Jean Amos
Impact in
-
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Congenital Ear and Nasal Anomalies
- Genomic variations and chromosomal abnormalities
Papers in
-
- Cystic Fibrosis Research Advances 13
- Tracheal and airway disorders 5
- Neonatal Respiratory Health Research 4
- Genetics 7
- Genomics and Rare Diseases 4
- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 3
- Congenital Ear and Nasal Anomalies 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Aubrey Milunsky (4 shared papers)Robert D. Oates (2 shared papers)Elias O. Da‐Silva (1 shared paper)Clinton T. Baldwin (1 shared paper)Christopher F. Hoth (1 shared paper)Michael Dean (5 shared papers)Marga Belle White (4 shared papers)Bernard Gerrard (4 shared papers)
- Journals
- Expert Review of Molecular Diagnostics (3 papers)Human Mutation (2 papers)Nature (2 papers)CHEST Journal (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- United StatesBrazilIsrael
In The Last Decade
Jean Amos
24 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 98
- Pulmonary and Respiratory Medicine 477
- Genetics 394
- Genetics 116
- Sensory Systems 51
- Molecular Biology 537
Countries citing papers authored by Jean Amos
This map shows the geographic impact of Jean Amos'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 Jean Amos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jean Amos more than expected).
Fields of papers citing papers by Jean Amos
This network shows the impact of papers produced by Jean Amos. 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 Jean Amos. The network helps show where Jean Amos may publish in the future.
Co-authors
The 25 scholars most cited alongside Jean Amos, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 385 | |
| 2 | 1990 | 287 | |
| 3 | 1994 | 140 | |
| 4 | 1993 | 121 | |
| 5 | 1990 | 92 | |
| 6 | 2002 | 89 | |
| 7 | 1996 | 39 | |
| 8 | 2002 | 32 | |
| 9 | 1987 | 29 | |
| 10 | 2004 | 25 | |
| 11 | 1998 | 10 | |
| 12 | 2004 | 10 | |
| 13 | 1984 | 10 | |
| 14 | 2004 | 8 | |
| 15 | 2004 | 7 | |
| 16 | 1992 | 7 | |
| 17 | 1991 | 6 | |
| 18 | 1993 | 5 | |
| 19 | 2003 | 5 | |
| 20 | 2005 | 4 |
About Jean Amos
Jean Amos is a scholar working on Pulmonary and Respiratory Medicine, Genetics, Molecular Biology, Genetics and Cellular and Molecular Neuroscience, having authored 24 papers that have together received 1.3k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (13 papers), Tracheal and airway disorders (5 papers), Genomics and Rare Diseases (4 papers), Neonatal Respiratory Health Research (4 papers), BRCA gene mutations in cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Congenital Ear and Nasal Anomalies (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (477 citations), Genetics (394 citations), Genetics (116 citations), Sensory Systems (51 citations) and Molecular Biology (537 citations). Jean Amos has collaborated with scholars based in United States, Brazil and Israel. Frequent co-authors include Aubrey Milunsky, Robert D. Oates, Elias O. Da‐Silva, Clinton T. Baldwin, Christopher F. Hoth, Michael Dean, Marga Belle White, Bernard Gerrard, Mark Leppert and Claudia Stewart. Their work appears in journals such as Expert Review of Molecular Diagnostics, Human Mutation, Nature, CHEST Journal and The Journal of Pediatrics.
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.