J.C. Murray

2.5k total citations · 1 hit paper
24 papers, 1.9k citations indexed

About

J.C. Murray is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, J.C. Murray has authored 24 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in J.C. Murray's work include Cleft Lip and Palate Research (4 papers), Angiogenesis and VEGF in Cancer (4 papers) and Craniofacial Disorders and Treatments (3 papers). J.C. Murray is often cited by papers focused on Cleft Lip and Palate Research (4 papers), Angiogenesis and VEGF in Cancer (4 papers) and Craniofacial Disorders and Treatments (3 papers). J.C. Murray collaborates with scholars based in United States, United Kingdom and Japan. J.C. Murray's co-authors include Peter W. Hewett, Elena V. Semina, Jacqueline Siegel‐Bartelt, John C. Carey, Pierre Bitoun, Nancy J. Leysens, Bernhard Zabel, Kent W. Small, Nicole A. Datson and Wallace L.M. Alward and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Advanced Drug Delivery Reviews.

In The Last Decade

J.C. Murray

23 papers receiving 1.8k citations

Hit Papers

Cloning and characterization of a novel bicoid-related ho... 1996 2026 2006 2016 1996 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.C. Murray United States 17 1.1k 747 169 154 151 24 1.9k
M C Johnston United States 14 654 0.6× 537 0.7× 149 0.9× 118 0.8× 51 0.3× 19 1.3k
James O’Sullivan United Kingdom 22 1.4k 1.3× 510 0.7× 103 0.6× 198 1.3× 74 0.5× 40 2.0k
Sanjeev S. Bhaskar United Kingdom 20 1.1k 1.1× 609 0.8× 84 0.5× 155 1.0× 55 0.4× 31 1.6k
Luitgard M. Neumann Germany 20 708 0.7× 1.0k 1.4× 207 1.2× 97 0.6× 68 0.5× 46 1.7k
Rika Kosaki Japan 25 1.3k 1.2× 846 1.1× 297 1.8× 185 1.2× 100 0.7× 113 2.3k
Lesley C. Adès Australia 23 915 0.9× 1.3k 1.7× 356 2.1× 120 0.8× 78 0.5× 58 2.2k
Éliane Chouery Lebanon 29 1.7k 1.6× 621 0.8× 188 1.1× 224 1.5× 277 1.8× 130 2.8k
Juan Carlos Zenteno Mexico 25 1.1k 1.0× 781 1.0× 198 1.2× 61 0.4× 88 0.6× 184 2.0k
Donald A. Glass United States 16 2.3k 2.2× 552 0.7× 225 1.3× 256 1.7× 100 0.7× 38 3.3k
B S Emanuel United States 30 1.8k 1.7× 1.1k 1.4× 243 1.4× 134 0.9× 60 0.4× 44 2.9k

Countries citing papers authored by J.C. Murray

Since Specialization
Citations

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

Fields of papers citing papers by J.C. Murray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.C. Murray. 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 J.C. Murray. The network helps show where J.C. Murray may publish in the future.

