Philip Stanier

9.7k total citations · 1 hit paper
122 papers, 6.0k citations indexed

About

Philip Stanier is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Philip Stanier has authored 122 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 75 papers in Genetics and 40 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Philip Stanier's work include Prenatal Screening and Diagnostics (37 papers), Genetic Syndromes and Imprinting (32 papers) and Epigenetics and DNA Methylation (30 papers). Philip Stanier is often cited by papers focused on Prenatal Screening and Diagnostics (37 papers), Genetic Syndromes and Imprinting (32 papers) and Epigenetics and DNA Methylation (30 papers). Philip Stanier collaborates with scholars based in United Kingdom, United States and France. Philip Stanier's 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 Michael A. Preece and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Philip Stanier

122 papers receiving 5.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Neural tube defects: recent advances, unsolved questions, and controversies

2013 415 citations Andrew J. Copp, Philip Stanier et al. profile →

Peers

Countries citing papers authored by Philip Stanier

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Philip Stanier

This figure shows the co-authorship network connecting the top 25 collaborators of Philip Stanier. A scholar is included among the top collaborators of Philip Stanier based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Philip Stanier. Philip Stanier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Familial Absent Uvula With Velopharyngeal Incompetence—A New Syndrome? 2019 ·The Cleft Palate-Craniofacial Journal ·Brian C. Sommerlad, (unknown), Melissa Lees, Erwin Pauws, Philip Stanier, Debbie Sell	1
2	Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young mice 2018 ·Scientific Reports ·Isabel R. Orriss, Stuart Lanham, Dawn Savery, Nicholas D. E. Greene, Philip Stanier, Richard O. C. Oreffo, Andrew J. Copp, Gabriel L. Galea	5
3	Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight 2011 ·UCL Discovery (University College London) ·Miho Ishida, David Monk, (unknown), Sayeda Abu‐Amero, Jer Pin Chong, (unknown), Marcus Pembrey, (unknown), J. R. Whittaker, Philip Stanier, (unknown)	1
4	Tbx22(null) mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes (vol 18, pg 4171, 2009) 2010 ·UCL Discovery (University College London) ·Erwin Pauws, Akihiko Hoshino, (unknown), (unknown), Christian E. Keller, P. Hammond, (unknown), (unknown), Philip Stanier	4
5	Genetics of human neural tube defects 2009 ·Human Molecular Genetics ·Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp	233
6	Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing 2008 ·Genome Research ·(unknown), Alexandre Wagschal, Philippe Arnaúd, (unknown), (unknown), Déborah Bourc’his, Stephen W. Scherer, Robert Feil, Philip Stanier, Gudrun E. Moore	73
7	Limited evolutionary conservation of imprinting in the human placenta 2006 ·Proceedings of the National Academy of Sciences ·David Monk, Philippe Arnaúd, Sophia Apostolidou, Frank Hills, Gavin Kelsey, Philip Stanier, Robert Feil, Gudrun E. Moore	202
8	Elevated maternal expression of the imprinted PHLDA2 gene is associated with low birth weight 2006 ·UCL Discovery (University College London) ·Sophia Apostolidou, Sayeda Abu‐Amero, Keelin O’Donoghue, Ólöf Birna Ólafsdóttir, (unknown), Jennifer M. Frost, (unknown), P. T. Loughna, Philip Stanier, (unknown)	6
9	Imprinted genes and their role in human fetal growth 2006 ·Cytogenetic and Genome Research ·Sayeda Abu‐Amero, David Monk, Sophia Apostolidou, Philip Stanier, Gudrun E. Moore	35
10	SNPs in the CpG island of NAP1L2: A possible link between DNA methylation and neural tube defects? 2002 ·American Journal of Medical Genetics ·Ute C. Rogner, Patrick Danoy, Fumihiko Matsuda, Gudrun E. Moore, Philip Stanier, Philip Avner	11
11	Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. 2002 ·Human Genetics ·David Monk, (unknown), Megan P. Hitchins, (unknown), Jill Clayton‐Smith, Samira Ismail, Sue Price, Michael Preece, Philip Stanier, (unknown)	63
12	ParalogousSm22α (Tagln) Genes Map to Mouse Chromosomes 1 and 9: Further Evidence for a Paralogous Relationship 1998 ·Genomics ·Philip Stanier, Shadi Abu‐Hayyeh, J. Murdoch, Jane Eddleston, Andrew J. Copp	24
13	Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues 1998 ·European Journal of Human Genetics ·Emma Wakeling, (unknown), Philip Stanier, M A Preece, Gudrun E. Moore	20
14	Localization of the mouse gene encoding tyrosine kinase receptor type 10 on distal Chromosome 1 1997 ·Mammalian Genome ·J. Murdoch, Jane Eddleston, Philip Stanier, Andrew J. Copp	1
15	A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R) 1997 ·Molecular and Cellular Probes ·Sayeda Abu‐Amero, Michael Preece, Emma Wakeling, Gudrun E. Moore, Philip Stanier	3
16	Expression of a common cellular phospholipase A2 by human intrauterine tissues 1993 ·Prostaglandins ·Phillip R. Bennett, Donna M. Slater, Philip Stanier, Gudrun E. Moore	7
17	Detection of human cytomegalovirus in peripheral mononuclear cells and urine samples using PCR 1992 ·Molecular and Cellular Probes ·Philip Stanier, Alan D. Kitchen, D.L. Taylor, A.S. Tyms	23
18	A new polymorphism at the DXS178 locus 1991 ·Nucleic Acids Research ·Philip Stanier, Robert Newton, Gudrun E. Moore	1
19	Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locus 1988 ·Human Genetics ·Philip Stanier, Xavier Estivill, Nicholas Lench, Robert Williamson	2
20	Linkage of the Col1A2 collagen gene to cystic fibrosis 1985 ·UCL Discovery (University College London) ·Peter Scambler, (unknown), Martin Farrall, Jimmy D. Bell, Philip Stanier, Nicholas Lench, George W. Bell, H. Kruyer, (unknown), R Williamson	1

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.

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