White matter hyperintensities and neurodegenerative dementias

by Sassi, Celeste
Published in Aging (Albany NY) (2019)

Investigating APOE, APP-Aβ metabolism genes and Alzheimer’s disease GWAS hits in brain small vessel ischemic disease

by Blumenau, Sonja, Foddis, Marco, Müller, Susanne, Holtgrewe, Manuel, Bentele, Kajetan, Berchtold, Daniel, Beule, Dieter, Dirnagl, Ulrich, Sassi, Celeste
Published in Sci Rep (2020)

A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy

by Sassi, Celeste, Capozzo, Rosa, Gibbs, Raphael, Crews, Cynthia, Zecca, Chiara, Arcuti, Simona, Copetti, Massimiliano, Barulli, Maria R., Brescia, Vincenzo, Singleton, Andrew B., Logroscino, Giancarlo
Published in J Alzheimers Dis (2016)

Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of Apulia

by Sassi, Celeste, Capozzo, Rosa, Hammer, Monia, Zecca, Chiara, Federoff, Monica, Blauwendraat, Cornelis, Bernstein, Nick, Ding, Jinhui, Gibbs, J. Raphael, Price, Timothy, Singleton, Andrew, Logroscino, Giancarlo
Published in Sci Rep (2021)

Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders

by Hammer, Monia B, Eleuch-Fayache, Ghada, Gibbs, J Raphael, Arepalli, Sampath K, Chong, Sean B, Sassi, Celeste, Bouhlal, Yosr, Hentati, Fayçal, Amouri, Rim, Singleton, Andrew B
Published in Eur J Neurol (2012)

Individual and temporal variability of the retina after chronic bilateral common carotid artery occlusion (BCCAO)

by Crespo-Garcia, Sergio, Reichhart, Nadine, Skosyrski, Sergej, Foddis, Marco, Wu, Jim, Figura, Aleksandar, Herrspiegel, Christina, Füchtemeier, Martina, Sassi, Celeste, Dirnagl, Ulrich, Joussen, Antonia M., Strauss, Olaf
Published in PLoS One (2018)

Correction: Individual and temporal variability of the retina after chronic bilateral common carotid artery occlusion (BCCAO)

by Crespo-Garcia, Sergio, Reichhart, Nadine, Skosyrski, Sergej, Foddis, Marco, Wu, Jim, Figura, Aleksandar, Herrspiegel, Christina, Füchtemeier, Martina, Sassi, Celeste, Dirnagl, Ulrich, Joussen, Antonia M., Strauss, Olaf
Published in PLoS One (2018)

An exploratory investigation of brain collateral circulation plasticity after cerebral ischemia in two experimental C57BL/6 mouse models

by Foddis, Marco, Winek, Katarzyna, Bentele, Kajetan, Mueller, Susanne, Blumenau, Sonja, Reichhart N, Nadine, Crespo-Garcia, Sergio, Harnett, Dermot, Ivanov, Andranik, Meisel, Andreas, Joussen, Antonia, Strauss, Olaf, Beule, Dieter, Dirnagl, Ulrich, Sassi, Celeste
Published in J Cereb Blood Flow Metab (2019)

Clinical and Genetic Analyses of Familial and Sporadic Frontotemporal Dementia Patients in Southern Italy

by Capozzo, Rosa, Sassi, Celeste, Hammer, Monia B., Arcuti, Simona, Zecca, Chiara, Barulli, Maria R., Tortelli, Rosanna, Gibbs, Raphael, Crews, Cynthia, Seripa, Davide, Carnicella, Francesco, Dell’Aquila, Claudia, Rossi, Marco, Tamma, Filippo, Valluzzi, Francesco, Brancasi, Bruno, Panza, Francesco, Singleton, Andrew B., Logroscino, Giancarlo
Published in Alzheimers Dement (2017)

Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease()

by Sassi, Celeste, Guerreiro, Rita, Gibbs, Raphael, Ding, Jinhui, Lupton, Michelle K., Troakes, Claire, Lunnon, Katie, Al-Sarraj, Safa, Brown, Kristelle S., Medway, Chirstopher, Lord, Jenny, Turton, James, Mann, David, Snowden, Julie, Neary, David, Harris, Jeniffer, Bras, Jose, Morgan, Kevin, Powell, John F., Singleton, Andrew, Hardy, John
Published 2014

Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease

by Sassi, Celeste, Guerreiro, Rita, Gibbs, Raphael, Ding, Jinhui, Lupton, Michelle K., Troakes, Claire, Al-Sarraj, Safa, Niblock, Michael, Gallo, Jean-Marc, Adnan, Jihad, Killick, Richard, Brown, Kristelle S., Medway, Christopher, Lord, Jenny, Turton, James, Bras, Jose, Morgan, Kevin, Powell, John F., Singleton, Andrew, Hardy, John
Published in Neurobiol Aging (2014)

Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity

by Hammer, Monia B., Eleuch-Fayache, Ghada, Schottlaender, Lucia V., Nehdi, Houda, Gibbs, J. Raphael, Arepalli, Sampath K., Chong, Sean B., Hernandez, Dena G., Sailer, Anna, Liu, Guoxiang, Mistry, Pramod K., Cai, Huaibin, Shrader, Ginamarie, Sassi, Celeste, Bouhlal, Yosr, Houlden, Henry, Hentati, Fayçal, Amouri, Rim, Singleton, Andrew B.
Published 2013

Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer’s Disease

by Sassi, Celeste, Ridge, Perry G., Nalls, Michael A., Gibbs, Raphael, Ding, Jinhui, Lupton, Michelle K., Troakes, Claire, Lunnon, Katie, Al-Sarraj, Safa, Brown, Kristelle S., Medway, Christopher, Lord, Jenny, Turton, James, Morgan, Kevin, Powell, John F., Kauwe, John S., Cruchaga, Carlos, Bras, Jose, Goate, Alison M., Singleton, Andrew B., Guerreiro, Rita, Hardy, John
Published in PLoS One (2016)

TREM2 Variants in Alzheimer's Disease

by Guerreiro, Rita, Wojtas, Aleksandra, Bras, Jose, Carrasquillo, Minerva, Rogaeva, Ekaterina, Majounie, Elisa, Cruchaga, Carlos, Sassi, Celeste, Kauwe, John S.K., Younkin, Steven, Hazrati, Lilinaz, Collinge, John, Pocock, Jennifer, Lashley, Tammaryn, Williams, Julie, Lambert, Jean-Charles, Amouyel, Philippe, Goate, Alison, Rademakers, Rosa, Morgan, Kevin, Powell, John, St. George-Hyslop, Peter, Singleton, Andrew, Hardy, John
Published 2012

A Paired RNAi and RabGAP Overexpression Screen Identifies Rab11 as a Regulator of β-Amyloid Production

by Udayar, Vinod, Buggia-Prévot, Virginie, Guerreiro, Rita L., Siegel, Gabriele, Rambabu, Naresh, Soohoo, Amanda L., Ponnusamy, Moorthi, Siegenthaler, Barbara, Bali, Jitin, Guerreiro, Rita, Brás, José, Sassi, Celeste, Gibbs, J. Raphael, Hernandez, Dena, Lupton, Michelle K., Brown, Kristelle, Morgan, Kevin, Powell, John, Singleton, Andrew, Hardy, John, Simons, Mikael, Ries, Jonas, Puthenveedu, Manojkumar A., Hardy, John, Thinakaran, Gopal, Rajendran, Lawrence
Published 2013

Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3

by Sassi, Celeste, Nalls, Michael A., Ridge, Perry G., Gibbs, Jesse R., Lupton, Michelle K., Troakes, Claire, Lunnon, Katie, Al-Sarraj, Safa, Brown, Kristelle S., Medway, Christopher, Lord, Jenny, Turton, James, Bras, Jose, Blumenau, Sonja, Thielke, Mareike, Josties, Christa, Freyer, Dorette, Dietrich, Annette, Hammer, Monia, Baier, Michael, Dirnagl, Ulrich, Morgan, Kevin, Powell, John F., Kauwe, John S., Cruchaga, Carlos, Goate, Alison M., Singleton, Andrew B., Guerreiro, Rita, Hodges, Angela, Hardy, John
Published in Neurobiol Aging (2018)

