Federico Santoni


AuthID: R-00K-H1R

Publications Awaiting Confirmation

1
TITLE: Trio analyses of patients with congenital hypopituitarism reveals novel candidate genes
AUTHORS: Correa, Fernanda de Azevedo; Habibi, Imen; Kolesinska, Zofia; Zouaghi, Yassine; Zhai, Jing; Phan Hug, Franziska; Antoniou, Maria Chiristina; Pignatelli, Duarte; Lang Muritano, Mariarosaria; Marek, Niedziela; l'Allemands, Dagmar; Papadakis, Georgios; Ameti, Adelina; Messina, Andrea; Niederlander, Nicolas J.; Boizot, Alexia; Santoni, Federico; Acierno, James S.; Pitteloud, Nelly;
PUBLISHED: 2023, SOURCE: HORMONE RESEARCH IN PAEDIATRICS, VOLUME: 96
INDEXED IN: WOS
2
TITLE: NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice
AUTHORS: Chachlaki, Konstantina; Messina, Andrea; Delli, Virginia; Leysen, Valerie; Maurnyi, Csilla; Huber, Chieko; Ternier, Gaetan; Skrapits, Katalin; Papadakis, Georgios; Shruti, Sonal; Kapanidou, Maria; Cheng, Xu; Acierno, James; Rademaker, Jesse; Rasika, Sowmyalakshmi; Quinton, Richard; Niedziela, Marek; L'Allemand, Dagmar; Pignatelli, Duarte; Dirlewander, Mirjam; Lang Muritano, Mariarosaria; Kempf, Patrick; Catteau Jonard, Sophie; Niederlaender, Nicolas J.; Ciofi, Philippe; Tena Sempere, Manuel; Garthwaite, John; Storme, Laurent; Avan, Paul; Hrabovszky, Erik; Carleton, Alan; Santoni, Federico; Giacobini, Paolo; Pitteloud, Nelly; Prevot, Vincent; ...More
PUBLISHED: 2022, SOURCE: SCIENCE TRANSLATIONAL MEDICINE, VOLUME: 14, ISSUE: 665
INDEXED IN: WOS

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