D R Booth

Author PubWeight™ 24.29‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Human lysozyme gene mutations cause hereditary systemic amyloidosis. Nature 1993 2.78
2 Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations. Rheumatology (Oxford) 2006 1.76
3 Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I. Kidney Int 1998 1.71
4 Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen alpha-chain variant in an English family. QJM 2000 1.45
5 An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1q. Arthritis Rheum 2000 1.41
6 Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. Q J Med 1994 1.06
7 Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy. Brain 1995 1.04
8 Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis. Brain 1999 1.02
9 Hereditary renal amyloidosis associated with variant lysozyme in a large English family. Nephrol Dial Transplant 1999 0.99
10 Intraoral condyloma acuminatum. Oral Surg Oral Med Oral Pathol 1974 0.93
11 Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosis. Genes Immun 2007 0.91
12 Hereditary cardiac amyloidosis associated with the transthyretin Ile122 mutation in a white man. Heart 1999 0.88
13 The role of SNPs in the α-chain of the IL-7R gene in CD4+ T-cell recovery in HIV-infected African patients receiving suppressive cART. Genes Immun 2011 0.85
14 Familial Mediterranean fever gene. N Engl J Med 1998 0.85
15 Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy. Ciba Found Symp 1996 0.84
16 The elusive multiple self-healing squamous epithelioma (MSSE) gene: further mapping, analysis of candidates, and loss of heterozygosity. Oncogene 2006 0.82
17 Voriconazole toxicity related to polymorphisms in CYP2C19. Intern Med J 2011 0.82
18 Transthyretin Ala97Ser is associated with familial amyloidotic polyneuropathy in a Chinese-Taiwanese family. Hum Mutat 2000 0.79
19 The early effects of segmental surgery on the human pulp. Int J Oral Surg 1975 0.79
20 Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg. Transplantation 2001 0.79
21 Dental maturity of children in Perth, Western Australia, and its application in forensic age estimation. J Clin Forensic Med 1999 0.78
22 CCR5-Δ32 genotype does not improve predictive value of IL28B polymorphisms for treatment response in chronic HCV infection. Genes Immun 2013 0.78
23 An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians. Mult Scler 2006 0.77
24 Hepatitis B--a personal view. Aust Dent J 1985 0.75
25 Odontological section of a bone tumour registry. Int J Oral Surg 1978 0.75
26 Vitreal deposits in Val71Ala transthyretin amyloidosis. Intern Med J 2012 0.75
27 Idiopathic coronal radiolucencies in unerupted permanent teeth. Case reports. Aust Dent J 1991 0.75
28 New units in haematology. Aust Dent J 1978 0.75