Prof. Valerie O'Leary
Prof. Valerie O'Leary
Charles University, Third Faculty of Medicine, Department of Medical Genetics
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Cited by
Cited by
Exercise-induced reversal of insulin resistance in obese elderly is associated with reduced visceral fat
VB O’Leary, CM Marchetti, RK Krishnan, BP Stetzer, F Gonzalez, ...
Journal of applied physiology 100 (5), 1584-1589, 2006
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a …
LC Brody, M Conley, C Cox, PN Kirke, MP McKeever, JL Mills, AM Molloy, ...
The American Journal of Human Genetics 71 (5), 1207-1215, 2002
MTRR and MTHFR polymorphism: link to Down syndrome?
VB O'Leary, A Parle‐McDermott, AM Molloy, PN Kirke, Z Johnson, ...
American journal of medical genetics 107 (2), 151-155, 2002
Exercise and diet enhance fat oxidation and reduce insulin resistance in older obese adults
TPJ Solomon, SN Sistrun, RK Krishnan, LF Del Aguila, CM Marchetti, ...
Journal of applied physiology 104 (5), 1313-1319, 2008
Impact of the MTHFR C677T polymorphism on risk of neural tube defects: case-control study
PN Kirke, JL Mills, AM Molloy, LC Brody, VB O'Leary, L Daly, S Murray, ...
Bmj 328 (7455), 1535-1536, 2004
Enhanced adiponectin multimer ratio and skeletal muscle adiponectin receptor expression following exercise training and diet in older insulin-resistant adults
VB O'Leary, AE Jorett, CM Marchetti, F Gonzalez, SA Phillips, TP Ciaraldi, ...
American Journal of Physiology-Endocrinology and Metabolism 293 (1), E421-E427, 2007
PARTICLE, a Triplex-Forming Long ncRNA, Regulates Locus-Specific Methylation in Response to Low-Dose Irradiation
AN O'Leary VB, Ovsepian SV, Carrascosa LG, Buske FA, Radulovic V, Niyazi M ...
Cell Reports 11 (3), 474-85, 2015
Decreased visfatin after exercise training correlates with improved glucose tolerance
J Haus, T Solomon, C Marchetti, V O'Leary, L Brooks, F Gonzalez, ...
Medicine+ Science in Sports+ Exercise 41 (6), 1255, 2009
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population
A Parle-McDermott, PN Kirke, JL Mills, AM Molloy, C Cox, VB O'Leary, ...
European journal of human genetics 14 (6), 768-772, 2006
The 19‐bp deletion polymorphism in intron‐1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population
A Parle‐McDermott, F Pangilinan, JL Mills, PN Kirke, ER Gibney, ...
American journal of medical genetics Part A 143 (11), 1174-1180, 2007
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects
F Pangilinan, AM Molloy, JL Mills, JF Troendle, A Parle-McDermott, ...
BMC medical genetics 13 (1), 1-19, 2012
Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association
VB O’Leary, JL Mills, F Pangilinan, PN Kirke, C Cox, M Conley, A Weiler, ...
Molecular genetics and metabolism 85 (3), 220-227, 2005
Analysis of the MTHFR 1298A→ C and 677C→ T polymorphisms as risk factors for neural tube defects
A Parle-McDermott, JL Mills, PN Kirke, VB O'Leary, DA Swanson, ...
Journal of human genetics 48 (4), 190-193, 2003
Retinol‐binding protein 4 (RBP4) protein expression is increased in omental adipose tissue of severely obese patients
KR Kelly, SR Kashyap, VB O'leary, J Major, PR Schauer, JP Kirwan
Obesity 18 (4), 663-666, 2010
The glucose-dependent insulinotropic polypeptide and glucose-stimulated insulin response to exercise training and diet in obesity
KR Kelly, LM Brooks, TPJ Solomon, SR Kashyap, VB O'Leary, JP Kirwan
American Journal of Physiology-Endocrinology and Metabolism 296 (6), E1269-E1274, 2009
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
A Parle‐McDermott, JL Mills, PN Kirke, C Cox, CC Signore, S Kirke, ...
American Journal of Medical Genetics Part A 132 (4), 365-368, 2005
Genome‐wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma
J Smida, H Xu, Y Zhang, D Baumhoer, S Ribi, M Kovac, I von Luettichau, ...
International journal of cancer 141 (4), 816-828, 2017
Reduced folate carrier polymorphisms and neural tube defect risk
VB O’Leary, F Pangilinan, C Cox, A Parle-McDermott, M Conley, ...
Molecular genetics and metabolism 87 (4), 364-369, 2006
Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population
DA Swanson, F Pangilinan, JL Mills, PN Kirke, M Conley, A Weiler, T Frey, ...
Birth Defects Research Part A: Clinical and Molecular Teratology 73 (4), 239-244, 2005
Distinctive role of KV1. 1 subunit in the biology and functions of low threshold K+ channels with implications for neurological disease
SV Ovsepian, M LeBerre, V Steuber, VB O'Leary, C Leibold, JO Dolly
Pharmacology & therapeutics 159, 93-101, 2016
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