Sequence and evolution of the FruR protein of Salmonella typhimurium: a pleiotropic transcriptional regulatory protein possessing both activator and repressor functions which is ho... von Vartak, N.B, Reizer, J, Reizer, A, Gripp, J.T, Groisman, E.A, Wu, L.-F, Tomich, J.M, Saier, M.H

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Sequence and evolution of the FruR protein of Salmonella typhimurium : A pleiotropic transcriptional regulatory protein possessing both activator and repressor functions which is h... von Vartak, N B, Reizer, J, Reizer, A, Gripp, J T, Groisman, E A, Wu, L-F, Tomich, J M, Saier, MH Jr

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Vibration and noise control using shunted piezoelectric transducers: A review von Gripp, J.A.B., Rade, D.A.

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Reanalysis of Clinical Exome Sequencing Data von Liu, Pengfei, Meng, Linyan, Normand, Elizabeth A, Xia, Fan, Song, Xiaofei, Ghazi, Andrew, Rosenfeld, Jill, Magoulas, Pilar L, Braxton, Alicia, Ward, Patricia, Dai, Hongzheng, Yuan, Bo, Bi, Weimin, Xiao, Rui, Wang, Xia, Chiang, Theodore, Vetrini, Francesco, He, Weimin, Cheng, Hanyin, Dong, Jie, Gijavanekar, Charul, Benke, Paul J, Bernstein, Jonathan A, Eble, Tanya, Eroglu, Yasemen, Erwin, Deanna, Escobar, Luis, Gibson, James B, Gripp, Karen, Kleppe, Soledad, Koenig, Mary K, Lewis, Andrea M, Natowicz, Marvin, Mancias, Pedro, Minor, LaKeesha, Scaglia, Fernando, Schaaf, Christian P, Streff, Haley, Vernon, Hilary, Uhles, Crescenda L, Zackai, Elaine H, Wu, Nan, Sutton, V. Reid, Beaudet, Arthur L, Muzny, Donna, Gibbs, Richard A, Posey, Jennifer E, Lalani, Seema, Shaw, Chad, Eng, Christine M, Lupski, James R, Yang, Yaping

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Global burden of influenza-associated lower respiratory tract infections and hospitalizations among adults: A systematic review and meta-analysis von Lafond, Kathryn E, Porter, Rachael M, Whaley, Melissa J, Suizan, Zhou, Ran, Zhang, Aleem, Mohammad Abdul, Thapa, Binay, Sar, Borann, Proschle, Viviana Sotomayor, Peng, Zhibin, Feng, Luzhao, Coulibaly, Daouda, Nkwembe, Edith, Olmedo, Alfredo, Ampofo, William, Saha, Siddhartha, Chadha, Mandeep, Mangiri, Amalya, Setiawaty, Vivi, Ali, Sami Sheikh, Chaves, Sandra S, Otorbaeva, Dinagul, Keosavanh, Onechanh, Saleh, Majd, Ho, Antonia, Alexander, Burmaa, Oumzil, Hicham, Baral, Kedar Prasad, Huang, Q Sue, Adebayo, Adedeji A, Al-Abaidani, Idris, von Horoch, Marta, Cohen, Cheryl, Tempia, Stefano, Mmbaga, Vida, Chittaganpitch, Malinee, Casal, Mariana, Dang, Duc Anh, Couto, Paula, Nair, Harish, Bresee, Joseph S, Olsen, Sonja J, Azziz-Baumgartner, Eduardo, Nuorti, J Pekka, Widdowson, Marc-Alain

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GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome von LaCroix, Amy J., Stabley, Deborah, Sahraoui, Rebecca, Adam, Margaret P., Mehaffey, Michele, Kernan, Kelly, Myers, Candace T., Fagerstrom, Carrie, Anadiotis, George, Akkari, Yassmine M., Robbins, Katherine M., Gripp, Karen W., Baratela, Wagner A.R., Bober, Michael B., Duker, Angela L., Doherty, Dan, Dempsey, Jennifer C., Miller, Daniel G., Kircher, Martin, Bamshad, Michael J., Nickerson, Deborah A., Mefford, Heather C., Sol-Church, Katia

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Costello syndrome: Clinical phenotype, genotype, and management guidelines von Gripp, Karen W., Morse, Lindsey A., Axelrad, Marni, Chatfield, Kathryn C., Chidekel, Aaron, Dobyns, William, Doyle, Daniel, Kerr, Bronwyn, Lin, Angela E., Schwartz, David D., Sibbles, Barbara J., Siegel, Dawn, Shankar, Suma P., Stevenson, David A., Thacker, Mihir M., Weaver, K. Nicole, White, Sue M., Rauen, Katherine A.

