Philip Stanier
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
Papers in
- Genetics 75
- Genetic Syndromes and Imprinting 32
- Cleft Lip and Palate Research 24
- Craniofacial Disorders and Treatments 19
- Congenital Ear and Nasal Anomalies 12
- Genomic variations and chromosomal abnormalities 10
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- Epigenetics and DNA Methylation 28
- Congenital heart defects research 9
- Co-authors
- Andrew J. Copp (24 shared papers)Gudrun E. Moore (60 shared papers)Nicholas D. E. Greene (13 shared papers)Sayeda Abu‐Amero (22 shared papers)Erwin Pauws (17 shared papers)David Monk (13 shared papers)Kit Doudney (10 shared papers)J. Murdoch (12 shared papers)
- Journals
- Genomics (11 papers)Human Molecular Genetics (10 papers)Human Genetics (6 papers)Journal of Medical Genetics (6 papers)European Journal of Human Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Philip Stanier
122 papers receiving 5.9k citations
Philip Stanier's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 2.8k
- Pediatrics, Perinatology and Child Health 1.3k
- Molecular Biology 3.2k
- Genetics 356
- Rheumatology 421
Countries citing papers authored by Philip Stanier
This map shows the geographic impact of Philip Stanier'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 Philip Stanier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philip Stanier more than expected).
Fields of papers citing papers by Philip Stanier
This network shows the impact of papers produced by Philip Stanier. 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 Philip Stanier. The network helps show where Philip Stanier may publish in the future.
Co-authors
The 25 scholars most cited alongside Philip Stanier, 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 122 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 490 | |
| 2 | Neural tube defects: recent advances, unsolved questions, and controversies Hit paper breakdown → | 2013 | 418 |
| 3 | 2004 | 294 | |
| 4 | 1987 | 278 | |
| 5 | 2009 | 232 | |
| 6 | 2001 | 207 | |
| 7 | 2006 | 202 | |
| 8 | 2013 | 197 | |
| 9 | 2011 | 150 | |
| 10 | 2007 | 128 | |
| 11 | 2006 | 114 | |
| 12 | 1997 | 114 | |
| 13 | 2014 | 109 | |
| 14 | 2006 | 107 | |
| 15 | 2000 | 106 | |
| 16 | 1989 | 103 | |
| 17 | 2001 | 85 | |
| 18 | 1991 | 84 | |
| 19 | 1988 | 82 | |
| 20 | 2001 | 81 |
About Philip Stanier
Philip Stanier is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Pulmonary and Respiratory Medicine, having authored 122 papers that have together received 6.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (35 papers), Genetic Syndromes and Imprinting (32 papers), Epigenetics and DNA Methylation (28 papers), Cleft Lip and Palate Research (24 papers), Craniofacial Disorders and Treatments (19 papers), Congenital Ear and Nasal Anomalies (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Congenital heart defects research (9 papers). The work is most often cited by research in Genetics (2.8k citations), Pediatrics, Perinatology and Child Health (1.3k citations), Molecular Biology (3.2k citations), Genetics (356 citations) and Rheumatology (421 citations). Philip Stanier has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Andrew J. Copp, Gudrun E. Moore, Nicholas D. E. Greene, Sayeda Abu‐Amero, Erwin Pauws, David Monk, Kit Doudney, J. Murdoch, Núria Setó‐Salvia and Sophia Apostolidou. Their work appears in journals such as Genomics, Human Molecular Genetics, Human Genetics, Journal of Medical 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.