19962019

Research output per year

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Research Output

2019

A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function: Human molecular genetics

Fratta, P., Ornaghi, F., Dati, G., Zambroni, D., Saveri, P., Belin, S., D'Adamo, P., Shy, M., Quattrini, A., Feltri, ML. & Wrabetz, L., 2019, In : Human Molecular Genetics. 28, 1, p. 124-132 9 p.

Research output: Contribution to journalArticle

A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function

Fratta, P., Ornaghi, F., Dati, G., Zambroni, D., Saveri, P., Belin, S., D'Adamo, P., Shy, M., Quattrini, A., Laura Feltri, M. & Wrabetz, L., Jan 1 2019, In : Human Molecular Genetics. 28, 1, p. 124-132 9 p.

Research output: Contribution to journalArticle

2018

Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia

Zanardi, A., Conti, A., Cremonesi, M., D'Adamo, P., Gilberti, M. E., Apostoli, P., Cannistraci, CV., Piperno, A., David, S. & Alessio, M., 2018, In : EMBO Molecular Medicine. 10, 1, p. 91-106 16 p.

Research output: Contribution to journalArticle

Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia

Zanardi, A., Conti, A., Cremonesi, M., D'Adamo, P., Gilberti, E., Apostoli, P., Cannistraci, C. V., Piperno, A., David, S. & Alessio, M., Jan 2018, In : EMBO Molecular Medicine. 10, 1, p. 91-106 16 p.

Research output: Contribution to journalArticle

2017

Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patients

Sauer, AV., Hernandez, RJ., Fumagalli, F., Bianchi, V., Poliani, PL., Dallatomasina, C., Riboni, E., Politi, LS., Tabucchi, A., Carlucci, F., Casiraghi, M., Carriglio, N., Cominelli, M., Forcellini, CA., Barzaghi, F., Ferrua, F., Minicucci, F., Medaglini, S., Leocani, L., la Marca, G. & 8 others, Notarangelo, L. D., Azzari, C., Comi, G., Baldoli, C., Canale, S., Sessa, M., D'Adamo, P. & Aiuti, A., 2017, In : Scientific Reports. 7, 9, 40136.

Research output: Contribution to journalArticle

Altered fronto-striatal functions in the Gdi1-null mouse model of X-linked Intellectual Disability

Morè, L., Künnecke, B., Yekhlef, L., Bruns, A., Marte, A., Fedele, E., Bianchi, V., Taverna, S., Gatti, S. & D'Adamo, P., 2017, In : Neuroscience. 344, 5, p. 346-359 14 p.

Research output: Contribution to journalArticle

A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility

Guarnieri, F. C., Pozzi, D., Raimondi, A., Fesce, R., Valente, M. M., Delvecchio, V. S., Van Esch, H., Matteoli, M., Benfenati, F., D'Adamo, P. & Valtorta, F., Dec 1 2017, In : Human Molecular Genetics. 26, 23, p. 4699-4714 16 p.

Research output: Contribution to journalArticle

A novel SYN1 missense mutation in non-syndromic X-linked intellectual disability affects synaptic vesicle life cycle, clustering and mobility

Guarnieri, FC., Pozzi, D., Raimondi, A., Fesce, R., Valente, MM., Delvecchio, VS., Van Esch, H., Matteoli, M., Benfenati, F., D'Adamo, P. & Valtorta, F., 2017, In : Human Molecular Genetics. 26, 23, p. 4699-4714 16 p.

