Mariangiola Baserga

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

Paolo Emidio Macchia, Paola Lapi, Heiko Krude et al. · Nature Genetics · 1998 · 502 citations

Life Sciences, Genetics, Molecular Genetics +16

Missense Mutation in the Transcription Factor NKX2–5: A Novel Molecular Event in the Pathogenesis of Thyroid Dysgenesis

Monica Dentice, Viviana Cordeddu, Annamaria Rosica et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 180 citations

Medicine, Genetics, Molecular Genetics +17

Risk factors for congenital hypothyroidism: results of a population case-control study (1997–2003)

Emanuela Medda, Antonella Olivieri, Maria Antonietta Stazi et al. · European Journal of Endocrinology · 2005 · 129 citations

Medicine, Endocrinology, Pediatrics +17

Cross-sectional reference data for phalangeal quantitative ultrasound from early childhood to young-adulthood according to gender, age, skeletal growth, and pubertal development

Giampiero I. Baroncelli, Giovanni Federico, M. Vignolo et al. · Bone · 2006 · 116 citations

Medicine, Anatomy, Pediatrics +16

Mutations in the Gene EncodingThyroid Transcription Factor-1 (TTF-1) Are Not a Frequent Cause of Congenital Hypothyroidism (CH) with Thyroid Dysgenesis

Paola Lapi, Paolo Emidio Macchia, Luca Chiovato et al. · Thyroid · 1997 · 79 citations

Life Sciences, Endocrinology, Genetics +14