Energy Resources and Development in Vietnam by England, Sarah B, Kammen, Daniel M

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Detection of Restriction Fragment Length Polymorphisms at the Centromeres of Human Chromosomes by Using Chromosome-Specific α Satellite DNA Probes: Implications for Development of... by Willard, Huntington F., Waye, John S., Skolnick, Mark H., Schwartz, Charles E., Powers, Vicki E., England, Sarah B.

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New technologies needed by ENGLAND, SARAH B., KAMMEN, DANIEL B.

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Genomic Organization of Alpha Satellite DNA on Human Chromosome 7: Evidence for Two Distinct Alphoid Domains on a Single Chromosome by Waye, John S., England, Sarah B., Willard, Huntington F.

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Clinical features and management of human monkeypox: a retrospective observational study in the UK by Adler, Hugh, Hine, Paul, Snell, Luke B, Osborne, Jane C, Rampling, Tommy, Beadsworth, Mike BJ, Dunning, Jake, Hunter, Ewan R, Jacobs, Michael, Khoo, Saye H, Porter, David, Porter, Robert J, Ratcliffe, Libuše, Schmid, Matthias L, Tunbridge, Anne J, Wingfield, Tom, Price, Nicholas M, Abouyannis, Mike, Al-Balushi, Asma, Aston, Stephen, Ball, Robert, Blanchard, Thomas J, Davies, Geraint, Gillespie, Angela, Hicks, Scott R, Hoyle, Marie-Claire, Ilozue, Chinenye, Mair, Luke, Marshall, Suzanne, Neary, Anne, Nsutebu, Emmanuel, Ryan, Hannah, Turtle, Lance, van Aartsen, Jon, Walker, Naomi F, Woolley, Stephen, Chawla, Anu, Smielewska, Anna, Benson, Cathryn, Brindley, Cheryl, Das, Urmi, Eyton-Chong, Chin K, Gnanalingham, Claire, Larru, Beatriz, McBride, Joanna, Oliver, Claire, Paul, Princy, Riordan, Andrew, Abrahamsen, Jennifer, Athan, Breda, Bhagani, Sanjay, Brown, Colin S, Carpenter, Oliver, Cropley, Ian, Hopkins, Susan, Joyce, Jessica, Lamb, Lucy, Lyons, Adrian, Mahungu, Tabitha, Mepham, Stephen, Mukwaira, Edina, Rodger, Alison, Williams, Alan, Allen, Denise, Dixon, Jill, Evans, Adam, McNicholas, Pauline, Price, D Ashley, Schwab, Uli, Ward, Margaret, Emonts, Marieke, Owens, Stephen, Douthwaite, Sam T, Goodman, Anna, MacMahon, Eithne, Nebbia, Gaia, Parsons, Joseph, Sullivan, Tadgh, Taj, Usman, van Nipsen tot Pannerden, Claire, Winslow, Helen, Zatyka, Ewa, Alozie-Otuka, Ekene, Beviz, Csaba, Ceesay, Yusupha, Gargee, Latchmin, Mitchell, Hannah, Tabios, Federico, Wigglesworth, Neil, Brooks, Tim, Dryden, Matthew, Furneaux, Jenna, Truelove, Elizabeth, Warrell, Clare E, Firth, Richard, Hobson, Gemma, Johnson, Christopher, Dewynter, Alison, Spence, Oliver, Hruby, Dennis E

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Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition by Martins Custodio, Helena, Clayton, Lisa M, Bellampalli, Ravishankara, Pagni, Susanna, Silvennoinen, Katri, Caswell, Richard, Brunklaus, Andreas, Guerrini, Renzo, Koeleman, Bobby P C, Lemke, Johannes R, Møller, Rikke S, Scheffer, Ingrid E, Weckhuysen, Sarah, Zara, Federico, Zuberi, Sameer, Kuchenbaecker, Karoline, Balestrini, Simona, Mills, James D, Sisodiya, Sanjay M

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Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype by Senum, Sarah R., Li, Ying (Sabrina) M., Benson, Katherine A., Joli, Giancarlo, Olinger, Eric, Lavu, Sravanthi, Madsen, Charles D., Gregory, Adriana V., Neatu, Ruxandra, Kline, Timothy L., Audrézet, Marie-Pierre, Outeda, Patricia, Nau, Cherie B., Meijer, Esther, Ali, Hamad, Steinman, Theodore I., Mrug, Michal, Phelan, Paul J., Watnick, Terry J., Peters, Dorien J.M., Ong, Albert C.M., Conlon, Peter J., Perrone, Ronald D., Cornec-Le Gall, Emilie, Hogan, Marie C., Torres, Vicente E., Sayer, John A., Harris, Peter C.

