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2020
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2024
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2022
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2016
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Upregulation of microRNA-96-5p is associated with adolescent idiopathic scoliosis and low bone mass phenotype.
Not available
S-EPMC9188568
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biostudies-literature
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A validated composite model to predict risk of curve progression in adolescent idiopathic scoliosis.
Not available
S-EPMC6948250
|
biostudies-literature
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Dysregulation of peripheral expression of the YWHA genes during conversion to psychosis.
Not available
S-EPMC7299951
|
biostudies-literature
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Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.
Not available
S-EPMC2771592
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biostudies-literature
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Effects of eight neuropsychiatric copy number variants on human brain structure.
Not available
S-EPMC8292542
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biostudies-literature
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Epigenome-wide analysis across the development span of pediatric acute lymphoblastic leukemia: backtracking to birth.
Not available
S-EPMC11515509
|
biostudies-literature
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CSHP Professional Practice Conference 2019: Poster Abstracts
Not available
S-EPMC6391241
|
biostudies-literature
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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Not available
S-EPMC6218476
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biostudies-literature
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Rare copy number variation in posttraumatic stress disorder.
Not available
S-EPMC9763110
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biostudies-literature
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Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Not available
S-EPMC5894477
|
biostudies-literature
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