Mary E. Deadman

2.8k total citations
41 papers, 2.1k citations indexed

About

Mary E. Deadman is a scholar working on Molecular Biology, Microbiology and Epidemiology. According to data from OpenAlex, Mary E. Deadman has authored 41 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 15 papers in Microbiology and 9 papers in Epidemiology. Recurrent topics in Mary E. Deadman's work include RNA and protein synthesis mechanisms (16 papers), Bacterial Infections and Vaccines (13 papers) and Glycosylation and Glycoproteins Research (10 papers). Mary E. Deadman is often cited by papers focused on RNA and protein synthesis mechanisms (16 papers), Bacterial Infections and Vaccines (13 papers) and Glycosylation and Glycoproteins Research (10 papers). Mary E. Deadman collaborates with scholars based in United Kingdom, Sweden and United States. Mary E. Deadman's co-authors include E. Richard Moxon, Derek W. Hood, Joanna Poulton, R. Mark Gardiner, Adèle Martin, J. Craig Venter, James C. Richards, Georg A. Holländer, Katherine Makepeace and Chris P. Ponting and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nucleic Acids Research.

In The Last Decade

Mary E. Deadman

41 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mary E. Deadman United Kingdom	23	1.3k	628	433	412	331	41	2.1k
Nobumichi Furuta Japan	14	1.3k 1.1×	221 0.4×	1.2k 2.8×	145 0.4×	97 0.3×	20	2.5k
Yuji Hidaka Japan	26	1.1k 0.9×	120 0.2×	311 0.7×	223 0.5×	20 0.1×	79	1.8k
Ian E. Gentle Germany	19	1.6k 1.3×	69 0.1×	272 0.6×	712 1.7×	86 0.3×	33	2.1k
Sven Müller‐Loennies Germany	23	634 0.5×	161 0.3×	187 0.4×	391 0.9×	10 0.0×	54	1.3k
Yoshio Yamakawa Japan	26	1.3k 1.0×	42 0.1×	226 0.5×	323 0.8×	25 0.1×	91	2.3k
Craig A. Strathdee Canada	24	961 0.8×	417 0.7×	231 0.5×	315 0.8×	7 0.0×	38	1.9k
Ryuji Yamaguchi Japan	22	864 0.7×	29 0.0×	414 1.0×	230 0.6×	95 0.3×	58	1.6k
Sue M. Travis United States	18	1.3k 1.0×	599 1.0×	216 0.5×	366 0.9×	14 0.0×	20	2.5k
Jörg Selzer Germany	12	1.1k 0.9×	75 0.1×	219 0.5×	845 2.1×	19 0.1×	14	2.5k
Henry Lackland United States	19	952 0.8×	42 0.1×	364 0.8×	212 0.5×	53 0.2×	33	2.2k

Countries citing papers authored by Mary E. Deadman

Since Specialization

Citations

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

Fields of papers citing papers by Mary E. Deadman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary E. Deadman. 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 Mary E. Deadman. The network helps show where Mary E. Deadman may publish in the future.

Co-authorship network of co-authors of Mary E. Deadman

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Börsch, Anastasiya, Stefano Maio, Sam Palmer, et al.. (2023). Combined multidimensional single-cell protein and RNA profiling dissects the cellular and functional heterogeneity of thymic epithelial cells. Nature Communications. 14(1). 4071–4071. 12 indexed citations

Handel, Adam E., Stanley Cheuk, Fatima Dhalla, et al.. (2022). Developmental dynamics of the neural crest–mesenchymal axis in creating the thymic microenvironment. Science Advances. 8(19). eabm9844–eabm9844. 10 indexed citations

Oftedal, Bergithe E, Stefano Maio, Adam E. Handel, et al.. (2021). The chaperonin CCT8 controls proteostasis essential for T cell maturation, selection, and function. Communications Biology. 4(1). 681–681. 10 indexed citations

Baran‐Gale, Jeanette, Michael D. Morgan, Stefano Maio, et al.. (2020). Ageing compromises mouse thymus function and remodels epithelial cell differentiation. eLife. 9. 120 indexed citations

Sansom, Stephen N., Saule Zhanybekova, Gretel Nusspaumer, et al.. (2014). Population and single-cell genomics reveal the Aire dependency, relief from Polycomb silencing, and distribution of self-antigen expression in thymic epithelia. Genome Research. 24(12). 1918–1931. 243 indexed citations

