RUSA Review Underway.(Reference and User Services Association) von Bennett, Denise Beaubien, Benham, Frances, Bonanni, Domenico P, Carr, Ruth A, Etschmaier, Gale S, Huling, Nancy, Kieft, Robert H, Kinyon, William R, Lyon, Elaine R, Neuman, Susan G, Davis, Larayne, Gutierrez, Michael

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ACMG clinical laboratory standards for next-generation sequencing von Rehm, Heidi L., Bale, Sherri J., Bayrak-Toydemir, Pinar, Berg, Jonathan S., Brown, Kerry K., Deignan, Joshua L., Friez, Michael J., Funke, Birgit H., Hegde, Madhuri R., Lyon, Elaine

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ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 von Richards, C. Sue, Bale, Sherri, Bellissimo, Daniel B., Das, Soma, Grody, Wayne W., Hegde, Madhuri R., Lyon, Elaine, Ward, Brian E.

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Assuring the quality of next-generation sequencing in clinical laboratory practice von Gargis, Amy S, Kalman, Lisa, Berry, Meredith W, Bick, David P, Dimmock, David P, Hambuch, Tina, Lu, Fei, Lyon, Elaine, Voelkerding, Karl V, Zehnbauer, Barbara A, Agarwala, Richa, Bennett, Sarah F, Chen, Bin, Chin, Ephrem L H, Compton, John G, Das, Soma, Farkas, Daniel H, Ferber, Matthew J, Funke, Birgit H, Furtado, Manohar R, Ganova-Raeva, Lilia M, Geigenmüller, Ute, Gunselman, Sandra J, Hegde, Madhuri R, Johnson, Philip L F, Kasarskis, Andrew, Kulkarni, Shashikant, Lenk, Thomas, Liu, C S Jonathan, Manion, Megan, Manolio, Teri A, Mardis, Elaine R, Merker, Jason D, Rajeevan, Mangalathu S, Reese, Martin G, Rehm, Heidi L, Simen, Birgitte B, Yeakley, Joanne M, Zook, Justin M, Lubin, Ira M

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Genotyping of Single-Nucleotide Polymorphisms by High-Resolution Melting of Small Amplicons von Liew, Michael, Pryor, Robert, Palais, Robert, Meadows, Cindy, Erali, Maria, Lyon, Elaine, Wittwer, Carl

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Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial von Thiele, Elizabeth A, Marsh, Eric D, French, Jacqueline A, Mazurkiewicz-Beldzinska, Maria, Benbadis, Selim R, Joshi, Charuta, Lyons, Paul D, Taylor, Adam, Roberts, Claire, Sommerville, Kenneth, Gunning, Boudewjin, Gawlowicz, Jacek, Lisewski, Pawel, Mazurkiewicz Beldzinska, Maria, Mitosek Szewczyk, Krystyna, Steinborn, Barbara, Zolnowska, Marta, Hughes, Elaine, McLellan, Ailsa, Benbadis, Selim, Ciliberto, Michael, Clark, Gary, Dlugos, Dennis, Filloux, Francis, Flamini, Robert, French, Jacqueline, Frost, Michael, Haut, Sheryl, Joshi, Charuta, Kapoor, Siddarth, Kessler, Sudha, Laux, Linda, Lyons, Paul, Marsh, Eric, Moore, David, Morse, Richard, Nagaraddi, Venkatesh, Rosenfeld, William, Seltzer, Laurie, Shellhaas, Renée, Sullivan, Joseph, Thiele, Elizabeth, Thio, Liu Lin, Wang, David, Wilfong, Angus

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Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15 von Cheng, Hanyin, Gottlieb, Leah, Marchi, Elaine, Kleyner, Robert, Bhardwaj, Puja, Rope, Alan F, Rosenheck, Sarah, Moutton, Sébastien, Philippe, Christophe, Eyaid, Wafaa, Alkuraya, Fowzan S, Toribio, Janet, Mena, Rafael, Prada, Carlos E, Stessman, Holly, Bernier, Raphael, Wermuth, Marieke, Kauffmann, Birgit, Blaumeiser, Bettina, Kooy, R Frank, Baralle, Diana, Mancini, Grazia M S, Conway, Simon J, Xia, Fan, Chen, Zhao, Meng, Linyan, Mihajlovic, Ljubisa, Marmorstein, Ronen, Lyon, Gholson J

