1000 genomes-based meta-analysis identifies 10 novel loci for kidney function

- Gorski, Mathias, van der Most, Peter J., Li, Yong, Sedaghat, S, Smith, AV, Sorice, R, Stengel, B, Stracke, S, Strauch, K, Toniolo, D, Uitterlinden, AG, Ulivi, S, Viikari, JS, Tayo, Bamidele, Voelker, U, Vollenweider, P, Voelzke, H, Vuckovic, D, Waldenberger, M, Wang, JJ, Yang, Q, Chasman, DI, Tromp, G, Snieder, H, Tin, Adrienne, Heid, IM, Fox, CS, Koettgen, A, Pattaro, C, Boeger, CA, Fuchsberger, C, Feitosa, Mary F., Aspelund, Thor, Attia, John, Biffar, Reiner, Bochud, Murielle, Boerwinkle, Eric, Borecki, Ingrid, Teumer, Alexander, Bottinger, Erwin P., Chen, Ming-Huei, Chouraki, Vincent, Ciullo, Marina, Coresh, Josef, Cornelis, Marilyn C., Curhan, Gary C., d'Adamo, Adamo P., Dehghan, Abbas, Dengler, Laura, Chu, Audrey Y., Ding, Jingzhong, Eiriksdottir, Gudny, Endlich, K, Enroth, S, Esko, T, Franco, OH, Gasparini, P, Gieger, C, Girotto, G, Gottesman, O, Li, Man, Gudnason, V, Gyllensten, U, Hancock, Stephen J., Harris, TB, Helmer, C, Hoellerer, S, Hofer, E, Hofman, A, Holliday, Elizabeth, Homuth, G, Mijatovic, Vladan, Hu, FB, Huth, C, Hutri-Kahonen, N, Hwang, S-J, Imboden, M, Johansson, A, Kahonen, M, Koenig, W, Kraemer, H, Kramer, BK, Nolte, Ilja M., Kumar, A, Kutalik, Z, Lambert, J-C, Launer, LJ, Lehtimaki, T, de Borst, M, Navis, G, Swertz, M, Liu, Y, Lohman, K, Cocca, Massimiliano, Loos, RJF, Lu, Y, Lyytikainen, L-P, McEvoy, Mark A., Meisinger, C, Meitinger, T, Metspalu, A, Metzger, M, Mihailov, E, Mitchell, P, Taliun, Daniel, Nauck, M, Oldehinkel, AJ, Olden, M, Penninx, BWJH, Pistis, G, Pramstaller, PP, Probst-Hensch, N, Raitakari, OT, Rettig, R, Ridker, PM, Gomez, Felicia, Rivadeneira, F, Robino, A, Rosas, SE, Ruderfer, D, Ruggiero, D, Saba, Y, Sala, C, Schmidt, H, Schmidt, R, Scott, Rodney J.

8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome

- Talseth-Palmer, Bente A., Scott, Rodney J., Vasen, Hans F. A., Wijnen, Juul T.

A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis

- Mechelli, Rosella, Umeton, Renato, Wellcome Trust Case Control Consortium 2,, Romano, Silvia, Salvetti, Marco, Ristori, Giovanni, Cox, Mathew B., Lechner-Scott, Jeannette S., Scott, Rodney J., Policano, Claudia, Annibali, Viviana, Coarelli, Giulia, Ricigliano, Vito A. G., Vittori, Danila, Fornasiero, Arianna, Buscarinu, Maria Chiara, International Multiple Sclerosis Genetics Consortium,

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 genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants

- Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.

