Raymond G. Fenwick

7.2k total citations · 2 hit papers
51 papers, 5.6k citations indexed

About

Raymond G. Fenwick is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Raymond G. Fenwick has authored 51 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 15 papers in Genetics and 11 papers in Epidemiology. Recurrent topics in Raymond G. Fenwick's work include Biochemical and Molecular Research (11 papers), HIV/AIDS drug development and treatment (10 papers) and Muscle Physiology and Disorders (8 papers). Raymond G. Fenwick is often cited by papers focused on Biochemical and Molecular Research (11 papers), HIV/AIDS drug development and treatment (10 papers) and Muscle Physiology and Disorders (8 papers). Raymond G. Fenwick collaborates with scholars based in United States, Canada and Netherlands. Raymond G. Fenwick's co-authors include C. Thomas Caskey, Antonio Pizzuti, David L. Nelson, Ying‐Hui Fu, Stephen Richards, Ying‐Hui Fu, Maura Pieretti, Jeanette J. A. Holden, Derek P.A. Kuhl and James S. Sutcliffe and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Raymond G. Fenwick

51 papers receiving 5.4k citations

Hit Papers

Variation of the CGG repe... 1991 2026 2002 2014 1991 1992 500 1000 1.5k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
    1991 1.6k citations Antonio Pizzuti, Stephen Richards et al. profile →
  2. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy
    1992 1.2k citations Ying‐Hui Fu, Antonio Pizzuti et al. Science profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raymond G. Fenwick United States 27 4.0k 2.3k 1.8k 786 520 51 5.6k
Bernard A. van Oost Netherlands 37 3.4k 0.8× 1.5k 0.6× 938 0.5× 392 0.5× 286 0.6× 134 6.4k
Grant R. Sutherland Australia 58 7.0k 1.8× 4.9k 2.1× 2.6k 1.4× 837 1.1× 259 0.5× 164 13.2k
Maria Anvret Sweden 39 2.5k 0.6× 1.3k 0.6× 1.4k 0.8× 215 0.3× 723 1.4× 125 4.7k
Lisbeth Tranebjærg Denmark 43 3.6k 0.9× 2.3k 1.0× 643 0.4× 417 0.5× 193 0.4× 163 6.7k
Jonathan A. Bernstein United States 28 3.8k 1.0× 2.2k 1.0× 767 0.4× 507 0.6× 169 0.3× 116 5.6k
Robert S. Sparkes United States 47 4.0k 1.0× 2.7k 1.2× 951 0.5× 405 0.5× 362 0.7× 205 9.8k
Gösta Holmgren Sweden 44 4.3k 1.1× 1.7k 0.7× 613 0.3× 401 0.5× 325 0.6× 165 6.6k
E. Schwinger Germany 40 2.7k 0.7× 2.0k 0.9× 1.3k 0.7× 391 0.5× 1.0k 2.0× 210 6.0k
Elizabeth Baker Australia 44 3.4k 0.9× 2.9k 1.3× 696 0.4× 681 0.9× 123 0.2× 116 6.7k
P. Pearson Netherlands 55 6.3k 1.6× 4.7k 2.0× 771 0.4× 234 0.3× 248 0.5× 209 10.7k

Countries citing papers authored by Raymond G. Fenwick

Since Specialization
Citations

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

Fields of papers citing papers by Raymond G. Fenwick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Raymond G. Fenwick. 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 Raymond G. Fenwick. The network helps show where Raymond G. Fenwick may publish in the future.

