Interrogation of STAT3 activation in patients with polyarticular juvenile arthritis von Wood, Stephanie Leigh, Branch, Justin, Vasquez, Pricilla, DeGuzman, Marietta M., Brown, Amanda, Sagcal Gironella, A. Carmela, Singla, Saimun, Ramirez, Andrea, Vogel, Tiphanie P.

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Immunogenicity of standard and extended dosing intervals of BNT162b2 mRNA vaccine von Payne, Rebecca P., Austin, James A., Skelly, Donal T., Meardon, Naomi, Faustini, Sian, Al-Taei, Saly, Moore, Shona C., Hering, Luisa M., Angyal, Adrienn, Brown, Rebecca, Nicols, Alexander R., Gillson, Natalie, Dobson, Susan L., Amini, Ali, Supasa, Piyada, Cross, Andrew, Bridges-Webb, Alice, Linder, Aline, Altmann, Thomas, Whitham, Rachel, Phillips, Eloise, Hargreaves, Alexander, Shields, Adrian, Foulkes, Sarah, Johnson, Sile, Wootton, Daniel G., Conlon, Christopher P., Matthews, Philippa C., Frater, John, Deeks, Alexandra S., Pollard, Andrew J., Brown, Anthony, Rowland-Jones, Sarah L., Mongkolsapaya, Juthathip, Hopkins, Susan, Dold, Christina, Richter, Alex, Carroll, Miles, Screaton, Gavin, de Silva, Thushan I., Turtle, Lance, Klenerman, Paul, Dunachie, Susanna, Abuelgasim, Hibatullah, Adland, Emily, Adlou, Syed, Akther, Hossain Delowar, Ansari, M. Azim, Arancibia-Cárcamo, Carolina V., Bayley, Martin, Brown, Helen, Chand, Meera, Chawla, Anu, Chinnakannan, Senthil, Cutteridge, Joseph, de Lara, Catherine, Denly, Lucy, Diffey, Ben, Dimitriadis, Stavros, Drake, Thomas M., Donnison, Timothy, Dupont, Maeva, Gardiner, Siobhan, Gilbert-Jarmillo, Javier, Goulder, Philip, Hackstein, Carl-Philipp, Hambleton, Sophie, Haniffa, Muzlifah, Haworth, Jenny, Holmes, Jennifer, Jämsén, Anni, Johnson, Sile, Jones, Chris, Kelly, Sinead, Kirk, Rosemary, Knight, Michael L., Lawrie, Allan, Lee, Lian, Lett, Lauren, Lim, Nicholas, Mentzer, Alexander J., O’Donnell, Denise, Payne, Brendan A.I., Provine, Nicholas, Robinson, Nichola, Romaniuk, Leigh, Simmons, Beatrice, Spegarova, Jarmila S., Stephenson, Emily, Subramaniam, Kris, Travis, Simon, Tucker, Stephanie, Watson, Adam, Watson, Lisa, Weeks, Esme, Wilson, Robert, Wood, Steven, Wright, Rachel, Xiao, Huiyuan, Zawia, Amira A.T.

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Adolescent Chlamydia Screening in Pediatric Primary Care: A Quality Improvement Project von Foppert, Leigh, Bowles, Wendy, Belardo, Haley, Zeno, Rosie, Hosley, Stephanie, Wood, Sarah

