Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
Vujkovic, Marijana, Keaton, Jacob M, Lynch, Julie A, Miller, Donald R, Zhou, Jin, Tcheandjieu, Catherine, Huffman, Jennifer E, Assimes, Themistocles L, Lorenz, Kimberly, Zhu, Xiang, Hilliard, Austin T, Judy, Renae L, Huang, Jie, Lee, Kyung M, Klarin, Derek, Pyarajan, Saiju, Danesh, John, Melander, Olle, Rasheed, Asif, Mallick, Nadeem H, Hameed, Shahid, Qureshi, Irshad H, Afzal, Muhammad Naeem, Malik, Uzma, Jalal, Anjum, Abbas, Shahid, Sheng, Xin, Gao, Long, Kaestner, Klaus H, Susztak, Katalin, Sun, Yan V, DuVall, Scott L, Cho, Kelly, Lee, Jennifer S, Gaziano, J Michael, Phillips, Lawrence S, Meigs, James B, Reaven, Peter D, Wilson, Peter W, Edwards, Todd L, Rader, Daniel J, Damrauer, Scott M, O'Donnell, Christopher J, Tsao, Philip S, Chang, Kyong-Mi, Voight, Benjamin F, Saleheen, Danish
Published in Nature genetics (01.07.2020)
Published in Nature genetics (01.07.2020)
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An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
Gervais, Olivier, Kawai, Yosuke, Tang, Ruqi, Atkinson, Elizabeth J., Carbone, Marco, de Andrade, Mariza, Byan, Jinyoung, Lazaridis, Konstantinos N., Siminovitch, Katherine A., Ma, Xiong, Affronti, Andrea, Almasio, Piero L., Benedetti, Antonio, Crocè, Lory Saveria, Donato, Francesca, Fabris, Luca, Lampertico, Pietro, Marzioni, Marco, Nagaoka, Shinya, Ohira, Hiromasa, Matsushita, Kouki, Kouno, Hirotaka, Ota, Hajime, Shimada, Masaaki, Komeda, Toshiki, Yamashita, Tsutomu, Takahashi, Hironao, Yamauchi, Kazuhiko, Hayashi, Shigeki, Watanabe, Yukio, Hirata, Keisuke, Kaneko, Shuichi, Arai, Kuniaki, Hashimoto, Etsuko, Umemura, Takeji, Seike, Masataka, Kanda, Tatsuo, Himoto, Takashi, Yasunami, Michio, Mizokami, Masashi, Yamamoto, Kazuhide, Ido, Akio, Harada, Kenichi, Nakanuma, Yasuni, Soejima, Yuji, Yagi, Shintaro, Tanaka, Tomohiro, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Lattari, Michael, Lopez, Alexander, Wolf, Sarah E., Balasubramanian, Suganthi, Khalid, Shareef, Maxwell, Evan K., Sturgess, Richard, Healey, Christopher, Kooner, Paul, Evans, Richard, Tibble, Jeremy A., Gorard, David A., Jones, Susan, Srivastava, Brijesh, Elphick, David, Sayer, Joanne, Carter, Martyn J., Koss, Konrad, Shah, Jayshri, Grimley, Charles, Gooding, Ian R., Williams, Simon, Cheent, Kuldeep, Marley, Richard, Ramage, John, Gordon, Harriet M., Ridpath, Jo, Abouda, George, Narain, Mark, Taylor-Robinson, Simon, Matthews, Helen C., Prince, Martin I., Bathgate, Andrew J., Dillon, John F., Collier, Jane, Aspinall, Richard, Douds, Andrew C., Booth, Jonathan, Hussaini, Hyder, Christie, John, Patanwala, Imran, Maltby, Julia, Singhal, Saket, Mitchison, Harriet, Jain, Sanjiv, Wright, Mark, Unitt, Esther, Grant, Allister, Mathew, Ray, Ramakrishnan, Subramaniam
Published in Journal of hepatology (01.09.2021)
Published in Journal of hepatology (01.09.2021)
