D Lillicrap

740 total citations
15 papers, 592 citations indexed

About

D Lillicrap is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, D Lillicrap has authored 15 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Hematology, 6 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in D Lillicrap's work include Hemophilia Treatment and Research (11 papers), Platelet Disorders and Treatments (7 papers) and Blood Coagulation and Thrombosis Mechanisms (6 papers). D Lillicrap is often cited by papers focused on Hemophilia Treatment and Research (11 papers), Platelet Disorders and Treatments (7 papers) and Blood Coagulation and Thrombosis Mechanisms (6 papers). D Lillicrap collaborates with scholars based in Canada, United Kingdom and Netherlands. D Lillicrap's co-authors include Scott A. Taylor, Megan E. Begbie, Colleen Notley, Shawn Tinlin, I. R. Peake, Man‐Chiu Poon, AR Giles, Bruce A. Schwartz, Elizabeth W. Murray and Irwin Walker and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

D Lillicrap

15 papers receiving 576 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D Lillicrap Canada 13 448 255 84 71 61 15 592
Ryukichi Ryo Japan 9 281 0.6× 102 0.4× 82 1.0× 38 0.5× 44 0.7× 24 405
John E. Lund United States 9 168 0.4× 83 0.3× 43 0.5× 84 1.2× 27 0.4× 14 430
Aruna B. Pawashe United States 10 355 0.8× 137 0.5× 128 1.5× 22 0.3× 61 1.0× 12 563
Ryan Fiehler United States 9 510 1.1× 99 0.4× 194 2.3× 66 0.9× 49 0.8× 9 671
Anjali Purkayastha United States 6 390 0.9× 94 0.4× 124 1.5× 60 0.8× 32 0.5× 7 517
Véronique Baccini France 8 256 0.6× 109 0.4× 112 1.3× 49 0.7× 13 0.2× 19 400
WH Kane United States 7 556 1.2× 103 0.4× 204 2.4× 47 0.7× 22 0.4× 7 705
William A. Dittman United States 10 404 0.9× 101 0.4× 92 1.1× 60 0.8× 28 0.5× 14 508
KA High United States 12 337 0.8× 155 0.6× 108 1.3× 77 1.1× 15 0.2× 17 477
Raffaella Toso United States 14 549 1.2× 76 0.3× 144 1.7× 104 1.5× 18 0.3× 23 613

Countries citing papers authored by D Lillicrap

Since Specialization
Citations

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

Fields of papers citing papers by D Lillicrap

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Lillicrap

This figure shows the co-authorship network connecting the top 25 collaborators of D Lillicrap. A scholar is included among the top collaborators of D Lillicrap 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 D Lillicrap. D Lillicrap 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.
2.
Begbie, Megan E., et al.. (2000). The Factor VIII acute phase response requires the participation of NFkappaB and C/EBP.. PubMed. 84(2). 216–22. 90 indexed citations
3.
Mueller, Christopher R., et al.. (1996). Role of the Liver-Enriched Transcription Factor Hepatocyte Nuclear Factor 1 in Transcriptional Regulation of the Factor VIII Gene. Molecular and Cellular Biology. 16(5). 1936–1945. 34 indexed citations
4.
Giannelli, F., et al.. (1994). Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994. Nucleic Acids Research. 22(17). 3534–3546. 38 indexed citations
5.
6.
Taylor, Scott A., et al.. (1994). Direct detection of a common inversion mutation in the genetic diagnosis of severe hemophilia A [see comments]. Blood. 84(7). 2202–2205. 22 indexed citations
7.
Peake, I. R., D Lillicrap, Victor Boulyjenkov, et al.. (1993). Report of a joint WHO/WFH meeting on the control of haemophilia. Blood Coagulation & Fibrinolysis. 4(2). 313–344. 81 indexed citations
8.
Peake, I. R., D Lillicrap, E Briët, et al.. (1993). Haemophilia: strategies for carrier detection and prenatal diagnosis.. PubMed. 71(3-4). 429–58. 57 indexed citations
9.
Giannelli, F., Katherine A. High, D Lillicrap, et al.. (1992). Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992. Nucleic Acids Research. 20(suppl). 2027–2063. 33 indexed citations
10.
Murray, Elizabeth W., AR Giles, & D Lillicrap. (1992). Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.. PubMed. 50(1). 199–207. 35 indexed citations
11.
Murray, Elizabeth W., et al.. (1991). Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease. Blood. 77(7). 1476–1483. 14 indexed citations
12.
Taylor, Scott A., et al.. (1991). Somatic mosaicism and female-to-female transmission in a kindred with hemophilia B (factor IX deficiency).. Proceedings of the National Academy of Sciences. 88(1). 39–42. 59 indexed citations
13.
Murray, Elizabeth W., et al.. (1991). Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease. Blood. 77(7). 1476–1483. 1 indexed citations
14.
Taylor, Sherryl A., et al.. (1990). A mutation adjacent to the beta cleavage site of factor IX (valine 182 to leucine) results in mild haemophilia Bm. British Journal of Haematology. 75(2). 217–221. 17 indexed citations
15.
Taylor, Sherryl A., Peter J. Bridge, & D Lillicrap. (1989). A BstXI polymorphism detected by the factor VIII genomic probe p.482.6 (F8C). Nucleic Acids Research. 17(15). 6426–6426. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ryukichi Ryo Breakdown of academic impact, for papers by John E. Lund Breakdown of academic impact, for papers by Aruna B. Pawashe Breakdown of academic impact, for papers by Ryan Fiehler Breakdown of academic impact, for papers by Anjali Purkayastha Breakdown of academic impact, for papers by Véronique Baccini Breakdown of academic impact, for papers by WH Kane Breakdown of academic impact, for papers by William A. Dittman Breakdown of academic impact, for papers by KA High Breakdown of academic impact, for papers by Raffaella Toso
Rankless by CCL
2026