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T-cell and antibody responses to first BNT162b2 vaccine dose in previously infected and SARS-CoV-2-naive UK health-care workers: a multicentre prospective cohort study von Angyal, Adrienn, Moore, Shona C, Payne, Rebecca P, Tipton, Tom, Rongkard, Patpong, Ali, Mohammad, Hering, Luisa M, Austin, James, Brown, Rebecca, Gillson, Natalie, Kilby, Jonathan A, Spegarova, Jarmila S, Hornsby, Hailey, Whitham, Rachel, Conlon, Christopher P, Jeffery, Katie, Dold, Christina, Ogbe, Ane, Brown, Helen, Hopkins, Susan, Rowland-Jones, Sarah L, Klenerman, Paul, Richter, Alex, Duncan, Christopher J A, Carroll, Miles, de Silva, Thushan I, Watson, Adam, Shields, Adrian, Richter, Alex, Nicols, Alexander, Webb-Bridges, Alice, Ogbe, Ane, Jämsén, Anni, Brown, Anthony, Dold, Christina, Duncan, Christopher, Conlon, Christopher, Skelly, Donal, Weeks, Esme, Sandhar, Gurjinder, Abuelgasim, Hibatullah, Xiao, Huiyuan, Spegarova, Jarmila, Tyerman, Jessica, Kilby, Jonathan, Turtle, Lance, Denly, Lucy, Hering, Luisa, Ansari, M. Azim, Pace, Matthew, Ali, Mohammad, Rongkard, Patpong, Klenerman, Paul, Goulder, Philip, Whitham, Rachel, Brown, Rebecca, Payne, Rebecca, Wilson, Robert, Gardiner, Siobhan, Longet, Stephanie, Dobson, Sue, Dunachie, Susanna, Adlou, Syed, de Silva, Thushan, Hall, Victoria, Lawrie, Allan, Smith, Nikki, Zawia, Amira, Fairman, Alex, Kirk, Rosemary, Marsh, Louise, Wood, Steven, Diffey, Benjamin, Jones, Chris, Lett, Lauren, Platt, Gareth, Subramaniam, Krishanthi, Wootton, Daniel, Payne, Brendan, Kelly, Sinead, Marston, Judith, Haniffa, Muzlifah, de Lara, Catherine, Donnison, Timothy, Hackstein, Carl-Philipp, Lee, Lian, Lim, Nicholas, Malone, Tom, Ramamurthy, Narayan, Sampson, Oliver, Eyre, David, Simmons, Beatrice, Stafford, Lizzie, Foulkes, Sarah, Wellington, Edgar, Gilbert-Jaramillo, Javier, Knight, Michael, Horner, Emily, Thaventhiran, James, Chalk, Jeremy

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Direct and reciprocal effects among social skills, vocabulary, and reading comprehension in first grade von Sparapani, Nicole, Connor, Carol McDonald, McLean, Leigh, Wood, Taffeta, Toste, Jessica, Day, Stephanie

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Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy von Parry, David A., Martin, Carol-Anne, Greene, Philip, Marsh, Joseph A., Blyth, Moira, Cox, Helen, Donnelly, Deirdre, Greenhalgh, Lynn, Greville-Heygate, Stephanie, Harrison, Victoria, Lachlan, Katherine, McKenna, Caoimhe, Quigley, Alan J., Rea, Gillian, Robertson, Lisa, Suri, Mohnish, Jackson, Andrew P.

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Stretch-activated ion channel TMEM63B associates with developmental and epileptic encephalopathies and progressive neurodegeneration von Vetro, Annalisa, Pelorosso, Cristiana, Balestrini, Simona, Masi, Alessio, Hambleton, Sophie, Argilli, Emanuela, Giubbolini, Simone, Barrick, Rebekah, Bergant, Gaber, Writzl, Karin, Bijlsma, Emilia K., Cacheiro, Pilar, Mei, Davide, Devlin, Anita, Machol, Keren, Mannaioni, Guido, Sakamoto, Masamune, Menezes, Manoj P., Courtin, Thomas, Sherr, Elliott, Parra, Riccardo, Richardson, Ruth, Roscioli, Tony, Scala, Marcello, von Stülpnagel, Celina, Smedley, Damian, Pochiero, Francesca, Ramesh, Venkateswaran, Capra, Valeria, Mancardi, Margherita, Keren, Boris, Mignot, Cyiril, Lulli, Matteo, Parks, Kendall, Griffin, Helen, Nigro, Vincenzo, Hirata, Yuko, Koichihara, Reiko, Peterlin, Borut, Maki, Ryuto, Nitta, Yohei, Ambrose, John C., Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boustred, Christopher R., Brittain, Helen, Brown, Matthew A., Caulfield, Mark J., Chan, Georgia C., Giess, Adam, Griffin, John N., Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Lakey, Anna, Lopez, Javier F., Maleady-Crowe, Fiona, Minneci, Federico, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Rahim, Tahrima, Rendon, Augusto, Sawant, Kushmita, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Zarowiecki, Magdalena, Torella, Annalaura, Tohyama, Jun, Hamada, Keisuke, Ogata, Kazuhiro, Sugie, Atsushi, van der Smagt, Jasper J., van Gassen, Koen, Valence, Stephanie, Vittery, Emma, Malone, Stephen, Kato, Mitsuhiro, Ratto, Gian Michele, Guerrini, Renzo

