Evolutionary History of the ADRB2 Gene in Humans

Por Wilson, Richard H., Moran, Colin N., Cole, John J., Pitsiladis, Yannis P., Bailey, Mark E.S.
Publicado em 2010

Should Physical Activity Recommendations Be Ethnicity-Specific? Evidence from a Cross-Sectional Study of South Asian and European Men

Por Celis-Morales, Carlos A., Ghouri, Nazim, Bailey, Mark E. S., Sattar, Naveed, Gill, Jason M. R.
Publicado em 2013

Gait Analysis in a Mecp2 Knockout Mouse Model of Rett Syndrome Reveals Early-Onset and Progressive Motor Deficits

Por Gadalla, Kamal K. E., Ross, Paul D., Riddell, John S., Bailey, Mark E. S., Cobb, Stuart R.
Publicado no PLoS One (2014)

Objective vs. Self-Reported Physical Activity and Sedentary Time: Effects of Measurement Method on Relationships with Risk Biomarkers

Por Celis-Morales, Carlos A., Perez-Bravo, Francisco, Ibañez, Luis, Salas, Carlos, Bailey, Mark E. S., Gill, Jason M. R.
Publicado em 2012

Plasma MicroRNA Levels Differ between Endurance and Strength Athletes

Por Wardle, Sophie L., Bailey, Mark E. S., Kilikevicius, Audrius, Malkova, Dalia, Wilson, Richard H., Venckunas, Tomas, Moran, Colin N.
Publicado no PLoS One (2015)

Characterisation of CDKL5 Transcript Isoforms in Human and Mouse

Por Hector, Ralph D., Dando, Owen, Landsberger, Nicoletta, Kilstrup-Nielsen, Charlotte, Kind, Peter C., Bailey, Mark E. S., Cobb, Stuart R.
Publicado no PLoS One (2016)

Development of a Novel AAV Gene Therapy Cassette with Improved Safety Features and Efficacy in a Mouse Model of Rett Syndrome

Por Gadalla, Kamal K.E., Vudhironarit, Thishnapha, Hector, Ralph D., Sinnett, Sarah, Bahey, Noha G., Bailey, Mark E.S., Gray, Steven J., Cobb, Stuart R.
Publicado no Mol Ther Methods Clin Dev (2017)

Insulin Resistance in Chileans of European and Indigenous Descent: Evidence for an Ethnicity x Environment Interaction

Por Celis-Morales, Carlos A., Perez-Bravo, Francisco, Ibañes, Luis, Sanzana, Ruth, Hormazabal, Edison, Ulloa, Natalia, Calvo, Carlos, Bailey, Mark E. S., Gill, Jason M. R.
Publicado em 2011

Improved MECP2 Gene Therapy Extends the Survival of MeCP2-Null Mice without Apparent Toxicity after Intracisternal Delivery

Por Sinnett, Sarah E., Hector, Ralph D., Gadalla, Kamal K.E., Heindel, Clifford, Chen, Daphne, Zaric, Violeta, Bailey, Mark E.S., Cobb, Stuart R., Gray, Steven J.
Publicado no Mol Ther Methods Clin Dev (2017)

Identification of novel common variants associated with chronic pain using conditional false discovery rate analysis with major depressive disorder and assessment of pleiotropic ef...

Por Johnston, Keira J. A., Adams, Mark J., Nicholl, Barbara I., Ward, Joey, Strawbridge, Rona J., McIntosh, Andrew M., Smith, Daniel J., Bailey, Mark E. S.
Publicado no Transl Psychiatry (2019)

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 inactivation...

