Activin A Balances Sertoli and Germ Cell Proliferation in the Fetal Mouse Testis by Mendis, Sirisha H.S, Meachem, Sarah J, Sarraj, Mai A, Loveland, Kate L

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Host Genetic Variants Potentially Associated With SARS-CoV-2: A Multi-Population Analysis by Smatti, Maria K, Al-Sarraj, Yasser A, Albagha, Omar, Yassine, Hadi M

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Correction: Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus by Elashi, Asma A, Toor, Salman M, Umlai, Umm-Kulthum Ismail, Al-Sarraj, Yasser A, Taheri, Shahrad, Suhre, Karsten, Abou-Samra, Abdul Badi, Albagha, Omar M E

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Genome-wide association study and meta-analysis of phytosterols identifies a novel locus for serum levels of campesterol by Alenbawi, Jamil, Al-Sarraj, Yasser A, Umlai, Umm-Kulthum I, Kadhi, Ayat, Hendi, Nagham N, Nemer, Georges, Albagha, Omar M E

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Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus by Elashi, Asma A, Toor, Salman M, Umlai, Umm-Kulthum Ismail, Al-Sarraj, Yasser A, Taheri, Shahrad, Suhre, Karsten, Abou-Samra, Abdul Badi, Albagha, Omar M E

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Genome-wide association study and polygenic score assessment of insulin resistance by Aliyu, Usama, Umlai, Umm-Kulthum Ismail, Toor, Salman M, Elashi, Asma A, Al-Sarraj, Yasser A, Abou Samra, Abdul Badi, Suhre, Karsten, Albagha, Omar M E

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Genome-wide association study identifies several loci for HEV seropositivity by Smatti, Maria K., Al-Sarraj, Yasser A., Albagha, Omar, Yassine, Hadi M.

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Fetal Testis Dysgenesis and Compromised Leydig Cell Function in Tgfbr3 (Betaglycan) Knockout Mice by Sarraj, Mai A, Escalona, Ruth M, Umbers, Alexandra, Chua, Hui Kheng, Small, Chris, Griswold, Mike, Loveland, Kate, Findlay, Jock K, Stenvers, Kaye L

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Betaglycan is required for the establishment of nephron endowment in the mouse by Walker, Kenneth A, Sims-Lucas, Sunder, Caruana, Georgina, Cullen-McEwen, Luise, Li, Jinhua, Sarraj, Mai A, Bertram, John F, Stenvers, Kaye L

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Estrogen-dependent gene expression in the mouse ovary by Liew, Seng H, Sarraj, Mai A, Drummond, Ann E, Findlay, Jock K

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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways by Cirulli, Elizabeth T., Lasseigne, Brittany N., Petrovski, Slavé, Sapp, Peter C., Dion, Patrick A., Leblond, Claire S., Couthouis, Julien, Lu, Yi-Fan, Wang, Quanli, Krueger, Brian J., Ren, Zhong, Keebler, Jonathan, Han, Yujun, Levy, Shawn E., Boone, Braden E., Wimbish, Jack R., Waite, Lindsay L., Jones, Angela L., Carulli, John P., Day-Williams, Aaron G., Staropoli, John F., Xin, Winnie W., Chesi, Alessandra, Raphael, Alya R., McKenna-Yasek, Diane, Cady, Janet, de Jong, J. M. B. Vianney, Kenna, Kevin P., Smith, Bradley N., Topp, Simon, Miller, Jack, Gkazi, Athina, Al-Chalabi, Ammar, van den Berg, Leonard H., Veldink, Jan, Silani, Vincenzo, Ticozzi, Nicola, Shaw, Christopher E., Baloh, Robert H., Appel, Stanley, Simpson, Ericka, Lagier-Tourenne, Clotilde, Pulst, Stefan M., Gibson, Summer, Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Grossman, Murray, Shneider, Neil A., Chung, Wendy K., Ravits, John M., Glass, Jonathan D., Sims, Katherine B., Van Deerlin, Vivianna M., Maniatis, Tom, Hayes, Sebastian D., Ordureau, Alban, Swarup, Sharan, Landers, John, Baas, Frank, Allen, Andrew S., Bedlack, Richard S., Harper, J. Wade, Gitler, Aaron D., Rouleau, Guy A., Brown, Robert, Harms, Matthew B., Cooper, Gregory M., Harris, Tim, Myers, Richard M., Goldstein, David B.

