Gudrun E. Moore
Impact in
- Genetics top 0.5%
- Genetic Syndromes and Imprinting
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Obstetrics and Gynecology top 1%
- Pregnancy and preeclampsia studies
Papers in
- Genetics 140
- Genetic Syndromes and Imprinting 87
- Cleft Lip and Palate Research 26
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 8
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- Prenatal Screening and Diagnostics 10
- Co-authors
- Philip Stanier (92 shared papers)Sayeda Nasreen Abu-Amero (36 shared papers)David Monk (33 shared papers)Michael A. Preece (24 shared papers)Jennifer M. Frost (11 shared papers)Phillip R. Bennett (20 shared papers)Megan Philippa Hitchins (17 shared papers)Miho Ishida (18 shared papers)
- Journals
- Journal of Medical Genetics (20 papers)Human Molecular Genetics (11 papers)The American Journal of Human Genetics (9 papers)Human Genetics (8 papers)European Journal of Human Genetics (7 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Gudrun E. Moore
205 papers receiving 8.6k citations
Gudrun E. Moore's Hit Papers
Peers
Comparison fields: 5 of 130
- Genetics 4.1k
- Obstetrics and Gynecology 632
- Pediatrics, Perinatology and Child Health 681
- Developmental Biology 68
- Immunology 581
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 208 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 430 | |
| 2 | Diagnosis and management of Silver–Russell syndrome: first international consensus statement Hit paper breakdown → | 2016 | 374 |
| 3 | 2010 | 273 | |
| 4 | 2013 | 250 | |
| 5 | 2001 | 220 | |
| 6 | 2006 | 209 | |
| 7 | 2007 | 206 | |
| 8 | 2010 | 192 | |
| 9 | 2008 | 172 | |
| 10 | 2003 | 166 | |
| 11 | 2010 | 149 | |
| 12 | 1995 | 147 | |
| 13 | 1998 | 144 | |
| 14 | 2007 | 142 | |
| 15 | 2012 | 137 | |
| 16 | 1997 | 132 | |
| 17 | 2012 | 132 | |
| 18 | 2015 | 128 | |
| 19 | 1997 | 127 | |
| 20 | 2000 | 125 |
About Gudrun E. Moore
Gudrun E. Moore is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Obstetrics and Gynecology, Public Health, Environmental and Occupational Health and Molecular Biology, having authored 208 papers that have together received 9k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (87 papers), Cleft Lip and Palate Research (26 papers), Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (10 papers), Spinal Dysraphism and Malformations (10 papers), Pregnancy and preeclampsia studies (9 papers), Genomics and Rare Diseases (8 papers) and Reproductive System and Pregnancy (7 papers). The work is most often cited by research in Genetics (4.1k citations), Obstetrics and Gynecology (632 citations), Pediatrics, Perinatology and Child Health (681 citations), Developmental Biology (68 citations) and Immunology (581 citations). Gudrun E. Moore has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Philip Stanier, Sayeda Nasreen Abu-Amero, David Monk, Michael A. Preece, Jennifer M. Frost, Phillip R. Bennett, Megan Philippa Hitchins, Miho Ishida, Kate Hardy and Antony D. Lighten. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Human Genetics 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.