A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma
Seviiri, Mathias, Law, Matthew H, Ong, Jue-Sheng, Gharahkhani, Puya, Fontanillas, Pierre, Olsen, Catherine M, Whiteman, David C, MacGregor, Stuart
Published in Nature communications (10.12.2022)
Published in Nature communications (10.12.2022)
Get full text
Journal Article
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma
Choquet, Hélène, Jiang, Chen, Yin, Jie, Kim, Yuhree, Hoffmann, Thomas J, Jorgenson, Eric, Asgari, Maryam M
Published in Communications biology (05.01.2024)
Published in Communications biology (05.01.2024)
Get full text
Journal Article
Genetic analyses identify widespread sex-differential participation bias
Pirastu, Nicola, Cordioli, Mattia, Nandakumar, Priyanka, Mignogna, Gianmarco, Abdellaoui, Abdel, Hollis, Benjamin, Kanai, Masahiro, Rajagopal, Veera M, Parolo, Pietro Della Briotta, Baya, Nikolas, Carey, Caitlin E, Karjalainen, Juha, Als, Thomas D, Van der Zee, Matthijs D, Day, Felix R, Ong, Ken K, Morisaki, Takayuki, de Geus, Eco, Bellocco, Rino, Okada, Yukinori, Børglum, Anders D, Joshi, Peter, Auton, Adam, Hinds, David, Neale, Benjamin M, Walters, Raymond K, Nivard, Michel G, Perry, John R B, Ganna, Andrea
Published in Nature genetics (01.05.2021)
Published in Nature genetics (01.05.2021)
Get full text
Journal Article
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti, Hassan S, Daghlas, Iyas, Lane, Jacqueline M, Huang, Yunru, Udler, Miriam S, Wang, Heming, Ollila, Hanna M, Jones, Samuel E, Kim, Jaegil, Wood, Andrew R, Weedon, Michael N, Aslibekyan, Stella, Garaulet, Marta, Saxena, Richa
Published in Nature communications (10.02.2021)
Published in Nature communications (10.02.2021)
Get full text
Journal Article
The genetic legacy of African Americans from Catoctin Furnace
Harney, Éadaoin, Micheletti, Steven, Bruwelheide, Karin S, Freyman, William A, Bryc, Katarzyna, Akbari, Ali, Jewett, Ethan, Comer, Elizabeth, Gates, Jr, Henry Louis, Heywood, Linda, Thornton, John, Curry, Roslyn, Esselmann, Samantha Ancona, Barca, Kathryn G, Sedig, Jakob, Sirak, Kendra, Olalde, Iñigo, Adamski, Nicole, Bernardos, Rebecca, Broomandkhoshbacht, Nasreen, Ferry, Matthew, Qiu, Lijun, Stewardson, Kristin, Workman, J Noah, Zalzala, Fatma, Mallick, Shop, Micco, Adam, Mah, Matthew, Zhang, Zhao, Rohland, Nadin, Mountain, Joanna L, Owsley, Douglas W, Reich, David
Published in Science (American Association for the Advancement of Science) (04.08.2023)
Published in Science (American Association for the Advancement of Science) (04.08.2023)
Get full text
Journal Article
Prevalence of Alpha-1 Antitrypsin Deficiency, Self-Reported Behavior Change, and Health Care Engagement Among Direct-to-Consumer Recipients of a Personalized Genetic Risk Report
Ashenhurst, James R., Nhan, Hoang, Shelton, Janie F., Wu, Shirley, Tung, Joyce Y., Elson, Sarah L., Stoller, James K., Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cameron, Briana, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Huber, Karen E., Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Kukar, Katelyn, Lane, Vanessa A., Lin, Keng-Han, Lowe, Maya, Luff, Marie K., McCreight, Jennifer C., McIntyre, Matthew H., McManus, Kimberly F., Micheletti, Steven J., Moreno, Meghan E., Mountain, Joanna L., Mozaffari, Sahar V., Nandakumar, Priyanka, Noblin, Elizabeth S., O’Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Tian, Chao, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter
Published in Chest (01.02.2022)
Published in Chest (01.02.2022)
Get full text
Journal Article
Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations
Thorpe, Hayley H. A., Fontanillas, Pierre, Pham, Benjamin K., Meredith, John J., Jennings, Mariela V., Courchesne-Krak, Natasia S., Vilar-Ribó, Laura, Bianchi, Sevim B., Mutz, Julian, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Heilbron, Karl, Gandhi, Pooja M., Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Lin, Keng-Han, Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Mountain, Joanna L., Nandakumar, Priyanka, Noblin, Elizabeth S., O’Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Hernandez, Alejandro, Wong, Corinna, Tchakouté, Christophe Toukam, Elson, Sarah L., Khokhar, Jibran Y., Abdellaoui, Abdel, Davis, Lea K., Palmer, Abraham A., Sanchez-Roige, Sandra
