Gudrun E. Moore
Impact in
- Genetics top 0.5%
- Genetic Syndromes and Imprinting
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
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- Prenatal Screening and Diagnostics
- Birth, Development, and Health
Papers in
- Genetics 82
- Genetic Syndromes and Imprinting 48
- Cleft Lip and Palate Research 16
- Craniofacial Disorders and Treatments 13
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 6
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- Epigenetics and DNA Methylation 32
- Co-authors
- Philip Stanier (60 shared papers)Sayeda Abu‐Amero (24 shared papers)Jennifer M. Frost (10 shared papers)David Monk (12 shared papers)Phillip R. Bennett (17 shared papers)Miho Ishida (16 shared papers)Kate Hardy (2 shared papers)Robert Winston (2 shared papers)
- Journals
- Journal of Medical Genetics (9 papers)Human Molecular Genetics (8 papers)Nucleic Acids Research (7 papers)Human Genetics (6 papers)American Journal of Obstetrics and Gynecology (5 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Gudrun E. Moore
136 papers receiving 5.5k citations
Peers
Comparison fields: 5 of 123
- Genetics 2.8k
- Pediatrics, Perinatology and Child Health 1.6k
- Obstetrics and Gynecology 393
- Molecular Biology 2.7k
- Cancer Research 302
Countries citing papers authored by Gudrun E. Moore
This map shows the geographic impact of Gudrun E. Moore'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 Gudrun E. Moore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gudrun E. Moore more than expected).
Fields of papers citing papers by Gudrun E. Moore
This network shows the impact of papers produced by Gudrun E. Moore. 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 Gudrun E. Moore. The network helps show where Gudrun E. Moore may publish in the future.
Co-authors
The 25 scholars most cited alongside Gudrun E. Moore, 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 136 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 265 | |
| 2 | 2001 | 214 | |
| 3 | 2006 | 214 | |
| 4 | 2013 | 211 | |
| 5 | 2007 | 197 | |
| 6 | 2010 | 196 | |
| 7 | 2008 | 153 | |
| 8 | 1998 | 146 | |
| 9 | 1995 | 146 | |
| 10 | 2010 | 141 | |
| 11 | 2007 | 138 | |
| 12 | 2012 | 129 | |
| 13 | 1997 | 128 | |
| 14 | 2006 | 119 | |
| 15 | 1997 | 119 | |
| 16 | 2000 | 115 | |
| 17 | 2006 | 115 | |
| 18 | 2007 | 104 | |
| 19 | 1987 | 97 | |
| 20 | 2006 | 89 |
About Gudrun E. Moore
Gudrun E. Moore is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 136 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (48 papers), Prenatal Screening and Diagnostics (42 papers), Epigenetics and DNA Methylation (32 papers), Cleft Lip and Palate Research (16 papers), Craniofacial Disorders and Treatments (13 papers), Genomic variations and chromosomal abnormalities (10 papers), Pregnancy and preeclampsia studies (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). The work is most often cited by research in Genetics (2.8k citations), Pediatrics, Perinatology and Child Health (1.6k citations), Obstetrics and Gynecology (393 citations), Molecular Biology (2.7k citations) and Cancer Research (302 citations). Gudrun E. Moore has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Philip Stanier, Sayeda Abu‐Amero, Jennifer M. Frost, David Monk, Phillip R. Bennett, Miho Ishida, Kate Hardy, Robert Winston, Antony D. Lighten and Sophia Apostolidou. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Nucleic Acids Research, Human Genetics and American Journal of Obstetrics and Gynecology.
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.