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Global Role and Burden of Influenza in Pediatric Respiratory Hospitalizations, 1982-2012: A Systematic Analysis von Lafond, Kathryn E, Nair, Harish, Rasooly, Mohammad Hafiz, Valente, Fátima, Booy, Robert, Rahman, Mahmudur, Kitsutani, Paul, Yu, Hongjie, Guzman, Guiselle, Coulibaly, Daouda, Armero, Julio, Jima, Daddi, Howie, Stephen R C, Ampofo, William, Mena, Ricardo, Chadha, Mandeep, Sampurno, Ondri Dwi, Emukule, Gideon O, Nurmatov, Zuridin, Corwin, Andrew, Heraud, Jean Michel, Noyola, Daniel E, Cojocaru, Radu, Nymadawa, Pagbajabyn, Barakat, Amal, Adedeji, Adebayo, von Horoch, Marta, Olveda, Remigio, Nyatanyi, Thierry, Venter, Marietjie, Mmbaga, Vida, Chittaganpitch, Malinee, Nguyen, Tran Hien, Theo, Andros, Whaley, Melissa, Azziz-Baumgartner, Eduardo, Bresee, Joseph, Campbell, Harry, Widdowson, Marc-Alain

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Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis von Khajuria, Rajiv K., Munschauer, Mathias, Ulirsch, Jacob C., Fiorini, Claudia, Ludwig, Leif S., McFarland, Sean K., Abdulhay, Nour J., Specht, Harrison, Keshishian, Hasmik, Mani, D.R., Jovanovic, Marko, Ellis, Steven R., Fulco, Charles P., Engreitz, Jesse M., Schütz, Sabina, Lian, John, Gripp, Karen W., Weinberg, Olga K., Pinkus, Geraldine S., Gehrke, Lee, Regev, Aviv, Lander, Eric S., Gazda, Hanna T., Lee, Winston Y., Panse, Vikram G., Carr, Steven A., Sankaran, Vijay G.

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Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy von Lee, Yu-Ri, Khan, Kamal, Armfield-Uhas, Kim, Srikanth, Sujata, Thompson, Nicola A., Pardo, Mercedes, Yu, Lu, Norris, Joy W., Peng, Yunhui, Gripp, Karen W., Aleck, Kirk A., Li, Chumei, Spence, Ed, Choi, Tae-Ik, Kwon, Soo Jeong, Park, Hee-Moon, Yu, Daseuli, Heo, Won Do, Mooney, Marie R., Baig, Shahid M., Wentzensen, Ingrid M., Telegrafi, Aida, McWalter, Kirsty, Moreland, Trevor, Roadhouse, Chelsea, Ramsey, Keri, Lyons, Michael J., Skinner, Cindy, Alexov, Emil, Katsanis, Nicholas, Stevenson, Roger E., Choudhary, Jyoti S., Adams, David J., Kim, Cheol-Hee, Davis, Erica E., Schwartz, Charles E.

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Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy von Aldinger, Kimberly A., Mosca, Stephen J., Tétreault, Martine, Dempsey, Jennifer C., Ishak, Gisele E., Hartley, Taila, Phelps, Ian G., Lamont, Ryan E., O’Day, Diana R., Basel, Donald, Gripp, Karen W., Baker, Laura, Stephan, Mark J., Bernier, Francois P., Boycott, Kym M., Majewski, Jacek, Parboosingh, Jillian S., Innes, A. Micheil, Doherty, Dan

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Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome von Bend, Eric G, Aref-Eshghi, Erfan, Everman, David B, Rogers, R Curtis, Cathey, Sara S, Prijoles, Eloise J, Lyons, Michael J, Davis, Heather, Clarkson, Katie, Gripp, Karen W, Li, Dong, Bhoj, Elizabeth, Zackai, Elaine, Mark, Paul, Hakonarson, Hakon, Demmer, Laurie A, Levy, Michael A, Kerkhof, Jennifer, Stuart, Alan, Rodenhiser, David, Friez, Michael J, Stevenson, Roger E, Schwartz, Charles E, Sadikovic, Bekim

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GestaltMatcher facilitates rare disease matching using facial phenotype descriptors von Hsieh, Tzung-Chien, Bar-Haim, Aviram, Moosa, Shahida, Ehmke, Nadja, Gripp, Karen W., Pantel, Jean Tori, Danyel, Magdalena, Mensah, Martin Atta, Horn, Denise, Rosnev, Stanislav, Fleischer, Nicole, Bonini, Guilherme, Hustinx, Alexander, Schmid, Alexander, Knaus, Alexej, Javanmardi, Behnam, Klinkhammer, Hannah, Lesmann, Hellen, Sivalingam, Sugirthan, Kamphans, Tom, Meiswinkel, Wolfgang, Ebstein, Frédéric, Krüger, Elke, Küry, Sébastien, Bézieau, Stéphane, Schmidt, Axel, Peters, Sophia, Engels, Hartmut, Mangold, Elisabeth, Kreiß, Martina, Cremer, Kirsten, Perne, Claudia, Betz, Regina C., Bender, Tim, Grundmann-Hauser, Kathrin, Haack, Tobias B., Wagner, Matias, Brunet, Theresa, Bentzen, Heidi Beate, Averdunk, Luisa, Coetzer, Kimberly Christine, Lyon, Gholson J., Spielmann, Malte, Schaaf, Christian P., Mundlos, Stefan, Nöthen, Markus M., Krawitz, Peter M.

