Sapkota, Yadav, Attia, John, Scott, Rodney J., Zondervan, Krina T., Montgomery, Grant W., Nyholt, Dale R., Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., Rahmioglu, Nilufer, MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P.. Oxford University Press; 2015. Genetic burden associated with varying degrees of disease severity in endometriosis.

Sapkota, Yadav, Low, Siew-Kee, Takahashi, Atsushi, Scott, Rodney J., Kubo, Michiaki, Zondervan, Krina T., Montgomery, Grant W., Nyholt, Dale R., Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P.. Oxford University Press; 2015. Association between endometriosis and the interleukin 1A (IL1A) locus.

Nyholt, Dale R., Low, Siew-Kee, Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Knichi, Nakamura, Yusuke, Anderson, Carl A., Zondervan, Krina T., Zembutsu, Hitoshi, Montgomery, Grant W., Painter Jodie N., Yun-Chul, Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G.. Nature Publishing Group; 2012. Genome-wide association meta-analysis identifies new endometriosis risk loci.

Lee, S. Hong, Harold, Denise, Nyholt, Dale R., Goddard, Michael E., Zondervan, Krina T., Williams, Julie, Montgomery, Grant W., Wray, Naomi R., Visscher, Peter M.. Oxford University Press; 2013. Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis.

Malik, Rainer, Freilinger, Tobias, Bis, Joshua C., Hopewell, Jemma C., Ferrari, Michel D., Rannikmae, Kristiina, Wessman, Maija, Kallela, Mikko, Kubisch, Christian, Fornage, Myriam, Meschia, James F., Lehtimäki, Terho, Winsvold, Bendik S., Sudlow, Cathie, Clarke, Robert, Chasman, Daniel I., Mitchell, Braxton D., Maguire, Jane, Kaprio, Jakko, Farrall, Martin, Raitakari, Olli T., Kurth, Tobias, Ikram, M. Arfan, Anttila, Verneri, Reiner, Alex P., Longstreth, W. T., Rothwell, Peter M., Strachan, David P., Sharma, Pankaj, Seshadri, Sudha, Quaye, Lydia, Cherkas, Lynn, Schürks, Markus, Rosand, Jonathan, Vander Heiden, Jason, Ligthart, Lannie, Boncoraglio, Giorgio B., Davey Smith, George, van Duijn, Cornelia M., Stefansson, Kari, Worrall, Bradford B., Nyholt, Dale R., Markus, Hugh S., van den Maagdenberg, Arn M. J. M., Cotsapas, Chris, Traylor, Matthew, Zwart, John A., Palotie, Aarno, Dichgans, Martin, de Vries, Boukje, Holliday, Elizabeth G., Terwindt, Gisela M., Sturm, Jonathan. Lippincott Williams & Wilkins; 2015. Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants.

Painter, Jodie N., O'Mara, Tracy A., Healey, Catherine S., Fridley, Brooke L., Børresen-Dale, Anne-Lise, Kristensen, Vessela N., Cox, Angela, Swerdlow, Anthony J., Orr, Nicholas, Bolla, Manjeet K., Wang, Qin, Palmieri Weber, Rachel, Chen, Zhihua, Kaufmann, Susanne, Shah, Mitul, French, Juliet D., Pharoah, Paul D. P., Dunning, Alison M., Tomlinson, Ian, Easton, Douglas F., Edwards, Stacey L., Thompson, Deborah J., Spurdle, Amanda B., Hillman, Kristine M., Walpole, Carina, Moya, Leire, Pollock, Pamela, Jones, Angela, Howarth, Kimberley, Martin, Lynn, Gorman, Maggie, Batra, Jyotsna, Hodgson, Shirley, National Study of Endometrial Cancer Genetics Group (NSECG), CHIBCHA Consortium, De Polanco, Ma. Magdalena Echeverry, Sans, Monica, Carracedo, Angel, Castellvi-Bel, Sergi, Rojas-Martinez, Augusto, Santos, Erika, Teixeira, Manuel R., Cheng, Timothy, Carvajal-Carmona, Luis, Shu, Xiao-Ou, Long, Jirong, Zheng, Wei, Xiang, Yong-Bing, The Australian National Endometrial Cancer Study Group (ANECS), Montgomery, Grant W., Webb, Penelope M., Scott, Rodney J., McEvoy, Mark, Lose, Felicity A., Attia, John, Holliday, Elizabeth, Martin, Nicholas G., Nyholt, Dale R., Henders, Anjali K., Fasching, Peter A., Hein, Alexander, Beckmann, Matthias W., Renner, Stefan P., Dörk, Thilo, Dennis, Joe, Hillemanns, Peter, Dürst, Matthias, Runnebaum, Ingo, Lambrechts, Diether, Coenegrachts, Lieve, Schrauwen, Stefanie, Amant, Frederic, Winterhoff, Boris, Dowdy, Sean C., Goode, Ellen L., Michailidou, Kyriaki, Teoman, Attila, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Werner, Henrica M. J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, Tzortzatos, Gerasimos, Mints, Miriam, Tyrer, Jonathan P., Tham, Emma, RENDOCAS, Hall, Per, Czene, Kamila, Liu, Jianjun, Li, Jingmei, Hopper, John L., Southey, Melissa C., Australian Ovarian Cancer Study (AOCS), Ekici, Arif B., Ahmed, Shahana, Ruebner, Matthias, Johnson, Nicola, Peto, Julian, Burwinkel, Barbara, Marme, Frederik, Brenner, Hermann, Dieffenbach, Aida K., Miendl, Alfons, Brauch, Hiltrud, The GENICA Network,, Ferguson, Kaltin, Lindblom, Annika, Depreeuw, Jeroen, Moisse, Matthieu, Chang-Claude, Jenny, Rudolph, Anja, Couch, Fergus J., Olsen, Janet E., Giles, Graham G., Bruinsma, Fiona, Cunnigham, Julie M.. Oxford University Press; 2015. Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk..