Gudrun E. Moore

9.5k total citations
135 papers, 5.4k citations indexed

About

Gudrun E. Moore is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gudrun E. Moore has authored 135 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 83 papers in Genetics, 74 papers in Molecular Biology and 56 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gudrun E. Moore's work include Genetic Syndromes and Imprinting (48 papers), Prenatal Screening and Diagnostics (47 papers) and Epigenetics and DNA Methylation (37 papers). Gudrun E. Moore is often cited by papers focused on Genetic Syndromes and Imprinting (48 papers), Prenatal Screening and Diagnostics (47 papers) and Epigenetics and DNA Methylation (37 papers). Gudrun E. Moore collaborates with scholars based in United Kingdom, United States and India. Gudrun E. Moore's co-authors include Philip Stanier, Sayeda Abu‐Amero, Jennifer M. Frost, David Monk, Phillip R. Bennett, Miho Ishida, Antony D. Lighten, Robert Winston, Kate Hardy and Philippe Arnaúd and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Gudrun E. Moore

135 papers receiving 5.3k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Gudrun E. Moore 3.0k 2.9k 1.8k 533 525 135 5.4k
Philip Stanier 3.6k 1.2× 2.9k 1.0× 1.5k 0.9× 327 0.6× 608 1.2× 122 6.0k
Brynn Levy 3.3k 1.1× 2.2k 0.8× 2.9k 1.6× 830 1.6× 519 1.0× 134 7.2k
Deborah E. McFadden 1.4k 0.5× 1.0k 0.4× 1.7k 0.9× 724 1.4× 481 0.9× 79 3.9k
Felix Beck 4.3k 1.4× 2.3k 0.8× 755 0.4× 1.0k 2.0× 1.2k 2.2× 160 7.3k
Monica Miozzo 1.9k 0.6× 1.2k 0.4× 669 0.4× 277 0.5× 466 0.9× 158 5.0k
Kenichiro Hata 6.8k 2.3× 3.3k 1.1× 1.9k 1.0× 916 1.7× 245 0.5× 228 8.8k
Raja Brauner 2.9k 1.0× 2.3k 0.8× 1.5k 0.8× 1.1k 2.2× 1.1k 2.1× 213 7.9k
J. M. Connor 1.5k 0.5× 1.3k 0.5× 1.4k 0.8× 275 0.5× 579 1.1× 105 5.8k
Aleksandar Rajkovic 2.1k 0.7× 2.2k 0.8× 723 0.4× 1.8k 3.3× 237 0.5× 117 5.6k
Philippe Touraine 2.4k 0.8× 1.6k 0.6× 516 0.3× 1.5k 2.8× 534 1.0× 195 6.1k

Countries citing papers authored by Gudrun E. Moore

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Gudrun E. Moore

This figure shows the co-authorship network connecting the top 25 collaborators of Gudrun E. Moore. A scholar is included among the top collaborators of Gudrun E. Moore 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 Gudrun E. Moore. Gudrun E. Moore is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Suntharalingham, Jenifer P., Ignacio del Valle, Federica Buonocore, et al.. (2025). The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development. Communications Biology. 8(1). 249–249. 1 indexed citations
2.
Kessler, Noah J., Miho Ishida, Charalambos Demetriou, et al.. (2022). Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo. Nucleic Acids Research. 50(12). 6735–6752. 7 indexed citations
3.
Sousa, Sérgio B., Fabiana Ramos, Paula Garcia, et al.. (2013). Intellectual disability, coarse face, relative macrocephaly, and cerebellar hypotrophy in two sisters. American Journal of Medical Genetics Part A. 164(1). 10–14. 8 indexed citations
4.
Kinsler, Veronica A., Glenn Anderson, B. Latimer, et al.. (2013). Immunohistochemical and ultrastructural features of congenital melanocytic naevus cells support a stem‐cell phenotype. British Journal of Dermatology. 169(2). 374–383. 17 indexed citations
5.
Padidela, Raja, et al.. (2011). The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight. Clinical Endocrinology. 76(2). 236–240. 13 indexed citations
6.
Monk, David, Philippe Arnaúd, Jennifer M. Frost, et al.. (2011). Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes. Nucleic Acids Research. 39(11). 4577–4586. 19 indexed citations
7.
Daelemans, Caroline, Matthew E. Ritchie, Guillaume Smits, et al.. (2010). High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta. BMC Genetics. 11(1). 25–25. 48 indexed citations
8.
Pauws, Erwin, Suresh I. Prajapati, Charles Keller, et al.. (2009). 06-P008 Loss of Tbx22 causes submucous cleft palate, ankyloglossia and choanal atresia. Mechanisms of Development. 126. S122–S122. 1 indexed citations
9.
Monk, David, Philippe Arnaúd, Jennifer M. Frost, et al.. (2009). Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression. Human Molecular Genetics. 18(16). 3066–3074. 60 indexed citations
10.
Wagschal, Alexandre, Philippe Arnaúd, Déborah Bourc’his, et al.. (2008). 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. Genome Research. 18(8). 1270–1281. 73 indexed citations
11.
Pauws, Erwin, Marius C. Jones, Manvendra K. Singh, et al.. (2007). TBX22 Missense Mutations Found in Patients with X-Linked Cleft Palate Affect DNA Binding, Sumoylation, and Transcriptional Repression. The American Journal of Human Genetics. 81(4). 700–712. 69 indexed citations
12.
Monk, David, Philippe Arnaúd, Sophia Apostolidou, et al.. (2006). Limited evolutionary conservation of imprinting in the human placenta. Proceedings of the National Academy of Sciences. 103(17). 6623–6628. 202 indexed citations
13.
Zhou, Haiyan, Martin Brockington, Heinz Jungbluth, et al.. (2006). Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies. The American Journal of Human Genetics. 79(5). 859–868. 79 indexed citations
14.
Rogner, Ute C., Patrick Danoy, Fumihiko Matsuda, et al.. (2002). SNPs in the CpG island of NAP1L2: A possible link between DNA methylation and neural tube defects?. American Journal of Medical Genetics. 110(3). 208–214. 11 indexed citations
15.
Moore, Gudrun E.. (2001). Breast cancer: early detection needed.. PubMed. 19(9). 39–39. 7 indexed citations
16.
Wakeling, Emma, et al.. (1998). Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues. European Journal of Human Genetics. 6(2). 158–164. 20 indexed citations
17.
Lighten, Antony D., Gudrun E. Moore, Robert Winston, & Kate Hardy. (1998). Routine addition of human insulin-like growth factor-I ligand could benefit clinical in-vitro fertilization culture. Human Reproduction. 13(11). 3144–3150. 138 indexed citations
18.
Lighten, Antony D., Kate Hardy, Robert Winston, & Gudrun E. Moore. (1997). Expression of mRNA for the insulin-like growth factors and their receptors in human preimplantation embryos. Molecular Reproduction and Development. 47(2). 134–139. 126 indexed citations
19.
Henderson, Deborah J., et al.. (1991). Trophoblast from anembryonic pregnancy has both a maternal and a paternal contribution to its genome. American Journal of Obstetrics and Gynecology. 165(1). 98–102. 4 indexed citations
20.
Ivens, Alasdair, Gudrun E. Moore, & R. Williamson. (1988). Molecular approaches to dysmorphology.. Journal of Medical Genetics. 25(7). 473–479. 5 indexed citations

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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