David Monk

1.9k total citations
23 papers, 1.2k citations indexed

About

David Monk is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David Monk has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 21 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David Monk's work include Genetic Syndromes and Imprinting (22 papers), Epigenetics and DNA Methylation (19 papers) and Prenatal Screening and Diagnostics (18 papers). David Monk is often cited by papers focused on Genetic Syndromes and Imprinting (22 papers), Epigenetics and DNA Methylation (19 papers) and Prenatal Screening and Diagnostics (18 papers). David Monk collaborates with scholars based in United Kingdom, Spain and United States. David Monk's co-authors include Gudrun E. Moore, Philip Stanier, Philippe Arnaúd, Frank Hills, Sophia Apostolidou, Robert Feil, Megan P. Hitchins, Andrew J. Wood, Rebecca J. Oakey and Gavin Kelsey and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Molecular and Cellular Biology.

In The Last Decade

David Monk

23 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
David Monk United Kingdom 18 963 874 646 100 64 23 1.2k
Salah Azzi France 19 930 1.0× 1.0k 1.1× 681 1.1× 61 0.6× 56 0.9× 28 1.3k
Hirotaka Wagatsuma Japan 9 820 0.9× 490 0.6× 274 0.4× 42 0.4× 286 4.5× 11 1.0k
Maryline Gagnebin Switzerland 9 465 0.5× 224 0.3× 92 0.1× 20 0.2× 257 4.0× 11 743
Yihua Bao China 15 391 0.4× 194 0.2× 205 0.3× 39 0.4× 30 0.5× 47 663
Joshua L. Everson United States 14 383 0.4× 256 0.3× 195 0.3× 37 0.4× 11 0.2× 21 607
Kathryn Lucchesi United States 8 336 0.3× 108 0.1× 149 0.2× 166 1.7× 17 0.3× 9 665
Sara Roos Sweden 11 299 0.3× 112 0.1× 560 0.9× 586 5.9× 42 0.7× 16 968
Ayako Tanae Japan 14 789 0.8× 345 0.4× 121 0.2× 23 0.2× 19 0.3× 67 1.1k
Saleh Mahmood United States 13 411 0.4× 109 0.1× 117 0.2× 21 0.2× 51 0.8× 23 585
Laëtitia Chotard Canada 5 413 0.4× 301 0.3× 147 0.2× 20 0.2× 52 0.8× 6 548

Countries citing papers authored by David Monk

Since Specialization
Citations

This map shows the geographic impact of David Monk'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 David Monk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Monk more than expected).

Fields of papers citing papers by David Monk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Monk. 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 David Monk. The network helps show where David Monk may publish in the future.

Co-authorship network of co-authors of David Monk

This figure shows the co-authorship network connecting the top 25 collaborators of David Monk. A scholar is included among the top collaborators of David Monk 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 David Monk. David Monk 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.
Monk, David. (2015). Genomic imprinting in the human placenta. American Journal of Obstetrics and Gynecology. 213(4). S152–S162. 82 indexed citations
2.
Ishida, Miho, David Monk, Sayeda Abu‐Amero, et al.. (2011). Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight. UCL Discovery (University College London). 1 indexed citations
3.
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
4.
Camprubí, Cristina & David Monk. (2011). Does Genomic Imprinting Play a Role in Autoimmunity?. Advances in experimental medicine and biology. 711. 103–116. 9 indexed citations
5.
Monk, David. (2010). Deciphering the cancer imprintome. Briefings in Functional Genomics. 9(4). 329–339. 28 indexed citations
6.
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
7.
Monk, David, et al.. (2008). Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues. Human Molecular Genetics. 17(21). 3263–3270. 13 indexed citations
8.
Wood, Andrew J., Roland G. Roberts, David Monk, et al.. (2007). A Screen for Retrotransposed Imprinted Genes Reveals an Association between X Chromosome Homology and Maternal Germ-Line Methylation. PLoS Genetics. 3(2). e20–e20. 102 indexed citations
9.
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
10.
Abu‐Amero, Sayeda, David Monk, Sophia Apostolidou, Philip Stanier, & Gudrun E. Moore. (2006). Imprinted genes and their role in human fetal growth. Cytogenetic and Genome Research. 113(1-4). 262–270. 35 indexed citations
11.
Peters, J., et al.. (2006). Imprinting control within the compact <i>Gnas</i> locus. Cytogenetic and Genome Research. 113(1-4). 194–201. 18 indexed citations
12.
Monk, David, R. Holanda Da Silva Sanches, Philippe Arnaúd, et al.. (2006). Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human. Human Molecular Genetics. 15(8). 1259–1269. 114 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.
Monk, David & Gudrun E. Moore. (2004). Intrauterine growth restriction—genetic causes and consequences. Seminars in Fetal and Neonatal Medicine. 9(5). 371–378. 52 indexed citations
15.
Kelsey, Gavin, Philippe Arnaúd, Michael A. Preece, et al.. (2003). Imprinted methylation profiles for proximal mouse Chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis. Mammalian Genome. 14(12). 805–816. 11 indexed citations
16.
Monk, David, Megan P. Hitchins, Jill Clayton‐Smith, et al.. (2002). Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.. Human Genetics. 111(4-5). 376–387. 63 indexed citations
17.
Hitchins, Megan P., David Monk, C.V. Beechey, et al.. (2002). DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed. Mammalian Genome. 13(12). 686–691. 20 indexed citations
18.
Hitchins, Megan P., David Monk, G. Bell, et al.. (2001). Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome. European Journal of Human Genetics. 9(2). 82–90. 52 indexed citations
19.
Monk, David, Emma Wakeling, Virginia K. Proud, et al.. (2000). Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome. The American Journal of Human Genetics. 66(1). 36–46. 107 indexed citations
20.
Abu‐Amero, Sayeda, Emma Wakeling, Megan P. Hitchins, et al.. (1999). The search for the gene for Silver‐Russell syndrome. Acta Paediatrica. 88(s433). 42–48. 15 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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