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Article

Ahlfors, H; Anyanwu, N; Pakanavicius, E; Dinischiotu, N; Lana-Elola, E; Watson-Scales, S; Tosh, J; ... Tybulewicz, VLJ; + view all (2019) Gene expression dysregulation domains are not a specific feature of Down syndrome. Nature Communications , 10 (1) , Article 2489. 10.1038/s41467-019-10129-9. Green open access
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Akcimen, F; Vural, A; Durmus, H; Cakar, A; Houlden, H; Parman, YG; Basak, AN; (2019) A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID. Journal of Human Genetics , 64 pp. 1141-1144. 10.1038/s10038-019-0652-y. Green open access
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Akram, H; Hariz, M; Zrinzo, L; (2019) Connectivity derived thalamic segmentation: Separating myth from reality. NeuroImage: Clinical , Article 101758. 10.1016/j.nicl.2019.101758. (In press). Green open access
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Al Shareef, SM; Basit, S; Li, S; Pfister, C; Pradervand, S; Lecendreux, M; Mayer, G; ... Tafti, M; + view all (2019) Kleine-Levin syndrome is associated with LMOD3 variants. Journal Of Sleep Research , 28 (3) , Article e12718. 10.1111/jsr.12718. Green open access
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Ambrosini, A; Quinlivan, R; Sansone, VA; Meijer, I; Schrijvers, G; Tibben, A; Padberg, G; ... Zittersteijn, A; + view all (2019) “Be an ambassador for change that you would like to see”: a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscular disease. Orphanet Journal of Rare Diseases , 14 , Article 126. 10.1186/s13023-019-1103-8. Green open access
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Anderhub, SJ; Mak, GW-Y; Gurden, MD; Faisal, A; Drosopoulos, K; Walsh, K; Woodward, HL; ... Linardopoulos, S; + view all (2019) High Proliferation Rate and a Compromised Spindle Assembly Checkpoint Confers Sensitivity to the MPS1 Inhibitor BOS172722 in Triple-Negative Breast Cancers. Molecular Cancer Therapeutics , 18 (10) pp. 1696-1707. 10.1158/1535-7163.MCT-18-1203. Green open access
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Andres-Alonso, M; Ammar, MR; Butnaru, I; Gomes, GM; Sanhueza, GA; Raman, R; Yuanxiang, P; ... Kreutz, MR; + view all (2019) SIPA1L2 controls trafficking and local signaling of TrkB-containing amphisomes at presynaptic terminals. Nature Communications , 10 , Article 5448. 10.1038/s41467-019-13224-z. Green open access
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Asgarian, Z; Magno, L; Ktena, N; Harris, KD; Kessaris, N; (2019) Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA. Stem Cell Reports 10.1016/j.stemcr.2019.09.008. (In press). Green open access
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Atkinson, BN; Steadman, D; Mahy, W; Zhao, Y; Sipthorp, J; Bayle, ED; Svensson, F; ... Fish, PV; + view all (2019) Scaffold-hopping identifies furano[2,3-d]pyrimidine amides as potent Notum inhibitors. Bioorganic & Medicinal Chemistry Letters , Article 126751. 10.1016/j.bmcl.2019.126751. (In press). Green open access
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Atkinson, BN; Steadman, D; Zhao, Y; Sipthorp, J; Vecchia, L; Ruza, RR; Jeganathan, F; ... Fish, PV; + view all (2019) Discovery of 2-phenoxyacetamides as inhibitors of the Wnt-depalmitoleating enzyme NOTUM from an X-ray fragment screen. MedChemComm 10.1039/c9md00096h. (In press). Green open access
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Attig, J; Ule, J; (2019) Genomic Accumulation of Retrotransposons Was Facilitated by Repressive RNA-Binding Proteins: A Hypothesis. Bioessays , Article e1800132. 10.1002/bies.201800132. (In press). Green open access