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Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype von Koenighofer, M., Hung, C. Y., McCauley, J. L., Dallman, J., Back, E. J., Mihalek, I., Gripp, K. W., Sol-Church, K., Rusconi, P., Zhang, Z., Shi, G-X., Andres, D. A., Bodamer, O. A.

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Constitutional LZTR1 mutation presenting with a unilateral vestibular schwannoma in a teenager von Gripp, K.W., Baker, L., Kandula, V., Piatt, J., Walter, A., Chen, Z., Messiaen, L.

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Assessing the gene–disease association of 19 genes with the RASopathies using the ClinGen gene curation framework von Grant, Andrew R., Cushman, Brandon J., Cavé, Hélène, Dillon, Mitchell W., Gelb, Bruce D., Gripp, Karen W., Lee, Jennifer A., Mason‐Suares, Heather, Rauen, Katherine A., Tartaglia, Marco, Vincent, Lisa M., Zenker, Martin

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Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP von Van Dijck, Anke, Vulto-van Silfhout, Anneke T., Cappuyns, Elisa, van der Werf, Ilse M., Mancini, Grazia M., Tzschach, Andreas, Bernier, Raphael, Gozes, Illana, Eichler, Evan E., Romano, Corrado, Lindstrand, Anna, Nordgren, Ann, Bakshi, Madhura, Wilson, Meredith, Berman, Yemina, Dickson, Rebecca, Fransen, Erik, Helsmoortel, Céline, Van den Ende, Jenneke, Van der Aa, Nathalie, van de Wijdeven, Marina J., Rosenblum, Jessica, Monteiro, Fabíola, Kok, Fernando, Quercia, Nada, Bowdin, Sarah, Dyment, David, Chitayat, David, Alkhunaizi, Ebba, Boonen, Susanne E., Keren, Boris, Jacquette, Aurelia, Faivre, Laurence, Bezieau, Stephane, Isidor, Bertrand, Rieß, Angelika, Moog, Ute, Lynch, Sally Ann, McVeigh, Terri, Elpeleg, Orly, Smeland, Marie Falkenberg, Fannemel, Madeleine, van Haeringen, Arie, Maas, Saskia M., Veenstra-Knol, H.E., Schouten, Meyke, Willemsen, Marjolein H., Marcelis, Carlo L., Ockeloen, Charlotte, van der Burgt, Ineke, Feenstra, Ilse, van der Smagt, Jasper, Jezela-Stanek, Aleksandra, Krajewska-Walasek, Malgorzata, González-Lamuño, Domingo, Anderlid, Britt-Marie, Malmgren, Helena, Nordenskjöld, Magnus, Hurst, Jane, Metcalfe, Kay, Mansour, Sahar, Lachlan, Katherine, Clayton-Smith, Jill, Hendon, Laura G., Abdulrahman, Omar A., Morrow, Eric, McMillan, Clare, Gerdts, Jennifer, Peeden, Joseph, Schrier Vergano, Samantha A., Valentino, Caitlin, Chung, Wendy K., Ozmore, Jillian R., Bedrosian-Sermone, Sandra, Treat, Kayla, Hughes, Susan Starling, Safina, Nicole, Le Pichon, Jean-Baptiste, McGuire, Marianne, Infante, Elena, Madan-Khetarpal, Suneeta, Desai, Sonal, Benke, Paul, Krokosky, Alyson, Cristian, Ingrid, Baker, Laura, Gripp, Karen, Stessman, Holly A., Eichenberger, Jacob, Jayakar, Parul, Manning, Melanie Ann, Slattery, Leah, Kvarnung, Malin, Kleefstra, Tjitske, de Vries, Bert B.A., Küry, Sébastien, Rosenfeld, Jill A., Meuwissen, Marije E., Vandeweyer, Geert, Kooy, R. Frank

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Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure von Mulchandani, Surabhi, Bhoj, Elizabeth J., Luo, Minjie, Powell-Hamilton, Nina, Jenny, Kim, Gripp, Karen W., Elbracht, Miriam, Eggermann, Thomas, Turner, Claire L.S., Temple, I. Karen, Mackay, Deborah J.G., Dubbs, Holly, Stevenson, David A., Slattery, Leah, Zackai, Elaine H., Spinner, Nancy B., Krantz, Ian D., Conlin, Laura K.

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Quantifying Order during Field-Driven Alignment of Colloidal Semiconductor Nanorods von Ratnaweera, Rivi J, Rodríguez Ortiz, Freddy A, Gripp, Nicholas J, Sheldon, Matthew T

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Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome von Gripp, Karen W., Robbins, Katherine M., Sobreira, Nara L., Witmer, P. Dane, Bird, Lynne M., Avela, Kristiina, Makitie, Outi, Alves, Daniela, Hogue, Jacob S., Zackai, Elaine H., Doheny, Kimberly F., Stabley, Deborah L., Sol-Church, Katia

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