Darren T. Oystreck

1.9k total citations
49 papers, 1.1k citations indexed

About

Darren T. Oystreck is a scholar working on Pathology and Forensic Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Darren T. Oystreck has authored 49 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Pathology and Forensic Medicine, 14 papers in Genetics and 13 papers in Molecular Biology. Recurrent topics in Darren T. Oystreck's work include Ophthalmology and Eye Disorders (21 papers), Genomic variations and chromosomal abnormalities (5 papers) and Craniofacial Disorders and Treatments (5 papers). Darren T. Oystreck is often cited by papers focused on Ophthalmology and Eye Disorders (21 papers), Genomic variations and chromosomal abnormalities (5 papers) and Craniofacial Disorders and Treatments (5 papers). Darren T. Oystreck collaborates with scholars based in Saudi Arabia, United States and South Africa. Darren T. Oystreck's co-authors include Thomas M. Bosley, Elizabeth C. Engle, Mustafa A. Salih, Ibrahim A. Alorainy, Khaled K. Abu‐Amero, Wai‐Man Chan, Caroline Andrews, Max A. Tischfield, Christopher J. Lyons and Robert P. Erickson and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

Darren T. Oystreck

47 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Darren T. Oystreck Saudi Arabia 19 451 386 336 197 171 49 1.1k
Emin Cumhur Şener Türkiye 15 375 0.8× 395 1.0× 184 0.5× 112 0.6× 89 0.5× 38 1.0k
Pei‐Lung Chen Taiwan 21 84 0.2× 530 1.4× 287 0.9× 145 0.7× 144 0.8× 102 1.4k
Chantal Daumerie Belgium 14 375 0.8× 233 0.6× 86 0.3× 112 0.6× 50 0.3× 25 1.0k
Jane S. Green Canada 19 256 0.6× 1.1k 2.8× 1.2k 3.6× 66 0.3× 119 0.7× 31 1.8k
Sarah MacKinnon United States 18 146 0.3× 448 1.2× 299 0.9× 84 0.4× 163 1.0× 33 891
Yoshifumi Kawanabe Japan 16 135 0.3× 658 1.7× 345 1.0× 251 1.3× 85 0.5× 51 1.4k
Julie Désir Belgium 19 73 0.2× 676 1.8× 529 1.6× 43 0.2× 99 0.6× 46 1.4k
Sibel Kantarci United States 15 126 0.3× 821 2.1× 1.0k 3.0× 49 0.2× 248 1.5× 23 1.8k
Guntram Borck Germany 27 68 0.2× 876 2.3× 681 2.0× 114 0.6× 113 0.7× 65 1.7k
Horia Stanescu United Kingdom 18 141 0.3× 536 1.4× 185 0.6× 90 0.5× 63 0.4× 42 1.3k

Countries citing papers authored by Darren T. Oystreck

Since Specialization
Citations

This map shows the geographic impact of Darren T. Oystreck'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 Darren T. Oystreck with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Darren T. Oystreck more than expected).

Fields of papers citing papers by Darren T. Oystreck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Darren T. Oystreck. 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 Darren T. Oystreck. The network helps show where Darren T. Oystreck may publish in the future.

