Peter N. Ray

12.1k citations

153 papers · 6.8k indexed · 1 hit paper · h-index 45

Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research 15
- Genetic Syndromes and Imprinting 12
- Genomics and Rare Diseases 11
Molecular Biology top 1%
- Muscle Physiology and Disorders 54
- RNA modifications and cancer 16
- Epigenetics and DNA Methylation 13
- RNA Research and Splicing 13
Genetics top 1%
- Neurogenetic and Muscular Disorders Research 15
- Genetic Syndromes and Imprinting 12
- Genomics and Rare Diseases 11
Cellular and Molecular Neuroscience top 2%
Cardiology and Cardiovascular Medicine top 2%
- Cardiomyopathy and Myosin Studies 19

Co-authors: Ronald G. Worton Arthur H.M. Burghes Henry J. Klamut Dennis E. Bulman Elizabeth E. Zubrzycka‐Gaarn Berivan Baskin Margaret Thompson George Karpati
Cited by: Genetics Molecular Biology
Journals: Neuromuscular Disorders (8 papers)Human Molecular Genetics (6 papers)Journal of Medical Genetics (5 papers)
Partner nations: Canada United States Sweden

In The Last Decade

Peter N. Ray

149 papers receiving 6.7k citations

Hit Papers

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Peers

Countries citing papers authored by Peter N. Ray

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

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

All Works

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20 of 20 papers shown

#	Work
1	De Novo Mutations Causing Shwachman-Diamond Syndrome and a Founder Mutation in SBDS in the French Canadian Population Leslie Steele,Johanna M. Rommens,Tracy Stockley,Berivan Baskin,Peter N. Ray	2014	3
2	Complex genomic rearrangements in the dystrophin gene due to replication‐based mechanisms Molecular Genetics & Genomic Medicine ·Berivan Baskin,Dimitri J. Stavropoulos,Valerie Bianca Galvan-Turner,Alexandr Kim,Martin Li,Leslie Steele,Christian R. Marshall,Edmond G. Lemire,Kym M. Boycott,William T. Gibson,Peter N. Ray	2014	17
3	Does Integration of Various Ion Channel Measurements Improve Diagnostic Performance in Cystic Fibrosis? Annals of the American Thoracic Society ·Chee Y. Ooi,Annie Dupuis,Tanja Gonska,Lynda Ellis,Ai Ni,Keith Jarvi,Sheelagh Martin,Peter N. Ray,Leslie Steele,Paul Kortan,Ruslan Dorfman,Melinda Solomon,Julian Zielenski,Mary Corey,Elizabeth Tullis,Peter R. Durie	2014	9
4	Genetic, cell biological, and clinical interrogation of theCFTR mutation c.3700 A>G (p.Ile1234Val) informs strategies for future medical intervention Genetics in Medicine ·Steven V. Molinski,Tanja Gonska,Ling Jun Huan,Berivan Baskin,Ibrahim Janahi,Peter N. Ray,Christine E. Bear	2014	29
5	High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome Human Genetics ·Berivan Baskin,Sanaa Choufani,Yi‐An Chen,Cheryl Shuman,Nicole Parkinson,Emmanuelle Lemyre,A. Micheil Innes,Dimitri J. Stavropoulos,Peter N. Ray,Rosanna Weksberg	2013	58
6	Eye and Brain Abnormalities in Congenital Muscular Dystrophies Caused by Fukutin-Related Protein Gene (FKRP) Mutations Pediatric Neurology ·Maina Kava,David Chitayat,Susan Blasér,Peter N. Ray,Jiri Vajsar	2013	12
7	Monoallelic Expression Determines Oncogenic Progression and Outcome in Benign and Malignant Brain Tumors Cancer Research ·Erin J. Walker,Cindy Zhang,Pedro Castelo‐Branco,Cynthia Hawkins,Novita Sarika N,Nataliya Zhukova,Noa Alon,Ana Novokmet,Berivan Baskin,Peter N. Ray,Christiane B. Knobbe‐Thomsen,Peter B. Dirks,Michael D. Taylor,Sidney Croul,David Malkin,Uri Tabori	2011	42
8	Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome Journal of Intellectual Disability Research ·Gregory Costain,Eva W.C. Chow,Peter N. Ray,Anne S. Bassett	2011	38