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DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders von Lessel, Ivana, Baresic, Anja, Chinn, Ivan K, May, Jonathan, Goenka, Anu, Chandler, Kate E, Posey, Jennifer E, Afenjar, Alexandra, Averdunk, Luisa, Bedeschi, Maria Francesca, Besnard, Thomas, Brager, Rae, Brick, Lauren, Brugger, Melanie, Brunet, Theresa, Byrne, Susan, Calle-Martín, Oscar de la, Capra, Valeria, Cardenas, Paul, Chappé, Céline, Chong, Hey J, Cogne, Benjamin, Conboy, Erin, Cope, Heidi, Courtin, Thomas, Deb, Wallid, Dilena, Robertino, Dubourg, Christèle, Elgizouli, Magdeldin, Fernandes, Erica, Fitzgerald, Kristi K, Gangi, Silvana, George-Abraham, Jaya K, Gucsavas-Calikoglu, Muge, Haack, Tobias B, Hadonou, Medard, Hanker, Britta, Hüning, Irina, Iascone, Maria, Isidor, Bertrand, Järvelä, Irma, Jin, Jay J, Jorge, Alexander A L, Josifova, Dragana, Kalinauskiene, Ruta, Kamsteeg, Erik-Jan, Keren, Boris, Kessler, Elena, Kölbel, Heike, Kozenko, Mariya, Kubisch, Christian, Kuechler, Alma, Leal, Suzanne M, Leppälä, Juha, Luu, Sharon M, Lyon, Gholson J, Madan-Khetarpal, Suneeta, Mancardi, Margherita, Marchi, Elaine, Mehta, Lakshmi, Menendez, Beatriz, Morel, Chantal F, Harasink, Sue Moyer, Nevay, Dayna-Lynn, Nigro, Vincenzo, Odent, Sylvie, Oegema, Renske, Pappas, John, Pastore, Matthew T, Perilla-Young, Yezmin, Platzer, Konrad, Powell-Hamilton, Nina, Rabin, Rachel, Rekab, Aisha, Rezende, Raissa C, Robert, Leema, Romano, Ferruccio, Scala, Marcello, Poths, Karin, Schrauwen, Isabelle, Sebastian, Jessica, Short, John, Sidlow, Richard, Sullivan, Jennifer, Szakszon, Katalin, Tan, Queenie K G, Wagner, Matias, Wieczorek, Dagmar, Yuan, Bo, Maeding, Nicole, Strunk, Dirk, Begtrup, Amber, Banka, Siddharth, Lupski, James R, Tolosa, Eva, Lessel, Davor

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Development and Evaluation of a Calibrator Material for Nucleic Acid-Based Assays for Diagnosing Aspergillosis von Lyon, G Marshall, Abdul-Ali, Deborah, Loeffler, Juergen, White, P Lewis, Wickes, Brian, Herrera, Monica L, Alexander, Barbara D, Baden, Lindsey R, Clancy, Cornelius, Denning, David, Nguyen, M Hong, Sugrue, Michele, Wheat, L Joseph, Wingard, John R, Donnelly, J Peter, Barnes, Rosemary, Patterson, Thomas F, Caliendo, Angela M

