T. Morris

657 total citations
11 papers, 529 citations indexed

About

T. Morris is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, T. Morris has authored 11 papers receiving a total of 529 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Public Health, Environmental and Occupational Health. Recurrent topics in T. Morris's work include DNA Repair Mechanisms (2 papers), Carcinogens and Genotoxicity Assessment (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). T. Morris is often cited by papers focused on DNA Repair Mechanisms (2 papers), Carcinogens and Genotoxicity Assessment (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). T. Morris collaborates with scholars based in United Kingdom, United States and Germany. T. Morris's co-authors include Mary F. Lyon, J. Thacker, Gary S. Stein, James C. Bonner, Daniel S. Greenspan, Janet L. Stein, Farhad Marashi, Eileen Hickey, Lee Weber and P. H. Glenister and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Genetics and Genetics Research.

In The Last Decade

T. Morris

11 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. Morris United Kingdom	10	349	177	146	101	88	11	529
Naoe Kotomura Japan	10	348 1.0×	121 0.7×	91 0.6×	46 0.5×	20 0.2×	19	431
K. Burkhart-Schultz United States	11	439 1.3×	149 0.8×	189 1.3×	121 1.2×	45 0.5×	14	571
R. Rathenberg Germany	7	189 0.5×	125 0.7×	64 0.4×	44 0.4×	50 0.6×	10	343
Jan Kudynowski Sweden	8	272 0.8×	187 1.1×	84 0.6×	160 1.6×	16 0.2×	10	546
Batoul Y. Abdallah United States	15	523 1.5×	322 1.8×	356 2.4×	107 1.1×	26 0.3×	18	845
Weng Kong Sung United States	8	416 1.2×	132 0.7×	25 0.2×	46 0.5×	120 1.4×	15	563
Yosuke Ichijima Japan	11	729 2.1×	174 1.0×	105 0.7×	104 1.0×	63 0.7×	12	823
J Frédéric Belgium	12	303 0.9×	203 1.1×	45 0.3×	110 1.1×	18 0.2×	41	515
Celia Alda-Catalinas United Kingdom	6	865 2.5×	118 0.7×	127 0.9×	46 0.5×	99 1.1×	7	952
Janet P. Sanford United States	10	725 2.1×	405 2.3×	33 0.2×	64 0.6×	47 0.5×	14	855

Countries citing papers authored by T. Morris

Since Specialization

Citations

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

Fields of papers citing papers by T. Morris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Morris

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

All Works

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11 of 11 papers shown

De‐la‐Torre, Pedro, Mina Zamani, Hina Khan, et al.. (2024). PKHD1L1, a gene involved in the stereocilia coat, causes autosomal recessive nonsyndromic hearing loss. Human Genetics. 143(3). 311–329. 3 indexed citations

Simpson, Paul, T. Morris, John R. K. Savage, & J. Thacker. (1993). High-resolution cytogenetic analysis of X-ray induced mutations of the HPRT gene of primary human fibroblasts. Cytogenetic and Genome Research. 64(1). 39–45. 13 indexed citations

Morris, T. & J. Thacker. (1993). Formation of large deletions by illegitimate recombination in the HPRT gene of primary human fibroblasts.. Proceedings of the National Academy of Sciences. 90(4). 1392–1396. 104 indexed citations

Ropers, Hans‐Hilger, Margaret A. Pericak‐Vance, & T. Morris. (1990). Report of the committee on the genetic constitution of chromosome 19. Cytogenetic and Genome Research. 55(1-4). 218–228. 23 indexed citations

Morris, T., Farhad Marashi, Lee Weber, et al.. (1986). Involvement of the 5'-leader sequence in coupling the stability of a human H3 histone mRNA with DNA replication.. Proceedings of the National Academy of Sciences. 83(4). 981–985. 68 indexed citations

Morris, T., et al.. (1970). Dose-response curve for X-ray-induced translocations in mouse spermatogonia II. Fractionated doses. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 9(4). 411–415. 31 indexed citations

Lyon, Mary F., et al.. (1970). Induction of translocations in mouse spermatogonia by X-ray doses divided into many small fractions. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 9(2). 219–223. 31 indexed citations

Lyon, Mary F. & T. Morris. (1969). Gene and chromosome mutation after large fractionated or unfractionated radiation doses to mouse spermatogonia. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 8(1). 191–198. 91 indexed citations

Morris, T.. (1968). The XO and OY chromosome constitutions in the mouse. Genetics Research. 12(2). 125–137. 88 indexed citations

10.

Lyon, Mary F., et al.. (1967). Occurrences and linkage relations of the mutant ‘extra-toes’ in the mouse. Genetics Research. 9(3). 383–385. 21 indexed citations

11.

Lyon, Mary F. & T. Morris. (1966). Mutation rates at a new set of specific loci in the mouse. Genetics Research. 7(1). 12–17. 56 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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