Daniel E. Hale

8.7k total citations
144 papers, 5.1k citations indexed

About

Daniel E. Hale is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Daniel E. Hale has authored 144 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 58 papers in Clinical Biochemistry and 48 papers in Genetics. Recurrent topics in Daniel E. Hale's work include Metabolism and Genetic Disorders (58 papers), Genomic variations and chromosomal abnormalities (36 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Daniel E. Hale is often cited by papers focused on Metabolism and Genetic Disorders (58 papers), Genomic variations and chromosomal abnormalities (36 papers) and Genetics and Neurodevelopmental Disorders (19 papers). Daniel E. Hale collaborates with scholars based in United States, United Kingdom and France. Daniel E. Hale's co-authors include Paul M. Coates, Charles A. Stanley, William R. Treem, Jannine D. Cody, Malcolm J. Bennett, Michael J. Bennett, A. Bhala, Piero Rinaldo, Colin Thorpe and J. P. Burke and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Daniel E. Hale

141 papers receiving 4.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Daniel E. Hale 2.7k 2.6k 943 901 785 144 5.1k
Louis J. Elsas 3.6k 1.3× 3.0k 1.2× 810 0.9× 842 0.9× 1.2k 1.5× 161 6.7k
Richard Koch 1.9k 0.7× 3.1k 1.2× 435 0.5× 1.5k 1.6× 935 1.2× 183 4.5k
Flemming Skovby 2.0k 0.7× 976 0.4× 1.3k 1.4× 613 0.7× 532 0.7× 126 5.3k
Barbara K. Burton 2.9k 1.1× 2.8k 1.1× 1.2k 1.3× 3.2k 3.6× 1.3k 1.7× 248 7.7k
Vivian E. Shih 1.6k 0.6× 2.0k 0.8× 389 0.4× 573 0.6× 818 1.0× 129 4.3k
Matthias R. Baumgartner 3.2k 1.2× 3.2k 1.2× 758 0.8× 1.0k 1.1× 879 1.1× 181 6.1k
P. Kay Lund 1.7k 0.6× 768 0.3× 500 0.5× 1.0k 1.2× 205 0.3× 59 4.5k
K. Bartlett 2.8k 1.0× 2.2k 0.9× 216 0.2× 1.0k 1.1× 398 0.5× 162 4.7k
Francjan J. van Spronsen 3.7k 1.4× 5.4k 2.1× 764 0.8× 3.1k 3.4× 992 1.3× 197 7.0k
Harvey L. Levy 4.3k 1.6× 6.8k 2.6× 1.2k 1.3× 2.5k 2.7× 2.3k 3.0× 313 10.5k

