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Number of items: 173.

A

Abramov, AY and Duchen, MR (2008) Mechanisms underlying the loss of mitochondrial membrane potential in glutamate excitotoxicity. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS , 1777 (7-8) 953 - 964. 10.1016/j.bbabio.2008.04.017.

Abramov, AY and Kasymov, VA and Zinchenko, VP (2008) Beta amyloid activates synthesis of nitric oxide in hyppocampal astrocytes and causes death of neurons. BIOL MEMBRANY , 25 (1) 11 - 17.

Aschar-Sobbi, R and Abramov, AY and Diao, C and Kargacin, ME and Kargacin, GJ and French, RJ and Pavlov, E (2008) High sensitivity, quantitative measurements of polyphosphate using a new DAPI-Based approach. J FLUORESC , 18 (5) 859 - 866. 10.1007/s10895-008-0315-4.

B

Bandopadhyay, R and Kumaran, R and Vandrovcova, J and Kingsbury, A and Lees, A (2008) DJ-1 (PARK7) mRNA levels in idiopathic Parkinson's disease. In: MOVEMENT DISORDERS. (pp. S11 - S11). WILEY-LISS

Baum, AE and Akula, N and Cabanero, M and Cardona, I and Corona, W and Klemens, B and Schulze, TG and Cichon, S and Rietschel, M and Noethen, MM and Georgi, A and Schumacher, J and Schwarz, M and Abou Jamra, R and Hoefels, S and Propping, P and Satagopan, J and Detera-Wadleigh, SD and Hardy, J and McMahon, FJ and Bipolar, NIMHGI (2008) A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. MOLECULAR PSYCHIATRY , 13 (2) 197 - 207. 10.1038/sj.mp.4002012.

Beck, J and Rohrer, JD and Campbell, T and Isaacs, A and Morrison, KE and Goodall, EF and Warrington, EK and Stevens, J and Revesz, T and Holton, J and Al-Sarraj, S and King, A and Scahill, R and Warren, JD and Fox, NC and Rossor, MN and Collinge, J and Mead, S (2008) A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. BRAIN , 131 706 - 720. 10.1093/brain/awm320.
An open access publication

Bennett, DLH and Groves, M and Blake, J and Holton, JL and King, RHM and Orrell, RW and Ginsberg, L and Reilly, MM (2008) The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study. J NEUROL NEUROSUR PS , 79 (12) 1376 - 1381.

Bertfield, DL and Jumma, O and Pitceathly, RDS and Sussman, JD (2008) Copper deficiency: an unusual case of myelopathy with neuropathy. ANN CLIN BIOCHEM , 45 434 - 435. 10.1258/acb.2008.007218.

Bettencourt, C and Fialho, RN and Santos, C and Montiel, R and Bruges-Armas, J and MacIel, P and Lima, M (2008) Segregation distortion of wild-type alleles at the Machado-Joseph disease locus: A study in normal families from the Azores islands (Portugal). Journal of Human Genetics , 53 (4) 333 - 339.

Bettencourt, C and Santos, C and Kay, T and Vasconcelos, J and Lima, M (2008) Analysis of segregation patterns in Machado-Joseph disease pedigrees. Journal of Human Genetics , 53 (10) 920 - 923.

Bhidayasiri, R and Ling, H (2008) Multiple system atrophy. Neurologist , 14 (4) 224 - 237. 10.1097/NRL.0b013e318167b93f.

Blom, ES and Holmans, P and Arepalli, S and Adighibe, O and Hamshere, ML and Gatz, M and Pedersen, NL and Bergem, ALM and Owen, MJ and Hollingworth, P and Goate, A and Williams, J and Lannfelt, L and Hardy, J and Vrieze, FW-D and Glaser, A (2008) Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS , 147B (6) 778 - 783. 10.1002/ajmg.b.30681.

