Peter Hickey
Peter Hickey
Senior Research Officer, Molecular Medicine Division, Walter and Eliza Hall Institute of Medical
Verified email at wehi.edu.au - Homepage
TitleCited byYear
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia—MLASA syndrome
LG Riley, S Cooper, P Hickey, J Rudinger-Thirion, M McKenzie, ...
The American Journal of Human Genetics 87 (1), 52-59, 2010
2012010
Saliva-derived DNA performs well in large-scale, high-density single-nucleotide polymorphism microarray studies
M Bahlo, J Stankovich, P Danoy, PF Hickey, BV Taylor, SR Browning, ...
Cancer Epidemiology and Prevention Biomarkers 19 (3), 794-798, 2010
492010
Genetic and epigenetic variation among inbred mouse littermates: identification of inter-individual differentially methylated regions
H Oey, L Isbel, P Hickey, B Ebaid, E Whitelaw
Epigenetics & chromatin 8 (1), 54, 2015
322015
X chromosome association testing in genome wide association studies
PF Hickey, M Bahlo
Genetic epidemiology 35 (7), 664-670, 2011
322011
Setdb1-mediated H3K9 methylation is enriched on the inactive X and plays a role in its epigenetic silencing
A Keniry, LJ Gearing, N Jansz, J Liu, AZ Holik, PF Hickey, SA Kinkel, ...
Epigenetics & chromatin 9 (1), 16, 2016
242016
Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease
BE Stranger, LE Brigham, R Hasz, M Hunter, C Johns, M Johnson, ...
Nature genetics 49 (12), 1664, 2017
182017
ALPK3-deficient cardiomyocytes generated from patient-derived induced pluripotent stem cells and mutant human embryonic stem cells display abnormal calcium handling and …
DG Phelan, DJ Anderson, SE Howden, RCB Wong, PF Hickey, K Pope, ...
European heart journal 37 (33), 2586-2590, 2016
152016
Spontaneous retrotransposon insertion into TNF 3′ UTR causes heart valve disease and chronic polyarthritis
D Lacey, P Hickey, BD Arhatari, LA O’Reilly, L Rohrbeck, H Kiriazis, ...
Proceedings of the National Academy of Sciences 112 (31), 9698-9703, 2015
142015
Neuronal brain-region-specific DNA methylation and chromatin accessibility are associated with neuropsychiatric trait heritability
LF Rizzardi, PF Hickey, VR DiBlasi, R Tryggvadóttir, CM Callahan, A Idrizi, ...
Nature neuroscience 22 (2), 307, 2019
8*2019
Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters
N Jansz, A Keniry, M Trussart, H Bildsoe, T Beck, ID Tonks, AW Mould, ...
Nature structural & molecular biology 25 (9), 766, 2018
8*2018
Smchd1 Targeting to the Inactive X Is Dependent on the Xist-HnrnpK-PRC1 Pathway
N Jansz, T Nesterova, A Keniry, M Iminitoff, PF Hickey, G Pintacuda, ...
Cell reports 25 (7), 1912-1923. e9, 2018
32018
A Novel Apparatus to Measure Knee Flexor Strength During Various Hamstring Exercises: A Reliability and Retrospective Injury Study
JT Hickey, PF Hickey, N Maniar, RG Timmins, MD Williams, CA Pitcher, ...
Journal of Orthopaedic & Sports Physical Therapy 48 (2), 72-80, 2018
22018
Novel and clinically practical measures of hamstring strength: The HamSling reliability and retrospective study
J Hickey, P Hickey, N Maniar, R Timmins, D Opar
Journal of Science and Medicine in Sport 20, e124, 2017
22017
Package ‘matrixStats’
H Bengtsson, HC Bravo, R Gentleman, O Hossjer, H Jaffee, D Jiang, ...
12018
The statistical analysis of high-throughput assays for studying DNA methylation
P HICKEY
12015
Coexpression patterns define epigenetic regulators associated with neurological dysfunction
L Boukas, JM Havrilla, PF Hickey, AR Quinlan, HT Bjornsson, KD Hansen
Genome research, 2019
2019
The Victorian Collaborative Autism Study: A family and community study of the genetics of autism spectrum disorder
I Scheffer, K Williams, C Green, K Pereira, N Brown, P Hickey, V Lukic, ...
Journal of Intellectual Disability Research 60 (7), 732, 2016
2016
Package ‘bsseq’
KD Hansen, P Hickey, MKD Hansen
2016
Genomics by the beach
PF Hickey, MD Robinson
Genome biology 15 (4), 304, 2014
2014
PW283 Identification and characterisation of a novel hypertrophic cardiomyopathy gene
D Phelan, G Wilson, J Sim, M Bahlo, P Hickey, P James, D du Sart, ...
Global Heart 1 (9), e316, 2014
2014
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Articles 1–20