Michael L. DiLuna

3.3k total citations
98 papers, 1.6k citations indexed

About

Michael L. DiLuna is a scholar working on Surgery, Neurology and Genetics. According to data from OpenAlex, Michael L. DiLuna has authored 98 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Surgery, 37 papers in Neurology and 21 papers in Genetics. Recurrent topics in Michael L. DiLuna's work include Craniofacial Disorders and Treatments (12 papers), Scoliosis diagnosis and treatment (12 papers) and Glioma Diagnosis and Treatment (10 papers). Michael L. DiLuna is often cited by papers focused on Craniofacial Disorders and Treatments (12 papers), Scoliosis diagnosis and treatment (12 papers) and Glioma Diagnosis and Treatment (10 papers). Michael L. DiLuna collaborates with scholars based in United States, Türkiye and United Kingdom. Michael L. DiLuna's co-authors include Murat Günel, Kristopher T. Kahle, Richard P. Lifton, Daniel Durán, Ketan R. Bulsara, Veronica Chiang, Jason K. Karimy, Jonathan Knisely, J. Marc Simard and Brian V. Nahed and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Neurology.

In The Last Decade

Michael L. DiLuna

91 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael L. DiLuna United States 21 707 362 348 269 219 98 1.6k
Évelyne Emery France 26 986 1.4× 381 1.1× 638 1.8× 293 1.1× 184 0.8× 114 2.1k
Vera Van Velthoven Germany 29 895 1.3× 480 1.3× 480 1.4× 166 0.6× 222 1.0× 94 2.3k
Mustafa Uzan Türkiye 25 614 0.9× 358 1.0× 280 0.8× 105 0.4× 223 1.0× 105 1.7k
Marie‐Claire Y. de Wit Netherlands 26 406 0.6× 204 0.6× 233 0.7× 244 0.9× 420 1.9× 69 1.9k
Matthew T. Whitehead United States 20 282 0.4× 246 0.7× 173 0.5× 180 0.7× 243 1.1× 125 1.7k
Samuel Ignacio Pascual Pascual Spain 28 825 1.2× 599 1.7× 403 1.2× 114 0.4× 643 2.9× 188 2.5k
Naci Koçer Türkiye 30 1.7k 2.4× 382 1.1× 236 0.7× 714 2.7× 131 0.6× 140 2.6k
Shih‐Shan Lang United States 19 471 0.7× 280 0.8× 139 0.4× 100 0.4× 157 0.7× 80 1.1k
Dong Ik Kim South Korea 21 582 0.8× 716 2.0× 207 0.6× 214 0.8× 72 0.3× 89 2.4k
Andrew D. Parent United States 26 832 1.2× 342 0.9× 258 0.7× 114 0.4× 300 1.4× 65 1.8k

Countries citing papers authored by Michael L. DiLuna

Since Specialization
Citations

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

Fields of papers citing papers by Michael L. DiLuna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael L. DiLuna. 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 Michael L. DiLuna. The network helps show where Michael L. DiLuna may publish in the future.

