Perceived health status among the new urban homeless von Ropers, Richard H., Boyer, Richard

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Unemployment and Political Partisanship: Support for the Null Hypothesis von Scott, Wilbur J., Ropers, Richard H.

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Perceived health status among the urban homeless von Ropers, Richard H, Boyer, Richard

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Creative educational use of existing community resources von Permaul, Janes S., Ropers, Richard H.

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Homelessness as a health risk von Ropers, R.H, Boyer, R

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Alcohol Training for Police Officers: Behavior or Attitude Change? von ROPERS, RICHARD H., CALKINS, RICHARD F.

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UNEMPLOYMENT AND POLITICAL ATTITUDES: AN EMPIRICAL ASSESSMENT von Koning, Steven M., Ropers, Richard H.

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Persistent Poverty: The American Dream Turned Nightmare von Hannon, James T.

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes von Hu, H, Haas, S A, Chelly, J, Van Esch, H, Raynaud, M, de Brouwer, A P M, Weinert, S, Froyen, G, Frints, S G M, Laumonnier, F, Zemojtel, T, Love, M I, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K L, Belet, S, van Roozendaal, K E P, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L B, Wieacker, P, Rodríguez Criado, G, Bondeson, M-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T J, Chen, W, Ropers, H-H, Kalscheuer, V M

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Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation von Jensen, Lars Riff, Amende, Marion, Gurok, Ulf, Moser, Bettina, Gimmel, Verena, Tzschach, Andreas, Janecke, Andreas R., Tariverdian, Gholamali, Chelly, Jamel, Fryns, Jean-Pierre, Van Esch, Hilde, Kleefstra, Tjitske, Hamel, Ben, Moraine, Claude, Gécz, Jozef, Turner, Gillian, Reinhardt, Richard, Kalscheuer, Vera M., Ropers, Hans-Hilger, Lenzner, Steffen

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De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome von Bainbridge, Matthew N, Hu, Hao, Muzny, Donna M, Musante, Luciana, Lupski, James R, Graham, Brett H, Chen, Wei, Gripp, Karen W, Jenny, Kim, Wienker, Thomas F, Yang, Yaping, Sutton, V Reid, Gibbs, Richard A, Ropers, H Hilger

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The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis von Colbert, Brett M., Lanting, Cris, Smeal, Molly, Blanton, Susan, Dykxhoorn, Derek M., Tang, Pei-Ciao, Getchell, Richard L., Velde, Hedwig, Fehrmann, Mirthe, Thorpe, Ryan, Chapagain, Prem, Elkhaligy, Heidy, Kremer, Hannie, Yntema, Helger, Haer-Wigman, Lonneke, Redfield, Shelby, Sun, Tieqi, Bruijn, Saskia, Plomp, Astrid, Goderie, Thadé, van de Kamp, Jiddeke, Free, Rolien H., Wassink-Ruiter, Jolien Klein, Widdershoven, Josine, Vanhoutte, Els, Rotteveel, Liselotte, Kriek, Marjolein, van Dooren, Marieke, Hoefsloot, Lies, de Gier, Heriette H. W., Schaefer, Amanda, Kolbe, Diana, Azaiez, Hela, Rabie, Grace, Aburayyan, Armal, Kawas, Mariana, Kanaan, Moien, Holder, Jourdan, Usami, Shin-ichi, Chen, Zhengyi, Dai, Pu, Holt, Jeffrey, Nelson, Rick, Choi, Byung Yoon, Shearer, Eliot, Smith, Richard J. H., Pennings, Ronald, Liu, Xue Zhong

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Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care von Mercuri, Eugenio, Finkel, Richard S., Muntoni, Francesco, Wirth, Brunhilde, Montes, Jacqueline, Main, Marion, Mazzone, Elena S., Vitale, Michael, Snyder, Brian, Quijano-Roy, Susana, Bertini, Enrico, Davis, Rebecca Hurst, Meyer, Oscar H., Simonds, Anita K., Schroth, Mary K., Graham, Robert J., Kirschner, Janbernd, Iannaccone, Susan T., Crawford, Thomas O., Woods, Simon, Qian, Ying, Sejersen, Thomas, Muntoni, Francesco, Wirth, Brunhilde, Tiziano, Francesco Danilo, Kirschner, Janbernd, Tizzano, Eduardo, Topaloglu, Haluk, Swoboda, Kathy, Laing, Nigel, Kayoko, Saito, Prior, Thomas, Chung, Wendy K., Wu, Shou-Mei, Montes, Jacqueline, Mazzone, Elena, Main, Marion, Coleman, Caron, Gee, Richard, Glanzman, Allan, Kroksmark, Anna-Karin, Krosschell, Kristin, Nelson, Leslie, Rose, Kristy, Stępień, Agnieszka, Vuillerot, Carole, Vitale, Michael, Snyder, Brian, Quijano-Roy, Susana, Dubousset, Jean, Farrington, David, Flynn, Jack, Halanski, Matthew, Hasler, Carol, Miladi, Lotfi, Reilly, Christopher, Roye, Benjamin, Sponseller, Paul, Yazici, Muharrem, Hurst, Rebecca, Bertini, Enrico, Tarrant, Stacey, Barja, Salesa, Bertoli, Simona, Crawford, Thomas, Foust, Kevin, Kyle, Barbara, Rodan, Lance, Roper, Helen, Seffrood, Erin, Swoboda, Kathryn, Szlagatys-Sidorkiewicz, Agnieszka

