Andrew J. Sharp
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities 33
- Genetic Syndromes and Imprinting 14
- Genetic Associations and Epidemiology 12
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 10
- Molecular Biology top 2%
- Epigenetics and DNA Methylation 21
- Congenital heart defects research 12
- Plant Science top 2%
- Chromosomal and Genetic Variations 21
- Cancer Research top 5%
- Co-authors
- Evan E. EichlerZe ChengDaniel PinkelDonna G. AlbertsonParas GargDavid RobinsonPatricia A. JacobsJeffrey A. Bailey
- Partner nations
- United StatesUnited KingdomSwitzerland
In The Last Decade
Andrew J. Sharp
101 papers receiving 6.4k citations
Hit Papers
Peers
Comparison fields: 5 of 170
- Genetics 4.1k
- Molecular Biology 3.7k
- Pediatrics, Perinatology and Child Health 908
- Plant Science 1.3k
- Cancer Research 440
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 6 | |
| 2 | 2022 | 12 | |
| 3 | 2022 | 79 | |
| 4 | 2021 | 18 | |
| 5 | 2021 | 21 | |
| 6 | 2019 | 49 | |
| 7 | 2017 | 63 | |
| 8 | 2016 | 101 | |
| 9 | 2013 | 17 | |
| 10 | 2012 | 25 | |
| 11 | 2011 | 219 | |
| 12 | 2010 | 25 | |
| 13 | 2010 | 28 | |
| 14 | 2008 | 12 | |
| 15 | 2008 | 207 | |
| 16 | 2007 | 185 | |
| 17 | 2006 | 231 | |
| 18 | Segmental Duplications and Copy-Number Variation in the Human Genomebreakdown → | 2005 | 678 |
| 19 | LINE repeats are associated with the spread of X inactivation | 2002 | 2 |
| 20 | 2001 | 9 |
About Andrew J. Sharp
Andrew J. Sharp is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 103 papers that have together received 6.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Epigenetics and DNA Methylation (21 papers), Chromosomal and Genetic Variations (21 papers), Genetic Syndromes and Imprinting (14 papers), Congenital heart defects research (12 papers), Genetic Associations and Epidemiology (12 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (10 papers). The work is most often cited by research in Genetics (4.1k citations), Molecular Biology (3.7k citations) and Pediatrics, Perinatology and Child Health (908 citations). Andrew J. Sharp has collaborated with scholars based in United States, United Kingdom and Switzerland. Frequent co-authors include Evan E. Eichler, Ze Cheng, Daniel Pinkel, Donna G. Albertson, Paras Garg, David Robinson, Patricia A. Jacobs, Jeffrey A. Bailey, L.M. Pertz and Corey T. Watson. Their work appears in journals such as PLoS Genetics, Human Genetics, Human Mutation, Human Molecular Genetics and The American 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.