Research output: Contribution to journalArticle

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Hinney, A., Kesselmeier, M., Jall, S., Volckmar, A-L., Föcker, M., Antel, J., [Unknown], GCAN., [Unknown], WTCCC., Heid, I. M., Winkler, T. W., Consortium, GIANT., Grant, S. F., [Unknown], EGG., Guo, Y., Bergen, A. W., Kaye, W., Berrettini, W. H., Hakonarson, H., Group, P. F. C., Foundation, C. H. O. PP. & 473 others, Herpertz-Dahlmann, B., de Zwaan, M., Herzog, W., Ehrlich, S., Zipfel, S., Egberts, K. M., Adan, R., Brandys, M., van Elburg, A. A., Boraska Perica, V., Müller, T. D., Tschöp, M. H., Zeggini, E., Bulik, C. M., Collier, D., Scherag, A., Hebebrand, J., Perica, V. B., Franklin, C. S., Floyd, J. A. B., Thornton, L. M., Huckins, L. M., Southam, L., Rayner, N. W., Tachmazidou, I., Klump, K. L., Treasure, J., Lewis, C. M., Schmidt, U., Tozzi, F., Iezebrink, K., Gorwood, P., Adan, R. A. H., Kas, M. J. H., Favaro, A., Santonastaso, P., Fernández-Aranda, F., Gratacos, M., Rybakowski, F., Dmitrzak-Weglarz, M., Kaprio, J., Keski-Rahkonen, A., Raevuori-Helkamaa, A., Van Furth, E. F., Slof-Op’t Landt, M. C. T., Hudson, J. I., Reichborn-Kjennerud, T., Knudsen, G. P. S., Monteleone, P., Kaplan, A. S., Karwautz, A., Berrettini, W. H., Li, D., Schork, N. J., Komaki, G., Ando, T., Inoko, H., Esko, T., Fischer, K., Männik, K., Metspalu, A., Baker, J. H., Cone, R. D., Dackor, J., DeSocio, J. E., Hilliard, C. E., O’Toole, J. K., Pantel, J., Szatkiewicz, J. P., Taico, C., Zerwas, S., Trace, S. E., Davis, O. S. P., Helder, S., Bühren, K., Burghardt, R., de Zwaan, M., Egberts, K., Imgart, H., Scherag, S., Boni, C., Ramoz, N., Versini, A., Brandys, M. K., Danner, U. N., de Kove, C., Hendriks, J., Koeleman, B. P. C., Ophoff, R. A., Strengman, E., van Elburg, A. A., Bruson, A., Clementi, M., Degortes, D., Forzan, M., Tenconi, E., Docampo, E., Jiménez-Murcia, G. E. S., Lissowska, J., Rajewski, A., Szeszenia-Dabrowska, N., Slopien, A., Hauser, J., Karhunen, L., Meulenbelt, I., Slagboom, P. E., Tortorella, A., Maj, M., Dedoussis, G., Dikeos, D., Gonidakis, F., Tziouvas, K., Tsitsika, A., Papezova, H., Slachtova, L., Martaskova, D., Kennedy, J. L., Levitan, R. D., Yilmaz, Z., Huemer, J., Koubek, D., Merl, E., Wagner, G., Lichtenstein, P., Breen, G., Cohen-Woods, S., Farmer, A., McGuffin, P., Cichon, S., Giegling, I., Herms, S., Rujescu, D., Schreiber, S., Wichmann, H. E., Christian, D., Sladek, R., Gambaro, G., Soranzo, N., Julia, A., Marsal, S., Rabionet, R., Gaborieau, V., Dick, D. M., Palotie, A., Ripatti, S., Widén, E., Andreassen, O. A., Espeseth, T., Lundervold, A., Reinvang, I., Steen, V. M., Le Hellard, S., Mattingsdal, M., Ntalla, I., Bencko, V., Foretova, L., Janout, V., Navratilova, M., Gallinger, S., Pinto, D., Scherer, S. W., Aschauer, H., Carlberg, L., Schosser, A., Alfredsson, L., Ding, B., Klareskog, L., Padyukov, L., Finan, C., Kalsi, G., Roberts, M., Logan, D. W., Peltonen, L., Ritchie, G. R. S., Barrett, J. C., Estivill, X., Sullivan, P. F., Collier, D. A., Anderson, C. A., McGinnis, R., Sambrook, J., Stephens, J., Ouwehand, W. H., McArdle, W. L., Ring, S. M., Strachan, D. P., Alexander, G., Conlon, P. J., Dominiczak, A., Duncanson, A., Hill, A., Langford, C., Lord, G., Maxwell, A. P., Morgan, L., Sandford, R. N., Sheerin, N., Vannberg, F. O., Blackburn, H., Chen, W-M., Edkins, S., Gillman, M., Gray, E., Hunt, S. E., Nengut, S-G., Potter, S., Rich, S. S., Simpkin, D., Whittaker, P., Adair, L. S., Ang, W., Atalay, M., van