Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study von Bowden, Sarah J, Bodinier, Barbara, Kalliala, Ilkka, Zuber, Verena, Vuckovic, Dragana, Doulgeraki, Triada, Whitaker, Matthew D, Wielscher, Matthias, Cartwright, Rufus, Tsilidis, Konstantinos K, Bennett, Phillip, Jarvelin, Marjo-Riitta, Flanagan, James M, Chadeau-Hyam, Marc, Kyrgiou, Maria

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A bird's-eye view of Italian genomic variation through whole-genome sequencing von Cocca, Massimiliano, Barbieri, Caterina, Concas, Maria Pina, Robino, Antonietta, Brumat, Marco, Gandin, Ilaria, Trudu, Matteo, Sala, Cinzia Felicita, Vuckovic, Dragana, Girotto, Giorgia, Matullo, Giuseppe, Polasek, Ozren, Kolčić, Ivana, Gasparini, Paolo, Soranzo, Nicole, Toniolo, Daniela, Mezzavilla, Massimo

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A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis von Bell, Steven, Rigas, Andreas S., Magnusson, Magnus K., Ferkingstad, Egil, Allara, Elias, Bjornsdottir, Gyda, Ramond, Anna, Sørensen, Erik, Halldorsson, Gisli H., Paul, Dirk S., Burgdorf, Kristoffer S., Eggertsson, Hannes P., Howson, Joanna M. M., Thørner, Lise W., Kristmundsdottir, Snaedis, Astle, William J., Erikstrup, Christian, Sigurdsson, Jon K., Vuckovic, Dragana, Dinh, Khoa M., Tragante, Vinicius, Surendran, Praveen, Pedersen, Ole B., Vidarsson, Brynjar, Jiang, Tao, Paarup, Helene M., Onundarson, Pall T., Akbari, Parsa, Nielsen, Kaspar R., Lund, Sigrun H., Juliusson, Kristinn, Magnusson, Magnus I., Frigge, Michael L., Oddsson, Asmundur, Olafsson, Isleifur, Kaptoge, Stephen, Hjalgrim, Henrik, Runarsson, Gudmundur, Wood, Angela M., Jonsdottir, Ingileif, Hansen, Thomas F., Sigurdardottir, Olof, Stefansson, Hreinn, Rye, David, Peters, James E., Westergaard, David, Holm, Hilma, Soranzo, Nicole, Banasik, Karina, Thorleifsson, Gudmar, Ouwehand, Willem H., Thorsteinsdottir, Unnur, Roberts, David J., Sulem, Patrick, Butterworth, Adam S., Gudbjartsson, Daniel F., Danesh, John, Brunak, Søren, Di Angelantonio, Emanuele, Ullum, Henrik, Stefansson, Kari

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Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss von Morgan, Anna, Vuckovic, Dragana, Krishnamoorthy, Navaneethakrishnan, Rubinato, Elisa, Ambrosetti, Umberto, Castorina, Pierangela, Franzè, Annamaria, Vozzi, Diego, La Bianca, Martina, Cappellani, Stefania, Di Stazio, Mariateresa, Gasparini, Paolo, Girotto, Giorgia

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Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss von Girotto, Giorgia, Abdulhadi, Khalid, Buniello, Annalisa, Vozzi, Diego, Licastro, Danilo, d'Eustacchio, Angela, Vuckovic, Dragana, Alkowari, Moza Khalifa, Steel, Karen P, Badii, Ramin, Gasparini, Paolo

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Expression and replication studies to identify new candidate genes involved in normal hearing function von Girotto, Giorgia, Vuckovic, Dragana, Buniello, Annalisa, Lorente-Cánovas, Beatriz, Lewis, Morag, Gasparini, Paolo, Steel, Karen P

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Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss von Espino Guarch, Meritxell, Font-Llitjós, Mariona, Murillo-Cuesta, Silvia, Errasti-Murugarren, Ekaitz, Celaya, Adelaida M, Girotto, Giorgia, Vuckovic, Dragana, Mezzavilla, Massimo, Vilches, Clara, Bodoy, Susanna, Sahún, Ignasi, González, Laura, Prat, Esther, Zorzano, Antonio, Dierssen, Mara, Varela-Nieto, Isabel, Gasparini, Paolo, Palacín, Manuel, Nunes, Virginia

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Biological age estimation using circulating blood biomarkers von Bortz, Jordan, Guariglia, Andrea, Klaric, Lucija, Tang, David, Ward, Peter, Geer, Michael, Chadeau-Hyam, Marc, Vuckovic, Dragana, Joshi, Peter K.