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Avery, J; Dowrick, T; Witkowska-Wrobel, A; Faulkner, M; Aristovich, KY; Holder, DS; (2019) Simultaneous EIT and EEG using frequency division multiplexing. Physiological Measurement , 40 (3) , Article 034007. 10.1088/1361-6579/ab0bbc. Green open access
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Bachmann, C; Noreen, F; Voermans, NC; Schar, PL; Vissing, J; Fock, JM; Bulk, S; ... Treves, S; + view all (2019) Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies. Human Mutation , 40 (7) pp. 962-974. 10.1002/humu.23745. Green open access
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Bajc Česnik, A; Darovic, S; Prpar Mihevc, S; Štalekar, M; Malnar, M; Motaln, H; Lee, Y-B; ... Rogelj, B; + view all (2019) Nuclear RNA foci from C9ORF72 expansion mutation form paraspeckle-like bodies. Journal of Cell Science , 132 (5) , Article 132: jcs224303. 10.1242/jcs.224303. Green open access
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Balint, B; Charlesworth, G; Stamelou, M; Carr, L; Mencacci, NE; Wood, NW; Bhatia, KP; (2019) Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy. European Journal of Neurology 10.1111/ene.13956. (In press). Green open access
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Bandres-Ciga, S; Ahmed, S; Sabir, MS; Blauwendraat, C; Adarmes-Gomez, AD; Bernal-Bernal, I; Bonilla-Toribio, M; ... Singleton, A; + view all (2019) The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight. Movement Disorders 10.1002/mds.27864. (In press).

Bandres-Ciga, S; Saez-Atienzar, S; Bonet-Ponce, L; Billingsley, K; Vitale, D; Blauwendraat, C; Gibbs, JR; ... Singleton, AB; + view all (2019) The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease. Movement Disorders , 34 (4) pp. 460-468. 10.1002/mds.27614.

Banerjee, G; Adams, ME; Jaunmuktane, Z; Lammie, GA; Turner, B; Wani, M; Sawhney, IMS; ... Werring, DJ; + view all (2019) Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura. Annals of Neurology , 85 (2) pp. 284-290. 10.1002/ana.25407. Green open access
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Belin, S; Ornaghi, F; Shackleford, GG; Wang, J; Scapin, C; Lopez-Anido, C; Silvestri, N; ... Wrabetz, L; + view all (2019) Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy. Human Molecular Genetics , 28 (8) pp. 1260-1273. 10.1093/hmg/ddy420. Green open access
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Bell, S; Rousseau, J; Peng, H; Aouabed, Z; Priam, P; Theroux, J-F; Jefri, M; ... Campeau, PM; + view all (2019) Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics , 104 (5) pp. 815-834. 10.1016/j.ajhg.2019.03.022. Green open access
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Betteridge, Z; Tansley, S; Shaddick, G; Chinoy, H; Cooper, RG; New, RP; Lilleker, JB; ... Winer, J; + view all (2019) Frequency, mutual exclusivity and clinical associations of myositis autoantibodies in a combined European cohort of idiopathic inflammatory myopathy patients. Journal of Autoimmunity , 101 pp. 48-55. 10.1016/j.jaut.2019.04.001. Green open access
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Billingsley, KJ; Barbosa, IA; Bandrés-Ciga, S; Quinn, JP; Bubb, VJ; Deshpande, C; Botia, JA; ... Koks, S; + view all (2019) Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset. npj Parkinson's Disease , 5 , Article 8. 10.1038/s41531-019-0080-x. Green open access
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Bonham, LW; Steele, NZR; Karch, CM; Broce, I; Geier, EG; Wen, NL; Momeni, P; ... International FTD-Genomics Consortium (IFGC), .; + view all (2019) Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia. Scientific Reports , 9 , Article 10854. 10.1038/s41598-019-46415-1. Green open access