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Computationally restoring the potency of a clinical antibody against Omicron von Desautels, Thomas A., Arrildt, Kathryn T., Zemla, Adam T., Lau, Edmond Y., Zhu, Fangqiang, Ricci, Dante, Cronin, Stephanie, Zost, Seth J., Binshtein, Elad, Scheaffer, Suzanne M., Dadonaite, Bernadeta, Petersen, Brenden K., Engdahl, Taylor B., Chen, Elaine, Handal, Laura S., Hall, Lynn, Goforth, John W., Vashchenko, Denis, Nguyen, Sam, Weilhammer, Dina R., Lo, Jacky Kai-Yin, Rubinfeld, Bonnee, Saada, Edwin A., Weisenberger, Tracy, Lee, Tek-Hyung, Whitener, Bradley, Case, James B., Ladd, Alexander, Silva, Mary S., Haluska, Rebecca M., Grzesiak, Emilia A., Earnhart, Christopher G., Hopkins, Svetlana, Bates, Thomas W., Thackray, Larissa B., Segelke, Brent W., Lillo, Antonietta Maria, Sundaram, Shivshankar, Bloom, Jesse D., Diamond, Michael S., Crowe, James E., Carnahan, Robert H., Faissol, Daniel M.

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Phenotypic and biochemical analysis of an international cohort of individuals with variants in NAA10 and NAA15 von Cheng, Hanyin, Gottlieb, Leah, Marchi, Elaine, Kleyner, Robert, Bhardwaj, Puja, Rope, Alan F, Rosenheck, Sarah, Moutton, Sébastien, Philippe, Christophe, Eyaid, Wafaa, Alkuraya, Fowzan S, Toribio, Janet, Mena, Rafael, Prada, Carlos E, Stessman, Holly, Bernier, Raphael, Wermuth, Marieke, Kauffmann, Birgit, Blaumeiser, Bettina, Kooy, R Frank, Baralle, Diana, Mancini, Grazia M S, Conway, Simon J, Xia, Fan, Chen, Zhao, Meng, Linyan, Mihajlovic, Ljubisa, Marmorstein, Ronen, Lyon, Gholson J

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Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group von Schmidt, Ryan J., Steeves, Marcie, Bayrak-Toydemir, Pinar, Benson, Katherine A., Coe, Bradley P., Conlin, Laura K., Ganapathi, Mythily, Garcia, John, Gollob, Michael H., Jobanputra, Vaidehi, Luo, Minjie, Ma, Deqiong, Maston, Glenn, McGoldrick, Kelly, Palculict, T. Blake, Pesaran, Tina, Pollin, Toni I., Qian, Emily, Rehm, Heidi L., Riggs, Erin R., Schilit, Samantha L.P., Sergouniotis, Panagiotis I., Tvrdik, Tatiana, Watkins, Nicholas, Zec, Lauren, Zhang, Wenying, Lebo, Matthew S., Byrne, Alicia, Spurdle, Amanda, Palculict, Blake, Coe, Bradley, Deqiong, Ma, Lyon, Elaine, Groopman, Emily, Qian, Emily, Puffenberger, Erik, Riggs, Erin, Couch, Fergus, Maston, Glenn, Dziadzio, Hannah, Harraway, James, Mester, Jessica, Garcia, John, Lerner-Ellis, Jordan, Benson, Katherine, Avello, Kayleigh, McGoldrick, Kelly, Conlin, Laura, Zec, Lauren, Steeves, Marcie, Richardson, Marcy, Lebo, Matt, Kelly, Melissa, Gollob, Michael, Luo, Minjie, Ganapathi, Mythily, Watkins, Nicholas, Niu, Nifang, Sergouniotis, Panagiotis, Bayrak-Toydemir, Pinar, Schmidt, Ryan, Schilit, Samantha, Richards, Sarah, Pesaran, Tina, Pollin, Toni, Jobanputra, Vaidehi, Zhang, Wenying, Chen, Wuyan, Fan, Yuxin

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Distinguishing different DNA heterozygotes by high-resolution melting von GRAHAM, Robert, LIEW, Michael, MEADOWS, Cindy, LYON, Elaine, WITTWER, Carl T

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The Science and Art of Clinical Genetic Variant Classification and Its Impact on Test Accuracy von Giles, Hunter H, Hegde, Madhuri R, Lyon, Elaine, Stanley, Christine M, Kerr, Iain D, Garlapow, Megan E, Eggington, Julie M

