Gudrun E. Moore
Impact in
- Genetics top 0.5%
- Genetic Syndromes and Imprinting
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
-
- Prenatal Screening and Diagnostics
- Birth, Development, and Health
Papers in
- Genetics 100
- Genetic Syndromes and Imprinting 61
- Cleft Lip and Palate Research 17
- Craniofacial Disorders and Treatments 13
- Genomic variations and chromosomal abnormalities 11
- Congenital Ear and Nasal Anomalies 8
- Genetics and Neurodevelopmental Disorders 8
-
- Prenatal Screening and Diagnostics 54
- Co-authors
- Philip Stanier (67 shared papers)Sayeda N Abu-Amero (24 shared papers)Jennifer M. Frost (10 shared papers)David Monk (14 shared papers)Phillip R. Bennett (18 shared papers)Miho Ishida (18 shared papers)Antony D. Lighten (3 shared papers)Kate Hardy (3 shared papers)
- Journals
- Journal of Medical Genetics (10 papers)Human Molecular Genetics (9 papers)The American Journal of Human Genetics (9 papers)Nucleic Acids Research (7 papers)European Journal of Human Genetics (6 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Gudrun E. Moore
165 papers receiving 7.4k citations
Gudrun E. Moore's Hit Papers
Peers
Comparison fields: 5 of 132
- Genetics 3.8k
- Pediatrics, Perinatology and Child Health 2.0k
- Obstetrics and Gynecology 511
- Molecular Biology 3.6k
- Genetics 299
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 166 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Diagnosis and management of Silver–Russell syndrome: first international consensus statement Hit paper breakdown → | 2016 | 369 |
| 2 | 2010 | 274 | |
| 3 | 2013 | 250 | |
| 4 | 2001 | 221 | |
| 5 | 2006 | 209 | |
| 6 | 2007 | 206 | |
| 7 | 2010 | 192 | |
| 8 | 2008 | 171 | |
| 9 | 2003 | 167 | |
| 10 | 1995 | 149 | |
| 11 | 2010 | 148 | |
| 12 | 1998 | 147 | |
| 13 | 2007 | 142 | |
| 14 | 2012 | 137 | |
| 15 | 1997 | 132 | |
| 16 | 2012 | 132 | |
| 17 | 1997 | 128 | |
| 18 | 2000 | 126 | |
| 19 | 2015 | 124 | |
| 20 | 2006 | 122 |
About Gudrun E. Moore
Gudrun E. Moore is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Obstetrics and Gynecology and Genetics, having authored 166 papers that have together received 7.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (61 papers), Prenatal Screening and Diagnostics (54 papers), Epigenetics and DNA Methylation (41 papers), Cleft Lip and Palate Research (17 papers), Craniofacial Disorders and Treatments (13 papers), Genomic variations and chromosomal abnormalities (11 papers), Congenital Ear and Nasal Anomalies (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (3.8k citations), Pediatrics, Perinatology and Child Health (2.0k citations), Obstetrics and Gynecology (511 citations), Molecular Biology (3.6k citations) and Genetics (299 citations). Gudrun E. Moore has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Philip Stanier, Sayeda N Abu-Amero, Jennifer M. Frost, David Monk, Phillip R. Bennett, Miho Ishida, Antony D. Lighten, Kate Hardy, Robert M L Winston and Sophia Apostolidou. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Nucleic Acids Research 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.