Katie Morrison

1.2k total citations
29 papers, 845 citations indexed

About

Katie Morrison is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Katie Morrison has authored 29 papers receiving a total of 845 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Pathology and Forensic Medicine and 6 papers in Genetics. Recurrent topics in Katie Morrison's work include Multiple Sclerosis Research Studies (8 papers), T-cell and B-cell Immunology (5 papers) and Polyamine Metabolism and Applications (4 papers). Katie Morrison is often cited by papers focused on Multiple Sclerosis Research Studies (8 papers), T-cell and B-cell Immunology (5 papers) and Polyamine Metabolism and Applications (4 papers). Katie Morrison collaborates with scholars based in United Kingdom, Canada and United States. Katie Morrison's co-authors include Yvonne H. Edwards, George C. Ebers, A. Dessa Sadovnick, Jane C. Sowden, Gabriele C. DeLuca, David A. Dyment, Giulio Disanto, Julia M. Morahan, Sreeram V. Ramagopalan and Adam E. Handel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Annals of Neurology.

In The Last Decade

Katie Morrison

29 papers receiving 823 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katie Morrison United Kingdom 15 330 273 248 205 150 29 845
H. M. Dosch Canada 13 269 0.8× 148 0.5× 222 0.9× 216 1.1× 28 0.2× 25 861
Thierry Vilboux United States 23 161 0.5× 628 2.3× 530 2.1× 77 0.4× 41 0.3× 49 1.2k
Andrew R. Baker United States 6 622 1.9× 347 1.3× 453 1.8× 95 0.5× 36 0.2× 7 1.0k
Laurent Delpy France 20 101 0.3× 304 1.1× 241 1.0× 622 3.0× 71 0.5× 37 1.2k
Scott Gurd Canada 11 52 0.2× 918 3.4× 439 1.8× 105 0.5× 154 1.0× 12 1.4k
Virginia Vega-Warner United States 16 143 0.4× 509 1.9× 195 0.8× 46 0.2× 43 0.3× 30 1.0k
Wanda E. Filipiak United States 8 71 0.2× 407 1.5× 234 0.9× 77 0.4× 23 0.2× 11 906
Gopesh Srivastava Hong Kong 15 78 0.2× 206 0.8× 37 0.1× 132 0.6× 37 0.2× 30 646
Ercan Mıhçı Türkiye 13 39 0.1× 383 1.4× 264 1.1× 44 0.2× 59 0.4× 65 759
Rhonda E. Schnur United States 20 58 0.2× 505 1.8× 333 1.3× 44 0.2× 39 0.3× 52 919

