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Friederike Ehrhart, Kelly J. M. Janssen, Susan L. Coort, Chris T. Evelo & Leopold M. G. Curfs. (2019) Prader-Willi syndrome and Angelman syndrome: Visualisation of the molecular pathways for two chromosomal disorders. The World Journal of Biological Psychiatry 20:9, pages 670-682.
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Articles from other publishers (7)
Cécile Louveau, Mimi-Caterina Turtulici, Angèle Consoli, Christine Poitou, Muriel Coupaye, Marie-Odile Krebs, Boris Chaumette & Anton Iftimovici. (2023) Prader–Willi syndrome: Symptoms and topiramate response in light of genetics. Frontiers in Neuroscience 17.
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Sanjukta Basak & Ajoy Basak. (2022) Proteins and proteases of Prader–Willi syndrome: a comprehensive review and perspectives. Bioscience Reports 42:6.
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Yanjie Duan, Lu Liu, Xiujuan Zhang, Xiuyun Jiang, Jin Xu & Qingbo Guan. (2021) Phenotypic spectrum and mechanism analysis of Schaff Yang syndrome. Medicine 100:24, pages e26309.
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Rachel Wevrick. (2020) Disentangling ingestive behavior-related phenotypes in Prader–Willi syndrome: Integrating information from nonclinical studies and clinical trials to better understand the pathophysiology of hyperphagia and obesity. Physiology & Behavior 219, pages 112864.
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Aaron L. Carrel & David B. Allen. 2018. Pediatric Endocrinology. Pediatric Endocrinology
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Tishani Methsala Wijesuriya, Leentje De Ceuninck, Delphine Masschaele, Matthea R Sanderson, Karin Vanessa Carias, Jan Tavernier & Rachel Wevrick. (2017) The Prader-Willi syndrome proteins MAGEL2 and necdin regulate leptin receptor cell surface abundance through ubiquitination pathways. Human Molecular Genetics 26:21, pages 4215-4230.
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Igor Pravdivyi, Klaus Ballanyi, William F. Colmers & Rachel Wevrick. (2015)
Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the
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