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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders by Gracia-Diaz, Carolina, Zhou, Yijing, Yang, Qian, Maroofian, Reza, Espana-Bonilla, Paula, Lee, Chul-Hwan, Zhang, Shuo, Padilla, Natàlia, Fueyo, Raquel, Waxman, Elisa A., Lei, Sunyimeng, Otrimski, Garrett, Li, Dong, Sheppard, Sarah E., Mark, Paul, Harr, Margaret H., Hakonarson, Hakon, Rodan, Lance, Jackson, Adam, Vasudevan, Pradeep, Powel, Corrina, Mohammed, Shehla, Maddirevula, Sateesh, Alzaidan, Hamad, Faqeih, Eissa A., Efthymiou, Stephanie, Turchetti, Valentina, Rahman, Fatima, Maqbool, Shazia, Salpietro, Vincenzo, Ibrahim, Shahnaz H., di Rosa, Gabriella, Houlden, Henry, Alharbi, Maha Nasser, Al-Sannaa, Nouriya Abbas, Bauer, Peter, Zifarelli, Giovanni, Estaras, Conchi, Hurst, Anna C. E., Thompson, Michelle L., Chassevent, Anna, Smith-Hicks, Constance L., de la Cruz, Xavier, Holtz, Alexander M., Elloumi, Houda Zghal, Hajianpour, M J, Rieubland, Claudine, Braun, Dominique, Banka, Siddharth, French, Deborah L., Heller, Elizabeth A., Saade, Murielle, Song, Hongjun, Ming, Guo-li, Alkuraya, Fowzan S., Agrawal, Pankaj B., Reinberg, Danny, Bhoj, Elizabeth J., Martínez-Balbás, Marian A., Akizu, Naiara

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Social and psychological adversity are associated with distinct mother and infant gut microbiome variations by Warner, Barbara B., Rosa, Bruce A., Ndao, I. Malick, Tarr, Phillip I., Miller, J. Philip, England, Sarah K., Luby, Joan L., Rogers, Cynthia E., Hall-Moore, Carla, Bryant, Renay E., Wang, Jacqueline D., Linneman, Laura A., Smyser, Tara A., Smyser, Christopher D., Barch, Deanna M., Miller, Gregory E., Chen, Edith, Martin, John, Mitreva, Makedonka

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An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy by Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O'Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry

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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism by Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta M., Kaur, Anupriya, Kaur, Parneet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia M.S., Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra E., Wilke, Martina, Thompson, Michelle L., Bebin, E. Martina, Bijlsma, Emilia K., Hoffer, Mariette J.V., Peeters-Scholte, Cacha, Slavotinek, Anne, Weiss, William A., Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Willaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Yachelevich, Naomi, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Klöckner, Chiara, Kamphausen, Susanne B., Abou Jamra, Rami, Arelin, Maria, Innes, A. Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damian, de Burca, Anna, Kini, Usha, Delatycki, Martin B., Gallacher, Lyndon, Yeung, Alison, Pais, Lynn, Field, Michael, Martin, Ellenore, Charles, Perrine, Courtin, Thomas, Keren, Boris, Iascone, Maria, Cereda, Anna, Poke, Gemma, Abadie, Véronique, Chalouhi, Christel, Parthasarathy, Padmini, Halliday, Benjamin J., Robertson, Stephen P., Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher T.