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Prolonged release oxycodone–naloxone for treatment of severe restless legs syndrome after failure of previous treatment: a double-blind, randomised, placebo-controlled trial with a... von Trenkwalder, Claudia, Prof, Beneš, Heike, MD, Grote, Ludger, MD, García-Borreguero, Diego, MD, Högl, Birgit, MD, Hopp, Michael, MD, Bosse, Björn, Dipl Stat, Oksche, Alexander, MD, Reimer, Karen, Prof, Winkelmann, Juliane, Prof, Allen, Richard P, PhD, Kohnen, Ralf, PhD

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Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1 von Roepman, Ronald, van Duijnhoven, Gerard, Rosenberg, Thomas, Pinckers, Alfred J. L. G., Bleeker-Wagemakers, Liesbeth M., Bergen, Arthur A. B., Post, Jan, Beck, Alfred, Reinhardt, Richard, Ropers, Hans-Hilger, Cremers, Frans P. M., Berger, Wolfgang

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Physician-Directed Patient Self-Management of Left Atrial Pressure in Advanced Chronic Heart Failure von RITZEMA, Jay, TROUGHTON, Richard, RICHARDS, Mark, EIGLER, Neal L, WHITING, James S, HAAS, Garrie J, HEYWOOD, J. Thomas, FRAMPTON, Christopher M, ABRAHAM, William T, MELTON, Lain, CROZIER, Ian, DOUGHTY, Robert, KRUM, Henry, WALTON, Anthony, ADAMSON, Philip, KAR, Saibal, SHAH, Prediman K

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Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation von Singh, Umashankar, Fohn, Laurel E., Wakayama, Teruhiko, Ohgane, Jun, Steinhoff, Christine, Lipkowitz, Bettina, Schulz, Ralph, Orth, Annie, Ropers, H. Hilger, Behringer, Richard R., Tanaka, Satoshi, Shiota, Kunio, Yanagimachi, Ryuzo, Nuber, Ulrike A., Fundele, Reinald

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Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus von Vikkula, Miikka, Madman, Edwin C.M, Lui, Vincent C.H, Zhidkova, Natalia I, Tiller, George E, Goldring, Mary B, van Beersum, Sylvia E.C, de Waal Malefijt, Maarten C, van den Hoogen, Frank H.J, Ropers, Hans-Hilger, Mayne, Richard, Cheah, Kathryn S.E, Olsen, Bjorn R, Warman, Matthew L, Brunner, Han G

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes von Hu, H, Haas, S.A, Chelly, J, Van Esch, Hilde, Raynaud, M, de Brouwer, A.P.M, Weinert, S, Froyen, Guy, Frints, S.G.M, Laumonnier, F, Zemojtel, T, Love, M.I, Richard, H, Emde, A.-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M.A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K.L, Belet, S, van Roozendaal, K.E.P, Jimenez-Pocquet, M, Moizard, M.-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L.B, Wieacker, P, Rodríguez Criado, G, Bondeson, M.-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, Jean-Pierre, Devriendt, Koenraad, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T.F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T.J, Chen, W, Ropers, H.-H, Kalscheuer, V.M

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes von Hu, H, Haas, SA, Chelly, J, Van Esch, H, Raynaud, M, De Brouwer, APM, Weinert, S, Froyen, G, Frints, SGM, Laumonnier, F, Zemojtel, T, Love, MI, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, MA, Gardner, A, Willis-Owen, S, Tan, C, Friend, KL, Belet, S, Van Roozendaal, KEP, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, Van Boemmel, A, Goeke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Mueller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bielenska, A, Ousager, LB, Wieacker, P, Criado, GR, Bondeson, M-L, Anneren, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, TF, Tzschach, A, Van Bokhoven, H, Gecz, J, Jentsch, TJ, Chen, W, Ropers, H-H, Kalscheuer, VM

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