Beijsterveldt, T., Bergen, N., Benke, K., Berry, D. J., Boomsma, D. I., Bradfield, J. P., Charoen, P., Coin, L., Cooper, C., Cousminer, D. L., Das, S., Davis, O. S., Dedoussis, G. V., Elliott, P., Evans, D. M., Feenstra, B., Flexeder, C., Frayling, T., Freathy, R. M., Gaillard, R., Geller, F., Grant, S. F., Groen-Blokhuis, M., Goh, L. K., Guxens, M., Hattersley, A. T., Haworth, C. M., Hadley, D., Heinrich, J., Hirschhorn, J. N., Hocher, B., Holloway, J. W., Holst, C., Hottenga, J. J., Horikoshi, M., Huikari, V., Hypponen, E., Iñiguez, C., Jaddoe, V. W., Jarvelin, M. R., Kaakinen, M., Kilpeläinen, T. O., Kirin, M., Kowgier, M., Lakka, H. M., Lakka, T. A., Lange, L. A., Lawlor, D. A., Lehtimäki, T., Lewin, A., Lindgren, C., Lindi, V., Maggi, R., Marsh, J., McCarthy, M. I., Melbye, M., Middeldorp, C., Millwood, I., Mohlke, K. L., Mook-Kanamori, D. O., Murray, J. C., Nivard, M., Nohr, E. A., Oken, E., Ong, K. K., O'Reilly, P. F., Palmer, L. J., Panoutsopoulou, K., Pararajasingham, J., Pearson, E. R., Pennell, C. E., Power, C., Price, T. S., Prokopenko, I., Raitakari, O. T., Rodriguez, A., Salem, R. M., Saw, S. M., Sebert, S., Siitonen, N., Simell, O., Sørensen, T. I., Sovio, U., Pourcain, B. S., Sunyer, J., Taal, H. R., Teo, Y. Y., Thiering, E., Tiesler, C., Timpson, N. J., Uitterlinden, A. G., Valcárcel, B., Warrington, N. M., White, S., Willemsen, G., Wilson, J. F., Yaghootkar, H., Elks, C. E., Perry, J. R., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Gudbjartsson, D. F., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F., Smith, A. V., Stolk, L., van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K., Smith, E. N., Ulivi, S., Warrington, M., Zgaga, L., Alavere, H., Amin, N., Aspelund, T., Bandinelli, S., Barroso, I., Berenson, G. S., Bergmann, S., Boerwinkle, E., Buring, J. E., Busonero, F., Campbell, H., Chanock, S. J., Chen, W., Cornelis, M. C., Couper, D., Coviello, A. D., d'Adamo, P., de Faire, U., de Geus, E. J., Deloukas, P., Döring, A., Davey Smith, G., Easton, D. F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ferrucci, L., Folsom, A. R., Foroud, T., Garcia, M., Gasparini, P., Gieger, C., Gudnason, V., Hall, P., Hankinson, S. E., Ferreli, L., Heath, A. C., Hernandez, D. G., Hofman, A., Hu, F. B., Illig, T., Järvelin, M. R., Johnson, A. D., Karasik, D., Khaw, K. T., Kiel, D. P., Kolcic, I., Kraft, P., Launer, L. J., Laven, J. S., Li, S., Liu, J., Levy, D., Martin, N. G., Mooser, V., Murray, S. S., Nalls, M. A., Navarro, P., Nelis, M., Ness, A. R., Northstone, K., Oostra, B. A., Peacock, M., Paré, G., Parker, A. N., Pedersen, N. L., Pharoah, P., Polasek, O., Plump, A. S., Pouta, A., Porcu, E., Rafnar, T., Rice, J. P., Rivadeneira, F., Rudan, I., Sala, C., Salomaa, V., Sanna, S., Schlessinger, D., Scuteri, A., Segrè, A. V., Shuldiner, A. R., Srinivasan, S. R., Tammesoo, M. L., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Tyrer, J., Uda, M., van Dam, R. M., van Meurs, J. B., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Weedon, M. N., Wichmann, H. E., Wright, A. F., Young, L., Zhai, G., Zhuang, W. V., Bierut, L. J., Boyd, H. A., Crisponi, L., Demerath, E. W., van Duijn, C. M., Econs, M. J., Harris, T. B., Hunter, D. J., Loos, R. J., Montgomery, G. W., Ridker, P. M., Spector, T. D., Streeten, E. A., Stefansson, K., Thorsteinsdottir, U., Widen, E., Murabito, J. M., Murray, A., Brandt, H., Crawford, S., Crow, S., Fichter, M. M., Halmi, K. A., Johnson, C., La Via, M., Mitchell, J., Strober, M., Rotondo, A., Woodside, D. B., Keel, P., Lilenfeld, L., Plotnicov, K. & Magistretti, P., 2017, In : Molecular Psychiatry. 22, 2, p. 192-201 10 p.

