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Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes
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Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes

Reid, Emma S ; Papandreou, Apostolos ; Drury, Suzanne ; Boustred, Christopher ; Yue, Wyatt W ; Wedatilake, Yehani ; Beesley, Clare ; Jacques, Thomas S ; Anderson, Glenn ; Abulhoul, Lara ; Broomfield, Alex ; Cleary, Maureen ; Grunewald, Stephanie ; Varadkar, Sophia M ; Lench, Nick ; Rahman, Shamima ; Gissen, Paul ; Clayton, Peter T ; Mills, Philippa B

Brain (London, England : 1878), 2016-11, Vol.139 (11), p.2844-2854 [Periódico revisado por pares]

England: Oxford University Press

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2
Expected value and prediction error abnormalities in depression and schizophrenia
Expected value and prediction error abnormalities in depression and schizophrenia
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Expected value and prediction error abnormalities in depression and schizophrenia

GRADIN, Victoria B ; KUMAR, Poornima ; WAITER, Gordon ; AHEARN, Trevor ; STICKLE, Catriona ; MILDERS, Marteen ; REID, Ian ; HALL, Jeremy ; STEELE, J. Douglas

Brain (London, England : 1878), 2011-06, Vol.134 (Pt 6), p.1751-1764 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Abnormal temporal difference reward-learning signals in major depression
Abnormal temporal difference reward-learning signals in major depression
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Abnormal temporal difference reward-learning signals in major depression

Kumar, P. ; Waiter, G. ; Ahearn, T. ; Milders, M. ; Reid, I. ; Steele, J. D.

Brain (London, England : 1878), 2008-08, Vol.131 (8), p.2084-2093 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
Progressive agrammatic aphasia without apraxia of speech as a distinct syndrome
Progressive agrammatic aphasia without apraxia of speech as a distinct syndrome
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Progressive agrammatic aphasia without apraxia of speech as a distinct syndrome

Tetzloff, Katerina A ; Duffy, Joseph R ; Clark, Heather M ; Utianski, Rene L ; Strand, Edythe A ; Machulda, Mary M ; Botha, Hugo ; Martin, Peter R ; Schwarz, Christopher G ; Senjem, Matthew L ; Reid, Robert I ; Gunter, Jeffrey L ; Spychalla, Anthony J ; Knopman, David S ; Petersen, Ronald C ; Jack, Clifford R ; Lowe, Val J ; Josephs, Keith A ; Whitwell, Jennifer L

Brain (London, England : 1878), 2019-08, Vol.142 (8), p.2466-2482 [Periódico revisado por pares]

England: Oxford University Press

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5
The evolution of primary progressive apraxia of speech
The evolution of primary progressive apraxia of speech
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The evolution of primary progressive apraxia of speech

JOSEPHS, Keith A ; DUFFY, Joseph R ; JACK, Clifford R ; WHITWELL, Jennifer L ; STRAND, Edythe A ; MACHULDA, Mary M ; SENJEM, Matthew L ; GUNTER, Jeffrey L ; SCHWARZ, Christopher G ; REID, Robert I ; SPYCHALLA, Anthony J ; LOWE, Val J

Brain (London, England : 1878), 2014-10, Vol.137 (Pt 10), p.2783-2795 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
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The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease

Bandopadhyay, Rina ; Kingsbury, Ann E. ; Cookson, Mark R. ; Reid, Andrew R. ; Evans, Ian M. ; Hope, Andrew D. ; Pittman, Alan M. ; Lashley, Tammaryn ; Canet‐Aviles, Rosa ; Miller, David W. ; McLendon, Chris ; Strand, Catherine ; Leonard, Andrew J. ; Abou‐Sleiman, Patrick M. ; Healy, Daniel G. ; Ariga, Hiroyashi ; Wood, Nicholas W. ; de Silva, Rohan ; Revesz, Tamas ; Hardy, John A. ; Lees, Andrew J.

Brain (London, England : 1878), 2004-02, Vol.127 (2), p.420-430 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathy
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathy
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Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathy

Bleakley, Lauren E ; McKenzie, Chaseley E ; Soh, Ming S ; Forster, Ian C ; Pinares-Garcia, Paulo ; Sedo, Alicia ; Kathirvel, Anirudh ; Churilov, Leonid ; Jancovski, Nikola ; Maljevic, Snezana ; Berkovic, Samuel F ; Scheffer, Ingrid E ; Petrou, Steven ; Santoro, Bina ; Reid, Christopher A

Brain (London, England : 1878), 2021-08, Vol.144 (7), p.2060-2073 [Periódico revisado por pares]

England: Oxford University Press

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8
Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy
Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy
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Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy

Abela, Lucia ; Gianfrancesco, Lorita ; Tagliatti, Erica ; Rossignoli, Giada ; Barwick, Katy ; Zourray, Clara ; Reid, Kimberley M ; Budinger, Dimitri ; Ng, Joanne ; Counsell, John ; Simpson, Arlo ; Pearson, Toni S ; Edvardson, Simon ; Elpeleg, Orly ; Brodsky, Frances M ; Lignani, Gabriele ; Barral, Serena ; Kurian, Manju A

Brain (London, England : 1878), 2024-06, Vol.147 (6), p.2023-2037 [Periódico revisado por pares]

England: Oxford University Press

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9
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia
Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia
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Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia

Newton, Timothy ; Allison, Rachel ; Edgar, James R ; Lumb, Jennifer H ; Rodger, Catherine E ; Manna, Paul T ; Rizo, Tania ; Kohl, Zacharias ; Nygren, Anders O H ; Arning, Larissa ; Schüle, Rebecca ; Depienne, Christel ; Goldberg, Lisa ; Frahm, Christiane ; Stevanin, Giovanni ; Durr, Alexandra ; Schöls, Ludger ; Winner, Beate ; Beetz, Christian ; Reid, Evan

Brain (London, England : 1878), 2018-05, Vol.141 (5), p.1286-1299 [Periódico revisado por pares]

England: Oxford University Press

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10
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome
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Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

Masellis, Mario ; Momeni, Parastoo ; Meschino, Wendy ; Heffner, Reid ; Elder, Joshua ; Sato, Christine ; Liang, Yan ; George-Hyslop, Peter St ; Hardy, John ; Bilbao, Juan ; Black, Sandra ; Rogaeva, Ekaterina

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3115-3123 [Periódico revisado por pares]

Oxford: Oxford University Press

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