Rhythms of life: circadian disruption and brain disorders across the lifespan

RW Logan, CA McClung - Nature Reviews Neuroscience, 2019 - nature.com
Many processes in the human body—including brain function—are regulated over the 24-
hour cycle, and there are strong associations between disrupted circadian rhythms (for …

Genomic imprinting and physiological processes in mammals

V Tucci, AR Isles, G Kelsey, AC Ferguson-Smith… - Cell, 2019 - cell.com
Complex multicellular organisms, such as mammals, express two complete sets of
chromosomes per nucleus, combining the genetic material of both parents. However …

Autism spectrum disorder: neuropathology and animal models

M Varghese, N Keshav, S Jacot-Descombes… - Acta …, 2017 - Springer
Autism spectrum disorder (ASD) has a major impact on the development and social
integration of affected individuals and is the most heritable of psychiatric disorders. An …

A multidisciplinary approach to the clinical management of Prader–Willi syndrome

J Duis, PJ van Wattum, A Scheimann… - Molecular genetics & …, 2019 - Wiley Online Library
Abstract Background Prader–Willi syndrome (PWS) is a complex neuroendocrine disorder
affecting approximately 1/15,000–1/30,000 people. Unmet medical needs of individuals with …

Box C/D small nucleolar RNA genes and the Prader‐Willi syndrome: a complex interplay

J Cavaillé - Wiley Interdisciplinary Reviews: RNA, 2017 - Wiley Online Library
The nucleolus of mammalian cells contains hundreds of box C/D small nucleolar RNAs
(SNORDs). Through their ability to base pair with ribosomal RNA precursors, most play …

[HTML][HTML] The emerging role of snoRNAs in human disease

X Zhang, C Wang, S Xia, F Xiao, J Peng, Y Gao, F Yu… - Genes & …, 2023 - Elsevier
Small nucleolar RNAs (snoRNAs) play critical roles in various biological processes. The
aberrant expression or depletion of snoRNAs is related to various diseases. In previous …

Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome

A Adhikari, NA Copping, B Onaga, MC Pride… - Neurobiology of learning …, 2019 - Elsevier
Prader-Willi syndrome (PWS) is an imprinted neurodevelopmental disease caused by a loss
of paternal genes on chromosome 15q11-q13. It is characterized by cognitive impairments …

Role of genomic imprinting in mammalian development

T Thamban, V Agarwaal, S Khosla - Journal of biosciences, 2020 - Springer
Non-mendelian inheritance refers to the group of phenomena and observations related to
the inheritance of genetic information that cannot be merely explained by Mendel's laws of …

Sleep consequences of prader-willi syndrome

R Itani, ES Gillett, IA Perez - Current Neurology and Neuroscience Reports, 2023 - Springer
Abstract Purpose of Review This paper reviews how sleep is impacted in patients with
Prader-Willi syndrome (PWS), focusing on sleep-related breathing disturbances and …

What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders?

J Salles, E Lacassagne, S Eddiry, N Franchitto… - Molecular …, 2021 - nature.com
Addictive disorders have been much investigated and many studies have underlined the
role of environmental factors such as social interaction in the vulnerability to and …