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Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Jurgens, Sean J, Choi, Seung Hoan, Morrill, Valerie N, Chaffin, Mark, Pirruccello, James P, Halford, Jennifer L, Weng, Lu-Chen, Nauffal, Victor, Roselli, Carolina, Hall, Amelia W, Oetjens, Matthew T, Lagerman, Braxton, vanMaanen, David P, Aragam, Krishna G, Lunetta, Kathryn L, Haggerty, Christopher M, Lubitz, Steven A, Ellinor, Patrick T
Published in Nature genetics (01.03.2022)
Published in Nature genetics (01.03.2022)
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Journal Article
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
Tcheandjieu, Catherine, Xiao, Ke, Tejeda, Helio, Lynch, Julie A, Ruotsalainen, Sanni, Bellomo, Tiffany, Palnati, Madhuri, Judy, Renae, Klarin, Derek, Kember, Rachel L, Verma, Shefali, Palotie, Aarno, Daly, Mark, Ritchie, Marylyn, Rader, Daniel J, Rivas, Manuel A, Assimes, Themistocles, Tsao, Philip, Damrauer, Scott, Priest, James R
Published in Nature genetics (01.06.2022)
Published in Nature genetics (01.06.2022)
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Journal Article
Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone
Kithcart, Aaron, Kim, Jee Hae, Ho, Andre Jo-Hao, Franklin, Matthew C., Romero Hernandez, Annabel, Botermans, Wouter, Meyer, Jonathan, Zhang, Dongqin, Kamat, Vishal, Garnova, Elena, Liu, Nina, Burczynski, Michael E., Rafique, Ashique, De, Tanima, Verweij, Niek, Pandit, Anita, Chalasani, Naga, Schwantes-An, Tae-Hwi, Ritchie, Marylyn D., Poindexter, Afiya, Hu-Sain, Khadijah, Ko, Yi-An, Vadivieso, Fred, Tran, Teo, Stephanowski, Julia, Zielinski, Monica, Haubein, Ned, Dunn, Joseph, Verma, Anurag, Kripke, Colleen Morse, Risman, Marjorie, Verma, Shefali S., Dudek, Scott, Boris, Derek, Buchanan, Adam, Carey, David J., Colonie, Ryan D., Davis, F. Daniel, Martin, Christa L., Meyer, Michelle, Mirshahi, Tooraj, Still, Christopher, Wagner, Jen, Williams, Marc, Abecasis, Goncalo, Coppola, Giovanni, Deubler, Andrew, Economides, Aris, Beechert, Christina, Forsythe, Caitlin, Gu, Zhenhua, Lattari, Michael, Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Sharma, Deepika, Staples, Jeffrey C., Balasubramanian, Suganthi, Bao, Suying, Eom, Gisu, Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Mansfield, Adam J., Nafde, Mona, Orelus, Max, Polanco, Tommy, Salerno, William, Dobbyn, Lee, Ferreira, Manuel Allen Revez, Ghosh, Arkopravo, Jorgenson, Eric, Kosmicki, Jack, Marchini, Jonathan, Moscati, Arden, Sidore, Carlo, Stahl, Eli, Watanabe, Kyoko, Ye, Bin, Ziyatdinov, Andrey, Ayer, Ariane, Guvenek, Aysegul, Hindy, George, Praveen, Kavita, Haas, Mary, Riaz, Moeen, Sosina, Olukayode, Akbari, Parsa, Nakka, Priyanka, Tzoneva, Gannie, Rodriguez-Flores, Juan, LeBlanc, Michelle G., Mighty, Jason, Mitnaul, Lyndon J., Nishtala, Nirupama, Baras, Aris, Mastaitis, Jason, Devalaraja-Narashimha, Kishor B., Rankin, Andrew J., Herman, Gary
Published in Nature (London) (19.09.2024)
Published in Nature (London) (19.09.2024)
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Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581]