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Bray, T; Jones, A; Bennett, A; Conaghan, P; Grainger, A; Hodgson, R; Hutchinson, C; ... Machado, P; + view all (2019) Recommendations for Acquisition and Interpretation of MRI of the Spine and Sacroiliac Joints in the Diagnosis of Axial Spondyloarthritis in the UK. Rheumatology , 58 (10) pp. 1831-1838. 10.1093/rheumatology/kez173. Green open access
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Briese, M; Haberman, N; Sibley, CR; Faraway, R; Elser, AS; Chakrabarti, AM; Wang, Z; ... Ule, J; + view all (2019) A systems view of spliceosomal assembly and branchpoints with iCLIP. Nature Structural and Molecular Biology , 26 (10) pp. 930-940. 10.1038/s41594-019-0300-4. Green open access
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Brittain, C; McCarthy, A; Irizarry, MC; McDermott, D; Biglan, K; Hoglinger, GU; Lorenzl, S; ... Gerpen, JV; + view all (2019) Severity dependent distribution of impairments in PSP and CBS: Interactive visualizations. Parkinsonism & Related Disorders , 60 pp. 138-145. 10.1016/j.parkreldis.2018.08.025. Green open access
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Bromage, DI; Taferner, S; He, Z; Ziff, OJ; Yellon, DM; Davidson, SM; (2019) Stromal cell-derived factor-1α signals via the endothelium to protect the heart against ischaemia-reperfusion injury. Journal of Molecular and Cellular Cardiology , 128 pp. 187-197. 10.1016/j.yjmcc.2019.02.002. Green open access
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Bugai, A; Quaresma, AJC; Friedel, CC; Lenasi, T; Düster, R; Sibley, CR; Fujinaga, K; ... Barborič, M; + view all (2019) P-TEFb Activation by RBM7 Shapes a Pro-survival Transcriptional Response to Genotoxic Stress. Molecular Cell , 74 10.1016/j.molcel.2019.01.033. Green open access
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Bugiardini, E; Khan, A; Phadke, R; Lynch, DS; Cortese, A; Feng, L; Gang, Q; ... Hanna, MG; + view all (2019) Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre. Neuromuscular Disorders , 29 (10) pp. 747-757. 10.1016/j.nmd.2019.08.003. Green open access
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Bugiardini, E; Pope, S; Feichtinger, RG; Poole, OV; Pittman, AM; Woodward, CE; Heales, S; ... Pitceathly, RDS; + view all (2019) Utility of Whole Blood Thiamine Pyrophosphate Evaluation in TPK1-Related Diseases. Journal Of Clinical Medicine , 8 (7) , Article 991. 10.3390/jcm8070991. Green open access
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Calautti, C; Jones, PS; Naccarato, M; Sharma, N; Carpenter, TA; Warburton, EA; Baron, J-C; (2019) Further evidence for a non-cortical origin of mirror movements after stroke. [Letter]. Brain , 142 (1) e1-e1. 10.1093/brain/awy308. Green open access
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Cappon, D; Beigi, M; Kefalopoulou, Z; Zrinzo, L; Candelario, J; Milabo, C; Akram, H; ... Jahanshahi, M; + view all (2019) Globus pallidal deep brain stimulation for Tourette syndrome: Effects on cognitive function. Parkinsonism & Related Disorders , 69 pp. 14-18. 10.1016/j.parkreldis.2019.10.013. Green open access
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Carr, AS; Shah, S; Choi, D; Blake, J; Phadke, R; Gilbertson, J; Whelan, CJ; ... Reilly, MM; + view all (2019) Spinal Stenosis in Familial Transthyretin Amyloidosis. Journal of Neuromuscular Diseases 10.3233/JND-180348. (In press). Green open access
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Carvalho, PD; Ferreira, RJO; Landewé, R; Vega-Morales, D; Salomon-Escoto, K; Veale, DJ; Chopra, A; ... Machado, PM; + view all (2019) Association of seventeen definitions of remission with functional status in a large clinical practice cohort of patients with rheumatoid arthritis. The Journal of Rheumatology , 46 (5) 10.3899/jrheum.181286. Green open access