Countries citing papers authored by Katie Morrison

Since Specialization
Citations

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

Fields of papers citing papers by Katie Morrison

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katie Morrison

This figure shows the co-authorship network connecting the top 25 collaborators of Katie Morrison. A scholar is included among the top collaborators of Katie Morrison 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 Katie Morrison. Katie Morrison 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.
Orton, Sarah-Michelle, Sreeram V Ramagopalan, Matthew R. Lincoln, et al.. (2011). Vitamin D metabolic pathway genes and risk of multiple sclerosis in Canadians. Journal of the Neurological Sciences. 305(1-2). 116–120. 50 indexed citations
2.
Watson, Corey T., Matthew R. Lincoln, S. V. Ramagopalan, et al.. (2011). Revisiting the T-cell receptor alpha/delta locus and possible associations with multiple sclerosis. Genes and Immunity. 12(2). 59–66. 6 indexed citations
3.
Ramagopalan, Sreeram V., David A. Dyment, M. Zameel Cader, et al.. (2011). Rare variants in the CYP27B1 gene are associated with multiple sclerosis. Annals of Neurology. 70(6). 881–886. 164 indexed citations
4.
Ramagopalan, S V, Lahiru Handunnetthi, Matthew R. Lincoln, et al.. (2010). Vitamin-D Receptor and 1-alpha-hydroxylase Genes in Risk and Outcome of Multiple Sclerosis in Canadians. Multiple Sclerosis Journal. 16. 271–271. 1 indexed citations
5.
Watson, Corey T., Sreeram V. Ramagopalan, Katie Morrison, George C. Ebers, & Felix Breden. (2010). IGHV4-39 deletion polymorphism does not associate with risk or outcome of multiple sclerosis. Journal of Neuroimmunology. 225(1-2). 164–166. 4 indexed citations
6.
Ramagopalan, Sreeram V., Katie Morrison, Adam E. Handel, et al.. (2009). Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families. Journal of Neuroimmunology. 212(1-2). 142–144. 1 indexed citations
7.
Ramagopalan, Sreeram V., David A. Dyment, Katie Morrison, et al.. (2008). Methylation of class II transactivator gene promoter IV is not associated with susceptibility to Multiple Sclerosis. BMC Medical Genetics. 9(1). 63–63. 16 indexed citations
8.
Willer, Cristen J., David A. Dyment, Stacey S. Cherny, et al.. (2007). A genome-wide scan in forty large pedigrees with multiple sclerosis. Journal of Human Genetics. 52(12). 955–962. 21 indexed citations
9.
Willer, Cristen J., Blanca Herrera, Katie Morrison, A. Dessa Sadovnick, & George C. Ebers. (2006). Association between microchimerism and multiple sclerosis in Canadian twins. Journal of Neuroimmunology. 179(1-2). 145–151. 33 indexed citations
10.
Sood, Raman, Patricia I. Bader, Marcy C. Speer, et al.. (2004). Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesis. Cytogenetic and Genome Research. 106(1). 61–67. 5 indexed citations
11.
Dyment, David A., J. L. Steckley, Katie Morrison, et al.. (2004). TCR β polymorphisms and multiple sclerosis. Genes and Immunity. 5(5). 337–342. 12 indexed citations
12.
Morrison, Katie, Charalambos Papapetrou, Frans A. Hol, et al.. (1998). Susceptibility to spina bifida; an association study of five candidate genes. Annals of Human Genetics. 62(5). 379–396. 95 indexed citations
13.
Sowden, Jane C., Hazel K. Smith, Katie Morrison, & Yvonne H. Edwards. (1998). Sequence comparisons and functional studies of the proximal promoter of the carbonic anhydrase 3 (CA3) gene. Gene. 214(1-2). 157–165. 6 indexed citations
14.
Sowden, Jane C., Katie Morrison, W. Putt, R. S. P. Beddington, & Yvonne H. Edwards. (1997). The identification of novel sequences expressed in the mouse notochord. Mammalian Genome. 8(1). 42–44. 4 indexed citations
15.
Sowden, Jane C., et al.. (1997). The caudal type homeobox protein CDX2 binds to the colon promoter of the carbonic anhydrase 1 gene. Genetics Research. 70(1). 79–89. 9 indexed citations
16.
Morrison, Katie. (1996). Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida. Human Molecular Genetics. 5(5). 669–674. 39 indexed citations
17.
Sowden, Jane C., et al.. (1996). The Caudal ‐Type Homeobox Protein Cdx‐2 Binds to the Colon Promoter of the Carbonic Anhydrase 1 Gene. European Journal of Biochemistry. 236(2). 670–681. 65 indexed citations
18.
Sowden, Jane C., Katie Morrison, Julian Schofield, W. Putt, & Yvonne J. K. Edwards. (1995). A Novel cDNA with Homology to an RNA Polymerase II Elongation Factor Maps to Human Chromosome 5q31 (TCEB1L) and to Mouse Chromosome 11 (Tceb1l). Genomics. 29(1). 145–151. 9 indexed citations
19.
Malaspina, Patrizia, Margaret Fox, James Dooley, et al.. (1993). A cosmid library specific for human Chromosome regions 6p21.3 and 6q27. Mammalian Genome. 4(9). 493–498. 7 indexed citations
20.
Tweedie, Susan, et al.. (1991). CAIII a marker for early myogenesis: Analysis of expression in cultured myogenic cells. Somatic Cell and Molecular Genetics. 17(3). 215–228. 12 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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