Research output: Contribution to journalArticle

Impaired αGDI Function in the X-Linked Intellectual Disability: The Impact on Astroglia Vesicle Dynamics

Potokar, M., Jorgačevski, J., Lacovich, V., Kreft, M., Vardjan, N., Bianchi, V., D'Adamo, P. & Zorec, R., 2017, In : Molecular Neurobiology. 54, 4, p. 2458-2468 11 p.

Research output: Contribution to journalArticle

Pharmacogenetics and induction/consolidation therapy toxicities in acute lymphoblastic leukemia patients treated with AIEOP-BFM ALL 2000 protocol

Franca, R., Rebora, P., Bertorello, N., Fagioli, F., Conter, V., Biondi, A., Colombini, A., Micalizzi, C., Zecca, M., Parasole, R., Petruzziello, F., Basso, G., Putti, M. C., Locatelli, F., d'Adamo, P., Valsecchi, M. G., Decorti, G. & Rabusin, M., Jan 1 2017, In : Pharmacogenomics Journal. 17, 1, p. 4-10 7 p.

Research output: Contribution to journalArticle

Pharmacogenetics and induction/consolidation therapy toxicities in acute lymphoblastic leukemia patients treated with AIEOP-BFM ALL 2000 protocol

Franca, R., Rebora, P., Bertorello, N., Fagioli, F., Conter, V., Biondi, A., Colombini, A., Micalizzi, C., Zecca, M., Parasole, R., Petruzziello, F., Basso, G., Putti, M. C., Locatelli, N., d'Adamo, P., Valsecchi, M. G., Decorti, G. & Rabusin, M., Jan 2017, In : Pharmacogenomics Journal. 17, 1, p. 4-10 7 p.

Research output: Contribution to journalArticle

Pharmacological Modulation of AMPAR Rescues Intellectual Disability-Like Phenotype in Tm4sf2-/yMice

Murru, L., Vezzoli, E., Longatti, A., Ponzoni, L., Falqui, A., Folci, A., Moretto, E., Bianchi, V., Braida, D., Sala, M., D'Adamo, P., Bassani, S., Francolini, M. & Passafaro, M., 2017, In : Cerebral Cortex. 27, 11, p. 5369-5384 16 p.

