Foto del docente

Fabiola Ceroni

Junior assistant professor (fixed-term)

Department of Pharmacy and Biotechnology

Academic discipline: BIO/18 Genetics

Publications

Cameli C, Viggiano M, Rochat MJ, Maresca A, Caporali L, Fiorini C, Palombo F, Magini P, Duardo RC, Ceroni F, Scaduto MC, Posar A, Seri M, Carelli V, Visconti P, Bacchelli E, Maestrini E., An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder., «JOURNAL OF CELLULAR AND MOLECULAR MEDICINE», 2021, 25, pp. 2459 - 2470 [Scientific article]Open Access

Holt R.J.; Young R.M.; Crespo B.; Ceroni F.; Curry C.J.; Bellacchio E.; Bax D.A.; Ciolfi A.; Simon M.; Fagerberg C.R.; van Binsbergen E.; De Luca A.; Memo L.; Dobyns W.B.; Mohammed A.A.; Clokie S.J.H.; Zazo Seco C.; Jiang Y.-H.; Sorensen K.P.; Andersen H.; Sullivan J.; Powis Z.; Chassevent A.; Smith-Hicks C.; Petrovski S.; Antoniadi T.; Shashi V.; Gelb B.D.; Wilson S.W.; Gerrelli D.; Tartaglia M.; Chassaing N.; Calvas P.; Ragge N.K., De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies, «AMERICAN JOURNAL OF HUMAN GENETICS», 2019, 105, pp. 640 - 657 [Scientific article]

Plaisancie J.; Ceroni F.; Holt R.; Zazo Seco C.; Calvas P.; Chassaing N.; Ragge N.K., Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia, «HUMAN GENETICS», 2019, 138, pp. 799 - 830 [Scientific article]

Ceroni F.; Aguilera-Garcia D.; Chassaing N.; Bax D.A.; Blanco-Kelly F.; Ramos P.; Tarilonte M.; Villaverde C.; da Silva L.R.J.; Ballesta-Martinez M.J.; Sanchez-Soler M.J.; Holt R.J.; Cooper-Charles L.; Bruty J.; Wallis Y.; McMullan D.; Hoffman J.; Bunyan D.; Stewart A.; Stewart H.; Lachlan K.; Fryer A.; McKay V.; Roume J.; Dureau P.; Saggar A.; Griffiths M.; Calvas P.; Ayuso C.; Corton M.; Ragge N.K., New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies, «HUMAN GENETICS», 2019, 138, pp. 1027 - 1042 [Scientific article]

Holt R.; Ceroni F.; Bax D.A.; Broadgate S.; Diaz D.G.; Santos C.; Gerrelli D.; Ragge N.K., New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders, «SCIENTIFIC REPORTS», 2017, 7, pp. 7975 - 7981 [Scientific article]

Prekovic S.; Durdevic D.F.; Csifcsak G.; Sveljo O.; Stojkovic O.; Jankovic M.; Koprivsek K.; Covill L.E.; Lucic M.; Van Den Broeck T.; Helsen C.; Ceroni F.; Claessens F.; Newbury D.F., Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation, «SCIENTIFIC REPORTS», 2016, 6, pp. 20369 - 20383 [Scientific article]

Simpson N.H.; Ceroni F.; Reader R.H.; Covill L.E.; Knight J.C.; Nudel R.; Monaco A.P.; Simonoff E.; Pickles A.; Slonims V.; Dworzynski K.; Everitt A.; Clark A.; Watson J.; Seckl J.; Cowie H.; Cohen W.; Nasir J.; Bishop D.V.M.; Simkin Z; Hennessy E.R.; Bolton P.F.; Conti-Ramsden G.; O'Hare A.; Baird G.; Fisher S.E.; Newbury D.F., Genome-wide analysis identifies a role for common copy number variants in specific language impairment, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2015, 23, pp. 1370 - 1377 [Scientific article]

Bacchelli E;Ceroni F;Pinto D;Lomartire S;Giannandrea M;D'Adamo P;Bonora E;Parchi P;Tancredi R;Battaglia A;Maestrini E, A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder., «JOURNAL OF NEURODEVELOPMENTAL DISORDERS», 2014, 6, Article number: 17 , pp. 1 - 11 [Scientific article]Open Access

Latest news

At the moment no news are available.