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

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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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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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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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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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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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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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Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity (vol 41, pg 449, 2020) 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, Amali, 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, 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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Evaluation of Pulse Counting for the Mars Organic Mass Analyzer (MOMA) Ion Trap Detection Scheme von Van Amerom, Friso H., Short, Tim, Brinckerhoff, William, Mahaffy, Paul, Kleyner, Igor, Cotter, Robert J., Pinnick, Veronica, Hoffman, Lars, Danell, Ryan M., Lyness, Eric I.

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