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Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits by Thareja, Gaurav, Al-Sarraj, Yasser, Belkadi, Aziz, Almotawa, Maryam, Suhre, Karsten, Albagha, Omar M. E.

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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study by Jabbari, Edwin, Koga, Shunsuke, Valentino, Rebecca R, Reynolds, Regina H, Ferrari, Raffaele, Tan, Manuela M X, Rowe, James B, Dalgard, Clifton L, Scholz, Sonja W, Dickson, Dennis W, Warner, Thomas T, Revesz, Tamas, Höglinger, Günter U, Ross, Owen A, Ryten, Mina, Hardy, John, Shoai, Maryam, Morris, Huw R, Mok, Kin Y., Murphy, David P., Al-Sarraj, Safa, Troakes, Claire, Gentleman, Steve M., Allinson, Kieren S.J., Jaunmuktane, Zane, Holton, Janice L., Lees, Andrew J., Morris, Christopher M., Compta, Yaroslau, Gelpi, Ellen, van Swieten, John C., Rajput, Alex, Ferguson, Leslie, Cookson, Mark R., Gibbs, J. Raphael, Blauwendraat, Cornelis, Ding, Jinhui, Chia, Ruth, Traynor, Bryan J., Pantelyat, Alexander, Viollet, Coralie, Pletnikova, Olga, Troncoso, Juan C., Rosenthal, Liana S., Boxer, Adam L., Respondek, Gesine, Arzberger, Thomas, Roeber, Sigrun, Giese, Armin, Burn, David J., Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, T.M. Hu, Michele

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Intravenous Thrombolysis With Tenecteplase in Patients With Large Vessel Occlusions: Systematic Review and Meta-Analysis by Katsanos, Aristeidis H., Safouris, Apostolos, Sarraj, Amrou, Magoufis, Georgios, Leker, Ronen R., Khatri, Pooja, Cordonnier, Charlotte, Leys, Didier, Shoamanesh, Ashkan, Ahmed, Niaz, Alexandrov, Andrei V., Tsivgoulis, Georgios

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Differential expression of TGFBR3 (betaglycan) in mouse ovary and testis during gonadogenesis by Sarraj, Mai A., Chua, Hui Kheng, Umbers, Alexandra, Loveland, Kate L., Findlay, Jock K., Stenvers, Kaye L.

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Endovascular Thrombectomy for Large Ischemic Stroke Across Ischemic Injury and Penumbra Profiles by Sarraj, Amrou, Hassan, Ameer E, Abraham, Michael G, Ortega-Gutierrez, Santiago, Kasner, Scott E, Hussain, Muhammad Shazam, Chen, Michael, Churilov, Leonid, Johns, Hannah, Sitton, Clark W, Yogendrakumar, Vignan, Ng, Felix C, Pujara, Deep K, Blackburn, Spiros, Sundararajan, Sophia, Hu, Yin C, Herial, Nabeel A, Arenillas, Juan F, Tsai, Jenny P, Budzik, Ronald F, Hicks, William J, Kozak, Osman, Yan, Bernard, Cordato, Dennis J, Manning, Nathan W, Parsons, Mark W, Cheung, Andrew, Hanel, Ricardo A, Aghaebrahim, Amin N, Wu, Teddy Y, Portela, Pere Cardona, Gandhi, Chirag D, Al-Mufti, Fawaz, Pérez de la Ossa, Natalia, Schaafsma, Joanna D, Blasco, Jordi, Sangha, Navdeep, Warach, Steven, Kleinig, Timothy J, Shaker, Faris, Al Shaibi, Faisal, Toth, Gabor, Abdulrazzak, Mohammad A, Sharma, Gagan, Ray, Abhishek, Sunshine, Jeffrey, Opaskar, Amanda, Duncan, Kelsey R, Xiong, Wei, Samaniego, Edgar A, Maali, Laith, Lechtenberg, Colleen G, Renú, Arturo, Vora, Nirav, Nguyen, Thanh, Fifi, Johanna T, Tjoumakaris, Stavropoula I, Jabbour, Pascal, Tsivgoulis, Georgios, Pereira, Vitor Mendes, Lansberg, Maarten G, DeGeorgia, Michael, Sila, Cathy A, Bambakidis, Nicholas, Hill, Michael D, Davis, Stephen M, Wechsler, Lawrence, Grotta, James C, Ribo, Marc, Albers, Greg W, Campbell, Bruce C

