Marcus Pembrey
Impact in
- Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics
-
- Birth, Development, and Health
- Prenatal Screening and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 27
- Genetics 61
- Genetics and Neurodevelopmental Disorders 23
- Genetic Syndromes and Imprinting 20
- Genomic variations and chromosomal abnormalities 13
- Hemoglobinopathies and Related Disorders 13
- Co-authors
- Lars Olov Bygren (5 shared papers)Jean Golding (23 shared papers)Gunnar Kaati (4 shared papers)Michael Sjöstróm (3 shared papers)Kate Northstone (14 shared papers)D. J. Weatherall (7 shared papers)Sören Edvinsson (3 shared papers)Anthony P. Monaco (4 shared papers)
- Journals
- Journal of Medical Genetics (26 papers)Human Genetics (9 papers)European Journal of Human Genetics (8 papers)The Lancet (8 papers)Archives of Disease in Childhood (7 papers)
- Partner nations
- United KingdomIndiaUnited States
In The Last Decade
Marcus Pembrey
165 papers receiving 10.4k citations
Marcus Pembrey's Hit Papers
Peers
Comparison fields: 5 of 161
- Sensory Systems 868
- Pediatrics, Perinatology and Child Health 2.6k
- Genetics 3.7k
- Genetics 1.0k
- Aging 139
Countries citing papers authored by Marcus Pembrey
This map shows the geographic impact of Marcus Pembrey'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 Marcus Pembrey with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcus Pembrey more than expected).
Fields of papers citing papers by Marcus Pembrey
This network shows the impact of papers produced by Marcus Pembrey. 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 Marcus Pembrey. The network helps show where Marcus Pembrey may publish in the future.
Co-authors
The 25 scholars most cited alongside Marcus Pembrey, 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 170 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Sex-specific, male-line transgenerational responses in humans Hit paper breakdown → | 2005 | 907 |
| 2 | 1993 | 451 | |
| 3 | 1998 | 382 | |
| 4 | 2007 | 360 | |
| 5 | 1995 | 354 | |
| 6 | 2011 | 338 | |
| 7 | 1992 | 309 | |
| 8 | 1998 | 305 | |
| 9 | 1996 | 283 | |
| 10 | 2005 | 281 | |
| 11 | 2008 | 275 | |
| 12 | 1997 | 251 | |
| 13 | 2013 | 236 | |
| 14 | 1998 | 222 | |
| 15 | 2014 | 220 | |
| 16 | 1998 | 199 | |
| 17 | 1995 | 198 | |
| 18 | 1991 | 171 | |
| 19 | 2014 | 159 | |
| 20 | 1995 | 155 |
About Marcus Pembrey
Marcus Pembrey is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Health, Toxicology and Mutagenesis, having authored 170 papers that have together received 11.2k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (27 papers), Birth, Development, and Health (23 papers), Genetics and Neurodevelopmental Disorders (23 papers), Genetic Syndromes and Imprinting (20 papers), Health, Environment, Cognitive Aging (16 papers), Genomic variations and chromosomal abnormalities (13 papers), Hearing, Cochlea, Tinnitus, Genetics (13 papers) and Hemoglobinopathies and Related Disorders (13 papers). The work is most often cited by research in Sensory Systems (868 citations), Pediatrics, Perinatology and Child Health (2.6k citations), Genetics (3.7k citations), Genetics (1.0k citations) and Aging (139 citations). Marcus Pembrey has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Lars Olov Bygren, Jean Golding, Gunnar Kaati, Michael Sjöstróm, Kate Northstone, D. J. Weatherall, Sören Edvinsson, Anthony P. Monaco, William Reardon and Jill Clayton‐Smith. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, European Journal of Human Genetics, The Lancet and Archives of Disease in Childhood.
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.