Gervais, Olivier, Kawai, Yosuke, Tang, Ruqi, Atkinson, Elizabeth J., Carbone, Marco, de Andrade, Mariza, Lazaridis, Konstantinos N., Siminovitch, Katherine A., Ma, Xiong, Affronti, Andrea, Almasio, Piero L., Cardinale, Vincenzo, Crocè, Lory Saveria, Donato, Francesca, Fabris, Luca, Mancuso, Clara, Nagaoka, Shinya, Matsushita, Kouki, Kouno, Hirotaka, Ota, Hajime, Shimada, Masaaki, Komeda, Toshiki, Yamashita, Tsutomu, Takahashi, Hironao, Yamauchi, Kazuhiko, Hayashi, Shigeki, Watanabe, Yukio, Hirata, Keisuke, Takikawa, Hajime, Onji, Morikazu, Kaneko, Shuichi, Arai, Kuniaki, Hashimoto, Etsuko, Umemura, Takeji, Seike, Masataka, Kanda, Tatsuo, Himoto, Takashi, Yasunami, Michio, Mizokami, Masashi, Yamamoto, Kazuhide, Ido, Akio, Harada, Kenichi, Nakanuma, Yasuni, Soejima, Yuji, Yagi, Shintaro, Tanaka, Tomohiro, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Lattari, Michael, Lopez, Alexander, Wolf, Sarah E., Balasubramanian, Suganthi, Khalid, Shareef, Maxwell, Evan K., Sturgess, Richard, Healey, Christopher, Evans, Richard, Gasem, Jaber, Tibble, Jeremy A., Gorard, David A., Jones, Susan, Mells, George, Mulcahy, Victoria, Srivastava, Brijesh, Elphick, David, Sayer, Joanne, Carter, Martyn J., Koss, Konrad, Shah, Jayshri, Grimley, Charles, Gooding, Ian R., Williams, Simon, Cheent, Kuldeep, Wong, Terry, Ramage, John, Gordon, Harriet M., Ridpath, Jo, Abouda, George, Narain, Mark, Matthews, Helen C., Prince, Martin I., Dillon, John F., Lee, Tom J.W., Collier, Jane, Aspinall, Richard, Booth, Jonathan, Hussaini, Hyder, Christie, John, Patanwala, Imran, Maltby, Julia, Singhal, Saket, Mitchison, Harriet, Ch'ng, Chin Lye, Jain, Sanjiv, Wright, Mark, Unitt, Esther, Grant, Allister, Mathew, Ray, Ramakrishnan, Subramaniam
Published in Journal of hepatology (01.02.2022)
Published in Journal of hepatology (01.02.2022)
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Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies
Cavazos, Taylor B, Kachuri, Linda, Graff, Rebecca E, Nierenberg, Jovia L, Thai, Khanh K, Alexeeff, Stacey, Van Den Eeden, Stephen, Corley, Douglas A, Kushi, Lawrence H, Hoffmann, Thomas J, Ziv, Elad, Habel, Laurel A, Jorgenson, Eric, Sakoda, Lori C, Witte, John S
Published in BMC medicine (06.10.2022)
Published in BMC medicine (06.10.2022)
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Journal Article
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults
Praveen, Kavita, Dobbyn, Lee, Gurski, Lauren, Ayer, Ariane H, Staples, Jeffrey, Mishra, Shawn, Bai, Yu, Kaufman, Alexandra, Moscati, Arden, Benner, Christian, Chen, Esteban, Chen, Siying, Popov, Alexander, Smith, Janell, Melander, Olle, Jones, Marcus B, Marchini, Jonathan, Balasubramanian, Suganthi, Zambrowicz, Brian, Drummond, Meghan C, Baras, Aris, Abecasis, Goncalo R, Ferreira, Manuel A, Stahl, Eli A, Coppola, Giovanni
Published in Communications biology (03.06.2022)
Published in Communications biology (03.06.2022)
