkan Okur, Mathieu Anheim, Nathalie Drouot, Christine Tranchant, Gabrielle Rudolf, Jamel Chelly, Katrina Tatton‐Brown, Cornelis Blauwendraat, Jean Paul Vonsattel, Etty Cortés, Roy N. Alcalay, Wendy K. Chung	29
6	A novel homozygous variant in TRAPPC2L results in a neurodevelopmental disorder and disrupts TRAPP complex function 2020 ·Journal of Medical Genetics ·(unknown), Volkan Okur, Priyanka Ahimaz, Miroslav P. Milev, Zaheer M. Valivullah, Jacob Hagen, (unknown), Wendy K. Chung, Michael Sacher, Mythily Ganapathi	10
7	Biallelic variants in AGMO with diminished enzyme activity are associated with a neurodevelopmental disorder 2019 ·Human Genetics ·Volkan Okur, Katrin Watschinger, Dmitriy Niyazov, Julie McCarrier, Donald Basel, Martin Hermann, Ernst R. Werner, Wendy K. Chung	11
8	Homozygous noncanonical splice variant in LSM1 in two siblings with multiple congenital anomalies and global developmental delay 2019 ·Molecular Case Studies ·Volkan Okur, Charles A. LeDuc, Edwin R. Guzman, Zaheer M. Valivullah, Kwame Anyane‐Yeboa, Wendy K. Chung	4
9	Clinical and genetic characterization of individuals with predicted deleterious PHIP variants 2019 ·Molecular Case Studies ·(unknown), Volkan Okur, Ashley Wilson, Erica H. Gerkes, Keri Ramsey, Jennifer Heeley, Jane Juusola, Antonio Vitobello, (unknown), Laurence Faivre, Wendy K. Chung	18
10	Biallelic variants in VARS in a family with two siblings with intellectual disability and microcephaly: case report and review of the literature 2018 ·Molecular Case Studies ·Volkan Okur, Mythily Ganapathi, Ashley Wilson, Wendy K. Chung	4
11	Pulmonary hypertension in patients with 9q34.3 microdeletion‐associated Kleefstra syndrome 2018 ·American Journal of Medical Genetics Part A ·Volkan Okur, Shannon N. Nees, Wendy K. Chung, Usha Krishnan	16
12	De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features 2016 ·Human Genetics ·Volkan Okur, Megan T. Cho, Lindsay B. Henderson, Kyle Retterer, Michael Schneider, (unknown), Dmitriy Niyazov, Meron Azage, Sharon E. Smith, Jonathan Picker, Sharyn A. Lincoln, Mark A. Tarnopolsky, Lauren Brady, Hans T. Björnsson, Carolyn Applegate, (unknown), Rebecca Willaert, Berivan Baskin, Jane Juusola, Wendy K. Chung	53
13	Isolated recessive nail dysplasia caused byFZD6mutations: report of three families and review of the literature 2016 ·Clinical and Experimental Dermatology ·(unknown), (unknown), Neil Wilson, Volkan Okur, Christian Cole, C. David Hansen, Kristin Bosse, Regina C. Betz, (unknown), Frances J.D. Smith	8
14	Novel splice-site and missense mutations in theALDH1A3gene underlying autosomal recessive anophthalmia/microphthalmia 2014 ·British Journal of Ophthalmology ·(unknown), Ersan Kalay, Cem Yıldırım, (unknown), (unknown), Bayram Toraman, (unknown), (unknown), Volkan Okur, N. Lale Şatıroğlu-Tufan, Nurten Akarsu	17
15	HIF1A as a major vascular endothelial growth factor regulator: do its polymorphisms have an association with age‐related macular degeneration? 2014 ·Clinical and Experimental Ophthalmology ·Volkan Okur, (unknown), Ebru Nevin Çetin, (unknown), (unknown), Cem Yıldırım	6

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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