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Lara Menzies
Lara Menzies
Clinical Genetics Consultant, Great Ormond Street Hospital
Bestätigte E-Mail-Adresse bei nhs.net
Titel
Zitiert von
Zitiert von
Jahr
Integrating evidence from neuroimaging and neuropsychological studies of obsessive-compulsive disorder: the orbitofronto-striatal model revisited
L Menzies, SR Chamberlain, AR Laird, SM Thelen, BJ Sahakian, ...
Neuroscience & Biobehavioral Reviews 32 (3), 525-549, 2008
13512008
The neuropsychology of obsessive compulsive disorder: the importance of failures in cognitive and behavioural inhibition as candidate endophenotypic markers
SR Chamberlain, AD Blackwell, NA Fineberg, TW Robbins, BJ Sahakian
Neuroscience & Biobehavioral Reviews 29 (3), 399-419, 2005
10872005
Probing compulsive and impulsive behaviors, from animal models to endophenotypes: a narrative review
NA Fineberg, MN Potenza, SR Chamberlain, HA Berlin, L Menzies, ...
Neuropsychopharmacology 35 (3), 591-604, 2010
7072010
Orbitofrontal dysfunction in patients with obsessive-compulsive disorder and their unaffected relatives
SR Chamberlain, L Menzies, A Hampshire, J Suckling, NA Fineberg, ...
Science 321 (5887), 421-422, 2008
6262008
Neurocognitive endophenotypes of obsessive-compulsive disorder
L Menzies, S Achard, SR Chamberlain, N Fineberg, CH Chen, ...
Brain 130 (12), 3223-3236, 2007
5522007
Impaired cognitive flexibility and motor inhibition in unaffected first-degree relatives of patients with obsessive-compulsive disorder
SR Chamberlain, NA Fineberg, LA Menzies, AD Blackwell, ET Bullmore, ...
American Journal of Psychiatry 164 (2), 335-338, 2007
5192007
White matter abnormalities in patients with obsessive-compulsive disorder and their first-degree relatives
L Menzies, GB Williams, SR Chamberlain, C Ooi, N Fineberg, J Suckling, ...
American Journal of Psychiatry 165 (10), 1308-1315, 2008
2352008
Tryptophan depletion disrupts the motivational guidance of goal-directed behavior as a function of trait impulsivity
R Cools, A Blackwell, L Clark, L Menzies, S Cox, TW Robbins
Neuropsychopharmacology 30 (7), 1362-1373, 2005
1772005
Endophenotypes of obsessive–compulsive disorder: rationale, evidence and future potential
SR Chamberlain, L Menzies
Expert review of neurotherapeutics 9 (8), 1133-1146, 2009
1632009
Grey matter abnormalities in trichotillomania: morphometric magnetic resonance imaging study
SR Chamberlain, LA Menzies, NA Fineberg, N Del Campo, J Suckling, ...
The British Journal of Psychiatry 193 (3), 216-221, 2008
1392008
Lifting the veil on trichotillomania
SR Chamberlain, L Menzies, BJ Sahakian, NA Fineberg
American Journal of Psychiatry 164 (4), 568-574, 2007
1292007
Effects of γ-aminobutyric acid–modulating drugs on working memory and brain function in patients with schizophrenia
L Menzies, C Ooi, S Kamath, J Suckling, P McKenna, P Fletcher, ...
Archives of general psychiatry 64 (2), 156-167, 2007
1232007
The effects of puberty on white matter development in boys
L Menzies, AL Goddings, KJ Whitaker, SJ Blakemore, RM Viner
Developmental cognitive neuroscience 11, 116-128, 2015
902015
Reduced brain white matter integrity in trichotillomania: a diffusion tensor imaging study
SR Chamberlain, A Hampshire, LA Menzies, E Garyfallidis, JE Grant, ...
Archives of General Psychiatry 67 (9), 965-971, 2010
902010
Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
K Ibañez, J Polke, RT Hagelstrom, E Dolzhenko, D Pasko, ERA Thomas, ...
The Lancet Neurology 21 (3), 234-245, 2022
892022
Nucleocytoplasmic transport of the RNA-binding protein CELF2 regulates neural stem cell fates
MJ MacPherson, SL Erickson, D Kopp, P Wen, MR Aghanoori, S Kedia, ...
Cell Reports 35 (10), 2021
192021
Pediatric epilepsy surgery from 2000 to 2018: Changes in referral and surgical volumes, patient characteristics, genetic testing, and postsurgical outcomes
MH Eriksson, KJ Whitaker, J Booth, RJ Piper, A Chari, P Martin Sanfilippo, ...
Epilepsia 64 (9), 2260-2273, 2023
152023
Genotype–phenotype correlation at codon 1740 of SETD2
R Rabin, A Radmanesh, IA Glass, WB Dobyns, KA Aldinger, JT Shieh, ...
American Journal of Medical Genetics Part A 182 (9), 2037-2048, 2020
142020
L1CAM variants cause two distinct imaging phenotypes on fetal MRI
A Accogli, S Goergen, G Izzo, K Mankad, K Krajden Haratz, C Parazzini, ...
Annals of clinical and translational neurology 8 (10), 2004-2012, 2021
112021
The effects of puberty on white matter development in boys. Dev. Cogn. Neurosci. 11, 116–128
L Menzies, AL Goddings, KJ Whitaker, SJ Blakemore, RM Viner
92015
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