T J Keen

1.3k total citations
27 papers, 994 citations indexed

About

T J Keen is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, T J Keen has authored 27 papers receiving a total of 994 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in T J Keen's work include Retinal Development and Disorders (14 papers), Photoreceptor and optogenetics research (5 papers) and Retinoids in leukemia and cellular processes (5 papers). T J Keen is often cited by papers focused on Retinal Development and Disorders (14 papers), Photoreceptor and optogenetics research (5 papers) and Retinoids in leukemia and cellular processes (5 papers). T J Keen collaborates with scholars based in United Kingdom, Norway and United States. T J Keen's co-authors include Chris F. Inglehearn, Alan C. Bird, C.F. Inglehearn, Shomi S. Bhattacharya, Shoumo Bhattacharya, Marcelle Jay, M Jay, G. B. Arden, Fred W. Fitzke and Rune Kleppe and has published in prestigious journals such as Ophthalmology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

T J Keen

27 papers receiving 962 citations

Peers

T J Keen
James S. Friedman United States
Alexander B. Quiambao United States
Michael H. Chaitin United States
C.F. Inglehearn United Kingdom
Guochun Xie United States
Elisabeth M. Bleeker‐Wagemakers Netherlands
Daniela Sanges Italy
Helene Achatz Germany
Fiona C. Mansergh Ireland
Yumi Ueki United States
James S. Friedman United States
T J Keen
Citations per year, relative to T J Keen T J Keen (= 1×) peers James S. Friedman

Countries citing papers authored by T J Keen

Since Specialization
Citations

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

Fields of papers citing papers by T J Keen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T J Keen

This figure shows the co-authorship network connecting the top 25 collaborators of T J Keen. A scholar is included among the top collaborators of T J Keen 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 J Keen. T J Keen 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.
2.
Gausdal, Gro, T J Keen, Camilla Krakstad, et al.. (2011). Cyclic AMP induces IPC leukemia cell apoptosis via CRE-and CDK-dependent Bim transcription. Cell Death and Disease. 2(12). e237–e237. 21 indexed citations
3.
Maita, Hiroshi, Hirotake Kitaura, T J Keen, et al.. (2004). PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor. Experimental Cell Research. 300(2). 283–296. 61 indexed citations
4.
Keen, T J, Moin Mohamed, Martin McKibbin, et al.. (2003). Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36. European Journal of Human Genetics. 11(5). 420–423. 46 indexed citations
5.
Downey, Louise, T J Keen, Michael J. Aldred, et al.. (2002). Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate. European Journal of Human Genetics. 10(12). 865–869. 26 indexed citations
6.
Downey, Louise, T J Keen, Emma Roberts, et al.. (2001). A New Locus for Autosomal Dominant Familial Exudative Vitreoretinopathy Maps to Chromosome 11p12-13. The American Journal of Human Genetics. 68(3). 778–781. 49 indexed citations
7.
Peacock, R., T J Keen, & Chris F. Inglehearn. (1997). Analysis of a Human Gene Homologous to Rat Ventral Prostate.1 Protein. Genomics. 46(3). 443–449. 20 indexed citations
8.
Keen, T J, et al.. (1997). Exclusion of CAG repeat expansion as the cause of disease in autosomal dominant retinitis pigmentosa families.. Journal of Medical Genetics. 34(2). 130–132. 3 indexed citations
9.
Keen, T J & Chris F. Inglehearn. (1996). Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration. Human Mutation. 8(4). 297–303. 77 indexed citations
10.
Reynolds, Paul A., et al.. (1996). Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities. Genes Chromosomes and Cancer. 17(3). 151–155. 16 indexed citations
11.
Keen, T J & Chris F. Inglehearn. (1996). Mutations and polymorphisms in the human peripherin‐RDS gene and their involvement in inherited retinal degeneration. Human Mutation. 8(4). 297–303. 12 indexed citations
12.
Keen, T J, et al.. (1995). A YAC Contig Spanning the Dominant Retinitis Pigmentosa Locus (RP9) on Chromosome 7p. Genomics. 28(3). 383–388. 15 indexed citations
13.
14.
Keen, T J, et al.. (1994). Retinal pattern dystrophy associated with a 4 bp insertion at codon 140 in the RDS-peripherin geneother. Human Molecular Genetics. 3(2). 367–368. 42 indexed citations
15.
Wroblewski, John J., John A. Wells, Anja Eckstein, et al.. (1994). Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa.. British Journal of Ophthalmology. 78(11). 831–836. 9 indexed citations
16.
Moore, Anthony T., F.W. Fitzke, M Jay, et al.. (1993). Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic study.. British Journal of Ophthalmology. 77(8). 473–479. 40 indexed citations
17.
Bashir, R., C.F. Inglehearn, T J Keen, et al.. (1992). Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP. Genomics. 14(1). 191–193. 4 indexed citations
18.
Moore, Anthony T., F.W. Fitzke, C.M. Kemp, et al.. (1992). Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.. British Journal of Ophthalmology. 76(8). 465–469. 62 indexed citations
19.
Inglehearn, Chris F., T J Keen, Rumaisa Bashir, et al.. (1992). A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosa. Human Molecular Genetics. 1(1). 41–45. 101 indexed citations
20.
Keen, T J, C.F. Inglehearn, Douglas H. Lester, et al.. (1991). Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site. Genomics. 11(1). 199–205. 129 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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