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  1. Article

    Open Access

    A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

    Genetic factors predictive of severe adolescent idiopathic scoliosis (AIS) are largely unknown. To identify genetic variation associated with severe AIS, we performed an exome-wide association study of 457 sev...

    Gabe Haller, Kevin McCall, Supak Jenkitkasemwong, Brooke Sadler… in Nature Communications (2018)

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  2. No Access

    Chapter

    The Genetics Contributing to Disorders Involving Congenital Scoliosis

    Congenital scoliosis (CS) is a congenital deformity of the spine, which can present as an isolated malformation, or part of a syndrome with other clinical features such as renal, cardiac, gastrointestinal, and...

    Nan Wu, Philip Giampietro, Kazuki Takeda in The Genetics and Development of Scoliosis (2018)