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        Clinical significance of circulating microRNAs as markers in detecting and predicting congenital heart defects in children

        In this study, we aimed to investigate the usefulness of miRNAs as biomarkers in diagnosing and predicting children with congenital heart defects (CHD), particularly in the context of multiple subtypes of CHD. ...

        Research

        Inhalational versus Intravenous Induction of Anesthesia in Children with a High Risk of Perioperative Respiratory Adverse Events: A Randomized Controlled Trial

        Anesthesiologists should consider using an intravenous propofol induction technique in children who are at high risk of experiencing perioperative respiratory adverse event ...

        Research

        Identification of the determinants of incomplete vaccination in Australian children

        Most parents are supportive of vaccination. Sociodemographic factors may contribute more to the risk of incomplete vaccination than attitudes or beliefs. ...

        Research

        Linking FANTOM5 CAGE peaks to annotations with CAGEscan

        Here, we present the production and quality control of CAGEscan libraries from 56 FANTOM5 RNA sources ...

        Research

        Risk factors for repetition of a deliberate self-harm episode within seven days in adolescents and young adults

        The risk of repetition of deliberate self-harm peaks in the first 7 days after a deliberate self-harm episode. ...

        Research

        Reactive aggression in young patients with ADHD—a critical role for small provocations

        ADHD is one of the most commonly diagnosed disorders in child and adolescent psychiatry and is characterized by attentional deficits, hyperactivity, and impulsivity ...

        Research

        MACROD2 gene associated with autistic-like traits in a general population sample

        The MACROD2 gene is a strong positional candidate risk factor for autistic-like traits in the general population ...

        Research

        TagDust2: A generic method to extract reads from sequencing data.

        Arguably the most basic step in the analysis of next generation sequencing data (NGS) involves the extraction of mappable reads from the raw reads... ...

        Research

        Lost in translation: translational interference from a recurrent mutation in exon 1 of MECP2

        Rett syndrome (RTT) is an X linked neuro-developmental disorder affecting mostly girls. Mutations in the coding region of MECP2 are found in 80% of classic... ...

        Research

        Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells

        Our data support a highly generalizable model in which enhancer transcription is the earliest event in successive waves of transcriptional change during... ...

        Research

        Gateways to the FANTOM5 promoter level mammalian expression atlas

        The FANTOM5 project investigates transcription initiation activities in more than 1,000 human and mouse primary cells, cell lines and tissues using CAGE. ...

        Research

        Oesophageal atresia and tracheo-oesophageal fistula in Western Australia: Prevalence and trends

        A recent international study reported a higher prevalence of oesophageal atresia with or without tracheo-oesophageal fistula (OA±TOF) in Western Australia (WA). ...

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