Moira Blyth
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 2
- Congenital Ear and Nasal Anomalies 2
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- Congenital heart defects research 2
- Chromatin Remodeling and Cancer 2
- Co-authors
- Diana Wellesley (3 shared papers)Danielle Howe (1 shared paper)James Gnanapragasam (1 shared paper)John A. Crolla (3 shared papers)Shuwen Huang (3 shared papers)David J. Bunyan (2 shared papers)I. Karen Temple (2 shared papers)Viv Maloney (2 shared papers)
- Journals
- European Journal of Medical Genetics (3 papers)Journal of Medical Genetics (2 papers)Burns (1 paper)Obstetrical & Gynecological Survey (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Moira Blyth
20 papers receiving 360 citations
Peers
Comparison fields: 5 of 47
- Developmental Biology 15
- Genetics 152
- Epidemiology 68
- Pediatrics, Perinatology and Child Health 36
- Pathology and Forensic Medicine 32
Countries citing papers authored by Moira Blyth
This map shows the geographic impact of Moira Blyth'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 Moira Blyth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moira Blyth more than expected).
Fields of papers citing papers by Moira Blyth
This network shows the impact of papers produced by Moira Blyth. 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 Moira Blyth. The network helps show where Moira Blyth may publish in the future.
Co-authors
The 25 scholars most cited alongside Moira Blyth, 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 | 2008 | 63 | |
| 2 | 2015 | 53 | |
| 3 | 2016 | 36 | |
| 4 | 2015 | 34 | |
| 5 | 2014 | 27 | |
| 6 | 2008 | 23 | |
| 7 | 2007 | 21 | |
| 8 | 2008 | 21 | |
| 9 | 2015 | 20 | |
| 10 | 2008 | 19 | |
| 11 | 2014 | 18 | |
| 12 | 2020 | 13 | |
| 13 | 2018 | 10 | |
| 14 | 2017 | 7 | |
| 15 | 2010 | 5 | |
| 16 | 2014 | 5 | |
| 17 | 2008 | 4 | |
| 18 | 2016 | 4 | |
| 19 | 2011 | 3 | |
| 20 | 2019 | 1 |
About Moira Blyth
Moira Blyth is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Genetics and Pediatrics, Perinatology and Child Health, having authored 22 papers that have together received 387 indexed citations. Recurring topics across this work include Congenital Heart Disease Studies (3 papers), Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Peptidase Inhibition and Analysis (2 papers), Chromatin Remodeling and Cancer (2 papers), Gestational Trophoblastic Disease Studies (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Developmental Biology (15 citations), Genetics (152 citations), Epidemiology (68 citations), Pediatrics, Perinatology and Child Health (36 citations) and Pathology and Forensic Medicine (32 citations). Moira Blyth has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Diana Wellesley, Danielle Howe, James Gnanapragasam, John A. Crolla, Shuwen Huang, David J. Bunyan, I. Karen Temple, Viv Maloney, Ghislaine Plessis and Amber Young. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, Burns, Obstetrical & Gynecological Survey and European Journal of 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.