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 clinical review of generalized overgrowth syndromes in the era of massively parallel sequencing

- Kamien, Benjamin, Ronan, Anne, Poke, Gemma, Sinnerbrink, Ingrid, Baynam, Gareth, Ward, Michelle, Gibson, William T., Dudding-Byth, Tracy, Scott, Rodney J.

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 Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

- Ni, Guiyan, Zeng, Jian, Smoller, Jordan W., ., Schizophrenia Working Group of the Psychiatric Genomics Consortium, ., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Yang, Jian, Visscher, Peter M., Wray, Naomi R., Henskens, Franz A., Loughland, Carmel M., Schall, Ulrich, Michie, Patricia T., Revez, Joana A., Scott, Rodney J., Wang, Ying, Zheng, Zhili, Ge, Tian, Restuadi, Restuadi, Kiewa, Jacqueline, Nyholt, Dale R., Coleman, Jonathan R. I.

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 molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia

- Li, Wen, Fan, Chun Chieh, Mäki-Marttunen, Tuomo, Thompson, Wesley K., Schork, Andrew J., Bettella, Francesco, Ripke, Stephan, Neal, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Djurovic, Srdjan, Dale, Andrew M., Andreassen, Ole A., Wang, Yunpeng

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 transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

- Wu, Lang, Shi, Wei, Al-Ejeh, Fares, Rozali, Esdy, Wang, Qin, Dennis, Joe, Li, Bingshan, Zeng, Chenjie, Feng, Helian, Gusev, Alexander, Barfield, Richard T., Andrulis, Irene L., Long, Jirong, Scott, Rodney J., Arndt, V, Aronson, KJ, Auer, PL, Barrdahl, M, Baynes, C, Beckmann, MW, Benitez, J, Bermisheva, M, Blomqvist, C, Guo, Xingyi, Bogdanova, NV, Bojesen, SE, Brauch, H, Brenner, H, Brinton, L, Broberg, P, Brucker, SY, Burwinkel, B, Caldés, T, Canzian, F, Michailidou, Kyriaki, Carter, BD, Castelao, JE, Chang-Claude, J, Chen, X, Cheng, TYD, Christiansen, H, Clarke, CL, Collée, M, Cornelissen, S, Couch, FJ, Beesley, Jonathan, Cox, D, Cox, A, Cross, SS, Cunningham, JM, Czene, K, Daly, MB, Devilee, P, Doheny, KF, Dörk, T, Dos-Santos-Silva, I, Bolla, Manjeet K., Dumont, M, Dwek, M, Eccles, DM, Eilber, U, Eliassen, AH, Engel, C, Eriksson, M, Fachal, L, Fasching, PA, Figueroa, J, Shu, Xiao-Ou, Flesch-Janys, D, Fletcher, O, Flyger, H, Fritschi, L, Gabrielson, M, Lu, Yingchang, Cai, Qiuyin

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

Age at first birth in women is genetically associated with increased risk of schizophrenia

- Ni, Guiyan, Gratten, Jacob, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Wray, Naomi R., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Bevilacqua, E, Bigdeli, TB, Black, DW, Bruggeman, R, Buccola, NG, Lee, Sang Hong, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Ripke, Stephan, Chan, RCK, Chen, RYL, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, D, Cohen, N, Cormican, P, Neale, Benjamin M., Craddock, N, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Corvin, Aiden, Djurovic, S, Donohoe, G, Drapeau, E, Walters, James T. R., Farh, Kai-How, Holmans, Peter A.

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