Research output: Contribution to journalArticle

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene

Ciammola, A., Carrera, P., Di Fonzo, A., Sassone, J., Villa, R., Poletti, B., Ferrari, M., Girotti, F., Monfrini, E., Buongarzone, G., Silani, V., Cinnante, C. M., Mignogna, M. L., D'Adamo, P. & Bonati, M. T., 2017, In : Parkinsonism and Related Disorders. 44, p. 142-146

Research output: Contribution to journalArticle

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene

Ciammola, A., Carrera, P., Di Fonzo, A., Sassone, J., Villa, R., Poletti, B., Ferrari, M., Girotti, F., Monfrini, E., Buongarzone, G., Silani, V., Cinnante, CM., Mignogna, ML., D'Adamo, P. & Bonati, MT., 2017, In : Parkinsonism and Related Disorders. 44, 3, p. 142-146 5 p.

Research output: Contribution to journalArticle

X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene

Ciammola, A., Carrera, P., Di Fonzo, A., Sassone, J., Villa, R., Poletti, B., Ferrari, M., Girotti, F., Monfrini, E., Buongarzone, G., Silani, V., Cinnante, C. M., Mignogna, M. L., D'Adamo, P. & Bonati, M. T., Nov 2017, In : Parkinsonism and Related Disorders. 44, p. 142-146 5 p.

Research output: Contribution to journalArticle

2016

2-Deoxy-D-glucose ameliorates PKD progression

Chiaravalli, M., Rowe, I. S. M-J., Mannella, V., Quilici, G., Canu, T., Bianchi, V., Gurgone, A., Antunes, S., D'Adamo, P., Esposito, A., Musco, G. & Boletta, A., 2016, In : Journal of the American Society of Nephrology. 27, 7, p. 1958-1969 12 p.

Research output: Contribution to journalArticle

Disruption of ArhGAP15 results in hyperactive Rac1, affects the architecture and function of hippocampal inhibitory neurons and causes cognitive deficits

Zamboni, V., Armentano, M., Saró, G., Ciraolo, E., Ghigo, A., Germena, G., Umbach, A., Valnegri, P., Passafaro, M., Carabelli, V., Gavello, D., Bianchi, V., D'Adamo, P., De Curtis, I., El-Assawi, N., Mauro, A., Priano, L., Ferri, N., Hirsch, E. & Merlo, G. R., Oct 7 2016, In : Scientific Reports. 6, 34877.

Research output: Contribution to journalArticle

Disruption of ArhGAP15 results in hyperactive Rac1, affects the architecture and function of hippocampal inhibitory neurons and causes cognitive deficits

Zamboni, V., Armentano, M., Saró, G., Ciraolo, E., Ghigo, A., Germena, G., Umbach, A., Valnegri, P., Passafaro, M., Carabelli, V., Gavello, D., Bianchi, V., D'Adamo, P., De Curtis, I., El-Assawi, N., Mauro, A., Priano, L., Ferri, N., Hirsch, E. & Merlo, G. R., Oct 7 2016, In : Scientific Reports. 6, 34877.

Research output: Contribution to journalArticle

Increased neuroplasticity and hippocampal microglia activation in a mice model of rapid antidepressant treatment

Muzio, L., Brambilla, V., Calcaterra, L., D'Adamo, P., Martino, G. & Benedetti, F., Sep 15 2016, In : Behavioural Brain Research. 311, p. 392-402 11 p.

Research output: Contribution to journalArticle

Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks

Pennucci, R., Talpo, F., Astro, V., Montinaro, V., Morè, L., Cursi, M., Castoldi, V., Chiaretti, S., Bianchi, V., Marenna, S., Cambiaghi, M., Tonoli, DI., Leocani, L., Biella, G., D'Adamo, P. & De Curtis, I., Feb 1 2016, In : Cerebral Cortex. 26, 2, p. 873-890 18 p.

