Fiona Connell

2.5k total citations
15 papers, 916 citations indexed

About

Fiona Connell is a scholar working on Oncology, Surgery and Molecular Biology. According to data from OpenAlex, Fiona Connell has authored 15 papers receiving a total of 916 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Oncology, 6 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in Fiona Connell's work include Lymphatic System and Diseases (10 papers), Vascular Malformations and Hemangiomas (5 papers) and Sympathectomy and Hyperhidrosis Treatments (4 papers). Fiona Connell is often cited by papers focused on Lymphatic System and Diseases (10 papers), Vascular Malformations and Hemangiomas (5 papers) and Sympathectomy and Hyperhidrosis Treatments (4 papers). Fiona Connell collaborates with scholars based in United Kingdom, Australia and Netherlands. Fiona Connell's co-authors include Peter Mortimer, Glen Brice, Sahar Mansour, Steve Jeffery, Pia Østergaard, Michael A. Simpson, Richard C. Trembath, Kamini Kalidas, Taija Mäkinen and Inés Martínez‐Corral and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Circulation Research.

In The Last Decade

Fiona Connell

15 papers receiving 894 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fiona Connell United Kingdom	10	503	296	213	197	175	15	916
Iwona Auer Canada	13	189 0.4×	114 0.4×	96 0.5×	175 0.9×	126 0.7×	28	714
Kelly L. Betterman Australia	10	406 0.8×	272 0.9×	118 0.6×	121 0.6×	48 0.3×	11	610
Shoichiro Takeishi Japan	12	298 0.6×	534 1.8×	55 0.3×	48 0.2×	275 1.6×	16	940
Leah DiMascio United States	7	206 0.4×	504 1.7×	55 0.3×	51 0.3×	253 1.4×	11	896
Brisa Palikuqi United States	10	126 0.3×	391 1.3×	101 0.5×	56 0.3×	78 0.4×	12	721
Spencer K. Sullivan United States	13	116 0.2×	360 1.2×	76 0.4×	51 0.3×	316 1.8×	22	714
Ngaire Elwood Australia	15	74 0.1×	465 1.6×	82 0.4×	123 0.6×	226 1.3×	44	846
Patrik Georgii‐Hemming Sweden	14	244 0.5×	409 1.4×	54 0.3×	37 0.2×	233 1.3×	17	778
Carrie Fitzpatrick United States	17	330 0.7×	465 1.6×	267 1.3×	61 0.3×	76 0.4×	33	1.3k
Angelika M. Dräger Netherlands	13	178 0.4×	205 0.7×	49 0.2×	38 0.2×	323 1.8×	22	784

Countries citing papers authored by Fiona Connell

Since Specialization

Citations

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

Fields of papers citing papers by Fiona Connell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fiona Connell

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

All Works

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15 of 15 papers shown

Athanasakis, Emmanouil, Sophie Dahoun, Ambroise Wonkam, et al.. (2013). Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. European Journal of Medical Genetics. 56(8). 404–410. 7 indexed citations

Gordon, Kristiana, Dörte Schulte, Glen Brice, et al.. (2013). Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema. Circulation Research. 112(6). 956–960. 125 indexed citations

Gordon, Kristiana, Fiona Connell, Glen Brice, et al.. (2012). FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update. Human Mutation. 34(1). 23–31. 54 indexed citations

Østergaard, Pia, Michael A. Simpson, Fiona Connell, et al.. (2011). Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nature Genetics. 43(10). 929–931. 348 indexed citations

Østergaard, Pia, Michael A. Simpson, Glen Brice, et al.. (2011). Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype. Journal of Medical Genetics. 48(4). 251–255. 85 indexed citations

Suri, Mohnish, Susan M. White, Nicole de Leeuw, et al.. (2011). Pierpont syndrome: A collaborative study. American Journal of Medical Genetics Part A. 155(9). 2203–2211. 13 indexed citations

Connell, Fiona, Glen Brice, Steve Jeffery, et al.. (2010). A new classification system for primary lymphatic dysplasias based on phenotype. Clinical Genetics. 77(5). 438–452. 62 indexed citations

Connell, Fiona, Kamini Kalidas, Pia Østergaard, et al.. (2009). Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia. Human Genetics. 127(2). 231–241. 67 indexed citations

Connell, Fiona, Pia Østergaard, Glen Brice, et al.. (2009). Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas. Human Genetics. 125(2). 237–237. 1 indexed citations

10.

Connell, Fiona, Glen Brice, Sahar Mansour, & Peter Mortimer. (2009). Presentation of childhood lymPhoedema. 5 indexed citations

11.

Connell, Fiona, Pia Østergaard, Glen Brice, et al.. (2008). Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas. Human Genetics. 124(6). 625–631. 68 indexed citations

12.

Connell, Fiona, Tessa Homfray, B. Thilaganathan, et al.. (2008). Congenital vascular malformations: A series of five prenatally diagnosed cases. American Journal of Medical Genetics Part A. 146A(20). 2673–2680. 6 indexed citations

13.

Connell, Fiona, Glen Brice, & Peter Mortimer. (2008). Phenotypic Characterization of Primary Lymphedema. Annals of the New York Academy of Sciences. 1131(1). 140–146. 36 indexed citations

14.

Connell, Fiona & Shirley Hodgson. (2005). Our evolving understanding of 22q.11 deletion syndrome. Developmental Medicine & Child Neurology. 47(12). 796–796. 1 indexed citations

15.

Layton, Judith E., Nathan E. Hall, Fiona Connell, Jennifer Venhorst, & Herbert Treutlein. (2001). Identification of Ligand-binding Site III on the Immunoglobulin-like Domain of the Granulocyte Colony-stimulating Factor Receptor. Journal of Biological Chemistry. 276(39). 36779–36787. 38 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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