Co-authorship network of co-authors of Michael L. DiLuna

This figure shows the co-authorship network connecting the top 25 collaborators of Michael L. DiLuna. A scholar is included among the top collaborators of Michael L. DiLuna 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 Michael L. DiLuna. Michael L. DiLuna 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.
2.
Jin, Sheng Chih, Rainelli Koumangoye, Stephanie M. Robert, et al.. (2021). Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelination. Clinical Genetics. 100(2). 176–186. 4 indexed citations
3.
Elsamadicy, Aladine A., Isaac G. Freedman, Andrew B. Koo, et al.. (2021). The Effects of Pulmonary Risk Factors on Hospital Resource Use After Posterior Spinal Fusion for Adolescent Idiopathic Scoliosis Correction. World Neurosurgery. 149. e737–e747. 2 indexed citations
4.
Elsamadicy, Aladine A., Isaac G. Freedman, Andrew B. Koo, et al.. (2020). Impact of Preoperative Anemia on Outcomes After Posterior Spinal Fusion for Adolescent Idiopathic Scoliosis. World Neurosurgery. 146. e214–e224. 3 indexed citations
5.
Koo, Andrew B., Jacky T. Yeung, Isaac G. Freedman, et al.. (2020). Clinical and economic burden of neurofibromatosis type 2 in the United States. Clinical Neurology and Neurosurgery. 197. 106053–106053. 2 indexed citations
6.
Elsamadicy, Aladine A., Andrew B. Koo, Megan Lee, et al.. (2020). Risk Factors Portending Extended Length of Stay After Suboccipital Decompression for Adult Chiari I Malformation. World Neurosurgery. 138. e515–e522. 2 indexed citations
7.
Antwi, Prince, Christopher S. Hong, Daniel Durán, et al.. (2018). A novel association of campomelic dysplasia and hydrocephalus with an unbalanced chromosomal translocation upstream of SOX9. Molecular Case Studies. 4(3). a002766–a002766. 6 indexed citations
8.
Fomchenko, Elena I., Daniel Durán, Sheng Chih Jin, et al.. (2018). De novo MYH9 mutation in congenital scalp hemangioma. Molecular Case Studies. 4(4). a002998–a002998. 7 indexed citations
9.
Chesler, David A., et al.. (2018). Non-syndromic single-suture craniosynostosis in triplets. Child s Nervous System. 34(6). 1241–1245. 3 indexed citations
10.
Karimy, Jason K., Jinwei Zhang, David B. Kurland, et al.. (2017). Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus. Nature Medicine. 23(8). 997–1003. 253 indexed citations
11.
Durán, Daniel, Sheng Chih Jin, Tyrone DeSpenza, et al.. (2016). Digenic mutations of human OCRL paralogs in Dent’s disease type 2 associated with Chiari I malformation. Human Genome Variation. 3(1). 16042–16042. 9 indexed citations
12.
Quon, Jennifer L., Ryan A. Grant, & Michael L. DiLuna. (2015). Multimodal evaluation of CSF dynamics following extradural decompression for Chiari malformation Type I. Journal of Neurosurgery Spine. 22(6). 622–630. 24 indexed citations
13.
Pfaff, Miles J., et al.. (2013). Transcranial nasoethmoidal dermoids: A review and rationale for approach. Journal of Plastic Reconstructive & Aesthetic Surgery. 66(12). 1725–1731. 7 indexed citations
14.
Beckett, Joel, Miles J. Pfaff, Michael L. DiLuna, & Derek M. Steinbacher. (2013). Dolichocephaly Without Sagittal Craniosynostosis. Journal of Craniofacial Surgery. 24(5). 1713–1715. 7 indexed citations
15.
Sanborn, Matthew R., Michael L. DiLuna, Robert G. Whitmore, & Phillip B. Storm. (2011). Fluoroscopically guided, transoral, closed reduction, and halo vest immobilization for an atypical C-1 fracture. Journal of Neurosurgery Pediatrics. 7(4). 380–382. 2 indexed citations
16.
DiLuna, Michael L., et al.. (2010). Primary Myxopapillary Ependymoma of the Medulla. Neurosurgery. 66(6). E1208–E1209. 9 indexed citations
17.
Bilgüvar, Kaya, Michael L. DiLuna, Matthew J. Bizzarro, et al.. (2009). COL4A1 Mutation in Preterm Intraventricular Hemorrhage. The Journal of Pediatrics. 155(5). 743–745. 47 indexed citations
18.
DiLuna, Michael L., Mohamad Bydon, Murat Günel, & Michele H. Johnson. (2009). Complications from cervical intra-arterial heroin injection: Figure 1. BMJ Case Reports. 2009. bcr2007118752–bcr2007118752. 1 indexed citations
19.
Tanrιöver, Gamze, et al.. (2008). PDCD10, THE GENE MUTATED IN CEREBRAL CAVERNOUS MALFORMATION 3, IS EXPRESSED IN THE NEUROVASCULAR UNIT. Neurosurgery. 62(4). 930–938. 30 indexed citations
20.
Güzel, Aslan, Mehmet Tatlı, Kaya Bilgüvar, et al.. (2007). Apparently novel genetic syndrome of pachygyria, mental retardation, seizure, and arachnoid cysts. American Journal of Medical Genetics Part A. 143A(7). 672–677. 8 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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