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Carvalho, PD; Machado, PM; (2019) How to investigate: Early axial spondyloarthritis. Best Practice & Research Clinical Rheumatology , 33 (4) , Article 101427. 10.1016/j.berh.2019.07.001. Green open access
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Castelo-Szekely, V; De Matos, M; Tusup, M; Pascolo, S; Ule, J; Gatfield, D; (2019) Charting DENR-dependent translation reinitiation uncovers predictive uORF features and links to circadian timekeeping via Clock. Nucleic Acids Research , 47 (10) pp. 5193-5209. 10.1093/nar/gkz261. Green open access
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Chan, E; Garritsen, E; Altendorff, S; Turner, D; Simister, R; Werring, DJ; Cipolotti, L; (2019) Additional Queen Square (QS) screening items improve the test accuracy of the Montreal Cognitive Assessment (MoCA) after acute stroke. Journal of the Neurological Sciences , 407 , Article 116442. 10.1016/j.jns.2019.116442. Green open access
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Chelban, V; Alsagob, M; Kloth, K; Chirita-Emandi, A; Vandrovcova, J; Maroofian, R; Davagnanam, I; ... Kaya, N; + view all (2019) Genetic and phenotypic characterization of NKX6-2-related spastic ataxia and hypomyelination. European Journal of Neurology 10.1111/ene.14082. (In press). Green open access
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Chelban, V; Bocchetta, M; Hassanein, S; Haridy, NA; Houlden, H; Rohrer, JD; (2019) An update on advances in magnetic resonance imaging of multiple system atrophy. Journal of Neurology , 266 (4) pp. 1036-1045. 10.1007/s00415-018-9121-3. Green open access
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Chelban, V; Wilson, MP; Warman Chardon, J; Vandrovcova, J; Zanetti, MN; Zamba-Papanicolaou, E; Efthymiou, S; ... SYNaPS Study Group, .; + view all (2019) PDXK mutations cause polyneuropathy responsive to PLP supplementation. Annals of Neurology 10.1002/ana.25524. (In press). Green open access
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Chen, Y; Dolt, KS; Kriek, M; Baker, T; Downey, P; Drummond, NJ; Canham, MA; ... Kunath, T; + view all (2019) Engineering synucleinopathy‐resistant human dopaminergic neurons by CRISPR‐mediated deletion of the SNCA gene. European Journal of Neuroscience , 49 (4) pp. 510-524. 10.1111/ejn.14286. Green open access
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Chen, Z; Houlden, H; Puzriakova, A; (2019) Spinocerebellar Ataxia Type 11. GeneReviews (In press). Green open access
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Chopek, JW; Hultborn, H; Brownstone, RM; (2019) Multistable properties of human subthalamic nucleus neurons in Parkinson's disease. Proceedings of the National Academy of Sciences (PNAS) , 116 (48) pp. 24326-24333. 10.1073/pnas.1912128116. Green open access
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Christopher, E; Poon, MTC; Glancz, LJ; Hutchinson, PJ; Kolias, AG; Brennan, PM; Afshari, FT; ... Zaben, M; + view all (2019) Outcomes following surgery in subgroups of comatose and very elderly patients with chronic subdural hematoma. Neurosurgical Review , 42 (2) 427`-431. 10.1007/s10143-018-0979-4. Green open access
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Ciccarelli, O; Cohen, JA; Reingold, SC; Weinshenker, G; (2019) Spinal cord involvement in multiple sclerosis and neuromyelitis optica spectrum disorders. Lancet Neurology , 18 (2) pp. 185-197. 10.1016/S1474-4422(18)30460-5. Green open access
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Clarke, BE; Gil, RS; Yip, J; Kalmar, B; Greensmith, L; (2019) Regional differences in the inflammatory and heat shock response in glia: implications for ALS. Cell Stress Chaperones 10.1007/s12192-019-01005-y. (In press). Green open access
