Effects of personalized endurance training on cellular age and vascular function in middle-aged sedentary women by Eigendorf, Julian, Melk, Anette, Haufe, Sven, Boethig, Dietmar, Berliner, Dominik, Kerling, Arno, Kueck, Momme, Stenner, Hedwig, Bara, Christoph, Stiesch, Meike, Schippert, Cordula, Hilfiker, Andres, Falk, Christine, Bauersachs, Johann, Thum, Thomas, Lichtinghagen, Ralf, Haverich, Axel, Hilfiker-Kleiner, Denise, Tegtbur, Uwe

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Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals by 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

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Used syringes analysis: A new approach to better-know what is injected by Nefau, Thomas, Karolak, Sara, Levi, Yves, Thibault, Vincent, Duplessy-Garcon, Catherine, Bara, Jean-Louis

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Amplification of mGlu 5 -Endocannabinoid Signaling Rescues Behavioral and Synaptic Deficits in a Mouse Model of Adolescent and Adult Dietary Polyunsaturated Fatty Acid Imbalance by Manduca, Antonia, Bara, Anissa, Larrieu, Thomas, Lassalle, Olivier, Joffre, Corinne, Layé, Sophie, Manzoni, Olivier J

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Blood Cytokine Profiles Associated with Distinct Patterns of Bronchopulmonary Dysplasia among Extremely Low Birth Weight Infants by D'Angio, Carl T., MD, Ambalavanan, Namasivayam, MD, Carlo, Waldemar A., MD, McDonald, Scott A., BS, Skogstrand, Kristin, PhD, Hougaard, David M., MD, DSc, Shankaran, Seetha, MD, Goldberg, Ronald N., MD, Ehrenkranz, Richard A., MD, Tyson, Jon E., MD, MPH, Stoll, Barbara J., MD, Das, Abhik, PhD, Higgins, Rosemary D., MD

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Protease activated receptor-2 expression and function in asthmatic bronchial smooth muscle by Allard, Benoit, Bara, Imane, Gilbert, Guillaume, Carvalho, Gabrielle, Trian, Thomas, Ozier, Annaig, Gillibert-Duplantier, Jennifer, Ousova, Olga, Maurat, Elise, Thumerel, Matthieu, Quignard, Jean-François, Girodet, Pierre-Olivier, Marthan, Roger, Berger, Patrick

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The UK Coalition Agreement of 2010: Who Won? by Quinn, Thomas, Bara, Judith, Bartle, John

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Cytokines Associated With Bronchopulmonary Dysplasia or Death in Extremely Low Birth Weight Infants by Ambalavanan, Namasivayam, Carlo, Waldemar A, D'Angio, Carl T, McDonald, Scott A, Das, Abhik, Schendel, Diana, Thorsen, Poul, Higgins, Rosemary D, Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network

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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 by 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

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Extreme Preterm Infant Rates of Overweight and Obesity at School Age in the SUPPORT Neuroimaging and Neurodevelopmental Outcomes Cohort by Heyne, Roy, Higgins, Rosemary D., Caplan, Michael S., Hensman, Angelita M., Vieira, Elisa, Alksninis, Barbara, Keszler, Mary Lenore, Leach, Theresa M., Watson, Victoria E., Fanaroff, Avroy A., Wilson-Costello, Deanne E., Newman, Nancy S., Taylor, H. Gerry, Zadell, Arlene, DiFiore, Julie, Bhola, Monika, Friedman, Harriet G., Bulas, Dorothy, Cotten, C. Michael, Gustafson, Kathryn E., Auten, Kathy J., Fisher, Kimberley A., Foy, Katherine A., Lohmeyer, Melody B., Malcolm, William F., Wallace, David K., Buchter, Susie, Piazza, Anthony J., Fritz, Sobha, Hale, Ellen C., Hutchinson, Amy K., Loggins, Yvonne, Archer, Stephanie Wilson, Papile, Lu-Ann, Tyson, Jon E., Duncan, Andrea Freeman, Dempsey, Allison G., Gail, Dorothy B., Kiley, James P., Newman, Jamie E., Auman, Jeanette O'Donnell, Hammond, Jane A., Poole, W. Kenneth, DeAnda, Maria Elena, Ball, M. Bethany, Goodlin, Gabrielle T., Fiascone, John M., McGowan, Elisabeth C., Furey, Anne, MacKinnon, Brenda L., Nylen, Ellen, Sibley, Cecelia, Ambalavanan, Namasivayam, Peralta-Carcelen, Myriam, Phillips, Vivien A., Biasini, Fred J., Patterson, Cryshelle S., Rector, Richard V., Rodriguez, Leslie, Whitley, Sally, Garey, Donna, Rasmussen, Maynard R., Fuller, Martha G., Akshoomoff, Natacha, Rich, Wade, Arnell, Kathy, Bridge, Renee, Bell, Edward F., Colaizy, Tarah T., Widness, John A., Klein, Jonathan M., Eastman, Diane L., Watterberg, Kristi L., Fuller, Janell, Rohr, Julie, Montman, Rebecca, Sánchez, Pablo J., Rosenfeld, Charles R., Salhab, Walid A., Adams, Sally S., Grau, Laura, Guzman, Alicia, Hensley, Gaynelle, Heyne, Elizabeth T., Hickman, Jackie F., Morgan, Janet S., Lee, Lizette E., Boatman, Catherine Twell, Yoder, Bradley A., Faix, Roger G., Winter, Sarah, Baker, Shawna, Osborne, Karen A., Rau, Carrie A., Cunningham, Sean, Shankaran, Seetha, Slovis, Thomas L., Billian, Elizabeth, Goldston, Laura A., Johnson, Mary