Bras, J and Guerreiro, R and Ribeiro, M and Morgadinho, A and Januario, C and Dias, M and Calado, A and Semedo, C and Oliveira, C and Hardy, J and Singleton, A (2008) Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2. BMC Neurology , 8 , Article 1. 10.1186/1471-2377-8-1.
An open access publication. A version is also available from UCL Discovery.

Bras, J and Singleton, A and Cookson, MR and Hardy, J (2008) Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease. FEBS J , 275 (23) 5767 - 5773. 10.1111/j.1742-4658.2008.06709.x.

Brundin, P and Li, JY and Holton, JL and Lindvall, O and Revesz, T (2008) Research in motion: the enigma of Parkinson's disease pathology spread. NAT REV NEUROSCI , 9 (10) 741 - 745. 10.1038/nrn2477.

C

Camargos, S and Scholz, S and Simón-Sánchez, J and Paisán-Ruiz, C and Lewis, P and Hernandez, D and Ding, J and Gibbs, JR and Cookson, MR and Bras, J and Guerreiro, R and Oliveira, CR and Lees, A and Hardy, J and Cardoso, F and Singleton, AB (2008) DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. The Lancet Neurology , 7 (3) 207 - 215.

Camargos, S and Scholz, S and Simon-Sanchez, J and Paisan-Ruiz, C and Lewis, P and Hernandez, D and Ding, J and Gibbs, JR and Cookson, MR and Bras, J and Guerreiro, R and Oliveira, CR and Lees, A and Hardy, J and Cardoso, F and Singleton, AB (2008) DYT16, a novel young-onset dystonia-parkinson ism disorder: identification of a segregating mutation in the stress-response protein PRKRA. LANCET NEUROL , 7 (3) 207 - 215. 10.1016/S1474-4422(08)70022-X.

Camargos, ST and Cardoso, F and Momeni, P and Gianetti, JG and Lees, A and Hardy, J and Singleton, A (2008) Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia. MOVEMENT DISORD , 23 (2) 299 - 302. 10.1002/mds.21842.

Campanella, M and Casswell, E and Chong, S and Farah, Z and Wieckowski, MR and Abramov, AY and Tinker, A and Duchen, MR (2008) Regulation of mitochondrial structure and function by the F1FO-ATPase inhibitor protein, IF1. CELL METAB , 8 (1) 13 - 25. 10.1016/j.cmet.2008.06.001.

Cano, SJ and Warner, TT and Thompson, AJ and Bhatia, KP and Fitzpatrick, R and Hobart, JC (2008) The Cervical Dystonia Impact Profile (CDIP-58): Can a Rasch developed patient reported outcome measure satisfy traditional psychometric criteria? HEALTH QUAL LIFE OUT , 6 , Article 58. 10.1186/1477-7525-6-58.
An open access publication

Carvajal-Carmona, L and Webb, E and Jaeger, E and Broderick, P and Spain, S and Howarth, K and Pittman, A and Consortium, CC and Houlston, R and Tomlinson, I (2008) A genome-wide association study of tag SNPs identify five novel colorectal cancer susceptibility loci. In: EJC SUPPLEMENTS. (pp. 10 - 10).

Cheeran, B and Talelli, P and Mori, F and Koch, G and Suppa, A and Edwards, M and Houlden, H and Bhatia, K and Greenwood, R and Rothwell, JC (2008) A common polymorphism in the brain-derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS. J PHYSIOL-LONDON , 586 (23) 5717 - 5725. 10.1113/jphysiol.2008.159905.
An open access publication

Cheeran, BJ and Talelli, P and Mori, F and Koch, G and Schneider, SA and Suppa, A and Edwards, M and Houlden, H and Greenwood, R and Rothwell, JC and Bhatia, KP (2008) Stimulation genomics: Identifying functional polymorphisms modulating LTP and LTD in human cerebral cortex and implications for levodopa induced dyskinesia in Parkinson's disease (PD). In: MOVEMENT DISORDERS. (pp. S20 - S20). WILEY-LISS

Clarimon, J and Pagonabarraga, J and Paisan-Ruiz, C and Campolongo, A and Pascual-Sedano, B and Marti-Masso, JF and Singleton, AB and Kulisevsky, J (2008) Tremor dominant parkinsonism: Clinical description and LRRK2 mutation screening. MOVEMENT DISORD , 23 (4) 518 - 523. 10.1002/mds.21771.

