Sigrid Wayne

1.3k total citations
19 papers, 543 citations indexed

About

Sigrid Wayne is a scholar working on Molecular Biology, Sensory Systems and Otorhinolaryngology. According to data from OpenAlex, Sigrid Wayne has authored 19 papers receiving a total of 543 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Sensory Systems and 3 papers in Otorhinolaryngology. Recurrent topics in Sigrid Wayne's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), RNA regulation and disease (5 papers) and Congenital heart defects research (4 papers). Sigrid Wayne is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), RNA regulation and disease (5 papers) and Congenital heart defects research (4 papers). Sigrid Wayne collaborates with scholars based in United States, Belgium and India. Sigrid Wayne's co-authors include Richard J. Smith, C. R. Srikumari Srisailapathy, Guy Van Camp, Ross I. S. Zbar, Robert A. Robinson, Rodney N. Nagoshi, Arabandi Ramesh, Paul Coucke, Kikuro Fukushima and A. Ramesh and has published in prestigious journals such as Genetics, Genome Research and Human Molecular Genetics.

In The Last Decade

Sigrid Wayne

18 papers receiving 537 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sigrid Wayne United States 11 364 344 115 74 55 19 543
Tzy-Wen L. Gong United States 14 292 0.8× 219 0.6× 108 0.9× 84 1.1× 45 0.8× 17 568
I Huber Netherlands 5 276 0.8× 245 0.7× 89 0.8× 63 0.9× 57 1.0× 7 439
Mohamed Drira Tunisia 12 517 1.4× 431 1.3× 192 1.7× 74 1.0× 119 2.2× 16 779
Laurence Jonard France 15 301 0.8× 379 1.1× 135 1.2× 90 1.2× 66 1.2× 36 742
TB Friedman United States 9 260 0.7× 238 0.7× 110 1.0× 46 0.6× 47 0.9× 9 407
Xuezhong Liu United States 11 350 1.0× 461 1.3× 87 0.8× 51 0.7× 45 0.8× 14 659
Achih Chen United States 6 355 1.0× 221 0.6× 154 1.3× 93 1.3× 84 1.5× 7 514
Marta Lucía Tamayo Colombia 11 338 0.9× 469 1.4× 89 0.8× 41 0.6× 31 0.6× 35 647
MB Petersen Greece 8 361 1.0× 369 1.1× 148 1.3× 89 1.2× 64 1.2× 10 645
Steve D.M. Brown United Kingdom 7 316 0.9× 354 1.0× 106 0.9× 63 0.9× 42 0.8× 8 522

Countries citing papers authored by Sigrid Wayne

Since Specialization
Citations

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

Fields of papers citing papers by Sigrid Wayne

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sigrid Wayne

This figure shows the co-authorship network connecting the top 25 collaborators of Sigrid Wayne. A scholar is included among the top collaborators of Sigrid Wayne 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 Sigrid Wayne. Sigrid Wayne 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.
Sharma, Arun, Sigrid Wayne, Marina N. Nikiforova, Jonas T. Johnson, & Rohan R. Walvekar. (2008). Two Sites of Head and Neck Squamous Cell Carcinoma: Utility of Loss of Heterozygosity. Annals of Otology Rhinology & Laryngology. 117(8). 591–593. 1 indexed citations
2.
Provenzano, Matthew J., Michael J. Hitchler, Matthew P. Fitzgerald, et al.. (2007). AP-2 participates in the transcriptional control of the amyloid precursor protein (APP) gene in oral squamous cell carcinoma. Experimental and Molecular Pathology. 83(2). 277–282. 6 indexed citations
3.
Wayne, Sigrid & Robert A. Robinson. (2006). Upper aerodigestive tract squamous dysplasia: correlation with p16, p53, pRb, and Ki-67 expression.. Archives of Pathology & Laboratory Medicine. 130(9). 1309–14. 10 indexed citations
4.
Wayne, Sigrid & Robert A. Robinson. (2006). Upper Aerodigestive Tract Squamous Dysplasia: Correlation With p16, p53, pRb, and Ki-67 Expression. Archives of Pathology & Laboratory Medicine. 130(9). 1309–1314. 9 indexed citations
5.
Leenheer, Els De, P.L.M. Huygen, Sigrid Wayne, et al.. (2002). DFNA10/EYA4 - The Clinical Picture. Advances in oto-rhino-laryngology. 61. 73–78. 11 indexed citations
6.
Wayne, Sigrid. (2001). Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus. Human Molecular Genetics. 10(3). 195–200. 166 indexed citations
7.
Leenheer, Els De, P.L.M. Huygen, Richard J. Smith, Sigrid Wayne, & W. R. J. Cremers. (2001). The DFNA10 Phenotype. Annals of Otology Rhinology & Laryngology. 110(9). 861–866. 17 indexed citations
8.
Verhoeven, Kristien, Toril Fagerheim, Sai Prasad, et al.. (2000). Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment. Human Genetics. 107(1). 7–11. 10 indexed citations
9.
Verhoeven, Kristien, Toril Fagerheim, Sai Prasad, et al.. (2000). Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment. Human Genetics. 107(1). 7–11. 4 indexed citations
10.
Zbar, Ross I. S., A. Ramesh, C. R. Srikumari Srisailapathy, et al.. (1998). Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss. Otolaryngology. 118(3). 333–337. 16 indexed citations
11.
Greinwald, John H., Sigrid Wayne, Daryl A. Scott, et al.. (1998). Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31. American Journal of Medical Genetics. 78(2). 107–113.
12.
Greinwald, John H., Sigrid Wayne, Daryl A. Scott, et al.. (1998). Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31. American Journal of Medical Genetics. 78(2). 107–113. 32 indexed citations
13.
Chen, Achih, Sigrid Wayne, Adam Bell, et al.. (1997). New gene for autosomal recessive non‐syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71(4). 467–471. 7 indexed citations
14.
Chen, Achih, Sigrid Wayne, Arabandi Ramesh, et al.. (1997). New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p. American Journal of Medical Genetics. 71(4). 467–471. 39 indexed citations
15.
Wayne, Sigrid. (1996). Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10. Human Molecular Genetics. 5(10). 1689–1692. 93 indexed citations
16.
Fukushima, Kikuro, A. Ramesh, C. R. Srikumari Srisailapathy, et al.. (1995). An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.. Genome Research. 5(3). 305–308. 42 indexed citations
17.
Johnson, Eric A., Sigrid Wayne, & Rodney N. Nagoshi. (1995). fs (1) Yb is required for ovary follicle cell differentiation in Drosophila melanogaster and has genetic interactions with the Notch group of neurogenic genes.. Genetics. 140(1). 207–217. 21 indexed citations
18.
19.
Jain, Pawan Kumar, Kunihiro Fukushima, Dilip Deshmukh, et al.. (1995). A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus. Human Molecular Genetics. 4(12). 2391–2394. 51 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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