Deborah Morrogh
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and rare skin diseases.
- Genomic variations and chromosomal abnormalities
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- Cutaneous Melanoma Detection and Management
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 2
- Congenital Ear and Nasal Anomalies 2
- Genetic and rare skin diseases. 1
-
- Congenital heart defects research 2
- Co-authors
- Rodger Palmer (3 shared papers)Richard H. Scott (3 shared papers)Jane A. Hurst (2 shared papers)Olga Slater (1 shared paper)Miho Ishida (2 shared papers)Estelle Chanudet (1 shared paper)Neil J. Sebire (1 shared paper)Philip Stanier (2 shared papers)
- Journals
- European Journal of Human Genetics (2 papers)Orphanet Journal of Rare Diseases (2 papers)Pediatric Nephrology (1 paper)Journal of Dental Research (1 paper)Blood (1 paper)
- Partner nations
- United KingdomNetherlandsGermany
In The Last Decade
Deborah Morrogh
13 papers receiving 569 citations
Peers
Comparison fields: 5 of 47
- Genetics 262
- Oncology 116
- Cell Biology 74
- Psychiatry and Mental health 58
- Molecular Biology 215
Countries citing papers authored by Deborah Morrogh
This map shows the geographic impact of Deborah Morrogh'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 Deborah Morrogh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deborah Morrogh more than expected).
Fields of papers citing papers by Deborah Morrogh
This network shows the impact of papers produced by Deborah Morrogh. 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 Deborah Morrogh. The network helps show where Deborah Morrogh may publish in the future.
Co-authors
The 25 scholars most cited alongside Deborah Morrogh, 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 | 2013 | 197 | |
| 2 | 2016 | 147 | |
| 3 | 2014 | 53 | |
| 4 | 2019 | 52 | |
| 5 | 2011 | 24 | |
| 6 | 2016 | 22 | |
| 7 | 2014 | 22 | |
| 8 | 2013 | 18 | |
| 9 | 2017 | 15 | |
| 10 | 2014 | 13 | |
| 11 | 2019 | 6 | |
| 12 | 2017 | 5 | |
| 13 | 2013 | 3 | |
| 14 | 2017 | 0 |
About Deborah Morrogh
Deborah Morrogh is a scholar working on Genetics, Molecular Biology, Plant Science, Genetics and Cellular and Molecular Neuroscience, having authored 14 papers that have together received 577 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Chromosomal and Genetic Variations (3 papers), Genetic Syndromes and Imprinting (2 papers), Congenital heart defects research (2 papers), Congenital Ear and Nasal Anomalies (2 papers) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Genetics (262 citations), Oncology (116 citations), Cell Biology (74 citations), Psychiatry and Mental health (58 citations) and Molecular Biology (215 citations). Deborah Morrogh has collaborated with scholars based in United Kingdom, Netherlands and Germany. Frequent co-authors include Rodger Palmer, Richard H. Scott, Jane A. Hurst, Olga Slater, Miho Ishida, Estelle Chanudet, Neil J. Sebire, Philip Stanier, Sayeda Abu‐Amero and Anna Thomas. Their work appears in journals such as European Journal of Human Genetics, Orphanet Journal of Rare Diseases, Pediatric Nephrology, Journal of Dental Research and Blood.
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.