David Monk
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
- Birth, Development, and Health
Papers in
- Genetics 56
- Genetic Syndromes and Imprinting 51
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 4
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- Prenatal Screening and Diagnostics 27
- Co-authors
- Andrea Riccio (11 shared papers)Thomas Eggermann (8 shared papers)Eamonn Richard Maher (7 shared papers)Deborah Mackay (7 shared papers)Marta Sánchez-Delgado (14 shared papers)Isabel Iglesias‐Platas (18 shared papers)Pablo Daniel Lapunzina (9 shared papers)Álex Martín-Trujillo (10 shared papers)
- Journals
- Clinical Epigenetics (9 papers)Epigenetics (7 papers)Journal of Medical Genetics (4 papers)Human Mutation (3 papers)Placenta (3 papers)
- Partner nations
- SpainUnited KingdomFrance
In The Last Decade
David Monk
70 papers receiving 3.3k citations
David Monk's Hit Papers
Peers
Comparison fields: 5 of 98
- Genetics 2.1k
- Pediatrics, Perinatology and Child Health 1.1k
- Molecular Biology 1.8k
- Obstetrics and Gynecology 119
- Cancer Research 141
Countries citing papers authored by David Monk
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
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.
All Works
Showing the 20 most-cited of 71 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Diagnosis and management of Silver–Russell syndrome: first international consensus statement Hit paper breakdown → | 2016 | 369 |
| 2 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact Hit paper breakdown → | 2019 | 297 |
| 3 | 2018 | 220 | |
| 4 | 2015 | 156 | |
| 5 | 2007 | 142 | |
| 6 | 2016 | 93 | |
| 7 | 2016 | 87 | |
| 8 | 2013 | 87 | |
| 9 | 2015 | 85 | |
| 10 | 2016 | 80 | |
| 11 | 2018 | 76 | |
| 12 | 2015 | 73 | |
| 13 | 2016 | 68 | |
| 14 | 2017 | 68 | |
| 15 | 2014 | 64 | |
| 16 | 2015 | 63 | |
| 17 | 2019 | 62 | |
| 18 | 2011 | 58 | |
| 19 | 2016 | 58 | |
| 20 | 2023 | 48 |
About David Monk
David Monk is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Pathology and Forensic Medicine and Obstetrics and Gynecology, having authored 71 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (51 papers), Epigenetics and DNA Methylation (37 papers), Prenatal Screening and Diagnostics (27 papers), Tumors and Oncological Cases (6 papers), RNA modifications and cancer (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Gestational Trophoblastic Disease Studies (4 papers). The work is most often cited by research in Genetics (2.1k citations), Pediatrics, Perinatology and Child Health (1.1k citations), Molecular Biology (1.8k citations), Obstetrics and Gynecology (119 citations) and Cancer Research (141 citations). David Monk has collaborated with scholars based in Spain, United Kingdom and France. Frequent co-authors include Andrea Riccio, Thomas Eggermann, Eamonn Richard Maher, Deborah Mackay, Marta Sánchez-Delgado, Isabel Iglesias‐Platas, Pablo Daniel Lapunzina, Álex Martín-Trujillo, Manel Esteller and Franck Court. Their work appears in journals such as Clinical Epigenetics, Epigenetics, Journal of Medical Genetics, Human Mutation and Placenta.
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.