Jac Charlesworth
Jac Charlesworth
Menzies Institute for Medical Research
Verified email at utas.edu.au - Homepage
Cited by
Cited by
Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes
HHH Göring, JE Curran, MP Johnson, TD Dyer, J Charlesworth, SA Cole, ...
Nature genetics 39 (10), 1208-1216, 2007
High dimensional endophenotype ranking in the search for major depression risk genes
DC Glahn, JE Curran, AM Winkler, MA Carless, JW Kent Jr, ...
Biological psychiatry 71 (1), 6-14, 2012
Genetic Analysis Workshop 17 mini-exome simulation
L Almasy, TD Dyer, JM Peralta, JW Kent, JC Charlesworth, JE Curran, ...
BMC proceedings 5 (9), 1-9, 2011
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytes
JC Charlesworth, JE Curran, MP Johnson, HHH Göring, TD Dyer, ...
BMC medical genomics 3 (1), 1-11, 2010
The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness
J Charlesworth, PL Kramer, T Dyer, V Diego, JR Samples, JE Craig, ...
Investigative ophthalmology & visual science 51 (7), 3509-3514, 2010
Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci
KP Burdon, DJ Coster, JC Charlesworth, RA Mills, KJ Laurie, C Giunta, ...
Human genetics 124 (4), 379-386, 2008
Genetic association of preeclampsia to the inflammatory response gene SEPS1
EK Moses, MP Johnson, L Třmmerdal, S Forsmo, JE Curran, LJ Abraham, ...
American journal of obstetrics and gynecology 198 (3), 336. e1-336. e5, 2008
A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis
J Field, SR Browning, LJ Johnson, P Danoy, MD Varney, BD Tait, ...
PloS one 5 (10), e13454, 2010
The genetics of multiple sclerosis
R Lin, J Charlesworth, I van der Mei, BV Taylor
Practical neurology 12 (5), 279-288, 2012
Genetic basis of neurocognitive decline and reduced white-matter integrity in normal human brain aging
DC Glahn, JW Kent, E Sprooten, VP Diego, AM Winkler, JE Curran, ...
Proceedings of the National Academy of Sciences 110 (47), 19006-19011, 2013
Low-frequency and rare-coding variation contributes to multiple sclerosis risk
M Mitrovič, NA Patsopoulos, AH Beecham, T Dankowski, A Goris, ...
Cell 175 (6), 1679-1687. e7, 2018
Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree
JC Charlesworth, TD Dyer, JM Stankovich, J Blangero, DA Mackey, ...
Investigative ophthalmology & visual science 46 (10), 3723-3729, 2005
Heritability of central corneal thickness in nuclear families
JA Landers, AW Hewitt, DP Dimasi, JC Charlesworth, T Straga, RAD Mills, ...
Investigative ophthalmology & visual science 50 (9), 4087-4090, 2009
Genetic determinants of mitochondrial content
JE Curran, MP Johnson, TD Dyer, HHH Göring, JW Kent, ...
Human molecular genetics 16 (12), 1504-1514, 2007
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
BJ Gu, J Field, S Dutertre, A Ou, TJ Kilpatrick, J Lechner-Scott, R Scott, ...
Human molecular genetics 24 (19), 5644-5654, 2015
An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3
J Zochling, F Newell, JC Charlesworth, P Leo, J Stankovich, A Cortes, ...
Arthritis research & therapy 16 (5), 1-7, 2014
Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis
Y Zhou, G Zhu, JC Charlesworth, S Simpson Jr, R Rubicz, HHH Göring, ...
Multiple Sclerosis Journal 22 (13), 1655-1664, 2016
A genome-wide analysis of'Bounty'descendants implicates several novel variants in migraine susceptibility
HC Cox, RA Lea, C Bellis, M Carless, TD Dyer, J Curran, J Charlesworth, ...
Neurogenetics 13 (3), 261-266, 2012
The role of the MTHFR gene in migraine
S Stuart, HC Cox, RA Lea, LR Griffiths
Headache: The Journal of Head and Face Pain 52 (3), 515-520, 2012
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