Cole, AR and Soutar, MP and Rembutsu, M and van Aalten, L and Hastie, CJ and McLauchlan, H and Peggie, M and Balastik, M and Lu, KP and Sutherland, C (2008) Relative resistance of Cdk5-phosphorylated CRMP2 to dephosphorylation. J Biol Chem , 283 (26) 18227 - 18237. 10.1074/jbc.M801645200.
An open access publication

Cookson, MR and Hardy, J and Lewis, PA (2008) Genetic Neuropathology of Parkinson's Disease. INT J CLIN EXP PATHO , 1 (3) 217 - 231.
An open access publication

D

Deng, JP and Lewis, PA and Greggio, E and Sluch, E and Beilina, A and Cookson, MR (2008) Structure of the ROC domain from the Parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric GTPase. P NATL ACAD SCI USA , 105 (5) 1499 - 1504. 10.1073/pnas.0709098105.

Devine, MJ and Lewis, PA (2008) Emerging pathways in genetic Parkinson's disease: tangles, Lewy bodies and LRRK2. FEBS J , 275 (23) 5748 - 5757. 10.1111/j.1742-4658.2008.06707.x.

Devine, MJ and Wilkinson, PA and Doherty, JF and Jarman, PR (2008) Neuroschistosomiasis presenting as brainstem encephalitis. NEUROLOGY , 70 (23) 2262 - 2264.

Di Bernardo, MC and Crowther-Swanepoel, D and Broderick, P and Webb, E and Sellick, G and Wild, R and Sullivan, K and Vijayakrishnan, J and Wang, Y and Pittman, AM and Sunter, NJ and Hall, AG and Dyer, MJ and Matutes, E and Dearden, C and Mainou-Fowler, T and Jackson, GH and Summerfield, G and Harris, RJ and Pettitt, AR and Hillmen, P and Allsup, DJ and Bailey, JR and Pratt, G and Pepper, C and Fegan, C and Allan, JM and Catovsky, D and Houlston, RS (2008) A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. Nat Genet , 40 (10) 1204 - 1210. 10.1038/ng.219.

Duncan, AJ and Sweeney, MG and Stern, E and Taylor, R and Woodward, C and Davis, MB and Hanna, MG and Rahman, S (2008) Comparative human mitochondrial genome analysis using the affymetrix Mitochip v2 and conventional cycle sequencing. In: NEUROMUSCULAR DISORDERS. (pp. 755 - 756). PERGAMON-ELSEVIER SCIENCE LTD

Duncan, AJ and Sweeney, MG and Stern, E and Taylor, RW and Woodward, C and Davis, MB and Hanna, MG and Rahman, S (2008) Identification of novel and recurrent mitochondrial DNA mutations in paediatric onset mitochondrial disease using the mitochip resequencing array. In: J INHERIT METAB DIS. (pp. 61 - 61). SPRINGER

Dunn, L and Vandrovcova, J and Malzer, E and Lees, AJ and Hardy, J and de Silva, R (2008) Investigation of tau gene-specific natural antisense transcript expression and splicing. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 30 - 30). BLACKWELL PUBLISHING

E

Espinoza, M and de Silva, R and Dickson, DW and Davies, P (2008) Differential incorporation of tau isoforms in Alzheimer's disease. J ALZHEIMERS DIS , 14 (1) 1 - 16.

Evans, A.H. (2008) Compulsive use of dopaminergic drugs in Parkinson's disease: a window into the role of dopamine in addiction and impulse control disorders. Doctoral thesis, UCL (University College London).