Research output: Contribution to journalArticle

Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination

Bolino, A., Piguet, F., Alberizzi, V., Pellegatta, M., Rivellini, C., Guerrero-Valero, M., Noseda, R., Brombin, C., Nonis, A., D'Adamo, P., Taveggia, C. & Previtali, S., Dec 1 2016, In : EMBO Molecular Medicine. 8, 12, p. 1438-1454 17 p.

Research output: Contribution to journalArticle

Synaptic dysfunction, memory deficits and hippocampal atrophy due to ablation of mitochondrial fission in adult forebrain neurons

Oettinghaus, B., Schulz, J. M., Restelli, L. M., Licci, M., Savoia, C., Schmidt, A., Schmitt, K., Grimm, A., Morè, L., Hench, J., Tolnay, M., Eckert, A., D'adamo, P., Franken, P., Ishihara, N., Mihara, K., Bischofberger, J., Scorrano, L. & Frank, S., Jan 1 2016, In : Cell Death and Differentiation. 23, 1, p. 18-28 11 p.

Research output: Contribution to journalArticle

2015

Down-sizing of neuronal network activity and density of presynaptic terminals by pathological acidosis are efficiently prevented by Diminazene Aceturate

de Ceglia, R., Chaabane, L., Biffi, E., Bergamaschi, A., Ferrigno, G., Amadio, S., Del Carro, U., Mazzocchi, N., Comi, G., Bianchi, V., Taverna, S., Forti, L., D'Adamo, P., Martino, G., Menegon, A. & Muzio, L., Mar 1 2015, In : Brain, Behavior, and Immunity. 45, p. 263-276 14 p.

Research output: Contribution to journalArticle

The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition

Mignogna, M. L., Giannandrea, M., Gurgone, A., Fanelli, F., Raimondi, F., Mapelli, L., Bassani, S., Fang, H., Van Anken, E., Alessio, M., Passafaro, M., Gatti, S., Esteban, J. A., Huganir, R. & D'Adamo, P., Mar 18 2015, In : Nature Communications. 6, 6504.

Research output: Contribution to journalArticle

2014

A CTNNA3 compound heterozygous deletion implicates a role for αt-catenin in susceptibility to autism spectrum disorder

Bacchelli, E., Ceroni, F., Pinto, D., Lomartire, S., Giannandrea, M., D'Adamo, P., Bonora, E., Parchi, P., Tancredi, R., Battaglia, A. & Maestrini, E., Jul 10 2014, In : Journal of Neurodevelopmental Disorders. 6, 1, 17.

Research output: Contribution to journalArticle

Increased dosage of RAB39B affects neuronal development and could explain the cognitive impairment in male patients with distal Xq28 copy number gains

Vanmarsenille, L., Giannandrea, M., Fieremans, N., Verbeeck, J., Belet, S., Raynaud, M., Vogels, A., Männik, K., Õunap, K., Jacqueline, V., Briault, S., Van Esch, H., D'Adamo, P. & Froyen, G., 2014, In : Human Mutation. 35, 3, p. 377-383 7 p.

Research output: Contribution to journalArticle

Mutations in RAB39B cause X-linked intellectual disability and early-onset parkinson disease with α-synuclein pathology

Wilson, G. R., Sim, J. C. H., McLean, C., Giannandrea, M., Galea, C. A., Riseley, J. R., Stephenson, S. E. M., Fitzpatrick, E., Haas, S. A., Pope, K., Hogan, K. J., Gregg, R. G., Bromhead, C. J., Wargowski, D. S., Lawrence, C. H., James, P. A., Churchyard, A., Gao, Y., Phelan, D. G., Gillies, G. & 13 others, Salce, N., Stanford, L., Marsh, A. P. L., Mignogna, M. L., Hayflick, S. J., Leventer, R. J., Delatycki, M. B., Mellick, G. D., Kalscheuer, V. M., D'Adamo, P., Bahlo, M., Amor, D. J. & Lockhart, P. J., Dec 4 2014, In : American Journal of Human Genetics. 95, 6, p. 729-735 7 p.