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The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease by Elhassan, Elhussein A E, Collins, Kane E, Heneghan, Sophia, Gilbert, Edmund, Yang, Hana, Senum, Sarah R, Schauer, Rachel S, Elbarougy, Doaa E, Madden, Stephen F, Murray, Susan L, Sadeghi-Alavijeh, Omid, Carmichael, Joshua, Gale, Daniel, Osman, Shohdan M, Kennedy, Claire, Griffin, Matthew D, Casserly, Liam, Moloney, Brona, O'Hara, Paul, Mallawaarachchi, Amali, Ciurli, Francesca, Graziano, Claudio, Wolff, Constantin A, Schönauer, Ria, LaManna, Gaetano, Durand, Axelle, Limou, Sophie, Halbritter, Jan, Capelli, Irene, McCann, Emma, Harris, Peter C, Cavalleri, Gianpiero L, Benson, Katherine A, Conlon, Peter J

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Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA by Earnest, Rebecca, Uddin, Rockib, Matluk, Nicholas, Renzette, Nicholas, Turbett, Sarah E., Siddle, Katherine J., Loreth, Christine, Adams, Gordon, Tomkins-Tinch, Christopher H., Petrone, Mary E., Rothman, Jessica E., Breban, Mallery I., Koch, Robert Tobias, Billig, Kendall, Fauver, Joseph R., Vogels, Chantal B.F., Bilguvar, Kaya, De Kumar, Bony, Landry, Marie L., Peaper, David R., Omerza, Greg, Grieser, Heather, Meak, Sim, Martha, John, Dewey, Hannah B., King, Ewa, Huard, Richard C., Novitsky, Vlad, Darpolor, Josephine, Manne, Akarsh, Kantor, Rami, Smole, Sandra C., Brown, Catherine M., Fink, Timelia, Lang, Andrew S., Gallagher, Glen R., Pitzer, Virginia E., Sabeti, Pardis C., Gabriel, Stacey, MacInnis, Bronwyn L., Altajar, Ahmad, DeJesus, Alexandra, Brito, Anderson, Watkins, Anne E., Muyombwe, Anthony, Blumenstiel, Brendan S., Neal, Caleb, Kalinich, Chaney C., Liu, Chen, Castaldi, Christopher, Pearson, Claire, Bernard, Clare, Nolet, Corey M., Buzby, Erika, Laszlo, Eva, Reagan, Faye L., Vicente, Gina, Rooke, Heather M., Munger, Heidi, Johnson, Hillary, Tikhonova, Irina R., Ott, Isabel M., Razeq, Jafar, Meldrim, James C., Brown, Jessica, Wang, Jianhui, Vostok, Johanna, Beauchamp, John P., Grimsby, Jonna L., Messer, Katelyn S., Vernest, Kyle, Green, Lisa M., Webber, Lori, Gagne, Luc, Ray, Marianne C., Fisher, Marissa E., Barter, Mary, Lee, Matthew D., DeFelice, Matthew T., Cipicchio, Michelle C., Smith, Natasha L., Fitzgerald, Nicholas A., Kerantzas, Nicholas, Hui, Pei, Harrington, Rachel, Haye, Rashida, Lynch, Ryan, Cofsky, Seana, Clancy, Selina, Mane, Shrikant, Ash, Stephanie, Baez, Stephanie, Fleming, Steve, Murphy, Steven, Alpert, Tara, Mandese, Zoe M., Adams, Mark D., Park, Daniel J., Lemieux, Jacob E., Grubaugh, Nathan D.

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Biomarkers of cardiometabolic complications in survivors of childhood acute lymphoblastic leukemia by Morel, Sophia, Léveillé, Pauline, Samoilenko, Mariia, Franco, Anita, England, Jade, Malaquin, Nicolas, Tu, Véronique, Cardin, Guillaume B., Drouin, Simon, Rodier, Francis, Lippé, Sarah, Krajinovic, Maja, Laverdière, Caroline, Sinnett, Daniel, Lefebvre, Geneviève, Levy, Emile, Marcil, Valérie

