Kết quả tìm kiếm - Celeste Sassi

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  1. 1
    Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity

    Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity Bằng Monia Hammer, Ghada Eleuch-Fayache, Lucía Schottlaender, Houda Nehdi, J. Raphael Gibbs, Sampath K. Arepalli, Sean Chong, Dena Hernández, Anna Sailer, Guoxiang Liu, Pramod K. Mistry, Huaibin Cai, Ginamarie Shrader, Celeste Sassi, Yosr Bouhlal, Henry Houlden, Fayçal Hentati, Rim Amouri, Andrew B. Singleton

    Được phát hành 2013
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    Artigo
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  2. 2
    Investigating the role of rare coding variability in Mendelian dementia genes ( APP , PSEN1 , PSEN2 , GRN , MAPT , and PRNP ) in late-onset Alzheimer's disease

    Investigating the role of rare coding variability in Mendelian dementia genes ( APP , PSEN1 , PSEN2 , GRN , MAPT , and PRNP ) in late-onset Alzheimer's disease Bằng Celeste Sassi, Rita Guerreiro, J. Raphael Gibbs, Joshua Shulman, Michelle K. Lupton, Claire Troakes, Safa Al‐Sarraj, Michael Niblock, Jean‐Marc Gallo, Jihad Adnan, Richard Killick, Kristelle Brown, Christopher Medway, Jenny Lord, James Turton, José Brás, Kevin Morgan, John Powell, Andrew Singleton, John Hardy

    Được phát hành 2014
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    Artigo
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  3. 3
    <i>TREM2</i> Variants in Alzheimer's Disease

    <i>TREM2</i> Variants in Alzheimer's Disease Bằng Rita Guerreiro, Aleksandra Wojtas, José Brás, Minerva M. Carrasquillo, Ekaterina Rogaeva, Elisa Majounie, Carlos Cruchaga, Celeste Sassi, John Kauwe, Steven G. Younkin, Lili‐Naz Hazrati, John Collinge, Jennifer M. Pocock, Tammaryn Lashley, Julie Williams, Jean‐Charles Lambert, Philippe Amouyel, Alison Goate, Rosa Rademakers, Kevin Morgan, John Powell, Peter St George‐Hyslop, Andrew Singleton, John Hardy

    Được phát hành 2012
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    Revisão
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  4. 4
    A Paired RNAi and RabGAP Overexpression Screen Identifies Rab11 as a Regulator of β-Amyloid Production

    A Paired RNAi and RabGAP Overexpression Screen Identifies Rab11 as a Regulator of β-Amyloid Production Bằng Vinod Udayar, Virginie Buggia-Prévot, Rita Guerreiro, Gabriele Siegel, Naresh Rambabu, Amanda L. Soohoo, Moorthi Ponnusamy, Barbara Siegenthaler, Jitin Bali, Mikael Simons, Jonas Ries, Manojkumar A. Puthenveedu, John Hardy, Gopal Thinakaran, Lawrence Rajendran, Rita Guerreiro, José Brás, Celeste Sassi, J. Raphael Gibbs, Dena Hernández, Michelle K. Lupton, Kristelle Brown, Kevin Morgan, John Powell, Andrew Singleton, John G. Hardy

    Được phát hành 2013
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    Artigo
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  5. 5
    Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience

    Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer’s disease resilience Bằng Perry G. Ridge, Celeste M. Karch, Simon Hsu, Ivan Arano, Craig C. Teerlink, Mark Ebbert, Josue D. Gonzalez Murcia, James M. Farnham, Anna R. Damato, Mariet Allen, Xue Wang, Oscar Harari, Victoria M. Fernandez, Rita Guerreiro, José Brás, John Hardy, Ronald G. Munger, Maria C. Norton, Celeste Sassi, Andrew Singleton, Steven G. Younkin, Dennis W. Dickson, Todd E. Golde, Nathan D. Price, Nilüfer Ertekin‐Taner, Carlos Cruchaga, Alison Goate, Christopher Corcoran, JoAnn T. Tschanz, Lisa Cannon‐Albright, John Kauwe

    Được phát hành 2017
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    Artigo
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  6. 6
    Missense variant in TREML2 protects against Alzheimer's disease