Research output: Contribution to journalArticle

RAB GTPases and RAB-interacting proteins and their role in the control of cognitive functions

D'Adamo, P., Masetti, M., Bianchi, V., Morè, L., Mignogna, M. L., Giannandrea, M. & Gatti, S., Oct 1 2014, In : Neuroscience and Biobehavioral Reviews. 46, P2, p. 302-314 13 p.

Research output: Contribution to journalArticle

2012

Forebrain deletion of αGDI in adult mice worsens the pre-synaptic deficit at cortico-lateral amygdala synaptic connections

Bianchi, V., Gambino, F., Muzio, L., Toniolo, D., Humeau, Y. & D'Adamo, P., Jan 23 2012, In : PLoS One. 7, 1, e29763.

Research output: Contribution to journalArticle

Growth defects and impaired cognitivebehavioral abilities in mice with knockout for Eif4h, a gene located in the mouse homolog of the williams-beuren syndrome critical region

Capossela, S., Muzio, L., Bertolo, A., Bianchi, V., Dati, G., Chaabane, L., Godi, C., Politi, L. S., Biffo, S., D'Adamo, P., Mallamaci, A. & Pannese, M., Mar 2012, In : American Journal of Pathology. 180, 3, p. 1121-1135 15 p.

Research output: Contribution to journalArticle

Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicity

Butti, E., Bacigaluppi, M., Rossi, S., Cambiaghi, M., Bari, M., Cebrian Silla, A., Brambilla, E., Musella, A., De Ceglia, R., Teneud, L., De Chiara, V., D'Adamo, P., Garcia-Verdugo, J. M., Comi, G., Muzio, L., Quattrini, A., Leocani, L., MacCarrone, M., Centonze, D. & Martino, G., 2012, In : Brain. 135, 11, p. 3320-3335 16 p.

Research output: Contribution to journalArticle

2010

Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly

Giannandrea, M., Bianchi, V., Mignogna, M. L., Sirri, A., Carrabino, S., D'Elia, E., Vecellio, M., Russo, S., Cogliati, F., Larizza, L., Ropers, H. H., Tzschach, A., Kalscheuer, V., Oehl-Jaschkowitz, B., Skinner, C., Schwartz, C. E., Gecz, J., Van Esch, H., Raynaud, M., Chelly, J. & 3 others, de Brouwer, A. P. M., Toniolo, D. & D'Adamo, P., Feb 12 2010, In : American Journal of Human Genetics. 86, 2, p. 185-195 11 p.

Research output: Contribution to journalArticle

Temporal gene expression profile of the hippocampus following trace fear conditioning

Sirri, A., Bianchi, V., Pelizzola, M., Mayhaus, M., Ricciardi-Castagnoli, P., Toniolo, D. & D'Adamo, P., Jan 13 2010, In : Brain Research. 1308, p. 14-23 10 p.

Research output: Contribution to journalArticle

2009

Cognitive impairment in Gdi1-deficient mice is associated with altered synaptic vesicle pools and short-term synaptic plasticity, and can be corrected by appropriate learning training

Bianchi, V., Farisello, P., Baldelli, P., Meskenaite, V., Milanese, M., Vecellio, M., Mühlemann, S., Lipp, H. P., Bonanno, G., Benfenati, F., Toniolo, D. & D'Adamo, P., 2009, In : Human Molecular Genetics. 18, 1, p. 105-117 13 p.

Research output: Contribution to journalArticle

2008

Hyperactivity and novelty-induced hyperreactivity in mice lacking Rac3

Corbetta, S., D'Adamo, P., Gualdoni, S., Braschi, C., Berardi, N. & de Curtis, I., Jan 25 2008, In : Behavioural Brain Research. 186, 2, p. 246-255 10 p.

