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David Booth
David Booth
Verified email at sydney.edu.au
Title
Cited by
Cited by
Year
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
26592011
IL28B is associated with response to chronic hepatitis C interferon-α and ribavirin therapy
V Suppiah, M Moldovan, G Ahlenstiel, T Berg, M Weltman, ML Abate, ...
Nature genetics 41 (10), 1100-1104, 2009
23062009
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis
DR Booth, M Sunde, V Bellotti, CV Robinson, WL Hutchinson, PE Fraser, ...
Nature 385 (6619), 787-793, 1997
12481997
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
WTCCC WTCCC2).
Nature Genetics, 2013
11362013
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis
HJ Lachmann, DR Booth, SE Booth, A Bybee, JA Gilbertson, JD Gillmore, ...
New England Journal of Medicine 346 (23), 1786-1791, 2002
7242002
Human lysozyme gene mutations cause hereditary systemic amyloidosis
MB Pepys, PN Hawkins, DR Booth, DM Vigushin, GA Tennent, AK Soutar, ...
Nature 362 (6420), 553-557, 1993
7171993
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Data analysis: Bahlo Melanie 2 Brown Matthew A 6 7 Browning Brian L 20 ...
Nature genetics 41 (7), 824-828, 2009
5072009
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
4422019
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations
HJ Lachmann, B Şengül, TU Yavuzşen, DR Booth, SE Booth, A Bybee, ...
Rheumatology 45 (6), 746-750, 2006
4142006
Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA …
E Aganna, F Martinon, PN Hawkins, JB Ross, DC Swan, DR Booth, ...
Arthritis & Rheumatism 46 (9), 2445-2452, 2002
3872002
Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci
NA Patsopoulos, ...
Annals of neurology 70 (6), 897-912, 2011
3292011
A high-density screen for linkage in multiple sclerosis
International Multiple Sclerosis Genetics Consortium
The American Journal of Human Genetics 77 (3), 454-467, 2005
3262005
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature genetics 47 (10), 1107-1113, 2015
3052015
Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever
I Touitou, T Sarkisian, M Medlej‐Hashim, M Tunca, A Livneh, D Cattan, ...
Arthritis & Rheumatism 56 (5), 1706-1712, 2007
2892007
MicroRNAs miR-17 and miR-20a inhibit T cell activation genes and are under-expressed in MS whole blood
MB Cox, MJ Cairns, KS Gandhi, AP Carroll, S Moscovis, GJ Stewart, ...
PloS one 5 (8), e12132, 2010
2692010
Amyloid P component. A critical review
MB Pepys, DR Booth, WL Hutchinson, JR Gallimore, IM Collins, ...
Amyloid 4 (4), 274-295, 1997
2491997
Potential role for Interleukin‐28B genotype in treatment decision‐making in recent hepatitis C virus infection
J Grebely, K Petoumenos, M Hellard, GV Matthews, V Suppiah, ...
Hepatology 52 (4), 1216-1224, 2010
2402010
The genetic basis of autosomal dominant familial Mediterranean fever
DR Booth, JD Gillmore, HJ Lachmann, SE Booth, A Bybee, M Soytürk, ...
Qjm 93 (4), 217-221, 2000
2282000
The role of the CD58 locus in multiple sclerosis
PL De Jager, C Baecher-Allan, LM Maier, AT Arthur, L Ottoboni, ...
Proceedings of the National Academy of Sciences 106 (13), 5264-5269, 2009
2142009
Antibodies to myelin oligodendrocyte glycoprotein in bilateral and recurrent optic neuritis
S Ramanathan, SW Reddel, A Henderson, JDE Parratt, M Barnett, ...
Neurology-Neuroimmunology Neuroinflammation 1 (4), 2014
2112014
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Articles 1–20