Anne Goodeve

8.5k total citations
114 papers, 4.3k citations indexed

About

Anne Goodeve is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Anne Goodeve has authored 114 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 99 papers in Hematology, 33 papers in Molecular Biology and 25 papers in Genetics. Recurrent topics in Anne Goodeve's work include Platelet Disorders and Treatments (62 papers), Hemophilia Treatment and Research (50 papers) and Blood groups and transfusion (37 papers). Anne Goodeve is often cited by papers focused on Platelet Disorders and Treatments (62 papers), Hemophilia Treatment and Research (50 papers) and Blood groups and transfusion (37 papers). Anne Goodeve collaborates with scholars based in United Kingdom, Italy and Netherlands. Anne Goodeve's co-authors include I. R. Peake, John T. Reilly, Peter R. Winship, Mamdooh Gari, G. A. Wilson, Rory Care, Gill Wilson, Elisabeth Vandenberghe, F E Preston and Giancarlo Castaman and has published in prestigious journals such as The Lancet, Blood and PLoS ONE.

In The Last Decade

Anne Goodeve

112 papers receiving 4.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anne Goodeve United Kingdom	36	3.6k	1.2k	917	395	376	114	4.3k
I. R. Peake United Kingdom	38	4.1k 1.1×	1.1k 0.9×	1.1k 1.2×	342 0.9×	352 0.9×	131	4.7k
Junji Nishioka Japan	31	1.7k 0.5×	533 0.4×	515 0.6×	345 0.9×	273 0.7×	99	3.0k
Lee‐Yung Shih Taiwan	30	1.7k 0.5×	1.2k 1.0×	776 0.8×	347 0.9×	114 0.3×	195	3.6k
Sally Killick United Kingdom	28	2.3k 0.7×	749 0.6×	894 1.0×	705 1.8×	292 0.8×	68	3.2k
Richard D. Press United States	31	1.9k 0.5×	550 0.4×	1.4k 1.5×	127 0.3×	139 0.4×	105	2.8k
Laszlo Bajzar Canada	27	2.5k 0.7×	563 0.5×	516 0.6×	147 0.4×	256 0.7×	38	3.5k
Frank Bridoux France	39	1.6k 0.5×	3.3k 2.7×	1.4k 1.5×	1.0k 2.6×	362 1.0×	165	5.8k
Stéphane Giraudier France	32	2.3k 0.7×	1.4k 1.1×	2.4k 2.6×	334 0.8×	106 0.3×	117	3.8k
Eric S. Winer United States	27	1.1k 0.3×	666 0.5×	585 0.6×	318 0.8×	340 0.9×	106	3.0k
Dominique Meyer France	35	2.8k 0.8×	533 0.4×	507 0.6×	788 2.0×	436 1.2×	106	3.9k

Countries citing papers authored by Anne Goodeve

Since Specialization

Citations

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

Fields of papers citing papers by Anne Goodeve

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Goodeve

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

All Works

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20 of 20 papers shown

Borgio, J. Francis, et al.. (2022). Phenotypic and Genotypic Signatures of VWF Exon 18 in Eastern Saudi Patients Previously Diagnosed with Type 1 von Willebrand Disease. International Journal of General Medicine. Volume 15. 5385–5394. 1 indexed citations

Jong, Annika de, Richard Dirven, Lisa D.S. Bloomer, et al.. (2020). Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms. Blood Advances. 4(13). 2979–2990. 7 indexed citations

Bowyer, Annette, H. Seidel, Philipp Westhofen, et al.. (2018). Evaluation of a semi‐automated von Willebrand factor multimer assay, the Hydragel 5 von Willebrand multimer, by two European Centers. Research and Practice in Thrombosis and Haemostasis. 2(4). 790–799. 31 indexed citations

Cairo, Athena H., Brian Dolan, Muriel Giansily‐Blaizot, et al.. (2015). Eahad-DB: a combined coagulation factor variant databases resource for the clinical and scientificcommunities. View. 1 indexed citations

