J.C. Murray

743 total citations
15 papers, 587 citations indexed

About

J.C. Murray is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology. According to data from OpenAlex, J.C. Murray has authored 15 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Rheumatology. Recurrent topics in J.C. Murray's work include Folate and B Vitamins Research (2 papers), Protein Interaction Studies and Fluorescence Analysis (1 paper) and Blood properties and coagulation (1 paper). J.C. Murray is often cited by papers focused on Folate and B Vitamins Research (2 papers), Protein Interaction Studies and Fluorescence Analysis (1 paper) and Blood properties and coagulation (1 paper). J.C. Murray collaborates with scholars based in United States, Norway and Australia. J.C. Murray's co-authors include K. Mills, Kenneth H. Buetow, Christian Bréchot, M C Kew, Mark A. Smith, Jonathan Israel, William T. London, Véronique Blanquet, Jorge S. López‐Camelo and George L. Wehby and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and American Journal of Epidemiology.

In The Last Decade

J.C. Murray

15 papers receiving 563 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J.C. Murray United States	10	266	178	91	87	78	15	587
A Bröcker-Vriends Netherlands	15	178 0.7×	177 1.0×	137 1.5×	73 0.8×	70 0.9×	26	842
H Mertens Netherlands	10	146 0.5×	87 0.5×	209 2.3×	88 1.0×	44 0.6×	22	738
D. Stirling United Kingdom	14	206 0.8×	337 1.9×	103 1.1×	58 0.7×	91 1.2×	26	889
Michael Lobell United States	13	202 0.8×	96 0.5×	142 1.6×	45 0.5×	42 0.5×	18	816
Dragana Janić Serbia	15	175 0.7×	111 0.6×	88 1.0×	142 1.6×	65 0.8×	70	722
Sylvie Martel France	19	580 2.2×	82 0.5×	197 2.2×	20 0.2×	101 1.3×	31	1.1k
Elizabeth O. Garner United States	8	157 0.6×	122 0.7×	237 2.6×	51 0.6×	129 1.7×	10	1.1k
R Davidson United Kingdom	9	159 0.6×	346 1.9×	120 1.3×	92 1.1×	45 0.6×	12	511
Lingmin Hu China	17	357 1.3×	86 0.5×	125 1.4×	91 1.0×	187 2.4×	46	845
Eng E United States	8	295 1.1×	63 0.4×	66 0.7×	25 0.3×	33 0.4×	12	701

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

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15 of 15 papers shown

Harrington, Patrick R., Lisa K. Naeger, Kirk M. Chan‐Tack, et al.. (2018). HCV genotype 4, 5 and 6: Distribution of viral subtypes and sustained virologic response rates in clinical trials of approved direct‐acting antiviral regimens. Journal of Viral Hepatitis. 25(8). 969–975. 9 indexed citations

Boyles, Abee L., Lisa A. DeRoo, Rolv T. Lie, et al.. (2010). Maternal Alcohol Consumption, Alcohol Metabolism Genes, and the Risk of Oral Clefts: A Population-based Case-Control Study in Norway, 1996-2001. American Journal of Epidemiology. 172(8). 924–931. 58 indexed citations

Wehby, George L., J.C. Murray, Eduardo E. Castilla, Jorge S. López‐Camelo, & Robert L. Ohsfeldt. (2009). Prenatal care effectiveness and utilization in Brazil. Health Policy and Planning. 24(3). 175–188. 78 indexed citations

Paola, Jorge Di, et al.. (2005). Platelet glycoprotein Ibα and integrin α2β1 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel. Journal of Thrombosis and Haemostasis. 3(7). 1511–1521. 26 indexed citations

Mathews, Katherine D., et al.. (1995). Phenotypic and Pathologic Evaluation of the myd Mouse. A Candidate Model for Facioscapulohumeral Dystrophy. Journal of Neuropathology & Experimental Neurology. 54(4). 607–607. 27 indexed citations

Murray, J.C., Val C. Sheffield, & Geoffrey M. Duyk. (1994). High resolution genetic maps incorporating multiple classes of short tandem repeat polymorphisms. The American Journal of Human Genetics. 55. 1 indexed citations

Nishimura, Darryl, A F Purchio, & J.C. Murray. (1993). Linkage Localization of TGFB2 and the Human Homeobox Gene HLX1 to Chromosome 1q. Genomics. 15(2). 357–364. 19 indexed citations

Mills, K., et al.. (1992). Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA). Human Molecular Genetics. 1(9). 779–779. 95 indexed citations

Murray, J.C., Gert‐Jan B. van Ommen, & R.J. Daniels. (1990). Report of the committee on the genetic constitution of chromosome 4. Cytogenetic and Genome Research. 55(1-4). 97–110. 34 indexed citations

10.

Beck, John S., Ruth Sager, & J.C. Murray. (1989). A Scal RFLP demonstrated for the GRO gene on chromosome 4. Nucleic Acids Research. 17(21). 8895–8895. 1 indexed citations

11.

Buetow, Kenneth H., J.C. Murray, Jonathan Israel, et al.. (1989). Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.. Proceedings of the National Academy of Sciences. 86(22). 8852–8856. 170 indexed citations

12.

Murray, J.C., et al.. (1988). A TaqI RFLP demonstrated for pIBS17 [D4S123], a single copy sequence on chromosome 4. Nucleic Acids Research. 16(6). 2743–2743. 2 indexed citations

13.

Carlock, L R, et al.. (1987). An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's Disease. Nucleic Acids Research. 15(1). 377–377. 8 indexed citations

14.

Ferrell, R E, Kenneth H. Buetow, John Darby, et al.. (1987). Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.. Journal of Medical Genetics. 24(9). 522–524. 2 indexed citations

15.

Murray, J.C., et al.. (1983). Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia.. Proceedings of the National Academy of Sciences. 80(19). 5951–5955. 57 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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