Everett, CM and Graves, TD and Lad, S and Jäger, HR and Thom, M and Isenberg, DA and Hanna, MG (2008) Aggressive CNS lupus vasculitis in the absence of systemic disease activity. Rheumatology (Oxford) , 47 (1) 107 - 109. 10.1093/rheumatology/kem264.

F

Fialho, D and Kullmann, DM and Hanna, MG and Schorge, S (2008) Non-genomic effects of sex hormones on CIC-1 may contribute to gender differences in myotonia congenita. In: NEUROMUSCULAR DISORDERS. (pp. 745 - 745). PERGAMON-ELSEVIER SCIENCE LTD

Fialho, D and Kullmann, DM and Hanna, MG and Schorge, S (2008) Non-genomic effects of sex hormones on CLC-1 may contribute to gender differences in myotonia congenita. NEUROMUSCULAR DISORD , 18 (11) 869 - 872. 10.1016/j.nmd.2008.07.004.

Fitzgerald, JC and Plun-Favreau, H (2008) Emerging pathways in genetic Parkinson's disease: Autosomal-recessive genes in Parkinson's disease - a common pathway? FEBS J , 275 (23) 5758 - 5766. 10.1111/j.1742-4658.2008.06708.x.

Fonteyn, EMR and Schmitz-Hubsch, T and Verstappen, CC and Baliko, L and Bloem, BR and Boesch, S and Bunn, L and Charles, P and Durr, A and Filla, A and Giunti, P and Globas, C and Klockgether, T and Melegh, B and Munneke, M and Pandolfo, M and de Rosa, A and Schols, L and Timmann, D and Kremer, BPH and van de Warrenburg, BPC (2008) Falls in spinocerebellar ataxias: Results of the EuroSCA fall study. In: MOVEMENT DISORDERS. (pp. S151 - S151). WILEY-LISS

G

Garrard, P and Martin, NH and Giunti, P and Cipolotti, L (2008) Cognitive and social cognitive functioning in spinocerebellar ataxia - A preliminary characterization. J NEUROL , 255 (3) 398 - 405. 10.1007/s00415-008-0680-6.

Garrard, P. and Martin, N.H. and Giunti, P. and Cipolotti, L. (2008) Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization. Journal of Neurology , 255 (3) pp. 398-405. 10.1007/s00415-008-0680-6.

Gilman, S and Wenning, G and Low, P and Brooks, D and Mathias, C and Trojanowski, J and Wood, NW and Colosimo, C and Durr, A and Fowler, C and Kaufmann, H and Klockgether, T and Lees, A and Poewe, W and Quinn, N and Revesz, T and Robertson, D and Sandroni, P and Seppi, K and Vidailhet, M (2008) Second consensus statement on the diagnosis of multiple system atrophy. In: NEUROLOGY. (pp. A229 - A229). LIPPINCOTT WILLIAMS & WILKINS

Gilman, S and Wenning, GK and Low, PA and Brooks, DJ and Mathias, CJ and Troianowski, JQ and Wood, NW and Colosimo, C and Durr, A and Fowler, CJ and Kaufmann, H and Klockgether, T and Lees, A and Poewe, W and Quinn, N and Revesz, T and Robertson, D and Sandroni, P and Seppi, K and Vidailhet, M (2008) Second consensus statement on the diagnosis of multiple system atrophy. In: MOVEMENT DISORDERS. (pp. S255 - S255). WILEY-LISS

Gilman, S and Wenning, GK and Low, PA and Brooks, DJ and Mathias, CJ and Trojanowski, JQ and Wood, NW and Colosimo, C and Duerr, A and Fowler, CJ and Kaufmann, H and Klockgether, T and Lees, A and Poewe, W and Quinn, N and Revesz, T and Robertson, D and Sandroni, P and Seppi, K and Vidailhet, M (2008) Second consensus statement on the diagnosis of multiple system atrophy. NEUROLOGY , 71 (9) 670 - 676.