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Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies von Iqbal, Maria, Maroofian, Reza, Çavdarlı, Büşranur, Riccardi, Florence, Field, Michael, Banka, Siddharth, Bubshait, Dalal K., Li, Yun, Hertecant, Jozef, Baig, Shahid Mahmood, Dyment, David, Efthymiou, Stephanie, Abdullah, Uzma, Makhdoom, Ehtisham Ul Haq, Ali, Zafar, Scherf de Almeida, Tobias, Molinari, Florence, Mignon-Ravix, Cécile, Chabrol, Brigitte, Antony, Jayne, Ades, Lesley, Pagnamenta, Alistair T., Jackson, Adam, Douzgou, Sofia, Beetz, Christian, Karageorgou, Vasiliki, Vona, Barbara, Rad, Aboulfazl, Baig, Jamshaid Mahmood, Sultan, Tipu, Alvi, Javeria Raza, Maqbool, Shazia, Rahman, Fatima, Toosi, Mehran Beiraghi, Ashrafzadeh, Farah, Imannezhad, Shima, Karimiani, Ehsan Ghayoor, Sarwar, Yasra, Khan, Sheraz, Jameel, Muhammad, Noegel, Angelika A., Budde, Birgit, Altmüller, Janine, Motameny, Susanne, Höhne, Wolfgang, Houlden, Henry, Nürnberg, Peter, Wollnik, Bernd, Villard, Laurent, Alkuraya, Fowzan Sami, Osmond, Matthew, Hussain, Muhammad Sajid, Yigit, Gökhan

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Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene von Yahya, Samar, Smith, Claire E.L., Poulter, James A., McKibbin, Martin, Arno, Gavin, Ellingford, Jamie, Kämpjärvi, Kati, Khan, Muhammad I., Cremers, Frans P.M., Hardcastle, Alison J., Castle, Bruce, Steel, David H.W., Webster, Andrew R., Black, Graeme C., El-Asrag, Mohammed E., Ali, Manir, Toomes, Carmel, Inglehearn, Chris F., Ingram, Stuart, Taylor, Rachel, Manson, Forbes, Sergouniotis, Panagiotis, Pontikos, Nikolas, Cheetham, Michael, Fiorentino, Alessia, Downes, Susan, Yu, Jing, Halford, Stephanie, Broadgate, Suzanne, van Heyningen, Veronica, 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, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, 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.

