Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets von Zhu, Zhihong, Zhang, Futao, Hu, Han, Bakshi, Andrew, Robinson, Matthew R, Powell, Joseph E, Montgomery, Grant W, Goddard, Michael E, Wray, Naomi R, Visscher, Peter M, Yang, Jian

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Signatures of negative selection in the genetic architecture of human complex traits von Zeng, Jian, de Vlaming, Ronald, Wu, Yang, Robinson, Matthew R., Lloyd-Jones, Luke R., Yengo, Loic, Yap, Chloe X., Xue, Angli, Sidorenko, Julia, McRae, Allan F., Powell, Joseph E., Montgomery, Grant W., Metspalu, Andres, Esko, Tonu, Gibson, Greg, Wray, Naomi R., Visscher, Peter M., Yang, Jian

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Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits von Wu, Yang, Zeng, Jian, Zhang, Futao, Zhu, Zhihong, Qi, Ting, Zheng, Zhili, Lloyd-Jones, Luke R., Marioni, Riccardo E., Martin, Nicholas G., Montgomery, Grant W., Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F., Yang, Jian

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Common SNPs explain a large proportion of the heritability for human height von Heath, Andrew C, Benyamin, Beben, Nyholt, Dale R, Goddard, Michael E, Gordon, Scott, Martin, Nicholas G, Henders, Anjali K, Madden, Pamela A, Visscher, Peter M, McEvoy, Brian P, Yang, Jian, Montgomery, Grant W

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Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits von Yang, Jian, Ferreira, Teresa, Morris, Andrew P, Medland, Sarah E, Madden, Pamela A F, Heath, Andrew C, Martin, Nicholas G, Montgomery, Grant W, Weedon, Michael N, Loos, Ruth J, Frayling, Timothy M, McCarthy, Mark I, Hirschhorn, Joel N, Goddard, Michael E, Visscher, Peter M

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Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets von Rahmioglu, Nilufer, Nyholt, Dale R, Morris, Andrew P, Missmer, Stacey A, Montgomery, Grant W, Zondervan, Krina T

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Identification of 55,000 Replicated DNA Methylation QTL von McRae, Allan F., Marioni, Riccardo E., Shah, Sonia, Yang, Jian, Powell, Joseph E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Bowdler, Lisa, Painter, Jodie N., Murphy, Lee, Martin, Nicholas G., Starr, John M., Wray, Naomi R., Deary, Ian J., Visscher, Peter M., Montgomery, Grant W.

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Genetic Regulation of Physiological Reproductive Lifespan and Female Fertility von McGrath, Isabelle M, Mortlock, Sally, Montgomery, Grant W

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Polygenic risk score phenome-wide association study reveals an association between endometriosis and testosterone von McGrath, Isabelle M, Montgomery, Grant W, Mortlock, Sally

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POT1 loss-of-function variants predispose to familial melanoma von Robles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S, Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, López-Otín, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A, Adams, David J

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Genotype-free demultiplexing of pooled single-cell RNA-seq von Xu, Jun, Falconer, Caitlin, Nguyen, Quan, Crawford, Joanna, McKinnon, Brett D, Mortlock, Sally, Senabouth, Anne, Andersen, Stacey, Chiu, Han Sheng, Jiang, Longda, Palpant, Nathan J, Yang, Jian, Mueller, Michael D, Hewitt, Alex W, Pébay, Alice, Montgomery, Grant W, Powell, Joseph E, Coin, Lachlan J M

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Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1 von Burdon, Kathryn P, Macgregor, Stuart, Hewitt, Alex W, Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A, Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C, Liu, Jimmy Z, Landers, John, Henders, Anjali K, Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R, Martin, Nicholas G, Montgomery, Grant W, Mitchell, Paul, Brown, Matthew A, Mackey, David A, Craig, Jamie E

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Gene expression profiles separate endometriosis lesion subtypes and indicate a sensitivity of endometrioma to estrogen suppressive treatments through elevated ESR2 expression von Marla, Sushma, Mortlock, Sally, Heinosalo, Taija, Poutanen, Matti, Montgomery, Grant W, McKinnon, Brett David

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Meta-analysis of telomere length in 19,713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect von Broer, Linda, Codd, Veryan, Nyholt, Dale R, Deelen, Joris, Mangino, Massimo, Willemsen, Gonneke, Albrecht, Eva, Amin, Najaf, Beekman, Marian, de Geus, Eco J C, Henders, Anjali, Nelson, Christopher P, Steves, Claire J, Wright, Margie J, de Craen, Anton J M, Isaacs, Aaron, Matthews, Mary, Moayyeri, Alireza, Montgomery, Grant W, Oostra, Ben A, Vink, Jacqueline M, Spector, Tim D, Slagboom, P Eline, Martin, Nicholas G, Samani, Nilesh J, van Duijn, Cornelia M, Boomsma, Dorret I

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The effect of X-linked dosage compensation on complex trait variation von Sidorenko, Julia, Kassam, Irfahan, Kemper, Kathryn E., Zeng, Jian, Lloyd-Jones, Luke R., Montgomery, Grant W., Gibson, Greg, Metspalu, Andres, Esko, Tonu, Yang, Jian, McRae, Allan F., Visscher, Peter M.

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Genome-wide DNA methylation profiling in whole blood reveals epigenetic signatures associated with migraine von Gerring, Zachary F, McRae, Allan F, Montgomery, Grant W, Nyholt, Dale R

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Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity von Mahajan, Anubha, Rodan, Aylin R., Le, Thu H., Gaulton, Kyle J., Haessler, Jeffrey, Stilp, Adrienne M., Kamatani, Yoichiro, Zhu, Gu, Sofer, Tamar, Puri, Sanjana, Schellinger, Jeffrey N., Chu, Pei-Lun, Cechova, Sylvia, van Zuydam, Natalie, Arnlov, Johan, Flessner, Michael F., Giedraitis, Vilmantas, Heath, Andrew C., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Madden, Pamela A.F., Montgomery, Grant W., Papanicolaou, George J., Reiner, Alex P., Sundström, Johan, Thornton, Timothy A., Lind, Lars, Ingelsson, Erik, Cai, Jianwen, Martin, Nicholas G., Kooperberg, Charles, Matsuda, Koichi, Whitfield, John B., Okada, Yukinori, Laurie, Cathy C., Morris, Andrew P., Franceschini, Nora

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

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DNA methylation profiles in monozygotic and dizygotic twins von Petronis, Art, Kaminsky, Zachary A, Tang, Thomas, Wang, Sun-Chong, Ptak, Carolyn, Oh, Gabriel H T, Wong, Albert H C, Feldcamp, Laura A, Virtanen, Carl, Halfvarson, Jonas, Tysk, Curt, McRae, Allan F, Visscher, Peter M, Montgomery, Grant W, Gottesman, Irving I, Martin, Nicholas G

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Genome-wide association study identifies loci affecting blood copper, selenium and zinc von Evans, David M, Zhu, Gu, Dy, Veronica, Heath, Andrew C, Madden, Pamela A F, Kemp, John P, McMahon, George, St Pourcain, Beate, Timpson, Nicholas J, Golding, Jean, Lawlor, Debbie A, Steer, Colin, Montgomery, Grant W, Martin, Nicholas G, Smith, George Davey, Whitfield, John B

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