Catherine Taylor

608 total citations
8 papers, 444 citations indexed

About

Catherine Taylor is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Catherine Taylor has authored 8 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Cognitive Neuroscience. Recurrent topics in Catherine Taylor's work include Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Catherine Taylor is often cited by papers focused on Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Catherine Taylor collaborates with scholars based in United Kingdom, United States and France. Catherine Taylor's co-authors include Peter Scambler, S. C. M. Daw, Judith Goodship, María Callias, Rob Willemsen, Ben A. Oostra, Eleni Stathopulu, Jeremy Turk, Matthew Kraman and Thomas Meitinger and has published in prestigious journals such as Nature Genetics, Genome Research and Human Molecular Genetics.

In The Last Decade

Catherine Taylor

8 papers receiving 436 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Catherine Taylor	325	272	95	63	46	8	444
Rachel D. Burnside	229 0.7×	460 1.7×	51 0.5×	29 0.5×	18 0.4×	26	576
Hiba Risheg	374 1.2×	403 1.5×	44 0.5×	14 0.2×	28 0.6×	13	640
Judith M. McKie	414 1.3×	213 0.8×	16 0.2×	97 1.5×	77 1.7×	9	460
Erica H. Gerkes	221 0.7×	203 0.7×	22 0.2×	55 0.9×	15 0.3×	14	386
Viv Maloney	256 0.8×	453 1.7×	29 0.3×	41 0.7×	26 0.6×	18	587
Val Davison	199 0.6×	120 0.4×	32 0.3×	36 0.6×	40 0.9×	10	368
Barbara Szomju	164 0.5×	154 0.6×	22 0.2×	30 0.5×	16 0.3×	13	312
Brandi Thompson	336 1.0×	107 0.4×	46 0.5×	9 0.1×	27 0.6×	11	415
James Colley	241 0.7×	383 1.4×	74 0.8×	17 0.3×	13 0.3×	13	539
Andy Itsara	338 1.0×	588 2.2×	67 0.7×	19 0.3×	9 0.2×	7	699

Countries citing papers authored by Catherine Taylor

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Taylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Taylor

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Taylor. A scholar is included among the top collaborators of Catherine 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 Catherine Taylor. Catherine 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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8 of 8 papers shown

Stathopulu, Eleni, María Callias, Catherine Taylor, et al.. (2003). Clinical features of boys with fragile X premutations and intermediate alleles. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 121B(1). 119–127. 123 indexed citations

McKie, Judith M., Roy Wadey, Helen Sutherland, Catherine Taylor, & Peter Scambler. (1998). Direct Selection of Conserved cDNAs from the DiGeorge Critical Region: Isolation of a Novel CDC45-Like Gene. Genome Research. 8(8). 834–841. 13 indexed citations

Sun, H. Sunny, et al.. (1997). Mapping of growth hormone releasing hormone receptor to swine chromosome 18. Animal Genetics. 28(5). 351–353. 8 indexed citations

Taylor, Catherine, Roy Wadey, Hilary O‘Donnell, et al.. (1997). Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related protein. Mammalian Genome. 8(5). 371–375. 16 indexed citations

Daw, S. C. M., Catherine Taylor, Matthew Kraman, et al.. (1996). A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Nature Genetics. 13(4). 458–460. 134 indexed citations

Rizzu, Patrizia, Elizabeth A. Lindsay, Catherine Taylor, et al.. (1996). Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans. Mammalian Genome. 7(9). 639–643. 24 indexed citations

Sutherland, Helen, R Wadey, Judith M. McKie, et al.. (1996). Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.. PubMed. 59(1). 23–31. 83 indexed citations

Wadey, Roy, S. C. M. Daw, Catherine Taylor, et al.. (1995). Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome. Human Molecular Genetics. 4(6). 1027–1033. 43 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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