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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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Earliest functional declines in Huntington disease von Beglinger, Leigh J, O'Rourke, Justin J.F, Wang, Chiachi, Langbehn, Douglas R, Duff, Kevin, Paulsen, Jane S

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Profiles of Foundational Learning Components among First Graders von Sparapani, Nicole, Connor, Carol McDonald, Day, Stephanie, Wood, Taffeta, Ingebrand, Sarah, McLean, Leigh, Phillips, Beth

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Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia von Morsy, Heba, Benkirane, Mehdi, Cali, Elisa, Zhelcheska, Kristina, Cipriani, Valentina, Galanaki, Evangelia, Maroofian, Reza, Efthymiou, Stephanie, Murphy, David, Banka, Siddharth, Clayton-Smith, Jill, Redman, Melody, Bassetti, Jennifer A., Nizon, Mathilde, Jamra, Rami Abu, Heruth, Marion, Krey, Ilona, Gburek-Augustat, Janina, Wieczorek, Dagmar, Mcentagart, Meriel, Goldenberg, Alice, Guyant-Marechal, Lucie, Garcia-Moreno, Hector, Giunti, Paola, Chabrol, Brigitte, Bacrot, Severine, Buissonnière, Roger, Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Melegh, Béla, Szabó, András, Sümegi, Katalin, Cossée, Mireille, Ziff, Monica, Butterfield, Russell, Hunt, David, Hanna, Michael, Koenig, Michel, Vandrovcova, Jana, Houlden, Henry, Arumugam, P., Baple, E.L., Bleda, M., Boardman-Pretty, F., Boissiere, J.M., Boustred, C.R., Brittain, H., Caulfield, M.J., Chan, G.C., Daugherty, L.C., Devereau, A., Foulger, R.E., Fowler, T., Furió-Tarí, P., Halai, D., Hamblin, A., Henderson, S., Holman, J.E., Hubbard, T.J.P., Ibáñez, K., Jackson, R., Jones, L.J., Kasperaviciute, D., Lahnstein, L., Leigh, S.E.A., Leong, I.U.S., Lopez, F.J., Maleady-Crowe, F., Mason, J., McDonagh, E.M., Moutsianas, L., Mueller, M., Murugaesu, N., Odhams, C.A., Patch, C., Perez-Gil, D., Pullinger, J., Rahim, T., Riesgo-Ferreiro, P., Rogers, T., Ryten, M., Savage, K., Scott, R.H., Siddiq, A., Sieghart, A., Smedley, D., Smith, K.R., Sosinsky, A., Stevens, H.E., Stuckey, A., Sultana, R., Thompson, S.R., Tucci, A., Walsh, E., Watters, S.A., Welland, M.J., Williams, E., Witkowska, K., Wood, S.M., Zarowiecki, M.

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Profiles of foundational learning skills among first graders von Sparapani, Nicole, Connor, Carol McDonald, Day, Stephanie, Wood, Taffeta, Ingebrand, Sarah, McLean, Leigh, Phillips, Beth

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Community change and resident needs: Designing a Participatory Action Research study in Metropolitan Boston von Arcaya, Mariana C., Schnake-Mahl, Alina, Binet, Andrew, Simpson, Shannon, Church, Maggie Super, Gavin, Vedette, Coleman, Bill, Levine, Shoshanna, Nielsen, Annika, Carroll, Leigh, Ursprung, Sanouri, Wood, Ben, Reeves, Halley, Keppard, Barry, Sportiche, Noemie, Partirdge, Jessie, Figueora, Jose, Frakt, Austin, Alfonzo, Mariel, Abreu, Dina, Abreu, Tatiana, Ambroise, Trena, Andrade, Eric, Barrientos, Eduardo, Baty, Arnetta, Baty, Carl, Benner, Katrina, Bennett, Clifton, Blanchette, Amy, Bongiovanni, Roseann, Cardile, Olivia, Corchado, Cristian, Dixon, Caleb, Dodson, Crystal, Dominguez, Juan, Durena, Mytha, Fiestas, Yrma, Genty, Josee, Graffam, Nicole, Gonzalez, Adela, Grigsby, Emma, Hayden, Patricia, Alvado, Stephanie Hernandez, Hernandez, Zuleyka, Hodes, Isaac, Johnson, Jarred, Keefe, Kathryn, Latimer, Krystle, Logg, Christina, Martinez, Nelson, Mboup, Khadijah, McPhorson, Doug, Meacham, Steve, Mohammed, Daynaba, Moss, Emily, O'Brien, Kathleen, Owens, Lisa, Partridge, Jessie, Johnson, Lillie Pearl, Power, Maria Belen, Rebelo, Taylee, Remy, Ronel, Roderigues, Gail, Sabtow, Qamar, Sanchez, Clarisa, Seeder, Andrew, Sepulveda, Ramon, West, Emma, Winters, Leah, Youmans, Tremayne

