Giovanni Coppola

Coppola Giovanni, Chinnathambi Subashchandrabose, Jiyong Lee Jason, Dombroski Beth A, Baker Matt C, Soto-Ortolaza Alexandra I, Lee Suzee E, Klein Eric, Huang Alden Y, Sears Renee, Lane Jessica R, Karydas Anna M, Kenet Robert O, Biernat Jacek, Wang Li-San, Cotman Carl W, Decarli Charles S, Levey Allan I, Ringman John M, Mendez Mario F, Chui Helena C, Le Ber Isabelle, Brice Alexis, Lupton Michelle K, Preza Elisavet, Lovestone Simon, Powell John, Graff-Radford Neill, Petersen Ronald C, Boeve Bradley F, Lippa Carol F, Bigio Eileen H, Mackenzie Ian, Finger Elizabeth, Kertesz Andrew, Caselli Richard J, Gearing Marla, Juncos Jorge L, Ghetti Bernardino, Spina Salvatore, Bordelon Yvette M, Tourtellotte Wallace W, Frosch Matthew P, Vonsattel Jean Paul G, Zarow Chris, Beach Thomas G, Albin Roger L, Lieberman Andrew P, Lee Virginia M, Trojanowski John Q, Van Deerlin Vivianna M, Bird Thomas D, Galasko Douglas R, Masliah Eliezer, White Charles L, Troncoso Juan C, Hannequin Didier, Boxer Adam L, Geschwind Michael D, Kumar Satish, Mandelkow Eva-Maria, Wszolek Zbigniew K, Uitti Ryan J, Dickson Dennis W, Haines Jonathan L, Mayeux Richard, Pericak-Vance Margaret A, Farrer Lindsay A, Farrer Lindsay A, Ross Owen A, Rademakers Rosa, Schellenberg Gerard D, Miller Bruce L, Mandelkow Eckhard, Geschwind Daniel H Evidence for a Role of The Rare p.A152T Variant in MAPT in increasing the Risk for FTD-Spectrum and Alzheimer's Diseases.. Human molecular genetics. 2012; .