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Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups by Kaivola, Karri, Shah, Zalak, Chia, Ruth, Scholz, Sonja W

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Synthesis of novel Fe3O4 nanostructures surrounded by Ti-MOF nanostructures as bioactive and efficient catalysts in three-component synthesis of new pyrazole derivatives by Qubais Saeed, Balsam, Waleed, Ibrahem, Chlib Alkaaby, Hussein Humedy, Farhan Jawad, Sabrean, Altimari, Usama S., Ahmed AL-Sarraj, Ziyad Shihab, Shbeeb, Ruwaida T., Hadrawi, Salema K., Suliman, Muath, Alshahrani, Mohammad Y.

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MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study by Valentino, Rebecca R, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Real, Raquel, Mok, Kin, Christopher, Elizabeth A, Lee, Edward B, Frosch, Matthew P, Molina-Porcel, Laura, Gefen, Tamar, Robinson, Andrew C, Kobylecki, Christopher, Rowe, James B, Beach, Thomas G, Teich, Andrew F, Keith, Julia L, Bodi, Istvan, Gearing, Marla, Arzberger, Thomas, Morris, Christopher M, White, Charles L, Mechawar, Naguib, MacKenzie, Ian R, McLean, Catriona, Wang, Shih-Hsiu J, Nagra, Rashed M, Kovacs, Gabor G, Giaccone, Giorgio, Ang, Lee-Cyn, Morris, Huw R, Hardy, John A, Dickson, Dennis W, Ross, Owen A, Warner, Thomas T, Boeve, Bradley F, Duara, Ranjan, Josephs, Keith A, Murray, Melissa E, Lyons, Kelly E, Whitwell, Jennifer L, Miller, Bruce, Schlereth, Athena, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Aldecoa, Iban, Gelpi, Ellen, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Bigio, Eileen H, Weintraub, Sandra, Schneider, Julie A, Chang, Koping, Troncoso, Juan C, Jones, Matthew, Richardson, Anna, Roncaroli, Federico, Snowden, Julie, Serrano, Geidy E, Goldman, James E, Leskinen, Sandra P, Masellis, Mario, King, Andrew, Al-Sarraj, Safa, Troakes, Claire, Hodges, John R, Kril, Jillian J, Kwok, John B, Roeber, Sigrun, Attems, Johannes, Thomas, Alan J, Evers, Bret M., Bieniek, Kevin F, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, Castellani, Rudolph J, Chaffee, Ann, Franklin, Erin, Jacobsen, Max, Keene, Dirk, Latimer, Caitlin S, Purohit, Dushyant P, Schantz, Aimee, Walker, Jamie, De Deyn, Peter P, Duyckaerts, Charles, Seilhean, Danielle, Turbant-Leclere, Sabrina, Nennesmo, Inger, Riehl, James, Nacmias, Benedetta, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

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Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants by Elfatih, Amal, Saad, Chadi, Mifsud, Borbala, Mbarek, Hamdi

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