Detection of Restriction Fragment Length Polymorphisms at the Centromeres of Human Chromosomes by Using Chromosome-Specific α Satellite DNA Probes: Implications for Development of... von 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 von 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 von Waye, John S., England, Sarah B., Willard, Huntington F.

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Localization of 24 cosmid clones on the human Y chromosome von Nagafuchi, Shigeo, Nakahori, Yutaka, Nakamura, Yusuke, England, Sarah B., Tamura, Takashi, Numabe, Hironao, Nakagome, Yasuo

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Molecular analysis of muscular dystrophy von Davies, K E, Kenwrick, S J, Patterson, M N, Smith, T J, Forrest, S M, Dorkins, H R, Cross, G S, England, S B

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Clinical features and management of human monkeypox: a retrospective observational study in the UK von 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 von 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 von 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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Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease von Claus, Laura R., Chen, Chuan, Stallworth, Jennifer, Turner, Joshua L., Slaats, Gisela G., Mabillard, Holly, Senum, Sarah R., Srikanth, Sujata, Flanagan-Steet, Heather, Louie, Raymond J., Silver, Josh, Lerner-Ellis, Jordan, Morel, Chantal, Mighton, Chloe, Sleutels, Frank, van Slegtenhorst, Marjon, van Ham, Tjakko, Brooks, Alice S., Dorresteijn, Eiske M., Barakat, Tahsin Stefan, Dahan, Karin, Demoulin, Nathalie, Goffin, Eric Jean, Olinger, Eric, 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, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Pereira, Mariana Buongermino, 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., Larsen, Martin, Hertz, Jens Michael, Lilien, Marc R., Obeidová, Lena, Stone, Hillarey K., Kerecuk, Larissa, Gurgu, Mihai, Yousef Yengej, Fjodor A., Ammerlaan, Carola M.E., Rookmaaker, Maarten B., Hanna, Christian, Rogers, R. Curtis, Duran, Karen, Peters, Edith, Sayer, John A., van Haaften, Gijs, Harris, Peter C., Ling, Kun, Mason, Jennifer M., van Eerde, Albertien M., Steet, Richard

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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders von 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 von 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 von 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 von 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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Unanticipated Therapeutic Value of the Patient-Centered Outcomes Research Institute (PCORI) Stakeholder Engagement Project for Homebound Older Adults von Sheehan, Orla C., Ritchie, Christine S., Garrett, Sarah B., Harrison, Krista L., Mickler, Alexandria, Eaton England, Ashley L., Sharma Basyal, Pragyashree, Garrigues, Sarah K., Leff, Bruce

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Biomarkers of cardiometabolic complications in survivors of childhood acute lymphoblastic leukemia von 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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Comparative transmissibility of SARS-CoV-2 variants Delta and Alpha in New England, USA von 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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Behavioural activation therapy for post-stroke depression: the BEADS feasibility RCT von 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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Efficacy of Dimethyl Fumarate in Young Adults with Relapsing-Remitting Multiple Sclerosis: Analysis of the DEFINE, CONFIRM, and ENDORSE Studies von 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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Individual-Level and Community-Level Predictors of Healthy Pregnancy Outcomes in Multigravid Black Women von Garr Barry, Valene, Martin, Samantha L, Schneider-Worthington, Camille, Zhao, Peinan, Woolfolk, Candice L, Foraker, Randi, Davis, Kia L, Kelly, Jeannie C, Raghuraman, Nandini, England, Sarah K, Carter, Ebony B

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A Home-Based Care Research Agenda by and for Homebound Older Adults and Caregivers von 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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