Tom Moore
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Evolution and Genetic Dynamics
- Obstetrics and Gynecology top 2%
- Pregnancy and preeclampsia studies
Papers in
- Genetics 31
- Genetic Syndromes and Imprinting 22
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
- Immunology 14
- Reproductive System and Pregnancy 14
- Co-authors
- Wolf Reik (5 shared papers)Gabriela S. Dveksler (4 shared papers)Miguel Constância (4 shared papers)Tessa J. Roseboom (1 shared paper)Claudine Junien (1 shared paper)LORNA GRINDLAY MOORE (1 shared paper)Anne Gabory (1 shared paper)Andrew S. McLellan (8 shared papers)
- Journals
- Reproduction (7 papers)Nature Genetics (4 papers)Placenta (4 papers)Human Molecular Genetics (3 papers)BioEssays (2 papers)
- Partner nations
- IrelandUnited KingdomGermany
In The Last Decade
Tom Moore
57 papers receiving 2.9k citations
Tom Moore's Hit Papers
Peers
Comparison fields: 5 of 111
- Genetics 1.4k
- Obstetrics and Gynecology 280
- Pediatrics, Perinatology and Child Health 321
- Immunology 257
- Bioengineering 31
Countries citing papers authored by Tom Moore
This map shows the geographic impact of Tom 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 Tom Moore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tom Moore more than expected).
Fields of papers citing papers by Tom Moore
This network shows the impact of papers produced by Tom 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 Tom Moore. The network helps show where Tom Moore may publish in the future.
Co-authors
The 25 scholars most cited alongside Tom 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genomic imprinting in mammalian development: a parental tug-of-war Hit paper breakdown → | 1991 | 1007 |
| 2 | 2013 | 291 | |
| 3 | 1997 | 218 | |
| 4 | 2000 | 159 | |
| 5 | 2014 | 109 | |
| 6 | 2012 | 90 | |
| 7 | 1998 | 88 | |
| 8 | 2005 | 81 | |
| 9 | 2001 | 80 | |
| 10 | 1996 | 71 | |
| 11 | 1996 | 69 | |
| 12 | 2007 | 64 | |
| 13 | 2005 | 58 | |
| 14 | 2006 | 47 | |
| 15 | 2005 | 45 | |
| 16 | 2013 | 45 | |
| 17 | 2002 | 35 | |
| 18 | 2005 | 34 | |
| 19 | 2011 | 34 | |
| 20 | 2001 | 32 |
About Tom Moore
Tom Moore is a scholar working on Genetics, Immunology, Obstetrics and Gynecology, Bioengineering and Pediatrics, Perinatology and Child Health, having authored 57 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (22 papers), Reproductive System and Pregnancy (14 papers), Pregnancy and preeclampsia studies (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Microbial Inactivation Methods (2 papers), Chromosomal and Genetic Variations (2 papers) and Cell Adhesion Molecules Research (2 papers). The work is most often cited by research in Genetics (1.4k citations), Obstetrics and Gynecology (280 citations), Pediatrics, Perinatology and Child Health (321 citations), Immunology (257 citations) and Bioengineering (31 citations). Tom Moore has collaborated with scholars based in Ireland, United Kingdom and Germany. Frequent co-authors include Wolf Reik, Gabriela S. Dveksler, Miguel Constância, Tessa J. Roseboom, Claudine Junien, LORNA GRINDLAY MOORE, Anne Gabory, Andrew S. McLellan, Abigail L. Fowden and Laurence D. Hurst. Their work appears in journals such as Reproduction, Nature Genetics, Placenta, Human Molecular Genetics and BioEssays.
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.