William Ted Brown
William Ted Brown
Institute for Basic Research
Verified email at sydney.edu.au
TitleCited byYear
Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome
M Eriksson, WT Brown, LB Gordon, MW Glynn, J Singer, L Scott, ...
Nature 423 (6937), 293, 2003
18182003
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
13592007
Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates
S Jacquemont, RJ Hagerman, M Leehey, J Grigsby, L Zhang, ...
The American Journal of Human Genetics 72 (4), 869-878, 2003
6832003
Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases.
AM Saunders, K Schmader, JC Breitner, MD Benson, WT Brown, ...
Lancet (London, England) 342 (8873), 710-711, 1993
5831993
Analysis of neocortex in three males with the fragile X syndrome
VJ Hinton, WT Brown, K Wisniewski, RD Rudelli
American journal of medical genetics 41 (3), 289-294, 1991
5521991
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study—preliminary data
DJ Allingham‐Hawkins, R Babul‐Hirji, D Chitayat, JJA Holden, KT Yang, ...
American journal of medical genetics 83 (4), 322-325, 1999
4831999
Adult fragile X syndrome
RD Rudelli, WT Brown, K Wisniewski, EC Jenkins, M Laure-Kamionowska, ...
Acta neuropathologica 67 (3-4), 289-295, 1985
4051985
Oxidative stress in autism: Increased lipid peroxidation and reduced serum levels of ceruloplasmin and transferrin-the antioxidant proteins
A Chauhan, V Chauhan, WT Brown, I Cohen
Life sciences 75 (21), 2539-2549, 2004
3882004
The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes
J Wegiel, I Kuchna, K Nowicki, H Imaki, J Wegiel, E Marchi, SY Ma, ...
Acta neuropathologica 119 (6), 755-770, 2010
3762010
Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles
SL Nolin, WT Brown, A Glicksman, GE Houck Jr, AD Gargano, A Sullivan, ...
The American Journal of Human Genetics 72 (2), 454-464, 2003
3692003
Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction
JA Brunberg, S Jacquemont, RJ Hagerman, EM Berry-Kravis, J Grigsby, ...
American Journal of Neuroradiology 23 (10), 1757-1766, 2002
3552002
Chromosome 21q21 sublocalisation of gene encoding beta-amyloid peptide in cerebral vessels and neuritic (senile) plaques of people with Alzheimer disease and Down syndrome
NK Robakis, HM Wisniewski, EC Jenkins, EA Devine-Gage, GE Houck, ...
The Lancet 329 (8529), 384-385, 1987
3161987
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome
D Goldgaber, LG Goldfarb, P Brown, DM Asher, WT Brown, S Lin, ...
Experimental neurology 106 (2), 204-206, 1989
3041989
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test
WT Brown, GE Houck, A Jeziorowska, FN Levinson, X Ding, C Dobkin, ...
Jama 270 (13), 1569-1575, 1993
3031993
Foetal thymic transplant in a case of DiGeorge's syndrome
WW Cleveland, BJ Fogel, WT Brown, HEM Kay
The Lancet 292 (7580), 1211-1214, 1968
2791968
Autism is associated with the fragile-X syndrome
WT Brown, EC Jenkins, E Friedman, J Brooks, K Wisniewski, S Raguthu, ...
Journal of autism and developmental disorders 12 (3), 303-308, 1982
2761982
Inheritance of mitral valve prolapse: effect of age and sex on gene expression
RB DEVEREUX, WTED BROWN, R KRAMER-FOX, I SACHS
Annals of internal medicine 97 (6), 826-832, 1982
2591982
Fragile X and autism: a multicenter survey
WT Brown, EC Jenkins, IL Cohen, GS Fisch, EG Wolf‐Schein, A Gross, ...
American Journal of Medical Genetics 23 (1‐2), 341-352, 1986
2121986
Decreased GABAA receptor expression in the seizure-prone fragile X mouse
A El Idrissi, XH Ding, J Scalia, E Trenkner, WT Brown, C Dobkin
Neuroscience letters 377 (3), 141-146, 2005
2052005
Familial transmission of the FMR1 CGG repeat.
SL Nolin, FA Lewis 3rd, LL Ye, GE Houck Jr, AE Glicksman, P Limprasert, ...
American journal of human genetics 59 (6), 1252, 1996
1971996
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