Browse by UCL people
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Number of items: 6.
Article
Brown, EE;
Blauwendraat, C;
Trinh, J;
Rizig, M;
Nalls, MA;
Leveille, E;
Ruskey, JA;
... International Parkinson Disease Genomics Consortium (IPDGC); + view all
(2020)
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease.
Neurobiology of Aging
10.1016/j.neurobiolaging.2020.07.002.
(In press).
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Chelban, V;
Tucci, A;
Lynch, DS;
Polke, JM;
Santos, L;
Jonvik, H;
Groppa, S;
... Houlden, H; + view all
(2017)
Truncating mutations in SPAST patients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia.
Journal of Neurology Neurosurgery and Psychiatry
, 88
(8)
10.1136/jnnp-2017-315796.
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McManus, IC;
Jonvik, H;
Richards, P;
Paice, E;
(2011)
Vocation and avocation: leisure activities correlate with professional engagement, but not burnout, in a cross-sectional survey of UK doctors.
BMC Medicine
, 9
, Article 100. 10.1186/1741-7015-9-100.
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Okubadejo, NU;
Rizig, M;
Ojo, OO;
Jonvik, H;
Oshinaike, O;
Brown, E;
Houlden, H;
(2018)
Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson disease.
PLOS ONE
, 13
(12)
, Article e0207984. 10.1371/journal.pone.0207984.
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Poole, OV;
Pizzamiglio, C;
Murphy, D;
Falabella, M;
Macken, WL;
Bugiardini, E;
Woodward, CE;
... Pitceathly, RDS; + view all
(2021)
Mitochondrial DNA analysis from exome sequencing data improves the diagnostic yield in neurological diseases.
Annals of Neurology
10.1002/ana.26063.
(In press).
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Wilson, Lindsay A;
Macken, William L;
Perry, Luke D;
Record, Christopher J;
Schon, Katherine R;
Frezatti, Rodrigo SS;
Raga, Sharika;
... Hanna, Michael G; + view all
(2023)
Neuromuscular disease genetics in under-represented populations: increasing data diversity.
Brain
, Article awad254. 10.1093/brain/awad254.
(In press).
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