R H McLean

652 total citations
24 papers, 441 citations indexed

About

R H McLean is a scholar working on Immunology, Genetics and Hematology. According to data from OpenAlex, R H McLean has authored 24 papers receiving a total of 441 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Immunology, 6 papers in Genetics and 6 papers in Hematology. Recurrent topics in R H McLean's work include Complement system in diseases (11 papers), Renal Diseases and Glomerulopathies (5 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers). R H McLean is often cited by papers focused on Complement system in diseases (11 papers), Renal Diseases and Glomerulopathies (5 papers) and Coagulation, Bradykinin, Polyphosphates, and Angioedema (5 papers). R H McLean collaborates with scholars based in United States, Italy and Canada. R H McLean's co-authors include Noorbibi K. Day, Robert A. Good, Hartmut Geiger, J A Winkelstein, D. Hoefnagel, B.J. Schmeckpeper, Kathleen E. Sullivan, M. A. Petri, Robin Wood and Robert J. Leggiadro and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Gastroenterology.

In The Last Decade

R H McLean

23 papers receiving 381 citations

Peers

R H McLean

IMMUN

HEMAT

NEPHR

GENET

RHEUM

G. Füst Hungary

S Bettoni Italy

Peters Dk United Kingdom

Eleonora Ballanti Italy

Emancipator Sn United States

G Di Muzio Italy

Rebecca Hyde United Kingdom

L. A. van Es Netherlands

Pilar Nozal Spain

Jing L. Marantz United States

G. Füst Hungary

R H McLean

268 ×1.0

IMMUN

94 ×0.8

HEMAT

48 ×0.5

NEPHR

73 ×0.8

GENET

92 ×1.1

RHEUM

Citations per year, relative to R H McLean R H McLean (= 1×) peers G. Füst

Countries citing papers authored by R H McLean

Since Specialization

Citations

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

Fields of papers citing papers by R H McLean

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R H McLean. 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 R H McLean. The network helps show where R H McLean may publish in the future.

Co-authorship network of co-authors of R H McLean

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

All Works

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20 of 20 papers shown

Venturella, Roberta, et al.. (2024). Quality of life improvements in women with uterine fibroids treated with relugolix combination therapy during the LIBERTY long‐term extension study: A descriptive subgroup analysis in women with anemia at baseline. International Journal of Gynecology & Obstetrics. 165(2). 431–441. 1 indexed citations

McLean, R H, G Niblack, Bruce A. Julian, et al.. (1994). Hemolytically inactive C4B complement allotype caused by a proline to leucine mutation in the C5-binding site.. Journal of Biological Chemistry. 269(44). 27727–27731. 8 indexed citations

Sullivan, Kathleen E., M. A. Petri, B.J. Schmeckpeper, R H McLean, & J A Winkelstein. (1994). Prevalence of a mutation causing C2 deficiency in systemic lupus erythematosus.. PubMed. 21(6). 1128–33. 50 indexed citations

Fasano, Mary Beth, et al.. (1992). A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotype.. Journal of Clinical Investigation. 90(4). 1180–1184. 5 indexed citations

McLean, R H, et al.. (1990). Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complement. Pediatric Nephrology. 4(6). 597–599. 30 indexed citations

Arnett, F C, Wilma Β. Bias, R H McLean, et al.. (1990). Connective tissue disease in southeast Georgia. A community based study of immunogenetic markers and autoantibodies.. PubMed. 17(8). 1029–35. 19 indexed citations

Rowe, Peter C., R H McLean, Robin Wood, Robert J. Leggiadro, & J A Winkelstein. (1989). Association of Homozygous C4B Deficiency with Bacterial Meningitis. The Journal of Infectious Diseases. 160(3). 448–451. 47 indexed citations

Wigley, Frederick M., et al.. (1987). Systemic sclerosis (scleroderma): clinical, genetic, and serologic subsets.. PubMed. 14(3). 512–8. 35 indexed citations

McLean, R H & D. Hoefnagel. (1980). Partial Lipodystrophy and Familial C3 Deficiency. Human Heredity. 30(3). 149–154. 29 indexed citations

10.

Kennedy, T. L., et al.. (1980). INTRAVENOUS METHYLPREDNISOLONE IN THE TREATMENT OF STEROID RESPONSIVE NEPHROTIC SYNDROME. Pediatric Research. 14(8). 1006–1006. 3 indexed citations

11.

McLean, R H, et al.. (1979). C3 Nephritic Factor Stabilization of the Classic C3 Convertase: A Role for C2 in C3 Nephritic Factor Activity. Experimental Biology and Medicine. 161(3). 358–363. 9 indexed citations

12.

McLean, R H, et al.. (1977). Normal complement in early poststreptococcal glomerulonephritis.. BMJ. 1(6072). 1326–1326. 4 indexed citations

13.

McLean, R H, Mitchell B. Lowenstein, & N Rothfield. (1977). HETEROZYGOUS C3 DEFICIENCY ASSOCIATED WITH A SYSTEMIC LUPUS ERYTHEMATOSUS-LIKE DISEASE. Pediatric Research. 11(4). 490–490. 8 indexed citations

14.

Hunt, Raegan, et al.. (1976). Proceedings: Cardiopulmonary manifestations of systemic lupus erythematosus (SLE).. PubMed. 18(5). 524–524. 1 indexed citations

15.

McLean, R H, et al.. (1975). The effect of anticomplementary substances on properdin in normal and C2-deficient sera.. PubMed. 19(3). 435–44. 8 indexed citations

16.

Westberg, N. Gunnar, et al.. (1973). Determination of Serum Properdin Levels by Immunodiffusion. International Archives of Allergy and Immunology. 44(1). 155–160. 7 indexed citations

17.

Day, Noorbibi K., et al.. (1973). DEVELOPMENT OF LUPUS ERYTHEMATOSUS. 12 indexed citations

18.

Day, Noorbibi K., et al.. (1973). The Association of Respiratory Infection, Recurrent Hematuria, and Focal Glomerulonephritis with Activation of the Complement System in the Cold. Journal of Clinical Investigation. 52(7). 1698–1706. 32 indexed citations

19.

Day, Noorbibi K., et al.. (1973). C2 Deficiency DEVELOPMENT OF LUPUS ERYTHEMATOSUS. Journal of Clinical Investigation. 52(7). 1601–1607. 91 indexed citations

20.

McLean, R H, et al.. (1972). The Immunoelectrophoretic Pattern of Properdin in Fresh and Aged Human Serum. Experimental Biology and Medicine. 141(2). 403–407. 11 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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