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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
29602011
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
23722009
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
WTCCC WTCCC2).
Nature Genetics, 2013
13252013
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
13131997
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study
M Tunca, H Ozdogan, O Kasapcopur, F Yalcinkaya, E Tutar, R Topaloglu, ...
Medicine (Baltimore) 84 (1), 1-11, 2005
10002005
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
8402019
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
7712002
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
7561993
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
5322009
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
5162006
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
4352002
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature genetics 47 (10), 1107-1113, 2015
3892015
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
3622005
Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci
NA Patsopoulos, ...
Annals of neurology 70 (6), 897-912, 2011
3602011
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
3232007
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
3012010
Amyloid P component. A critical review
MB Pepys, DR Booth, WL Hutchinson, JR Gallimore, IM Collins, ...
Amyloid 4 (4), 274-295, 1997
2651997
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
2512000
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
2472010
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
2382009
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