Cox Dw

713 total citations
11 papers, 502 citations indexed

About

Cox Dw is a scholar working on Molecular Biology, Cancer Research and Nutrition and Dietetics. According to data from OpenAlex, Cox Dw has authored 11 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Cancer Research and 4 papers in Nutrition and Dietetics. Recurrent topics in Cox Dw's work include Protease and Inhibitor Mechanisms (5 papers), Trace Elements in Health (4 papers) and Biochemical and Structural Characterization (2 papers). Cox Dw is often cited by papers focused on Protease and Inhibitor Mechanisms (5 papers), Trace Elements in Health (4 papers) and Biochemical and Structural Characterization (2 papers). Cox Dw collaborates with scholars based in Canada, United States and Italy. Cox Dw's co-authors include Magne K. Fagerhol, Elias I. Traboulsi, E. Ferda Perçin, M. Sarfarazi, Ayse G. Koçak-Altintas, Jane C. Sowden, Bharati Bapat, A.J. Rutherford, Mustafa Kemal Arıcı and Ernest Cutz and has published in prestigious journals such as Nature Genetics, Human Mutation and Cytogenetic and Genome Research.

In The Last Decade

Cox Dw

11 papers receiving 477 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cox Dw Canada	10	237	153	110	75	69	11	502
Jennifer M. Lu-Kuo United States	9	259 1.1×	39 0.3×	25 0.2×	44 0.6×	32 0.5×	9	516
M. Wick Germany	10	444 1.9×	100 0.7×	159 1.4×	17 0.2×	77 1.1×	12	857
Romulo Martin Brena United States	16	852 3.6×	132 0.9×	232 2.1×	32 0.4×	85 1.2×	19	1.1k
Deborah Bielser United States	7	387 1.6×	73 0.5×	57 0.5×	15 0.2×	48 0.7×	7	536
Satoru Takahashi Japan	10	268 1.1×	27 0.2×	37 0.3×	71 0.9×	81 1.2×	12	466
Daniel J. Schroen United States	8	351 1.5×	193 1.3×	225 2.0×	15 0.2×	51 0.7×	11	641
Małgorzata Jarmuż‐Szymczak Poland	18	573 2.4×	151 1.0×	181 1.6×	37 0.5×	29 0.4×	64	781
G D Billingsley Canada	9	276 1.2×	166 1.1×	94 0.9×	15 0.2×	51 0.7×	12	404
Fiona McLaughlin United Kingdom	12	440 1.9×	56 0.4×	46 0.4×	31 0.4×	90 1.3×	19	653
Joseph W. Towner United States	9	324 1.4×	313 2.0×	49 0.4×	43 0.6×	17 0.2×	17	660

Countries citing papers authored by Cox Dw

Since Specialization

Citations

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

Fields of papers citing papers by Cox Dw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cox Dw. 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 Cox Dw. The network helps show where Cox Dw may publish in the future.

Co-authorship network of co-authors of Cox Dw

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

1.

Dw, Cox, et al.. (2003). Genetic variation in the promoter and 5′ UTR of the copper transporter, ATP7B, in patients with Wilson disease. Clinical Genetics. 64(5). 429–432. 20 indexed citations

2.

Perçin, E. Ferda, Mustafa Kemal Arıcı, A.J. Rutherford, et al.. (2000). Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Nature Genetics. 25(4). 397–401. 222 indexed citations

3.

Orrù, Sandro, Gordon R. Thomas, Annalisa Loizedda, Cox Dw, & L. Contu. (1997). 24 bp deletion and Ala1278 to val mutation of the ATP7B gene in a Sardinian family with Wilson disease. Human Mutation. 10(1). 84–85. 9 indexed citations

4.

Dw, Cox. (1996). Molecular advances in Wilson disease.. PubMed. 14. 245–64. 29 indexed citations

5.

Bull, Peter C., et al.. (1993). Isolation of new probes in the region of the Wilson disease locus, 13q14.2→q14.3. Cytogenetic and Genome Research. 64(1). 12–17. 9 indexed citations

6.

Dw, Cox. (1986). Ethnic differences in reactions to drugs and xenobiotics. Clinical and molecular studies of alpha 1-antitrypsin deficiency.. PubMed. 214. 373–84. 1 indexed citations

7.

Dw, Cox. (1981). New variants of alpha 1-antitrypsin: comparison of Pi typing techniques.. Europe PMC (PubMed Central). 33(3). 354–65. 39 indexed citations

8.

Fagerhol, Magne K. & Cox Dw. (1981). The Pi polymorphism: genetic, biochemical, and clinical aspects of human alpha 1-antitrypsin.. PubMed. 11. 1–62, 371. 128 indexed citations

9.

Cutz, Ernest & Cox Dw. (1979). Alpha 1-antitrypsin deficiency: the spectrum of pathology and pathophysiology.. PubMed. 5. 1–39. 15 indexed citations

10.

Dw, Cox. (1978). Genetic variation of alpha 1-antitrypsin.. PubMed. 30(6). 660–2. 16 indexed citations

11.

Dw, Cox. (1975). The effect of neuraminidase on genetic variants of alpha anitrypsin.. PubMed. 27(2). 165–77. 14 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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