T Blunt

2.5k total citations · 2 hit papers
10 papers, 2.1k citations indexed

About

T Blunt is a scholar working on Molecular Biology, Hematology and Oncology. According to data from OpenAlex, T Blunt has authored 10 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Hematology and 3 papers in Oncology. Recurrent topics in T Blunt's work include DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (4 papers) and Blood groups and transfusion (4 papers). T Blunt is often cited by papers focused on DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (4 papers) and Blood groups and transfusion (4 papers). T Blunt collaborates with scholars based in United Kingdom, United States and Canada. T Blunt's co-authors include Stephen P. Jackson, Penny A. Jeggo, Tanya Gottlieb, Guillermo E. Taccioli, Frederick W. Alt, Jocelyne Demengeot, Ryushin Mizuta, Alan R. Lehmann, A. Priestley and Graeme C.M. Smith and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

T Blunt

10 papers receiving 2.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation

1995 725 citations T Blunt, Guillermo E. Taccioli et al. Cell profile →
Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombination

1994 555 citations Guillermo E. Taccioli, Tanya Gottlieb et al. Science profile →

Peers

Countries citing papers authored by T Blunt

Since Specialization

Citations

This map shows the geographic impact of T Blunt'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 T Blunt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T Blunt more than expected).

Fields of papers citing papers by T Blunt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T Blunt

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Molecular and Biochemical Characterization of xrs Mutants Defective in Ku80 1997 ·Molecular and Cellular Biology ·Belinda K. Singleton, A. Priestley, Herdis Steingrimsdottir, David A. Gell, T Blunt, Stephen P. Jackson, Alan R. Lehmann, Penny A. Jeggo	149
2	Identification of a nonsense mutation in the carboxyl-terminal region of DNA-dependent protein kinase catalytic subunit in the scid mouse. 1996 ·Proceedings of the National Academy of Sciences ·T Blunt, David A. Gell, M. Fox, Guillermo E. Taccioli, Alan R. Lehmann, Stephen P. Jackson, Penny A. Jeggo	283
3	Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation breakdown → 1995 ·Cell ·T Blunt, (unknown), Guillermo E. Taccioli, Graeme C.M. Smith, Jocelyne Demengeot, Tanya Gottlieb, Ryushin Mizuta, A. J. Varghese, Frederick W. Alt, Penny A. Jeggo, Stephen P. Jackson	725
4	A YAC Contig Encompassing the XRCC5 (Ku80) DNA Repair Gene and Complementation of Defective Cells by YAC Protoplast Fusion 1995 ·Genomics ·T Blunt, Guillermo E. Taccioli, Anne Priestley, Majid Hafezparast, Trevor J. McMillan, Jing Liu, (unknown), (unknown), Frederick W. Alt, Stephen P. Jackson, Erwin Schurr, Alan R. Lehmann, Penny A. Jeggo	13
5	DNA-dependent protein kinase activity is absent in xrs-6 cells: implications for site-specific recombination and DNA double-strand break repair. 1995 ·Proceedings of the National Academy of Sciences ·(unknown), Tanya Gottlieb, T Blunt, Penny A. Jeggo, Stephen P. Jackson	306
6	Ku80: product of the XRCC5 gene and its role in DNA repair and V(D)J recombination breakdown → 1994 ·Science ·Guillermo E. Taccioli, Tanya Gottlieb, T Blunt, A. Priestley, Jocelyne Demengeot, Ryushin Mizuta, Alan R. Lehmann, Frederick W. Alt, Stephen P. Jackson, Penelope A. Jeggo	555
7	Serotype Switching in a Partially Deleted RHD Gene 1994 ·Vox Sanguinis ·T Blunt, Geoff Daniels, B. Carritt	46
8	Lack of RH C/E expression in the Rhesus D– phenotype is the result of a gene deletion 1994 ·Annals of Human Genetics ·T Blunt, (unknown), Geoff Daniels, B. Carritt	21
9	Serotype Switching in a Partially Deleted RHD Gene 1994 ·Vox Sanguinis ·T Blunt, Geoff Daniels, B. Carritt	11
10	Rh null phenotypes are not due to a gross deletion and can occure on different Rh genetic backgrounds 1993 ·Annals of Human Genetics ·B. Carritt, T Blunt, Neil D. Avent, Geoff Daniels, (unknown)	16

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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