A L Bloom

621 total citations
23 papers, 413 citations indexed

About

A L Bloom is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, A L Bloom has authored 23 papers receiving a total of 413 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Hematology, 7 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in A L Bloom's work include Hemophilia Treatment and Research (16 papers), Platelet Disorders and Treatments (10 papers) and Cancer-related gene regulation (6 papers). A L Bloom is often cited by papers focused on Hemophilia Treatment and Research (16 papers), Platelet Disorders and Treatments (10 papers) and Cancer-related gene regulation (6 papers). A L Bloom collaborates with scholars based in United Kingdom, Canada and France. A L Bloom's co-authors include I. R. Peake, P Bignell, Graham R. Standen, J. Evan Sadler, Brenda Furlong, I R Peake, R. James Matthews, J. C. Giddings, David Lillicrap and D. J. Bowen and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

A L Bloom

23 papers receiving 387 citations

Peers

A L Bloom
van Eys J United States
A Pollak United States
V. Bony France
Mark Velangi United Kingdom
Erin L. Kuether United States
van Eys J United States
A L Bloom
Citations per year, relative to A L Bloom A L Bloom (= 1×) peers van Eys J

Countries citing papers authored by A L Bloom

Since Specialization
Citations

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

Fields of papers citing papers by A L Bloom

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A L Bloom. 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 A L Bloom. The network helps show where A L Bloom may publish in the future.

Co-authorship network of co-authors of A L Bloom

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

All Works

20 of 20 papers shown
1.
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
2.
Bloom, A L. (1991). The evolution and future of haemophilia therapy. Transfusion Medicine. 1(1). 5–12. 4 indexed citations
3.
Bowen, D. J., Cameron Webb, I. R. Peake, & A L Bloom. (1991). Aatll polymorphism in von Willebrand factor gene at codon 471. Nucleic Acids Research. 19(11). 3159–3159. 5 indexed citations
4.
Bloom, A L. (1991). Progress in the Clinical Management of Haemophilia. Thrombosis and Haemostasis. 66(1). 166–177. 17 indexed citations
5.
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
6.
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
9.
Furlong, R. A., et al.. (1989). Anti‐idiotypes to factor VIII antibodies and their possible role in the pathogenesis and treatment of factor VIII inhibitors. British Journal of Haematology. 71(1). 85–90. 14 indexed citations
10.
Peake, I R, et al.. (1989). Factor IX Cardiff: a variant factor IX protein that shows abnormal activation is caused by an arginine to cysteine substitution at position 145. British Journal of Haematology. 72(4). 556–560. 13 indexed citations
11.
Lillicrap, David, et al.. (1989). Defective propeptide processing and abnormal activation underlie the molecular pathology of factor IX Troed‐y‐Rhiw. British Journal of Haematology. 72(2). 208–215. 16 indexed citations
12.
Peake, I R, et al.. (1988). Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms. British Journal of Haematology. 70(1). 77–84. 16 indexed citations
13.
Matthews, R. James, I R Peake, A L Bloom, & D S Anson. (1988). Carrier detection through the use of abnormal deletion junction fragments in a case of haemophilia B involving complete deletion of the factor IX gene.. Journal of Medical Genetics. 25(11). 779–780. 1 indexed citations
14.
Matthews, R. James, D S Anson, I R Peake, & A L Bloom. (1987). Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.. Journal of Clinical Investigation. 79(3). 746–753. 24 indexed citations
15.
Lillicrap, David, et al.. (1986). Comparison of phenotypic assessment and the use of two restriction fragment length polymorphisms in the diagnosis of the carrier state in haemophilia B. British Journal of Haematology. 62(3). 557–565. 16 indexed citations
16.
Yoshioka, Akira, et al.. (1985). Immunoassays of factor IX antigen using monoclonal antibodies. British Journal of Haematology. 59(2). 265–275. 30 indexed citations
17.
Peake, I. R., Brenda Furlong, & A L Bloom. (1984). CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY). The Lancet. 323(8371). 242–243. 49 indexed citations
18.
Bloom, A L. (1983). Haemophilia: Benefits of cloning genes for clotting factors. Nature. 303(5917). 474–475. 8 indexed citations
19.
Bloom, A L & I. R. Peake. (1977). FACTOR VIII AND ITS INHERITED DISORDERS. British Medical Bulletin. 33(3). 219–224. 10 indexed citations
20.
Beck, Peter, J. C. Giddings, & A L Bloom. (1970). INHIBITOR OF FACTOR VIII IN MILD HAEMOPHILIA. British Journal of Haematology. 18(1). 107–107. 1 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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