A national disgrace von Noon, Ian

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The Lived Experience and Legacy of Pragmatics for Deaf and Hard of Hearing Children von Young, Alys, Szarkowski, Amy, Ferguson-Coleman, Emma, Freeman, Darlene, Lindow-Davies, Candace, Davies, Ron, Hopkins, Karen, Noon, Ian, Rogers, Katherine, Russell, Jane, Seaver, Leeanne, Vesey, Kathy

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The Lived Experience and Legacy of Pragmatics for Deaf and Hard of Hearing Children von Young, Alys, Szarkowski, Amy, Ferguson-Coleman, Emma, Freeman, Darlene, Lindow-Davies, Candace, Davies, Ron, Hopkins, Karen, Noon, Ian, Rogers, Katherine, Russell, Jane, Seaver, Leeanne, Vesey, Kathy

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Method of testing a parking brake von Ian Noon, Stephen Price

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Method of testing a parking brake von Ian Noon, Stephen Price

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Method of testing a parking brake von Ian Noon, Stephen Price

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A Central Role for the ERK-Signaling Pathway in Controlling Schwann Cell Plasticity and Peripheral Nerve Regeneration In Vivo von Napoli, Ilaria, Noon, Luke A., Ribeiro, Sara, Kerai, Ajay P., Parrinello, Simona, Rosenberg, Laura H., Collins, Melissa J., Harrisingh, Marie C., White, Ian J., Woodhoo, Ashwin, Lloyd, Alison C.

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The use of natural antioxidants to combat lipid oxidation in O/W emulsions von Noon, John, Mills, Tom B., Norton, Ian T.

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USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder von Hao, Yi-Heng, Fountain, Michael D., Fon Tacer, Klementina, Xia, Fan, Bi, Weimin, Kang, Sung-Hae L., Patel, Ankita, Rosenfeld, Jill A., Le Caignec, Cédric, Isidor, Bertrand, Krantz, Ian D., Noon, Sarah E., Pfotenhauer, Jean P., Morgan, Thomas M., Moran, Rocio, Pedersen, Robert C., Saenz, Margarita S., Schaaf, Christian P., Potts, Patrick Ryan

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Actors with Multiple Roles: Pleiotropic Enhancers and the Paradigm of Enhancer Modularity von Sabarís, Gonzalo, Laiker, Ian, Preger-Ben Noon, Ella, Frankel, Nicolás

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Germline gain-of-function mutations in AFF4 cause a developmental syndrome functionally linking the super elongation complex and cohesin von Izumi, Kosuke, Nakato, Ryuichiro, Zhang, Zhe, Edmondson, Andrew C, Noon, Sarah, Dulik, Matthew C, Rajagopalan, Ramakrishnan, Venditti, Charles P, Gripp, Karen, Samanich, Joy, Zackai, Elaine H, Deardorff, Matthew A, Clark, Dinah, Allen, Julian L, Dorsett, Dale, Misulovin, Ziva, Komata, Makiko, Bando, Masashige, Kaur, Maninder, Katou, Yuki, Shirahige, Katsuhiko, Krantz, Ian D

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The use of antioxidant rutin hydrate Pickering particles to combat lipid oxidation in O/W emulsions von Noon, John, Mills, Tom B., Norton, Ian T.

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Quantifying Ecological Integrity of Terrestrial Systems to Inform Management of Multiple-Use Public Lands in the United States von Carter, Sarah K., Fleishman, Erica, Leinwand, Ian I. F., Flather, Curtis H., Carr, Natasha B., Fogarty, Frank A., Leu, Matthias, Noon, Barry R., Wohlfeil, Martha E., Wood, David J. A.

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Microwave-Assisted Nanonization of Poorly Water-Soluble Curcumin von Aditya, Nayak P, Hamilton, Ian E, Noon, John, Norton, Ian T

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The Density of Regulatory Information Is a Major Determinant of Evolutionary Constraint on Noncoding DNA in Drosophila von Sabarís, Gonzalo, Ortíz, Daniela M, Laiker, Ian, Mayansky, Ignacio, Naik, Sujay, Cavalli, Giacomo, Stern, David L, Preger-Ben Noon, Ella, Frankel, Nicolás