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ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma
Praveen, Kavita, Patel, Gaurang C, Gurski, Lauren, Ayer, Ariane H, Persaud, Trikaladarshi, Still, Matthew D, Miloscio, Lawrence, Van Zyl, Tavé, Di Gioia, Silvio Alessandro, Brumpton, Ben, Krebs, Kristi, Åsvold, Bjørn Olav, Chen, Esteban, Chavali, Venkata R M, Fury, Wen, Gudiseva, Harini V, Hyde, Sarah, Jorgenson, Eric, Lefebvre, Stephanie, Li, Dadong, Li, Alexander, Mclninch, James, Patel, Brijeshkumar, Rabinowitz, Jeremy S, Salowe, Rebecca, Schurmann, Claudia, Seidelin, Anne-Sofie, Stahl, Eli, Sun, Dylan, Teslovich, Tanya M, Tybjærg-Hansen, Anne, Willer, Cristen, Waldron, Scott, Walley, Sabrina, Yang, Hua, Zaveri, Sarthak, Hu, Ying, Hveem, Kristian, Melander, Olle, Milani, Lili, Stender, Stefan, O'Brien, Joan M, Jones, Marcus B, Abecasis, Gonçalo R, Cantor, Michael N, Weyne, Jonathan, Karalis, Katia, Economides, Aris, Della Gatta, Giusy, Ferreira, Manuel A, Yancopoulos, George D, Baras, Aris, Romano, Carmelo, Coppola, Giovanni
Published in Communications biology (03.10.2022)
Published in Communications biology (03.10.2022)
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PMS2CL interference leading to erroneous identification of a pathogenic PMS2 variant in Black patients
Cappadocia, Jacqueline, Aiello, Lisa B., Kelley, Michael J., Katona, Bryson W., Verma, Anurag, Brock, Ashlei, DerOhannessian, Stephanie, Dudek, Scott, Drivas, Theodore, Haubein, Ned, Hu-Sain, Khadijah, Judy, Renae, Ko, Yi-An, Livingstone, Meghan, Morrel, Linda, Morse, Colleen, Risman, Marjorie, Tran, Teo, Vadivieso, Fred, Weaver, JoEllen, Rader, Daniel J., Ritchie, Marylyn D., Feldman, Michael D., Beechert, Christina, Fuller, Erin D., Lopez, Alexander, Overton, John D., Padilla, Maria Sotiropoulos, Manoochehri, Kia, Schleicher, Thomas D., Widom, Louis, Wolf, Sarah E., Banerjee, Nilanjana, Cantor, Michael, Li, Dadong, Malhotra, Sameer, Sharma, Deepika, Staples, Jeffrey, Bai, Xiaodong, Bao, Suying, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Lanche, Rouel, Mansfield, Adam J., Maxwell, Evan K., O’Keeffe, Sean, Orelus, Max, Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Salerno, William, Staples, Jeffrey C., Sun, Kathie, Backman, Joshua, Damask, Amy, Ferreira, Manuel Allen Revez, Ghosh, Arkopravo, Gurski, Lauren, Jorgenson, Eric, Kang, Hyun Min, Kessler, Michael, Kosmicki, Jack, Li, Alexander, Lin, Nan, Locke, Adam, Mbatchou, Joelle, Moscati, Arden, Paulding, Charles, Sidore, Carlo, Stahl, Eli, Ye, Bin, Coppola, Giovanni, Bovijn, Jonas, Siminovitch, Katherine, Praveen, Kavita, Lotta, Luca A., Kapoor, Manav, Verweij, Niek, Sosina, Olukayode, Akbari, Parsa, Nakka, Priyanka, Gokhale, Sujit, De, Tanima, Rajagopal, Veera, Shuldiner, Alan, Tzoneva, Gannie, Rodriguez-Flores, Juan, Jones, Marcus B., LeBlanc, Michelle G., Mighty, Jason, Mitnaul, Lyndon J., Nishtala, Nirupama, Rana, Nadia, Hernandez, Jaimee, Abecasis, Goncalo, Baras, Aris, Deubler, Andrew, Economides, Aris, Lotta, Luca A.