A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes

- Hondow, Heather L., Fox, Stephen B., Mitchell, Gillian, Scott, Rodney J., Beshay, Victoria, Wong, Stephen Q., kConFab Investigators,, Dobrovic, Alexander

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 polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis

- Field, Judith, Browning, Sharon R., Lechner-Scott, Jeanette, Moscato, Pablo, Scott, Rodney J., Stewart, Graeme J., Kilpatrick, Trevor J., Foote, Simon J., Bahlo, Melanie, Butzkueven, Helmut, Wiley, James, Booth, David R., Johnson, Laura J., Taylor, Bruce V., Brown, Matthew A., Rubio, Justin P., Stankovich, Jim, Danoy, Patrick, Varney, Michael D,, Tait, Brian D., Kaushal, S. Gandhi, Charlesworth, Jac C., Heard, Robert N., The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)

A simple migration/invasion workflow using an automated live-cell imager

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

A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis

- Riveros, Carlos, Mellor, Drew, Vucic, Stephen, Stewart, Graeme J., Williams, David W., Scott, Rodney J., Lechner-Scott, Jeannette, Booth, David R., Moscato, Pablo, ANZgene Multiple Sclerosis Genetics Consortium, Gandhi, Kaushal S., McKay, Fiona C., Cox, Mathew B., Berretta, Regina, Vaezpour, S. Yahya, Inostroza-Ponta, Mario, Broadley, Simon A., Heard, Robert N.

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

Alteration of miRNA-mRNA interactions in lymphocytes of individuals with schizophrenia

- Geaghan, Michael P., Atkins, Joshua R., Brichta, Alan M., Tooney, Paul A., Scott, Rodney J., Carr, Vaughan J., Cairns, Murray J.

Altered expression of the plasminogen activation pathway in peripheral blood mononuclear cells in multiple sclerosis: possible pathomechanism of matrix metalloproteinase activation

- Cox, Mathew B., Bowden, Nikola A., Scott, Rodney J., Lechner-Scott, Jeannette

Altered gene expression in the amygdala in schizophrenia: up-regulation of genes located in the cytomatrix active zone

- Weidenhofer, Judith, Bowden, Nikola A., Scott, Rodney J., Tooney, Paul A.

Altered gene expression in the superior temporal gyrus in schizophrenia

- Bowden, Nikola A., Scott, Rodney J., Tooney, Paul A.

Altered neural signaling and immune pathways in peripheral blood mononuclear cells of schizophrenia patients with cognitive impairment: a transcriptome analysis

- Wu, Jing Qin, Green, Melissa J., Gardiner, Erin J., Tooney, Paul A., Scott, Rodney J., Carr, Vaughan J., Cairns, Murray J.

An X-linked haplotype of Neandertal origin is present among all non-African populations

- Yotova, Vania, Lefebvre, Jean-Francois, Avogbe, Patrice Hodonou, Chabi, Nicodeme, Dicko, Mamoudou Hama, Kou' Santa Amouzou , Emile Sabiba, Sanni, Ambaliou, Roberts-Thomson, June, Boettcher, Barry, Scott, Rodney J., Labuda, Damian, Moreau, Claudia, Gbeha, Elias, Hovhannesyan, Kristine, Bourgeois, Stephane, Bédarida, Sandra, Azevedo, Luisa, Amorim, Antonio, Sarkisian, Tamara

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

- Thompson, Bryony A., Spurdle, Amanda B., du Sart, Desiree, Fabre, Aurelie, Farrell, Michael P., Farrington, Susan M., Frayling, Ian M., Frebourg, Thierry, Goldgar, David E., Heinen, Christopher D., Holinski-Feder, Elke, Kohonen-Corish, Maija, Plazzer, John-Paul, Robinson, Kristina Lagerstedt, Leung, Suet Yi, Martins, Alexandra, Moller, Pat, Morak, Monika, Nystrom, Minna, Peltomaki, Paivi, Pineda, Marta, Qi, Ming, Ramesar, Rajkumar, Greenblatt, Marc S., Rasmussen, Lene Juel, Royer-Pokora, Brigitte, Scott, Rodney J., Sijmons, Rolf, Tavtigian, Sean V., Tops, Carli M., Weber, Thomas, Wijnen, Juul, Woods, Michael O., Macrae, Finlay, Akagi, Kiwamu, Genuardi, Maurizio, Al-Mulla, Fahd, Bapat, Bharati, Bernstein, Inge, Capellá, Gabriel, den Dunnen, John T.