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Shared genetic architecture links schizophrenia with hemispheric white matter microstructure
Schizophrenia is a highly heterogeneous psychiatric disorder affecting ~1% of the global population, typically emerging in ...
Telomere length and polygenic risk scores (PRS) are linked to idiopathic pulmonary fibrosis (IPF) risk, especially in noncarriers of rare genetic variants. The study identified rare damaging variants ...
Most cancers are not driven by a single gene mutation, but rather an accumulation of mutations that develop over the evolution of tumor growth. While mouse models are useful for identifying cancer ...
Please provide your email address to receive an email when new articles are posted on . NASHVILLE, Tenn. — An analysis of germline susceptibility to renal cell carcinoma revealed considerable ...
UCLA Health researchers have created a comprehensive map showing how eight different genetic mutations associated with autism spectrum disorder affect early brain development, providing new insights ...
Despite the development of cutting-edge genetic testing techniques and considerable progress in our understanding of the genetic basis of idiopathic pulmonary fibrosis (IPF), missing heritability and ...
Forty-five years ago adult AL was incurable. Since then we have discovered the striking heterogeneity of AL and its importance in selecting therapy, resulting in cure of increasing numbers of patients ...
Large genetic study links telomere-related polygenic risk to distinct idiopathic pulmonary fibrosis subgroups, improving disease prediction.
Using cortical organoids from individuals with autism, researchers tracked gene activity over development. Early ...
C syndrome, also known as Opitz trigonocephaly syndrome (OTCS) or C Syndrome, is a rare and heterogeneous genetic disorder with a broad range of severity. It was ...
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