Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease

Lesage, Suzanne ; Bras, Jose ; Cormier-Dequaire, Florence ; Condroyer, Christel ; Nicolas, Aude ; Darwent, Lee ; Guerreiro, Rita ; Majounie, Elisa ; Federoff, Monica ; Heutink, Peter ; Wood, Nicholas W ; Gasser, Thomas ; Hardy, John ; Tison, François ; Singleton, Andrew ; Brice, Alexis

United States: American Academy of Neurology

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Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

Paisán-Ruiz, Coro ; Guevara, Rocio ; Federoff, Monica ; Hanagasi, Hasmet ; Sina, Fardaz ; Elahi, Elahe ; Schneider, Susanne A. ; Schwingenschuh, Petra ; Bajaj, Nin ; Emre, Murat ; Singleton, Andrew B. ; Hardy, John ; Bhatia, Kailash P. ; Brandner, Sebastian ; Lees, Andrew J. ; Houlden, Henry

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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Correction of depression‐associated circadian rhythm abnormalities is associated with lithium response in bipolar disorder

Federoff, Monica ; McCarthy, Michael J. ; Anand, Amit ; Berrettini, Wade H. ; Bertram, Holli ; Bhattacharjee, Abesh ; Calkin, Cynthia V. ; Conroy, Carla ; Coryell, William H. ; D'Arcangelo, Nicole ; DeModena, Anna ; Fisher, Carrie ; Feeder, Scott ; Frazier, Nicole ; Frye, Mark A. ; Gao, Keming ; Garnham, Julie ; Gershon, Elliot S. ; Alliey‐Rodriguez, Ney ; Glazer, Kara ; Goes, Fernando ; Karberg, Toyomi ; Harrington, Gloria ; Jakobsen, Petter ; Kamali, Masoud ; Kelly, Marisa ; Leckband, Susan G. ; Lohoff, Falk ; Maihofer, Adam X. ; McInnis, Melvin G. ; Mondimore, Francis ; Morken, Gunnar ; Nurnberger, John I. ; Oedegaard, Ketil J. ; Ritchey, Megan ; Ryan, Kelly ; Schinagle, Martha ; Schoeyen, Helle ; Schwebel, Candice ; Shaw, Martha ; Shilling, Paul D. ; Slaney, Claire ; Stautland, Andrea ; Tarwater, Bruce ; Calabrese, Joseph R. ; Alda, Martin ; Nievergelt, Caroline M. ; Zandi, Peter P. ; Kelsoe, John R.

Denmark: Wiley Subscription Services, Inc

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LRP10 in α-synucleinopathies

Pihlstrøm, Lasse ; Schottlaender, Lucia ; Chelban, Viorica ; Houlden, Henry ; Al-Sarraj, Safa ; Arzberger, Thomas ; Bettencourt, Conceicao ; Bhatia, Kailash ; Dickson, Dennis W ; Federoff, Monica ; Gelpi, Ellen ; Gentleman, Steve ; Hardy, John ; Holton, Janice ; Huitinga, Inge ; Levey, Allan ; Mann, David ; Meissner, Wassilios ; Morris, Huw ; Morris, Chris ; Pittman, Alan ; Rascol, Olivier ; Riederer, Peter ; Rogaeva, Ekaterina ; Ross, Owen ; Scholtz, Sonja ; Singleton, Andrew B ; Trojanowski, John ; Vandrovcova, Jana ; Warner, Tom ; Wood, Nick

England: Elsevier Ltd

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ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies

Blauwendraat, Cornelis ; Nalls, Mike A. ; Federoff, Monica ; Pletnikova, Olga ; Ding, Jinhui ; Letson, Christopher ; Geiger, Joshua T. ; Gibbs, J. Raphael ; Hernandez, Dena G. ; Troncoso, Juan C. ; Simón‐Sánchez, Javier ; Scholz, Sonja W.

United States: Wiley Subscription Services, Inc

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Lack of replication of association between GIGYF2 variants and Parkinson disease

Bras, Jose ; Simón-Sánchez, Javier ; Federoff, Monica ; Morgadinho, Ana ; Januario, Cristina ; Ribeiro, Maria ; Cunha, Luis ; Oliveira, Catarina ; Singleton, Andrew B.

Oxford: Oxford University Press

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ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies: Mutational Analysis In ADORA1

Blauwendraat, Cornelis ; Nalls, Mike A. ; Federoff, Monica ; Pletnikova, Olga ; Ding, Jinhui ; Letson, Christopher ; Geiger, Joshua T. ; Gibbs, J. Raphael ; Hernandez, Dena G. ; Troncoso, Juan C. ; Simón-Sánchez, Javier ; Scholz, Sonja W.

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Genetic and phenotypic characterization of complex hereditary spastic paraplegia

Kara, Eleanna ; Tucci, Arianna ; Manzoni, Claudia ; Lynch, David S ; Elpidorou, Marilena ; Bettencourt, Conceicao ; Chelban, Viorica ; Manole, Andreea ; Hamed, Sherifa A ; Haridy, Nourelhoda A ; Federoff, Monica ; Preza, Elisavet ; Hughes, Deborah ; Pittman, Alan ; Jaunmuktane, Zane ; Brandner, Sebastian ; Xiromerisiou, Georgia ; Wiethoff, Sarah ; Schottlaender, Lucia ; Proukakis, Christos ; Morris, Huw ; Warner, Tom ; Bhatia, Kailash P ; Korlipara, L.V. Prasad ; Singleton, Andrew B ; Hardy, John ; Wood, Nicholas W ; Lewis, Patrick A ; Houlden, Henry

Oxford University Press 2016

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Multiple System Atrophy: Moving towards a Multi-mechanistic Hypothesis

Federoff, Monica

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Early-Onset L-dopa-Responsive Parkinsonism with Pyramidal Signs Due to ATP13A2, PLA2G6, FBX07 and Spatacsin Mutations

PAISAN-RUIZ, Coro ; GUEVARA, Rocio ; SINGLETON, Andrew B ; HARDY, John ; BHATIA, Kailash P ; BRANDNER, Sebastian ; LEES, Andrew J ; HOULDEN, Henry ; FEDEROFF, Monica ; HANAGASI, Hasmet ; SINA, Fardaz ; ELAHI, Elahe ; SCHNEIDER, Susanne A ; SCHWINGENSCHUH, Petra ; BAJAJ, Nin ; EMRE, Murat

Hoboken, NJ: Wiley

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