Gary Shutler

2.9k total citations · 1 hit paper
23 papers, 2.3k citations indexed

About

Gary Shutler is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Gary Shutler has authored 23 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Gary Shutler's work include Genetic Neurodegenerative Diseases (7 papers), RNA modifications and cancer (6 papers) and DNA Repair Mechanisms (5 papers). Gary Shutler is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), RNA modifications and cancer (6 papers) and DNA Repair Mechanisms (5 papers). Gary Shutler collaborates with scholars based in Canada, United States and Netherlands. Gary Shutler's co-authors include Robert G. Korneluk, Catherine Tsilfidis, Mani S. Mahadevan, Bé Wieringa, Pieter J. de Jong, Gert Jansen, Chris T. Amemiya, S. Leblond, Luc A. Sabourin and Catherine Neville and has published in prestigious journals such as Nature, Science and Nucleic Acids Research.

In The Last Decade

Gary Shutler

22 papers receiving 2.2k citations

Hit Papers

Myotonic Dystrophy Mutation: an Unstable CTG Repeat in th... 1992 2026 2003 2014 1992 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gary Shutler Canada 13 1.9k 1.5k 539 532 219 23 2.3k
A. Vandenberghe France 20 676 0.4× 530 0.3× 242 0.4× 273 0.5× 38 0.2× 55 1.3k
Jayne Leggo United Kingdom 19 798 0.4× 596 0.4× 264 0.5× 399 0.8× 80 0.4× 31 1.6k
Geneviève Gourdon France 30 2.5k 1.3× 1.7k 1.1× 340 0.6× 310 0.6× 223 1.0× 79 2.8k
Peter O'Connell United States 14 808 0.4× 356 0.2× 265 0.5× 295 0.6× 56 0.3× 17 1.4k
Nobutada Tachi Japan 16 789 0.4× 619 0.4× 234 0.4× 150 0.3× 56 0.3× 86 1.3k
Sahar Al‐Mahdawi United Kingdom 25 1.5k 0.8× 1.1k 0.7× 196 0.4× 242 0.5× 311 1.4× 52 1.9k
D Paul United States 7 969 0.5× 510 0.3× 198 0.4× 137 0.3× 24 0.1× 8 1.4k
Aı̈da Metzenberg United States 16 660 0.4× 230 0.1× 41 0.1× 225 0.4× 59 0.3× 19 1.2k
Marjolein H. Willemsen Netherlands 20 1.3k 0.7× 238 0.2× 48 0.1× 1.5k 2.8× 68 0.3× 43 2.4k
S. Igarashi Japan 12 1.3k 0.7× 1.3k 0.9× 530 1.0× 323 0.6× 28 0.1× 26 1.9k

Countries citing papers authored by Gary Shutler

Since Specialization
Citations

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

Fields of papers citing papers by Gary Shutler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gary Shutler

This figure shows the co-authorship network connecting the top 25 collaborators of Gary Shutler. A scholar is included among the top collaborators of Gary Shutler 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 Gary Shutler. Gary Shutler 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.
Coyle, Heather Miller, Gary Shutler, Stephen L. Abrams, et al.. (2003). A Simple DNA Extraction Method for Marijuana Samples Used in Amplified Fragment Length Polymorphism (AFLP) Analysis. Journal of Forensic Sciences. 48(2). 1–5. 27 indexed citations
2.
Sweet, D & Gary Shutler. (1999). Analysis of Salivary DNA Evidence from a Bite Mark on a Body Submerged in Water. Journal of Forensic Sciences. 44(5). 1069–1072. 45 indexed citations
3.
Shutler, Gary, et al.. (1996). Genomic Structure of the Human D-Site Binding Protein (DBP) Gene. Genomics. 34(3). 334–339. 8 indexed citations
4.
Mahadevan, Mani S., Stephen Baird, J Bailly, et al.. (1995). Isolation of a Novel G Protein-Coupled Receptor (GPR4) Localized to Chromosome 19q13.3. Genomics. 30(1). 84–88. 40 indexed citations
5.
Jansen, Gert, Pieter J. de Jong, Chris T. Amemiya, et al.. (1992). Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q. Genomics. 13(3). 509–517. 30 indexed citations
6.
Aslanidis, Charalampos, Gert Jansen, Chris T. Amemiya, et al.. (1992). Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Nature. 355(6360). 548–551. 405 indexed citations
7.
Shutler, Gary, Robert G. Korneluk, Catherine Tsilfidis, et al.. (1992). Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region. Genomics. 13(3). 518–525. 19 indexed citations
8.
Mahadevan, Mani S., Catherine Tsilfidis, Luc A. Sabourin, et al.. (1992). Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene. Science. 255(5049). 1253–1255. 1340 indexed citations breakdown →
9.
Tsilfidis, Catherine, Gary Shutler, Mani S. Mahadevan, & Robert G. Korneluk. (1991). A frequent Hincll polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118). Nucleic Acids Research. 19(5). 1157–1157. 5 indexed citations
10.
Tsilfidis, Catherine, Gary Shutler, S. Leblond, & Robert G. Korneluk. (1991). An Sstl RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3. Nucleic Acids Research. 19(5). 1158–1158. 4 indexed citations
11.
Shutler, Gary, Catherine Tsilfidis, S. Leblond, & Robert G. Korneluk. (1991). RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3. Nucleic Acids Research. 19(5). 1158–1158. 4 indexed citations
12.
Shutler, Gary, S. Leblond, J Bailly, et al.. (1991). An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3. Nucleic Acids Research. 19(5). 1159–1159. 4 indexed citations
13.
Shutler, Gary, Alex MacKenzie, Han G. Brunner, et al.. (1991). Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy. Genomics. 9(3). 500–504. 15 indexed citations
14.
Tsilfidis, Catherine, A.E. MacKenzie, Gary Shutler, et al.. (1991). D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.. PubMed. 49(5). 961–5. 12 indexed citations
15.
Budowle, B, et al.. (1990). Hae III—A Suitable Restriction Endonuclease for Restriction Fragment Length Polymorphism Analysis of Biological Evidence Samples. Journal of Forensic Sciences. 35(3). 530–536. 30 indexed citations
16.
Budowle, Bruce, John S. Waye, Gary Shutler, & F. Samuel Baechtel. (1990). Hae III--a suitable restriction endonuclease for restriction fragment length polymorphism analysis of biological evidence samples.. PubMed. 35(3). 530–6. 32 indexed citations
17.
Waye, John S., Lawrence A. Presley, Bruce Budowle, Gary Shutler, & R.M. Fourney. (1989). A simple and sensitive method for quantifying human genomic DNA in forensic specimen extracts.. PubMed. 7(8). 852–5. 168 indexed citations
18.
Shutler, Gary, et al.. (1988). Bloodstain characterization in the EAP, Hp, Hb, AK and Glo I typing systems using minigels and the PhastSystem™. Forensic Science International. 39(1). 97–104. 2 indexed citations
19.
Shutler, Gary. (1980). A Study on the Inter-Relationship Between Fingerprint Developing Techniques and Bloodstain Identification and Typing Methods. Canadian Society of Forensic Science Journal. 13(1). 1–8. 3 indexed citations
20.
Shutler, Gary, et al.. (1980). Characterizing Human Seminal Fluid in the ABO, Lewis and Phosphoglucomutase Typing Systems. Canadian Society of Forensic Science Journal. 13(4). 11–15. 1 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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