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Sanaa Eddiry

Paul Sabatier University

10

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242

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Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory.

2021
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SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.

2021 Genetics in Medicine
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Ghrelin uses the GHS-R1a/Gi/cAMP pathway and induces differentiation only in mature osteoblasts. This ghrelin pathway is impaired in AIS patients

2020 Biochemistry and biophysics reports
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What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders

2020 Molecular Psychiatry
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Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

2017 Journal of Clinical Investigation
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Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.

2016 Stem Cell Research
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Impairment of adipose tissue in Prader-Willi syndrome rescued by growth hormone treatment.

2014 International Journal of Obesity
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