David Monk

1.9k citations

23 papers · 1.2k · h-index 18

Impact in

Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics
- Birth, Development, and Health
Genetics top 2%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 22
- Genetic Syndromes and Imprinting 22
- Genomic variations and chromosomal abnormalities 2
Molecular Biology 21
- Epigenetics and DNA Methylation 19
- RNA modifications and cancer 2
- Muscle Physiology and Disorders 1

Co-authors: Gudrun E. Moore (12 shared papers)Philip Stanier (13 shared papers)Philippe Arnaúd (5 shared papers)Frank Hills (3 shared papers)Sophia Apostolidou (3 shared papers)Robert Feil (3 shared papers)Megan P. Hitchins (5 shared papers)Andrew J. Wood (4 shared papers)
Journals: Human Molecular Genetics (4 papers)The American Journal of Human Genetics (3 papers)Cytogenetic and Genome Research (2 papers)Mammalian Genome (2 papers)Briefings in Functional Genomics (1 paper)
Partner nations: United Kingdom Spain United States

In The Last Decade

David Monk

23 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside David Monk, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David Monk Line = papers co-authored together David Monk links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Limited evolutionary conservation of imprinting in the human placenta Proceedings of the National Academy of Sciences ·David Monk, Philippe Arnaúd, Sophia Apostolidou, Frank Hills, Gavin Kelsey, Philip Stanier, Robert Feil, Gudrun E. Moore	2006	202
2	Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human Human Molecular Genetics ·David Monk, R. Holanda Da Silva Sanches, Philippe Arnaúd, Sophia Apostolidou, Frank Hills, S. Abu-Amero, Adele Murrell, Helmut Friess, Wolf Reik, Philip Stanier, Miguel Constância, Gudrun E. Moore	2006	114
3	Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome The American Journal of Human Genetics ·David Monk, Emma Wakeling, Virginia K. Proud, Megan P. Hitchins, Sayeda Abu‐Amero, Philip Stanier, Michael A. Preece, Gudrun E. Moore	2000	106
4	A Screen for Retrotransposed Imprinted Genes Reveals an Association between X Chromosome Homology and Maternal Germ-Line Methylation PLoS Genetics ·Andrew J. Wood, Roland G. Roberts, David Monk, Gudrun E. Moore, Reiner Schulz, Rebecca J. Oakey	2007	102
5	Genomic imprinting in the human placenta American Journal of Obstetrics and Gynecology ·David Monk	2015	83
6	Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies The American Journal of Human Genetics ·Haiyan Zhou, Martin Brockington, Heinz Jungbluth, David Monk, Philip Stanier, Caroline A. Sewry, Gudrun E. Moore, Francesco Muntoni	2006	80
7	Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. Human Genetics ·David Monk, Louise Bentley, Megan P. Hitchins, Rachael Myler, Jill Clayton‐Smith, Samira Ismail, Sue Price, Michael Preece, Philip Stanier, Gudrun Moore	2002	63
8	Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression Human Molecular Genetics ·David Monk, Philippe Arnaúd, Jennifer M. Frost, Frank Hills, Philip Stanier, Robert Feil, Gudrun E. Moore	2009	60
9	Transcript- and tissue-specific imprinting of a tumour suppressor gene Human Molecular Genetics ·Reiner Schulz, Ruth B. McCole, Kathryn Woodfine, Andrew J. Wood, Mandeep Chahal, David Monk, Gudrun E. Moore, Rebecca J. Oakey	2008	51
10	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 ·Megan P. Hitchins, David Monk, G. Bell, Zehra Ali, Michael A. Preece, Philip Stanier, Gudrun E. Moore	2001	51
11	Intrauterine growth restriction—genetic causes and consequences Seminars in Fetal and Neonatal Medicine ·David Monk, Gudrun E. Moore	2004	51
12	Imprinted genes and their role in human fetal growth Cytogenetic and Genome Research ·Sayeda Abu‐Amero, David Monk, Sophia Apostolidou, Philip Stanier, Gudrun E. Moore	2006	35
13	Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight The American Journal of Human Genetics ·Miho Ishida, David Monk, Andrew Duncan, Sayeda Abu‐Amero, Jiehan Chong, Susan M. Ring, Marcus Pembrey, Peter C. Hindmarsh, John C. Whittaker, Philip Stanier, Gudrun E. Moore	2012	35
14	Genomic Imprinting of Dopa decarboxylase in Heart and Reciprocal Allelic Expression with Neighboring Grb10 Molecular and Cellular Biology ·Trevelyan R. Menheniott, Kathryn Woodfine, Reiner Schulz, Andrew J. Wood, David Monk, Andrew S. Giraud, H. Scott Baldwin, Gudrun E. Moore, Rebecca J. Oakey	2007	34
15	Deciphering the cancer imprintome Briefings in Functional Genomics ·David Monk	2010	28
16	DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed Mammalian Genome ·Megan P. Hitchins, Louise Bentley, David Monk, C.V. Beechey, Jo Peters, Gavin Kelsey, Fumitoshi Ishino, Michael A. Preece, Philip Stanier, Gudrun E. Moore	2002	20
17	Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes Nucleic Acids Research ·David Monk, Philippe Arnaúd, Jennifer M. Frost, Andrew J. Wood, Michael Cowley, Alejandro Martin-Trujillo, Amy Guillaumet-Adkins, Isabel Iglesias‐Platas, Cristina Camprubí, Déborah Bourc’his, Robert Feil, Gudrun E. Moore, Rebecca J. Oakey	2011	19
18	Imprinting control within the compact <i>Gnas</i> locus Cytogenetic and Genome Research ·J. Peters, Rebecca J. Holmes, David Monk, C.V. Beechey, Gudrun E. Moore, Catherine Williamson	2006	18
19	The search for the gene for Silver‐Russell syndrome Acta Paediatrica ·GE Moore, Sayeda Abu‐Amero, Emma Wakeling, Megan P. Hitchins, David Monk, Philip Stanier, M A Preece	1999	15
20	Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissues Human Molecular Genetics ·Layla Parker-Katiraee, Eleni Bousiaki, David Monk, Gudrun E. Moore, Kazuhiko Nakabayashi, Stephen W. Scherer	2008	13

About David Monk

David Monk is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 23 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (22 papers), Epigenetics and DNA Methylation (19 papers), Prenatal Screening and Diagnostics (18 papers), RNA modifications and cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Hibiscus Plant Research Studies (1 paper), Muscle Physiology and Disorders (1 paper) and Cynara cardunculus studies (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (531 citations), Genetics (837 citations), Molecular Biology (838 citations), Obstetrics and Gynecology (79 citations) and Cancer Research (55 citations). David Monk has collaborated with scholars based in United Kingdom, Spain and United States. Frequent 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. Their work appears in journals such as Human Molecular Genetics, The American Journal of Human Genetics, Cytogenetic and Genome Research, Mammalian Genome and Briefings in Functional Genomics.

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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