Stein Jason L, Medland Sarah E, Vasquez Alejandro Arias, Hibar Derrek P, Senstad Rudy E, Winkler Anderson M, Toro Roberto, Appel Katja, Bartecek Richard, Bergmann Orjan, Bernard Manon, Brown Andrew A, Cannon Dara M, Chakravarty M Mallar, Christoforou Andrea, Domin Martin, Grimm Oliver, Hollinshead Marisa, Holmes Avram J, Homuth Georg, Hottenga Jouke-Jan, Langan Camilla, Lopez Lorna M, Hansell Narelle K, Hwang Kristy S, Kim Sungeun, Laje Gonzalo, Lee Phil H, Liu Xinmin, Loth Eva, Lourdusamy Anbarasu, Mattingsdal Morten, Mohnke Sebastian, Maniega Susana Muñoz, Nho Kwangsik, Nugent Allison C, O'Brien Carol, Papmeyer Martina, Pütz Benno, Ramasamy Adaikalavan, Rasmussen Jerod, Rijpkema Mark, Risacher Shannon L, Roddey J Cooper, Rose Emma J, Ryten Mina, Shen Li, Sprooten Emma, Strengman Eric, Teumer Alexander, Trabzuni Daniah, Turner Jessica, van Eijk Kristel, van Erp Theo G M, van Tol Marie-Jose, Wittfeld Katharina, Wolf Christiane, Woudstra Saskia, Aleman Andre, Alhusaini Saud, Almasy Laura, Binder Elisabeth B, Brohawn David G, Cantor Rita M, Carless Melanie A, Corvin Aiden, Czisch Michael, Curran Joanne E, Davies Gail, de Almeida Marcio A A, Delanty Norman, Depondt Chantal, Duggirala Ravi, Dyer Thomas D, Erk Susanne, Fagerness Jesen, Fox Peter T, Freimer Nelson B, Gill Michael, Göring Harald H H, Hagler Donald J, Hoehn David, Holsboer Florian, Hoogman Martine, Hosten Norbert, Jahanshad Neda, Johnson Matthew P, Kasperaviciute Dalia, Kent Jack W, Kochunov Peter, Lancaster Jack L, Lawrie Stephen M, Liewald David C, Mandl René, Matarin Mar, Mattheisen Manuel, Meisenzahl Eva, Melle Ingrid, Moses Eric K, Mühleisen Thomas W, Nauck Matthias, Nöthen Markus M, Olvera Rene L, Pandolfo Massimo, Pike G Bruce, Puls Ralf, Reinvang Ivar, Rentería Miguel E, Rietschel Marcella, Roffman Joshua L, Royle Natalie A, Rujescu Dan, Savitz Jonathan, Schnack Hugo G, Schnell Knut, Seiferth Nina, Smith Colin, Steen Vidar M, Valdés Hernández Maria C, Van den Heuvel Martijn, van der Wee Nic J, Van Haren Neeltje E M, Veltman Joris A, Völzke Henry, Walker Robert, Westlye Lars T, Whelan Christopher D, Agartz Ingrid, Boomsma Dorret I, Cavalleri Gianpiero L, Dale Anders M, Djurovic Srdjan, Drevets Wayne C, Hagoort Peter, Hall Jeremy, Heinz Andreas, Jack Clifford R, Foroud Tatiana M, Le Hellard Stephanie, Macciardi Fabio, Montgomery Grant W, Poline Jean Baptiste, Porteous David J, Sisodiya Sanjay M, Starr John M, Sussmann Jessika, Toga Arthur W, Veltman Dick J, Walter Henrik, Weiner Michael W, Weiner Michael W, Weiner Michael W, Weiner Michael W, Weiner Michael W, Bis Joshua C, Ikram M Arfan, Smith Albert V, Gudnason Vilmundur, Tzourio Christophe, Vernooij Meike W, Launer Lenore J, Decarli Charles, Seshadri Sudha, Seshadri Sudha, Seshadri Sudha, Andreassen Ole A, Apostolova Liana G, Bastin Mark E, Blangero John, Brunner Han G, Buckner Randy L, Cichon Sven, Coppola Giovanni, de Zubicaray Greig I, Deary Ian J, Donohoe Gary, de Geus Eco J C, Espeseth Thomas, Fernández Guillén, Glahn David C, Grabe Hans J, Hardy John, Hulshoff Pol Hilleke E, Jenkinson Mark, Kahn René S, McDonald Colm, McIntosh Andrew M, McMahon Francis J, McMahon Katie L, Meyer-Lindenberg Andreas, Morris Derek W, Müller-Myhsok Bertram, Nichols Thomas E, Ophoff Roel A, Paus Tomas, Pausova Zdenka, Penninx Brenda W, Potkin Steven G, Sämann Philipp G, Saykin Andrew J, Schumann Gunter, Smoller Jordan W, Wardlaw Joanna M, Weale Michael E, Martin Nicholas G, Franke Barbara, Wright Margaret J, Thompson Paul M Identification of common variants associated with human hippocampal and intracranial volumes.. Nature genetics. 2012; 44(5): 552-561.

Ringman John M, Fithian Andrew T, Gylys Karen, Cummings Jeffrey L, Coppola Giovanni, Elashoff David, Pratico Domenico, Moskovitz Jackob, Bitan Gal Plasma Methionine Sulfoxide in Persons with Familial Alzheimer's Disease Mutations.. Dementia and geriatric cognitive disorders. 2012; 33(4): 219-225.

Khan Baber K, Yokoyama Jennifer S, Takada Leonel T, Sha Sharon J, Rutherford Nicola J, Fong Jamie C, Karydas Anna M, Wu Teresa, Ketelle Robin S, Baker Matthew C, Hernandez Mariely-Dejesus, Coppola Giovanni, Geschwind Daniel H, Rademakers Rosa, Lee Suzee E, Rosen Howard J, Rabinovici Gil D, Seeley William W, Rankin Katherine P, Boxer Adam L, Miller Bruce L Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion.. Journal of neurology, neurosurgery, and psychiatry. 2012; 83(4): 358-64.

Juknat Ana, Pietr Maciej, Kozela Ewa, Rimmerman Neta, Levy Rivka, Coppola Giovanni, Geschwind Daniel, Vogel Zvi Differential transcriptional profiles mediated by exposure to the cannabinoids cannabidiol and Δ(9) -tetrahydrocannabinol in BV-2 microglial cells.. British journal of pharmacology. 2012; 165(8): 2512-28.

