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: 2017 | 2015 | 2012 | 2010 | 2009 | 2008 | 2006 | 2005 | 2004
Number of items: 10.

2017

Couto, J. M. (2017) Biofilms for babies: introducing microbes and biofilms to preschool-aged children. Journal of Microbiology and Biology Education, 18(1), (doi:10.1128/jmbe.v18i1.1273) (PMID:28512515) (PMCID:PMC5410756)

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)

Wigg, K. G. et al. (2005) Investigation of the relationship of attention deficit hyperactivity disorder to the EKN1 gene on chromosome 15q21. Scientific Studies of Reading, 9(3), pp. 261-283. (doi:10.1207/s1532799xssr0903_5)

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 Mon Jun 26 02:33:54 2017 BST.
Jump to: Articles
Number of items: 10.

Articles

Couto, J. M. (2017) Biofilms for babies: introducing microbes and biofilms to preschool-aged children. Journal of Microbiology and Biology Education, 18(1), (doi:10.1128/jmbe.v18i1.1273) (PMID:28512515) (PMCID:PMC5410756)

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. et al. (2005) Investigation of the relationship of attention deficit hyperactivity disorder to the EKN1 gene on chromosome 15q21. Scientific Studies of Reading, 9(3), pp. 261-283. (doi:10.1207/s1532799xssr0903_5)

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 Mon Jun 26 02:33:54 2017 BST.