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Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study by Sun, Jiangming, Borné, Yan, Edsfeldt, Andreas, Wang, Yunpeng, Pan, Mengyu, Melander, Olle, Engström, Gunnar, Gonçalves, Isabel

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Quality of care at childbirth during the COVID-19 pandemic in Belgium: a cross-sectional study based on WHO standards by Galle, Anna, Berghman, Helga, D’Hauwers, Silke, Vaerewijck, Nele, Valente, Emanuelle Pessa, Mariani, Ilaria, Bomben, Arianna, delle Vedove, Stefano, Lazzerini, Marzia, König-Bachmann, Martina, Zenzmaier, Christoph, Imola, Simon, D'Costa, Elisabeth, Galle, Anna, D’Hauwers, Silke, Kolokotroni, Ourania, Hadjigeorgiou, Eleni, Karanikola, Maria, Middleton, Nicos, Eteocleous, Ioli Orphanide, Zirovnicka, Lenka Laubrova, Kramná, Miloslava, Virginie, Rozée, Rochebrochard, Elise de La, Kristina, Antigoni Sarantaki, Metallinou, Dimitra, Lykeridou, Aikaterini, Lazzerini, Marzia, Valente, Emanuelle Pessa, Mariani, Ilaria, Bomben, Arianna, Vedove, Stefano Delle, Morano, Sandra, Nespoli, Antonella, Fumagalli, Simona, Pumpure, Elizabete, Rezeberga, Dace, Jakovicka, Dārta, Jansone-Šantare, Gita, Šibalova, Anna, Voitehoviča, Elīna, Krēsliņa, Dārta, Liepinaitienė, Alina, Kondrakova, Andželika, Mizgaitienė, Marija, Juciūtė, Simona, Arendt, Maryse, Tasch, Barbara, Lopriore, Enrico, Akker, Thomas Van den, Baranowska, Barbara, Tataj-Puzyna, Urszula, Szlendak, Beata, Pawlicka, Paulina, Costa, Raquel, Barata, Catarina, Santos, Teresa, Dias, Heloísa, Pinto, Tiago Miguel, Marques, Sofia, Meireles, Ana, Oliveira, Joana, Pereira, Mariana, Nunes, Maria Arminda, Otelea, Marina Ruxandra, Drglin, Zalka, Bohinec, Anja, Brigidi, Serena, Oliden, Alejandra, Castañeda, Lara Martín, Elden, Helen, Linden, Karolina, Zaigham, Mehreen, Labrusse, Claire de, Abderhalden-Zellweger, Alessia, Pfund, Anouck, Thorn, Harriet, Grylka, Susanne, Gemperle, Michael, Mueller, Antonia

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Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium by Wan, Xuesi, Perry, James, Zhang, Haichen, Jin, Feng, Ryan, Kathleen A, Van Hout, Cristopher, Reid, Jeffrey, Overton, John, Baras, Aris, Han, Zhe, Streeten, Elizabeth, Li, Yanbing, Mitchell, Braxton D, Shuldiner, Alan R, Fu, Mao

