OS-021-YI Molecular phenotype of chronic antibody-mediated rejection in liver transplant biopsies von Engel, Bastian, Alaswad, Ahmed, Campos-Murguia, Alejandro, Zoodsma, Martijn, Höffer, Anne, Chihab, Kinan, Bosselmann, Emily, Heinrich, Sophia, Hartleben, Björn, Jonigk, Danny, Hallensleben, Michael, Murielle, Verboom, Geffers, Robert, Wedemeyer, Heiner, Xu, Chengjian, Mensah, Angelina, Kirchner, Theresa, Jaeckel, Elmar, Li, Yang, Taubert, Richard

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Relevance and Narrative (Research) – An International Symposium“, Bergische Universität Wuppertal, 30.09.-02.10.2014 von Daniel Becker, Anne-Catherine Höffer

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Relational Bureaucracy: Structuring Reciprocal Relationships into Roles von Gittell, Jody Hoffer, Douglass, Anne

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Classifying aerosol type using in situ surface spectral aerosol optical properties von Schmeisser, Lauren, Andrews, Elisabeth, Ogren, John A, Sheridan, Patrick, Jefferson, Anne, Sharma, Sangeeta, Kim, Jeong Eun, Sherman, James P, Sorribas, Mar, Kalapov, Ivo, Arsov, Todor, Angelov, Christo, Mayol-Bracero, Olga L, Labuschagne, Casper, Kim, Sang-Woo, Hoffer, András, Lin, Neng-Huei, Chia, Hao-Ping, Bergin, Michael, Sun, Junying, Liu, Peng, Wu, Hao

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Activity of Vincristine and Irinotecan in Diffuse Anaplastic Wilms Tumor and Therapy Outcomes of Stage II to IV Disease: Results of the Children's Oncology Group AREN0321 Study von Daw, Najat C, Chi, Yueh-Yun, Kalapurakal, John A, Kim, Yeonil, Hoffer, Fredric A, Geller, James I, Perlman, Elizabeth J, Ehrlich, Peter F, Mullen, Elizabeth A, Warwick, Anne B, Grundy, Paul E, Paulino, Arnold C, Gratias, Eric, Ward, Deborah, Anderson, James R, Khanna, Geetika, Tornwall, Brett, Fernandez, Conrad V, Dome, Jeffrey S

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A potential gain-of-function variant of SLC9A6 leads to endosomal alkalinization and neuronal atrophy associated with Christianson Syndrome von Ilie, Alina, Gao, Andy Y.L., Boucher, Annie, Park, Jaeok, Berghuis, Albert M., Hoffer, Mariëtte J.V., Hilhorst-Hofstee, Yvonne, McKinney, R. Anne, Orlowski, John

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Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study von Groot‐van der Mooren, Maurike, Graaf, Gert, Weijerman, Michel E, Hoffer, Mariette J. V, Knijnenburg, Jeroen, Kevie‐Kersemaekers, Anne‐Marie M. F, Kooper, Angelique J. A, Voorhoeve, Els, Sikkema‐Raddatz, Birgit, Zutven, Laura J. C. M, Srebniak, Malgorzata Ilona, Huijsdens‐van Amsterdam, Karin, Engelen, John J. M, Smeets, Dominique, Kaam, Anton H, Cornel, Martina C

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Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome von van der Laan, Liselot, Rooney, Kathleen, Alders, Mariëlle, Relator, Raissa, McConkey, Haley, Kerkhof, Jennifer, Levy, Michael A, Lauffer, Peter, Aerden, Mio, Theunis, Miel, Legius, Eric, Tedder, Matthew L, Vissers, Lisenka E L M, Koene, Saskia, Ruivenkamp, Claudia, Hoffer, Mariette J V, Wieczorek, Dagmar, Bramswig, Nuria C, Herget, Theresia, González, Vanesa López, Santos-Simarro, Fernando, Tørring, Pernille M, Denomme-Pichon, Anne-Sophie, Isidor, Bertrand, Keren, Boris, Julia, Sophie, Schaefer, Elise, Francannet, Christine, Maillard, Pierre-Yves, Misra-Isrie, Mala, Van Esch, Hilde, Mannens, Marcel M A M, Sadikovic, Bekim, van Haelst, Mieke M, Henneman, Peter

