P.J. McAlpine

2.7k total citations
68 papers, 1.4k citations indexed

About

P.J. McAlpine is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, P.J. McAlpine has authored 68 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 29 papers in Molecular Biology and 12 papers in Hematology. Recurrent topics in P.J. McAlpine's work include Genomic variations and chromosomal abnormalities (15 papers), Erythrocyte Function and Pathophysiology (10 papers) and Blood groups and transfusion (9 papers). P.J. McAlpine is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Erythrocyte Function and Pathophysiology (10 papers) and Blood groups and transfusion (9 papers). P.J. McAlpine collaborates with scholars based in Canada, United States and United Kingdom. P.J. McAlpine's co-authors include T.B. Shows, Claude Boucheix, A.J. Pakstis, J.L. Hamerton, D. A. HOPKINSON, Harry Harris, Robert Miller, T.B. Shows, P. W. Allderdice and Arnold H. Greenberg and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and The Journal of Pediatrics.

In The Last Decade

P.J. McAlpine

65 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P.J. McAlpine Canada 22 692 549 168 162 149 68 1.4k
Sharon Dana United States 21 1.1k 1.5× 453 0.8× 183 1.1× 63 0.4× 35 0.2× 27 1.5k
Dexter T. Duncan United States 8 1.1k 1.5× 252 0.5× 152 0.9× 40 0.2× 44 0.3× 12 1.6k
Christophe Rachez France 24 2.2k 3.2× 1.1k 1.9× 139 0.8× 146 0.9× 70 0.5× 35 3.1k
Lee Carpenter United Kingdom 26 1.7k 2.4× 286 0.5× 313 1.9× 112 0.7× 64 0.4× 36 2.4k
Zoya Galcheva-Gargova United States 14 1.1k 1.6× 567 1.0× 205 1.2× 78 0.5× 17 0.1× 29 1.9k
Y. Takagi Japan 20 941 1.4× 607 1.1× 68 0.4× 46 0.3× 30 0.2× 37 1.6k
Susan Zollman United States 19 1.1k 1.6× 527 1.0× 123 0.7× 133 0.8× 29 0.2× 21 1.9k
Rami Skaliter Israel 15 1.6k 2.4× 304 0.6× 133 0.8× 44 0.3× 36 0.2× 19 2.3k
Xiangyuan Wang United States 24 1.5k 2.1× 553 1.0× 50 0.3× 104 0.6× 126 0.8× 43 2.0k
Alain Mir United States 12 932 1.3× 165 0.3× 73 0.4× 114 0.7× 198 1.3× 14 1.4k

