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Donald L. Atkinson

Observed names: D Atkinson, D L Atkinson, D. Atkinson, D. L. Atkinson, D.L. Atkinson, Donald Atkinson, Donald J. Atkinson
Institution: University of Utah
ORCID: 0009-0003-7421-890X
Observed ORCID: 0009-0003-7421-890X
OpenAlex ID: A5110093180
Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel
1996 · M. C. Sanguinetti, M. E. Curran, et al. · Nature · 1,764
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1996 · Q. Wang, M.E. Curran, et al. · Nature Genetics · 1,759
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
1995 · Qing Wang, Jiaxiang Shen, et al. · Cell · 1,686
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Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
1993 · Amanda K. Ewart, Colleen A. Morris, et al. · Nature Genetics · 1,143
LIM-kinase1 Hemizygosity Implicated in Impaired Visuospatial Constructive Cognition
1996 · J.Michael Frangiskakis, Amanda K Ewart, et al. · Cell · 559
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Linkage of a Cardiac Arrhythmia, the Long QT Syndrome, and the Harvey ras -1 Gene
1991 · Mark Keating, Donald Atkinson, et al. · Science · 519
Molecular Basis of the Long-QT Syndrome Associated with Deafness
1997 · Igor Splawski, Katherine W. Timothy, et al. · New England Journal of Medicine · 349
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Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
1994 · Changan Jiang, Donald Atkinson, et al. · Nature Genetics · 270
Platelet-activating factor acetylhydrolase deficiency. A missense mutation near the active site of an anti-inflammatory phospholipase.
1996 · D M Stafforini, K Satoh, et al. · Journal of Clinical Investigation · 267
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Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene.
1994 · A K Ewart, W Jin, et al. · Journal of Clinical Investigation · 221
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Normal newt limb regeneration requires matrix metalloproteinase function
2005 · Vladimir Vinarsky, Donald L. Atkinson, et al. · Developmental Biology · 211
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Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.
1991 · M Keating, C Dunn, et al. · PubMed · 109
Autophagy Ablation in Adipocytes Induces Insulin Resistance and Reveals Roles for Lipid Peroxide and Nrf2 Signaling in Adipose-Liver Crosstalk
2018 · Jinjin Cai, Karla M. Pires, et al. · Cell Reports · 107
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Metabolically Active Human Brown Adipose Tissue Derived Stem Cells
2013 · Francisco J Silva, Dolly J Holt, et al. · Stem Cells · 73
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Locus heterogeneity of autosomal dominant long QT syndrome.
1993 · M Curran, D Atkinson, et al. · Journal of Clinical Investigation · 68
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Multi-Tissue Microarray Analysis Identifies a Molecular Signature of Regeneration
2012 · Sarah E. Mercer, Chia-Ho Cheng, et al. · PLoS ONE · 43
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Ceramides Increase Fatty Acid Utilization in Intestinal Progenitors to Enhance Stemness and Increase Tumor Risk
2023 · Ying Li, Bhagirath Chaurasia, et al. · Gastroenterology · 41
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Cellular electroporation induces dedifferentiation in intact newt limbs
2006 · Donald L. Atkinson, Tamara J. Stevenson, et al. · Developmental Biology · 31
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Tissue inhibitor of metalloproteinase 1 regulates matrix metalloproteinase activity during newt limb regeneration
2005 · Tamara J. Stevenson, Vladimir Vinarsky, et al. · Developmental Dynamics · 31
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Gene expression signatures in the newt irises during lens regeneration
2007 · Evgeny Makarev, Mindy K. Call, et al. · FEBS Letters · 30
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Identification of a Paracrine Signaling Mechanism Linking CD34high Progenitors to the Regulation of Visceral Fat Expansion and Remodeling
2019 · Márcio Buffolo, Karla Maria Pires, et al. · Cell Reports · 16
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Ceramide-induced FGF13 impairs systemic metabolic health
2025 · Jamal Naderi, Amanda Kelsey Johnson, et al. · Cell Metabolism · 15
A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemia
2022 · Christopher A. Simeone, Joseph L. Wilkerson, et al. · npj Genomic Medicine · 13
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Evaluation of Multiple Biological Therapies for Ischemic Cardiac Disease
2016 · Amalia A. Winters, Sophia Bou-Ghannam, et al. · Cell Transplantation · 13
George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.
1997 · I Splawski, K W Timothy, et al. · PubMed · 9
Works count: 27
Citation count: 8,777
H-index: 19
I10-index: 23
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