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Medicine

D-Index
98
Citations
25172
World Ranking
9043
National Ranking
4660

Overview

Charles A. Stanley is affiliated with the Children's Hospital of Philadelphia in the United States, focusing primarily on medical research in the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their work spans various subfields including Endocrinology, Diabetes and Metabolism, Genetics, Surgery, Molecular Biology, and Physiology.

The scientist's research topics cover a broad range of areas within metabolic and endocrine conditions, with significant attention given to:

  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Diabetes Management and Research
  • Diabetes and associated disorders
  • Pancreatic function and diabetes
  • Diet and metabolism studies
  • Metabolism, Diabetes, and Cancer
  • Neuroblastoma Research and Treatments

Among their recent scholarly contributions are the following papers:

  • International Guidelines for the Diagnosis and Management of Hyperinsulinism, 2023, published in Hormone Research in Paediatrics
  • Decreased KATP Channel Activity Contributes to the Low Glucose Threshold for Insulin Secretion of Rat Neonatal Islets, 2021, published in Endocrinology
  • New approaches to screening and management of neonatal hypoglycemia based on improved understanding of the molecular mechanism of hypoglycemia, 2023, published in Frontiers in Pediatrics
  • Advances in Understanding the Mechanism of Transitional Neonatal Hypoglycemia and Implications for Management, 2022, published in Clinics in Perinatology
  • Localized islet nuclear enlargement hyperinsulinism (LINE-HI) due to ABCC8 and GCK mosaic mutations, 2022, published in European Journal of Endocrinology

Frequent publication venues for their work include:

  • Hormone Research in Paediatrics
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Endocrinology
  • Frontiers in Pediatrics
  • Clinics in Perinatology

Collaborative research efforts have involved several co-authors with repeated joint publications, such as:

  • Diva D. De León
  • Kara E. Boodhansingh
  • Paul Thornton
  • Katherine Lord
  • Tricia R. Bhatti

Best Publications

  • Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene.

    Charles A. Stanley;Yen K. Lieu;Betty Y.L. Hsu;Alberto B. Burlina

  • Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation

    B Glaser;P Kesavan;M Heyman;E Davis

  • A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

    Hakon Hakonarson;Struan F A Grant;Jonathan P. Bradfield;Luc Marchand

  • Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children

    Paul S. Thornton;Charles A. Stanley;Diva D. De Leon;Deborah Harris

  • Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts.

    William R. Treem;Charles A. Stanley;David N. Finegold;Daniel E. Hale

  • Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.

    K. E. Snider;S. Becker;L. Boyajian;S.-L. Shyng

  • Effect of tri-iodothyronine replacement on the metabolic and pituitary responses to starvation.

    David F. Gardner;Michael M. Kaplan;Charles A. Stanley;Robert D. Utiger

  • Medium-chain acyl-CoA dehydrogenase deficiency.

    Piero Rinaldo;John J. O'Shea;Paul M. Coates;Daniel E. Hale

  • A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.

    A Nestorowicz;N Inagaki;T Gonoi;K P Schoor

  • Carnitine deficiency disorders in children.

    Charles A. Stanley

  • Mutations in the Sulfonylurea Receptor Gene Are Associated with Familial Hyperinsulinism in Ashkenazi Jews

    Ann Nestorowicz;Beth Anne Wilson;Kathleen P. Schoor;Hiroshi Inoue

  • Multiple Phenotypes in Phosphoglucomutase 1 Deficiency

    Laura C. Tegtmeyer;Stephan Rust;Monique van Scherpenzeel;Bobby G. Ng

  • From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

    Zhi Wei;Kai Wang;Hui Qi Qu;Haitao Zhang

  • Mechanisms of Disease: advances in diagnosis and treatment of hyperinsulinism in neonates

    Diva D De León;Charles A Stanley

  • Diagnosis and Localization of Focal Congenital Hyperinsulinism by 18F-Fluorodopa PET Scan

    Olga T. Hardy;Miguel Hernandez-Pampaloni;Janet R. Saffer;Mariko Suchi

  • Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.

    Daniel E Hale;Mark L Batshaw;Paul M Coates;Frank E Frerman

  • Hyperinsulinism in infants and children

    Charles A. Stanley

  • New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.

    Stanley Ca

  • Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels

    Charles A Stanley;Daniel E Hale;Paul M Coates;Carole L Hall;Carole L Hall

  • Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.

    Charles A. Stanley

Frequent Co-Authors

N. Scott Adzick
N. Scott Adzick Children's Hospital of Philadelphia
Michael J. Bennett
Michael J. Bennett University Hospital Southampton NHS Foundation Trust
Franz M. Matschinsky
Franz M. Matschinsky University of Pennsylvania
Thomas J. Smith
Thomas J. Smith Johns Hopkins University School of Medicine
Benjamin Glaser
Benjamin Glaser Hebrew University of Jerusalem
Marc Yudkoff
Marc Yudkoff Children's Hospital of Philadelphia
Abass Alavi
Abass Alavi University of Pennsylvania
Dimitri S. Monos
Dimitri S. Monos Children's Hospital of Philadelphia
Itzhak Nissim
Itzhak Nissim Children's Hospital of Philadelphia
Hakon Hakonarson
Hakon Hakonarson Children's Hospital of Philadelphia

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