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 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 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

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.

Association of zinc level and polymorphism in MMP-7 gene with prostate cancer in Polish population

- Bialkowska, Katarzyna, Marciniak, Wojciech, Cybulski, Cezary, Huzarski, Tomasz, Gronwald, Jacek, Debniak, Tadeusz, Scott, Rodney J., Lubinski, Jan, Jakubowska, Anna, Muszynska, Magdalena, Baszuk, Piotr, Gupta, Satish, Jaworska-Bieniek, Katarzyna, Sukiennicki, Grzegorz, Durda, Katarzyna, Gromowski, Tomasz, Prajzendanc, Karolina

BRCA1/2 mutations are not a common cause of malignant melanoma in the Polish population

- Debniak, Tadeusz, Scott, Rodney J., Malinska, Karolina, Kiedrowicz, Magdalena, Rogoza-Janiszewska, Emilia, Rudnicka, Helena, Deptula, Jakub, Domagala, Paweo, Kluzniak, Wojciech, Lener, Marcin R., Lubinski, Jan, Górski, Bohdan, Masojc, Bartoomiej, Kram, Andrzej, Maleszka, Romuald, Cybulski, Cezary, Paszkowska-Szczur, Katarzyna, Kashyap, Aniruddh, Murawa, Dawid

CD36-a plausible modifier of disease phenotype in familial adenomatous polyposis

- Holmes, Merran, Connor, Toni, Oldmeadow, Christopher, Pockney, Peter G., Scott, Rodney J., Talseth-Palmer, Bente A.

Cortical brain abnormalities in 4474 individuals with schizophrenia and 5098 control subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) consortium

- van Erp, Theo G. M., Walton, Esther, Hibar, Derek P., Schmaal, Lianne, Jiang, Wenhao, Glahn, David C., Pearlson, Godfrey D., Yao, Nailin, Fukunaga, Masaki, Hashimoto, Ryota, Okada, Naohiro, Yamamori, Hidenaga, Bustillo, Juan R., Clark, Vincent P., Agartz, Ingrid, Mueller, Bryon A., Cahn, Wiepke, de Zwarte, Sonja M. C., Hulshoff Pol, Hilleke E., Kahn, René S., Ophoff, Roel A., van Haren, Neeltje E. M., Andreassen, Ole A., Dale, Anders M., Loughland, Carmel, Henskens, Frans A., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Cairns, Murray J., Tooney, Paul A., Rasser, Paul E., Cooper, Gavin

Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA

- Kennedy, Daniel W., White, Nicole M., Benton, Miles C., Fox, Andrew, Scott, Rodney J., Griffiths, Lyn R., Mengersen, Kerrie, Lea, Rodney A.

Differing contributions of classical risk factors to type 2 diabetes in multi-ethnic Malaysian populations

- Abdullah, Noraidatulakma, Murad, Nor Azian Abdul, Attia, John, Oldmeadow, Christopher, Kamaruddin, Mohd Arman, Jalal, Nazihah Abd, Ismail, Norliza, Jamal, Rahman, Scott, Rodney J., Holliday, Elizabeth G.

DNA methylation changes in CD4+ T cells isolated from multiple sclerosis patients on dimethyl fumarate

- Maltby, Vicki E., Lea, Rodney A., Ribbons, Karen A., Sanders, Katherine A., Kennedy, Daniel, Min, Myintzu, Scott, Rodney J., Lechner-Scott, Jeannette

Epigenetically reprogrammed methylation landscape drives the DNA self-assembly and serves as a universal cancer biomarker

- Ibn Sina, Abu Ali, Carrascosa, Laura G., Korbie, Darren, Trau, Matt, Liang, Ziyu, Grewal, Yadveer S., Wardiana, Andri, Shiddiky, Muhammad J. A., Gardiner, Robert A., Samaratunga, Hemamali, Gandhi, Maher K., Scott, Rodney J.

