Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences

Por Czyz, Witold, Morahan, Julia M, Ebers, George C, Ramagopalan, Sreeram V
Publicado em 2012

The Effect of Single Nucleotide Polymorphisms from Genome Wide Association Studies in Multiple Sclerosis on Gene Expression

Por Handel, Adam E., Handunnetthi, Lahiru, Berlanga, Antonio J., Watson, Corey T., Morahan, Julia M., Ramagopalan, Sreeram V.
Publicado em 2010

Month of birth, vitamin D and risk of immune-mediated disease: a case control study

Por Disanto, Giulio, Chaplin, George, Morahan, Julia M, Giovannoni, Gavin, Hyppönen, Elina, Ebers, George C, Ramagopalan, Sreeram V
Publicado em 2012

Genomic Regions Associated with Multiple Sclerosis Are Active in B Cells

Por Disanto, Giulio, Sandve, Geir Kjetil, Berlanga-Taylor, Antonio J., Morahan, Julia M., Dobson, Ruth, Giovannoni, Gavin, Ramagopalan, Sreeram V.
Publicado em 2012

Seasonal Distribution of Psychiatric Births in England

Por Disanto, Giulio, Morahan, Julia M., Lacey, Melanie V., DeLuca, Gabriele C., Giovannoni, Gavin, Ebers, George C., Ramagopalan, Sreeram V.
Publicado em 2012

Vitamin D receptor binding, chromatin states and association with multiple sclerosis

Por Disanto, Giulio, Sandve, Geir Kjetil, Berlanga-Taylor, Antonio J., Ragnedda, Giammario, Morahan, Julia M., Watson, Corey T., Giovannoni, Gavin, Ebers, George C., Ramagopalan, Sreeram V.
Publicado em 2012

Heterogeneity in Multiple Sclerosis: Scratching the Surface of a Complex Disease

Por Disanto, Giulio, Berlanga, Antonio J., Handel, Adam E., Para, Andrea E., Burrell, Amy M., Fries, Anastasia, Handunnetthi, Lahiru, De Luca, Gabriele C., Morahan, Julia M.
Publicado em 2011

Functional analysis of missense variants in the TRESK (KCNK18) K(+) channel

Por Andres-Enguix, Isabelle, Shang, Lijun, Stansfeld, Phillip J., Morahan, Julia M., Sansom, Mark S. P., Lafrenière, Ronald G., Roy, Bishakha, Griffiths, Lyn R., Rouleau, Guy A., Ebers, George C., Cader, Zameel M., Tucker, Stephen J.
Publicado em 2012

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene

Por Dyment, David A., Cader, M. Zameel, Chao, Michael J., Lincoln, Matthew R., Morrison, Katie M., Disanto, Giulio, Morahan, Julia M., De Luca, Gabriele C., Sadovnick, A. Dessa, Lepage, Pierre, Montpetit, Alexandre, Ebers, George C., Ramagopalan, Sreeram V.
Publicado em 2012

A ChIP-seq defined genome-wide map of vitamin D receptor binding: Associations with disease and evolution

Por Ramagopalan, Sreeram V., Heger, Andreas, Berlanga, Antonio J., Maugeri, Narelle J., Lincoln, Matthew R., Burrell, Amy, Handunnetthi, Lahiru, Handel, Adam E., Disanto, Giulio, Orton, Sarah-Michelle, Watson, Corey T., Morahan, Julia M., Giovannoni, Gavin, Ponting, Chris P., Ebers, George C., Knight, Julian C.
Publicado em 2010