Gilman, S and Wenning, GK and Low, PA and Brooks, DJ and Mathias, CJ and Trojanowski, JQ and Wood, NW and Colosimo, C and Durr, A and Fowler, CJ and Kaufmann, H and Klockgether, T and Lees, A and Poewe, W and Quinn, N and Revesz, T and Robertson, D and Sandroni, P and Seppi, K and Vidailhet, M (2008) Second consensus statement on the diagnosis of multiple system atrophy. In: MOVEMENT DISORDERS. (pp. S255 - S255). WILEY-LISS

Granata, A and Watson, R and Collinson, LM and Schiavo, G and Warner, TT (2008) The dystonia-associated protein torsinA modulates synaptic vesicle recycling. J BIOL CHEM , 283 (12) 7568 - 7579. 10.1074/jbc.M704097200.
An open access publication

Graves, TD and Hanna, MG (2008) Episodic ataxia: SLC1A3 and CACNB4 do not explain the apparent genetic heterogeneity. J NEUROL , 255 (7) 1097 - 1099. 10.1007/s00415-008-0844-4.

Graves, TD and Imbrici, P and Kors, EE and Terwindt, GM and Eunson, LH and Frants, RR and Haan, J and Ferrari, MD and Goadsby, PJ and Hanna, MG and van den Maagdenberg, AMJM and Kullmann, DM (2008) Premature stop codons in a facilitating EF-hand splice variant of Ca(v)2.1 cause episodic ataxia type 2. NEUROBIOL DIS , 32 (1) 10 - 15. 10.1016/j.nbd.2008.06.002.

Graves, TD and Morris, H and Zuberi, S and Hanna, MG and Kullmann, DM and Schorge, S (2008) Episodic ataxia type 1 in twins: Genotype-phenotype correlation. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 344 - 344). B M J PUBLISHING GROUP

Graves, TD and Zuberi, SM and Morris, H and Schorge, S and Kullmann, DM and Hanna, MG (2008) Episodic ataxia type 1 in identical twins. In: NEUROMUSCULAR DISORDERS. (pp. 746 - 746). PERGAMON-ELSEVIER SCIENCE LTD

Graves, TD and Zuberi, SM and Morris, H and Schorge, S and Kullmann, DM and Hanna, MG (2008) Episodic ataxia type 1 in identical twins: genotype-phenotype correlation. In: JOURNAL OF NEUROLOGY. (pp. 16 - 16). DR DIETRICH STEINKOPFF VERLAG

Guerreiro, RJ and Santana, I and Bras, JM and Revesz, T and Rebelo, O and Ribeiro, MH and Santiago, B and Oliveira, CR and Singleton, A and Hardy, J (2008) Novel progranulin mutation: Screening for PGRN mutations in a Portuguese series of FTD/CBS cases. MOVEMENT DISORD , 23 (9) 1269 - 1273. 10.1002/mds.22078.

Guerreiro, RJ and Schymick, JC and Crews, C and Singleton, A and Hardy, J and Traynor, BJ (2008) TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis. PLOS ONE , 3 (6) , Article e2450. 10.1371/journal.pone.0002450.
An open access publication. A version is also available from UCL Discovery.

H

Hall, AM and Unwin, RJ and Hanna, MG and Duchen, MR (2008) Renal function and mitochondrial cytopathy (MC): more questions than answers. QJM-INT J MED , 101 (10) 755 - 766. 10.1093/qjmed/hcn060.

Hardy, J (2008) Race, genetics, and medicine at a crossroads. LANCET S85 - S89.

Hardy, J (2008) ALZHEIMER'S DISEASE: GENETICS TO PATHOGENESIS. In: Ragaini, R, (ed.) INTERNATIONAL SEMINAR ON NUCLEAR WAR AND PLANETARY EMERGENCIES - 38TH SESSION. (pp. 355 - 363). WORLD SCIENTIFIC PUBL CO PTE LTD

Hardy, J and Low, N and Singleton, A (2008) Whole genome association studies: Deciding when persistence becomes perseveration. AM J MED GENET B , 147B (2) 131 - 133. 10.1002/ajmg.b.30568.

