Peter N. Ray
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Glioma Diagnosis and Treatment
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 1%
- Muscle Physiology and Disorders
- Retinal Development and Disorders
Papers in
- Genetics 59
- Genomics and Rare Diseases 17
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 10
- Glioma Diagnosis and Treatment 6
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- Muscle Physiology and Disorders 53
- Co-authors
- Ronald G. Worton (22 shared papers)Arthur H.M. Burghes (10 shared papers)Dennis E. Bulman (14 shared papers)Henry J. Klamut (10 shared papers)Elizabeth E. Zubrzycka‐Gaarn (7 shared papers)Berivan Baskin (21 shared papers)Margaret W. Thompson (3 shared papers)George Karpati (4 shared papers)
- Journals
- Neuromuscular Disorders (8 papers)Human Molecular Genetics (6 papers)Nature (5 papers)Journal of Medical Genetics (5 papers)Human Mutation (4 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Peter N. Ray
155 papers receiving 9.4k citations
Peter N. Ray's Hit Papers
Peers
Comparison fields: 5 of 134
- Genetics 1.4k
- Genetics 2.8k
- Molecular Biology 4.1k
- Clinical Biochemistry 129
- Pediatrics, Perinatology and Child Health 242
Countries citing papers authored by Peter N. Ray
This map shows the geographic impact of Peter N. Ray'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 Peter N. Ray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter N. Ray more than expected).
Fields of papers citing papers by Peter N. Ray
This network shows the impact of papers produced by Peter N. Ray. 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 Peter N. Ray. The network helps show where Peter N. Ray may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter N. Ray, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 155 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1988 | 584 | |
| 2 | 1997 | 470 | |
| 3 | Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test Hit paper breakdown → | 2017 | 440 |
| 4 | Whole-genome sequencing of quartet families with autism spectrum disorder Hit paper breakdown → | 2015 | 410 |
| 5 | 2013 | 381 | |
| 6 | 1985 | 324 | |
| 7 | 2016 | 286 | |
| 8 | 1988 | 257 | |
| 9 | 2015 | 243 | |
| 10 | 1987 | 223 | |
| 11 | 1995 | 214 | |
| 12 | Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation. | 1990 | 203 |
| 13 | 2008 | 201 | |
| 14 | 2013 | 194 | |
| 15 | 2010 | 162 | |
| 16 | 2010 | 136 | |
| 17 | 1986 | 133 | |
| 18 | Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers. | 1992 | 126 |
| 19 | 2010 | 120 | |
| 20 | 1988 | 104 |
About Peter N. Ray
Peter N. Ray is a scholar working on Genetics, Molecular Biology, Genetics, Biochemistry and Cellular and Molecular Neuroscience, having authored 155 papers that have together received 9.9k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (53 papers), Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (12 papers), Genetic Syndromes and Imprinting (10 papers), Cystic Fibrosis Research Advances (7 papers), Lysosomal Storage Disorders Research (6 papers), Glioma Diagnosis and Treatment (6 papers) and Amino Acid Enzymes and Metabolism (6 papers). The work is most often cited by research in Genetics (1.4k citations), Genetics (2.8k citations), Molecular Biology (4.1k citations), Clinical Biochemistry (129 citations) and Pediatrics, Perinatology and Child Health (242 citations). Peter N. Ray has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Ronald G. Worton, Arthur H.M. Burghes, Dennis E. Bulman, Henry J. Klamut, Elizabeth E. Zubrzycka‐Gaarn, Berivan Baskin, Margaret W. Thompson, George Karpati, Thomas W. Prior and Patricia E. McAndrew. Their work appears in journals such as Neuromuscular Disorders, Human Molecular Genetics, Nature, Journal of Medical Genetics and Human Mutation.
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.