Rebecca C. Tyler

833 total citations
19 papers, 624 citations indexed

About

Rebecca C. Tyler is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Rebecca C. Tyler has authored 19 papers receiving a total of 624 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Ophthalmology. Recurrent topics in Rebecca C. Tyler's work include Ocular Disorders and Treatments (5 papers), Congenital Ear and Nasal Anomalies (4 papers) and Glaucoma and retinal disorders (3 papers). Rebecca C. Tyler is often cited by papers focused on Ocular Disorders and Treatments (5 papers), Congenital Ear and Nasal Anomalies (4 papers) and Glaucoma and retinal disorders (3 papers). Rebecca C. Tyler collaborates with scholars based in United States, Canada and Taiwan. Rebecca C. Tyler's co-authors include Elena V. Semina, Linda M. Reis, Tanya Bardakjian, Adele Schneider, Kala F. Schilter, Ulrich Broeckel, Omar Abdul‐Rahman, Sanaa Muheisen, Jeffrey C. Murray and Alex V. Levin and has published in prestigious journals such as Human Molecular Genetics, Investigative Ophthalmology & Visual Science and Journal of Medical Genetics.

In The Last Decade

Rebecca C. Tyler

18 papers receiving 618 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rebecca C. Tyler United States 13 375 334 144 116 115 19 624
Joe Rainger United Kingdom 11 289 0.8× 251 0.8× 55 0.4× 71 0.6× 64 0.6× 18 499
Oscar F. Chacón‐Camacho Mexico 12 348 0.9× 211 0.6× 156 1.1× 46 0.4× 60 0.5× 62 533
Terri L. Young United States 16 371 1.0× 171 0.5× 344 2.4× 44 0.4× 371 3.2× 20 870
Kathy Williamson United Kingdom 5 318 0.8× 258 0.8× 51 0.4× 129 1.1× 56 0.5× 8 572
V. Ventruto Italy 17 479 1.3× 288 0.9× 54 0.4× 81 0.7× 52 0.5× 48 792
Prasuna Paluru United States 17 334 0.9× 104 0.3× 328 2.3× 32 0.3× 391 3.4× 20 889
Siddharth R. Vora United States 11 340 0.9× 107 0.3× 37 0.3× 58 0.5× 29 0.3× 21 527
Kala F. Schilter United States 8 222 0.6× 144 0.4× 72 0.5× 34 0.3× 70 0.6× 23 363
Muneera Alshammari Saudi Arabia 14 473 1.3× 406 1.2× 44 0.3× 32 0.3× 14 0.1× 18 749
Ghislaine Plessis France 18 431 1.1× 341 1.0× 33 0.2× 129 1.1× 11 0.1× 31 810

Countries citing papers authored by Rebecca C. Tyler

Since Specialization
Citations

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

Fields of papers citing papers by Rebecca C. Tyler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca C. Tyler

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

All Works

19 of 19 papers shown
1.
2.
Udani, Rupa, Kala F. Schilter, Rebecca C. Tyler, et al.. (2023). A novel variant of TNNC1 associated with severe dilated cardiomyopathy causing infant mortality and stillbirth: a case of germline mosaicism. Journal of Genetics. 102(1). 2 indexed citations
3.
Langlo, Christopher S., Honey V. Reddi, Kala F. Schilter, et al.. (2021). Long-term retinal imaging of a case of suspected congenital rubella infection. American Journal of Ophthalmology Case Reports. 25. 101241–101241. 5 indexed citations
4.
Сорокина, Елена А., Sanaa Muheisen, Linda M. Reis, et al.. (2018). PITX2 deficiency and associated human disease: insights from the zebrafish model. Human Molecular Genetics. 27(10). 1675–1695. 40 indexed citations
5.
Reis, Linda M., Rebecca C. Tyler, Eric Weh, et al.. (2016). Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies. Clinical Genetics. 90(4). 378–382. 13 indexed citations
6.
Reis, Linda M., Rebecca C. Tyler, Eric Weh, et al.. (2016). Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.. PubMed. 22. 1229–1238. 10 indexed citations
7.
Reis, Linda M., Rebecca C. Tyler, & Elena V. Semina. (2014). Identification of a novel C-terminal extension mutation in EPHA2 in a family affected with congenital cataract.. PubMed. 20. 836–42. 17 indexed citations
8.
Reis, Linda M., Rebecca C. Tyler, Sanaa Muheisen, et al.. (2013). Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes. Human Genetics. 132(7). 761–770. 70 indexed citations
9.
Weh, Eric, Linda M. Reis, Rebecca C. Tyler, et al.. (2013). Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. Clinical Genetics. 86(2). 142–148. 33 indexed citations
10.
Reis, Linda M., Rebecca C. Tyler, Kala F. Schilter, et al.. (2012). PITX2 and FOXC1 spectrum of mutations in ocular syndromes. European Journal of Human Genetics. 20(12). 1224–1233. 108 indexed citations
11.
Reis, Linda M., Rebecca C. Tyler, Kala F. Schilter, et al.. (2011). BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome. Human Genetics. 130(4). 495–504. 87 indexed citations
12.
Reis, Linda M., et al.. (2011). VSX2 mutations in autosomal recessive microphthalmia.. PubMed. 17. 2527–32. 25 indexed citations
13.
Reis, Linda M., Rebecca C. Tyler, Adele Schneider, et al.. (2010). FOXE3 plays a significant role in autosomal recessive microphthalmia. American Journal of Medical Genetics Part A. 152A(3). 582–590. 44 indexed citations
14.
Reis, Linda M., Rebecca C. Tyler, Adele Schneider, Tanya Bardakjian, & Elena V. Semina. (2010). Examination of SOX2 in variable ocular conditions identifies a recurrent deletion in microphthalmia and lack of mutations in other phenotypes.. PubMed. 16. 768–73. 15 indexed citations
15.
Schneider, Adele, Tanya Bardakjian, Linda M. Reis, Rebecca C. Tyler, & Elena V. Semina. (2009). Novel SOX2 mutations and genotype–phenotype correlation in anophthalmia and microphthalmia. American Journal of Medical Genetics Part A. 149A(12). 2706–2715. 86 indexed citations
16.
Reis, Linda M., Rebecca C. Tyler, Omar Abdul‐Rahman, et al.. (2008). Mutation analysis of B3GALTL in Peters Plus syndrome. American Journal of Medical Genetics Part A. 146A(20). 2603–2610. 46 indexed citations
17.
Zinkevich, Natalya S., D.V. Bosenko, Rebecca C. Tyler, & Elena V. Semina. (2006). Studies of Zebrafish pitx2 Demonstrate Conservation of Expression and Function With the Human Gene. Investigative Ophthalmology & Visual Science. 47(13). 5631–5631.
18.
Bosenko, D.V., Natalya S. Zinkevich, Rebecca C. Tyler, Brian A. Link, & Elena V. Semina. (2004). Sequence and expression of zebrafish optineurin gene suggests conserved function in vertebrate eye. Investigative Ophthalmology & Visual Science. 45(13). 4408–4408. 1 indexed citations
19.
Maltby, Edna L., et al.. (1997). A report of a child with a deletion (9)(q34.3): a recognisable phenotype?. Journal of Medical Genetics. 34(7). 610–612. 21 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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