Alan E H Emery
Impact in
- Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research
- Molecular Biology top 1%
- Muscle Physiology and Disorders
- Nuclear Structure and Function
- RNA Research and Splicing
Papers in
- Genetics 20
- Neurogenetic and Muscular Disorders Research 19
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 13
- Genomics and Rare Diseases 8
-
- Metabolism and Genetic Disorders 9
- Co-authors
- Fritz E. DreifussR. SkinnerJ.A. SofaerD. BurtHans MoserSusan HollowayA. M. DavieMia Nelson
- Journals
- Journal of Medical Genetics (41 papers)Neuromuscular Disorders (30 papers)Journal of the Neurological Sciences (11 papers)Clinical Genetics (9 papers)The Lancet (8 papers)
- Partner nations
- United KingdomUnited StatesPoland
In The Last Decade
Alan E H Emery
186 papers receiving 6.5k citations
Hit Papers
Peers
Comparison fields: 5 of 185
- Genetics 1.2k
- Molecular Biology 4.7k
- Cellular and Molecular Neuroscience 1.1k
- Cardiology and Cardiovascular Medicine 1.0k
- Rehabilitation 266
Countries citing papers authored by Alan E H Emery
This map shows the geographic impact of Alan E H Emery'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 Alan E H Emery with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alan E H Emery more than expected).
Fields of papers citing papers by Alan E H Emery
This network shows the impact of papers produced by Alan E H Emery. 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 Alan E H Emery. The network helps show where Alan E H Emery may publish in the future.
Co-authors
The 25 scholars most cited alongside Alan E H Emery, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | The mummy state. | 2005 | 1 |
| 2 | Neuromuscular disorders : clinical and molecular genetics | 1998 | 57 |
| 3 | Medical genetics—Past, present, future | 1985 | 25 |
| 4 | Human Gene Mapping 7: Cytogenetics and Cell Genetics. | 1984 | 0 |
| 5 | Psychological aspects of genetic counselling | 1984 | 47 |
| 6 | Cytogenetics of the Mammalian X Chromosome | 1984 | 74 |
| 7 | 1983 | 100 | |
| 8 | Genetics and human variation | 1983 | 7 |
| 9 | 1980 | 73 | |
| 10 | 1977 | 20 | |
| 11 | Registers for the detection and prevention of genetic disease : proceedings of a workshop held in Albany, New York, October 13, 1975 | 1976 | 1 |
| 12 | 1975 | 23 | |
| 13 | 1975 | 4 | |
| 14 | 1975 | 1 | |
| 15 | 1973 | 7 | |
| 16 | 1973 | 30 | |
| 17 | 1970 | 8 | |
| 18 | 1970 | 31 | |
| 19 | 1968 | 16 | |
| 20 | 1965 | 10 |
About Alan E H Emery
Alan E H Emery is a scholar working on Genetics, Clinical Biochemistry, Cellular and Molecular Neuroscience, Genetics and Molecular Biology, having authored 196 papers that have together received 7.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (50 papers), Genetic Neurodegenerative Diseases (19 papers), Nuclear Structure and Function (19 papers), Neurogenetic and Muscular Disorders Research (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Adipose Tissue and Metabolism (10 papers), Metabolism and Genetic Disorders (9 papers) and Genomics and Rare Diseases (8 papers). The work is most often cited by research in Genetics (1.2k citations), Molecular Biology (4.7k citations), Cellular and Molecular Neuroscience (1.1k citations), Cardiology and Cardiovascular Medicine (1.0k citations) and Rehabilitation (266 citations). Alan E H Emery has collaborated with scholars based in United Kingdom, United States and Poland. Frequent co-authors include Fritz E. Dreifuss, R. Skinner, J.A. Sofaer, D. Burt, Hans Moser, Susan Holloway, A. M. Davie, Mia Nelson, J. S. Lawrence and Muriel Watt. Their work appears in journals such as Journal of Medical Genetics, Neuromuscular Disorders, Journal of the Neurological Sciences, Clinical Genetics and The Lancet.
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.