Ringman John M, Coppola Giovanni, Elashoff David, Rodriguez-Agudelo Yaneth, Medina Luis D, Gylys Karen, Cummings Jeffrey L, Cole Greg M Cerebrospinal fluid biomarkers and proximity to diagnosis in preclinical familial Alzheimer's disease.. Dementia and geriatric cognitive disorders. 2012; 33(1): 1-5.

Lunnon Katie, Ibrahim Zina, Proitsi Petroula, Lourdusamy Anbarasu, Newhouse Stephen, Sattlecker Martina, Furney Simon, Saleem Muzamil, Soininen Hilkka, Kłoszewska Iwona, Mecocci Patrizia, Tsolaki Magda, Vellas Bruno, Coppola Giovanni, Geschwind Daniel, Simmons Andrew, Lovestone Simon, Dobson Richard, Hodges Angela Mitochondrial Dysfunction and Immune Activation are Detectable in Early Alzheimer's Disease Blood.. Journal of Alzheimer's disease : JAD. 2012; 83(4): .

Fogel Brent L, Lee Ji Yong, Lane Jessica, Wahnich Amanda, Chan Sandy, Huang Alden, Osborn Greg E, Klein Eric, Mamah Catherine, Perlman Susan, Geschwind Daniel H, Coppola Giovanni Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia.. Movement disorders : official journal of the Movement Disorder Society. 2012; 27(3): 442-6.

Blesch Armin, Lu Paul, Tsukada Shingo, Alto Laura Taylor, Roet Kasper, Coppola Giovanni, Geschwind Dan, Tuszynski Mark H Conditioning lesions before or after spinal cord injury recruit broad genetic mechanisms that sustain axonal regeneration: Superiority to camp-mediated effects.. Experimental neurology. 2011; 98(1): .

Ma Chi H E, Brenner Gary J, Omura Takao, Samad Omar A, Costigan Michael, Inquimbert Perrine, Niederkofler Vera, Salie Rishard, Sun Chia Chi, Lin Herbert Y, Arber Silvia, Coppola Giovanni, Woolf Clifford J, Samad Tarek A The BMP coreceptor RGMb promotes while the endogenous BMP antagonist noggin reduces neurite outgrowth and peripheral nerve regeneration by modulating BMP signaling.. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2011; 31(50): 18391-400.

Coppola Giovanni, Burnett Ryan, Perlman Susan, Versano Revital, Gao Fuying, Plasterer Heather, Rai Myriam, Saccá Francesco, Filla Alessandro, Lynch David R, Rusche James R, Gottesfeld Joel M, Pandolfo Massimo, Geschwind Daniel H A gene expression phenotype in lymphocytes from Friedreich ataxia patients.. Annals of neurology. 2011; 70(5): 790-804.

Ma Chi Him Eddie, Omura Takao, Cobos Enrique J, Latrémolière Alban, Ghasemlou Nader, Brenner Gary J, van Veen Ed, Barrett Lee, Sawada Tomokazu, Gao Fuying, Coppola Giovanni, Gertler Frank, Costigan Michael, Geschwind Dan, Woolf Clifford J Accelerating axonal growth promotes motor recovery after peripheral nerve injury in mice.. The Journal of clinical investigation. 2011; 121(11): 4332-47.

DeJesus-Hernandez Mariely, Mackenzie Ian R, Boeve Bradley F, Boxer Adam L, Baker Matt, Rutherford Nicola J, Nicholson Alexandra M, Finch NiCole A, Flynn Heather, Adamson Jennifer, Kouri Naomi, Wojtas Aleksandra, Sengdy Pheth, Hsiung Ging-Yuek R, Karydas Anna, Seeley William W, Josephs Keith A, Coppola Giovanni, Geschwind Daniel H, Wszolek Zbigniew K, Feldman Howard, Knopman David S, Petersen Ronald C, Miller Bruce L, Dickson Dennis W, Boylan Kevin B, Graff-Radford Neill R, Rademakers Rosa Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.. Neuron. 2011; 72(2): 245-56.