Co-authorship network of co-authors of J.C. Murray

This figure shows the co-authorship network connecting the top 25 collaborators of J.C. Murray. A scholar is included among the top collaborators of J.C. Murray 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 J.C. Murray. J.C. Murray 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.
Robinson, Kelsey, Sarah W. Curtis, Justin Paschall, et al.. (2025). Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios. The American Journal of Human Genetics. 112(11). 2679–2692.
2.
Petrin, Aline, Erliang Zeng, Mary Ann Thomas, et al.. (2023). DNA methylation differences in monozygotic twins with Van der Woude syndrome. SHILAP Revista de lepidopterología. 4. 2 indexed citations
3.
Cooper, M.E., et al.. (2007). Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. Journal of Perinatology. 27(11). 672–680. 50 indexed citations
4.
Dobbs, Stephen, Laurence Brown, David Ireland, et al.. (2000). Platelet-derived endothelial cell growth factor expression and angiogenesis in cervical intraepithelial neoplasia and squamous cell carcinoma of the cervix. Annals of Diagnostic Pathology. 4(5). 286–292. 16 indexed citations
5.
Martin, Stewart G. & J.C. Murray. (2000). Gene-transfer systems for human endothelial cells. Advanced Drug Delivery Reviews. 41(2). 223–233. 16 indexed citations
6.
Dubrovsky, Alberto, et al.. (2000). Bacterial expression of full-length and truncated forms of cytokine EMAP-2 and cytokine-like domain of mammalian tyrosyl-tRNA synthetase. Biopolymers and Cell. 16(3). 229–235. 9 indexed citations
7.
Yoshiura, Koh-ichiro, Junichiro Machida, Sandra Daack‐Hirsch, et al.. (1998). Characterization of a Novel Gene Disrupted by a Balanced Chromosomal Translocation t(2;19)(q11.2;q13.3) in a Family with Cleft Lip and Palate. Genomics. 54(2). 231–240. 57 indexed citations
8.
Семина, Е. В., Robert S. Reiter, & J.C. Murray. (1997). Isolation of a New Homeobox Gene Belonging to the Pitx/Rieg Family: Expression During Lens Development and Mapping to the Aphakia Region on Mouse Chromosome 19. Human Molecular Genetics. 6(12). 2109–2116. 163 indexed citations
9.
Kavanagh, G.M., et al.. (1997). The scleroatrophic syndrome of Huriez. British Journal of Dermatology. 137(1). 114–118. 12 indexed citations
10.
Semina, Elena V., Rebecca S. Reiter, Nancy J. Leysens, et al.. (1996). Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nature Genetics. 14(4). 392–399. 720 indexed citations breakdown →
11.
Gastier, Julie M., Thomas Brody, Jacqueline C. Pulido, et al.. (1996). Development of a Screening Set for New (CAG/CTG)nDynamic Mutations. Genomics. 32(1). 75–85. 35 indexed citations
12.
Munger, Ronald G., Paul A. Romitti, Sandra Daack‐Hirsch, et al.. (1996). Maternal alcohol use and risk of orofacial cleft birth defects. Teratology. 54(1). 27–33. 108 indexed citations
13.
Murray, J.C. & J Carmichael. (1995). Targeting solid tumours: challenges, disappointments, and opportunities. Advanced Drug Delivery Reviews. 17(1). 117–127. 22 indexed citations
14.
Hewett, Peter W. & J.C. Murray. (1993). Human Lung Microvessel Endothelial Cells: Isolation, Culture, and Characterization. Microvascular Research. 46(1). 89–102. 59 indexed citations
15.
Hewett, Peter W., J.C. Murray, Elizabeth Price, M.E. Watts, & M. Woodcock. (1993). Isolation and characterization of microvessel endothelial cells from human mammary adipose tissue. In Vitro Cellular & Developmental Biology - Animal. 29(4). 325–331. 61 indexed citations
16.
Hewett, Peter W. & J.C. Murray. (1993). Human microvessel endothelial cells: Isolation, culture and characterization. In Vitro Cellular & Developmental Biology - Animal. 29(11). 823–830. 81 indexed citations
17.
Hewett, Peter W. & J.C. Murray. (1993). Immunomagnetic purification of human microvessel endothelial cells using Dynabeads coated with monoclonal antibodies to PECAM-1.. PubMed. 62(2). 451–4. 65 indexed citations
18.
Padanilam, Babu J., H. Scott Stadler, K. Mills, et al.. (1992). Characterization of the human HOX 7 cDNA and identification of polymorphic markers. Human Molecular Genetics. 1(6). 407–410. 44 indexed citations
19.
Murray, J.C.. (1992). Vascular damage and tumour response. European Journal of Cancer. 28(10). 1593–1594. 4 indexed citations
20.
Kittur, Smita, John A. Phillips, J.C. Murray, et al.. (1989). Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.. PubMed. 44(1). 48–50. 8 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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