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Mark E. S. Bailey
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Year
Rett syndrome: revised diagnostic criteria and nomenclature
JL Neul, WE Kaufmann, DG Glaze, J Christodoulou, AJ Clarke, ...
Annals of neurology 68 (6), 944-950, 2010
15182010
Objective vs. self-reported physical activity and sedentary time: Effects of measurement method on relationships with risk biomarkers
CA Celis-Morales, F Perez-Bravo, L Ibañez, C Salas, MES Bailey, ...
PLoS One 7 (5), e36345, 2012
6142012
Association of disrupted circadian rhythmicity with mood disorders, subjective wellbeing, and cognitive function: a cross-sectional study of 91 105 participants from the UK Biobank
LM Lyall, CA Wyse, N Graham, A Ferguson, DM Lyall, B Cullen, ...
The Lancet Psychiatry 5 (6), 507-514, 2018
3442018
Association analysis of the ACTN3 R577X polymorphism and complex quantitative body composition and performance phenotypes in adolescent Greeks
CN Moran, N Yang, MES Bailey, A Tsiokanos, A Jamurtas, DG MacArthur, ...
European Journal of Human Genetics 15 (1), 88-93, 2006
2952006
Genome-wide analysis of over 106,000 individuals identifies 9 neuroticism-associated loci
DJ Smith, V Escott-Price, G Davies, MES Bailey, LC Conde, J Ward, ...
bioRxiv, 032417, 2015
2882015
A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG) n repeat
CA Boucher, SK King, N Carey, R Krahe, CL Winchester, S Rahman, ...
Human molecular genetics 4 (10), 1919-1925, 1995
2341995
Genetics of psoriasis: paternal inheritance and a locus on chromosome 6p
AD Burden, S Javed, M Bailey, M Hodgins, M Connor, D Tillman
Journal of investigative dermatology 110 (6), 958-960, 1998
2151998
Genome-wide Association Study of Multisite Chronic Pain in UK Biobank
KJA Johnston, MJ Adams, BI Nicholl, J Ward, R Strawbridge, A Ferguson, ...
bioRxiv, 502807, 2018
2022018
Improved survival and reduced phenotypic severity following AAV9/MECP2 gene transfer to neonatal and juvenile male Mecp2 knockout mice
KKE Gadalla, MES Bailey, RC Spike, PD Ross, KT Woodard, SN Kalburgi, ...
Molecular Therapy 21 (1), 18-30, 2012
1732012
MeCP2 and Rett syndrome - reversibility and potential avenues for therapy.
KKE Gadalla, MES Bailey, SR Cobb
Biochemical Journal - BJ Disease 439, 1-14, 2011
1392011
Association analysis of ACE and ACTN3 in Elite Caucasian and East Asian Swimmers.
G Wang, E Mikami, LL Chiu, A de Perini, M Deason, N Fuku, M Miyachi, ...
Medicine and science in sports and exercise, 2012
1332012
Mutation screening in Rett syndrome patients
F Xiang, S Buervenich, P Nicolao, MES Bailey, Z Zhang, M Anvret
Journal of medical genetics 37 (4), 250-255, 2000
1322000
Correlation between clinical severity in patients with Rett syndrome with a p. R168X or p. T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome …
H Archer, J Evans, H Leonard, L Colvin, D Ravine, J Christodoulou, ...
Journal of medical genetics 44 (2), 148-152, 2007
1282007
Adverse metabolic and mental health outcomes associated with shiftwork in a population-based study of 277,168 workers in UK biobank
CA Wyse, CA Celis Morales, N Graham, Y Fan, J Ward, AM Curtis, ...
Annals of medicine 49 (5), 411-420, 2017
1192017
Dietary intake, FTO genetic variants and adiposity: a combined analysis of over 16,000 children and adolescents
Q Qi, MK Downer, TO Kilpeläinen, HR Taal, SJ Barton, I Ntalla, M Standl, ...
Diabetes, db141629, 2015
1192015
Plasma microRNA levels differ between endurance and strength athletes
SL Wardle, MES Bailey, A Kilikevicius, D Malkova, RH Wilson, ...
PloS one 10 (4), e0122107, 2015
1112015
Novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide.
RJ Strawbridge, J Ward, A Ferguson, N Graham, RJ Shaw, B Cullen, ...
bioRxiv, 451971, 2018
109*2018
Insulin resistance in Chileans of European and indigenous descent: evidence for an ethnicity x environment interaction
CA Celis-Morales, F Perez-Bravo, L Ibañes, R Sanzana, E Hormazabal, ...
PloS one 6 (9), e24690, 2011
1072011
Synaptic plasticity deficits in an experimental model of rett syndrome: long-term potentiation saturation and its pharmacological reversal
SM Weng, F McLeod, MES Bailey, SR Cobb
Neuroscience 180, 314-321, 2011
1072011
Familial Ménière's disease: clinical and genetic aspects
AW Morrison, MES Bailey, GAJ Morrison
Journal of Laryngology and Otology 123 (01), 29-37, 2009
1062009
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Articles 1–20