A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology
- Creator: Talseth-Palmer, B. A. , Bowden, N. A. , Scott, R. J. , Meldrum, C. , Nicholl, J. , Thompson, E. , Friend, K. , Liebelt, J. , Bratkovic, D. , Haan, E. , Yu, S.
- Resource Type: journal article
- Date: 2009
Altered expression of brain related genes in lymphocytes in schizophrenia
- Creator: Bowden, N. A. , Weidenhofer, J. C. , Scott, R. J. , Todd, J. , Case, V. , Schall, U. , Tooney, P. A.
- Resource Type: conference paper
- Date: 2004
Analysis of the global methylation status of human spermatozoa and its association with the tendency of these cells to enter apoptosis
- Creator: Barzideh, J. , Scott, R. J. , Aitken, R. J.
- Resource Type: journal article
- Date: 2013
Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
- Creator: van der Luijt, B. , Devilee, P. , EMBRACE, , Easton, D. F. , Peock, S. , Frost, D. , Platte, R. , Ellis, S. D. , Fineberg, E. , Evans, D. G. , Lalloo, F. , Eeles, R. , Jacobs, C. , Adlard, J. , Davidson, R. , Eccles, D. , Cole, T. , Cook, J. , Godwin, A. , Bove, B. , GEMO Study Collaborators, , Stoppa-Lyonnet, D. , Caux-Moncoutier, V. , Coupier, I. , Peyrat, J.-P. , Vennin, P. , Muller, D. , Fricker, J. P. , Venat-Bouvet, L. , Johannsson, O. Th. , Isaacs, C. , Schmutzler, R. , Wappenschmidt, B. , Meindl, A. , Arnold, N. , Varon-Mateeva, R. , Niederacher, D. , Sutter, C. , Deissler, H. , Preisler-Adams, S. , Simard, J. , Soucy, P. , Durocher, F. , Chenevix-Trench, G. , Beesley, J. , Chen, X. , ConFab, K. , Rebbeck, T. , Couch, F. , Wang, X. , Lindor, N. , Fredericksen, Z. , Pankratz, V. S. , Peterlongo, P. , Bonanni, B. , Fortuzzi, S. , Peissel, B. , Szabo, C. , Mai, P. L. , Loud, J. T. , Lubinski, J. , Jakubowska, A. , Rozkrut, D. , Antoniou, A. , Hamann, U. , Scott, R. J. , McGuffog, L. , Healy, S. , Sinilnikova, O. M. , Rennert, G. , Lejbkowicz, F. , Flugelman, A. , Andrulis, I. L. , Glendon, G. , Ozcelik, H. , Thomassen, M. , Paligo, M. , Aretini, P. , Kantala, J. , Aroer, B. , Von Wachenfeldt, A. , Liljegren, A. , Loman, N. , Herbst, K. , Kristoffersson, U. , Rosenquist, R. , Karlsson, P. , Stenmark-Askmalm, M. , Melin, B. , Nathanson, K. L. , Domchek, S. M. , Byrski, T. , Huzarski, T. , Gronwald, J. , Menkiszak, J. , Cybulski, C. , Serrano, P. , Osorio, A. , Cajal, T. R. , Tsitlaidou, M. , Benitez, J. , Gilbert, M. , Rookus, M. , Aalfs, C. M. , Kluijt, I. , Boessenkool-Pape, J. L. , Meijers-Heijboer, H. E. J. , Oosterwijk, J. C. , Van Asperen, C. J. , Blok, M. J. , Nelen, M. R. , Van Den Ouweland, A. M. W. , Seynaeve, C.
- Resource Type: journal article
- Date: 2012
BRAF and NRAS mutational status are prognostically important in thick and locally advanced cutaneous melanoma
- Creator: Vilain, R. , Braye, S. G. , Ashman, L. , Scott, R. J.
- Resource Type: conference paper
- Date: 2011
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
- Creator: Acikyol, B. , Graham, R. M. , Trinder, D. , House, M. J. , Olynyk, J. K. , Scott, R. J. , Milward, E. A. , Johnstone, D. M.
