Foto del docente

Marco Seri

Professor

Department of Medical and Surgical Sciences

Academic discipline: MED/03 Medical Genetics

Head of Scuola di Specializzazione Genetica Medica (DI 68/2015)

Publications

C. Evangelisti;F. Bianco;L. M. Pradella;A. Puliti;A. Goldoni;I. Sbrana;M. Rossi;M. Vargiolu;M. Seri;G. Romeo;V. Stanghellini;R. de Giorgio;E. Bonora, Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways, «NEUROGASTROENTEROLOGY AND MOTILITY», 2012, 24, pp. 497 - 508 [Scientific article]

Panza E; Knowles CH; Graziano C; Thapar N; Burns AJ; Seri M; Stanghellini V; De Giorgio R., Genetics of human enteric neuropathies., «PROGRESS IN NEUROBIOLOGY», 2012, 96, pp. 176 - 189 [Scientific article]

Garavelli L.; Zollino M.; Cerruti Mainardi P.; Gurrieri F.; Rivieri F.; Soli F.; Verri R.; Albertini E.; Favaron E.; Zignani M.; Orteschi D.; Bianchi P.; Faravelli F.; Forzano F.; Seri M.; Wischmeijer A.; Turchetti D.; Pompilii E.; Gnoli M.; Cocchi G.; Mazzanti L.; Bergamaschi R.; De Brasi D.; Sperandeo M.P.; Mari F.; Uliana V.; Mostardini R.; Cecconi M.; Grasso M.; Sassi S.; Sebastio G.; Renieri A.; Silengo M.; Bernasconi S.; Wakamatsu N.; Neri G., Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature, «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2009, 149A, pp. 417 - 426 [Scientific article]

Balbi P; Seri M; Ceccherini I; Uggetti C; Casale R; Fundarò C; Caroli F; Santoro L., Adult-onset Alexander disease : Report on a family., «JOURNAL OF NEUROLOGY», 2008, 255(1), pp. 24 - 30 [Scientific article]

Pecci A; Panza E; Pujol-Moix N; Klersy C; Di Bari F; Bozzi V; Gresele P; Lethagen S; Fabris F; Dufour C; Granata A; Doubek M; Pecoraro C; Koivisto PA; Heller PG; Iolascon A; Alvisi P; Schwabe D; De Candia E; Rocca B; Russo U; Ramenghi U; Noris P; Seri M; Balduini CL; Savoia A., Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease., «HUMAN MUTATION», 2008, 29(3), pp. 409 - 417 [Scientific article]

Graziano C.; D'Elia AV.; Mazzanti L.; Moscano F.; Guidelli Guidi S.; Scarano E.; Turchetti D.; Franzoni E.; Romeo G.; Damante G.; Seri M., A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation, «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2007, 143, pp. 1802 - 1805 [Scientific article]

Deglincerti A; De Giorgio R; Cefle K; Devoto M; Pippucci T; Castegnaro G; Panza E; Barbara G; Cogliandro RF; Mungan Z; Palanduz S; Corinaldesi R; Romeo G; Seri M; Stanghellini V., A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24., «EUROPEAN JOURNAL OF HUMAN GENETICS», 2007, 15, pp. 889 - 897 [Scientific article]

Savoia A; Dufour C; Locatelli F; Noris P; Ambaglio C; Rosti V; Zecca M; Ferrari S; di Bari F; Corcione A; Di Stazio M; Seri M; Balduini CL., Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations., «HAEMATOLOGICA», 2007, 92, pp. 1186 - 1193 [Scientific article]

De Giorgio R; Seri M; van Eys G., Deciphering chronic intestinal pseudo-obstruction: do mice help to solve the riddle?, «GASTROENTEROLOGY», 2007, 6, pp. 2052 - 2055 [Scientific article]

Caroli F; Biancheri R; Seri M; Rossi A; Pessagno A; Bugiani M; Corsolini F; Savasta S; Romano S; Antonelli C; Romano A; Pareyson D; Gambero P; Uziel G; Ravazzolo R; Ceccherini I; Filocamo M., GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease., «CLINICAL GENETICS», 2007, 72, pp. 427 - 433 [Scientific article]

L. Longo; E. Panza; F. Schena; M. Seri; M. Devoto; G. Romeo; C. Bini; G. Pappalardo; G.P. Tonini; P. Perri., Genetic Predisposition to Familial Neuroblastoma: Identification of Two Novel Genomic Regions at 2p and 12p., «HUMAN HEREDITY», 2007, 63(3-4), pp. 205 - 211 [Scientific article]

Emanuela Scarano; Laura Mazzanti; Marco Seri; Rosalba Bergamaschi; Chiara Matteucci; Pamela Magini; Manuela de Gregori; Roberto Ciccone; Orsetta Zuffardi; Alessandro Cicognani, Interstitial 6q deletion: a new patient with empty sella and GH deficiency, in: , «HORMONE RESEARCH», 2007, 68, pp. 198 - 198 (atti di: 46th Annual Meeting of the ESPE, Helsinki, 2007) [Abstract]

S. Sanna-Cherchi; G. Caridi; P.L. Weng; M. Dagnino; M. Seri; A. Konka; D. Somenzi; A. Carrea; C. Izzi; D. Casu; L. Allegri; K.M. Schmidt-Ott; J. Barasch; F. Scolari; R. Ravazzolo; G.M. Ghiggeri; A.G. Gharavi., Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33., «AMERICAN JOURNAL OF HUMAN GENETICS», 2007, 80(3), pp. 539 - 549 [Scientific article]

Jaijo T; Aller E; Beneyto M; Najera C; Graziano C; Turchetti D; Seri M; Ayuso C; Baiget M; Moreno F; Morera C; Perez-Garrigues H; Millan JM., MYO7A mutation screening in Usher syndrome type I patients from diverse origins., «JOURNAL OF MEDICAL GENETICS», 2007, 44 [Scientific article]

Panza E; Seri M; Barbara G; Castegnaro G; Romeo G; Stanghellini V; Corinaldesi R; De Giorgio R., Molecular genetics of human enteric neuropathies., in: , «NEUROGASTROENTEROLOGY AND MOTILITY», 2007, 19-supplement 3, pp. 17 - 17 (atti di: 21st international symposium on neurogastroenterology and motility, Jeju, Korea, September, 2-5) [Abstract]