Daniel E. Hale
Impact in
- Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
-
- Neonatal Health and Biochemistry
Papers in
-
- Peroxisome Proliferator-Activated Receptors 16
- Mitochondrial Function and Pathology 15
- Biochemical and Molecular Research 14
- Congenital heart defects research 13
-
- Metabolism and Genetic Disorders 56
- Co-authors
- Charles A. Stanley (18 shared papers)Paul M. Coates (19 shared papers)William R. Treem (9 shared papers)Jannine D. Cody (39 shared papers)Michael J. Bennett (15 shared papers)A. Bhala (6 shared papers)Piero Rinaldo (8 shared papers)J. P. Burke (2 shared papers)
- Journals
- Pediatric Research (13 papers)Journal of Inherited Metabolic Disease (7 papers)The Journal of Pediatrics (7 papers)Human Genetics (6 papers)PEDIATRICS (4 papers)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Daniel E. Hale
142 papers receiving 4.9k citations
Peers
Comparison fields: 5 of 134
- Clinical Biochemistry 2.6k
- Pediatrics, Perinatology and Child Health 650
- Molecular Biology 2.5k
- Physiology 850
- Biochemistry 246
Countries citing papers authored by Daniel E. Hale
This map shows the geographic impact of Daniel E. Hale'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 Daniel E. Hale with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel E. Hale more than expected).
Fields of papers citing papers by Daniel E. Hale
This network shows the impact of papers produced by Daniel E. Hale. 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 Daniel E. Hale. The network helps show where Daniel E. Hale may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniel E. Hale, 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 147 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1988 | 259 | |
| 2 | 1999 | 217 | |
| 3 | 1990 | 205 | |
| 4 | 1995 | 181 | |
| 5 | 1985 | 181 | |
| 6 | 1983 | 177 | |
| 7 | 1992 | 160 | |
| 8 | 1992 | 156 | |
| 9 | 1995 | 147 | |
| 10 | 1994 | 123 | |
| 11 | 1997 | 110 | |
| 12 | 1985 | 104 | |
| 13 | 2004 | 104 | |
| 14 | Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. | 1996 | 103 |
| 15 | 1999 | 94 | |
| 16 | 1986 | 88 | |
| 17 | 1995 | 87 | |
| 18 | 1988 | 86 | |
| 19 | 2011 | 84 | |
| 20 | Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiency. | 1991 | 78 |
About Daniel E. Hale
Daniel E. Hale is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Endocrinology, Diabetes and Metabolism and Pediatrics, Perinatology and Child Health, having authored 147 papers that have together received 5.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (56 papers), Genomic variations and chromosomal abnormalities (33 papers), Genetics and Neurodevelopmental Disorders (18 papers), Peroxisome Proliferator-Activated Receptors (16 papers), Mitochondrial Function and Pathology (15 papers), Biochemical and Molecular Research (14 papers), Congenital heart defects research (13 papers) and Diet and metabolism studies (13 papers). The work is most often cited by research in Clinical Biochemistry (2.6k citations), Pediatrics, Perinatology and Child Health (650 citations), Molecular Biology (2.5k citations), Physiology (850 citations) and Biochemistry (246 citations). Daniel E. Hale has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include Charles A. Stanley, Paul M. Coates, William R. Treem, Jannine D. Cody, Michael J. Bennett, A. Bhala, Piero Rinaldo, J. P. Burke, Colin Thorpe and Arnold W. Strauss. Their work appears in journals such as Pediatric Research, Journal of Inherited Metabolic Disease, The Journal of Pediatrics, Human Genetics and 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.