P Bignell

895 total citations
15 papers, 285 citations indexed

About

P Bignell is a scholar working on Hematology, Genetics and Genetics. According to data from OpenAlex, P Bignell has authored 15 papers receiving a total of 285 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Hematology, 5 papers in Genetics and 4 papers in Genetics. Recurrent topics in P Bignell's work include Platelet Disorders and Treatments (7 papers), Blood Coagulation and Thrombosis Mechanisms (5 papers) and Blood groups and transfusion (5 papers). P Bignell is often cited by papers focused on Platelet Disorders and Treatments (7 papers), Blood Coagulation and Thrombosis Mechanisms (5 papers) and Blood groups and transfusion (5 papers). P Bignell collaborates with scholars based in United Kingdom, Australia and India. P Bignell's co-authors include A L Bloom, Graham R. Standen, J. Evan Sadler, I. R. Peake, D. J. Bowen, V V Kakkar, Anna Schuh, Joseph Chacko, Sally Killick and Simon J. McGowan and has published in prestigious journals such as Blood, The Journal of Clinical Endocrinology & Metabolism and British Journal of Haematology.

In The Last Decade

P Bignell

13 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P Bignell United Kingdom 7 211 93 83 38 24 15 285
Ana Rebeca Jaloma‐Cruz Mexico 9 217 1.0× 50 0.5× 51 0.6× 88 2.3× 6 0.3× 26 297
Suely M. Rezende United Kingdom 9 273 1.3× 84 0.9× 48 0.6× 22 0.6× 60 2.5× 10 313
Irene Corrales Spain 10 110 0.5× 27 0.3× 36 0.4× 46 1.2× 38 1.6× 18 188
S. Fattoum France 12 269 1.3× 328 3.5× 51 0.6× 39 1.0× 8 0.3× 39 432
Yongrong Lai China 8 137 0.6× 127 1.4× 17 0.2× 55 1.4× 11 0.5× 25 269
I. A. Mochtar Netherlands 8 360 1.7× 101 1.1× 32 0.4× 27 0.7× 30 1.3× 21 415
Andréia A. Canalli Brazil 10 184 0.9× 228 2.5× 20 0.2× 84 2.2× 30 1.3× 21 321
Roberta Marra Italy 9 116 0.5× 148 1.6× 37 0.4× 61 1.6× 10 0.4× 24 335
Maria Patrizia Bicocchi Italy 12 169 0.8× 45 0.5× 124 1.5× 189 5.0× 11 0.5× 24 420
Elisabeth Thorelli Sweden 6 308 1.5× 146 1.6× 34 0.4× 9 0.2× 10 0.4× 7 325

Countries citing papers authored by P Bignell

Since Specialization
Citations

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

Fields of papers citing papers by P Bignell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Bignell

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

All Works

15 of 15 papers shown
1.
Fratter, Carl, Will Lester, Charles Percy, et al.. (2025). The diagnostic utility of genetic testing in inherited thrombocytopenia: regional multicenter tertiary experience. Research and Practice in Thrombosis and Haemostasis. 9(3). 102869–102869.
2.
Collins, Annie, Nicola Curry, P Bignell, et al.. (2021). Factor VIII levels and bleeding according to factor 8 (F8) mutation in pregnant carriers of haemophilia A: a multicentre retrospective cohort study. British Journal of Haematology. 193(2). 397–400. 6 indexed citations
3.
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Alatzoglou, Kyriaki S., Nicholas Rogers, P Bignell, et al.. (2014). SOX3 Deletion in Mouse and Human Is Associated With Persistence of the Craniopharyngeal Canal. The Journal of Clinical Endocrinology & Metabolism. 99(12). E2702–E2708. 26 indexed citations
6.
Roy, Noémi, Saul Myerson, Anna Schuh, et al.. (2011). Cardiac iron overload in transfusion‐dependent patients with myelodysplastic syndromes. British Journal of Haematology. 154(4). 521–524. 48 indexed citations
7.
Salehi, Rasoul, Christopher A. Fisher, P Bignell, Gilda Eslami, & John Old. (2010). Identification of Three Novel Mutations [−41 (A>C), codon 24 (–G), and IVS-I-109 (−T)], in a Study of β-Thalassemia Alleles in the Isfahan Region of Iran. Hemoglobin. 34(1). 115–120. 6 indexed citations
8.
Dreau, Hélène, H Jackson, P Bignell, et al.. (2010). Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family. Hemoglobin. 34(1). 110–114. 5 indexed citations
9.
Bowen, D. J., Philip Thomas, Cameron Webb, et al.. (2008). Facile and rapid analysis of three DNA polymorphisms within the human factor IX gene using the polymerase chain reaction. British Journal of Haematology. 77(4). 559–560. 6 indexed citations
10.
Grundy, C, P Bignell, Drake C. Mitchell, et al.. (1993). A novel nonsense mutation in the protein C (PROC) gene (Trp-29?Term) causing recurrent venous thrombosis. Human Genetics. 91(2). 196–196. 4 indexed citations
11.
Girolami, Antonio, Paolo Simioni, Bruno Girolami, et al.. (1993). A novel dysfunctional protein C (Protein C Padua 2) associated with a thrombotic tendency: substitution of Cys for Arg‐1 results in a strongly reduced affinity for binding of Ca++. British Journal of Haematology. 85(3). 521–527. 22 indexed citations
12.
Grundy, C, et al.. (1993). A Gla domain mutation (Arg 15???Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis. Blood Coagulation & Fibrinolysis. 4(2). 345–348. 5 indexed citations
13.
Standen, Graham R., P Bignell, D. J. Bowen, I. R. Peake, & A L Bloom. (1990). Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequence. British Journal of Haematology. 76(2). 242–249. 27 indexed citations
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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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2026