Louise Tilley

725 total citations
20 papers, 331 citations indexed

About

Louise Tilley is a scholar working on Hematology, Physiology and Molecular Biology. According to data from OpenAlex, Louise Tilley has authored 20 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Hematology, 14 papers in Physiology and 5 papers in Molecular Biology. Recurrent topics in Louise Tilley's work include Blood groups and transfusion (14 papers), Erythrocyte Function and Pathophysiology (11 papers) and Alzheimer's disease research and treatments (3 papers). Louise Tilley is often cited by papers focused on Blood groups and transfusion (14 papers), Erythrocyte Function and Pathophysiology (11 papers) and Alzheimer's disease research and treatments (3 papers). Louise Tilley collaborates with scholars based in United Kingdom, Japan and United States. Louise Tilley's co-authors include Kevin Morgan, Noor Kalsheker, Shane Grimsley, Geoff Daniels, Linda Morgan, Joyce Poole, James Lowe, P. Marsters, Joe Grainger and John H. Xuereb and has published in prestigious journals such as Blood, Nature Cell Biology and British Journal of Haematology.

In The Last Decade

Louise Tilley

19 papers receiving 322 citations

Peers

Louise Tilley

PHYSI

HEMAT

GENET

Stefan D. Jevtic Canada

Simona Signorini Italy

Cameron J. McDonald Australia

Sadahiko Iwamoto Japan

Kuan‐I Lee Taiwan

Lisa Philp Australia

Teresa Ramírez Mexico

Yuliya Kucherenko Germany

Salvo Danilo Lombardo Italy

Yumiko Takei Japan

Stefan D. Jevtic Canada

Louise Tilley

108 ×0.5

PHYSI

57 ×0.3

HEMAT

122 ×1.5

27 ×0.4

GENET

13 ×0.3

GENET

Citations per year, relative to Louise Tilley Louise Tilley (= 1×) peers Stefan D. Jevtic

Countries citing papers authored by Louise Tilley

Since Specialization

Citations

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

Fields of papers citing papers by Louise Tilley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Louise Tilley

This figure shows the co-authorship network connecting the top 25 collaborators of Louise Tilley. A scholar is included among the top collaborators of Louise Tilley 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 Louise Tilley. Louise Tilley 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

Tilley, Louise, et al.. (2025). Homozygosity for a novel A4GALT allele resulting in the rare p phenotype in an Indian blood donor. Vox Sanguinis. 120(5). 509–512.

Tilley, Louise. (2025). An update on the RHAG blood group system. Immunohematology. 41(1). 1–3. 1 indexed citations

Tilley, Louise, et al.. (2025). Modelling co-development between the somites and neural tube in human trunk-like structures. Nature Cell Biology. 27(12). 2049–2062. 1 indexed citations

Tilley, Louise, Vanja Karamatic Crew, Tosti J. Mankelow, et al.. (2024). Deletions in the MAL gene result in loss of Mal protein, defining the rare inherited AnWj-negative blood group phenotype. Blood. 144(26). 2735–2747. 3 indexed citations

Dulski, Jarosław, Witold Sołtan, Michał Schinwelski, et al.. (2016). Clinical variability of neuroacanthocytosis syndromes—a series of six patients with long follow-up. Clinical Neurology and Neurosurgery. 147. 78–83. 18 indexed citations

Tilley, Louise & Shane Grimsley. (2014). Is Next Generation Sequencing the future of blood group testing?. Transfusion and Apheresis Science. 50(2). 183–188. 31 indexed citations

Tilley, Louise, et al.. (2014). The RHD(1227G>A) DEL‐associated allele is the most prevalent DEL allele in Australian D– blood donors with C+ and/or E+ phenotypes. Transfusion. 54(11). 2931–2940. 24 indexed citations

Tilley, Louise, et al.. (2010). RhD variant caused by an in‐frame triplet duplication in the RHD gene. Transfusion. 51(3). 570–573. 10 indexed citations

Tilley, Louise, Joyce Poole, K. Ridgwell, et al.. (2009). A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein. Vox Sanguinis. 98(2). 151–159. 30 indexed citations

10.

Hustinx, Hein, Joyce Poole, Peter Bugert, et al.. (2008). Molecular basis of the Rh antigen RH48 (JAL). Vox Sanguinis. 96(3). 234–239. 9 indexed citations

11.

Klempíř, Jiří, Jan Roth, Kateřina Zárubová, et al.. (2007). The McLeod syndrome without acanthocytes. Parkinsonism & Related Disorders. 14(4). 364–366. 9 indexed citations

12.

Poole, Joyce, Louise Tilley, Frances A. Spring, et al.. (2007). Two missense mutations in the CD44 gene encode two new antigens of the Indian blood group system. Transfusion. 47(7). 1306–1311. 13 indexed citations

13.

Tilley, Louise, et al.. (2006). Sequence variation in the 5′ untranslated region of the human A4GALT gene is associated with, but does not define, the P1 blood‐group polymorphism. Vox Sanguinis. 90(3). 198–203. 15 indexed citations

14.

Tilley, Louise, et al.. (2006). SI37 Two Novel D Genes of the Rh Blood Group System Producing D Variant Phenotypes. Transfusion Medicine. 16(s1). 21–22. 2 indexed citations

15.

Zeman, Adam, et al.. (2005). McLeod Syndrome: life-long neuropsychiatric disorder due to a novel mutation of the XK gene. Psychiatric Genetics. 15(4). 291–293. 10 indexed citations

16.

Pinto-Cardoso, Sandra, Todd E. DeFor, Louise Tilley, et al.. (2004). Patient interleukin‐18 GCG haplotype associates with improved survival and decreased transplant‐related mortality after unrelated‐donor bone marrow transplantation. British Journal of Haematology. 126(5). 704–710. 25 indexed citations

17.

Morgan, Kevin, Federico Licastro, Louise Tilley, et al.. (2001). Polymorphism in the alpha1-antichymotrypsin (ACT) gene promoter: effect on expression in transfected glial and liver cell lines and plasma ACT concentrations. Human Genetics. 109(3). 303–310. 25 indexed citations

18.

Wood, Neil, Leigh Keen, Louise Tilley, & Jeff L. Bidwell. (2001). Determination of cytokine regulatory haplotypes by induced heteroduplex analysis of DNA. Journal of Immunological Methods. 249(1-2). 191–198. 10 indexed citations

19.

Tilley, Louise, Kevin Morgan, Joe Grainger, et al.. (1999). Evaluation of polymorphisms in the presenilin-1 gene and the butyrylcholinesterase gene as risk factors in sporadic Alzheimer's disease. European Journal of Human Genetics. 7(6). 659–663. 49 indexed citations

20.

Tilley, Louise, Kevin Morgan, & Noor Kalsheker. (1998). Genetic risk factors in Alzheimer's disease.. Molecular Pathology. 51(6). 293–304. 46 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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