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Author/Creator Forzan, Monica

1. Catechol‐O‐Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta‐Analysis of Previously Published Studies. (22nd October 2017)

Authors:
Collantoni, Enrico; Solmi, Marco; Gallicchio, Davide; Santonastaso, Paolo; Meneguzzo, Paolo; Carvalho, Andrè F.; Stubbs, Brendon; Clementi, Maurizio; Pinato, Claudia; Forzan, Monica; Cassina, Matteo; Fontana, Francesca; Piva, Ivana; Siani, Roberta; Salvo, Pierandrea; Tenconi, Elena; Veronese, Nic...
Journal:
European eating disorders review
Issue:
Volume 25:Number 6(2017)
Page Start:
524
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Functional connectivity correlates of response inhibition impairment in anorexia nervosa. (30th January 2016)

Authors:
Collantoni, Enrico; Michelon, Silvia; Tenconi, Elena; Degortes, Daniela; Titton, Francesca; Manara, Renzo; Clementi, Maurizio; Pinato, Claudia; Forzan, Monica; Cassina, Matteo; Santonastaso, Paolo; Favaro, Angela
Journal:
Psychiatry research
Issue:
Volume 247(2016)
Page Start:
9
Record Type:
Journal Article
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4. Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies. (16th February 2020)

Authors:
Munn‐Chernoff, Melissa A.; Johnson, Emma C.; Chou, Yi‐Ling; Coleman, Jonathan R.I.; Thornton, Laura M.; Walters, Raymond K.; Yilmaz, Zeynep; Baker, Jessica H.; Hübel, Christopher; Gordon, Scott; Medland, Sarah E.; Watson, Hunna J.; Gaspar, Héléna A.; Bryois, Julien; Hinney, Anke; Leppä, Virpi M.;...
Journal:
Addiction biology
Issue:
Volume 26:Number 1(2021)
Page Start:
n/a
Record Type:
Journal Article
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5. The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas. Issue 5 (6th March 2019)

Authors:
Trevisson, Eva; Morbidoni, Valeria; Forzan, Monica; Daolio, Cecilia; Fumini, Valentina; Parrozzani, Raffaele; Cassina, Matteo; Midena, Edoardo; Salviati, Leonardo; Clementi, Maurizio
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 5(2019)
Page Start:
n/a
Record Type:
Journal Article
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