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How has Sara E. Pinney's publication output changed over time?
ScholarIQpublication output · 2008–2020
Output grew0% over the shown period — from 1 works in 2008 to 1 in 2020.
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1
1
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200820092011201320142016201720192020
What are the most-cited papers on Sara E. Pinney?
ScholarIQmost cited works
Epigenetic mechanisms in the development of type 2 diabetes
Sara E. Pinney, Rebecca A. Simmons
S93802863. 2009203 Citations
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations
Sara E. Pinney, Courtney MacMullen, Susan Becker, Yu-Wen Lin, Cheryl E. Hanna, Paul Thornton, Arupa Ganguly, Show‐Ling Shyng, Charles A. Stanley
S114430552. 2008202 CitationsOPEN ACCESS
DNA methylation and its role in the pathogenesis of diabetes
Amita Bansal, Sara E. Pinney
S118758356. 2017161 Citations
Exendin-4 increases histone acetylase activity and reverses epigenetic modifications that silence Pdx1 in the intrauterine growth retarded rat
Sara E. Pinney, Lane J. Jaeckle Santos, Yilong Han, Doris A. Stoffers, Rebecca A. Simmons
Diabetologia. 2011132 CitationsOPEN ACCESS
Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence
Sara E. Pinney, Jennifer Oliver‐Krasinski, Linda M. Ernst, Nkecha Hughes, Puja Patel, Doris A. Stoffers, Pierre Russo, Diva D. De León
The Journal of Clinical Endocrinology & Metabolism. 201196 CitationsOPEN ACCESS
Related on ScholarIQ
Children's Hospital of Philadelphia
Institution
Epigenetic mechanisms in the development of type 2 diabetes
Paper
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations
Paper
DNA methylation and its role in the pathogenesis of diabetes
Paper
Exendin-4 increases histone acetylase activity and reverses epigenetic modifications that silence Pdx1 in the intrauterine growth retarded rat
Paper
Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence
Paper