Published in Neuropsychopharmacology (New York, N.Y.) (01.09.2024)
Published in Neuropsychopharmacology (New York, N.Y.) (01.09.2024)
Get full text
Journal Article
Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant
Kmiecik, Matthew J, Micheletti, Steven, Coker, Daniella, Heilbron, Karl, Shi, Jingchunzi, Stagaman, Keaton, Filshtein Sonmez, Teresa, Fontanillas, Pierre, Shringarpure, Suyash, Wetzel, Madeleine, Rowbotham, Helen M, Cannon, Paul, Shelton, Janie F, Hinds, David A, Tung, Joyce Y, Holmes, Michael V, Aslibekyan, Stella, Norcliffe-Kaufmann, Lucy
Published in Brain (London, England : 1878) (28.05.2024)
Published in Brain (London, England : 1878) (28.05.2024)
Get full text
Journal Article
Genetic neurodevelopmental clustering and dyslexia
Ciulkinyte, Austeja, Mountford, Hayley S., Fontanillas, Pierre, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bowes, Jonathan, Bryc, Katarzyna, Chaudhary, Ninad S., Coker, Daniella, Das, Sayantan, DelloRusso, Emily, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Freyman, Will, Fuller, Zach, German, Chris, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan, Liang, Yanyu, Lin, Keng-Han, Llamas, Bianca A., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Nandakumar, Priyanka, Nguyen, Dominique T., O’Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Reynoso, Alexandra, Saini, Shubham, Schumacher, Morgan, Selcer, Leah, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Su, Qiaojuan Jane, Tat, Susana A., Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Wong, Corinna D., Bates, Timothy C., Martin, Nicholas G., Fisher, Simon E., Luciano, Michelle
Published in Molecular psychiatry (15.07.2024)
Published in Molecular psychiatry (15.07.2024)
Get full text
Journal Article
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
Liyanage, Upekha E., MacGregor, Stuart, Bishop, D. Timothy, Shi, Jianxin, An, Jiyuan, Ong, Jue Sheng, Han, Xikun, Scolyer, Richard A., Martin, Nicholas G., Medland, Sarah E., Byrne, Enda M., Green, Adèle C., Saw, Robyn P.M., Thompson, John F., Stretch, Jonathan, Spillane, Andrew, Jiang, Yunxuan, Tian, Chao, Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cameron, Briana, Coker, Daniella, Cuellar Partida, Gabriel, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Huber, Karen E., Jewett, Ethan M., Kleinman, Aaron, Kukar, Katelyn, Lin, Keng-Han, Lowe, Maya, Luff, Marie K., McCreight, Jennifer C., McIntyre, Matthew H., McManus, Kimberly F., Micheletti, Steven J., Moreno, Meghan E., Mountain, Joanna L., Mozaffari, Sahar V., Nandakumar, Priyanka, Noblin, Elizabeth S., O'Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Gordon, Scott G., Duffy, David L., Olsen, Catherine M., Whiteman, David C., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Law, Matthew H.
Published in Journal of investigative dermatology (01.06.2022)
Published in Journal of investigative dermatology (01.06.2022)
Get full text
Journal Article
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia
Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D, Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E, Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B, Monaco, Anthony P, Stein, John F, Gruen, Jeffrey R, Olson, Richard K, Willcutt, Erik G, DeFries, John C, Pennington, Bruce F, Smith, Shelley D, Wright, Margaret J, Martin, Nicholas G, Auton, Adam, Bates, Timothy C, Fisher, Simon E, Luciano, Michelle
Published in Nature genetics (01.03.2023)
Published in Nature genetics (01.03.2023)
Get full text
Journal Article
Using a polygenic score in a family design to understand genetic influences on musicality
Wesseldijk, Laura W., Abdellaoui, Abdel, Gordon, Reyna L., Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Faaborg, Anna, Fuller, Shirin T., Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Jewett, Ethan M., Kukar, Katelyn, Lin, Keng-Han, Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Mountain, Joanna L., Nandakumar, Priyanka, Noblin, Elizabeth S., O’Connell, Jared, Huang, Yunru, Petrakovitz, Aaron A., Lane, Vanessa, Petrakovitz, Aaron, Kim, Joanne S., Poznik, G. David, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Hernandez, Alejandro, Wong, Corinna, Tchakouté, Christophe Toukam, Ullén, Fredrik, Mosing, Miriam A.