Erythrocyte microRNA sequencing reveals differential expression in relapsing-remitting multiple sclerosis

- Groen, Kira, Maltby, Vicki E., Lea, Rodney A., Sanders, Katherine A., Fink, J. Lynn, Scott, Rodney J., Tajouri, Lotti, Lechner-Scott, Jeannette

Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

- Ni, Guiyan, Moser, Gerhard, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Henskens, Frans A., Loughland, Carmel A., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Wray, Naomi R., Lee, S. Hong

Extracellular matrix (ECM) activates β-catenin signaling in uterine fibroids

- Ko, Yi-An, Jamaluddin, M. Fairuz B., Adebayo, Mariam, Bajwa, Preety, Scott, Rodney J., Dharmarajan, Arunasalam M., Nahar, Pravin, Tanwar, Pradeep S.

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

- Lee, James J., Wedow, Robbee, Okbay, Aysu, Kong, Edward, Maghzian, Omeed, Zacher, Meghan, Nguyen-Viet, Tuan Anh, Bowers, Peter, Sidorenko, Julia, Karlsson Linnér, Richard, Fontana, Mark Alan, Kundu, Tushar, Lee, Chanwook, Li, Hui, Li, Ruoxi, Royer, Rebecca, Timshel, Pascal N., Walters, Raymond K., Willoughby, Emily A., Yengo, Loïc, Agee, Michelle, Oldmeadow, Christopher, Holliday, Elizabeth G., Scott, Rodney J., Attia, John R.

Gene expression profiles in whole blood and associations with metabolic dysregulation in obesity

- Cox, Amanda J., Zhang, Ping, Evans, Tiffany J., Scott, Rodney J., Cripps, Allan W., West, Nicholas P.

Genetic overlap between endometriosis and endometrial cancer: Evidence from cross-disease genetic correlation and GWAS meta-analyses

- Painter, Jodie N., O'Mara, Tracy A., Henders, Anjali K., Attia, John, McEvoy, Mark, Holliday, Elizabeth G., Scott, Rodney J., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Morris, Andrew P., Rübner, Matthias, Hall, P, Czene, K, Dörk, T, Dürst, M, Hillemanns, P, Runnebaum, I, Lambrechts, D, Amant, F, Annibali, D, Cheng, Timothy H. T., Depreeuw, J, Vanderstichele, A, Goode, EL, Cunningham, JM, Dowdy, SC, Winham, SJ, Trovik, J, Hoivik, E, Werner, HMJ, Krakstad, C, Gorman, Maggie, Ashton, Katie, Otton, Geoffrey, Proietto, Tony, Tham, E, Mints, M, Ahmed, S, Healey, CS, Shah, M, Pharoah, PDP, Dunning, AM, Martin, Lynn, Dennis, J, Bolla, MK, Michailidou, K, Wang, Q, Tyrer, JP, Hopper, JL, Peto, J, Swerdlow, AJ, Burwinkel, B, Brenner, H, Hodson, Shirley, Meindl, A, Brauch, H, Lindblom, A, Chang-Claude, J, Couch, FJ, Giles, GG, Kristensen, VN, Cox, A, Zondervan, KT, Nyholt, DR, Jones, Angela, Macgregor, S, Montgomery, GW, Martin, Nnicholas G., Gordon, Scott

Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders

- Ligthart, Symen, Vaez, Ahmad, Võsa, Urmo, Stathopoulou, Maria G., de Vries, Paul S., Prins, Bram P., Van der Most, Peter J., Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M., Wu, Ying, Karlsson, Robert, Barbalic, Maja, Lin, Honghuang, Pool, René, Zhu, Gu, Macé, Aurélien, Sidore, Carlo, Trompet, Stella, Mangino, Massimo, Sabater-Lleal, Maria, Oldmeadow, Christopher, Holliday, Elizabeth G., Attia, John R., Scott, Rodney J., McEvoy, Mark

Genome-wide DNA methylation changes in CD19⁺ B cells from relapsing-remitting multiple sclerosis patients

- Maltby, Vicki E., Lea, Rodney A., Graves, Moira C., Sanders, Katherine A., Benton, Miles C., Tajouri, Lotti, Scott, Rodney J., Lechner-Scott, Jeannette