Hardy, J and Low, N and Singleton, A (2008) Whole genome association studies: Deciding when persistence becomes perseveration. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics , 147 (2) 131 - 133.

Hardy, J and Singleton, A (2008) The HapMap - Charting a course for genetic discovery in neurological diseases. ARCH NEUROL-CHICAGO , 65 (3) 319 - 321.

Harrower, T and Stewart, JD and Hudson, G and Houlden, H and Warner, G and O'Donovan, DG and Findlay, LJ and Taylor, RW and De Silva, R and Chinnery, PF (2008) POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease. ARCH NEUROL-CHICAGO , 65 (1) 133 - 136.

Healy, DG and Falchi, M and O'Sullivan, SS and Bonifati, V and Durr, A and Bressman, S and Brice, A and Aasly, J and Zabetian, CP and Goldwurm, S and Ferreira, JJ and Tolosa, E and Kay, DM and Klein, C and Williams, DR and Marras, C and Lang, AE and KWszolek, Z and Berciano, J and Schapira, AHV and Lynch, T and Bhatia, KP and Gasser, T and Lees, AJ and Wood, NW and Int LRRK2 Consortium, (2008) Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. LANCET NEUROL , 7 (7) 583 - 590. 10.1016/S1474-4422(08)70117-0.
An open access publication

Healy, DG and Goadsby, PJ and Kitchen, ND and Yousry, T and Hanna, MG (2008) Spontaneous intracranial hypotension, hygromata and haematomata. J NEUROL NEUROSUR PS , 79 (4) 442 - 442. 10.1136/jnnp.2007.132019.

Healy, DG and Wood, NW and Schapira, AH (2008) Test for LRRK2 mutations in patients with Parkinson's disease. Pract Neurol , 8 (6) 381 - 385. 10.1136/jnnp.2008.162420.

Holton, JL and Schneider, SA and Gandhi, S and Ganesharajah, T and Strand, C and Shashidharan, P and Barreto, J and Wood, NW and Lees, AJ and Bhatia, KP and Revesz, T (2008) Neuropathology of primary dystonia unrelated to DYT1 mutations. In: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. (pp. 28 - 28). BLACKWELL PUBLISHING

Holton, JL and Schneider, SA and Ganesharajah, T and Gandhi, S and Strand, C and Shashidharan, P and Barreto, J and Wood, NW and Lees, AJ and Bhatia, KP and Revesz, T (2008) Neuropathology of primary adult-onset dystonia. NEUROLOGY , 70 (9) 695 - 699.

Holton, JL and Schneider, SA and Ganesharajah, T and Gandhi, S and Strand, C and Shashidharan, P and Barreto, J and Wood, NW and Lees, AL and Bhatia, KP and Revesz, T (2008) Neuropathology of primary adult onset non-DYT1 dystonia. In: JOURNAL OF NEUROLOGY. (pp. 98 - 98). DR DIETRICH STEINKOPFF VERLAG

Houlden, H and Johnson, J and Gardner-Thorpe, C and Lashley, T and Hernandez, D and Singleton, AB and Holton, J and Revesz, T and Davis, MB and Giunti, P and Wood, NW (2008) Tau tubulin kinase 2, implicated by tau phosphorylation, contains mutations that segregate with spinocerebellar ataxia type II. In: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. (pp. 344 - 344). B M J PUBLISHING GROUP

Houlden, H and Johnson, J and Gardner-Thorpe, C and Lashley, T and Hernandez, D and Worth, P and Singleton, AB and Hilton, DA and Holton, J and Revesz, T and Davis, MB and Giunti, P and Wood, NW (2008) Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 (Nature Genetics (2007) 39, (1434-1436)). Nature Genetics , 40 (2) 255 - 255.

