Carrie Hanscom
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Animal Genetics and Reproduction 1
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- Congenital heart defects research 3
- DNA Repair Mechanisms 1
- Co-authors
- Michael E. Talkowski (10 shared papers)Cynthia C. Morton (6 shared papers)James F. Gusella (7 shared papers)Vamsee Pillalamarri (5 shared papers)Jill A. Rosenfeld (4 shared papers)Zehra Ordulu (3 shared papers)Shahrin Pereira (2 shared papers)Colby Chiang (3 shared papers)
- Journals
- The American Journal of Human Genetics (4 papers)Current Protocols in Human Genetics (1 paper)Prenatal Diagnosis (1 paper)Human Genetics (1 paper)New England Journal of Medicine (1 paper)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Carrie Hanscom
10 papers receiving 474 citations
Peers
Comparison fields: 5 of 58
- Genetics 316
- Pediatrics, Perinatology and Child Health 118
- Reproductive Medicine 31
- Sensory Systems 13
- Cancer Research 36
Countries citing papers authored by Carrie Hanscom
This map shows the geographic impact of Carrie Hanscom'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 Carrie Hanscom with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carrie Hanscom more than expected).
Fields of papers citing papers by Carrie Hanscom
This network shows the impact of papers produced by Carrie Hanscom. 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 Carrie Hanscom. The network helps show where Carrie Hanscom may publish in the future.
Co-authors
The 25 scholars most cited alongside Carrie Hanscom, 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 | 2011 | 121 | |
| 2 | 2012 | 120 | |
| 3 | 2019 | 67 | |
| 4 | 2013 | 52 | |
| 5 | 2015 | 37 | |
| 6 | 2014 | 28 | |
| 7 | 2014 | 27 | |
| 8 | 2014 | 18 | |
| 9 | 2016 | 14 | |
| 10 | 2017 | 9 |
About Carrie Hanscom
Carrie Hanscom is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Genetics, having authored 10 papers that have together received 493 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers), Chromosomal and Genetic Variations (3 papers), Congenital heart defects research (3 papers), Prenatal Screening and Diagnostics (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), DNA Repair Mechanisms (1 paper) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Genetics (316 citations), Pediatrics, Perinatology and Child Health (118 citations), Reproductive Medicine (31 citations), Sensory Systems (13 citations) and Cancer Research (36 citations). Carrie Hanscom has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Michael E. Talkowski, Cynthia C. Morton, James F. Gusella, Vamsee Pillalamarri, Jill A. Rosenfeld, Zehra Ordulu, Shahrin Pereira, Colby Chiang, Carl Ernst and Ian Blumenthal. Their work appears in journals such as The American Journal of Human Genetics, Current Protocols in Human Genetics, Prenatal Diagnosis, Human Genetics and New England Journal of Medicine.
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.