N.E. Morton
Impact in
- Genetics top 1%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities
- Genetic and phenotypic traits in livestock
- Molecular Biology top 10%
- DNA Repair Mechanisms
Papers in
- Genetics 25
- Genetic Associations and Epidemiology 12
- Genetic Mapping and Diversity in Plants and Animals 8
- Nutrition, Genetics, and Disease 4
- Evolution and Genetic Dynamics 2
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- Bioinformatics and Genomic Networks 4
- Epigenetics and DNA Methylation 2
- Co-authors
- Jean-Marc Lalouel (3 shared papers)P. A. Jacobs (1 shared paper)Gillian Turner (1 shared paper)Stephanie L. Sherman (1 shared paper)D. C. Rao (9 shared papers)Andrew Collins (10 shared papers)Stanley W. Wright (1 shared paper)R Lew (3 shared papers)
- Journals
- Human Heredity (11 papers)Annals of Human Genetics (5 papers)Genomics (2 papers)Journal of Medical Genetics (2 papers)Genes and Immunity (1 paper)
- Partner nations
- United StatesUnited KingdomSweden
In The Last Decade
N.E. Morton
51 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 123
- Genetics 1.3k
- Molecular Biology 833
- Cancer Research 158
- Physiology 207
- Plant Science 292
Countries citing papers authored by N.E. Morton
This map shows the geographic impact of N.E. Morton'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 N.E. Morton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N.E. Morton more than expected).
Fields of papers citing papers by N.E. Morton
This network shows the impact of papers produced by N.E. Morton. 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 N.E. Morton. The network helps show where N.E. Morton may publish in the future.
Co-authors
The 25 scholars most cited alongside N.E. Morton, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1991 | 427 | |
| 2 | 1981 | 331 | |
| 3 | 1984 | 315 | |
| 4 | 1981 | 103 | |
| 5 | 2000 | 101 | |
| 6 | 1999 | 97 | |
| 7 | Genetic studies on cystic fibrosis in Hawaii. | 1968 | 90 |
| 8 | 1977 | 85 | |
| 9 | Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information. | 1985 | 74 |
| 10 | 1994 | 68 | |
| 11 | Combined segregation and linkage analysis of Graves disease with a thyroid autoantibody diathesis. | 1994 | 63 |
| 12 | CEPH(ヒト多形性研究センター)共同製作ヒト1番染色体連鎖地図 | 1991 | 54 |
| 13 | Variability of human linkage data. | 1978 | 51 |
| 14 | 1984 | 49 | |
| 15 | 1983 | 47 | |
| 16 | 2004 | 39 | |
| 17 | 1977 | 31 | |
| 18 | 2001 | 27 | |
| 19 | 1995 | 25 | |
| 20 | 2008 | 24 |
About N.E. Morton
N.E. Morton is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Hematology, having authored 55 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (12 papers), Genetic Mapping and Diversity in Plants and Animals (8 papers), Nutrition, Genetics, and Disease (4 papers), Bioinformatics and Genomic Networks (4 papers), Cardiac electrophysiology and arrhythmias (2 papers), Evolution and Genetic Dynamics (2 papers), Epigenetics and DNA Methylation (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (833 citations), Cancer Research (158 citations), Physiology (207 citations) and Plant Science (292 citations). N.E. Morton has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Jean-Marc Lalouel, P. A. Jacobs, Gillian Turner, Stephanie L. Sherman, D. C. Rao, Andrew Collins, Stanley W. Wright, R Lew, S Yee and Irving I. Gottesman. Their work appears in journals such as Human Heredity, Annals of Human Genetics, Genomics, Journal of Medical Genetics and Genes and Immunity.
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.