Houlden, H and Johnson, J and Gardner-Thorpe, C and Lashley, T and Hernandez, D and Worth, P and Singleton, AB and Hilton, DA and Holton, J and Revesz, T and Davis, MB and Giunti, P and Wood, NW (2008) Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 (vol 39, pg 1434, 2007). NAT GENET , 40 (2) 255 - 255.

Houlden, H and Laura, M and Wavrant-De Vrieze, F and Blake, J and Wood, N and Reilly, MM (2008) Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2. NEUROLOGY , 71 (21) 1660 - 1668. 10.1212/01.wnl.0000319696.14225.67.

Houlston, RS and Webb, E and Broderick, P and Pittman, AM and Di Bernardo, MC and Lubbe, S and Chandler, I and Vijayakrishnan, J and Sullivan, K and Penegar, S and Colorectal Cancer Association Study Consortium, and Carvajal-Carmona, L and Howarth, K and Jaeger, E and Spain, SL and Walther, A and Barclay, E and Martin, L and Gorman, M and Domingo, E and Teixeira, AS and CoRGI Consortium, and Kerr, D and Cazier, JB and Niittymäki, I and Tuupanen, S and Karhu, A and Aaltonen, LA and Tomlinson, IP and Farrington, SM and Tenesa, A and Prendergast, JG and Barnetson, RA and Cetnarskyj, R and Porteous, ME and Pharoah, PD and Koessler, T and Hampe, J and Buch, S and Schafmayer, C and Tepel, J and Schreiber, S and Völzke, H and Chang-Claude, J and Hoffmeister, M and Brenner, H and Zanke, BW and Montpetit, A and Hudson, TJ and Gallinger, S and International Colorectal Cancer Genetic Association Consortium, and Campbell, H and Dunlop, MG (2008) Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet , 40 (12) 1426 - 1435. 10.1038/ng.262.

Huang, Y and Song, YJC and Murphy, K and Holton, JL and Lashley, T and Revesz, T and Gai, WP and Halliday, G (2008) LRRK2 and parkin immunoreactivity in multiple system atrophy inclusions. ACTA NEUROPATHOL , 116 (6) 639 - 646. 10.1007/s00401-008-0446-3.

I

Ince, PG and Clark, B and Holton, J and Revesz, T and Wharton, SB (2008) Diseases of movement and system degenerations. In: Love, S and Louis, DN and Ellison, DW, (eds.) Greenfield's neuropathology. (889 - 1030). Hodder Arnold: London.

J

Jackson, TL and Hussain, A and Morley, AMS and Sullivan, PM and Hodgetts, A and El-Osta, A and Hillenkamp, J and Charles, SJ and Sheard, R and Williamson, TH and Kumar, A and Laidlaw, DAH and Woon, WH and Costen, MJ and Luff, AJ and Marshall, J (2008) Scleral Hydraulic Conductivity and Macromolecular Diffusion in Patients with Uveal Effusion Syndrome. INVEST OPHTH VIS SCI , 49 (11) 5033 - 5040. 10.1167/iovs.08-1980.

Jaeger, E and Webb, E and Howarth, K and Carvajal-Carmona, L and Rowan, A and Broderick, P and Walther, A and Spain, S and Pittman, A and Kemp, Z and Sullivan, K and Heinimann, K and Lubbe, S and Domingo, E and Barclay, E and Martin, L and Gorman, M and Chandler, I and Vijayakrishnan, J and Wood, W and Papaemmanuil, E and Penegar, S and Qureshi, M and Farrington, S and Tenesa, A and Cazier, J-B and Kerr, D and Gray, R and Peto, J and Dunlop, M and Campbell, H and Thomas, H and Houlston, R and Tomlinson, I and Consortium, CORGI (2008) Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. NATURE GENETICS , 40 (1) 26 - 28. 10.1038/ng.2007.41.

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