Mark E.S. Bailey - Concepedia

Author

Mark E.S. Bailey

Also Known As

Bailey, Mark, Cobb, Stuart R., M Bailey, M E Bailey, M E S Bailey, M. Bailey, M. E. S. BAILEY, M. E. S. Bailey, M. E.S. Bailey, M.E.S. Bailey

139

Publications

7.3K

Citations

H-Index

148

Concepts

All Affiliations

University of Glasgow Karolinska Institutet University of Edinburgh Cardiff University Charing Cross Hospital

About

Mark E.S. Bailey is an author at University of Glasgow specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	27	2.1K
2	Public Health	9	9	851
3	Health Sciences	6	6	361
4	Natural Sciences	5	5	171
5	Education	3	3	98

Mark E.S. Bailey

Publications

6.6K

Citations

H-Index

Page 1

	Year	Citations
Rett syndrome: Revised diagnostic criteria and nomenclature Jeffrey L. Neul, Walter E. Kaufmann, Daniel G. Glaze, Annals of Neurology	2010	1.4K
Objective vs. Self-Reported Physical Activity and Sedentary Time: Effects of Measurement Method on Relationships with Risk Biomarkers Carlos Celis‐Morales, Francisco Pérez‐Bravo, Luis Ibáñez, PLoS ONE	2012	479
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 Laura M. Lyall, Cathy Wyse, Nicholas Graham, The Lancet Psychiatry Mental HealthSocial SciencesPsychologyMood SymptomCircadian Rhythm	2018	387
Genome-wide association study of multisite chronic pain in UK Biobank Keira J.A. Johnston, Mark J. Adams, Barbara I. Nicholl, PLoS Genetics GeneticsPolygenic RiskGenetic EpidemiologyMultiomicsGenetic Foundation	2019	268
Association analysis of the ACTN3 R577X polymorphism and complex quantitative body composition and performance phenotypes in adolescent Greeks Colin N. Moran, Nan Yang, Mark E.S. Bailey, European Journal of Human Genetics Association AnalysisAdolescent GreeksPhysical ActivityBody CompositionGenotype-phenotype Association	2006	199
A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)<sub>n</sub> repeat Catherine Boucher, Stephanie King, Nessa Carey, Human Molecular Genetics	1995	184
Genetics of Psoriasis: Paternal Inheritance and a Locus on Chromosome 6p A. David Burden, Malcolm B. Hodgins, David M. Tillman, Journal of Investigative Dermatology Paternal InheritanceGenetic DisorderMedicineGeneticsMolecular Genetics	1998	163
Improved Survival and Reduced Phenotypic Severity Following AAV9/MECP2 Gene Transfer to Neonatal and Juvenile Male Mecp2 Knockout Mice Kamal K.E. Gadalla, Mark E.S. Bailey, R.C. Spike, Molecular Therapy	2012	153
Comparison of Genome Screens for Two Independent Cohorts Provides Replication of Suggestive Linkage of Bone Mineral Density to 3p21 and 1p36 Scott G. Wilson, Peter Reed, Aruna T. Bansal, The American Journal of Human Genetics Genome-wide Association StudySuggestive LinkageGeneticsGenetic EpidemiologyBone Mineral Density	2003	135
Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide Rona J. Strawbridge, Joey Ward, Amy Ferguson, EBioMedicine Genome-wide Association StudyPsychiatryGeneticsPsychiatric GeneticsSuicide	2019	122

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