Characterizing the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort

- Abdullah, N., Abdul Murad, N. A., Scott, R. J., Holliday, E. G., Attia, J., Oldmeadow, C., Mohd Haniff, E. A., Syafruddin, S. E., Abd Jalal, N., Ismail, N., Ishak, M., Jamal, R.

Characterising the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort

- Abdullah, N., Abdul Murad, N., Scott, R. J., Holliday, E. G., Attia, J., Oldmeadow, C., Mohd Haniff, E. A., Syafruddin, S. E., Abd Jalal, N., Ismail, N., Ishak, M., Jamal, R.

Predicting type 2 diabetes using genetic and environmental risk factors in a multi-ethnic Malaysian cohort

- Abdullah, N., Abdul Murad, N. A., Jamal, R., Scott, R. J., Holliday, E. G., Mohd Haniff, E. A., Syafruddin, S. E., Attia, J., Oldmeadow, C., Kamaruddin, M. A., Abd Jalal, N., Ismail, N., Ishak, M.

Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation

- Acikyol, B., Graham, R. M., Trinder, D., House, M. J., Olynyk, J. K., Scott, R. J., Milward, E. A., Johnstone, D. M.

Estrogen receptor polymorphisms and the risk of endometrial cancer

- Ashton, K. A., Proietto, A., Otton, G., Symonds, I., McEvoy, M., Attia, J., Gilbert, M., Hamann, U., Scott, R. J.

Differential gene expression and cytokine production from neutrophils in asthma phenotypes

- Baines, K. J., Simpson, J. L., Bowden, N. A., Scott, R. J., Gibson, P. G.

Analysis of the global methylation status of human spermatozoa and its association with the tendency of these cells to enter apoptosis

- Barzideh, J., Scott, R. J., Aitken, R. J.

Downstream effects of reduction in nucleotide excision repair in response to cisplatin treatment in melanoma

- Bowden, N. A., Ashton, K. A., Avery-Kiejda, K. A., Zhang, X. D., Hersey, P., Scott, R. J.

Altered expression of brain related genes in lymphocytes in schizophrenia

- Bowden, N. A., Weidenhofer, J. C., Scott, R. J., Todd, J., Case, V., Schall, U., Tooney, P. A.

Low-level parental mosaicism in an apparent de novo case of Peutz-Jeghers syndrome

- Butel-Simoes, G. I., Spigelman, A. D., Scott, R. J., Vilain, R. E.

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)

- Davies, G., Armstrong, N., van der Lee, S. J., Le Hellard, S., Liu, T., Marioni, R. E., Oldmeadow, C., Postmus, I., Smith, A. V., Smith, J. A., Thalamuthu, A., Thomson, R., Bis, J. C., Holliday, E. G., Scott, R. J., Attia, J. R., Schofield, P. W., Bressler, J., Chouraki, V., Giddaluru, S., Hofer, E., Ibrahim-Verbaas, C. A., Kirin, M., Lahti, J.

Common variants of DNA repair genes and malignant melanoma

- Debniak, T., Scott, R. J., Kowalska, E., Jakubowska, A., Gronwald, J., Wokolorczyk, D., Maleszka, R., Kładny, J., Lubinski, J., Gorski, B., Cybulskia, C., van de Wetering, T., Serrano-Fernandez, P., Huzarski, T., Byrski, T., Nagay, L., Dębniak, B.

Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis

- Dudding, T., Heron, J., Thakkinstian, A., Nurk, E., Golding, J., Pembrey, M., Ring, S. M., Attia, J., Scott, R. J.

New EPCAM founder deletion in Polish population

- Dymerska, D., Gołębiewska, K., Szwiec, M., Kilar, E., Huzarski, T., Byrski, T., Lubiński, J., Kurzawski, G., Kuświk, M., Rudnicka, H., Scott, R. J., Billings, R., Pławski, A., Boruń, P., Siołek, M., Kozak-Klonowska, B.

Vitamin D receptor variants and the malignant melanoma risk: a population-based study

- Gapska, P., Scott, R. J., Maleszka, R., Sulikowski, M., Lubinski, J., Debniak, T., Serrano-Fernandez, P., Mirecka, A., Rassoud, I., Gorski, B., Cybulski, C., Huzarski, T., Byrski, T., Nagay, L.

Vitamin D receptor variants and breast cancer risk in the Polish population

- Gapska, P., Scott, R. J., Dębniak, T., Serrano-Fernandez, P., Huzarski, T., Byrski, T., Kładny, J., Gronwald, J., Górski, B., Cybulski, C., Lubinski, J.

Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells

- Gardiner, E., Beveridge, N. J., Wu, J. Q., Carr, V., Scott, R. J., Tooney, P. A., Cairns, M. J.

Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis

- Graves, M. C., Benton, M., Lea, R. A., Boyle, M., Tajouri, L., Macartney-Coxson, D., Scott, R. J., Lechner-Scott, J.

Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia

- Green, M. J., Cairns, M. J., Wu, J., Dragovic, M., Jablensky, A., Tooney, P. A., Scott, R. J., Carr, V. J.

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

- Ibrahim-Verbaas, C. A., Bressler, J., Chibnik, L. B., Liu, Y., Vitart, V., Kirin, M., Petrovic, K., Polasek, O., Zgaga, L., Fawns-Ritchie, C., Hoffmann, P., Karjalainen, J., Debette, S., Oldmeadow, C., Holliday, E. G., Scott, R. J., Attia, J. R., Schofield, P. W., Schuur, M., Smith, A. V., Bis, J. C., Davies, G., Trompet, S., Smith, J. A., Wolf, C.