Erica Andersen
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
-
- Genomics and Chromatin Dynamics 4
- Cancer-related gene regulation 3
- Epigenetics and DNA Methylation 3
- Genetics 9
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Sarah T. South (6 shared papers)Erik C. Thorland (5 shared papers)Erin Rooney Riggs (4 shared papers)Athena M. Cherry (2 shared papers)Gordana Raca (2 shared papers)Sibel Kantarci (2 shared papers)Deborah Ritter (2 shared papers)Swaroop Aradhya (2 shared papers)
- Journals
- Molecular and Cellular Biology (3 papers)Genetics in Medicine (2 papers)Human Mutation (2 papers)European Journal of Human Genetics (2 papers)Journal of Visualized Experiments (2 papers)
- Partner nations
- United StatesAustriaCanada
In The Last Decade
Erica Andersen
26 papers receiving 1.5k citations
Erica Andersen's Hit Papers
Peers
Comparison fields: 5 of 73
- Genetics 601
- Pediatrics, Perinatology and Child Health 254
- Aging 23
- Developmental Neuroscience 31
- Pathology and Forensic Medicine 131
Countries citing papers authored by Erica Andersen
This map shows the geographic impact of Erica Andersen'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 Erica Andersen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Erica Andersen more than expected).
Fields of papers citing papers by Erica Andersen
This network shows the impact of papers produced by Erica Andersen. 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 Erica Andersen. The network helps show where Erica Andersen may publish in the future.
Co-authors
The 25 scholars most cited alongside Erica Andersen, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) Hit paper breakdown → | 2019 | 923 |
| 2 | 2005 | 145 | |
| 3 | 2018 | 51 | |
| 4 | 2021 | 39 | |
| 5 | 2021 | 35 | |
| 6 | 2014 | 31 | |
| 7 | 2006 | 31 | |
| 8 | 2013 | 30 | |
| 9 | 2011 | 30 | |
| 10 | 2013 | 27 | |
| 11 | 2021 | 26 | |
| 12 | 2017 | 23 | |
| 13 | 2017 | 21 | |
| 14 | 2012 | 20 | |
| 15 | 2010 | 18 | |
| 16 | 2018 | 16 | |
| 17 | 2010 | 10 | |
| 18 | 2020 | 10 | |
| 19 | 2019 | 8 | |
| 20 | 2019 | 3 |
About Erica Andersen
Erica Andersen is a scholar working on Molecular Biology, Genetics, Cell Biology, Pathology and Forensic Medicine and Oncology, having authored 28 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers), Genomics and Chromatin Dynamics (4 papers), Zebrafish Biomedical Research Applications (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Cancer-related gene regulation (3 papers), Epigenetics and DNA Methylation (3 papers) and Lymphoma Diagnosis and Treatment (3 papers). The work is most often cited by research in Genetics (601 citations), Pediatrics, Perinatology and Child Health (254 citations), Aging (23 citations), Developmental Neuroscience (31 citations) and Pathology and Forensic Medicine (131 citations). Erica Andersen has collaborated with scholars based in United States, Austria and Canada. Frequent co-authors include Sarah T. South, Erik C. Thorland, Erin Rooney Riggs, Athena M. Cherry, Gordana Raca, Sibel Kantarci, Deborah Ritter, Swaroop Aradhya, Ankita Patel and Hutton M. Kearney. Their work appears in journals such as Molecular and Cellular Biology, Genetics in Medicine, Human Mutation, European Journal of Human Genetics and Journal of Visualized Experiments.
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.