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Shah, Sonia, Roselli, Carolina, Lin, Honghuang, Fatemifar, Ghazaleh, Hedman, Åsa K, Morley, Michael P, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Ärnlöv, Johan, Backman, Joshua D, Biggs, Mary L, Bloom, Heather L, Brown, Michael R, Buckbinder, Leonard, Chasman, Daniel I, Chen, Xing, Chen, Xu, Chung, Jonathan, Chutkow, William, Delgado, Graciela E, Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C, Dunn, Michael E, Felix, Stephan B, Finan, Chris, Ghanbari, Mohsen, Ghasemi, Sahar, Giedraitis, Vilmantas, Giulianini, Franco, Gottdiener, John S, Gross, Stefan, Guðbjartsson, Daníel F, van der Harst, Pim, Hyde, Craig L, Ingelsson, Erik, Jukema, J Wouter, Khaw, Kay-Tee, Kleber, Marcus E, Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, London, Barry, Lovering, Ruth C, Luan, Jian'an, Magnusson, Patrik, Mahajan, Anubha, Melander, Olle, Mordi, Ify R, Morgan, Thomas, Morris, Andrew D, Morris, Andrew P, Morrison, Alanna C, Nagle, Michael W, Niessner, Alexander, O'Donoghue, Michelle L, Owens, Anjali T, Palmer, Colin N A, Parry, Helen M, Portilla-Fernandez, Eliana, Psaty, Bruce M, Rice, Kenneth M, Ridker, Paul M, Romaine, Simon P R, Salo, Perttu, Salomaa, Veikko, Smith, Nicholas L, Stender, Steen, Stott, David J, Svensson, Per, Taylor, Kent D, Teumer, Alexander, Thorgeirsson, Guðmundur, Thorsteinsdottir, Unnur, Tyl, Benoit, Uitterlinden, Andre G, Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A, Wang, Xiaosong, Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L, Xing, Heming, Yerges-Armstrong, Laura M, Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, Samani, Nilesh J, Malarstig, Anders, Asselbergs, Folkert W, Kuchenbaecker, Karoline, Lang, Chim C, Stefansson, Kari, Smith, J Gustav, Swerdlow, Daniel I, Lumbers, R Thomas
Published in Nature communications (2020)
Published in Nature communications (2020)
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Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
Horowitz, Julie E, Kosmicki, Jack A, Damask, Amy, Sharma, Deepika, Roberts, Genevieve H L, Justice, Anne E, Banerjee, Nilanjana, Coignet, Marie V, Yadav, Ashish, Leader, Joseph B, Marcketta, Anthony, Park, Danny S, Lanche, Rouel, Maxwell, Evan, Knight, Spencer C, Bai, Xiaodong, Guturu, Harendra, Sun, Dylan, Baltzell, Asher, Kury, Fabricio S P, Backman, Joshua D, Girshick, Ahna R, O'Dushlaine, Colm, McCurdy, Shannon R, Partha, Raghavendran, Mansfield, Adam J, Turissini, David A, Li, Alexander H, Zhang, Miao, Mbatchou, Joelle, Watanabe, Kyoko, Gurski, Lauren, McCarthy, Shane E, Kang, Hyun M, Dobbyn, Lee, Stahl, Eli, Verma, Anurag, Sirugo, Giorgio, Ritchie, Marylyn D, Jones, Marcus, Balasubramanian, Suganthi, Siminovitch, Katherine, Salerno, William J, Shuldiner, Alan R, Rader, Daniel J, Mirshahi, Tooraj, Locke, Adam E, Marchini, Jonathan, Overton, John D, Carey, David J, Habegger, Lukas, Cantor, Michael N, Rand, Kristin A, Hong, Eurie L, Reid, Jeffrey G, Ball, Catherine A, Baras, Aris, Abecasis, Gonçalo R, Ferreira, Manuel A R