- Resource Type: journal article
- Date: 2013
cDNA analysis of the BRCA1 unclassified variant c.5194-12G > A (letter)
- Creator: Wong-Brown, M. W. , McPhillips, M. L. , Hipwell, M. , Pecenpetelovska, G. , Dooley, S. , Meldrum, C. , Scott, R. J.
- Resource Type: journal article
- Date: 2013
Characterising the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort
- Creator: 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.
- Resource Type: journal article
- Date: 2015
Characterizing the genetic risk for type 2 diabetes in a Malaysian multi-ethnic cohort
- Creator: 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.
- Resource Type: journal article
- Date: 2015
Common variants of DNA repair genes and malignant melanoma
- Creator: 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.
- Resource Type: journal article
- Date: 2008
Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening
- Creator: Kurlapska, A. , Serrano-Fernández, P. , Rogoza-Mateja, W. , Scott, R. J. , Lubiński, J. , Baszuk, P. , Gupta, S. , Starzyńska, T. , Małecka-Panas, E. , Dabrowski, A. , Dębniak, T. , Kurzawski, G. , Suchy, J.
- Resource Type: journal article
- Date: 2015
Differential gene expression and cytokine production from neutrophils in asthma phenotypes
- Creator: Baines, K. J. , Simpson, J. L. , Bowden, N. A. , Scott, R. J. , Gibson, P. G.
- Resource Type: journal article
- Date: 2010
Downstream effects of reduction in nucleotide excision repair in response to cisplatin treatment in melanoma
- Creator: Bowden, N. A. , Ashton, K. A. , Avery-Kiejda, K. A. , Zhang, X. D. , Hersey, P. , Scott, R. J.
- Resource Type: conference paper
- Date: 2011
Estrogen receptor polymorphisms and the risk of endometrial cancer
- Creator: Ashton, K. A. , Proietto, A. , Otton, G. , Symonds, I. , McEvoy, M. , Attia, J. , Gilbert, M. , Hamann, U. , Scott, R. J.
- Resource Type: journal article
- Date: 2009
Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis
- Creator: Dudding, T. , Heron, J. , Thakkinstian, A. , Nurk, E. , Golding, J. , Pembrey, M. , Ring, S. M. , Attia, J. , Scott, R. J.
- Resource Type: journal article
- Date: 2008
Familial recurrence risks for multiple sclerosis in Australia
- Creator: O'Gorman, C. , Freeman, S. , Kilpatrick, T. J. , Lechner-Scott, J. , Moscato, P. , Perreau, V. M. , Scott, R. J. , Stankovich, J. , Stewart, G. J. , Chapman, C. , Marriot, M. , Tanner, M. , Taylor, B. V. , Tubridy, N. , Wiley, J. , Butzkueven, H. , Broadley, S. A. , Bahlo, M. , Booth, D. R. , Brown, M. A. , Foote, S. J. , Griffiths, L. R.
- Resource Type: journal article
- Date: 2011
Fetal growth and risk of childhood acute lymphoblastic leukemia: results from an Australian case-control study
- Creator: Milne, E. , Royle, J. A. , de Klerk , N. H. , Blair, E. , Bailey, H. , Cole, C. , Attia, J. , Scott, R. J. , Armstrong, B. K.
- Resource Type: journal article
- Date: 2009
Gene profiling in the amygdala in schizophrenia
- Creator: Weidenhofer, J. , Bowden, N. A. , Scott, R. J. , Tooney, P. A.
- Resource Type: conference paper
- Date: 2004
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949)
- Creator: 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.
- Resource Type: journal article
- Date: 2015
Genetic polymorphisms and childhood acute lymphoblastic leukemia: GWAS of the ESCALE study (SFCE)
- Creator: Orsi, L. , Rudant, J. , Michel, G. , Sirvent, N. , Chastagner, P. , Ducassou, S. , Rialland, X. , Hémon, D. , Milne, E. , Scott, R. J. , Baruchel, A. , Clavel, J. , Bonaventure, A. , Goujon-Bellec, S. , Corda, E. , Evans, T. J. , Petit, A. , Bertrand, Y. , Nelken, B. , Robert, A.
- Resource Type: journal article
- Date: 2012