A population-based study revealed reasons behind elevated suicide risk, attempted suicides, and other selfharm, which require special health care, among a and young adults with autism spectrum disorders. Comorbid disorders, ...
Dec 10, 2020
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A study headed by researchers from the Danish project iPSYCH and the Broad Institute in the U.S., has found the first common genetic risk variants for autism and uncovered genetic differences in clinical subgroups of autism. ...
Feb 27, 2019
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Later-born siblings of children with autism spectrum disorder (ASD) or attention-deficit/hyperactivity disorder (ADHD) are at elevated risk for both disorders, a new study led by Meghan Miller, assistant professor in the ...
Dec 10, 2018
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Babies exposed in the womb to the majority of medications that target neurotransmitter systems, including typical targets of antidepressants and antipsychotic drugs, are not any more likely to develop autism than non-exposed ...
Oct 31, 2018
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(HealthDay)—Pregnant women who have any form of diabetes may face higher odds that their child could develop autism, a new study suggests.
Jun 25, 2018
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A new study finds children born to mothers who had a larger waist size before pregnancy may be more likely to have autism than those whose mothers had a smaller pre-pregnancy waist. The research results will be presented ...
Mar 19, 2018
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Scientists have long tried to pin down the causes of autism spectrum disorder. Recent studies have expanded the search for genetic links from identifying genes toward epigenetics, the study of factors that control gene expression ...
Jan 16, 2018
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A protein called disrupted-in-schizophrenia 1, encoded by the DISC1 gene, has been established as a genetic risk factor for a wide array of psychiatric disorders, including schizophrenia, bipolar disorder, major depression, ...
Dec 14, 2017
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Taking multivitamins during early pregnancy may be associated with a reduced risk of autism spectrum disorder (ASD) in children compared with mothers who do not take multivitamins, finds a study published in The BMJ today.
Oct 4, 2017
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Huntington's disease, cystic fibrosis, and muscular dystrophy are all diseases that can be traced to a single mutation. Diagnosis in asymptomatic patients for these diseases is relatively easy—you have the mutation? Then ...
Aug 31, 2017
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