PHYLLIS J. McALPINE
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Hematology top 10%
- Blood groups and transfusion
Papers in
- Genetics 29
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 5
- Hematology 13
- Blood groups and transfusion 10
- Co-authors
- David A. Hopkinson (3 shared papers)Harry Harris (3 shared papers)Penelope W. Allderdice (5 shared papers)JOHN L. HAMERTON (12 shared papers)A Shalev (1 shared paper)Arnold H. Greenberg (1 shared paper)Thomas B. Shows (9 shared papers)Margaret W. Thompson (1 shared paper)
- Journals
- Annals of Human Genetics (8 papers)Transfusion (5 papers)Genomics (5 papers)Vox Sanguinis (4 papers)Human Genetics (3 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
PHYLLIS J. McALPINE
59 papers receiving 980 citations
Peers
Comparison fields: 5 of 103
- Genetics 398
- Hematology 113
- Molecular Biology 500
- Genetics 69
- Clinical Biochemistry 43
Countries citing papers authored by PHYLLIS J. McALPINE
This map shows the geographic impact of PHYLLIS 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 PHYLLIS 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 PHYLLIS J. McALPINE more than expected).
Fields of papers citing papers by PHYLLIS J. McALPINE
This network shows the impact of papers produced by PHYLLIS 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 PHYLLIS J. McALPINE. The network helps show where PHYLLIS J. McALPINE may publish in the future.
Co-authors
The 25 scholars most cited alongside PHYLLIS 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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 96 | |
| 2 | 1974 | 96 | |
| 3 | 1980 | 77 | |
| 4 | 1997 | 76 | |
| 5 | 1967 | 66 | |
| 6 | 1970 | 49 | |
| 7 | The 1979 catalog of human genes and chromosome assignments. | 1980 | 43 |
| 8 | 1970 | 41 | |
| 9 | 1974 | 39 | |
| 10 | 1994 | 32 | |
| 11 | 1991 | 31 | |
| 12 | 1985 | 28 | |
| 13 | 1990 | 27 | |
| 14 | Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. | 1986 | 24 |
| 15 | 1988 | 23 | |
| 16 | 2008 | 23 | |
| 17 | 1977 | 22 | |
| 18 | 1988 | 21 | |
| 19 | 1973 | 20 | |
| 20 | 2008 | 20 |
About PHYLLIS J. McALPINE
PHYLLIS J. McALPINE is a scholar working on Genetics, Hematology, Molecular Biology, Physiology and Immunology, having authored 76 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Blood groups and transfusion (10 papers), Erythrocyte Function and Pathophysiology (10 papers), Pancreatic function and diabetes (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Biochemical and Molecular Research (4 papers), Glycosylation and Glycoproteins Research (4 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Genetics (398 citations), Hematology (113 citations), Molecular Biology (500 citations), Genetics (69 citations) and Clinical Biochemistry (43 citations). PHYLLIS J. McALPINE has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include David A. Hopkinson, Harry Harris, Penelope W. Allderdice, JOHN L. HAMERTON, A Shalev, Arnold H. Greenberg, Thomas B. Shows, Margaret W. Thompson, E. Gordon Murphy and Hiroko Kaita. Their work appears in journals such as Annals of Human Genetics, Transfusion, Genomics, Vox Sanguinis and Human 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.