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Clout, AE; Della Pasqua, O; Hanna, MG; Orlu, M; Pitceathly, RDS; (2019) Drug repurposing in neurological diseases: an integrated approach to reduce trial and error. Journal of Neurology, Neurosurgery and Psychiatry , 90 (11) pp. 1270-1275. 10.1136/jnnp-2019-320879. Green open access
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Coenen, VA; Schlaepfer, TE; Varkuti, B; Schuurman, PR; Reinacher, PC; Voges, J; Zrinzo, L; ... Hariz, M; + view all (2019) Surgical decision making for deep brain stimulation should not be based on aggregated normative data mining. Brain Stimulation 10.1016/j.brs.2019.07.014. (In press). Green open access
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Coleman, JRI; Bryois, J; Gaspar, HA; Jansen, PR; Savage, JE; Skene, N; Plomin, R; ... Breen, G; + view all (2019) Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals. Molecular Psychiatry , 24 pp. 182-197. 10.1038/s41380-018-0040-6. Green open access
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Cortese, A; Simone, R; Sullivan, R; Vandrovcova, J; Tariq, H; Yan, YW; Humphrey, J; ... Houlden, H; + view all (2019) Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia. Nature Genetics , 51 (4) pp. 649-658. 10.1038/s41588-019-0372-4. Green open access
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Cortese, A; Wilcox, JE; Polke, JM; Poh, R; Skorupinska, M; Rossor, AM; Laura, M; ... Reilly, MM; + view all (2019) Targeted next-generation sequencing panels in the diagnosis of Charcot-Marie-Tooth disease. Neurology 10.1212/WNL.0000000000008672. (In press). Green open access
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Craven, CL; Chapman, MD; D'Antona, L; Thompson, SD; Lakdawala, N; Zetterberg, H; Watkins, LD; (2019) Lumbar drains can affect CSF biomarker levels. [Letter]. Journal of Clinical Pathology , 72 (1) pp. 91-92. 10.1136/jclinpath-2018-205296. Green open access
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Crerar, H; Scott-Solomon, E; Bodkin-Clarke, C; Andreassi, C; Hazbon, M; Logie, E; Cano-Jaimez, M; ... Riccio, A; + view all (2019) Regulation of NGF Signaling by an Axonal Untranslated mRNA. Neuron 10.1016/j.neuron.2019.02.011. (In press). Green open access
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D'Antona, L; Matharu, M; (2019) Identifying and managing refractory migraine: barriers and opportunities? The Journal of Headache and Pain , 20 , Article 89. 10.1186/s10194-019-1040-x. Green open access
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D’Antona, L; McHugh, JA; Ricciardi, F; Thorne, LW; Matharu, MS; Watkins, LD; Toma, AK; (2019) Association of Intracranial Pressure and Spontaneous Retinal Venous Pulsation. JAMA Neurology 10.1001/jamaneurol.2019.2935. (In press).

David, G; Mohammadi, S; Martin, AR; Cohen-Adad, J; Weiskopf, N; Thompson, A; Freund, P; (2019) Traumatic and nontraumatic spinal cord injury: pathological insights from neuroimaging. Nature Reviews Neurology , 15 pp. 718-731. 10.1038/s41582-019-0270-5. Green open access
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David, G; Seif, M; Huber, E; Hupp, M; Rosner, J; Dietz, V; Weiskopf, N; ... Freund, P; + view all (2019) In vivo evidence of remote neural degeneration in the lumbar enlargement after cervical injury. Neurology , 92 (12) e1367-e1377. 10.1212/WNL.0000000000007137. Green open access
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Dayal, V; Grover, T; Tripoliti, E; Milabo, C; Salazar, M; Candelario-McKeown, J; Athauda, D; ... Foltynie, T; + view all (2019) Short Versus Conventional Pulse-Width Deep Brain Stimulation in Parkinson's Disease: A Randomized Crossover Comparison. Movement Disorders 10.1002/mds.27863. (In press).