Rosen Ezra Y, Wexler Eric M, Versano Revital, Coppola Giovanni, Gao Fuying, Winden Kellen D, Oldham Michael C, Martens Lauren Herl, Zhou Ping, Farese Robert V, Geschwind Daniel H Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling.. Neuron. 2011; 71(6): 1030-42.

Nicholson Garth, Lenk Guy M, Reddel Stephen W, Grant Adrienne E, Towne Charles F, Ferguson Cole J, Simpson Ericka, Scheuerle Angela, Yasick Michelle, Hoffman Stuart, Blouin Randall, Brandt Carla, Coppola Giovanni, Biesecker Leslie G, Batish Sat D, Meisler Miriam H Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P₂ phosphatase FIG4.. Brain : a journal of neurology. 2011; 134(Pt 7): 1959-71.

Tang Bin, Seredenina Tamara, Coppola Giovanni, Kuhn Alexandre, Geschwind Daniel H, Luthi-Carter Ruth, Thomas Elizabeth A Gene expression profiling of R6/2 transgenic mice with different CAG repeat lengths reveals genes associated with disease onset and progression in Huntington's disease.. Neurobiology of disease. 2011; 42(3): 459-67.

Sleiman Sama F, Langley Brett C, Basso Manuela, Berlin Jill, Xia Li, Payappilly Jimmy B, Kharel Madan K, Guo Hengchang, Marsh J Lawrence, Thompson Leslie Michels, Mahishi Lata, Ahuja Preeti, MacLellan W Robb, Geschwind Daniel H, Coppola Giovanni, Rohr Jürgen, Ratan Rajiv R Mithramycin is a gene-selective Sp1 inhibitor that identifies a biological intersection between cancer and neurodegeneration.. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2011; 31(18): 6858-70.

Cenik Basar, Sephton Chantelle F, Dewey Colleen M, Xian Xunde, Wei Shuguang, Yu Kimberley, Niu Wenze, Coppola Giovanni, Coughlin Sarah E, Lee Suzee E, Dries Daniel R, Almeida Sandra, Geschwind Daniel H, Gao Fen-Biao, Miller Bruce L, Farese Robert V, Posner Bruce A, Yu Gang, Herz Joachim Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia.. The Journal of biological chemistry. 2011; 286(18): 16101-8.

Zai Laila, Ferrari Christina, Dice Carlie, Subbaiah Sathish, Havton Leif A, Coppola Giovanni, Geschwind Daniel, Irwin Nina, Huebner Eric, Strittmatter Stephen M, Benowitz Larry I Inosine augments the effects of a Nogo receptor blocker and of environmental enrichment to restore skilled forelimb use after stroke.. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2011; 31(16): 5977-88.

Thomas Elizabeth A, Coppola Giovanni, Tang Bin, Kuhn Alexandre, Kim SoongHo, Geschwind Daniel H, Brown Timothy B, Luthi-Carter Ruth, Ehrlich Michelle E In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons.. Human molecular genetics. 2011; 20(6): 1049-60.

Marques Fernanda, Sousa João C, Coppola Giovanni, Gao Fuying, Puga Renato, Brentani Helena, Geschwind Daniel H, Sousa Nuno, Correia-Neves Margarida, Palha Joana A Transcriptome signature of the adult mouse choroid plexus.. Fluids and barriers of the CNS. 2011; 8(1): 10.

Coppola Giovanni Designing, performing, and interpreting a microarray-based gene expression study.. Methods in molecular biology (Clifton, N.J.). 2011; 793(1): 417-39.

Newbern Jason M, Li Xiaoyan, Shoemaker Sarah E, Zhou Jiang, Zhong Jian, Wu Yaohong, Bonder Daniel, Hollenback Steven, Coppola Giovanni, Geschwind Daniel H, Landreth Gary E, Snider William D Specific functions for ERK/MAPK signaling during PNS development.. Neuron. 2011; 69(1): 91-105.

Gumy Laura F, Yeo Giles S H, Tung Yi-Chun Loraine, Zivraj Krishna H, Willis Dianna, Coppola Giovanni, Lam Brian Y H, Twiss Jeffery L, Holt Christine E, Fawcett James W Transcriptome analysis of embryonic and adult sensory axons reveals changes in mRNA repertoire localization.. RNA (New York, N.Y.). 2011; 17(1): 85-98.