Lydia E. McMorrow
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- Renal and related cancers
- RNA Research and Splicing
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 5
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- Genomics and Chromatin Dynamics 3
- Co-authors
- Theresa A. Freeman (2 shared papers)Robert G. Nagele (2 shared papers)Hsin‐Yi Lee (2 shared papers)Yue Hao (1 shared paper)Thomas Moulton (1 shared paper)Na‐Sheng Lin (1 shared paper)Lawrence M. Weiss (1 shared paper)Francine R. Dembitzer (1 shared paper)
- Journals
- Journal of Medical Genetics (3 papers)Cancer (1 paper)Nature Genetics (1 paper)Science (1 paper)American Journal of Hematology (1 paper)
- Partner nations
- United StatesAustraliaCanada
In The Last Decade
Lydia E. McMorrow
22 papers receiving 669 citations
Peers
Comparison fields: 5 of 61
- Genetics 320
- Molecular Biology 505
- Pediatrics, Perinatology and Child Health 137
- Cancer Research 80
- Developmental Biology 11
Countries citing papers authored by Lydia E. McMorrow
This map shows the geographic impact of Lydia E. McMorrow'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 Lydia E. McMorrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lydia E. McMorrow more than expected).
Fields of papers citing papers by Lydia E. McMorrow
This network shows the impact of papers produced by Lydia E. McMorrow. 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 Lydia E. McMorrow. The network helps show where Lydia E. McMorrow may publish in the future.
Co-authors
The 25 scholars most cited alongside Lydia E. McMorrow, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 271 | |
| 2 | 1995 | 136 | |
| 3 | 1999 | 92 | |
| 4 | 1993 | 35 | |
| 5 | 1986 | 21 | |
| 6 | 1987 | 18 | |
| 7 | 1974 | 15 | |
| 8 | Development and progression of karyotypic variability in melanoma K1735 following X-irradiation. | 1985 | 14 |
| 9 | 1992 | 13 | |
| 10 | 1980 | 13 | |
| 11 | 1995 | 10 | |
| 12 | 1996 | 10 | |
| 13 | 1984 | 10 | |
| 14 | Growth of granulopoietic bone marrow cells of RF mice. | 1980 | 9 |
| 15 | Animal model of human disease: myelogenous leukemia in the RF mouse. | 1982 | 7 |
| 16 | Irradiation-induced marker chromosomes in a metastasizing murine tumor. | 1988 | 6 |
| 17 | 1988 | 4 | |
| 18 | 1991 | 4 | |
| 19 | 1980 | 4 | |
| 20 | Lack of chromosomal breakage in congenital rubella. | 1973 | 3 |
About Lydia E. McMorrow
Lydia E. McMorrow is a scholar working on Genetics, Molecular Biology, Plant Science, Hematology and Genetics, having authored 22 papers that have together received 699 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers), Chromosomal and Genetic Variations (4 papers), Genomics and Chromatin Dynamics (3 papers), Acute Myeloid Leukemia Research (2 papers), Acute Lymphoblastic Leukemia research (2 papers), Cancer Genomics and Diagnostics (2 papers) and Cancer-related Molecular Pathways (2 papers). The work is most often cited by research in Genetics (320 citations), Molecular Biology (505 citations), Pediatrics, Perinatology and Child Health (137 citations), Cancer Research (80 citations) and Developmental Biology (11 citations). Lydia E. McMorrow has collaborated with scholars based in United States, Australia and Canada. Frequent co-authors include Theresa A. Freeman, Robert G. Nagele, Hsin‐Yi Lee, Yue Hao, Thomas Moulton, Na‐Sheng Lin, Lawrence M. Weiss, Francine R. Dembitzer, Benjamin Tycko and William L. Gerald. Their work appears in journals such as Journal of Medical Genetics, Cancer, Nature Genetics, Science and American Journal of Hematology.
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.