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Phenotypes and genotypes in individuals with SMC1A variants von Huisman, Sylvia, Mulder, Paul A., Redeker, Egbert, Bader, Ingrid, Bisgaard, Anne‐Marie, Brooks, Alice, Cereda, Anna, Cinca, Constanza, Clark, Dinah, Cormier‐Daire, Valerie, Deardorff, Matthew A., Diderich, Karin, Elting, Mariet, van Essen, Anthonie, FitzPatrick, David, Gervasini, Cristina, Gillessen‐Kaesbach, Gabriele, Girisha, Katta M., Hilhorst‐Hofstee, Yvonne, Hopman, Saskia, Horn, Denise, Isrie, Mala, Jansen, Sandra, Jespersgaard, Cathrine, Kaiser, Frank J., Kaur, Maninder, Kleefstra, Tjitske, Krantz, Ian D., Lakeman, Phillis, Landlust, Annemiek, Lessel, Davor, Michot, Caroline, Moss, Jo, Noon, Sarah E., Oliver, Chris, Parenti, Ilaria, Pie, Juan, Ramos, Feliciano J., Rieubland, Claudine, Russo, Silvia, Selicorni, Angelo, Tümer, Zeynep, Vorstenbosch, Rieneke, Wenger, Tara L., van Balkom, Ingrid, Piening, Sigrid, Wierzba, Jolanta, Hennekam, Raoul C.

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Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic von Mehta, Devanshi, Noon, Sarah E., Schwartz, Emily, Wilkens, Alisha, Bedoukian, Emma C., Scarano, Irene, Crenshaw III, E. Bryan, Krantz, Ian D.

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A de novo SATB2 mutation in monozygotic twins with cleft palate, dental anomalies, and developmental delay von Schwartz, Emily, Wilkens, Alisha, Noon, Sarah E., Krantz, Ian D., Wu, Yaning

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DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies von Ji, Jianling, Lee, Hane, Argiropoulos, Bob, Dorrani, Naghmeh, Mann, John, Martinez-Agosto, Julian A, Gomez-Ospina, Natalia, Gallant, Natalie, Bernstein, Jonathan A, Hudgins, Louanne, Slattery, Leah, Isidor, Bertrand, Le Caignec, Cédric, David, Albert, Obersztyn, Ewa, Wiśniowiecka-Kowalnik, Barbara, Fox, Michelle, Deignan, Joshua L, Vilain, Eric, Hendricks, Emily, Horton Harr, Margaret, Noon, Sarah E, Jackson, Jessi R, Wilkens, Alisha, Mirzaa, Ghayda, Salamon, Noriko, Abramson, Jeff, Zackai, Elaine H, Krantz, Ian, Innes, A Micheil, Nelson, Stanley F, Grody, Wayne W, Quintero-Rivera, Fabiola

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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance von Kaiser, Frank J., Ansari, Morad, Braunholz, Diana, Concepción Gil-Rodríguez, María, Decroos, Christophe, Wilde, Jonathan J., Fincher, Christopher T., Kaur, Maninder, Bando, Masashige, Amor, David J., Atwal, Paldeep S., Bahlo, Melanie, Bowman, Christine M., Bradley, Jacquelyn J., Brunner, Han G., Clark, Dinah, Del Campo, Miguel, Di Donato, Nataliya, Diakumis, Peter, Dubbs, Holly, Dyment, David A., Eckhold, Juliane, Ernst, Sarah, Ferreira, Jose C., Francey, Lauren J., Gehlken, Ulrike, Guillén-Navarro, Encarna, Gyftodimou, Yolanda, Hall, Bryan D., Hennekam, Raoul, Hudgins, Louanne, Hullings, Melanie, Hunter, Jennifer M., Yntema, Helger, Innes, A. Micheil, Kline, Antonie D., Krumina, Zita, Lee, Hane, Leppig, Kathleen, Lynch, Sally Ann, Mallozzi, Mark B., Mannini, Linda, Mckee, Shane, Mehta, Sarju G., Micule, Ieva, Mohammed, Shehla, Moran, Ellen, Mortier, Geert R., Moser, Joe-Ann S., Noon, Sarah E., Nozaki, Naohito, Nunes, Luis, Pappas, John G., Penney, Lynette S., Pérez-Aytés, Antonio, Petersen, Michael B., Puisac, Beatriz, Revencu, Nicole, Roeder, Elizabeth, Saitta, Sulagna, Scheuerle, Angela E., Schindeler, Karen L., Siu, Victoria M., Stark, Zornitza, Strom, Samuel P., Thiese, Heidi, Vater, Inga, Willems, Patrick, Williamson, Kathleen, Wilson, Louise C., Hakonarson, Hakon, Quintero-Rivera, Fabiola, Wierzba, Jolanta, Musio, Antonio, Gillessen-Kaesbach, Gabriele, Ramos, Feliciano J., Jackson, Laird G., Shirahige, Katsuhiko, Pié, Juan, Christianson, David W., Krantz, Ian D., Fitzpatrick, David R., Deardorff, Matthew A.

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