Gökhan Uyanık

2.8k total citations
42 papers, 1.2k citations indexed

About

Gökhan Uyanık is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gökhan Uyanık has authored 42 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gökhan Uyanık's work include Muscle Physiology and Disorders (9 papers), Mitochondrial Function and Pathology (7 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Gökhan Uyanık is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Mitochondrial Function and Pathology (7 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Gökhan Uyanık collaborates with scholars based in Germany, Türkiye and Austria. Gökhan Uyanık's co-authors include William B. Dobyns, Ute Hehr, Eva Klopocki, Denise Horn, Kerstin Kutsche, Déborah Morris-Rosendahl, Thomas D. Cushion, Daniela T. Pilz, Mark I. Rees and Haluk Topaloğlu and has published in prestigious journals such as Nature Genetics, PLoS ONE and Brain.

In The Last Decade

Gökhan Uyanık

41 papers receiving 1.2k citations

Peers

Gökhan Uyanık
Jean‐Baptiste Rivière Canada
Yoann Saillour France
Norimasa Mitsuma Japan
Carlos Cardoso France
Saad Al Shahwan Saudi Arabia
Emmanuelle Buhler France
Lam Son Nguyen Australia
Konstantinos Zarbalis United States
Tatsuro Kumada Japan
Pedro Mancías United States
Jean‐Baptiste Rivière Canada
Gökhan Uyanık
Citations per year, relative to Gökhan Uyanık Gökhan Uyanık (= 1×) peers Jean‐Baptiste Rivière

Countries citing papers authored by Gökhan Uyanık

Since Specialization
Citations

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

Fields of papers citing papers by Gökhan Uyanık

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gökhan Uyanık

This figure shows the co-authorship network connecting the top 25 collaborators of Gökhan Uyanık. A scholar is included among the top collaborators of Gökhan Uyanık 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 Gökhan Uyanık. Gökhan Uyanık 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.
Uyanık, Gökhan, et al.. (2025). Precise Gene Editing Technologies in Retinal Applications. Advances in experimental medicine and biology. 1468. 119–123. 1 indexed citations
2.
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Haschka, Judith, Katharina M. Roetzer, Gökhan Uyanık, et al.. (2022). Identifying adult hypophosphatasia in the rheumatology unit. Osteologie/Osteology. 31(3). 227–228. 1 indexed citations
4.
Uyanık, Gökhan, et al.. (2022). How Did SARS-CoV-2 Pandemic Affect the Cats’ Health in Hatay Province? A retrospective study. Topics in companion animal medicine. 50. 100696–100696. 1 indexed citations
5.
Heibl, Sonja, Bettina Gisslinger, Peter Bettelheim, et al.. (2020). Clinical, Hematologic, Biologic and Molecular Characteristics of Patients with Myeloproliferative Neoplasms and a Chronic Myelomonocytic Leukemia-Like Phenotype. Cancers. 12(7). 1891–1891. 4 indexed citations
6.
Fratzl‐Zelman, Nadja, Sonja Gamsjaeger, Stéphane Blouin, et al.. (2020). Alterations of bone material properties in adult patients with X-linked hypophosphatemia (XLH). Journal of Structural Biology. 211(3). 107556–107556. 25 indexed citations
7.
Zenz, Peter, Christian Wurnig, Alfred Engel, et al.. (2018). HFE hemochromatosis screening in patients with severe hip osteoarthritis: A prospective cross-sectional study. PLoS ONE. 13(11). e0207415–e0207415. 4 indexed citations
8.
Roetzer, Katharina M., Gökhan Uyanık, A. Brehm, et al.. (2017). Novel familial mutation of LRP5 causing high bone mass: Genetic analysis, clinical presentation, and characterization of bone matrix mineralization. Bone. 107. 154–160. 18 indexed citations
9.
Bierhals, Tatjana, et al.. (2013). Pontocerebellar hypoplasia type 2 and TSEN2: Review of the literature and two novel mutations. European Journal of Medical Genetics. 56(6). 325–330. 23 indexed citations
10.
Cushion, Thomas D., William B. Dobyns, Jonathan G.L. Mullins, et al.. (2013). Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain. 136(2). 536–548. 101 indexed citations
11.
Kortüm, Fanny, Soma Das, Déborah Morris-Rosendahl, et al.. (2011). The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. Journal of Medical Genetics. 48(6). 396–406. 179 indexed citations
12.
Najm, Juliane, Denise Horn, Isabella Wimplinger, et al.. (2008). Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics. 40(9). 1065–1067. 202 indexed citations
13.
Yiş, Uluç, Gökhan Uyanık, Semra Hız Kurul, et al.. (2006). A case of Walker–Warburg syndrome resulting from a homozygous POMT1 mutation. European Journal of Paediatric Neurology. 11(1). 46–49. 10 indexed citations
14.
Koch, Horst J., et al.. (2006). Relation between Laterality and Immune Response after Acute Cerebral Ischemia. NeuroImmunoModulation. 13(1). 8–12. 18 indexed citations
15.
Koch, Horst, et al.. (2005). Memantine: A Therapeutic Approach in Treating Alzheimers and Vascular Dementia. PubMed. 4(5). 499–506. 18 indexed citations
16.
Hahn, Andrew D., et al.. (2004). X-Linked Lissencephaly with Abnormal Genitalia Associated with Renal Phosphate Wasting. Neuropediatrics. 35(3). 202–205. 13 indexed citations
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Tercanli, Sevgi, et al.. (2000). Increased Nuchal Translucency in a Case of Long-Chain 3-Hydroxyacyl- Coenzyme A Dehydrogenase Deficiency. Fetal Diagnosis and Therapy. 15(6). 322–325. 6 indexed citations
19.
Buguet, Alain, Sylvie Bisser, E. Omer Burgert, et al.. (1996). <i>BaI</i>l and <i>Msp</i>I Polymorphisms of the Dopamine D3 Receptor Gene in African Blacks and Caucasians. Human Heredity. 46(1). 58–60. 8 indexed citations
20.
Griffon, Nathalie, M.A. Crocq, Caroline Pilon, et al.. (1996). Dopamine D3 receptor gene: Organization, transcript variants, and polymorphism associated with schizophrenia. American Journal of Medical Genetics. 67(1). 63–70. 59 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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