Elizabeth C. Engle

9.2k total citations
112 papers, 4.4k citations indexed

About

Elizabeth C. Engle is a scholar working on Pathology and Forensic Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Elizabeth C. Engle has authored 112 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Pathology and Forensic Medicine, 42 papers in Genetics and 38 papers in Molecular Biology. Recurrent topics in Elizabeth C. Engle's work include Ophthalmology and Eye Disorders (56 papers), Craniofacial Disorders and Treatments (21 papers) and Axon Guidance and Neuronal Signaling (16 papers). Elizabeth C. Engle is often cited by papers focused on Ophthalmology and Eye Disorders (56 papers), Craniofacial Disorders and Treatments (21 papers) and Axon Guidance and Neuronal Signaling (16 papers). Elizabeth C. Engle collaborates with scholars based in United States, United Kingdom and Saudi Arabia. Elizabeth C. Engle's co-authors include Wai‐Man Chan, Max A. Tischfield, Caroline Andrews, Joseph L. Demer, Thomas M. Bosley, Darren T. Oystreck, Robert A. Clark, David G. Hunter, Alan H. Beggs and Irène Gottlob and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Elizabeth C. Engle

108 papers receiving 4.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elizabeth C. Engle United States	39	1.9k	1.7k	1.2k	799	631	112	4.4k
M. Leppert United States	40	2.8k 1.5×	1.4k 0.9×	1.4k 1.2×	188 0.2×	646 1.0×	169	6.1k
Hideki Garren United States	28	1.4k 0.7×	1.3k 0.8×	467 0.4×	191 0.2×	527 0.8×	59	4.6k
Leopoldo Zelante Italy	41	3.4k 1.8×	440 0.3×	964 0.8×	310 0.4×	201 0.3×	160	6.5k
Irene H. Maumenee United States	47	3.4k 1.8×	544 0.3×	1.9k 1.6×	501 0.6×	522 0.8×	143	6.3k
Hirotomo Saitsu Japan	43	4.2k 2.2×	353 0.2×	2.8k 2.4×	721 0.9×	849 1.3×	430	7.7k
O. D. Wiestler Germany	41	2.1k 1.1×	876 0.5×	305 0.3×	290 0.4×	620 1.0×	100	4.8k
Stefan Isenmann Germany	38	3.6k 1.9×	280 0.2×	504 0.4×	316 0.4×	1.3k 2.1×	125	6.1k
Erdem Tüzün Türkiye	32	1.1k 0.6×	700 0.4×	1.1k 0.9×	241 0.3×	809 1.3×	248	6.4k
Gudrun Nürnberg Germany	44	2.9k 1.5×	205 0.1×	1.6k 1.4×	895 1.1×	451 0.7×	93	5.1k
Ehud Hauben Israel	29	912 0.5×	788 0.5×	352 0.3×	113 0.1×	714 1.1×	51	3.7k

Countries citing papers authored by Elizabeth C. Engle

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth C. Engle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth C. Engle. 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 Elizabeth C. Engle. The network helps show where Elizabeth C. Engle may publish in the future.

Co-authorship network of co-authors of Elizabeth C. Engle

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth C. Engle. A scholar is included among the top collaborators of Elizabeth C. Engle 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 Elizabeth C. Engle. Elizabeth C. Engle 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

Bolar, Divya S., Bobby S. Korn, Don O. Kikkawa, et al.. (2024). The influence of orbital architecture on strabismus in craniosynostosis. Journal of American Association for Pediatric Ophthalmology and Strabismus. 28(1). 103812–103812. 1 indexed citations

Jurgens, Julie A., Brenda J. Barry, Gabrielle Lemire, et al.. (2021). Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain development. European Journal of Human Genetics. 29(5). 816–826. 12 indexed citations

Thiffault, Isabelle, Laura Cross, Shivarajan Amudhavalli, et al.. (2019). MAGEL2 ‐related disorders: A study and case series. Clinical Genetics. 96(6). 493–505. 27 indexed citations

An, Disi, Shuvadeep Maity, Matthew F. Rose, et al.. (2019). Stem cell-derived cranial and spinal motor neurons reveal proteostatic differences between ALS resistant and sensitive motor neurons. eLife. 8. 24 indexed citations

Nugent, Alicia, Jong G. Park, Yan Wei, et al.. (2017). Mutant α2-chimaerin signals via bidirectional ephrin pathways in Duane retraction syndrome. Journal of Clinical Investigation. 127(5). 1664–1682. 19 indexed citations

Brownstein, Catherine A., Robin J. Kleiman, Elizabeth C. Engle, et al.. (2016). Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports. American Journal of Medical Genetics Part A. 170(5). 1165–1173. 14 indexed citations

Smpokou, Patroula, et al.. (2014). Menkes disease in affected females: The clinical disease spectrum. American Journal of Medical Genetics Part A. 167(2). 417–420. 22 indexed citations

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

Saito, Yoshiaki, Kenji Sugai, Eiji Nakagawa, et al.. (2013). Pontine Malformation, Undecussated Pyramidal Tracts, and Regional Polymicrogyria: A New Syndrome. Pediatric Neurology. 50(4). 384–388. 6 indexed citations

10.

Cederquist, G., Anna Łuchniak, Max A. Tischfield, et al.. (2012). An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human Molecular Genetics. 21(26). 5484–5499. 95 indexed citations

11.

Desai, Jigar, et al.. (2012). Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). Gene Expression Patterns. 12(5-6). 180–188. 16 indexed citations

12.

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

13.

Rankin, Jessica K., Caroline Andrews, Wai‐Man Chan, & Elizabeth C. Engle. (2010). HOXA1 mutations are not a common cause of Möbius syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 14(1). 78–80. 10 indexed citations

14.

Engle, Elizabeth C., et al.. (2009). Clinical features associated with an I126M α2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 13(3). 245–248. 12 indexed citations

15.

Miyake, Noriko, et al.. (2009). CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome. American Journal of Medical Genetics Part A. 152A(1). 215–217. 22 indexed citations

16.

Andrews, Caroline, et al.. (2008). Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 12(4). 381–389. 12 indexed citations

17.

Pieh, Christina, Hans H. Goebel, Elizabeth C. Engle, & Irène Gottlob. (2003). Congenital fibrosis syndrome associated with central nervous system abnormalities. Graefe s Archive for Clinical and Experimental Ophthalmology. 241(7). 546–553. 20 indexed citations

18.

Nakano, Motoi, Koki Yamada, Emin Cumhur Şener, et al.. (2001). Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2. Nature Genetics. 29(3). 315–320. 148 indexed citations

19.

Engle, Elizabeth C., Louis M. Kunkel, Linda A. Specht, & Alan H. Beggs. (1994). Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12. Nature Genetics. 7(1). 69–73. 75 indexed citations

20.

Engle, Elizabeth C., et al.. (1982). Differential effects of antibiotics inhibiting gyrase. Journal of Bacteriology. 149(1). 92–98. 60 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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