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

by Messerschmidt, Clemens, Foddis, Marco, Blumenau, Sonja, Müller, Susanne, Bentele, Kajetan, Holtgrewe, Manuel, Kun-Rodrigues, Celia, Alonso, Isabel, do Carmo Macario, Maria, Morgadinho, Ana Sofia, Velon, Ana Graça, Santo, Gustavo, Santana, Isabel, Mönkäre, Saana, Kuuluvainen, Liina, Schleutker, Johanna, Pöyhönen, Minna, Myllykangas, Liisa, Senatore, Assunta, Berchtold, Daniel, Winek, Katarzyna, Meisel, Andreas, Pavlovic, Aleksandra, Kostic, Vladimir, Dobricic, Valerija, Lohmann, Ebba, Hanagasi, Hasmet, Guven, Gamze, Bilgic, Basar, Bras, Jose, Guerreiro, Rita, Beule, Dieter, Dirnagl, Ulrich, Sassi, Celeste
Published in Sci Rep (2021)

ABCA7 p.G215S as potential protective factor for Alzheimer's disease

by Sassi, Celeste, Nalls, Michael A., Ridge, Perry G., Gibbs, Jesse R., Ding, Jinhui, Lupton, Michelle K., Troakes, Claire, Lunnon, Katie, Al-Sarraj, Safa, Brown, Kristelle S., Medway, Christopher, Clement, Naomi, Lord, Jenny, Turton, James, Bras, Jose, Almeida, Maria R., Holstege, Henne, Louwersheimer, Eva, van der Flier, Wiesje M., Scheltens, Philip, Van Swieten, John C., Santana, Isabel, Oliveira, Catarina, Morgan, Kevin, Powell, John F., Kauwe, John S., Cruchaga, Carlos, Goate, Alison M., Singleton, Andrew B., Guerreiro, Rita, Hardy, John
Published in Neurobiol Aging (2016)

Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

by Ridge, Perry G., Karch, Celeste M., Hsu, Simon, Arano, Ivan, Teerlink, Craig C., Ebbert, Mark T. W., Gonzalez Murcia, Josue D., Farnham, James M., Damato, Anna R., Allen, Mariet, Wang, Xue, Harari, Oscar, Fernandez, Victoria M., Guerreiro, Rita, Bras, Jose, Hardy, John, Munger, Ronald, Norton, Maria, Sassi, Celeste, Singleton, Andrew, Younkin, Steven G., Dickson, Dennis W., Golde, Todd E., Price, Nathan D., Ertekin-Taner, Nilüfer, Cruchaga, Carlos, Goate, Alison M., Corcoran, Christopher, Tschanz, JoAnn, Cannon-Albright, Lisa A., Kauwe, John S. K.
Published in Genome Med (2017)

Correction to: Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

by Ridge, Perry G., Karch, Celeste M., Hsu, Simon, Arano, Ivan, Teerlink, Craig C., Ebbert, Mark T. W., Murcia, Josue D. Gonzalez, Farnham, James M., Damato, Anna R., Allen, Mariet, Wang, Xue, Harari, Oscar, Fernandez, Victoria M., Guerreiro, Rita, Bras, Jose, Hardy, John, Munger, Ronald, Norton, Maria, Sassi, Celeste, Singleton, Andrew, Younkin, Steven G., Dickson, Dennis W., Golde, Todd E., Price, Nathan D., Ertekin-Taner, Nilüfer, Cruchaga, Carlos, Goate, Alison M., Corcoran, Christopher, Tschanz, JoAnn, Cannon-Albright, Lisa A., Kauwe, John S. K.
Published in Genome Med (2018)