Gomez, Keith, Anne Goodeve, Geoffrey Kemball‐Cook, et al.. (2014). The EAHAD coagulation factor variant databases. Surrey Research Insight Open Access (The University of Surrey). 1 indexed citations

Eikenboom, Jeroen, Augusto B. Federici, Richard Dirven, et al.. (2013). VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease. Blood. 121(12). 2336–2339. 84 indexed citations

Abuzenadah, Adel, Ulrich Budde, Türkiz Gursel, et al.. (2013). Identification and characterisation of mutations associated with von Willebrand disease in a Turkish patient cohort. Thrombosis and Haemostasis. 110(8). 264–274. 7 indexed citations

Rossetti, Liliana Carmen, R. Bianco, Irene Larripa, et al.. (2012). Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B. Thrombosis and Haemostasis. 109(1). 24–33. 31 indexed citations

Goodeve, Anne, David J. Perry, Martin Hill, et al.. (2012). Genetics of haemostasis. Haemophilia. 18(s4). 73–80. 6 indexed citations

10.

Castaman, Giancarlo, Sofia H. Giacomelli, Maria Elisa Mancuso, et al.. (2011). Deep intronic variations may cause mild hemophilia A. Journal of Thrombosis and Haemostasis. 9(8). 1541–1548. 54 indexed citations

11.

Bowyer, Annette, Anne Goodeve, Ri Liesner, et al.. (2011). p.Tyr365Cys change in factor VIII: haemophilia A, but not as we know it. British Journal of Haematology. 154(5). 618–625. 17 indexed citations

12.

Hickson, Nicholas, Daniel J. Hampshire, Peter R. Winship, et al.. (2010). von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels. Journal of Thrombosis and Haemostasis. 8(9). 1986–1993. 14 indexed citations

13.

Sung, Hye Youn, et al.. (2009). Tribbles-1 and -2 are tumour suppressors, down-regulated in human acute myeloid leukaemia. Immunology Letters. 130(1-2). 115–124. 34 indexed citations

14.

Rossetti, Liliana Carmen, et al.. (2004). Analysis of factor VIII gene intron 1 inversion in Argentinian families with severe haemophilia A and a review of the literature. Blood Coagulation & Fibrinolysis. 15(7). 569–572. 19 indexed citations

15.

Rossetti, Liliana Carmen, Anne Goodeve, Irene Larripa, & Carlos Daniel De Brasi. (2004). Homeologous recombination between AluSx-sequences as a cause of hemophilia. Human Mutation. 24(5). 440–440. 30 indexed citations

16.

Curtis, Diana, Miranda Durkie, Anne Goodeve, et al.. (1999). A study of Wilson disease mutations in Britain. Human Mutation. 14(4). 304–311. 64 indexed citations

17.

Goodeve, Anne, et al.. (1998). Rapid genotypic diagnosis of type 2A von Willebrand's disease by heteroduplex analysis. Clinical & Laboratory Haematology. 20(3). 177–178. 1 indexed citations

18.

Goodeve, Anne, Giuseppe Tagariello, Ampaiwan Chuansumrit, F. E. Preston, & I R Peake. (1996). A rapid and cost effective method for analysis of dinucleotide repeat polymorphisms in the factor VIII gene. Blood Coagulation & Fibrinolysis. 7(7). 672–677. 18 indexed citations

19.

Chuansumrit, Ampaiwan, Anne Goodeve, Werasak Sasanakul, et al.. (1995). DNA polymorphisms for carrier detection of hemophilia in Thailand.. PubMed. 26 Suppl 1. 201–6. 1 indexed citations

20.

Lees, Janice F., et al.. (1992). Detection of EBV DNA in post‐nasal space biopsy tissue from asymptomatic EBV‐seropositive individuals. Journal of Medical Virology. 37(1). 30–38. 17 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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