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Ling, Helen, Morris, Huw R, Neal, James W, Lees, Andrew J ORCID: 0000-0002-2476-4385, Hardy, John, Holton, Janice L, Revesz, Tamas and Williams, David DR
(2017)
Mixed pathologies including chronic traumatic encephalopathy account for dementia in retired association football (soccer) players.
ACTA NEUROPATHOLOGICA, 133 (3).
pp. 337-352.
Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M, Brady, Stefen, Holton, Janice L, Pittman, Alan M ORCID: 0000-0002-8112-2987, Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David et al (show 20 more authors)
(2016)
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
Neurobiology of aging, 47.
218.e1-218.e9.
Jabbari, Edwin, Woodside, John, Tan, Manuela MX, Shoai, Maryam, Pittman, Alan, Ferrari, Raffaele, Mok, Kin Y, Zhang, David, Reynolds, Regina H, de Silva, Rohan et al (show 13 more authors)
(2018)
Variation at the <i>TRIM11</i> locus modifies progressive supranuclear palsy phenotype.
ANNALS OF NEUROLOGY, 84 (4).
pp. 485-496.
Goldfinger, Marc H, Ling, Helen, Tilley, Bension S, Liu, Alan KL, Davey, Karen, Holton, Janice L, Revesz, Tamas and Gentleman, Steve M
(2018)
The aftermath of boxing revisited: identifying chronic traumatic encephalopathy pathology in the original Corsellis boxer series.
ACTA NEUROPATHOLOGICA, 136 (6).
pp. 973-974.
Jabbari, Edwin ORCID: 0000-0001-6844-882X, Woodside, John, Tan, Manuela MX ORCID: 0000-0001-5835-669X, Pavese, Nicola ORCID: 0000-0002-6801-6194, Bandmann, Oliver, Ghosh, Boyd CP, Massey, Luke A, Capps, Erica, Warner, Tom T ORCID: 0000-0001-6195-6995, Lees, Andrew J ORCID: 0000-0002-2476-4385 et al (show 5 more authors)
(2019)
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.
Movement disorders : official journal of the Movement Disorder Society, 34 (9).
pp. 1307-1314.
Sailer, Anna, Scholz, Sonja W, Nalls, Michael A, Schulte, Claudia, Federoff, Monica, Price, T Ryan, Lees, Andrew ORCID: 0000-0002-2476-4385, Ross, Owen A, Dickson, Dennis W, Mok, Kin et al (show 35 more authors)
(2016)
A genome-wide association study in multiple system atrophy.
NEUROLOGY, 87 (15).
pp. 1591-1598.