Research output: Contribution to journalArticle

2005

Aquaporin-8 is involved in water transport in isolated superficial colonocytes from rat proximal colon

Laforenza, U., Cova, E., Gastaldi, G., Tritto, S., Grazioli, M., LaRusso, N. F., Splinter, P. L., D'Adamo, P., Tosco, M. & Ventura, U., Oct 2005, In : Journal of Nutrition. 135, 10, p. 2329-2336 8 p.

Research output: Contribution to journalArticle

2004

Accelerated extinction of conditioned taste aversion in P301L tau transgenic mice

Pennanen, L., Welzl, H., D'Adamo, P., Nitsch, R. M. & Götz, J., Apr 2004, In : Neurobiology of Disease. 15, 3, p. 500-509 10 p.

Research output: Contribution to journalArticle

DNA variants in the human RAB3A gene are not associated with autism

D'Adamo, P., Bacchelli, E., Blasi, F., Lipp, H. P., Toniolo, D. & Maestrini, E., Apr 2004, In : Genes, Brain and Behavior. 3, 2, p. 123-124 2 p.

Research output: Contribution to journalArticle

Midlatency auditory event-related potentials in mice: Comparison to midlatency auditory ERPs in humans

Umbricht, D., Vyssotky, D., Latanov, A., Nitsch, R., Brambilla, R., D'Adamo, P. & Lipp, H. P., Sep 3 2004, In : Brain Research. 1019, 1-2, p. 189-200 12 p.

Research output: Contribution to journalArticle

2002

Deletion of the mental retardation gene Gdi1 impairs associative memory and alters social behavior in mice

D'Adamo, P., Welzl, H., Papadimitriou, S., Di Barletta, M. R., Tiveron, C., Tatangelo, L., Pozzi, L., Chapman, P. F., Knevett, S. G., Ramsay, M. F., Valtorta, F., Leoni, C., Menegon, A., Wolfer, D. P., Lipp, H. P. & Toniolo, D., Oct 1 2002, In : Human Molecular Genetics. 11, 21, p. 2567-2580 14 p.

Research output: Contribution to journalArticle

2001

Conditioned taste aversion as a learning and memory paradigm

Welzl, H., D'Adamo, P. & Lipp, H. P., Nov 8 2001, In : Behavioural Brain Research. 125, 1-2, p. 205-213 9 p.

Research output: Contribution to journalArticle

2000

A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

Meloni, I., Bruttini, M., Longo, I., Mari, F., Rizzolio, F., D'Adamo, P., Denvriendt, K., Fryns, J. P., Toniolo, D. & Renieri, A., 2000, In : American Journal of Human Genetics. 67, 4, p. 982-985 4 p.

Research output: Contribution to journalArticle

X-linked non-specific mental retardation

Toniolo, D. & D'Adamo, P., Jun 1 2000, In : Current Opinion in Genetics and Development. 10, 3, p. 280-285 6 p.

Research output: Contribution to journalArticle

1998

Erratum: Mutations in GDI1 are responsible for X-linked non-specific mental retardation (Nature Genetics (1998) 19 (134-139))

D'Adamo, P., Menegon, A., Nigro, C. L., Grasso, M., Gulisano, M., Tamanini, F., Bienvenu, T., Gedeon, A. K., Oostra, B., Wu, S. K., Tandon, A., Valtorta, F., Batch, W. E., Chelly, J. & Toniolo, D., 1998, In : Nature Genetics. 19, 3, p. 303 1 p.

Research output: Contribution to journalArticle

Mutations in GDI1 are responsible for X-linked non-specific mental retardation

D'Adamo, P., Menegon, A., Nigro, C. L., Grasso, M., Gulisano, M., Tamanini, F., Bienvenu, T., Gedeon, A. K., Oostra, B., Wu, S. K., Tandon, A., Valtorta, F., Balch, W. E., Chelly, J. & Toniolo, D., 1998, In : Nature Genetics. 19, 2, p. 134-139 6 p.

Research output: Contribution to journalArticle