Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity
Shelton, Janie F., Shastri, Anjali J., Ye, Chelsea, Weldon, Catherine H., Filshtein-Sonmez, Teresa, Coker, Daniella, Symons, Antony, Esparza-Gordillo, Jorge, Aslibekyan, Stella, Auton, Adam
Published in Nature genetics (01.06.2021)
Published in Nature genetics (01.06.2021)
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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)
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The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste
Shelton, Janie F., Shastri, Anjali J., Fletez-Brant, Kipper, Aslibekyan, Stella, Auton, Adam
Published in Nature genetics (01.02.2022)
Published in Nature genetics (01.02.2022)
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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Iwaki, Hirotaka, Lake, Julie, Solsberg, Caroline Warly, Leonard, Hampton, Makarious, Mary B., Tan, Eng-King, Singleton, Andrew B., Bandres-Ciga, Sara, Noyce, Alastair J., Blauwendraat, Cornelis, Nalls, Mike A., Foo, Jia Nee, Mata, Ignacio
Published in Nature genetics (01.01.2024)
Published in Nature genetics (01.01.2024)
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Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects
Krohn, Lynne, Heilbron, Karl, Blauwendraat, Cornelis, Reynolds, Regina H., Yu, Eric, Senkevich, Konstantin, Rudakou, Uladzislau, Estiar, Mehrdad A., Gustavsson, Emil K., Brolin, Kajsa, Ruskey, Jennifer A., Freeman, Kathryn, Asayesh, Farnaz, Chia, Ruth, Arnulf, Isabelle, Hu, Michele T. M., Montplaisir, Jacques Y., Gagnon, Jean-François, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Šonka, Karel, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Biscarini, Francesco, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel-Döring, Friederike, Cochen De Cock, Valérie, Monaca, Christelle Charley, Heidbreder, Anna, Ferini-Strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley F., Scholz, Sonja W., Ryten, Mina, Bandres-Ciga, Sara, Noyce, Alastair, Cannon, Paul, Pihlstrøm, Lasse, Nalls, Mike A., Singleton, Andrew B., Rouleau, Guy A., Postuma, Ronald B., Gan-Or, Ziv
Published in Nature communications (05.12.2022)
Published in Nature communications (05.12.2022)
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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)
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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)
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Configuring and Verifying Reverberation Chambers for Testing Cellular Wireless Devices
Remley, Kate A., Dortmans, Jos, Weldon, Catherine, Horansky, Robert D., Meurs, Thomas B., Chih-Ming Wang, Williams, Dylan F., Holloway, Christopher L., Wilson, Perry F.
Published in IEEE transactions on electromagnetic compatibility (01.06.2016)
Published in IEEE transactions on electromagnetic compatibility (01.06.2016)
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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)
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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) (03.06.2024)
Published in Brain (London, England : 1878) (03.06.2024)
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Genetic neurodevelopmental clustering and dyslexia
Ciulkinyte, Austeja, Mountford, Hayley S, Fontanillas, Pierre, 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)
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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)
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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)
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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease
Wightman, Douglas P, Jansen, Iris E, Savage, Jeanne E, Shadrin, Alexey A, Bahrami, Shahram, Holland, Dominic, Rongve, Arvid, Børte, Sigrid, Winsvold, Bendik S, Martinsen, Amy E, Skogholt, Anne Heidi, Willer, Cristen, Bråthen, Geir, Bosnes, Ingunn, Nielsen, Jonas Bille, Fritsche, Lars G, Thomas, Laurent F, Pedersen, Linda M, Gabrielsen, Maiken E, Meisingset, Tore Wergeland, Zhou, Wei, Proitsi, Petroula, Dobson, Richard, Velayudhan, Latha, Sealock, Julia M, Pedersen, Nancy L, Reynolds, Chandra A, Karlsson, Ida K, Magnusson, Sigurdur, Stefansson, Hreinn, Thordardottir, Steinunn, Jonsson, Palmi V, Snaedal, Jon, Zettergren, Anna, Kern, Silke, Waern, Margda, Zetterberg, Henrik, Blennow, Kaj, Stordal, Eystein, Zwart, John-Anker, Selnes, Per, Saltvedt, Ingvild, Sando, Sigrid B, Ulstein, Ingun, Djurovic, Srdjan, Fladby, Tormod, Aarsland, Dag, Ripke, Stephan, Stefansson, Kari, Posthuma, Danielle, Aslibekyan, Stella, Babalola, Elizabeth, Bielenberg, Jessica, 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, Hicks, Barry, Hinds, David A, Huber, Karen E, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Kukar, Katelyn, Lane, Vanessa, 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 Nature genetics (01.09.2021)
Published in Nature genetics (01.09.2021)
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Healthcare professionals’ perspectives of the provision of, and challenges for, eating, drinking and psychological support post stroke: findings from semistructured interviews across India
Jones, Stephanie P, Injety, Ranjit J, Pandian, Jeyaraj D, Ratra, Sanjali, Sylaja, PN, Babu, Veena, Srivastava, MV Padma, Sharma, Sakshi, Sharma, Sudhir, Webster, Jemin, Koirala, Amrit, Kaushal, Pawna, Kulkarni, Girish Baburao, Dixit, Anand, Sharma, Arvind, Prajapati, Jagruti, Weldon, Jo Catherine, Kuroski, Jennifer A, Watkins, Caroline Leigh, Lightbody, Catherine Elizabeth, Pandian, Jeyaraj D, Padma Srivastava, MV, Sylaja, PN, Watkins, Dame Caroline, Boaden, Liz, Cadilhac, Dominique, Clegg, Andy, Forshaw, Denise, Gabbay, Mark, Georgiou, Rachel, Gibson, Jo, Hackett, Maree, Jones, Steph, Lightbody, Liz, Middleton, Sandy, Prescott, Gordon, Sanders, Caroline, Sharma, Anil, Walker, Marion
Published in BMJ open (25.10.2023)
Published in BMJ open (25.10.2023)
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MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups
Jin, Jin, Zhan, Jianan, Zhang, Jingning, Zhao, Ruzhang, O’Connell, Jared, Jiang, Yunxuan, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Cuellar Partida, Gabriel, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan, Lin, Keng-Han, Llamas, Bianca A., Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Nandakumar, Priyanka, Nguyen, Dominique T., Noblin, Elizabeth S., O’Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Reynoso, Alexandra, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Su, Qiaojuan Jane, Tat, Susana A., Tchakouté, Christophe Toukam, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Wong, Corinna D., Buyske, Steven, Gignoux, Christopher, Haiman, Christopher, Kenny, Eimear E., Kooperberg, Charles, North, Kari, Koelsch, Bertram L., Wojcik, Genevieve, Zhang, Haoyu, Chatterjee, Nilanjan
Published in Cell genomics (10.04.2024)
Published in Cell genomics (10.04.2024)
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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)
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FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression
Puan, Kia Joo, San Luis, Boris, Yusof, Nurhashikin, Kumar, Dilip, Andiappan, Anand Kumar, Lee, Wendy, Cajic, Samanta, Vuckovic, Dragana, Chan, Jing De, Döllner, Tobias, Hou, Han Wei, Jiang, Yunxuan, Tian, Chao, Rapp, Erdmann, Poidinger, Michael, Wang, De Yun, Soranzo, Nicole, Lee, Bernett, Rötzschke, Olaf
Published in Communications biology (02.07.2021)
Published in Communications biology (02.07.2021)
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