P N Ray

986 total citations
17 papers, 783 citations indexed

About

P N Ray is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, P N Ray has authored 17 papers receiving a total of 783 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Genetics. Recurrent topics in P N Ray's work include Muscle Physiology and Disorders (11 papers), Neurogenetic and Muscular Disorders Research (5 papers) and RNA modifications and cancer (3 papers). P N Ray is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Neurogenetic and Muscular Disorders Research (5 papers) and RNA modifications and cancer (3 papers). P N Ray collaborates with scholars based in Canada, United States and Netherlands. P N Ray's co-authors include Ronald G. Worton, R. G. Worton, Suman B. Gangopadhyay, Henry J. Klamut, Elizabeth E. Zubrzycka‐Gaarn, George Karpati, Paul C. Holland, Yannick Pouliot, Stirling Carpenter and Sharon Bodrug and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Genetics.

In The Last Decade

P N Ray

15 papers receiving 771 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P N Ray Canada 13 643 225 136 116 107 17 783
G K Suthers Australia 11 587 0.9× 283 1.3× 107 0.8× 112 1.0× 102 1.0× 18 717
Lau A.J. Blonden Netherlands 12 727 1.1× 219 1.0× 157 1.2× 93 0.8× 114 1.1× 15 861
Eri Kondo-Iida Japan 8 842 1.3× 105 0.5× 99 0.7× 209 1.8× 113 1.1× 13 939
Dominique Récan France 20 1.3k 2.1× 700 3.1× 107 0.8× 137 1.2× 113 1.1× 33 1.6k
Jeffrey Murray United Kingdom 7 605 0.9× 284 1.3× 141 1.0× 100 0.9× 51 0.5× 8 766
Chris A. Feener United States 8 601 0.9× 118 0.5× 55 0.4× 111 1.0× 142 1.3× 8 712
Steven G. Webster United States 4 995 1.5× 154 0.7× 124 0.9× 114 1.0× 129 1.2× 6 1.2k
Hiroko Wada Japan 14 461 0.7× 109 0.5× 177 1.3× 36 0.3× 43 0.4× 27 561
Rita C.M. Pavanello Brazil 18 899 1.4× 154 0.7× 210 1.5× 303 2.6× 93 0.9× 50 1.0k
P.M. Grootscholten Netherlands 13 1.2k 1.9× 268 1.2× 517 3.8× 167 1.4× 144 1.3× 15 1.4k

Countries citing papers authored by P N Ray

Since Specialization
Citations

This map shows the geographic impact of P 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 P 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 P N Ray more than expected).

Fields of papers citing papers by P N Ray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P 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 P N Ray. The network helps show where P N Ray may publish in the future.

Co-authorship network of co-authors of P N Ray

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

All Works

17 of 17 papers shown
1.
Vajsar, Jiri, Thomas Balslev, P N Ray, J. Siegel‐Bartelt, & Venita Jay. (1998). Congenital cytoplasmic body myopathy with survival motor neuron gene deletion or Werdnig-Hoffmann disease. Neurology. 51(3). 873–875. 12 indexed citations
2.
Costa, Teresa, Marie Lambert, Ikuko Teshima, et al.. (1998). Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex. American Journal of Medical Genetics. 75(1). 40–44. 35 indexed citations
3.
Costa, Teresa, Wenda Greer, G Rysiecki, J. Raymond Buncic, & P N Ray. (1997). Monozygotic twins discordant for Aicardi syndrome.. Journal of Medical Genetics. 34(8). 688–691. 17 indexed citations
4.
Pillers, De‐Ann M., Dennis E. Bulman, Richard G. Weleber, et al.. (1993). Dystrophin expression in the human retina is required for normal function as defined by electroretinography. Nature Genetics. 4(1). 82–86. 134 indexed citations
5.
Wijmenga, Cisca, L. Sandkuijl, Petra Moerer, et al.. (1992). Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.. PubMed. 51(2). 411–5. 50 indexed citations
6.
Clarke, J. T. R., Peter J. Wilson, C. Phillip Morris, et al.. (1992). Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.. PubMed. 51(2). 316–22. 36 indexed citations
7.
Bapat, Bharati, John Groffen, & P N Ray. (1991). The human tyrosine kinase gene (FER) detects an RFLP with Bgll. Nucleic Acids Research. 19(15). 4310–4310.
8.
Clarke, Joe T.R., et al.. (1991). Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl.. PubMed. 49(2). 289–97. 39 indexed citations
9.
Worton, Ronald G., Dennis E. Bulman, Elizabeth E. Zubrzycka‐Gaarn, & P N Ray. (1990). Genetic and Biochemical Determinations in the Pre-Transplant Workup and in the Post-Transplant Assessment Period. Advances in experimental medicine and biology. 280. 219–226.
10.
Bodrug, Sharon, Jacquelyn Roberson, Lester Weiss, et al.. (1990). Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.. Journal of Medical Genetics. 27(7). 426–432. 33 indexed citations
11.
Klamut, Henry J., Suman B. Gangopadhyay, R. G. Worton, & P N Ray. (1990). Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy gene.. Molecular and Cellular Biology. 10(1). 193–205. 125 indexed citations
12.
Karpati, George, Yannick Pouliot, Elizabeth E. Zubrzycka‐Gaarn, et al.. (1989). Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation.. PubMed. 135(1). 27–32. 181 indexed citations
13.
Ray, P N, et al.. (1988). The problem of Duchenne muscular dystrophy. Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 319(1194). 275–284. 2 indexed citations
14.
Bodrug, Sharon, et al.. (1987). Molecular Analysis of a Constitutional X-Autosome Translocation in a Female with Muscular Dystrophy. Science. 237(4822). 1620–1624. 70 indexed citations
15.
Thomas, Nick, P N Ray, Ronald G. Worton, & Peter S. Harper. (1986). Molecular deletion analysis in Duchenne muscular dystrophy.. Journal of Medical Genetics. 23(6). 509–515. 21 indexed citations
16.
17.
Worton, Ronald G., et al.. (1986). Analysis of an X-autosome Translocation Responsible for X-linked Muscular Dystrophy. Cold Spring Harbor Symposia on Quantitative Biology. 51(0). 345–348. 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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