Predicting traumatic brain injury outcomes using a posterior dominant rhythm von Cleri, Nathaniel A, Saadon, Jordan R, Zheng, Xuwen, Swarna, Sujith A, Zhang, Jason, Vagal, Vaibhav, Wang, Cassie, Kleyner, Robert S, Mikell, Charles B, Mofakham, Sima

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Capecitabine-Induced Enterocolitis von Khan, Muzammil, Kleyner, Robert, Abbasi, Sadia, Haider, Asim

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ITPR1 -associated spinocerebellar ataxia with craniofacial features-additional evidence for germline mosaicism von Kleyner, Robert, Ung, Nathaniel, Arif, Mohammad, Marchi, Elaine, Amble, Karen, Gavin, Maureen, Madrid, Ricardo, Lyon, Gholson

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Autosomal recessive SLC30A9 variants in a proband with a cerebrorenal syndrome and no parental consanguinity von Kleyner, Robert, Arif, Mohammad, Marchi, Elaine, Horowitz, Naomi, Haworth, Andrea, King, Brian, Gavin, Maureen, Amble, Karen, Velinov, Milen, Lyon, Gholson J

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Autosomal recessive SLC30A9 variants in a Proband with a Cerebro-Renal Syndrome and No Parental Consanguinity von Kleyner, Robert, Mohammad, Arif, Marchi, Elaine, Horowitz, Naomi, Haworth, Andrea, King, Brian, Amble, Karen, Gavin, Maureen, Velinov, Milen, Lyon, Gholson J

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KBG syndrome involving a single-nucleotide duplication in ANKRD11 von Kleyner, Robert, Malcolmson, Janet, Tegay, David, Ward, Kenneth, Maughan, Annette, Maughan, Glenn, Nelson, Lesa, Wang, Kai, Robison, Reid, Lyon, Gholson J

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PillHarmonics: An Orchestrated Pharmacogenetics Medication Clinical Decision Support Service von Dolin, Robert H, Shenvi, Edna, Alvarez, Carla, Barrows, Jr, Randolph C, Boxwala, Aziz, Lee, Benson, Nathanson, Brian H, Kleyner, Yelena, Hagemann, Rachel, Hongsermeier, Tonya, Kapusnik-Uner, Joan, Lakdawala, Adnan, Shalaby, James

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Changed In Translation: Greek Actives Become Gothic Passives von Kleyner, Svetlana

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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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Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies von Cheng, Hanyin, Dharmadhikari, Avinash V., Varland, Sylvia, Ma, Ning, Domingo, Deepti, Kleyner, Robert, Rope, Alan F., Yoon, Margaret, Stray-Pedersen, Asbjørg, Posey, Jennifer E., Crews, Sarah R., Eldomery, Mohammad K., Akdemir, Zeynep Coban, Lewis, Andrea M., Sutton, Vernon R., Rosenfeld, Jill A., Conboy, Erin, Agre, Katherine, Xia, Fan, Walkiewicz, Magdalena, Longoni, Mauro, High, Frances A., van Slegtenhorst, Marjon A., Mancini, Grazia M.S., Finnila, Candice R., van Haeringen, Arie, den Hollander, Nicolette, Ruivenkamp, Claudia, Naidu, Sakkubai, Mahida, Sonal, Palmer, Elizabeth E., Murray, Lucinda, Lim, Derek, Jayakar, Parul, Parker, Michael J., Giusto, Stefania, Stracuzzi, Emanuela, Romano, Corrado, Beighley, Jennifer S., Bernier, Raphael A., Küry, Sébastien, Nizon, Mathilde, Corbett, Mark A., Shaw, Marie, Gardner, Alison, Barnett, Christopher, Armstrong, Ruth, Kassahn, Karin S., Van Dijck, Anke, Vandeweyer, Geert, Kleefstra, Tjitske, Schieving, Jolanda, Jongmans, Marjolijn J., de Vries, Bert B.A., Pfundt, Rolph, Kerr, Bronwyn, Rojas, Samantha K., Boycott, Kym M., Person, Richard, Willaert, Rebecca, Eichler, Evan E., Kooy, R. Frank, Yang, Yaping, Wu, Joseph C., Lupski, James R., Arnesen, Thomas, Cooper, Gregory M., Chung, Wendy K., Gecz, Jozef, Stessman, Holly A.F., Meng, Linyan, Lyon, Gholson J.