Por Archer, Hayley, Evans, Julie, Leonard, Helen, Colvin, Lyn, Ravine, David, Christodoulou, John, Williamson, Sarah, Charman, Tony, Bailey, Mark E S, Sampson, Julian, de Klerk, Nicholas, Clarke, Angus
Publicado em 2007

CDKL5 variants: Improving our understanding of a rare neurologic disorder

Por Hector, Ralph D., Kalscheuer, Vera M., Hennig, Friederike, Leonard, Helen, Downs, Jenny, Clarke, Angus, Benke, Tim A., Armstrong, Judith, Pineda, Mercedes, Bailey, Mark E.S., Cobb, Stuart R.
Publicado no Neurol Genet (2017)

Genome-wide association study of multisite chronic pain in UK Biobank

Por Johnston, Keira J. A., Adams, Mark J., Nicholl, Barbara I., Ward, Joey, Strawbridge, Rona J., Ferguson, Amy, McIntosh, Andrew M., Bailey, Mark E. S., Smith, Daniel J.
Publicado no PLoS Genet (2019)

FTO genotype and adiposity in children: physical activity levels influence the effect of the risk genotype in adolescent males

Por Scott, Robert A, Bailey, Mark E S, Moran, Colin N, Wilson, Richard H, Fuku, Noriyuki, Tanaka, Masashi, Tsiokanos, Athanasios, Jamurtas, Athanasios Z, Grammatikaki, Evangelia, Moschonis, George, Manios, Yannis, Pitsiladis, Yannis P
Publicado em 2010

Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes

Por Ross, Paul D., Guy, Jacky, Selfridge, Jim, Kamal, Bushra, Bahey, Noha, Tanner, K. Elizabeth, Gillingwater, Thomas H., Jones, Ross A., Loughrey, Christopher M., McCarroll, Charlotte S., Bailey, Mark E.S., Bird, Adrian, Cobb, Stuart
Publicado no Hum Mol Genet (2016)

Rett Syndrome: Revised Diagnostic Criteria and Nomenclature

Por Neul, Jeffrey L., Kaufmann, Walter E., Glaze, Daniel G., Christodoulou, John, Clarke, Angus J., Bahi-Buisson, Nadia, Leonard, Helen, Bailey, Mark E. S., Schanen, N. Carolyn, Zappella, Michele, Renieri, Alessandra, Huppke, Peter, Percy, Alan K.
Publicado em 2010

Novel genome-wide associations for anhedonia, genetic correlation with psychiatric disorders, and polygenic association with brain structure

Por Ward, Joey, Lyall, Laura M., Bethlehem, Richard A. I., Ferguson, Amy, Strawbridge, Rona J., Lyall, Donald M., Cullen, Breda, Graham, Nicholas, Johnston, Keira J. A., Bailey, Mark E. S., Murray, Graham K., Smith, Daniel J.
Publicado no Transl Psychiatry (2019)

Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UK Biobank

Por Strawbridge, Rona J., Ward, Joey, Bailey, Mark E.S., Cullen, Breda, Ferguson, Amy, Graham, Nicholas, Johnston, Keira J.A., Lyall, Laura M., Pearsall, Robert, Pell, Jill, Shaw, Richard J., Tank, Rachana, Lyall, Donald M., Smith, Daniel J.
Publicado no Arterioscler Thromb Vasc Biol (2020)

Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia

Por Ward, Joey, Strawbridge, Rona J., Bailey, Mark E. S., Graham, Nicholas, Ferguson, Amy, Lyall, Donald M., Cullen, Breda, Pidgeon, Laura M., Cavanagh, Jonathan, Mackay, Daniel F., Pell, Jill P., O’Donovan, Michael, Escott-Price, Valentina, Smith, Daniel J.
Publicado no Transl Psychiatry (2017)

The role of neuromedin U in adiposity regulation. Haplotype analysis in European children from the IDEFICS Cohort

Por Gianfagna, Francesco, Grippi, Claudio, Ahrens, Wolfgang, Bailey, Mark E. S., Börnhorst, Claudia, De Henauw, Stefan, Foraita, Ronja, Koni, Anna C., Krogh, Vittorio, Mårild, Staffan, Molnár, Dénes, Moreno, Luis, Pitsiladis, Yannis, Russo, Paola, Siani, Alfonso, Tornaritis, Michael, Veidebaum, Toomas, Iacoviello, Licia
Publicado no PLoS One (2017)