Andrew J. Sharp
Impact in
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Psychiatry and Mental health top 2%
- Epilepsy research and treatment
Papers in
- Genetics 70
- Genomic variations and chromosomal abnormalities 37
- Genetic Associations and Epidemiology 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genetic Syndromes and Imprinting 8
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 5
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- Epigenetics and DNA Methylation 18
- Genomics and Phylogenetic Studies 7
- Co-authors
- Evan E. Eichler (14 shared papers)Daniel Pinkel (4 shared papers)Donna G. Albertson (4 shared papers)Paras Garg (16 shared papers)Patricia A. Jacobs (3 shared papers)David Robinson (2 shared papers)Jeffrey A. Bailey (2 shared papers)Lisa M. Pertz (2 shared papers)
- Journals
- The American Journal of Human Genetics (8 papers)Journal of Medical Genetics (7 papers)Human Mutation (7 papers)Nature Communications (7 papers)PLoS Genetics (7 papers)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Andrew J. Sharp
98 papers receiving 8.8k citations
Andrew J. Sharp's Hit Papers
Peers
Comparison fields: 5 of 131
- Genetics 5.5k
- Psychiatry and Mental health 707
- Pediatrics, Perinatology and Child Health 492
- Molecular Biology 1.9k
- Developmental Neuroscience 91
Countries citing papers authored by Andrew J. Sharp
This map shows the geographic impact of Andrew J. Sharp'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 Andrew J. Sharp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew J. Sharp more than expected).
Fields of papers citing papers by Andrew J. Sharp
This network shows the impact of papers produced by Andrew J. Sharp. 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 Andrew J. Sharp. The network helps show where Andrew J. Sharp may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew J. Sharp, 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 99 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Fine-scale structural variation of the human genome Hit paper breakdown → | 2005 | 753 |
| 2 | Segmental Duplications and Copy-Number Variation in the Human Genome Hit paper breakdown → | 2005 | 752 |
| 3 | Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Hit paper breakdown → | 2008 | 629 |
| 4 | 2006 | 484 | |
| 5 | 2008 | 476 | |
| 6 | 2009 | 466 | |
| 7 | 2000 | 326 | |
| 8 | 2015 | 262 | |
| 9 | 2009 | 261 | |
| 10 | 2008 | 257 | |
| 11 | 2006 | 253 | |
| 12 | 2013 | 221 | |
| 13 | 2006 | 218 | |
| 14 | 2007 | 210 | |
| 15 | 2008 | 179 | |
| 16 | 2011 | 177 | |
| 17 | 2016 | 166 | |
| 18 | 2007 | 150 | |
| 19 | 2015 | 148 | |
| 20 | 1999 | 146 |
About Andrew J. Sharp
Andrew J. Sharp is a scholar working on Genetics, Molecular Biology, Immunology and Allergy, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 99 papers that have together received 9.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (37 papers), Epigenetics and DNA Methylation (18 papers), Genetic Associations and Epidemiology (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genetic Syndromes and Imprinting (8 papers), Genomics and Rare Diseases (7 papers), Genomics and Phylogenetic Studies (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (5.5k citations), Psychiatry and Mental health (707 citations), Pediatrics, Perinatology and Child Health (492 citations), Molecular Biology (1.9k citations) and Developmental Neuroscience (91 citations). Andrew J. Sharp has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Evan E. Eichler, Daniel Pinkel, Donna G. Albertson, Paras Garg, Patricia A. Jacobs, David Robinson, Jeffrey A. Bailey, Lisa M. Pertz, Corey T. Watson and Stuart H. Schwartz. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, Human Mutation, Nature Communications and PLoS 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.