    Missense variant in TREML2 protects against Alzheimer's disease Bằng Bruno A. Benítez, Sheng Chih Jin, Rita Guerreiro, Rob Graham, Jenny Lord, Denise Harold, Rebecca Sims, Jean‐Charles Lambert, J. Raphael Gibbs, José Brás, Celeste Sassi, Oscar Harari, Sarah Bertelsen, Michelle K. Lupton, John Powell, Céline Bellenguez, Kristelle Brown, Christopher Medway, Patrick C. G. Haddick, Marcel P. van der Brug, Tushar Bhangale, Ward Ortmann, Tim Behrens, Richard Mayeux, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Gerard D. Schellenberg, Jonathan L. Haines, James Turton, Anne Braae, Imelda Barber, Anne M. Fagan, David M. Holtzman, John C. Morris, Julie Williams, John S.K. Kauwe, Philippe Amouyel, Kevin Morgan, Andy Singleton, John Hardy, Alison Goate, Carlos Cruchaga

    Được phát hành 2013
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    Artigo
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  7. 7
    Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3

    Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3 Bằng Celeste Sassi, Michael A. Nalls, Perry G. Ridge, J. Raphael Gibbs, Michelle K. Lupton, Claire Troakes, Katie Lunnon, Safa Al‐Sarraj, Kristelle Brown, Christopher Medway, Jenny Lord, James Turton, José Brás, Sonja Blumenau, Mareike Thielke, Christa Josties, Dorette Freyer, A. Dietrich, Monia Hammer, Michael Baier, Ulrich Dirnagl, Kevin Morgan, John Powell, John S.K. Kauwe, Carlos Cruchaga, Alison Goate, Andrew B. Singleton, Rita Guerreiro, Angela Hodges, John Hardy, Peter Passmore, David Craig, Janet M. Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Emma Vardy, Nigel M. Hooper, David Mann, Stuart Pickering‐Brown, Kristelle Brown, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes

    Được phát hành 2018
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    Artigo
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  8. 8
    ABCA7 p.G215S as potential protective factor for Alzheimer's disease

    ABCA7 p.G215S as potential protective factor for Alzheimer's disease Bằng Celeste Sassi, Michael A. Nalls, Perry G. Ridge, J. Raphael Gibbs, Joshua Shulman, Michelle K. Lupton, Claire Troakes, Katie Lunnon, Safa Al‐Sarraj, Kristelle Brown, Christopher Medway, Naomi Clement, Jenny Lord, James Turton, José Brás, Maria Rosário Almeida, Henne Holstege, Eva Louwersheimer, Wiesje M. van der Flier, Philip Scheltens, John C. van Swieten, Isabel Santana, Catarina R. Oliveira, Kevin Morgan, John Powell, John S.K. Kauwe, Carlos Cruchaga, Alison Goate, Andrew B. Singleton, Rita Guerreiro, John Hardy, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Emma Vardy, Nigel M. Hooper, David Mann, Stuart Pickering‐Brown, Kristelle Brown, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes

    Được phát hành 2016
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    Artigo
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  9. 9
    Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

    Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease Bằng Carlos Cruchaga, Celeste M. Karch, Sheng Chih Jin, Bruno A. Benítez, Yefei Cai, Rita Guerreiro, Oscar Harari, Joanne Norton, John Budde, Sarah Bertelsen, Amanda T. Jeng, Breanna Cooper, Tara Skorupa, David Carrell, Denise Levitch, Simon Hsu, Jiyoon Choi, Mina Ryten, John Hardy, Mina Ryten, Daniah Trabzuni, Michael E. Weale, Adaikalavan Ramasamy, Colin Smith, Celeste Sassi, José Brás, J. Raphael Gibbs, Dena G. Hernandez, Michelle K. Lupton, John Powell, Paola Forabosco, Perry G. Ridge, Christopher Corcoran, JoAnn T. Tschanz, Maria C. Norton, Ronald G. Munger, Cameron Schmutz, Maegan Leary, F. Yesim Demirci, Mikhil Bamne, Xingbin Wang, Oscar L. López, Mary Ganguli, Christopher Medway, James Turton, Jenny Lord, Anne Braae, Imelda Barber, Kristelle Brown, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, David Mann, Stuart Pickering‐Brown, Kristelle Brown, Noor Kalsheker, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes, Pau Pástor, Oswaldo Lorenzo‐Betancor, Zoran Brkanac, Erick R. Scott, Eric J. Topol, Kevin Morgan, Ekaterina Rogaeva, Andrew B. Singleton, John Hardy, M. Ilyas Kamboh, Peter St George‐Hyslop, Nigel J. Cairns, John C. Morris, John Kauwe, Alison Goate

    Được phát hành 2013
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    Artigo
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