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Number of items: 9.


Wilson, Duncan, Ambler, Gareth, Shakeshaft, Clare, Brown, Martin M, Charidimou, Andreas, Salman, Rustam Al-Shahi, Lip, Gregory YH ORCID: 0000-0002-7566-1626, Cohen, Hannah, Banerjee, Gargi, Houlden, Henry
et al (show 11 more authors) (2018) Cerebral microbleeds and intracranial haemorrhage risk in patients anticoagulated for atrial fibrillation after acute ischaemic stroke or transient ischaemic attack (CROMIS-2): a multicentre observational cohort study. LANCET NEUROLOGY, 17 (6). 539 - 547.


Wilson, Duncan, Ambler, Gareth, Banerjee, Gargi, Shakeshaft, Clare, Cohen, Hannah, Yousry, Tarek A, Salman, Rustam Al-Shahi, Lip, Gregory YH ORCID: 0000-0002-7566-1626, Houlden, Henry, Brown, Martin M
et al (show 4 more authors) (2019) Early versus late anticoagulation for ischaemic stroke associated with atrial fibrillation: multicentre cohort study. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 90 (3). 320 - 325.


Banerjee, Gargi, Wilson, Duncan, Ambler, Gareth, Hostettler, Isabel Charlotte, Shakeshaft, Clare, Cohen, Hannah, Yousry, Tarek, Salman, Rustam Al-Shahi, Lip, Gregory YH ORCID: 0000-0002-7566-1626, Houlden, Henry
et al (show 5 more authors) (2020) Longer term stroke risk in intracerebral haemorrhage survivors. Journal of Neurology, Neurosurgery and Psychiatry, 91 (8). 840 - 845.


Blauwendraat, Cornelis, Faghri, Faraz, Pihlstrom, Lasse, Geiger, Joshua T, Elbaz, Alexis, Lesage, Suzanne, Corvol, Jean-Christophe, May, Patrick, Nicolas, Aude, Abramzon, Yevgeniya
et al (show 31 more authors) (2017) NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiology of Aging, 57. 247.e9 - 247.e13.


Jabbari, Edwin, Woodside, John, Guo, Tong, Magdalinou, Nadia K, Chelban, Viorica, Athauda, Dilan, Lees, Andrew J ORCID: 0000-0002-2476-4385, Foltynie, Thomas, Houlden, Henry, Church, Alistair
et al (show 4 more authors) (2019) Proximity extension assay testing reveals novel diagnostic biomarkers of atypical parkinsonian syndromes. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 90 (7). 768 - 773.


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.


Fernandez-Santiago, Ruben, Martin-Flores, Nuria, Antonelli, Francesca, Cerquera, Catalina, Moreno, Veronica, Bandres-Ciga, Sara, Manduchi, Elisabetta, Tolosa, Eduard, Singleton, Andrew B, Moore, Jason H
et al (show 153 more authors) (2019) SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease. MOVEMENT DISORDERS, 34 (9). 1333 - 1344.


Almarzouki, Abeer, Wilson, Duncan, Ambler, Gareth, Shakeshaft, Clare, Cohen, Hannah, Yousry, Tarek, Salman, Rustam Al-Shahi, Lip, Gregory YH ORCID: 0000-0002-7566-1626, Houlden, Henry, Brown, Martin M
et al (show 3 more authors) (2020) Sensitivity and specificity of blood-fluid levels for oral anticoagulant-associated intracerebral haemorrhage. SCIENTIFIC REPORTS, 10 (1).


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 37 more authors) (2016) A genome-wide association study in multiple system atrophy. NEUROLOGY, 87 (15). 1591 - 1598.

This list was generated on Mon Oct 19 00:27:41 2020 BST.