Published in Nature genetics (01.04.2022)
Published in Nature genetics (01.04.2022)
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Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
Mansour Aly, Dina, Dwivedi, Om Prakash, Prasad, Rashmi B, Käräjämäki, Annemari, Hjort, Rebecka, Thangam, Manonanthini, Åkerlund, Mikael, Mahajan, Anubha, Udler, Miriam S, Florez, Jose C, McCarthy, Mark I, Brosnan, Julia, Melander, Olle, Carlsson, Sofia, Hansson, Ola, Tuomi, Tiinamaija, Groop, Leif, Ahlqvist, Emma
Published in Nature genetics (01.11.2021)
Published in Nature genetics (01.11.2021)
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Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Li, Yong, Wuttke, Matthias, Winkler, Thomas W., Chai, Jin-Fang, Chu, Audrey Y., Cocca, Massimiliano, Feitosa, Mary F., Hoppmann, Anselm, Horn, Katrin, Li, Man, Nutile, Teresa, Tin, Adrienne, Tayo, Bamidele O., Bakker, Stephan J.L., Banas, Bernhard, Biggs, Mary L., Bottinger, Erwin P., Brenner, Hermann, Chalmers, John, Chee, Miao-Ling, Degenhardt, Frauke, Eckardt, Kai-Uwe, Ghanbari, Mohsen, Gieger, Christian, Hofer, Edith, Xian Foo, Valencia Hui, Hutri-Kähönen, Nina, Ikram, M. Arfan, Kähönen, Mika, Khor, Chiea-Chuen, Koenig, Wolfgang, Kramer, Holly, Krämer, Bernhard K., Kühnel, Brigitte, Lange, Leslie A., Franke, Lude, van der Harst, Pim, Navis, Gerjan, Snieder, Harold, Swertz, Morris, Wolffenbuttel, Bruce H.R., Wijmenga, Cisca, Abecasis, Goncalo, Baras, Aris, Coppola, Giovanni, Economides, Aris, Lotta, Luca A., Overton, John D., Reid, Jeffrey G., Beechert, Christina, Forsythe, Caitlin, Gu, Zhenhua, Lattari, Michael, Padilla, Maria Sotiropoulos, Toledo, Karina, Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Barnard, Leland, Blumenfeld, Andrew, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Mitnaul, Lyndon J., Loos, Ruth J.F., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Milaneschi, Yuri, Mishra, Pashupati P., Mychaleckyj, Josyf C., Nikus, Kjell, Nolte, Ilja M., O’Donoghue, Michelle L., Pendergrass, Sarah A., Penninx, Brenda W.J.H., Preuss, Michael H., Psaty, Bruce M., Raitakari, Olli T., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rosenkranz, Alexander R., Rossing, Peter, Sedaghat, Sanaz, Taylor, Kent D., Tremblay, Johanne, Völker, Uwe, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Wong, Tien-Yin, Snieder, Harold, Böger, Carsten A., Köttgen, Anna, Heid, Iris M.
