Gary Shutler

2.9k citations

23 papers · 2.3k indexed · 1 hit paper · h-index 13

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments

Papers in

Cellular and Molecular Neuroscience 7
- Genetic Neurodegenerative Diseases 7
Molecular Biology 19
- RNA modifications and cancer 6
- DNA Repair Mechanisms 5
- Fungal and yeast genetics research 4
- Biochemical and Molecular Research 3
- DNA and Nucleic Acid Chemistry 3
- Mitochondrial Function and Pathology 2

Co-authors: Robert G. Korneluk Catherine Tsilfidis Mani S. Mahadevan Bé Wieringa Pieter J. de Jong Gert Jansen Chris T. Amemiya S. Leblond
Journals: Nucleic Acids Research (5 papers)Genomics (5 papers)Journal of Forensic Sciences (4 papers)Science (1 paper)Nature (1 paper)
Partner nations: Canada United States Netherlands

In The Last Decade

Gary Shutler

22 papers receiving 2.2k citations

Hit Papers

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Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene 1992 · 1.3k citations

Peers

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

The 25 scholars most cited alongside Gary Shutler, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gary Shutler Line = papers co-authored together Gary Shutler links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A Simple DNA Extraction Method for Marijuana Samples Used in Amplified Fragment Length Polymorphism (AFLP) Analysis Journal of Forensic Sciences ·Heather Miller Coyle, Gary Shutler, Stephen L. Abrams, JC Aster, Christian Warouw, Carll Ladd, Timothy M. Palmbach, Hsin‐Chen Lee	2003	27
2	Analysis of Salivary DNA Evidence from a Bite Mark on a Body Submerged in Water Journal of Forensic Sciences ·D Sweet, Gary Shutler	1999	45
3	Genomic Structure of the Human D-Site Binding Protein (DBP) Gene Genomics ·Gary Shutler, Erwin Frey, Xiaolin Kang, Robert G. Korneluk, Christopher R. Mueller	1996	8
4	Isolation of a Novel G Protein-Coupled Receptor (GPR4) Localized to Chromosome 19q13.3 Genomics ·Mani S. Mahadevan, Stephen Baird, J Bailly, Gary Shutler, Luc A. Sabourin, Catherine Tsilfidis, Catherine Neville, Monica Narang, Robert G. Korneluk	1995	40
5	Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q Genomics ·Gert Jansen, Pieter J. de Jong, Chris T. Amemiya, Charalampos Aslanidis, Duncan J. Shaw, H G Harley, J. David Brook, Denis Doni, Robert G. Korneluk, Catherine Tsilfidis, Gary Shutler, Rosella Hermens, Ranjamin Amin, Hubert J.M. Smeets, Bé Wieringa	1992	30
6	Cloning of the essential myotonic dystrophy region and mapping of the putative defect Nature ·Charalampos Aslanidis, Gert Jansen, Chris T. Amemiya, Gary Shutler, Mani S. Mahadevan, Catherine Tsilfidis, Kristoffer Sakseide, Jennifer Alleman, Ranjamin Amin, J. Beiler, Jessica L. Buxton, Keith Johnson, H. Smeets, Gregory G. Lennon, A.V. Carrano, Robert G. Korneluk, Bé Wieringa, Pieter J. de Jong	1992	405
7	Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region Genomics ·Gary Shutler, Robert G. Korneluk, Catherine Tsilfidis, Mani S. Mahadevan, J Bailly, H. Smeets, Gert Jansen, Bé Wieringa, Frans P. Lohman, Charalampos Aslanidis, Pieter J. de Jong	1992	19
8	Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene Science ·Mani S. Mahadevan, Catherine Tsilfidis, Luc A. Sabourin, Gary Shutler, Chris T. Amemiya, Gert Jansen, Catherine Neville, Monica Narang, Juana Barceló, Kim O'Hoy, S. Leblond, O. V. Peneva, Pieter J. de Jong, Bé Wieringa, Robert G. Korneluk Hit paper breakdown →	1992	1340
9	A frequent Hincll polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118) Nucleic Acids Research ·Catherine Tsilfidis, Gary Shutler, Mani S. Mahadevan, Robert G. Korneluk	1991	5
10	An Sstl RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3 Nucleic Acids Research ·Catherine Tsilfidis, Gary Shutler, S. Leblond, Robert G. Korneluk	1991	4
11	RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3 Nucleic Acids Research ·Gary Shutler, Catherine Tsilfidis, S. Leblond, Robert G. Korneluk	1991	4
12	An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3 Nucleic Acids Research ·Gary Shutler, S. Leblond, J Bailly, Alex MacKenzie, Catherine Tsilfidis, Robert G. Korneluk	1991	4
13	Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy Genomics ·Gary Shutler, Alex MacKenzie, Han G. Brunner, Bé Wieringa, Peter J. de Jong, Frans P. Lohman, S. Leblond, J Bailly, Robert G. Korneluk	1991	15
14	D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q. PubMed ·Catherine Tsilfidis, A.E. MacKenzie, Gary Shutler, S. Leblond, J Bailly, Keith Johnson, R. Williamson, J. Siegel‐Bartelt, Robert G. Korneluk, Peggy Shelbourne	1991	12
15	Hae III—A Suitable Restriction Endonuclease for Restriction Fragment Length Polymorphism Analysis of Biological Evidence Samples Journal of Forensic Sciences ·B Budowle, Nicholas Cunha Peres Rodrigues, Gary Shutler, F. Samuel Baechtel	1990	30
16	Hae III--a suitable restriction endonuclease for restriction fragment length polymorphism analysis of biological evidence samples. PubMed ·Bruce Budowle, John S. Waye, Gary Shutler, F. Samuel Baechtel	1990	32
17	A simple and sensitive method for quantifying human genomic DNA in forensic specimen extracts. PubMed ·John S. Waye, Lawrence A. Presley, Bruce Budowle, Gary Shutler, R.M. Fourney	1989	168
18	Bloodstain characterization in the EAP, Hp, Hb, AK and Glo I typing systems using minigels and the PhastSystem™ Forensic Science International ·Gary Shutler, Chen Ping Yu	1988	2
19	A Study on the Inter-Relationship Between Fingerprint Developing Techniques and Bloodstain Identification and Typing Methods Canadian Society of Forensic Science Journal ·Gary Shutler	1980	3
20	Characterizing Human Seminal Fluid in the ABO, Lewis and Phosphoglucomutase Typing Systems Canadian Society of Forensic Science Journal ·Gary Shutler, H. S. Howard	1980	1

About Gary Shutler

Gary Shutler is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Safety Research and Ecology, having authored 23 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), RNA modifications and cancer (6 papers), DNA Repair Mechanisms (5 papers), Forensic and Genetic Research (4 papers), Fungal and yeast genetics research (4 papers), Biochemical and Molecular Research (3 papers), DNA and Nucleic Acid Chemistry (3 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.5k citations), Neurology (539 citations), Molecular Biology (1.9k citations), Genetics (532 citations) and Cardiology and Cardiovascular Medicine (219 citations). Gary Shutler has collaborated with scholars based in Canada, United States and Netherlands. Frequent 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. Their work appears in journals such as Nucleic Acids Research, Genomics, Journal of Forensic Sciences, Science and Nature.

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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