Bipolar disorder
Bipolar disorder (BP), also known as manic-depressive illness, affects approximately 1%–
2% of the adult population. The disorder is characterized by cyclic disturbances of mood …
2% of the adult population. The disorder is characterized by cyclic disturbances of mood …
[PDF][PDF] and functional signatures of 16p11. 2 reciprocal genomic disorder across mouse brain and human neuronal models
Summary Chromosome 16p11. 2 reciprocal genomic disorder, resulting from recurrent copy-
number variants (CNVs), involves intellectual disability, autism spectrum disorder (ASD) …
number variants (CNVs), involves intellectual disability, autism spectrum disorder (ASD) …
Вариабельность генетических маркеров шизофрении и болезни Альцгеймера в популяциях Северной Евразии
АВ Бочарова - 2021 - elibrary.ru
Полученные в работе результаты расширяют представления о генетической
компоненте ШЗ и БА. С помощью разнообразных методов анализа большая часть …
компоненте ШЗ и БА. С помощью разнообразных методов анализа большая часть …
[HTML][HTML] Расстройства аутистического спектра: факторы риска, особенности диагностики и терапии
ИА Марценковский… - Международный …, 2018 - cyberleninka.ru
В статье обсуждаются современные представления о взаимодействии генного
полиморфизма и средовых факторов при манифестации расстройств аутистического …
полиморфизма и средовых факторов при манифестации расстройств аутистического …
[图书][B] Seeking Cures: Design of Therapies for Genetically Determined Diseases
M Smith - 2013 - books.google.com
Progress in molecular and cellular biology has greatly enhanced our ability to accurately
diagnose diseases that are caused by gene mutations, changes in genome structures, and …
diagnose diseases that are caused by gene mutations, changes in genome structures, and …
Convolutional neural network visualization for identification of risk genes in bipolar disorder
Q Yue, J Yang, Q Shu, M Bai… - Current Molecular …, 2020 - ingentaconnect.com
Background: Bipolar disorder (BD) is a type of chronic emotional disorder with a complex
genetic structure. However, its genetic molecular mechanism is still unclear, which makes it …
genetic structure. However, its genetic molecular mechanism is still unclear, which makes it …
An Entropy-Regularized Framework for Detecting Copy Number Variants
M Mohammadi, F Farahi - IEEE Transactions on Biomedical …, 2018 - ieeexplore.ieee.org
The detection of DNA copy number variants (CNVs) is essential for the diagnosis and
prognosis of multiple diseases including cancer. Array-based comparative genomic …
prognosis of multiple diseases including cancer. Array-based comparative genomic …
[PDF][PDF] TAOK2β represses translation via phosphorylation of eEF2 and ameliorates exaggerated protein synthesis in a mouse model of 16p11. 2 microdeletion-driven …
M Henis, T Rücker, R Scharrenberg, M Richter… - scholar.archive.org
Abstract Microdeletions in the 16p11. 2 region of the human genome are frequently
associated with autism spectrum disorders (ASDs), but how these genomic rearrangements …
associated with autism spectrum disorders (ASDs), but how these genomic rearrangements …
[PDF][PDF] Педіатричний делірій при розладах аутистичного спектра. Клінічний і генетичний поліморфізм, зв'язок з онтогенетичними епілептичними …
ІА Марценковський, ІІ Марценковська, ГВ Макаренко… - 2021 - rimon.in.ua
Психотичні симптоми діагностуються в 3–16% підлітків і молодих дорослих з
розладами аутистичного спектра (РАС) і викликають дискусії щодо їх …
розладами аутистичного спектра (РАС) і викликають дискусії щодо їх …
Genomic and Epigenomic Insights into Nutrition and Brain Disorders.
M Joy Dauncey - Nutrients, 2013 - search.ebscohost.com
Considerable evidence links many neuropsychiatric, neurodevelopmental and
neurodegenerative disorders with multiple complex interactions between genetics and …
neurodegenerative disorders with multiple complex interactions between genetics and …