Co-authorship network of co-authors of Raymond G. Fenwick

This figure shows the co-authorship network connecting the top 25 collaborators of Raymond G. Fenwick. A scholar is included among the top collaborators of Raymond G. Fenwick 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 Raymond G. Fenwick. Raymond G. Fenwick 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.
Strom, Charles M., Beryl Crossley, Joy B. Redman, et al.. (2007). Molecular testing for Fragile X Syndrome: Lessons learned from 119,232 tests performed in a clinical laboratory. Genetics in Medicine. 9(1). 46–51. 42 indexed citations
2.
Fenwick, Raymond G., et al.. (2006). Hyponatremia resulting from Arginine Vasopressin Receptor 2 gene mutation. Pediatric Nephrology. 22(3). 463–466. 20 indexed citations
3.
4.
Ahmed, Syed A., et al.. (2005). Nine Novel Germline Gene Variants in the RET Proto-Oncogene Identified in Twelve Unrelated Cases. Journal of Molecular Diagnostics. 7(2). 283–288. 23 indexed citations
5.
Batanian, Jacqueline R., David H. Ledbetter, & Raymond G. Fenwick. (1998). A Simple VNTR-PCR Method for Detecting Maternal Cell Contamination in Prenatal Diagnosis. Genetic Testing. 2(4). 347–350. 23 indexed citations
6.
Guida, Marco, et al.. (1996). Southern transfer protocol for confirmation of Huntington disease. Clinical Chemistry. 42(10). 1711–1712. 18 indexed citations
7.
8.
Demarchi, J, et al.. (1994). A robotics-assisted procedure for large scale cystic fibrosis mutation analysis. Human Mutation. 4(4). 281–290. 52 indexed citations
9.
Fu, Ying‐Hui, David L. Friedman, Stephen Richards, et al.. (1993). Decreased Expression of Myotonin-Protein Kinase Messenger RNA and Protein in Adult Form of Myotonic Dystrophy. Science. 260(5105). 235–238. 249 indexed citations
10.
Bies, Roger D., C. Thomas Caskey, & Raymond G. Fenwick. (1992). An intact cysteine-rich domain is required for dystrophin function.. Journal of Clinical Investigation. 90(2). 666–672. 61 indexed citations
11.
Caskey, C. Thomas, Antonio Pizzuti, Ying‐Hui Fu, Raymond G. Fenwick, & David L. Nelson. (1992). Triplet repeat mutations in human disease. Science. 256(5058). 784–789. 312 indexed citations
12.
Hoffman, Eric P., Carlos García, Jeffrey S. Chamberlain, et al.. (1991). Is the carboxyl‐terminus of dystrophin required for membrane association? A novel, severe case of duchenne muscular dystrophy. Annals of Neurology. 30(4). 605–610. 80 indexed citations
13.
14.
Krizman, David B., Joseph Jankovic, P Steuber, et al.. (1991). 9p monosomy in a patient with Gilles de la Tourette's syndrome. Neurology. 41(9). 1513–1513. 35 indexed citations
15.
Howell, Robin E., et al.. (1990). A transforming Kirsten ras oncogene in an oral squamous carcinoma. Journal of Oral Pathology and Medicine. 19(7). 301–305. 16 indexed citations
16.
Howell, Robin E., et al.. (1989). Loss of Harvey ras heterozygosity in oral squamous carcinoma. Journal of Oral Pathology and Medicine. 18(2). 79–83. 15 indexed citations
17.
Mirabelli, Christopher K., Cheng-Hsiung Huang, Raymond G. Fenwick, & Stanley T. Crooke. (1985). Quantitative measurement of single- and double-strand breakage of DNA in Escherichia coli by the antitumor antibiotics bleomycin and talisomycin. Antimicrobial Agents and Chemotherapy. 27(4). 460–467. 32 indexed citations
18.
Fuscoe, James C., Raymond G. Fenwick, David H. Ledbetter, & C. Thomas Caskey. (1983). Deletion and amplification of the HGPRT locus in Chinese hamster cells.. Molecular and Cellular Biology. 3(6). 1086–1096. 138 indexed citations
19.
Fenwick, Raymond G.. (1980). Reversion of a mutation affecting the molecular weight of HGPRT: Intragenic suppression and localization of X-linked genes. Somatic Cell and Molecular Genetics. 6(4). 477–494. 19 indexed citations
20.
Fenwick, Raymond G. & Roy Curtiss. (1973). Conjugal Deoxyribonucleic Acid Replication by Escherichia coli K-12: Effect of Nalidixic Acid. Journal of Bacteriology. 116(3). 1236–1246. 17 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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