Dr Jillian Couto

  • Research Associate in Molecular Environmental Genomic Method (Infrastructure and Environment)

telephone: 01413306311
email: Jillian.Couto@glasgow.ac.uk

Publications

List by: Type | Date

Jump to: 2015 | 2012 | 2010 | 2009 | 2008 | 2006 | 2005 | 2004
Number of items: 8.

2015

Couto, J. M., Ijaz, U. Z., Phoenix, V. R., Schirmer, M., and Sloan, W. T. (2015) Metagenomic sequencing unravels gene fragments with phylogenetic signatures of O2-tolerant NiFe membrane-bound hydrogenases in lacustrine sediment. Current Microbiology, 71(2), pp. 296-302. (doi:10.1007/s00284-015-0846-2) (PMID:26044993) (PMCID:PMC4486115)

2012

Morales Montero, F. et al. (2012) Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity. Human Molecular Genetics, 21(16), pp. 3558-3567. (doi:10.1093/hmg/dds185)

2010

Couto, J.M. et al. (2010) Association of reading disabilities with regions marked by acetylated H3 histones inKIAA0319. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B(2), pp. 447-462. (doi:10.1002/ajmg.b.30999)

2009

Couto, J., Gomez, L., Wigg, K., Ickowicz, A., Pathare, T., Malone, M., Kennedy, J.L., Schachar, R., and Barr, C.L. (2009) Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biological Psychiatry, 66(4), pp. 368-375. (doi:10.1016/j.biopsych.2009.02.016)

2008

Couto, J. et al. (2008) The KIAA0319-Like(KIAA0319L)gene on chromosome 1p34 as a candidate for reading disabilities. Journal of Neurogenetics, 22(4), pp. 295-313. (doi:10.1080/01677060802354328)

2006

Wang, Y., Gracheva, E.O., Richmond, J., Kawano, T., Couto, J.M., Calarco, J.A., Vijayaratnam, V., Jin, Y., and Zhen, M. (2006) The C2H2 zinc-finger protein SYD-9 is a putative posttranscriptional regulator for synaptic transmission. Proceedings of the National Academy of Sciences of the United States of America, 103(27), pp. 10450-10455. (doi:10.1073/pnas.0602073103)

2005

Zai, G., King, N., Wigg, K., Couto, J., Wong, G.W.H., Honer, W.G., Barr, C.L., and Kennedy, J.L. (2005) Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia. Genes, Brain and Behavior, 4(1), pp. 2-9. (doi:10.1111/j.1601-183X.2004.00089.x)

2004

Wigg, K.G., Couto, J., Feng, Y., Anderson, B., Cate-Carter, T.D., Macciardi, F., Tannock, R., Lovett, M.W., Humphries, T.W., and Barr, C.L. (2004) Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Molecular Psychiatry, 9(12), pp. 1111-1121. (doi:10.1038/sj.mp.4001543)

This list was generated on Tue Mar 28 20:42:00 2017 BST.
Jump to: Articles
Number of items: 8.

Articles

Couto, J. M., Ijaz, U. Z., Phoenix, V. R., Schirmer, M., and Sloan, W. T. (2015) Metagenomic sequencing unravels gene fragments with phylogenetic signatures of O2-tolerant NiFe membrane-bound hydrogenases in lacustrine sediment. Current Microbiology, 71(2), pp. 296-302. (doi:10.1007/s00284-015-0846-2) (PMID:26044993) (PMCID:PMC4486115)

Morales Montero, F. et al. (2012) Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity. Human Molecular Genetics, 21(16), pp. 3558-3567. (doi:10.1093/hmg/dds185)

Couto, J.M. et al. (2010) Association of reading disabilities with regions marked by acetylated H3 histones inKIAA0319. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 153B(2), pp. 447-462. (doi:10.1002/ajmg.b.30999)

Couto, J., Gomez, L., Wigg, K., Ickowicz, A., Pathare, T., Malone, M., Kennedy, J.L., Schachar, R., and Barr, C.L. (2009) Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p. Biological Psychiatry, 66(4), pp. 368-375. (doi:10.1016/j.biopsych.2009.02.016)

Couto, J. et al. (2008) The KIAA0319-Like(KIAA0319L)gene on chromosome 1p34 as a candidate for reading disabilities. Journal of Neurogenetics, 22(4), pp. 295-313. (doi:10.1080/01677060802354328)

Wang, Y., Gracheva, E.O., Richmond, J., Kawano, T., Couto, J.M., Calarco, J.A., Vijayaratnam, V., Jin, Y., and Zhen, M. (2006) The C2H2 zinc-finger protein SYD-9 is a putative posttranscriptional regulator for synaptic transmission. Proceedings of the National Academy of Sciences of the United States of America, 103(27), pp. 10450-10455. (doi:10.1073/pnas.0602073103)

Zai, G., King, N., Wigg, K., Couto, J., Wong, G.W.H., Honer, W.G., Barr, C.L., and Kennedy, J.L. (2005) Genetic study of the myelin oligodendrocyte glycoprotein (MOG) gene in schizophrenia. Genes, Brain and Behavior, 4(1), pp. 2-9. (doi:10.1111/j.1601-183X.2004.00089.x)

Wigg, K.G., Couto, J., Feng, Y., Anderson, B., Cate-Carter, T.D., Macciardi, F., Tannock, R., Lovett, M.W., Humphries, T.W., and Barr, C.L. (2004) Support for EKN1 as the susceptibility locus for dyslexia on 15q21. Molecular Psychiatry, 9(12), pp. 1111-1121. (doi:10.1038/sj.mp.4001543)

This list was generated on Tue Mar 28 20:42:00 2017 BST.