Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

- McLaughlin, Russell L., Schijven, Dick, Schall, Ulrich, Scott, Rodney J., van Rheenen, Wouter, van Eijk, Kristel R., O'Brien, Margaret, Project MinE GWAS Consortium,, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Khan, René S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, van den Berg, Leonard H., Luykx, Jurjen J.

Genome-wide miRNA, gene and methylation analysis of triple negative breast cancer to identify changes associated with lymph node metastases

- Avery-Kiejda, Kelly A., Mathe, Andrea, Scott, Rodney J.

Identification of endothelin-converting enzyme-2 as an autoantigen in autoimmune polyendocrine syndrome type 1

- Smith-Anttila, Casey J. A., Bensing, Sophie, Fransson, Anette, Nordmark, Gunnel, Rönnblom, Lars, Meloni, Antonella, Scott, Rodney J., Hökfelt, Tomas, Crock, Patricia A., Kämpe, Olle, Alimohammadi, Mohammad, Dalin, Frida, Oscarson, Mikael, Zhang, Ming-Dong, Perheentupa, Jaakko, Husebye, Eystein S., Gustafsson, Jan, Björklund, Peyman

Identification of gene loci that overlap between schizophrenia and educational attainment

- Le Hellard, Stephanie, Wang, Yunpeng, Schork, Andrew J., Thompson, Wesley K., Dale, Anders M., Djurovic, Srdjan, Andreassen, Ole A., Cairns, Murray J., Henskens, Frans, Kelly, Brian J., Loughland, Carmel, Michie, Patricia T., Witoelar, Aree, Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Zuber, Verena, Bettella, Francesco, Hugdahl, Kenneth, Espeseth, Thomas, Steen, Vidar M., Melle, Ingrid, Desikan, Rahul

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

- Milne, Roger L., Kuchenbaecker, Karoline B., Jiang, Xia, Rostamianfar, Asha, Finucane, Hilary, Bolla, Manjeet K., McGuffog, Lesley, Wang, Qin, Aalfs, Cora M., ABCTB Investigators, Braye, Stephen, Forbes, John, Michailidou, Kyriaki, Scott, Rodney J., Beesley, Jonathan, Kar, Siddhartha, Lindström, Sara, Hui, Shirley, Lemaçon, Audrey, Soucy, Penny, Dennis, Joe

Initial investigations of simple and multifactorial drug-gene interactions related to methotrexate in a community cohort

- Dias, Thilani H., Biswas, Mohitosh, Daneshi, Nilofar, Holliday, Elizabeth, Hancock, Stephen, Munro, Irene, Kerr, Karen, Attia, John, Scott, Rodney J., Milward, Elizabeth A.

Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy

- Najdawi, Fedaa, Crook, Ashley, Sioson, Loretta, Ahadi, Masha, Turchini, John, Clarkson, Adele, Hogg, Russell, Valmadre, Sue, Gard, Greg, Dooley, Susan J., Scott, Rodney J., Fox, Stephen B., Maidens, Jayne, Field, Michael, Gill, Anthony J., McEvoy, Christopher, Fellowes, Andrew, Pickett, Justine, Ho, Musei, Nevell, David, McIlroy, Kirsten, Sheen, Amy

Prevalence of clinically actionable genotypes and medication exposure of older adults in the community

- Daneshi, Nilofar, Holliday, Elizabeth, Hancock, Stephen, Schneider, Jennifer J., Scott, Rodney J., Attia, John, Milward, Elizabeth A.

Promoter methylation pattern controls corticotropin releasing hormone gene activity in human trophoblasts

- Pan, Xin, Bowman, Maria, Scott, Rodney J., Fitter, John, Smith, Roger, Zakar, Tamas

Serum 25(OH)D concentration, common variants of the VDR gene and lung cancer occurrence

- Gromowski, Tomasz, Gapska, Paulina, Kaczmarek, Katarzyna, Jaworska-Bieniek, Katarzyna, Paszkowska-Szczur, Katarzyna, Waloszczyk, Piotr, Lubinski, Jan, Debniak, Tadeusz, Scott, Rodney J., Kaklewski, Krzysztof, Marciniak, Wojciech, Durda, Katarzyna, Lener, Marcin, Górski, Bohdan, Cybulski, Cezary, Sukiennicki, Grzegorz

The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation

- Strumidło, Agnieszka, Skiba, Sylwia, Scott, Rodney J., Lubiński, Jan

Thyroid cancer in a patient with Lynch syndrome - case report and literature review