De Giorgio, F; Maduro, C; Fisher, EMC; Acevedo-Arozena, A; (2019) Transgenic and physiological mouse models give insights into different aspects of amyotrophic lateral sclerosis. Disease Models & Mechanisms , 12 (1) , Article dmm037424. 10.1242/dmm.037424. Green open access
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de Paiva, ARB; Lynch, DS; Melo, US; Lucato, LT; Freua, F; de Assis, BDR; Barcelos, I; ... Kok, F; + view all (2019) PUS3 mutations are associated with intellectual disability, leukoencephalopathy, and nephropathy. Neurology Genetics , 5 (1) , Article e306. 10.1212/NXG.0000000000000306. Green open access
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Dias, CM; Punetha, J; Zheng, C; Mazaheri, N; Rad, A; Efthymiou, S; Petersen, A; ... Maroofian, R; + view all (2019) Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. American Journal of Human Genetics , 105 (5) pp. 1048-1056. 10.1016/j.ajhg.2019.09.025. Green open access
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Doneddu, PE; Cocito, D; Manganelli, F; Fazio, R; Briani, C; Filosto, M; Benedetti, L; ... Italian CIDP Database study group; + view all (2019) Atypical CIDP: diagnostic criteria, progression and treatment response. Data from the Italian CIDP Database. Journal of Neurology, Neurosurgery & Psychiatry , 90 (2) pp. 125-132. 10.1136/jnnp-2018-318714. Green open access
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Efthymiou, S; Salpietro, V; Malintan, N; Poncelet, M; Kriouile, Y; Fortuna, S; De Zorzi, R; ... Houlden, H; + view all (2019) Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination. Brain 10.1093/brain/awz248. (In press). Green open access
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Efthymiou, S; Salpietro, V; Pironti, E; Bonsignore, M; Ferrazzoli, V; Di Rosa, G; Houlden, H; (2019) A de novo truncating mutation in ASXL1 associated with segmental overgrowth. Journal of Genetics , 98 (5) , Article 108. 10.1007/s12041-019-1155-5. Green open access
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Elia, N; Palmio, J; Castañeda, MS; Shieh, PB; Quinonez, M; Suominen, T; Hanna, MG; ... Cannon, SC; + view all (2019) Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4. Neurology , 92 e1-e11. 10.1212/WNL.0000000000007185. Green open access
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Faraway, R; Ule, J; (2019) The origin of neural microexons. Nature Ecology & Evolution , 3 pp. 526-527. 10.1038/s41559-019-0818-1. Green open access
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Feeney, CL; Lim, A; Fagan, E; Blain, A; Bright, A; Maddison, J; Devine, H; ... McFarland, R; + view all (2019) A case-comparison study of pregnant women with mitochondrial disease - what to expect. BJOG: An International Journal of Obstetrics & Gynaecology 10.1111/1471-0528.15667. (In press). Green open access
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Ferreira, RJO; Carvalho, PD; Ndosi, M; Duarte, C; Chopra, A; Murphy, E; van der Heijde, D; ... da Silva, JAP; + view all (2019) Impact of patient global assessment on achieving remission in patients with rheumatoid arthritis: a multinational study using the METEOR database. Arthritis Care & Research , 71 (10) pp. 1317-1325. 10.1002/acr.23866. Green open access
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Fish, PV; Steadman, D; Bayle, ED; Whiting, P; (2019) New approaches for the treatment of Alzheimer's disease. Bioorganic & Medicinal Chemistry Letters , 29 (2) pp. 125-133. 10.1016/j.bmcl.2018.11.034. Green open access