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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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THE ENGLISH VERSIONS OF THE FRIDAY LEGEND: THREE AND TWELVE von IVANOV, SERGEY, KLEYNER, SVETLANA

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Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity

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Paralog Studies Augment Gene Discovery: DDX and DHX Genes von Paine, Ingrid, Posey, Jennifer E, Grochowski, Christopher M, Jhangiani, Shalini N, Rosenheck, Sarah, Kleyner, Robert, Marmorale, Taylor, Yoon, Margaret, Wang, Kai, Robison, Reid, Cappuccio, Gerarda, Pinelli, Michele, Magli, Adriano, Akdemir, Zeynep Coban, Hui, Joannie, Yeung, Wai Lan, Wong, Bibiana K.Y, Ortega, Lucia, Bekheirnia, Mir Reza, Bierhals, Tatjana, Hempel, Maja, Johannsen, Jessika, Santer, Rene, Aktas, Dilek, Alikasifoglu, Mehmet, Bozdogan, Sevcan, Aydin, Hatip, Karaca, Ender, Bayram, Yavuz, Ityel, Hadas, Dorschner, Michael, White, Janson J, Wilichowski, Ekkehard, Wortmann, Saskia B, Casella, Erasmo B, Kitajima, Joao Paulo, Kok, Fernando, Monteiro, Fabiola, Muzny, Donna M, Bamshad, Michael, Gibbs, Richard A, Sutton, V. Reid, Van Esch, Hilde, Brunetti-Pierri, Nicola, Hildebrandt, Friedhelm, Brautbar, Ariel, Van den Veyver, Ignatia B, Glass, Ian, Lessel, Davor, Lyon, Gholson J, Lupski, James R

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Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity von Cheng, Hanyin, Capponi, Simona, Wakeling, Emma, Marchi, Elaine, Li, Quan, Zhao, Mengge, Weng, Chunhua, Stefan, Piatek G, Ahlfors, Helena, Kleyner, Robert, Rope, Alan, Lumaka, Aime, Lukusa, Prosper, Devriendt, Koenraad, Vermeesch, Joris, Posey, Jennifer E, Palmer, Elizabeth E, Murray, Lucinda, Leon, Eyby, Diaz, Jullianne, Worgan, Lisa, Mallawaarachchi, Amalia, Vogt, Julie, de Munnik, Sonja A, Dreyer, Lauren, Baynam, Gareth, Ewans, Lisa, Stark, Zornitza, Lunke, Sebastian, Goncalves, Ana R, Soares, Gabriela, Oliveira, Jorge, Fassi, Emily, Willing, Marcia, Waugh, Jeff L, Faivre, Laurence, Riviere, Jean-Baptiste, Moutton, Sebastien, Mohammed, Shehla, Payne, Katelyn, Walsh, Laurence, Begtrup, Amber, Sacoto, Maria J. Guillen, Douglas, Ganka, Alexander, Nora, Buckley, Michael F, Mark, Paul R, Ades, Lesley C, Sandaradura, Sarah A, Lupski, James R, Roscioli, Tony, Agrawal, Pankaj B, Kline, Antonie D, Wang, Kai, Timmers, H.T. Marc, Lyon, Gholson J

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SCN8A mutation in a child presenting with seizures and developmental delays von Malcolmson, Janet, Kleyner, Robert, Tegay, David, Adams, Whit, Ward, Kenneth, Coppinger, Justine, Nelson, Lesa, Meisler, Miriam H, Wang, Kai, Robison, Reid, Lyon, Gholson J

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Capecitabine-Induced Enterocolitis von Khan, Muzammil, Kleyner, Robert, Abbasi, Sadia, Haider, Asim

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Science of opportunity: Heliophysics on the FASTSAT mission and STP-S26 von Rowland, Douglas E, Collier, Michael R, Sigwarth, John B, Jones, Sarah L, Hill, Joanne K, Benson, Robert, Choi, Michael, Chornay, Dennis, Cooper, John, Feng, Steven, Gill, Nathaniel, Goodloe, Colby, Han, Lawrence, Hancock, Holly, Hunsaker, Floyd, Jones, Noble, Keller, John W, Klenzing, Jeffrey, Kleyner, Igor, Moore, Tom, Ogilvie, Keith, Pfaff, Robert, Price, Tracy, Roman, Joe, Rodruiguez, Marcello, Rozmarynowski, Paul, Saulino, Mark, Sheikh, Salman, Simms, Ken, Yew, Alvin, Young, Eric, Kujawski, Joseph, Boudreaux, Mark, Casas, Joseph, Myre, David, Smith, Billy

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Tumor necrosis factor alpha leads to increased cell surface expression of CXCR4 in SK-N-MC cells von Rostasy, Kevin, Gorgun, Gullue, Kleyner, Yelena, Garcia, Anthony, Kramer, Michael, Melanson, Suzanne M, Mathys, Jean Marie, Yiannoutsos, Constantin, Skolnik, Paul R, Navia, Bradford A

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Cell-Specific Expression of the Lark Rna-Binding Protein in Drosophila Results in Morphological and Circadian Behavioral Phenotypes von SCHROEDER, ANDREW J., GENOVA, GINKA K., ROBERTS, MARY A., KLEYNER, YELENA, SUH, JOOWON, JACKSON, F. ROB

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