Renée Carroll

904 total citations
8 papers, 188 citations indexed

About

Renée Carroll is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Renée Carroll has authored 8 papers receiving a total of 188 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in Renée Carroll's work include Genetics and Neurodevelopmental Disorders (3 papers), interferon and immune responses (1 paper) and Virus-based gene therapy research (1 paper). Renée Carroll is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), interferon and immune responses (1 paper) and Virus-based gene therapy research (1 paper). Renée Carroll collaborates with scholars based in Australia, Germany and United States. Renée Carroll's co-authors include Jozef Gécz, Charles H. Norris, Benoît Laurent, John B. Moeschler, Katrin Õunap, Michael Field, Yang Shi, Emily Brookes, Charles E. Schwartz and Mark Corbett and has published in prestigious journals such as Neurology, Human Molecular Genetics and Neuropharmacology.

In The Last Decade

Renée Carroll

8 papers receiving 188 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Renée Carroll Australia	6	124	82	48	19	16	8	188
Rita Teek Estonia	9	126 1.0×	124 1.5×	34 0.7×	14 0.7×	14 0.9×	14	221
Alexis Lupien‐Meilleur Canada	4	112 0.9×	88 1.1×	97 2.0×	40 2.1×	32 2.0×	5	217
Jana Neupauerová Czechia	10	78 0.6×	68 0.8×	83 1.7×	23 1.2×	13 0.8×	14	203
Donna Villasana United States	2	137 1.1×	93 1.1×	94 2.0×	70 3.7×	14 0.9×	2	237
Stephanie Lussier United States	6	109 0.9×	40 0.5×	38 0.8×	12 0.6×	25 1.6×	15	263
Anne Hempelmann Germany	8	124 1.0×	74 0.9×	125 2.6×	108 5.7×	14 0.9×	8	236
Mohammad Saharul Islam Japan	7	130 1.0×	95 1.2×	31 0.6×	8 0.4×	4 0.3×	11	250
Yongxin Wen China	9	160 1.3×	102 1.2×	29 0.6×	23 1.2×	38 2.4×	16	251
Anna Mikhailov Canada	7	102 0.8×	104 1.3×	24 0.5×	5 0.3×	13 0.8×	16	194
Ranjana Verma United States	10	151 1.2×	103 1.3×	36 0.8×	33 1.7×	3 0.2×	12	272

Countries citing papers authored by Renée Carroll

Since Specialization

Citations

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

Fields of papers citing papers by Renée Carroll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renée Carroll

This figure shows the co-authorship network connecting the top 25 collaborators of Renée Carroll. A scholar is included among the top collaborators of Renée Carroll 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 Renée Carroll. Renée Carroll 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

1.

Carroll, Renée, Marie Shaw, Maria Arvio, et al.. (2020). Two novel intragenic variants in the FMR1 gene in patients with suspect clinical diagnosis of Fragile X syndrome and no CGG repeat expansion. European Journal of Medical Genetics. 63(10). 104010–104010. 4 indexed citations

2.

Jolly, Lachlan A., Ying Sun, Renée Carroll, Claire C. Homan, & Jozef Gécz. (2018). Robust imaging and gene delivery to study human lymphoblastoid cell lines. Journal of Human Genetics. 63(9). 945–955. 1 indexed citations

3.

Carroll, Renée, Raman Kumar, Marie Shaw, et al.. (2017). Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restriction. European Journal of Human Genetics. 25(9). 1078–1082. 6 indexed citations

4.

Corbett, Mark, Samantha J. Turner, Alison Gardner, et al.. (2017). Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. European Journal of Medical Genetics. 60(8). 437–443. 8 indexed citations

5.

Corbett, Mark, Susannah T. Bellows, Melody Li, et al.. (2016). DominantKCNA2mutation causes episodic ataxia and pharmacoresponsive epilepsy. Neurology. 87(19). 1975–1984. 67 indexed citations

6.

Brookes, Emily, Benoît Laurent, Katrin Õunap, et al.. (2015). Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity. Human Molecular Genetics. 24(10). 2861–2872. 51 indexed citations

7.

Palmer, Elizabeth E., Melanie Leffler, Carolyn Rogers, et al.. (2015). New insights into Brunner syndrome and potential for targeted therapy. Clinical Genetics. 89(1). 120–127. 29 indexed citations

8.

Norris, Charles H., et al.. (1977). Kanamycin priming for audiogenic seizures in mice. Neuropharmacology. 16(5). 375–380. 22 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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