David Monk
Impact in
-
- Prenatal Screening and Diagnostics
- Birth, Development, and Health
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Prenatal Screening and Diagnostics 21
- Genetics 27
- Genetic Syndromes and Imprinting 27
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Gudrun E. Moore (14 shared papers)Philip Stanier (16 shared papers)Sophia Apostolidou (5 shared papers)Frank A. Hills (4 shared papers)Philippe Arnaud (5 shared papers)Megan Philippa Hitchins (7 shared papers)Robert Feil (3 shared papers)Gavin Kelsey (3 shared papers)
- Journals
- Human Molecular Genetics (4 papers)The American Journal of Human Genetics (4 papers)Cytogenetic and Genome Research (2 papers)Mammalian Genome (2 papers)Advances in experimental medicine and biology (1 paper)
- Partner nations
- United KingdomSpainUnited States
In The Last Decade
David Monk
28 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 81
- Pediatrics, Perinatology and Child Health 693
- Genetics 999
- Obstetrics and Gynecology 162
- Molecular Biology 1.0k
- Cancer Research 80
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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 209 | |
| 2 | 2000 | 126 | |
| 3 | 2015 | 124 | |
| 4 | 2006 | 120 | |
| 5 | 2007 | 99 | |
| 6 | 2015 | 97 | |
| 7 | 2006 | 96 | |
| 8 | 2009 | 72 | |
| 9 | 2002 | 69 | |
| 10 | 2001 | 58 | |
| 11 | 2008 | 55 | |
| 12 | 2004 | 52 | |
| 13 | 2002 | 47 | |
| 14 | 2006 | 42 | |
| 15 | 2012 | 39 | |
| 16 | 2007 | 38 | |
| 17 | 2007 | 36 | |
| 18 | 2010 | 31 | |
| 19 | 2001 | 25 | |
| 20 | 2002 | 23 |
About David Monk
David Monk is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Clinical Biochemistry and Obstetrics and Gynecology, having authored 28 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (27 papers), Epigenetics and DNA Methylation (22 papers), Prenatal Screening and Diagnostics (21 papers), Renal and related cancers (2 papers), RNA modifications and cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Cynara cardunculus studies (1 paper) and Pregnancy and preeclampsia studies (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (693 citations), Genetics (999 citations), Obstetrics and Gynecology (162 citations), Molecular Biology (1.0k citations) and Cancer Research (80 citations). David Monk has collaborated with scholars based in United Kingdom, Spain and United States. Frequent co-authors include Gudrun E. Moore, Philip Stanier, Sophia Apostolidou, Frank A. Hills, Philippe Arnaud, Megan Philippa Hitchins, Robert Feil, Gavin Kelsey, Sayeda N Abu-Amero and Michael A. Preece. Their work appears in journals such as Human Molecular Genetics, The American Journal of Human Genetics, Cytogenetic and Genome Research, Mammalian Genome and Advances in experimental medicine and biology.
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.