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Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study by Schon, Katherine R, Horvath, Rita, Wei, Wei, Calabrese, Claudia, Tucci, Arianna, Ibañez, Kristina, Ratnaike, Thiloka, Pitceathly, Robert D S, Bugiardini, Enrico, Quinlivan, Rosaline, Hanna, Michael G, Clement, Emma, Ashton, Emma, Sayer, John A, Brennan, Paul, Josifova, Dragana, Izatt, Louise, Fratter, Carl, Nesbitt, Victoria, Barrett, Timothy, McMullen, Dominic J, Smith, Audrey, Deshpande, Charulata, Smithson, Sarah F, Festenstein, Richard, Canham, Natalie, Caulfield, Mark, Houlden, Henry, Rahman, Shamima, Chinnery, Patrick F, Ambrose, John C, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R, Brittain, Helen, Caulfield, Mark J, Chan, Georgia C, Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J P, Jackson, Rob, Jones, Louise J, Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E A, Leong, Ivonne U S, Lopez, Javier F, Maleady-Crowe, Fiona, McEntegart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C, O’Donovan, Peter, Odhams, Chris A, Patch, Christine, Buonerimo Pereira, Mariana, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C, Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R A, Thompson, Simon R, Tucci, Arianna, Welland, Matthew J, Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M

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Efficacy of Dimethyl Fumarate in Young Adults with Relapsing-Remitting Multiple Sclerosis: Analysis of the DEFINE, CONFIRM, and ENDORSE Studies by Amezcua, Lilyana, Mao-Draayer, Yang, Vargas, Wendy S., Farber, Rebecca, Schaefer, Sara, Branco, Filipe, England, Sarah M., Belviso, Nicholas, Lewin, James B., Mendoza, Jason P., Shankar, Sai L.

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Behavioural activation therapy for post-stroke depression: the BEADS feasibility RCT by Thomas, Shirley A, Drummond, Avril Er, Lincoln, Nadina B, Palmer, Rebecca L, das Nair, Roshan, Latimer, Nicholas R, Hackney, Gemma L, Mandefield, Laura, Walters, Stephen J, Hatton, Rachael D, Cooper, Cindy L, Chater, Timothy F, England, Timothy J, Callaghan, Patrick, Coates, Elizabeth, Sutherland, Katie E, Eshtan, Sarah Jacob, Topcu, Gogem

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A Home-Based Care Research Agenda by and for Homebound Older Adults and Caregivers by Leff, Bruce, Sheehan, Orla C., Harrison, Krista L., Eaton England, Ashley, Mickler, Alex, Basyal, Pragyashree Sharma, Garrigues, Sarah K., Schuchman, Mattan, Perissinotto, Carla, Garrett, Sarah B., Ritchie, Christine S.

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Management, Outcomes, and Predictors of Mortality of Cryptococcus Infection in Patients Without Human Immunodeficiency Virus: A Multicenter Study in 46 Hospitals in Australia and N... by Coussement, Julien, Heath, Christopher H, Roberts, Matthew B, Lane, Rebekah J, Spelman, Tim, Smibert, Olivia C, Longhitano, Anthony, Morrissey, C Orla, Nield, Blake, Tripathy, Monica, Davis, Joshua S, Kennedy, Karina J, Lynar, Sarah A, Crawford, Lucy C, Crawford, Simeon J, Smith, Benjamin J, Gador-Whyte, Andrew P, Haywood, Rose, Mahony, Andrew A, Howard, Julia C, Walls, Genevieve B, O’Kane, Gabrielle M, Broom, Matthew T, Keighley, Caitlin L, Bupha-Intr, Olivia, Cooley, Louise, O’Hern, Jennifer A, Jackson, Justin D, Morris, Arthur J, Bartolo, Caroline, Tramontana, Adrian R, Grimwade, Katherine C, Au Yeung, Victor, Chean, Roy, Woolnough, Emily, Teh, Benjamin W, Slavin, Monica A, Chen, Sharon C A, Alcorn, Kylie, Beardsley, Justin, Bloch, Aaron, Crowe, Amy, Doyle, Wendy, England, Michelle, Griffin, David, Hamilton, Kate, Korman, Tony M, Madigan, Victoria, McGann, Hugh, Pratt, William, Sparham, Sarah, Van Hal, Sebastiaan, Waters, Prue, Williams, Eloise

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FSH receptor (FSHR) expression in human extragonadal reproductive tissues and the developing placenta, and the impact of its deletion on pregnancy in mice by Stilley, Julie A W, Christensen, Debora E, Dahlem, Kristin B, Guan, Rongbin, Santillan, Donna A, England, Sarah K, Al-Hendy, Ayman, Kirby, Patricia A, Segaloff, Deborah L

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