Search Results - DONALDSON, John Y.

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    Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer by Rebbeck, Timothy R, Mitra, Nandita, Wan, Fei, Sinilnikova, Olga M, Healey, Sue, McGuffog, Lesley, Mazoyer, Sylvie, Chenevix-Trench, Georgia, Nathanson, Katherine L, Kushnir, Anya, Zidan, Jamal, Ehrencrona, Hans, Stenmark-Askmalm, Marie, Melin, Beatrice, Huo, Dezheng, Olopade, Olufunmilayo I, Odunsi, Kunle, Domchek, Susan M, Karlan, Beth Y, Walsh, Christine, Chung, Wendy K, Janavicius, Ramunas, Steele, Linda, Ejlertsen, Bent, Hansen, Thomas v. O, Benitez, Javier, Godino, Javier, Duran, Mercedes, Weitzel, Jeffrey N, Bobolis, Kristie A, Peissel, Bernard, Genuardi, Maurizio, Manoukian, Siranoush, Pensotti, Valeria, Gismondi, Viviana, Fostira, Florentia, Frost, Debra, Platte, Radka, Davidson, Rosemarie, Eccles, Diana, Hodgson, Shirley, Porteous, Mary E, Izatt, Louise, Donaldson, Alan, Ellis, Steve, Schmutzler, Rita Katharina, Becker, Alexandra, Engel, Christoph, Mundhenke, Christoph, Niederacher, Dieter, Fleisch, Markus, Sutter, Christian, Gadzicki, Dorothea, Varon-Mateeva, Raymonda, Gehrig, Andrea, Weber, Bernhard H, Mazoyer, Sylvie, Gauthier-Villars, Marion, Peyrat, Jean-Philippe, Muller, Danièle, De Paepe, Anne, De Leeneer, Kim, Piedmonte, Marion, Rodriguez, Gustavo, Blank, Stephanie V, Azodi, Masoud, Phillips, Kelly-Anne, de la Hoya, Miguel, Romero, Atocha, Aittomäki, Kristiina, Oosterwijk, Jan C, Wijnen, Juul T, Ausems, Margreet G. E. M, Aalfs, Cora M, Kwong, Ava, Darder, Esther, Blanco, Ignacio, Durda, Katarzyna, Sukiennicki, Grzegorz, Byrski, Tomasz, Toloczko-Grabarek, Aleksandra, Arason, Adalgeir, Laframboise, Rachel, Agata, Simona, Lee, Min Hyuk, Park, Sue K, Lindor, Noralane M, Tischkowitz, Marc, Vijai, Joseph, Offit, Kenneth, Rau-Murthy, Rohini, Fink-Retter, Anneliese, Singer, Christian F, Pfeiler, Georg, Senter, Leigha, Pedersen, Inge Sokilde, Sunde, Lone, Thomassen, Mads, Teo, Soo-Hwang, Hulick, Peter J

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    Overview of the DESI Legacy Imaging Surveys by Dey, Arjun, Schlegel, David J., Lang, Dustin, Blum, Robert, Burleigh, Kaylan, Findlay, Joseph R., Juneau, Stéphanie, Levi, Michael, McGreer, Ian, Meisner, Aaron, Myers, Adam D., Moustakas, John, Patej, Anna, Schlafly, Edward F., Valdes, Francisco, Weaver, Benjamin A., Yèche, Christophe, Zou, Hu, Zhou, Xu, Abareshi, Behzad, Abbott, T. M. C., Abolfathi, Bela, Alvarez, A., Annis, James, Ansarinejad, Behzad, Aubert, Marie, Beechert, Jacqueline, BenZvi, Segev Y., Beutler, Florian, Bielby, Richard M., Bolton, Adam S., Buckley-Geer, Elizabeth J., Butler, Karen, Calamida, Annalisa, Carlberg, Raymond G., Carter, Paul, Casas, Ricard, Castander, Francisco J., Comparat, Johan, Dickinson, Mark, Ding, Zhejie, Duckworth, Christopher J., Eftekharzadeh, Sarah, Etourneau, Thomas, Fitzpatrick, Mike, Font-Ribera, Andreu, Fulmer, Leah, Gänsicke, Boris T., Gaztanaga, Enrique, George, Koshy, A Gontcho, Satya Gontcho, Green, Gregory, Guy, Julien, James, David J., Jannuzi, Buell T., Karkar, Sonia, Kueter-Young, Andrea, Lan, Ting-Wen, Lauer, Tod R., Lee, Jae Hyeon, Levasseur, Laurence Perreault, Li, Ting S., Mann, Justin L., Martínez-Vázquez, C. E., Martini, Paul, du Mas des Bourboux, Hélion, McManus, Sean, Meier, Tobias Gabriel, Narayan, Gautham, Newman, Jeffrey A., Nie, Jundan, Nord, Brian, Norman, Dara J., Palanque-Delabrouille, Nathalie, Poppett, Claire L., Poremba, Megan R., Prakash, Abhishek, Rabinowitz, David, Raichoor, Anand, Ross, Nicholas P., Rudnick, Gregory, Safonova, Sasha, Sánchez, F. Javier, Shan, Huanyuan, Slepian, Zachary, Soto, Christian, Staten, Ryan, Stupak, Robert J., Summers, David L., Tie, Suk Sien, Tirado, H., Vargas-Magaña, Mariana, Wechsler, Risa H., Yang, Jinyi, Yang, Qian, Zaritsky, Dennis, Zhang, Kai, Zhang, Tianmeng, Zhou, Rongpu, Zhou, Zhimin

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    SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile by Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, 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, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

    Published in Genetics in medicine
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    Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy by Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Basinger, Alice A., Ceulemans, Sophia, Charles, Perrine, McRae, Jeremy F., Rajan, Diana, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Ahmed, Munaza, Anjum, Uruj, Armstrong, Ruth, Barnicoat, Angela, Bennett, Chris, Blair, Edward, Blyth, Moira, Bourdon, Louise, Brady, Angela, Burn, John, Canham, Natalie, Cilliers, Deirdre, Clayton-Smith, Jill, Coates, Andrea, Cooper, Nicola, Dabir, Tabib, Davies, Sally, Dean, John, Devlin, Gemma, Donnai, Dian, Donnelly, Carina, Evans, Karenza, Fendick, Tina, Goodship, Judith, Green, Andrew, Harrison, Lucy, Holden, Simon, Jarvis, Joanna, Johnson, Diana, Jones, Elizabeth, Kumar, V. K. Ajith, Lachlan, Katherine, Langman, Caroline, Maye, Una, McMullan, Dominic J., McWilliam, Catherine, Metcalfe, Kay, Norman, Andrew, Ogilvie, Caroline, Park, Soo-Mi, Phipps, Julie, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Ross, Alison, Sampson, Julian, Shannon, Nora, Skitt, Zara, Stewart, Fiona, Stewart, Helen, Swaminathan, Ganesh Jawahar, Taylor, Cat, Tein, Mark, Treacy, Becky, Vandersteen, Anthony, Wallwark, Sarah, Waters, Jonathon, Weber, Astrid, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Parker, Michael, FitzPatrick, David R., Demurger, Florence, Eiset, Saga Elise, Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Jonasson, Amy R., Kok, Fernando, Marcelis, Carlo L.M., McWalter, Kirsty, Mercimek-Andrews, Saadet, Person, Richard, Ramelli, Gian Paolo, Rauch, Anita, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Trauner, Doris A., Vogel, Ida, Widjaja, Elysa, Zak, Jaroslav, Banka, Siddharth, Rodan, Lance H.

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