Emily Fassi
Impact in
-
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Congenital Ear and Nasal Anomalies
-
- Genetic factors in colorectal cancer
Papers in
- Genetics 2
- Genomics and Rare Diseases 1
- BRCA gene mutations in cancer 1
- Congenital Ear and Nasal Anomalies 1
-
- Congenital heart defects research 1
- Co-authors
- Marwan Shinawi (2 shared papers)Linda Manwaring (1 shared paper)Beth A. Kozel (1 shared paper)Charles W. Goss (1 shared paper)Dustin Baldridge (1 shared paper)Dorothy K. Grange (1 shared paper)Elise Fiala (1 shared paper)Jennifer Heeley (1 shared paper)
- Journals
- American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)Genetics in Medicine (1 paper)Molecular Genetics & Genomic Medicine (1 paper)Journal of Genetic Counseling (1 paper)
- Partner nations
- United States
In The Last Decade
Emily Fassi
4 papers receiving 114 citations
Peers
Comparison fields: 5 of 32
- Genetics 79
- Genetics 9
- Pathology and Forensic Medicine 11
- Aging 1
- Cell Biology 8
Countries citing papers authored by Emily Fassi
This map shows the geographic impact of Emily Fassi'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 Emily Fassi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily Fassi more than expected).
Fields of papers citing papers by Emily Fassi
This network shows the impact of papers produced by Emily Fassi. 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 Emily Fassi. The network helps show where Emily Fassi may publish in the future.
Co-authors
The 16 scholars most cited alongside Emily Fassi, 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 | 2017 | 66 | |
| 2 | 2018 | 20 | |
| 3 | 2020 | 19 | |
| 4 | 2017 | 9 |
About Emily Fassi
Emily Fassi is a scholar working on Genetics, Molecular Biology, Genetics, Pathology and Forensic Medicine and Pulmonary and Respiratory Medicine, having authored 4 papers that have together received 114 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (1 paper), Cancer Genomics and Diagnostics (1 paper), Tracheal and airway disorders (1 paper), BRCA gene mutations in cancer (1 paper), Genetic factors in colorectal cancer (1 paper), Cellular transport and secretion (1 paper), Congenital Ear and Nasal Anomalies (1 paper) and Congenital heart defects research (1 paper). The work is most often cited by research in Genetics (79 citations), Genetics (9 citations), Pathology and Forensic Medicine (11 citations), Aging (1 citation) and Cell Biology (8 citations). Emily Fassi has collaborated with scholars based in United States. Frequent co-authors include Marwan Shinawi, Linda Manwaring, Beth A. Kozel, Charles W. Goss, Dustin Baldridge, Dorothy K. Grange, Elise Fiala, Jennifer Heeley, Marcia Willing and Sarah M. Brown. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Genetics in Medicine, Molecular Genetics & Genomic Medicine and Journal of Genetic Counseling.
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.