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Candidate Sequence Variants and Fetal Hemoglobin in Children with Sickle Cell Disease Treated with Hydroxyurea

Overview of attention for article published in PLOS ONE, February 2013
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Title
Candidate Sequence Variants and Fetal Hemoglobin in Children with Sickle Cell Disease Treated with Hydroxyurea
Published in
PLOS ONE, February 2013
DOI 10.1371/journal.pone.0055709
Pubmed ID
Authors

Nancy S. Green, Katherine L. Ender, Farzana Pashankar, Catherine Driscoll, Patricia J. Giardina, Craig A. Mullen, Lorraine N. Clark, Deepa Manwani, Jennifer Crotty, Sergey Kisselev, Kathleen A. Neville, Carolyn Hoppe, Sandra Barral

Abstract

Fetal hemoglobin level is a heritable complex trait that strongly correlates swith the clinical severity of sickle cell disease. Only few genetic loci have been identified as robustly associated with fetal hemoglobin in patients with sickle cell disease, primarily adults. The sole approved pharmacologic therapy for this disease is hydroxyurea, with effects largely attributable to induction of fetal hemoglobin.

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The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 70 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Italy 1 1%
Canada 1 1%
Unknown 68 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 15 21%
Researcher 8 11%
Student > Master 8 11%
Other 6 9%
Professor 4 6%
Other 17 24%
Unknown 12 17%
Readers by discipline Count As %
Medicine and Dentistry 18 26%
Biochemistry, Genetics and Molecular Biology 16 23%
Agricultural and Biological Sciences 13 19%
Pharmacology, Toxicology and Pharmaceutical Science 2 3%
Nursing and Health Professions 2 3%
Other 4 6%
Unknown 15 21%