Countries citing papers authored by P.J. McAlpine

Since Specialization
Citations

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

Fields of papers citing papers by P.J. McAlpine

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P.J. McAlpine

This figure shows the co-authorship network connecting the top 25 collaborators of P.J. McAlpine. A scholar is included among the top collaborators of P.J. McAlpine 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 P.J. McAlpine. P.J. McAlpine 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.
Hansen, C., J.N.B. Shrestha, R. J. Parker, et al.. (2003). Genetic diversity among Canadienne, Brown Swiss, Holstein and Jersey cattle based on mitochondrial D-loop sequence variation. Canadian Journal of Animal Science. 83(1). 39–44. 2 indexed citations
2.
White, Julia A., P.J. McAlpine, Stylianos E. Antonarakis, et al.. (1997). NOMENCLATURE. Genomics. 45(2). 468–471. 69 indexed citations
3.
Huie, Maryann L., Michael Menaker, P.J. McAlpine, & Rochelle Hirschhorn. (1996). Identification of an E689K substitution as the molecular basis of the human acid α‐glucosidase type 4 allozyme (GAA*4). Annals of Human Genetics. 60(5). 365–368. 16 indexed citations
4.
Marles, Sandra L., et al.. (1993). Identification of an uncommon haptoglobin type using DNA and protein analysis. Human Genetics. 92(4). 364–366. 5 indexed citations
5.
Allderdice, P. W., et al.. (1991). Complementation by two non‐homologous recombinant chromosomes 3. American Journal of Medical Genetics. 39(4). 396–398. 15 indexed citations
6.
Allderdice, P. W., et al.. (1991). The cloned butyrylcholinesterase (BCHE) gene maps to a single chromosome site, 3q26. Genomics. 11(2). 452–454. 88 indexed citations
7.
McAlpine, P.J., et al.. (1991). Polymorphism detected by multiple RENS in the human coagulation factor II (F2) gene. Nucleic Acids Research. 19(1). 193–193. 2 indexed citations
8.
McAlpine, P.J., et al.. (1991). The butyrylcholinesterase gene (BCHE) at 3q26.2 shows two RFLPs. Nucleic Acids Research. 19(18). 5088–5088. 3 indexed citations
9.
Zelinski, Teresa, Gail Coghlan, Cheryl R. Greenberg, P.J. McAlpine, & M. Lewis. (1989). Evidence that SE is distal to LU on chromosome 19q. Transfusion. 29(4). 304–305. 4 indexed citations
10.
Lewis, M., Hiroko Kaita, Sylvia Philipps, et al.. (1988). The Swann Phenotype 700:4,‐41; Genetic Studies. Vox Sanguinis. 54(3). 184–187. 4 indexed citations
11.
Wong, Paul, Marc Schroeder, M. Lewis, et al.. (1988). Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter: F13A:HLA:GL01:cen gene order. Human Genetics. 79(3). 228–230. 5 indexed citations
12.
Chodirker, Bernard N., et al.. (1988). Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16. American Journal of Medical Genetics. 31(1). 145–151. 7 indexed citations
13.
Zelinski, Teresa, Hiroko Kaita, M. Lewis, et al.. (1988). The Colton blood group locus. Transfusion. 28(5). 435–438. 7 indexed citations
14.
Lewis, M., Hiroko Kaita, Gail Coghlan, et al.. (1988). The chromosome 19 linkage group LDLR, C3, LW, APOC2, LU, SE in man. Annals of Human Genetics. 52(2). 137–144. 18 indexed citations
15.
Zelinski, Teresa, et al.. (1988). Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1. Genomics. 2(2). 154–156. 16 indexed citations
16.
McAlpine, P.J., T.B. Shows, Robert Miller, & A.J. Pakstis. (1985). The 1985 catalog of mapped genes and report of the nomenclature committee. Cytogenetic and Genome Research. 40(1-4). 8–66. 58 indexed citations
17.
Shows, T.B. & P.J. McAlpine. (1978). The catalog of human genes and chromosome assignments. Cytogenetic and Genome Research. 22(1-6). 132–145. 14 indexed citations
18.
McAlpine, P.J., Hiroko Kaita, & M. Lewis. (1978). Is the <i>DIA</i><sub>1</sub> locus linked to the <i>P </i>blood group locus?. Cytogenetic and Genome Research. 22(1-6). 629–632. 7 indexed citations
19.
McAlpine, P.J., et al.. (1974). Genetic Markers in Blood in a Canadian Eskimo Population with a Comparison of Allele Frequencies in Circumpolar Populations. Human Heredity. 24(2). 114–143. 35 indexed citations
20.
Thompson, Margaret, E. Gordon Murphy, & P.J. McAlpine. (1967). An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy. The Journal of Pediatrics. 71(1). 82–93. 61 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Sharon Dana Breakdown of academic impact, for papers by Dexter T. Duncan Breakdown of academic impact, for papers by Christophe Rachez Breakdown of academic impact, for papers by Lee Carpenter Breakdown of academic impact, for papers by Zoya Galcheva-Gargova Breakdown of academic impact, for papers by Y. Takagi Breakdown of academic impact, for papers by Susan Zollman Breakdown of academic impact, for papers by Rami Skaliter Breakdown of academic impact, for papers by Xiangyuan Wang Breakdown of academic impact, for papers by Alain Mir
Rankless by CCL
2026