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Multiple loci on 8q24 associated with prostate cancer susceptibility von Al Olama, Ali Amin, Kote-Jarai, Zsofia, Giles, Graham G, Guy, Michelle, Morrison, Jonathan, Severi, Gianluca, Leongamornlert, Daniel A, Tymrakiewicz, Malgorzata, Jhavar, Sameer, Saunders, Ed, Hopper, John L, Southey, Melissa C, Muir, Kenneth R, English, Dallas R, Dearnaley, David P, Ardern-Jones, Audrey T, Hall, Amanda L, O'Brien, Lynne T, Wilkinson, Rosemary A, Sawyer, Emma, Lophatananon, Artitaya, Horwich, Alan, Huddart, Robert A, Khoo, Vincent S, Parker, Christopher C, Woodhouse, Christopher J, Thompson, Alan, Christmas, Tim, Ogden, Chris, Cooper, Colin, Donovan, Jenny L, Hamdy, Freddie C, Neal, David E, Eeles, Rosalind A, Easton, Douglas F

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Identification of seven new prostate cancer susceptibility loci through a genome-wide association study von Eeles, Rosalind A, Kote-Jarai, Zsofia, Al Olama, Ali Amin, Giles, Graham G, Guy, Michelle, Severi, Gianluca, Muir, Kenneth, Hopper, John L, Henderson, Brian E, Haiman, Christopher A, Schleutker, Johanna, Hamdy, Freddie C, Neal, David E, Donovan, Jenny L, Stanford, Janet L, Ostrander, Elaine A, Ingles, Sue A, John, Esther M, Thibodeau, Stephen N, Schaid, Daniel, Park, Jong Y, Spurdle, Amanda, Clements, Judith, Dickinson, Joanne L, Maier, Christiane, Vogel, Walther, Dörk, Thilo, Rebbeck, Timothy R, Cooney, Kathleen A, Cannon-Albright, Lisa, Chappuis, Pierre O, Hutter, Pierre, Zeegers, Maurice, Kaneva, Radka, Zhang, Hong-Wei, Lu, Yong-Jie, Foulkes, William D, English, Dallas R, Leongamornlert, Daniel A, Tymrakiewicz, Malgorzata, Morrison, Jonathan, Ardern-Jones, Audrey T, Hall, Amanda L, O'Brien, Lynne T, Wilkinson, Rosemary A, Saunders, Edward J, Page, Elizabeth C, Sawyer, Emma J, Edwards, Stephen M, Dearnaley, David P, Huddart, Robert A, Khoo, Vincent S, Parker, Christopher C, Van As, Nicholas, Woodhouse, Christopher J, Thompson, Alan, Christmas, Tim, Ogden, Chris, Cooper, Colin S, Southey, Melissa C, Lophatananon, Artitaya, Liu, Jo-Fen, Kolonel, Laurence N, Le Marchand, Loic, Wahlfors, Tiina, Tammela, Teuvo L, Auvinen, Anssi, Lewis, Sarah J, Cox, Angela, FitzGerald, Liesel M, Koopmeiners, Joseph S, Karyadi, Danielle M, Kwon, Erika M, Stern, Mariana C, Corral, Roman, Joshi, Amit D, Shahabi, Ahva, McDonnell, Shannon K, Sellers, Thomas A, Pow-Sang, Julio, Chambers, Suzanne, Aitken, Joanne, Gardiner, R A (Frank), Batra, Jyotsna, Kedda, Mary Anne, Lose, Felicity, Polanowski, Andrea, Patterson, Briony, Serth, Jürgen, Meyer, Andreas, Luedeke, Manuel, Stefflova, Klara, Ray, Anna M, Lange, Ethan M, Farnham, Jim, Khan, Humera, Slavov, Chavdar, Mitkova, Atanaska, Cao, Guangwen, Easton, Douglas F

