P.J. McAlpine
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Hematology top 10%
- Blood groups and transfusion
Papers in
-
- Glycosylation and Glycoproteins Research 4
- Biochemical and Molecular Research 4
- DNA Repair Mechanisms 3
- Genetics 29
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 5
- Co-authors
- D. A. HOPKINSON (3 shared papers)Harry Harris (3 shared papers)P. W. Allderdice (5 shared papers)J.L. Hamerton (13 shared papers)A Shalev (1 shared paper)Arnold H. Greenberg (1 shared paper)T.B. Shows (9 shared papers)E. Gordon Murphy (1 shared paper)
- Journals
- Annals of Human Genetics (8 papers)Transfusion (4 papers)Genomics (4 papers)Vox Sanguinis (4 papers)Journal of Medical Genetics (3 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
P.J. McAlpine
53 papers receiving 926 citations
Peers
Comparison fields: 5 of 97
- Genetics 375
- Hematology 103
- Molecular Biology 467
- Genetics 65
- Clinical Biochemistry 43
Countries citing papers authored by P.J. McAlpine
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
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-authors
The 25 scholars most cited alongside P.J. McAlpine, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1974 | 96 | |
| 2 | 1991 | 95 | |
| 3 | 1980 | 78 | |
| 4 | 1997 | 76 | |
| 5 | 1967 | 66 | |
| 6 | 1970 | 49 | |
| 7 | The 1979 catalog of human genes and chromosome assignments. | 1980 | 43 |
| 8 | 1970 | 40 | |
| 9 | 1974 | 38 | |
| 10 | 1991 | 32 | |
| 11 | 1994 | 31 | |
| 12 | 1990 | 27 | |
| 13 | 1985 | 23 | |
| 14 | Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. | 1986 | 23 |
| 15 | 1988 | 21 | |
| 16 | 1988 | 21 | |
| 17 | 2008 | 20 | |
| 18 | 1973 | 20 | |
| 19 | 1977 | 19 | |
| 20 | 2002 | 19 |
About P.J. McAlpine
P.J. McAlpine is a scholar working on Molecular Biology, Genetics, Hematology, Physiology and Surgery, having authored 69 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Erythrocyte Function and Pathophysiology (9 papers), Blood groups and transfusion (9 papers), Pancreatic function and diabetes (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Glycosylation and Glycoproteins Research (4 papers), Biochemical and Molecular Research (4 papers) and DNA Repair Mechanisms (3 papers). The work is most often cited by research in Genetics (375 citations), Hematology (103 citations), Molecular Biology (467 citations), Genetics (65 citations) and Clinical Biochemistry (43 citations). P.J. McAlpine has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include D. A. HOPKINSON, Harry Harris, P. W. Allderdice, J.L. Hamerton, A Shalev, Arnold H. Greenberg, T.B. Shows, E. Gordon Murphy, Margaret Thompson and Albert E. Chudley. Their work appears in journals such as Annals of Human Genetics, Transfusion, Genomics, Vox Sanguinis and Journal of Medical Genetics.
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.