Marcus E Pembrey
Impact in
- Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Hemoglobinopathies and Related Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 75
- Genetics and Neurodevelopmental Disorders 29
- Genetic Syndromes and Imprinting 22
- Genomic variations and chromosomal abnormalities 15
- Hemoglobinopathies and Related Disorders 14
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- Birth, Development, and Health 32
- Co-authors
- Jean Golding (33 shared papers)Lars Olov Bygren (4 shared papers)Gunnar Kaati (3 shared papers)Michael Sjöstróm (3 shared papers)Kate Northstone (21 shared papers)David John Weatherall (7 shared papers)Sören Edvinsson (2 shared papers)William Reardon (12 shared papers)
- Journals
- Journal of Medical Genetics (26 papers)The Lancet (14 papers)Human Genetics (10 papers)Wellcome Open Research (9 papers)European Journal of Human Genetics (9 papers)
- Partner nations
- United KingdomIndiaUnited States
In The Last Decade
Marcus E Pembrey
189 papers receiving 12.6k citations
Marcus E Pembrey's Hit Papers
Peers
Comparison fields: 5 of 168
- Sensory Systems 926
- Genetics 4.3k
- Pediatrics, Perinatology and Child Health 2.7k
- Genetics 1.1k
- Hematology 882
Countries citing papers authored by Marcus E Pembrey
This map shows the geographic impact of Marcus E 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 E 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 E Pembrey more than expected).
Fields of papers citing papers by Marcus E Pembrey
This network shows the impact of papers produced by Marcus E 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 E Pembrey. The network helps show where Marcus E Pembrey may publish in the future.
Co-authors
The 25 scholars most cited alongside Marcus E 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 197 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants Hit paper breakdown → | 2007 | 1188 |
| 2 | Sex-specific, male-line transgenerational responses in humans Hit paper breakdown → | 2005 | 918 |
| 3 | 1993 | 463 | |
| 4 | 1998 | 380 | |
| 5 | Bayesian refinement of association signals for 14 loci in 3 common diseases Hit paper breakdown → | 2012 | 366 |
| 6 | 2007 | 357 | |
| 7 | 1995 | 356 | |
| 8 | 2011 | 348 | |
| 9 | 1992 | 330 | |
| 10 | 1998 | 309 | |
| 11 | 2008 | 295 | |
| 12 | 2005 | 295 | |
| 13 | 1997 | 261 | |
| 14 | 2014 | 236 | |
| 15 | 2013 | 235 | |
| 16 | 1998 | 228 | |
| 17 | 1995 | 204 | |
| 18 | 1998 | 202 | |
| 19 | 1995 | 177 | |
| 20 | 1991 | 171 |
About Marcus E Pembrey
Marcus E Pembrey is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology and Health, Toxicology and Mutagenesis, having authored 197 papers that have together received 13.5k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (33 papers), Birth, Development, and Health (32 papers), Genetics and Neurodevelopmental Disorders (29 papers), Health, Environment, Cognitive Aging (23 papers), Genetic Syndromes and Imprinting (22 papers), Genomic variations and chromosomal abnormalities (15 papers), Hemoglobinopathies and Related Disorders (14 papers) and Hearing, Cochlea, Tinnitus, Genetics (13 papers). The work is most often cited by research in Sensory Systems (926 citations), Genetics (4.3k citations), Pediatrics, Perinatology and Child Health (2.7k citations), Genetics (1.1k citations) and Hematology (882 citations). Marcus E Pembrey has collaborated with scholars based in United Kingdom, India and United States. Frequent co-authors include Jean Golding, Lars Olov Bygren, Gunnar Kaati, Michael Sjöstróm, Kate Northstone, David John Weatherall, Sören Edvinsson, William Reardon, Anthony P. Monaco and Jill Clayton‐Smith. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Human Genetics, Wellcome Open Research and European Journal of Human Genetics.
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.