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Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency von Zawerton, Ash, Mignot, Cyril, Sigafoos, Ashley, Blackburn, Patrick R., Haseeb, Abdul, McWalter, Kirsty, Ichikawa, Shoji, Nava, Caroline, Keren, Boris, Charles, Perrine, Marey, Isabelle, Tabet, Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca, Gaetan, Schluth-Bolard, Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto, Maria J., Schnur, Rhonda E., Zhu, Zehua, Poisson, Alice, El Chehadeh, Salima, Alembik, Yves, Bruel, Ange-Line, Lehalle, Daphné, Nambot, Sophie, Moutton, Sébastien, Odent, Sylvie, Jaillard, Sylvie, Dubourg, Christèle, Hilhorst-Hofstee, Yvonne, Barbaro-Dieber, Tina, Ortega, Lucia, Bhoj, Elizabeth J., Masser-Frye, Diane, Bird, Lynne M., Lindstrom, Kristin, Ramsey, Keri M., Narayanan, Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G., Akilapa, Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H., Klein Wassink-Ruiter, Jolien S., Bijlsma, Emilia, Hoffer, Mariëtte, Vargas, Marcelo, Wojcik, Antonina, Cherik, Florian, Francannet, Christine, Rosenfeld, Jill A., Machol, Keren, Scott, Daryl A., Bacino, Carlos A., Wang, Xia, Clark, Gary D., Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H., Akay, Ela, Chang, Richard C., Bressi, Rebekah, Sanchez Russo, Rossana, Srour, Myriam, Russell, Laura, Goyette, Anne-Marie E., Dupuis, Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Joseph, Maries, Nizon, Mathilde, Cogné, Benjamin, Kuechler, Alma, Piton, Amélie, Klee, Eric W., Lefebvre, Véronique, Clark, Karl J., Depienne, Christel

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OVERVIEW OF THE NOAA/ESRL FEDERATED AEROSOL NETWORK von Andrews, Elisabeth, Sheridan, Patrick J., Ogren, John A., Hageman, Derek, Jefferson, Anne, Wendell, Jim, Alástuey, Andrés, Alados-Arboledas, Lucas, Bergin, Michael, Ealo, Marina, Hallar, A. Gannet, Hoffer, András, Kalapov, Ivo, Keywood, Melita, Kim, Jeongeun, Kim, Sang-Woo, Kolonjari, Felicia, Labuschagne, Casper, Lin, Neng-Huei, Macdonald, AnneMarie, Mayol-Bracero, Olga L., McCubbin, Ian B., Pandolfi, Marco, Reisen, Fabienne, Sharma, Sangeeta, Sherman, James P., Sorribas, Mar, Sun, Junying

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Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis von Fenwick, Aimee L., Kliszczak, Maciej, Cooper, Fay, Murray, Jennie, Sanchez-Pulido, Luis, Twigg, Stephen R.F., Goriely, Anne, McGowan, Simon J., Miller, Kerry A., Taylor, Indira B., Logan, Clare, Bozdogan, Sevcan, Danda, Sumita, Dixon, Joanne, Elsayed, Solaf M., Elsobky, Ezzat, Gardham, Alice, Hoffer, Mariette J.V., Koopmans, Marije, McDonald-McGinn, Donna M., Santen, Gijs W.E., Savarirayan, Ravi, de Silva, Deepthi, Vanakker, Olivier, Wall, Steven A., Wilson, Louise C., Yuregir, Ozge Ozalp, Zackai, Elaine H., Ponting, Chris P., Jackson, Andrew P., Wilkie, Andrew O.M., Niedzwiedz, Wojciech, Bicknell, Louise S.

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Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group von Ehrlich, Peter F., Chi, Yueh‐Yun, Chintagumpala, Murali M., Hoffer, Fredric A., Perlman, Elizabeth J., Kalapurakal, John A., Tornwall, Brett, Warwick, Anne, Shamberger, Robert C., Khanna, Geetika, Hamilton, Thomas E., Gow, Kenneth W., Paulino, Arnold C., Gratias, Eric J., Mullen, Elizabeth A., Geller, James I., Grundy, Paul E., Fernandez, Conrad V., Dome, Jeffrey S.

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Cochlear Implants in Neurologically Impaired Children: A Survey of Health-Related Quality of Life von Anne, Samantha, Schwartz, Seth Roslow, McCoy, Jennifer L., Haberkamp, Thomas, Hoffer, Michael E., Chi, David H.

