Amy E. Roberts
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 1%
- Protein Tyrosine Phosphatases
- Congenital heart defects research
- Protein Kinase Regulation and GTPase Signaling
Papers in
- Genetics 47
- Genomics and Rare Diseases 29
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 7
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- Protein Tyrosine Phosphatases 31
- Congenital heart defects research 21
- Co-authors
- Bruce D. Gelb (9 shared papers)Judith E Allanson (3 shared papers)Marco Tartaglia (6 shared papers)Raju Kucherlapati (8 shared papers)Mary Ella Pierpont (6 shared papers)Erica Tworog‐Dube (8 shared papers)Jacqueline A. Noonan (3 shared papers)Benjamin G. Neel (4 shared papers)
- Journals
- The American Journal of Human Genetics (10 papers)Genetics in Medicine (6 papers)Circulation Genomic and Precision Medicine (5 papers)Proceedings of the National Academy of Sciences (4 papers)Journal of the American Heart Association (3 papers)
- Partner nations
- United StatesItalyCanada
In The Last Decade
Amy E. Roberts
118 papers receiving 11.1k citations
Amy E. Roberts's Hit Papers
Peers
Comparison fields: 5 of 134
- Genetics 3.8k
- Molecular Biology 4.9k
- Cardiology and Cardiovascular Medicine 1.6k
- Clinical Biochemistry 246
- Epidemiology 1.3k
Countries citing papers authored by Amy E. Roberts
This map shows the geographic impact of Amy E. Roberts'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 Amy E. Roberts with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amy E. Roberts more than expected).
Fields of papers citing papers by Amy E. Roberts
This network shows the impact of papers produced by Amy E. Roberts. 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 Amy E. Roberts. The network helps show where Amy E. Roberts may publish in the future.
Co-authors
The 25 scholars most cited alongside Amy E. Roberts, 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 120 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Aneurysm Syndromes Caused by Mutations in the TGF-β Receptor Hit paper breakdown → | 2006 | 1274 |
| 2 | De novo mutations in histone-modifying genes in congenital heart disease Hit paper breakdown → | 2013 | 745 |
| 3 | Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies Hit paper breakdown → | 2014 | 733 |
| 4 | De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies Hit paper breakdown → | 2015 | 629 |
| 5 | Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands Hit paper breakdown → | 2017 | 628 |
| 6 | Noonan syndrome Hit paper breakdown → | 2013 | 611 |
| 7 | 2006 | 484 | |
| 8 | 2010 | 476 | |
| 9 | Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association Hit paper breakdown → | 2018 | 450 |
| 10 | 2008 | 336 | |
| 11 | Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability Hit paper breakdown → | 2017 | 334 |
| 12 | 2009 | 257 | |
| 13 | 2019 | 233 | |
| 14 | 2006 | 210 | |
| 15 | 2008 | 174 | |
| 16 | 2014 | 157 | |
| 17 | 2014 | 146 | |
| 18 | 2015 | 139 | |
| 19 | 2012 | 132 | |
| 20 | 2014 | 128 |
About Amy E. Roberts
Amy E. Roberts is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Epidemiology and Pediatrics, Perinatology and Child Health, having authored 120 papers that have together received 11.5k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (31 papers), Genomics and Rare Diseases (29 papers), Congenital Heart Disease Studies (23 papers), Congenital heart defects research (21 papers), Cardiomyopathy and Myosin Studies (17 papers), Genomic variations and chromosomal abnormalities (13 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Pulmonary Hypertension Research and Treatments (4 papers). The work is most often cited by research in Genetics (3.8k citations), Molecular Biology (4.9k citations), Cardiology and Cardiovascular Medicine (1.6k citations), Clinical Biochemistry (246 citations) and Epidemiology (1.3k citations). Amy E. Roberts has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Bruce D. Gelb, Judith E Allanson, Marco Tartaglia, Raju Kucherlapati, Mary Ella Pierpont, Erica Tworog‐Dube, Jacqueline A. Noonan, Benjamin G. Neel, Elizabeth Irene Pierpont and Jonathan G. Seidman. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Circulation Genomic and Precision Medicine, Proceedings of the National Academy of Sciences and Journal of the American Heart Association.
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.