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Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease von Xu, Yu, Vuckovic, Dragana, Ritchie, Scott C., Akbari, Parsa, Jiang, Tao, Grealey, Jason, Butterworth, Adam S., Ouwehand, Willem H., Roberts, David J., Di Angelantonio, Emanuele, Danesh, John, Soranzo, Nicole, Inouye, Michael

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Automated calibration of consensus weighted distance-based clustering approaches using sharp von Bodinier, Barbara, Vuckovic, Dragana, Rodrigues, Sabrina, Filippi, Sarah, Chiquet, Julien, Chadeau-Hyam, Marc

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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals von 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, Alver, Maris, Bao, Yanchun, Clark, David W., Day, Felix R., Furlotte, Nicholas A., Joshi, Peter K., Kemper, Kathryn E., Kleinman, Aaron, Langenberg, Claudia, Mägi, Reedik, Trampush, Joey W., Verma, Shefali Setia, Wu, Yang, Lam, Max, Zhao, Jing Hua, Zheng, Zhili, Boardman, Jason D., Campbell, Harry, Freese, Jeremy, Harris, Kathleen Mullan, Hayward, Caroline, Herd, Pamela, Kumari, Meena, Lencz, Todd, Luan, Jian’an, Malhotra, Anil K., Metspalu, Andres, Milani, Lili, Ong, Ken K., Perry, John R. B., Porteous, David J., Ritchie, Marylyn D., Smart, Melissa C., Smith, Blair H., Tung, Joyce Y., Wareham, Nicholas J., Wilson, James F., Beauchamp, Jonathan P., Conley, Dalton C., Esko, Tõnu, Lehrer, Steven F., Magnusson, Patrik K. E., Oskarsson, Sven, Pers, Tune H., Robinson, Matthew R., Thom, Kevin, Watson, Chelsea, Chabris, Christopher F., Meyer, Michelle N., Laibson, David I., Yang, Jian, Johannesson, Magnus, Koellinger, Philipp D., Turley, Patrick, Visscher, Peter M., Benjamin, Daniel J., Cesarini, David

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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N., Lee, James J., Kong, Augustine, Yengo, Loic, Cesarini, David, Turley, Patrick, Visscher, Peter M., Beauchamp, Jonathan P., Benjamin, Daniel J., Young, Alexander I.

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Advances in understanding the pathogenesis of hereditary macrothrombocytopenia von Collins, Janine, Astle, William J., Megy, Karyn, Mumford, Andrew D., Vuckovic, Dragana

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Machine Learning for Identification of High-Risk Clonal Haematopoiesis Using Blood Count Data von Dunn, William G, Withnell, Isabella, Gu, Muxin, Quiros, Pedro, Cheloor Kovilakam, Sruthi, Marando, Ludovica, Fabre, Margarete, Mohorianu, Irina, Vuckovic, Dragana, Vassiliou, George

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Hair-Derived Exposome Exploration of Cardiometabolic Health: Piloting a Bayesian Multitrait Variable Selection Approach von Wada, Rin, Peng, Feng-Jiao, Lin, Chia-An, Vermeulen, Roel, Iglesias-González, Alba, Palazzi, Paul, Bodinier, Barbara, Streel, Sylvie, Guillaume, Michèle, Vuckovic, Dragana, Dagnino, Sonia, Chiquet, Julien, Appenzeller, Brice M R, Chadeau-Hyam, Marc

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Polygenic Germline Risk of Common Haematological Traits Drives Clonal Selection on JAK2 V617F and Development of Myeloproliferative Neoplasms von Nangalia, Jyoti, Guo, Jing, Walter, Klaudia, Quiros, Pedro, Gu, Muxin, Baxter, E Joanna, Danesh, John, Di Angelantonio, Emanuele, Roberts, David, Guglielmelli, Paola, Harrison, Claire N, Godfrey, Anna L, Green, Anthony R, Vassiliou, George, Vuckovic, Dragana, Soranzo, Nicole

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Educational patterning in biological health seven years apart: Findings from the Tromsø Study von Neufcourt, Lola, Castagné, Raphaële, Wilsgaard, Tom, Grimsgaard, Sameline, Chadeau-Hyam, Marc, Vuckovic, Dragana, Ugarteche-Perez, Ainhoa, Farbu, Erlend Hoftun, Sandanger, Torkjel M, Delpierre, Cyrille, Kelly-Irving, Michelle

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Association of hair polychlorinated biphenyls and multiclass pesticides with obesity, diabetes, hypertension and dyslipidemia in NESCAV study von Peng, Feng-Jiao, Lin, Chia-An, Wada, Rin, Bodinier, Barbara, Iglesias-González, Alba, Palazzi, Paul, Streel, Sylvie, Guillaume, Michèle, Vuckovic, Dragana, Chadeau-Hyam, Marc, Appenzeller, Brice M.R.

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Inherited polygenic effects on common hematological traits influence clonal selection on JAK2V617F and the development of myeloproliferative neoplasms von Guo, Jing, Walter, Klaudia, Quiros, Pedro M., Gu, Muxin, Baxter, E. Joanna, Danesh, John, Di Angelantonio, Emanuele, Roberts, David, Guglielmelli, Paola, Harrison, Claire N., Godfrey, Anna L., Green, Anthony R., Vassiliou, George S., Vuckovic, Dragana, Nangalia, Jyoti, Soranzo, Nicole

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Hair-Derived Exposome Exploration of Cardiometabolic Health: Piloting a Bayesian Multitrait Variable Selection Approach von Wada, Rin, Peng, Feng-Jiao, Lin, Chia-An, Vermeulen, Roel, Iglesias-González, Alba, Palazzi, Paul, Bodinier, Barbara, Streel, Sylvie, Guillaume, Michèle, Vuckovic, Dragana, Dagnino, Sonia, Chiquet, Julien, Appenzeller, Brice M. R., Chadeau-Hyam, Marc

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