Indira B. Taylor

1.3k total citations
14 papers, 703 citations indexed

About

Indira B. Taylor is a scholar working on Genetics, Molecular Biology and Developmental Biology. According to data from OpenAlex, Indira B. Taylor has authored 14 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Developmental Biology. Recurrent topics in Indira B. Taylor's work include Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (5 papers) and Connective tissue disorders research (3 papers). Indira B. Taylor is often cited by papers focused on Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (5 papers) and Connective tissue disorders research (3 papers). Indira B. Taylor collaborates with scholars based in United Kingdom, Netherlands and Denmark. Indira B. Taylor's co-authors include Andrew O.M. Wilkie, Anne Goriely, Steven A. Wall, Gil McVean, Simon J. McGowan, Susanne P. Pfeifer, Sahan V. Rannan‐Eliya, Inge A. Olesen, Grete Krag Jacobsen and Ewa Rajpert-De Meyts and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Indira B. Taylor

14 papers receiving 690 citations

Peers

Indira B. Taylor

GENET

SURGE

Mark Clement-Jones United Kingdom

Georg Klaus Hinkel Germany

Olivier Pichon France

Anita S. Kulharya United States

Carmelilia De Bernardo Italy

Sayoko Fujimura Japan

Anthony Argentaro Australia

Marie‐France Portnoï France

Andreas Hehr Germany

A. Rodewald Germany

Mark Clement-Jones United Kingdom

Indira B. Taylor

593 ×1.3

550 ×1.3

GENET

83 ×1.0

SURGE

17 ×0.3

132 ×2.8

Citations per year, relative to Indira B. Taylor Indira B. Taylor (= 1×) peers Mark Clement-Jones

Countries citing papers authored by Indira B. Taylor

Since Specialization

Citations

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

Fields of papers citing papers by Indira B. Taylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Indira B. Taylor. 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 Indira B. Taylor. The network helps show where Indira B. Taylor may publish in the future.

Co-authorship network of co-authors of Indira B. Taylor

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

All Works

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14 of 14 papers shown

Giannoulatou, Eleni, Gil McVean, Indira B. Taylor, et al.. (2013). Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline. Proceedings of the National Academy of Sciences. 110(50). 20152–20157. 58 indexed citations

Wiberg, Akira, Marc C. Swan, Tracy Lester, et al.. (2013). The Fibroblast Growth Factor Receptor 2 p.Ala172Phe Mutation in Pfeiffer Syndrome—History Repeating Itself. American Journal of Medical Genetics Part A. 161(5). 1158–1163. 5 indexed citations

Goriely, Anne, Geoffrey J. Maher, Joohyun Lim, et al.. (2012). PATERNAL AGE EFFECT AND SELFISH MUTATIONS. Schizophrenia Research. 136. S4–S4. 1 indexed citations

Furniss, Dominic, Shih‐hsin Kan, Indira B. Taylor, et al.. (2009). Genetic screening of 202 individuals with congenital limb malformations and requiring reconstructive surgery. Journal of Medical Genetics. 46(11). 730–735. 28 indexed citations

Goriely, Anne, Indira B. Taylor, Inge A. Olesen, et al.. (2009). Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors. Nature Genetics. 41(11). 1247–1252. 155 indexed citations

Bochukova, Elena G., Tony Roscioli, Dale J. Hedges, et al.. (2008). Rare mutations ofFGFR2causing apert syndrome: identification of the first partial gene deletion, and anAluelement insertion from a new subfamily. Human Mutation. 30(2). 204–211. 39 indexed citations

Furniss, Dominic, Laura A. Lettice, Indira B. Taylor, et al.. (2008). A variant in the sonic hedgehog regulatory sequence (ZRS) is associated with triphalangeal thumb and deregulates expression in the developing limb. Human Molecular Genetics. 17(16). 2417–2423. 61 indexed citations

Taylor, Indira B., et al.. (2007). Fibroblast growth factor receptor 3 (FGFR3) mutation in a verrucous epidermal naevus associated with mild facial dysmorphism. British Journal of Dermatology. 156(6). 1353–1356. 16 indexed citations

Wilkie, Andrew O.M., Elena G. Bochukova, Indira B. Taylor, et al.. (2007). Clinical dividends from the molecular genetic diagnosis of craniosynostosis†. American Journal of Medical Genetics Part A. 143A(16). 1941–1949. 66 indexed citations

10.

Twigg, Stephen R.F., Kazuya Matsumoto, Alexa Kidd, et al.. (2006). The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males. The American Journal of Human Genetics. 78(6). 999–1010. 73 indexed citations

11.

Wilkie, Andrew O.M., Elena G. Bochukova, Indira B. Taylor, et al.. (2006). Clinical dividends from the molecular genetic diagnosis of craniosynostosis. American Journal of Medical Genetics Part A. 140A(23). 2631–2639. 80 indexed citations

12.

Mavrogiannis, Lampros A., Indira B. Taylor, Sally Davies, et al.. (2005). Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype. European Journal of Human Genetics. 14(2). 151–158. 52 indexed citations

13.

Rannan‐Eliya, Sahan V., et al.. (2004). Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis. Human Genetics. 115(3). 200–207. 48 indexed citations

14.

Ravel, Thomy de, et al.. (2004). A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome. European Journal of Human Genetics. 13(4). 503–505. 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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