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Behavioral Deficits at 18-22 Months of Age Are Associated with Early Cerebellar Injury and Cognitive and Language Performance in Children Born Extremely Preterm by Dempsey, Allison, Caplan, Michael S., Laptook, Abbot R., Vohr, Betty R., Hensman, Angelita M., Alksninis, Barbara, Cashore, Bill, Francis, Kim, Gingras, Dan, Walsh, Michele C., Newman, Nancy S., Zadell, Arlene, Yalcinkaya, Gulgun, Bulas, Dorothy, Foy, Katherine A., Freedman, Sharon F., Lohmeyer, Melody B., Carlton, David P., Adams-Chapman, Ira, Piazza, Anthony J., LaRossa, Maureen Mulligan, Higgins, Rosemary D., Sokol, Gregory M., Dusick, Anna M., Lemons, James A., Wilson, Leslie D., Hamer, Faithe, Cook, Ann B., Herron, Dianne E., Minnich, Heike M., Berberich, Mary Anne, Das, Abhik, Newman, Jamie E., Auman, Jeanette O'Donnell, Pickett, James W., Van Meurs, Krisa P., Stevenson, David K., Ball, M. Bethany, Pyle, Renee P., Weiss, Hali E., Frantz, Ivan D., McGowan, Elisabeth C., Brussa, Ana, Carlo, Waldemar A., Hopkins, Maria, Johnston, Kristen C., Patterson, Cryshelle S., Soong, Amanda, Vaucher, Yvonne E., Lukasik, Meghan, Pontillo, Deborah, Wilkes, James, Colaizy, Tarah T., Johnson, Karen J., Calejo, Maria, Frade Eguaras, Silvia M., Berkowits, Michelle Harwood, Hiriart-Fajardo, Sylvia, Mathews, Elaine O., Pierre, Helina, Stroerger, Alexandra, Ohls, Robin K., Lowe, Jean, Laroia, Nirupama, Myers, Gary J., Reubens, Linda J., Johnson, Julie Babish, Gelbard, Harris, Kushner, Emily, Wang, David, Salhab, Walid A., Heyne, Roy J., Allen, James, Guzman, Alicia, Hensley, Gaynelle, Hickman, Jackie F., Solis, Araceli, Torres, Lizette E., Kennedy, Kathleen A., Evans, Patricia W., Alaniz, Nora I., Harris, Beverly Foley, Jiminez, Margarita, McDavid, Georgia E., Morris, Brenda H., Reddoch, Stacy, Wright, Sharon L., Yoder, Bradley A., Baker, Shawna, Bird, Karie, Bullwinkle, Anna E., Burnett, Jill, Osborne, Karen A., Steele, R. Edison, Weaver-Lewis, Kimberlee, Peters, Nancy J., Chiu, Korinne, Goldstein, Donald J., Sood, Beena G., Johnson, Mary

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Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants by Hartnett, M Elizabeth, Morrison, Margaux A, Smith, Silvia, Yanovitch, Tammy L, Young, Terri L, Colaizy, Tarah, Momany, Allison, Dagle, John, Carlo, Waldemar A, Clark, Erin A S, Page, Grier, Murray, Jeff, DeAngelis, Margaret M, Cotten, C Michael

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Patients Regret Their Choice of Therapy Significantly Less Frequently after Robot-Assisted Radical Prostatectomy as Opposed to Open Radical Prostatectomy: Patient-Reported Results... by Wolff, Ingmar, Burchardt, Martin, Gilfrich, Christian, Peter, Julia, Baunacke, Martin, Thomas, Christian, Huber, Johannes, Gillitzer, Rolf, Sikic, Danijel, Fiebig, Christian, Steinestel, Julie, Schifano, Paola, Löbig, Niklas, Bolenz, Christian, Distler, Florian A, Huettenbrink, Clemens, Janssen, Maximilian, Schilling, David, Barakat, Bara, Harke, Nina N, Fuhrmann, Christian, Manseck, Andreas, Wagenhoffer, Robert, Geist, Ekkehard, Blair, Lisa, Pfitzenmaier, Jesco, Reinhardt, Bettina, Hoschke, Bernd, Burger, Maximilian, Bründl, Johannes, Schnabel, Marco J, May, Matthias