9	Recurrent Focal Copy-Number Changes and Loss of Heterozygosity Implicate Two Noncoding RNAs and One Tumor Suppressor Gene at Chromosome 3q13.31 in Osteosarcoma Cancer Research ·Ivan Pašić,Adam Shlien,Adam D. Durbin,Dimitrios J. Stavropoulos,Berivan Baskin,Peter N. Ray,Ana Novokmet,David Malkin	2010	126
10	Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4 Neuromuscular Disorders ·Berivan Baskin,William T. Gibson,Peter N. Ray	2010	18
11	Strategy for Comprehensive Molecular Testing for Duchenne and Becker Muscular Dystrophies Genetic Testing ·Tracy Stockley,A. M. Amanov,Natalie Bulgin,Peter N. Ray	2006	28
12	Analysis of the glucocerebrosidase gene in Parkinson's disease Movement Disorders ·Christine Sato,Angharad R. Morgan,Anthony E. Lang,Shabnam Salehi‐Rad,Toshitaka Kawarai,Yan Meng,Peter N. Ray,Lindsay A. Farrer,Peter St George‐Hyslop,Ekaterina Rogaeva	2004	91
13	Duchenne Muscular Dystrophy: Current Knowledge, Treatment, and Future Prospects Clinical Orthopaedics and Related Research ·W. Douglas Biggar,Henry J. Klamut,Sara Abdelghani,Daniel Stevens,Peter N. Ray	2002	34
14	Status of joint forest management in Tripura. Indian Forester ·Peter N. Ray	2000	1
15	Alternative splicing regulates the nuclear or cytoplasmic localization of dystrophin Dp71 FEBS Letters ·Vinh Adams,Cecilia Montáñez,Peter N. Ray,Perry L. Howard,Francisco García‐Sierra,Dominique Mornet,Bulmaro Cisneros	2000	32
16	Reply to Migeon. The American Journal of Human Genetics ·Joe T.R. Clarke,Peter J. Wilson,C. Phillip Morris,John J. Hopwood,Robert I. Richards,Grant R. Sutherland,Peter N. Ray	1993	0
17	Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy Human Molecular Genetics ·Alissa V. Winnard,Christopher J. Klein,Daniel D. Coovert,Thomas W. Prior,Audrey C. Papp,Pamela J. Snyder,Dennis E. Bulman,Peter N. Ray,Patricia McAndrew,Wendy King,Richard T. Moxley,Jerry R. Mendell,Arthur H.M. Burghes	1993	84
18	Immunogold labelling of dystrophin in human muscle, using an antibody to the last 17 amino acids of the C-terminus Neuromuscular Disorders ·Michael J. Cullen,John Walsh,L. V. B. Nicholson,J.B. Harris,Elizabeth E. Zubrzycka‐Gaarn,Peter N. Ray,R. G. Worton	1991	27
19	Molecular structure of the human asparagine synthetase gene Genomics ·Yi Ping Zhang,Marie Lambert,Claire Louise Simons,Elsa Viridiana Severo Garnica,Peter N. Ray,Irene L. Andrulis	1989	27
20	Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy. Journal of Medical Genetics ·A. Mizulov,Agnieszka Olechnicka,Sabine Czenna,Peter N. Ray,Ch. Verellen-Dumoulin,R. G. Worton	1986	11

About Peter N. Ray

Peter N. Ray is a scholar working on Genetics, Genetics and Molecular Biology, having authored 153 papers that have together received 6.8k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (54 papers), Cardiomyopathy and Myosin Studies (19 papers), RNA modifications and cancer (16 papers), Neurogenetic and Muscular Disorders Research (15 papers), Epigenetics and DNA Methylation (13 papers), RNA Research and Splicing (13 papers), Genetic Syndromes and Imprinting (12 papers) and Genomics and Rare Diseases (11 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (5.3k citations) and Genetics (1.8k citations). Peter N. Ray has collaborated with scholars based in Canada, United States and Sweden. Frequent co-authors include Ronald G. Worton, Arthur H.M. Burghes, Henry J. Klamut, Dennis E. Bulman, Elizabeth E. Zubrzycka‐Gaarn, Berivan Baskin, Margaret Thompson, George Karpati, Louise R. Simard and Patricia McAndrew. Their work appears in journals such as Neuromuscular Disorders, Human Molecular Genetics, Journal of Medical Genetics, Nature and Molecular and Cellular Biology.

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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