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  1. Article

    Open Access

    A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis

    JI Arostegui, R Rabionet, A Remesal, A Mensa-Vilaro, S Murias… in Pediatric Rheumatology (2015)

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    Article

    A genome-wide association study of anorexia nervosa

    Anorexia nervosa (AN) is a complex and heritable eating disorder characterized by dangerously low body weight. Neither candidate gene studies nor an initial genome-wide association study (GWAS) have yielded si...

    V Boraska, C S Franklin, J A B Floyd, L M Thornton, L M Huckins… in Molecular Psychiatry (2014)