Sadarangani, Manish, Martin Callaghan, Claire Jones, et al.. (2012). Construction of Opa-Positive and Opa-Negative Strains of Neisseria meningitidis to Evaluate a Novel Meningococcal Vaccine. PLoS ONE. 7(12). e51045–e51045. 7 indexed citations

Engskog, Mikael K.R., Mary E. Deadman, Jianjun Li, Derek W. Hood, & Elke K. H. Schweda. (2011). Detailed structural features of lipopolysaccharide glycoforms in nontypeable Haemophilus influenzae strain 2019. Carbohydrate Research. 346(10). 1241–1249. 8 indexed citations

Engskog, Mikael K.R., Hakan Yıldırım, Jianjun Li, et al.. (2009). A dual role for the lex2 locus: identification of galactosyltransferase activity in non-typeable Haemophilus influenzae strains 1124 and 2019. Carbohydrate Research. 344(5). 632–641. 2 indexed citations

Gerlach, Gabriele, Mark Anthony, Mary E. Deadman, et al.. (2009). Transposon insertion in a serine-specific minor tRNA coding sequence affects intraperitoneal survival of Haemophilus influenzae in the infant rat model. International Journal of Medical Microbiology. 300(4). 218–228. 3 indexed citations

10.

Moxon, E. Richard, et al.. (2008). Haemophilus influenzae biofilms: hypothesis or fact?. Trends in Microbiology. 16(3). 95–100. 33 indexed citations

11.

Cody, Alison J., David Field, Edward J. Feil, et al.. (2003). High rates of recombination in otitis media isolates of non-typeable Haemophilus influenzae1. Infection Genetics and Evolution. 3(1). 57–66. 54 indexed citations

12.

Adam, Rüdiger, Dirk Lindemann, Tobias A. Oelschlaeger, et al.. (2002). The avian chorioallantoic membrane in ovo – a useful model for bacterial invasion assays. International Journal of Medical Microbiology. 292(3-4). 267–275. 20 indexed citations

13.

Herbert, Mark, Samuel L. Hayes, Mary E. Deadman, et al.. (2002). Signature Tagged Mutagenesis of Haemophilus influenzae identifies genes required for in vivo survival. Microbial Pathogenesis. 33(5). 211–223. 49 indexed citations

14.

High, Nicola J., Mary E. Deadman, Derek W. Hood, & E. Richard Moxon. (1996). The identification a novel gene required for lipopolysaccharide biosynthesis byHaemophilus influenzaeRM7004, using transposon Tn916 mutagenesis. FEMS Microbiology Letters. 145(3). 325–331. 14 indexed citations

15.

Hood, Derek W., Mary E. Deadman, Hussein Masoud, et al.. (1996). Use of the complete genome sequence information of Haemophilus influenzae strain Rd to investigate lipopolysaccharide biosynthesis. Molecular Microbiology. 22(5). 951–965. 131 indexed citations

16.

Poulton, Joanna, Mary E. Deadman, Laurence A. Bindoff, et al.. (1993). Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form. Human Molecular Genetics. 2(1). 23–30. 133 indexed citations

17.

High, Nicola J., Mary E. Deadman, & E. Richard Moxon. (1993). The role of a repetitive DNA motif (5′‐CAAT‐3′) in the variable expression of the Haemophilus influenzae lipopolysaccharide epitope αGal(1–4)βGal. Molecular Microbiology. 9(6). 1275–1282. 86 indexed citations

18.

Maskell, Duncan J., Marika Szabo, Mary E. Deadman, & E. Richard Moxon. (1992). The gal locus from Haemophilus influenzae: cloning, sequencing and the use of gal mutants to study lipopolysaccharide. Molecular Microbiology. 6(20). 3051–3063. 38 indexed citations

19.

Poulton, Joanna, Mary E. Deadman, Douglass M. Turnbull, Brian Lake, & R M Gardiner. (1991). Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non‐invasive diagnosis of mitochondrial myopathy. Clinical Genetics. 39(1). 33–38. 16 indexed citations

20.

Poulton, Joanna, Mary E. Deadman, & R M Gardiner. (1989). Tandem direct duplications of mitochondrial DNA in mitochondrial myopathy: analysis of nucleotide sequence and tissue distribution. Nucleic Acids Research. 17(24). 10223–10229. 39 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