Daryl A. Scott
Impact in
- Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
- Otorhinolaryngology top 1%
- Ear Surgery and Otitis Media
Papers in
-
- Congenital heart defects research 20
- RNA modifications and cancer 11
- Genetics 40
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 8
- Co-authors
- Lawrence P. Karniski (2 shared papers)Val C. Sheffield (7 shared papers)Rong Wang (1 shared paper)Annelies de Klein (10 shared papers)Dick Tibboel (10 shared papers)Ashley M. Holder (6 shared papers)Sau Wai Cheung (12 shared papers)Iustin V. Tabarean (1 shared paper)
- Journals
- Human Molecular Genetics (7 papers)PLoS ONE (5 papers)European Journal of Human Genetics (4 papers)Journal of Medical Genetics (4 papers)American Journal of Medical Genetics Part A (34 papers)
- Partner nations
- United StatesGermanyNetherlands
In The Last Decade
Daryl A. Scott
96 papers receiving 3.9k citations
Peers
Comparison fields: 5 of 135
- Sensory Systems 797
- Otorhinolaryngology 224
- Neurology 356
- Genetics 955
- Molecular Biology 1.6k
Countries citing papers authored by Daryl A. Scott
This map shows the geographic impact of Daryl A. Scott'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 Daryl A. Scott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daryl A. Scott more than expected).
Fields of papers citing papers by Daryl A. Scott
This network shows the impact of papers produced by Daryl A. Scott. 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 Daryl A. Scott. The network helps show where Daryl A. Scott may publish in the future.
Co-authors
The 25 scholars most cited alongside Daryl A. Scott, 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 99 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 441 | |
| 2 | 2010 | 282 | |
| 3 | 2006 | 231 | |
| 4 | 2014 | 185 | |
| 5 | 2007 | 162 | |
| 6 | 2000 | 146 | |
| 7 | 1998 | 142 | |
| 8 | 2007 | 140 | |
| 9 | 2009 | 133 | |
| 10 | 2000 | 113 | |
| 11 | Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagen. | 1994 | 109 |
| 12 | 1997 | 99 | |
| 13 | 2015 | 95 | |
| 14 | 2010 | 84 | |
| 15 | 2010 | 75 | |
| 16 | 2012 | 69 | |
| 17 | 2007 | 68 | |
| 18 | 2002 | 67 | |
| 19 | 2012 | 66 | |
| 20 | 2011 | 65 |
About Daryl A. Scott
Daryl A. Scott is a scholar working on Molecular Biology, Genetics, Surgery, Pulmonary and Respiratory Medicine and Sensory Systems, having authored 99 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Congenital heart defects research (20 papers), Congenital Diaphragmatic Hernia Studies (19 papers), Hearing, Cochlea, Tinnitus, Genetics (12 papers), Tracheal and airway disorders (11 papers), RNA modifications and cancer (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Congenital Anomalies and Fetal Surgery (7 papers). The work is most often cited by research in Sensory Systems (797 citations), Otorhinolaryngology (224 citations), Neurology (356 citations), Genetics (955 citations) and Molecular Biology (1.6k citations). Daryl A. Scott has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Lawrence P. Karniski, Val C. Sheffield, Rong Wang, Annelies de Klein, Dick Tibboel, Ashley M. Holder, Sau Wai Cheung, Iustin V. Tabarean, Eliezer Masliah and Subhojit Roy. Their work appears in journals such as Human Molecular Genetics, PLoS ONE, European Journal of Human Genetics, Journal of Medical Genetics and American Journal of Medical Genetics Part A.
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.