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Outcomes based on histopathologic response to preoperative chemotherapy in children with bilateral Wilms tumor: A prospective study (COG AREN0534) von Chintagumpala, Murali M., Perlman, Elizabeth J., Tornwall, Brett, Chi, Yueh‐Yun, Kim, Yeonil, Hoffer, Fredric A., Kalapurakal, John A., Warwick, Anne B., Shamberger, Robert C., Khanna, Geetika, Hamilton, Thomas E., Gow, Kenneth W., Paulino, Arnold C., Gratias, Eric J., Mullen, Elizabeth A., Geller, James I., Fernandez, Conrad V., Ritchey, Michael L., Grundy, Paul E., Dome, Jeffrey S., Ehrlich, Peter F.

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Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data von Shi, Huwenbo, Kichaev, Gleb, Pasaniuc, Bogdan

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Preventing Episodic Migraine With Caloric Vestibular Stimulation: A Randomized Controlled Trial von Wilkinson, David, Ade, Kristen K., Rogers, Lesco L., Attix, Deborah K., Kuchibhatla, Maragatha, Slade, Martin D., Smith, Lanty L., Poynter, Kathryn P., Laskowitz, Daniel T., Freeman, Marshall C., Hoffer, Michael E., Saper, Joel R., Scott, Dianne L., Sakel, Mohamed, Calhoun, Anne H., Black, Robert D.

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High throughput qPCR analyses suggest that Enterobacterales of French sheep and cow cheese rarely carry genes conferring resistances to critically important antibiotics for human m... von Delannoy, Sabine, Hoffer, Corine, Tran, Maï-Lan, Madec, Jean-Yves, Brisabois, Anne, Fach, Patrick, Haenni, Marisa

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Putting genome-wide sequencing in neonates into perspective von van der Sluijs, Pleuntje J., Aten, Emmelien, Barge-Schaapveld, Daniela Q. C. M., Bijlsma, Emilia K., Bökenkamp-Gramann, Regina, Donker Kaat, Laura, van Doorn, Remco, van de Putte, Dietje Fransen, van Haeringen, Arie, ten Harkel, Arend D. J., Hilhorst-Hofstee, Yvonne, Hoffer, Mariette J. V., den Hollander, Nicolette S., van Ierland, Yvette, Koopmans, Marije, Kriek, Marjolein, Moghadasi, Setareh, Nibbeling, Esther A. R., Peeters-Scholte, Cacha M. P. C. D., Potjer, Thomas P., van Rij, Maartje, Ruivenkamp, Claudia A. L., Rutten, Julie W., Steggerda, Sylke J., Suerink, Manon, Tan, Ratna N. G. B., van der Tuin, Karin, Visser, Remco, van der Werf –’t Lam, Anne-Sophie, Williams, Monique, Witlox, Ruben, Santen, Gijs W. E.

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Kidney Preservation and Wilms Tumor Development in Children with Diffuse Hyperplastic Perilobar Nephroblastomatosis: A Report from the Children’s Oncology Group Study AREN0534 von Ehrlich, Peter F., Tornwall, Brett, Chintagumpala, Murali M., Chi, Yueh-Yun, Hoffer, Fredric A., Perlman, Elizabeth J., Kalapurakal, John A., Warwick, Anne, Shamberger, Robert C., Khanna, Geetika, Hamilton, Thomas E., Gow, Kenneth W., Paulino, Arnold C., Gratias, Eric J., Mullen, Elizabeth A., Geller, James I., Fernandez, Conrad V., Dome, Jeffrey S.

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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism von Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta M., Kaur, Anupriya, Kaur, Parneet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia M.S., Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra E., Wilke, Martina, Thompson, Michelle L., Bebin, E. Martina, Bijlsma, Emilia K., Hoffer, Mariette J.V., Peeters-Scholte, Cacha, Slavotinek, Anne, Weiss, William A., Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Willaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Yachelevich, Naomi, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Klöckner, Chiara, Kamphausen, Susanne B., Abou Jamra, Rami, Arelin, Maria, Innes, A. Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damian, de Burca, Anna, Kini, Usha, Delatycki, Martin B., Gallacher, Lyndon, Yeung, Alison, Pais, Lynn, Field, Michael, Martin, Ellenore, Charles, Perrine, Courtin, Thomas, Keren, Boris, Iascone, Maria, Cereda, Anna, Poke, Gemma, Abadie, Véronique, Chalouhi, Christel, Parthasarathy, Padmini, Halliday, Benjamin J., Robertson, Stephen P., Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher T.

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