- Fazekas-Lavu, Monika, Parker, Andrew, Spigelman, Allan D., Scott, Rodney J., Epstein, Richard J., Jensen, Michael, Samaras, Katherine

Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

- Hansen, Maren F., Johansen, Jostein, Sjursen, Wenche, Sylvander, Anna E., Bjørnevoll, Inga, Talseth-Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn

A common variant at the 14q32 endometrial cancer risk locus activates AKT1 through YY1 binding

- Painter, Jodie N., Kaufmann, Susanne, Hoivik, Erling A., Goode, Ellen L., Scott, Rodney J., Tomlinson, Ian, Dunning, Alison M., Easton, Douglas F., French, Juliet D., Salvesen, Helga B., Pollock, Pamela M., Thompson, Deborah J., O'Mara, Tracy A., Spurdle, Amanda B., Edwards, Stacey L., Hillman, Kristine M., Sivakumaran, Haran, Darabi, Hatef, Cheng, Timothy H.T., Pearson, John, Kazakoff, Stephen, Waddell, Nicola

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

- de Vries, P. S., Chasman, D. I., Hottenga, J. J., Trompet, S, Müller-Nurasyid, M., Zhao, J. H., Brody, J. A., Kleber, M. E., Guo, X., Wang, J. J., Auer, P. L., Attia, John R., Sabater-Lleal, M., Yanek, L. R., Ahluwalia, T. S., Lahti, J., Venturini, C., Tanaka, T., Bielak, L. F., Joshi, P. K., Rocanin-Arjo, A., Kolcic, I., Navarro, P., Chen, M. H., Rose, L. M., Oldmeadow, Christopher, Riess, H., Mazur, J., Basu, S., Goel, A., Yang, Q., Ghanbari, M., Gonneke, Willemsen, Rumley, A., Huffman, J. E., Fiorillo, E., de Craen, A. J. M., Grotevendt, A., Scott, R., Taylor, K. D., Delgado, G. E., Yao, J., Kifley, A., Kooperberg, C., Qayyum, R., Steri, M., Lopez, L., Berentzen, T. L., Räikkönen, K., Mangino, M., Bandinelli, S., Peyser, P. A., Wild, S., Trégouët, D. A., Wright, A. F., Marten, J., Tang, W., Zemunik, T., Morrison, A. C., Sennblad, B., Tofler, G., de Maat, M. P. M., De Geus, E. J. C., Lowe, G. D., Zoledziewska, M., Sattar, N., Binder, H., Teumer, A., Völker, U., Waldenberger, M., Khaw, K. T., Scott, Rodney J., Marioni, R. E., Grossmann, V.

A novel polymorphic repeat in the upstream regulatory region of the estrogen-induced gene EIG121 is not associated with the risk of developing breast or endometrial cancer

- Bolton, Katherine A., Holliday, Elizabeth G., Attia, John, Bowden, Nikola A., Avery-Kiejda, Kelly A., Scott, Rodney J.

A polymorphic repeat in the IGF1 promoter influences the risk of endometrial cancer

- Bolton, Katherine A., Avery-Kiejda, Kelly A., Holliday, Elizabeth G., Attia, John, Bowden, Nikola A., Scott, Rodney J.

A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.

- Hungate, Eric A., Vora, Sapana R., Rudant, Jéremie, Orsi, Laurent, Clavel, Jacqueline, Milne, Elizabeth, Scott, Rodney J., Pui, Ching-Hon, Cox, Nancy J., Loh, Mignon L., Yang, Jun J., Skol, Andrew D., Gamazon, Eric R., Onel, Kenan, Moriyama, Takaya, Best, Timothy, Hulur, Imge, Lee, Younghee, Evans, Tiffany-Jane, Ellinghaus, Eva, Stanulla, Martin

Associations between methylenetetrahydrofolate reductase polymorphisms, serum homocysteine levels, and incident cortical cataract

- Tan, Ava Grace, Kifley, Annette, Klein, Barbara E. K., Cheng, Ching-Yu, Iyengar, Sudha K., Wang, Jie Jin, Mitchell, Paul, Rochtchina, Elena, Flood, Victoria M., Cumming, Robert G., Jun, Gyungah, Holliday, Elizabeth G., Scott, Rodney J., Teo, Yik Ying

Comparison of the QuantiGene 2.0 assay and real-time RT-PCR in the detection of p53 isoform mRNA expression in formalin-fixed paraffin-embedded tissues- a preliminary study

- Morten, Brianna C., Scott, Rodney J., Avery-Kiejda, Kelly A.