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Neuronal intranuclear inclusion disease is genetically heterogeneous von Chen, Zhongbo, Yan Yau, Wai, Jaunmuktane, Zane, Tucci, Arianna, Sivakumar, Prasanth, Gagliano Taliun, Sarah A., Turner, Chris, Efthymiou, Stephanie, Ibáñez, Kristina, Sullivan, Roisin, Bibi, Farah, Athanasiou‐Fragkouli, Alkyoni, Bourinaris, Thomas, Zhang, David, Revesz, Tamas, Lashley, Tammaryn, DeTure, Michael, Dickson, Dennis W., Josephs, Keith A., Gelpi, Ellen, Kovacs, Gabor G., Halliday, Glenda, Rowe, Dominic B., Blair, Ian, Tienari, Pentti J., Suomalainen, Anu, Fox, Nick C., Wood, Nicholas W., Lees, Andrew J., Haltia, Matti J., Hardy, John, Ryten, Mina, Vandrovcova, Jana, Houlden, Henry

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Cardiac Investigations in Sudden Unexpected Death in DEPDC5-Related Epilepsy von Bacq, Alexandre, Roussel, Delphine, Bonduelle, Thomas, Zagaglia, Sara, Maletic, Marina, Ribierre, Théo, Adle-Biassette, Homa, Marchal, Cécile, Jennesson, Mélanie, An, Isabelle, Picard, Fabienne, Navarro, Vincent, Sisodiya, Sanjay M, Baulac, Stéphanie

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Nautilus Field Season Overview von Raineault, Nicole A., Gee, Lindsay, Heffron, Erin, Kane, Renato, Peters, Colleen, Gandulla, Stephanie, Waters, Sarah, Schmidt, Val, Marcus, Clint, Ballard, Robert D., Mayer, Larry, Broad, Kenneth, Richmond, Kristof, Shapiro, Beth, Lim, Darlene S.S., Breier, John A., Chan, Eric, Chernov, Josh, Cohen, Tamar, Deans, Matthew, Garcia, Angela, German, Christopher R., Hauer, Michelle, Hu, Sarah, Huber, Julie A., Nawotniak, Shannon Kobs, Lees, David, Lowe, Justin, Lubetkin, Megan, Marsh, Leigh, Milesi, Vincent, Miller, Matthew J., Mirmalek, Zara, Saunders, Miles, Sharif, Khaled, Shields, Ashley, Shock, Everett, Smith, Amy, Sylva, Sean, Auscavitch, Steven, Pockalny, Robert, Konrad, Kevin, Humphreys, Jennifer, Clark, Timothy B., Fundis, Allison, Matthews, Russ, Brennan, Michael L., Schorer, Lonnie, Lickliter-Mundon, Megan, Marx, Deborah, Wishnak, Samantha, Delgado, James P., Trippe, Edward, Hill, John H., Miller, Doug, Jacques, Christopher, Sudek, Mareike, Spathias, Hanae, Coward, Georgia, Que, Nerelle, Roman, Christopher, Petruncio, Emil, Weinnig, Alexis, Coleman, Dwight F., Georgian, Samuel, Richards, Holly, Roletto, Jan, Lipski, Danielle, Graiff, Kaitlin, Williams, Gary, Cochrane, Guy, Stock, Jennifer, Tezak, Sage, King, Chad, Brown, Jennifer, Burton, Erica, Kahn, Amanda, Hartwell, Anne, Wood, Amity, Hardin, Dane

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