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Fisher, EMC; Bannerman, DM; (2019) Mouse models of neurodegeneration: Know your question, know your mouse. Science Translational Medicine , 11 (493) , Article eaaq1818. 10.1126/scitranslmed.aaq1818. Green open access
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Forstner, AJ; Awasthi, S; Wolf, C; Maron, E; Erhardt, A; Czamara, D; Eriksson, E; ... Schumacher, J; + view all (2019) Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. Molecular Psychiatry 10.1038/s41380-019-0590-2. (In press). Green open access
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Foti, S; Hargreaves, I; Carrington, S; Kiely, AP; Houlden, H; Holton, J; (2019) Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson’s disease. Scientific Reports , 9 , Article 6559. 10.1038/s41598-019-42902-7. Green open access
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Fratta, P; Ornaghi, F; Dati, G; Zambroni, D; Saveri, P; Belin, S; D'Adamo, P; ... Wrabetz, L; + view all (2019) A nonsense mutation in Myelin Protein Zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function. Human Molecular Genetics , 28 (1) pp. 124-132. 10.1093/hmg/ddy336. Green open access
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Giagkou, N; Bhatia, KP; Höglinger, GU; Stamelou, M; (2019) Chapter Thirteen - Genetic mimics of the non-genetic atypical parkinsonian disorders – the ‘atypical’ atypical. International Review of Neurobiology , 149 pp. 327-351. 10.1016/bs.irn.2019.10.008.

GlobalSurg Collaborative; (2019) Global variation in anastomosis and end colostomy formation following left-sided colorectal resection. BJS Open , 3 (3) pp. 403-414. 10.1002/bjs5.50138. Green open access
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Glover, IS; Baker, SN; (2019) Multimodal stimuli modulate rapid visual responses during reaching. Journal of Neurophysiology , 122 (5) pp. 1894-1908. 10.1152/jn.00158.2019. Green open access
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Gomes, C; Cunha, C; Nascimento, F; Ribeiro, JA; Vaz, AR; Brites, D; (2019) Cortical Neurotoxic Astrocytes with Early ALS Pathology and miR-146a Deficit Replicate Gliosis Markers of Symptomatic SOD1G93A Mouse Model. Molecular Neurobiology , 56 (3) pp. 2137-2158. 10.1007/s12035-018-1220-8. Green open access
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Gomez-Suaga, P; Perez-Nievas, BG; Glennon, EB; Lau, DHW; Paillusson, S; Morotz, GM; Cali, T; ... Miller, CCJ; + view all (2019) The VAPB-PTPIP51 endoplasmic reticulum-mitochondria tethering proteins are present in neuronal synapses and regulate synaptic activity. Acta Neuropathologica Communications , 7 , Article 35. 10.1186/s40478-019-0688-4. Green open access
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Goto-Silva, L; McShane, MP; Salinas, S; Kalaidzidis, Y; Schiavo, G; Zerial, M; (2019) Retrograde transport of Akt by a neuronal Rab5-APPL1 endosome. Scientific Reports , 9 (1) , Article 2433. 10.1038/s41598-019-38637-0. Green open access
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Granger, N; Luján Feliu-Pascual, A; Spicer, C; Ricketts, S; Hitti, R; Forman, O; Hersheson, J; (2019) Charcot-Marie-Tooth type 4B2 demyelinating neuropathy in miniature Schnauzer dogs caused by a novel splicing SBF2 (MTMR13) genetic variant: a new spontaneous clinical model. PeerJ , 7 , Article e7983. 10.7717/peerj.7983. Green open access
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Granno, S; Nixon-Abell, J; Berwick, DC; Tosh, J; Heaton, G; Almudimeegh, S; Nagda, Z; ... Harvey, K; + view all (2019) Downregulated Wnt/β-catenin signalling in the Down syndrome hippocampus. Scientific Reports , 9 (1) , Article 7322. 10.1038/s41598-019-43820-4. Green open access
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