Countries citing papers authored by Daniel E. Hale

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Daniel E. Hale

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel E. Hale. A scholar is included among the top collaborators of Daniel E. Hale based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Daniel E. Hale. Daniel E. Hale is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Oser, Tamara K., Sean M. Oser, Kanthi Bangalore Krishna, et al.. (2020). Challenges and Successes in Raising a Child With Type 1 Diabetes and Autism Spectrum Disorder: Mixed Methods Study. Journal of Medical Internet Research. 22(6). e17184–e17184. 9 indexed citations
2.
López-Alvarenga, Juan Carlos, Geetha Chittoor, Solomon F.D. Paul, et al.. (2020). Acanthosis nigricans as a composite marker of cardiometabolic risk and its complex association with obesity and insulin resistance in Mexican American children. PLoS ONE. 15(10). e0240467–e0240467. 8 indexed citations
3.
Shah, Amy S., Laure El ghormli, Samuel S. Gidding, et al.. (2018). Prevalence of arterial stiffness in adolescents with type 2 diabetes in the TODAY cohort: Relationships to glycemic control and other risk factors. Journal of Diabetes and its Complications. 32(8). 740–745. 27 indexed citations
4.
Farook, Vidya S., Lavanya Reddivari, Srinivas Mummidi, et al.. (2017). Genetics of serum carotenoid concentrations and their correlation with obesity-related traits in Mexican American children. American Journal of Clinical Nutrition. 106(1). 52–58. 16 indexed citations
5.
Foster, Byron A., et al.. (2015). A Positive Deviance Approach to Early Childhood Obesity: Cross-Sectional Characterization of Positive Outliers. Childhood Obesity. 11(3). 281–288. 21 indexed citations
6.
Foster, Byron A., et al.. (2015). A randomized clinical trial of the effects of parent mentors on early childhood obesity: Study design and baseline data. Contemporary Clinical Trials. 45(Pt B). 164–169. 16 indexed citations
7.
Forman, Michele R., Yeyi Zhu, Ladia M. Hernandez, et al.. (2014). Arm Span and Ulnar Length Are Reliable and Accurate Estimates of Recumbent Length and Height in a Multiethnic Population of Infants and Children under 6 Years of Age. Journal of Nutrition. 144(9). 1480–1487. 22 indexed citations
8.
Willi, Steven M., Kathryn Hirst, Russell Jago, et al.. (2012). Cardiovascular risk factors in multi‐ethnic middle school students: the HEALTHY primary prevention trial. Pediatric Obesity. 7(3). 230–239. 34 indexed citations
9.
Cody, Jannine D., et al.. (2009). A gene dosage map of Chromosome 18: A map with clinical utility. Genetics in Medicine. 11(11). 778–782. 14 indexed citations
10.
Heard, Patricia, et al.. (2009). High resolution genomic analysis of 18q− using oligo‐microarray comparative genomic hybridization (aCGH). American Journal of Medical Genetics Part A. 149A(7). 1431–1437. 42 indexed citations
11.
Medina, Rolando, Patricia Heard, Erika Carter, et al.. (2009). Psychiatric syndromes in individuals with chromosome 18 abnormalities. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(3). 837–845. 10 indexed citations
12.
Horbinski, Craig, Patricia Heard, Malini Sathanoori, et al.. (2008). Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication. American Journal of Medical Genetics Part A. 146A(22). 2898–2904. 18 indexed citations
13.
Dawson, D. Brian, Lewis Waber, Daniel E. Hale, & Michael J. Bennett. (1995). Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency. The Journal of Pediatrics. 126(1). 69–71. 37 indexed citations
14.
Sewell, A, J. Herwig, H. Böhles, et al.. (1993). A new case of short-chain acyl-CoA dehydrogenase deficiency with isolated ethylmalonic aciduria. European Journal of Pediatrics. 152(11). 922–924. 41 indexed citations
15.
Coates, Paul M., Yasuhiro Indo, D S Young, Daniel E. Hale, & Kay Tanaka. (1992). Immunochemical Characterization of Variant Medium-Chain Acyl-CoA Dehydrogenase in Fibroblasts from Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Pediatric Research. 31(1). 34–38. 23 indexed citations
16.
Indo, Yasuhiro, Paul M. Coates, Daniel E. Hale, & Kay Tanaka. (1991). Immunochemical Characterization of Variant Long-Chain Acyl-CoA Dehydrogenase in Cultured Fibroblasts from Nine Patients with Long-Chain Acyl-CoA Dehydrogenase Deficiency. Pediatric Research. 30(3). 211–215. 20 indexed citations
17.
Corkey, Barbara E., J.F. Geschwind, Jude T. Deeney, et al.. (1991). Ca2+ responses to interleukin 1 and tumor necrosis factor in cultured human skin fibroblasts. Possible implications for Reye syndrome.. Journal of Clinical Investigation. 87(3). 778–786. 33 indexed citations
18.
Dionisi‐Vici, Carlo, Enrico Bertini, C. Bachmann, et al.. (1991). Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. The Journal of Pediatrics. 118(5). 744–746. 55 indexed citations
19.
Hale, Daniel E., Charles A. Stanley, & Paul M. Coates. (1990). Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay.. PubMed. 321. 333–48. 12 indexed citations
20.
Hale, Daniel E., et al.. (1988). Medium-Chain Acyl-CoA Dehydrogenase Deficiency. New England Journal of Medicine. 319(20). 1308–1313. 167 indexed citations

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.

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