Published in Scientific reports (29.08.2022)
Published in Scientific reports (29.08.2022)
Get full text
Journal Article
CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice
Sanchez-Roige, Sandra, Jennings, Mariela V, Thorpe, Hayley H A, Mallari, Jazlene E, van der Werf, Lieke C, Bianchi, Sevim B, Huang, Yuye, Lee, Calvin, Mallard, Travis T, Barnes, Samuel A, Wu, Jin Yi, Barkley-Levenson, Amanda M, Boussaty, Ely C, Snethlage, Cedric E, Schafer, Danielle, Babic, Zeljana, Winters, Boyer D, Watters, Katherine E, Biederer, Thomas, Mackillop, James, Stephens, David N, Elson, Sarah L, Fontanillas, Pierre, Khokhar, Jibran Y, Young, Jared W, Palmer, Abraham A
Published in Translational psychiatry (12.05.2023)
Published in Translational psychiatry (12.05.2023)
Get full text
Journal Article
Genome-wide association analysis and replication in 810,625 individuals with varicose veins
Ahmed, Waheed-Ul-Rahman, Kleeman, Sam, Ng, Michael, Wang, Wei, Auton, Adam, Lee, Regent, Handa, Ashok, Zondervan, Krina T, Wiberg, Akira, Furniss, Dominic
Published in Nature communications (02.06.2022)
Published in Nature communications (02.06.2022)
Get full text
Journal Article
A Polygenic Score for Type 2 Diabetes Improves Risk Stratification Beyond Current Clinical Screening Factors in an Ancestrally Diverse Sample
Ashenhurst, James R, Sazonova, Olga V, Svrchek, Olivia, Detweiler, Stacey, Kita, Ryosuke, Babalola, Liz, McIntyre, Matthew, Aslibekyan, Stella, Fontanillas, Pierre, Shringarpure, Suyash, Pollard, Jeffrey D, Koelsch, Bertram L
Published in Frontiers in genetics (26.04.2022)
Published in Frontiers in genetics (26.04.2022)
Get full text
Journal Article
Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy
Krebs, Kristi, Bovijn, Jonas, Zheng, Neil, Lepamets, Maarja, Censin, Jenny C., Jürgenson, Tuuli, Särg, Dage, Abner, Erik, Laisk, Triin, Luo, Yang, Skotte, Line, Geller, Frank, Feenstra, Bjarke, Wang, Wei, Auton, Adam, Agee, Michelle, Aslibekyan, Stella, Bell, Robert K., Bryc, Katarzyna, Clark, Sarah K., Elson, Sarah L., Fletez-Brant, Kipper, Fontanillas, Pierre, Furlotte, Nicholas A., Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Huber, Karen E., Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K., Luff, Marie K., McCreight, Jennifer C., McIntyre, Matthew H., McManus, Kimberly F., Mountain, Joanna L., Mozaffari, Sahar V., Nandakumar, Priyanka, Noblin, Elizabeth S., Northover, Carrie A.M., O’Connell, Jared, Petrakovitz, Aaron A., Pitts, Steven J., Poznik, G. David, Sathirapongsasuti, J. Fah, Shastri, Anjali J., Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y., Tunney, Robert J., Vacic, Vladimir, Wang, Xin, Zare, Amir S., Raychaudhuri, Soumya, Esko, Tõnu, Metspalu, Andres, Laur, Sven, Roden, Dan M., Wei, Wei-Qi, Holmes, Michael V., Lindgren, Cecilia M., Phillips, Elizabeth J., Mägi, Reedik, Milani, Lili, Fadista, João
Published in American journal of human genetics (01.10.2020)
Published in American journal of human genetics (01.10.2020)
Get full text
Journal Article
The genetic architecture of dog ownership: large-scale genome-wide association study in 97,552 European-ancestry individuals
Gong, Tong, Karlsson, Robert, Yao, Shuyang, Magnusson, Patrik K E, Ajnakina, Olesya, Steptoe, Andrew, Bhatta, Laxmi, Brumpton, Ben, Kumar, Ashish, Mélen, Erik, Lin, Keng-Han, Tian, Chao, Fall, Tove, Almqvist, Catarina
Published in G3 : genes - genomes - genetics (2024)
Published in G3 : genes - genomes - genetics (2024)
Get full text
Journal Article
Characterizing mood disorders in the AFFECT study: a large, longitudinal, and phenotypically rich genetic cohort in the US
Dalby, Maria, Vitezic, Morana, Plath, Niels, Hammer-Helmich, Lene, Jiang, Yunxuan, Tian, Chao, Dhamija, Devika, Wilson, Catherine H, Hinds, David, Sullivan, Patrick F, Buckholtz, Joshua W, Smoller, Jordan W
Published in Translational psychiatry (25.03.2022)
Published in Translational psychiatry (25.03.2022)
Get full text
Journal Article
A population-specific reference panel for improved genotype imputation in African Americans
O'Connell, Jared, Yun, Taedong, Moreno, Meghan, Li, Helen, Litterman, Nadia, Kolesnikov, Alexey, Noblin, Elizabeth, Chang, Pi-Chuan, Shastri, Anjali, Dorfman, Elizabeth H, Shringarpure, Suyash, Auton, Adam, Carroll, Andrew, McLean, Cory Y
Published in Communications biology (05.11.2021)
Published in Communications biology (05.11.2021)
Get full text
Journal Article