Comment on “Genomic Hypomethylation in the Human Germline Associates with Selective Structural Mutability in the Human Genome”

Por Watson, Corey T., Garg, Paras, Sharp, Andrew J.
Publicado em 2013

Genomic organization of duplicated short wave-sensitive and long wave-sensitive opsin genes in the green swordtail, Xiphophorus helleri

Por Watson, Corey T, Lubieniecki, Krzysztof P, Loew, Ellis, Davidson, William S, Breden, Felix
Publicado em 2010

Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs

Por Watson, Corey T., Disanto, Giulio, Breden, Felix, Giovannoni, Gavin, Ramagopalan, Sreeram V.
Publicado em 2012

The Genetics of Microdeletion and Microduplication Syndromes: An Update

Por Watson, Corey T., Marques-Bonet, Tomas, Sharp, Andrew J., Mefford, Heather C.
Publicado no Annu Rev Genomics Hum Genet (2014)

Age-Associated Hyper-Methylated Regions in the Human Brain Overlap with Bivalent Chromatin Domains

Por Watson, Corey T., Disanto, Giulio, Sandve, Geir Kjetil, Breden, Felix, Giovannoni, Gavin, 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

Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC Exposure

Por Watson, Corey T, Szutorisz, Henrietta, Garg, Paras, Martin, Qammarah, Landry, Joseph A, Sharp, Andrew J, Hurd, Yasmin L
Publicado no Neuropsychopharmacology (2015)

DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation

Por Bala Tannan, Neeta, Brahmachary, Manisha, Garg, Paras, Borel, Christelle, Alnefaie, Randah, Watson, Corey T., Thomas, N. Simon, Sharp, Andrew J.
Publicado em 2014

Genome-wide12 DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer’s disease

Por Watson, Corey T., Roussos, Panos, Garg, Paras, Ho, Daniel J., Azam, Nidha, Katsel, Pavel L., Haroutunian, Vahram, Sharp, Andrew J.
Publicado no Genome Med (2016)

Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye

Por Murphy, Taylor R., Vihtelic, Thomas S., Ile, Kristina E., Watson, Corey T., Willer, Gregory B., Gregg, Ronald G., Bankaitis, Vytas A., Hyde, David R.
Publicado em 2011

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

IGHV1-69 polymorphism modulates anti-influenza antibody repertoires, correlates with IGHV utilization shifts and varies by ethnicity

Por Avnir, Yuval, Watson, Corey T., Glanville, Jacob, Peterson, Eric C., Tallarico, Aimee S., Bennett, Andrew S., Qin, Kun, Fu, Ying, Huang, Chiung-Yu, Beigel, John H., Breden, Felix, Zhu, Quan, Marasco, Wayne A.
Publicado no Sci Rep (2016)

Erratum: IGHV1-69 polymorphism modulates anti-influenza antibody repertoires, correlates with IGHV utilization shifts and varies by ethnicity

Por Avnir, Yuval, Watson, Corey T., Glanville, Jacob, Peterson, Eric C., Tallarico, Aimee S., Bennett, Andrew S., Qin, Kun, Fu, Ying, Huang, Chiung-Yu, Beigel, John H., Breden, Felix, Zhu, Quan, Marasco, Wayne A.
Publicado no Sci Rep (2016)

Mechanisms Underlying Metabolic and Neural Defects in Zebrafish and Human Multiple Acyl-CoA Dehydrogenase Deficiency (MADD)

Por Song, Yuanquan, Selak, Mary A., Watson, Corey T., Coutts, Christopher, Scherer, Paul C., Panzer, Jessica A., Gibbs, Sarah, Scott, Marion O., Willer, Gregory, Gregg, Ronald G., Ali, Declan W., Bennett, Michael J., Balice-Gordon, Rita J.
Publicado em 2009

Complete Haplotype Sequence of the Human Immunoglobulin Heavy-Chain Variable, Diversity, and Joining Genes and Characterization of Allelic and Copy-Number Variation

Por Watson, Corey T., Steinberg, Karyn M., Huddleston, John, Warren, Rene L., Malig, Maika, Schein, Jacqueline, Willsey, A. Jeremy, Joy, Jeffrey B., Scott, Jamie K., Graves, Tina A., Wilson, Richard K., Holt, Robert A., Eichler, Evan E., Breden, Felix
Publicado em 2013

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

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

Por Joshi, Ricky S., Garg, Paras, Zaitlen, Noah, Lappalainen, Tuuli, Watson, Corey T., Azam, Nidha, Ho, Daniel, Li, Xin, Antonarakis, Stylianos E., Brunner, Han G., Buiting, Karin, Cheung, Sau Wai, Coffee, Bradford, Eggermann, Thomas, Francis, David, Geraedts, Joep P., Gimelli, Giorgio, Jacobson, Samuel G., Le Caignec, Cedric, de Leeuw, Nicole, Liehr, Thomas, Mackay, Deborah J., Montgomery, Stephen B., Pagnamenta, Alistair T., Papenhausen, Peter, Robinson, David O., Ruivenkamp, Claudia, Schwartz, Charles, Steiner, Bernhard, Stevenson, David A., Surti, Urvashi, Wassink, Thomas, Sharp, Andrew J.
Publicado no Am J Hum Genet (2016)