Published in Kidney international (01.04.2021)
Published in Kidney international (01.04.2021)
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GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms
Ward, Lucas D, Tu, Ho-Chou, Quenneville, Chelsea B, Tsour, Shira, Flynn-Carroll, Alexander O, Parker, Margaret M, Deaton, Aimee M, Haslett, Patrick A J, Lotta, Luca A, Verweij, Niek, Ferreira, Manuel A R, Baras, Aris, Hinkle, Gregory, Nioi, Paul
Published in Nature communications (27.07.2021)
Published in Nature communications (27.07.2021)
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Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals
Kember, Rachel L., Merikangas, Alison K., Verma, Shefali S., Verma, Anurag, Judy, Renae, Abecasis, Goncalo, Baras, Aris, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Lotta, Luca, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Schleicher, Thomas D., Padilla, Maria Sotiropoulos, Toledo, Karina, Widom, Louis, Wolf, Sarah E., Pradhan, Manasi, Manoochehri, Kia, Ulloa, Ricardo H., Bai, Xiaodong, Balasubramanian, Suganthi, Barnard, Leland, Blumenfeld, Andrew, Eom, Gisu, Habegger, Lukas, Hahn, Young, Hawes, Alicia, Khalid, Shareef, Maxwell, Evan K., Salerno, William, Staples, Jeffrey C., Yadav, Ashish, Jones, Marcus B., Mitnaul, Lyndon J., Damrauer, Scott M., Ritchie, Marylyn D., Rader, Daniel J., Bućan, Maja
Published in Biological psychiatry (1969) (01.02.2021)
Published in Biological psychiatry (1969) (01.02.2021)
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Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
Deaton, Aimee M, Parker, Margaret M, Ward, Lucas D, Flynn-Carroll, Alexander O, BonDurant, Lucas, Hinkle, Gregory, Akbari, Parsa, Lotta, Luca A, Baras, Aris, Nioi, Paul
Published in Scientific reports (03.11.2021)
Published in Scientific reports (03.11.2021)
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Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study
Sun, Jiangming, Borné, Yan, Edsfeldt, Andreas, Wang, Yunpeng, Pan, Mengyu, Melander, Olle, Engström, Gunnar, Gonçalves, Isabel
Published in Stroke (1970) (01.05.2023)
Published in Stroke (1970) (01.05.2023)
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Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection
Zhang, Chao, Verma, Anurag, Feng, Yuanqing, Melo, Marcelo C R, McQuillan, Michael, Hansen, Matthew, Lucas, Anastasia, Park, Joseph, Ranciaro, Alessia, Thompson, Simon, Rubel, Meagan A, Campbell, Michael C, Beggs, William, Hirbo, Jibril, Wata Mpoloka, Sununguko, George Mokone, Gaonyadiwe, Nyambo, Thomas, Wolde Meskel, Dawit, Belay, Gurja, Fokunang, Charles, Njamnshi, Alfred K, Omar, Sabah A, Williams, Scott M, Rader, Daniel J, Ritchie, Marylyn D, de la Fuente-Nunez, Cesar, Sirugo, Giorgio, Tishkoff, Sarah A
Published in Proceedings of the National Academy of Sciences - PNAS (24.05.2022)
Published in Proceedings of the National Academy of Sciences - PNAS (24.05.2022)
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Thrombotic risk determined by rare and common SERPINA1 variants in a population‐based cohort study
Manderstedt, Eric, Halldén, Christer, Lind‐Halldén, Christina, Elf, Johan, Svensson, Peter J., Engström, Gunnar, Melander, Olle, Baras, Aris, Lotta, Luca A., Zöller, Bengt, Abecasis, Goncalo, Cantor, Michael, Coppola, Giovanni, Economides, Aris, Overton, John D., Reid, Jeffrey G., Shuldiner, Alan, Beechert, Christina, Forsythe, Caitlin, Fuller, Erin D., Gu, Zhenhua, Lattari, Michael, Lopez, Alexander, Manoochehri, Kia, Overton, John D., Padilla, Maria Sotiropoulos, Pradhan, Manasi, Schleicher, Thomas D., Ulloa, Ricardo H., Widom, Louis, Wolf, Sarah E., Bai, Xiaodong, Balasubramanian, Suganthi, Blumenfeld, Andrew, Boutkov, Boris, Eom, Gisu, Habegger, Lukas, Hawes, Alicia, Khalid, Shareef, Krasheninina, Olga, Lanche, Rouel, Mansfield, Adam J., Maxwell, Evan K., Nafde, Mrunali, O’Keeffe, Sean, Orelus, Max, Panea, Razvan, Polanco, Tommy, Rasool, Ayesha, Reid, Jeffrey G., Salerno, William, Staples, Jeffrey C., Jones, Marcus B., Mighty, Jason, Mitnaul, Lyndon J.
Published in Journal of thrombosis and haemostasis (01.06.2022)
Published in Journal of thrombosis and haemostasis (01.06.2022)
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