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Cytokines and Neurodevelopmental Outcomes in Extremely Low Birth Weight Infants by Carlo, Waldemar A., MD, McDonald, Scott A., BS, Tyson, Jon E., MD, MPH, Stoll, Barbara J., MD, Ehrenkranz, Richard A., MD, Shankaran, Seetha, MD, Goldberg, Ronald N., MD, Das, Abhik, PhD, Schendel, Diana, PhD, Thorsen, Poul, MD, Skogstrand, Kristin, PhD, Hougaard, David M., MD, Oh, William, MD, Laptook, Abbot R., MD, Duara, Shahnaz, MD, Fanaroff, Avroy A., MD, Donovan, Edward F., MD, Korones, Sheldon B., MD, Stevenson, David K., MD, Papile, Lu-Ann, MD, Finer, Neil N., MD, O’Shea, T. Michael, MD, MPH, Poindexter, Brenda B., MD, MS, Wright, Linda L., MD, Ambalavanan, Namasivayam, MD, Higgins, Rosemary D., MD

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Population-scale analysis of common and rare genetic variation associated with hearing loss in adults by 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

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Strategies to minimise and monitor biases and imbalances by arm in surgical cluster randomised trials: evidence from ChEETAh, a trial in seven low- and middle-income countries by Ahogni, Didier, Ahounou, Aristide, Boukari, K. Alassan, Gbehade, Oswald, Hessou, Thierry K., Nindopa, Sinama, Nontonwanou, M. J. Bienvenue, Guessou, Nafissatou Orou, Sambo, Arouna, Tchati, Sorekou Victoire, Tchogo, Affisatou, Tobome, Semevo Romaric, Yanto, Parfait, Gandaho, Isidore, Hadonou, Armel, Hinvo, Simplice, Hodonou, Montcho Adrien, Tamou, Sambo Bio, Lawani, Souliath, Kandokponou, Covalic Melic Bokossa, Dossou, Francis Moise, Gaou, Antoine, Goudou, Roland, Kouroumta, Marie-Claire, Lawani, Ismail, Malade, Enrif, Dikao, Anne Stredy Mkoh, Nsilu, Joel Nzuwa, Ogouyemi, Pencome, Akpla, Marcelin, Mitima, Nathan Bisimwa, Kovohouande, Blaise, Kpangon, Cyrille, Loupeda, Stephane Laurent, Agbangla, Mamonde Victorin, Hedefoun, Sena Emmanuel, Mavoha, Thierry, Ngaguene, Juvenal, Rugendabanga, Janvier, Soton, Rish Romaric, Totin, Martin, Agbadebo, Mouhamed, Akpo, Irene, Dewamon, Hubert, Djeto, Martin, Hada, Aissatou, Hollo, Monsede, Houndji, Albert, Houndote, Anasthasie, Hounsa, Sylvestre, Kpatchassou, Expedit, Yome, Hugues, Alidou, Mohamed Moussa, Bara, Eric Jerry, Yovo, B. T. Bonheur Dossou, Guinnou, Robert, Hamadou, Souleymane, Kola, H. Pauline, Moussa, Nabil, Cakpo, Boniface, Etchisse, Lolyta, Hatangimana, Emery, Muhindo, Moise, Sanni, Katia, Yevide, Agossou Barthelemy, Agossou, Hermann, Musengo, Fiston Basirwa, Behanzin, Hulrich, Seto, Djifid Morel, Alia, Bill Armstrong, Alitonou, Arnaud, Mehounou, Y. Edith, Agbanda, Lucien, Attinon, Julien, Gbassi, Marcel, Hounsou, Nounagnon Rene, Acquah, Regina, Banka, Charles, Esssien, Derick, Hussey, Romeo, Mustapha, Yakubu, Nunoo-Ghartey, Kojo, Yeboah, Grace, Aniakwo, Luke A., Adjei, Margarey N. M., Adofo-Asamoah, Yvonne, Agyapong, Meshach M., Agyen, Thomas, Alhassan, Baba A. B., Amoako-Boateng, Mabel P., Appiah, Anthony Baffour, Ashong, Josephine, Awindaogo, Joseph K., Brimpong, Benjamin B., Dayie, Makafui S. C. J. K., Enti, Donald, Ghansah, Wendy W., Gyamfi, Jude E., Koggoh, Patience, Kpankpari, Richard

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Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies by 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

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