Co-authorship network of co-authors of Darren T. Oystreck

This figure shows the co-authorship network connecting the top 25 collaborators of Darren T. Oystreck. A scholar is included among the top collaborators of Darren T. Oystreck 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 Darren T. Oystreck. Darren T. Oystreck 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.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Darren T. Oystreck, Arif O. Khan, & Thomas M. Bosley. (2014). Microdeletions involving Chromosomes 12 and 22 Associated with Syndromic Duane Retraction Syndrome. Ophthalmic Genetics. 35(3). 162–169. 3 indexed citations
2.
MacKinnon, Sarah, Darren T. Oystreck, Caroline Andrews, et al.. (2014). Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome. Ophthalmology. 121(7). 1461–1468. 50 indexed citations
3.
Chew, Sheena, Ravikumar Balasubramanian, Wai‐Man Chan, et al.. (2013). A novel syndrome caused by the E410K amino acid substitution in the neuronal β-tubulin isotype 3. Brain. 136(2). 522–535. 81 indexed citations
4.
Bosley, Thomas M., Khaled K. Abu‐Amero, & Darren T. Oystreck. (2013). Congenital cranial dysinnervation disorders. Current Opinion in Ophthalmology. 24(5). 398–406. 28 indexed citations
5.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Mustafa A. Salih, et al.. (2013). Ophthalmologic Observations in a Patient with Partial Mosaic Trisomy 8. Ophthalmic Genetics. 34(4). 249–253. 2 indexed citations
6.
Oystreck, Darren T., et al.. (2013). Variable Ptosis after Botulinum Toxin Type A Injection with Positive Ice Test Mimicking Ocular Myasthenia Gravis. Journal of Neuro-Ophthalmology. 33(2). 169–171. 4 indexed citations
7.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Ali Hellani, et al.. (2013). Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome. Ophthalmic Genetics. 36(2). 99–104. 3 indexed citations
8.
Abu‐Amero, Khaled K., Altaf A. Kondkar, Mustafa A. Salih, et al.. (2012). Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder. Ophthalmic Genetics. 34(1-2). 90–96. 17 indexed citations
9.
Webb, Bryn D., Sherin Shaaban, Harald Gaspar, et al.. (2012). HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1 Mice. The American Journal of Human Genetics. 91(1). 171–179. 53 indexed citations
10.
Oystreck, Darren T., José Morales, Imtiaz A. Chaudhry, et al.. (2012). Visual Loss in Orbitofacial Neurofibromatosis Type 1. Ophthalmology. 119(10). 2168–2173. 13 indexed citations
11.
Oystreck, Darren T., Elizabeth C. Engle, & Thomas M. Bosley. (2011). Recent Progress in Understanding Congenital Cranial Dysinnervation Disorders. Journal of Neuro-Ophthalmology. 31(1). 69–77. 54 indexed citations
12.
Bosley, Thomas M., Mustafa A. Salih, Ibrahim A. Alorainy, et al.. (2011). The neurology of carbonic anhydrase type II deficiency syndrome. Brain. 134(12). 3502–3515. 27 indexed citations
13.
Chaudhry, Imtiaz A., José Morales, Farrukh A. Shamsi, et al.. (2011). Orbitofacial neurofibromatosis: clinical characteristics and treatment outcome. Eye. 26(4). 583–592. 24 indexed citations
14.
Salih, Mustafa A., Darren T. Oystreck, Yasser H. Al‐Faky, et al.. (2010). Congenital Myasthenic Syndrome Due to Homozygous CHRNE Mutations: Report of Patients in Arabia. Journal of Neuro-Ophthalmology. 31(1). 42–47. 15 indexed citations
15.
Oystreck, Darren T., et al.. (2009). Comparison of the Accommodative Response in Amblyopic and Non-Amblyopic Eyes. Investigative Ophthalmology & Visual Science. 50(13). 4704–4704. 2 indexed citations
16.
Oystreck, Darren T., Arif O. Khan, Nada Al Tassan, et al.. (2009). Synergistic Divergence: A Distinct Ocular Motility Dysinnervation Pattern. Investigative Ophthalmology & Visual Science. 50(11). 5213–5213. 14 indexed citations
17.
Khan, Arif O., Darren T. Oystreck, M. Kœnig, & Mustafa A. Salih. (2007). Ophthalmic features of ataxia telangiectasia–like disorder. Journal of American Association for Pediatric Ophthalmology and Strabismus. 12(2). 186–189. 18 indexed citations
18.
Khan, Arif O. & Darren T. Oystreck. (2006). Clinical Characteristics of Bilateral Duane Syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 10(3). 198–201. 19 indexed citations
19.
Khan, M. Javed & Darren T. Oystreck. (2006). Fixation Preference for the Affected Eye in Patients With Unilateral Duane Syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 10(3). 275–276. 4 indexed citations
20.
Tischfield, Max A., Thomas M. Bosley, Mustafa A. Salih, et al.. (2005). Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nature Genetics. 37(10). 1035–1037. 206 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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