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Developing a curriculum for advanced fellowship training in complex cancer for the UK von Mohan, Helen, Harji, Deena, Drami, Ioanna, Griffiths, Ben, Larkins, Kirsten, Boyle, Kirsten, Daniels, Ian R., Baker, Richard, Jenkins, John T., Evans, Martyn, Burns, Elaine, Sutton, Paul, Simpson, Alastair, Mirnezami, Alex, Parkin, Edward, Kapur, Sandeep, Coyne, Peter, Harris, Dean, Tiernan, Jim, Stearns, Adam, Shaikh, Irshad, Dattani, Mitt, McArthur, David, Fearnhead, Nicola, Quirke, Ned, Quyn, Aaron, Tekkis, Paris, Schizas, Alexis, Lyons, Ann, Lee, Jack, Chowdhury, Abeed, Smolarek, Sebastian, Mitchell, Peter, Peristerakis, Ioannis, Sagar, Peter, Collins, Danielle

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Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms von Badner, J A, Koller, D, Foroud, T, Edenberg, H, Nurnberger, J I, Zandi, P P, Willour, V L, McMahon, F J, Potash, J B, Hamshere, M, Grozeva, D, Green, E, Kirov, G, Jones, I, Jones, L, Craddock, N, Morris, D, Segurado, R, Gill, M, Sadovnick, D, Remick, R, Keck, P, Kelsoe, J, Ayub, M, MacLean, A, Blackwood, D, Liu, C-Y, Gershon, E S, McMahon, W, Lyon, G J, Robinson, R, Ross, J, Byerley, W

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Predicting phenotypic severity of uncertain gene variants in the RET proto-oncogene von Crockett, David K, Piccolo, Stephen R, Ridge, Perry G, Margraf, Rebecca L, Lyon, Elaine, Williams, Marc S, Mitchell, Joyce A

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Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) von Lin, Angela E., Scimone, Eleanor R., Thom, Robyn P., Balaguru, Duraisamy, Kinane, T. Bernard, Moschovis, Peter P., Cohen, Michael S., Tan, Weizhen, Hague, Cole D., Dannheim, Katelyn, Levitsky, Lynne L., Lilly, Evelyn, DiGiacomo, Daniel V., Masse, Kara M., Kadzielski, Sarah M., Zar‐Kessler, Claire A., Ginns, Leo C., Neumeyer, Ann M., Colvin, Mary K., Elder, Jack S., Learn, Christopher P., Mou, Hongmei, Weagle, Kathryn M., Buch, Karen A., Butler, William E., Alhadid, Kenda, Musolino, Patricia L., Sultana, Sadia, Bandyopadhyay, Dhrubajyoti, Rapalino, Otto, Peacock, Zachary S., Chou, Elizabeth L., Heidary, Gena, Dorfman, Aaron T., Morris, Shaine A., Bergin, James D., Rayment, Jonathan H., Schimmenti, Lisa A., Lindsay, Mark E., Acosta, Luisa Paredes, Bassetti, Jennifer A., Bowdin, Sarah, Bress, Joy A., Camarda, Joseph A., Chiu, Joanne S., Corrales, C. Eduardo, Costain, Gregory, Dinulos, Mary Beth P., Devanagondi, Rajiv, Doherty, Emily S., Dykes, John, Duhaime, Ann‐Christine, English, Robert F., Fieg, Elizabeth, Friedman, Nora D. B., Garabedian, Carl P., Glowacki, Samantha, Gottlieb, Barbara R., Griffin, Mary Hope, Hayes, Frances J., Hicks, Stephanie R., Hinze, Alicia M., Jason, Brigette A., Krier, Joel, Lindgren, Kristen, Lyons, Michael, Majid, Adnan, Mannem, Hannah C., McDonald, Marie, Misra, Vinod, Morgan, Amy, Nath, Barbara J., Ploutz, Michele, Prijoles, Eloise J., Pulsifer, Margaret B., Quesnel, Alicia M., Rajabi, Farrah, Rohanizadegan, Mersedeh, Rosales, Ana Maria, Rothermel, Holly, Schussler, Edith, Sellars, Elizabeth A., Shieh, Joseph, Sherrill, Stephanie, Taska‐Tench, Heidi, Thompson, Matthew, Tiller, George E., Vallee, Stephanie E., Viskochil, David, Ware, Stephanie, Whooten, Rachel C., Yang, Samuel, Zackai, Elaine H., Zakaria, Dala

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