Intronic TP53 polymorphisms are associated with increased Δ133TP53 transcript, immune infiltration and cancer risk

- Eiholzer, Ramona A., Mehta, Sunali, Kazantseva, Marina, Drummond, Catherine J., McKinney, Cushla, Young, Katie, Slater, David, Morten, Brianna C., Avery-Kiejda, Kelly A., Lasham, Annette, Fleming, Nicholas, Morrin, Helen R., Reader, Karen, Royds, Janice A., Landmann, Michael, Petrich, Simone, Reddel, Roger, Huschtscha, Lily, Taha, Ahmad, Hung, Noelyn A., Slatter, Tania L., Braithwaite, Antony W.

The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis

- Lukkunaprasit, Thitiya, Rattanasiri, Sasivimol, Turongkaravee, Saowalak, Suvannang, Naravut, Ingsathit, Atiporn, Attia, John, Thakkinstian, Ammarin

Estimating effect sizes and expected replication probabilities from GWAS summary statistics

- Holland, Dominic, Wang, Yunpeng, Dale, Anders M., Tooney, Paul A., Thompson, Wesley K., Schork, Andrew, Chen, Chi-Hua, Lo, Min-Tzu, Witoelar, Aree, Werge, Thomas, O'Donovan, Michael, Andreassen, Ole A.

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer

- Chen, Maxine M., O'Mara, Tracy A., Cheng, Timothy H. T., Cook, Linda S., Crous-Bou, Marta, Doherty, Jennifer, Friedenreich, Christine M., Garcia-Closas, Montserrat, Gaudet, Mia M., Gorman, Maggie, Haiman, Christopher, Hankinson, Susan E., Thompson, Deborah J., Holliday, Elizabeth G., Painter, Jodie N., Australian National Endometrial Cancer Study Group (ANECS),, Attia, John, Black, Amanda, Brinton, Louise, Chanock, Stephen, Chen, Chu

Prediction of breast cancer risk based on profiling with common genetic variants

- Mavaddat, Nasim, Pharoah, Paul D. P., Michailidou, Kyriaki, Tyrer, Jonathan, Brook, Mark N., Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Dunning, Alison M., Shah, Mitul, Luben, Robert, Brown, Judith, Bojesen, Stig E., Nordestgaard, Børge G., Nielsen, Sune F., Flyger, Henrik, Czene, Kamila, Darabi, Hatef, Eriksson, Mikael, Peto, Julian, Dos-Santos-Silva, Isabel, Dudbridge, Frank, Scott, Rodney, Yang, Rui

The effect of a muscarinic receptor 1 gene variant on grey matter volume in schizophrenia

- Cropley, Vanessa L., Scarr, Elizabeth, Fornito, Alex, Klauser, Paul, Bousman, Chad A., Scott, Rodney, Cairns, Murray J., Tooney, Paul A., Pantelis, Christos, Dean, Brian

Genome-wide association study of kidney function decline in individuals of European descent.

- Gorski, Mathias, Tin, Adreienne, Hamet, Pavel, Köttgen, Anna, Kao, W. H., Fox, Caroline S., Böger, Carsten A., Tremblay, Johanne, Woodward, Marc, Aspelund, Thor, Eiriksdottir, Gudney, Gudnason, Vilmundur, Harris, Tamara B,, Launer, Lenore J., Smith, Albert V., Mitchell, Braxton D., Garnaas, Maija, O'Connell, Jeffrey R., Shuldiner, Alan R., Coresh, Josef, Li, Man, Freudenberger, Paul, Hofer, Edith, Schmidt, Helena, Schmidt, Reinhold, Holliday, Elizabeth G., Mitchell, Paul, McMahon, Gearoid M., Wang, Jie Jin, de Boer, Ian H,, Li, Guo, Siscovick, David S., Kutalik, Zoltan, Corre, Tanguy, Vollenweider, Peter, Waeber, Gerard, Gupta, Jayanta, Kanetsky, Peter A,, Chu, Audrey Y,, Hwang, Shih-Jen, Olden, Matthias, Yang, Qiong, de Andrade, Mariza, Atkinson, Elizabeth J., Kardia, Sharon L. R., Turner, Stephen T,, Stafford, Jeanette M., Ding, Jingzhong, Liu, Yongmei, Tayo, Bamidele O., Barlassina, Cristina, Cusi, Daniele, Salvi, Erika, Staessen, Jan A., Ridker, Paul M., Grallert, Harald, Meisinger, Christa, Müller-Nurasyid, Martina, Krämer, Bernhard K., Kramer, Holly, Pattaro, Cristian, Rosas, Sylvia E., Nolte, Ilja M., Penninx, Brenda W., Snieder, Harold, Fabiola Del Greco, M., Franke, Andre, Nöthlings, Ute, Lieb, Wolfgang, Bakker, Stehan J. L., Gansevoort, Ron T., Teumer, Alexander, van der Harst, Pim, Dehghan, Abbas, Franco, Oscar H., Hofman, Albert, Rivadeneira, Fernando, Sedaghat, Sanaz, Uitterlinden, Andre G., Coassin, Stefan, Haun, Margot, Kollerits, Barbara, Chasman, Daniel I., Kronenberg, Florian, Paulweber, Bernhard, Aumann, Nicole, Endlich, Karlhans, Pietzner, Mike, Völker, Uwe, Rettig, Rainer, Chouraki, Vincent, Helmer, Catherine, Lambert, Jean-Charles, Chalmers, John, Metzger, Marie, Stengel, Benedicte, Lehtimäki, Terho, Lyytikäinen, Leo-Pekka, Raitakari, Olli, Johnson, Andrew, Parsa, Afshin, Bochud, Murielle, Heid, Iris M., Goessling, Wolfram

Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis

- Cox, Mathew B., Ban, Maria, Bowden, Nikola A., Baker, Amie, Scott, Rodney J., Lechner-Scott, Jeannette

GGN1 in the testis and ovary and its variance within the Australian fertile and infertile male population

- Jamsai, D., Sarraj, M. A., Merriner, D. J., Drummond, A. E., Jones, K. T., McLachlan, R. I., O'Bryan, M. K.

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

- 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.

How to use an article about genetic association. A: background concepts

- Attia, John, Ioannidis, John P. A., Thakkinstian, Ammarin, McEvoy, Mark, Scott, Rodney J., Minelli, Cosetta, Thompson, John, Infante-Rivard, Claire, Guyatt, Gordon

Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c-KIT

- Foster, R., Byrnes, E., Ashman, L. K., Meldrum, C., Griffith, R., Ross, G., Upjohn, E., Braue, A., Scott, R., Varigos, G., Ferrao, P.

Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysis

- Dudding, T., Heron, J., Thakkinstian, A., Nurk, E., Golding, J., Pembrey, M., Ring, S. M., Attia, J., Scott, R. J.

Identification and interrogation of highly informative single nucleotide polymorphism sets defined by bacterial multilocus sequence typing databases

- Robertson, Gail A., Thiruvenkataswamy, Venugopal, Shilling, Hayden, Price, Erin P., Huygens, Flavia, Henskens, Frans A., Giffard, Philip M.