Classification of non-bacterial osteitis : Retrospective study of clinical, immunological and genetic aspects in 89 patients by JANSSON, A, RENNER, E. D, BELOHRADSKY, B. H, RAMSER, J, MAYER, A, HABAN, M, MEINDL, A, GROTE, V, DIEBOLD, J, JANSSON, V, SCHNEIDER, K

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Keratinocyte growth factor supports pulmonary innate immune defense through maintenance of alveolar antimicrobial protein levels and macrophage function by Gardner, Jason C, Wu, Huixing, Noel, John G, Ramser, Benjamin J, Pitstick, Lori, Saito, Atsushi, Nikolaidis, Nikolaos M, McCormack, Francis X

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Deficits in pattern separation and dentate gyrus proliferation after rodent lateral fluid percussion injury by Correll, Erika A., Ramser, Benjamin J., Knott, Maxon V., McCullumsmith, Robert E., McGuire, Jennifer L., Ngwenya, Laura B.

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The DNA sequence of human chromosome 21 by Sakaki, Y, Hattori, M, Fujiyama, A, Taylor, T. D, Watanabe, H, Yada, T, Park, H.-S, Toyoda, A, Ishii, K, Totoki, Y, Choi, D.-K, Soeda, E, Ohki, M, Takagi, T, Taudien, S, Blechschmidt, K, Polley, A, Menzel, U, Delabar, J, Kumpf, K, Lehmann, R, Patterson, D, Reichwald, K, Rump, A, Schillhabel, M, Schudy, A, Zimmermann, W, Rosenthal, A, Kudoh, J, Shibuya, K, Kawasaki, K, Asakawa, S, Shintani, A, Sasaki, T, Nagamine, K, Mitsuyama, S, Antonarakis, S. E, Minoshima, S, Shimizu, N, Nordsiek, G, Hornischer, K, Brandt, P, Scharfe, M, Schön, O, Desario, A, Reichelt, J, Kauer, G, Blöcker, H, Ramser, J, Beck, A, Klages, S, Hennig, S, Riesselmann, L, Dagand, E, Haaf, T, Wehrmeyer, S, Borzym, K, Gardiner, K, Nizetic, D, Francis, F, Lehrach, H, Reinhardt, R, Yaspo, M.-L

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Thermal injury of the skin induces G-CSF-dependent attenuation of EPO-mediated STAT signaling and erythroid differentiation arrest in mice by Noel, John G., Ramser, Benjamin J., Cancelas, Jose A., McCormack, Francis X., Gardner, Jason C.

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A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9) by Ramser, J, Winnepenninckx, B, Lenski, C, Errijgers, V, Platzer, M, Schwartz, C E, Meindl, A, Kooy, R F

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Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores by Leslie, Goska, Dennis, Joe, Yang, Xin, Adlard, Julian, Agnarsson, Bjarni A, Ahmed, Munaza, Aittomäki, Kristiina, Arnold, Norbert, Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B, Barwell, Julian, Belotti, Muriel, Berthet, Pascaline, Boonen, Susanne E, Borg, Åke, Brennan, Paul, Brewer, Carole, Bucalo, Agostino, Buys, Saundra S, Campbell, Ian, Cassingham, Hayley, Christensen, Lise Lotte, Claes, Kathleen B M, Coppa, Anna, Damante, Giuseppe, Davidson, Rosemarie, De Leeneer, Kim, de Putter, Robin, Del Valle, Jesús, Ding, Yuan Chun, Domchek, Susan M, Donaldson, Alan, Eason, Jacqueline, Eeles, Ros, Evans, D Gareth, Feliubadaló, Lidia, Gehrig, Andrea, Giraud, Sophie, Godwin, Andrew K, Gregory, Helen, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V O, Hentschel, Julia, Horvath, Judit, Izquierdo, Angel, Jensen, Uffe Birk, John, Esther M, Kruse, Torben A, Lautrup, Charlotte, Lesueur, Fabienne, Manoukian, Siranoush, Meindl, Alfons, Monteiro, Alvaro N, Morrison, Patrick J, Muranen, Taru A, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Niederacher, Dieter, Olah, Edith, Olopade, Olufunmilayo I, Palli, Domenico, Parsons, Michael T, Pedersen, Inge Sokilde, Perez-Segura, Pedro, Petersen, Annabeth H, Pinto, Pedro, Pottinger, Caroline, Ramser, Juliane, Rantala, Johanna, Robson, Mark, Rogers, Mark T, Sánchez de Abajo, Ana María, Shah, Payal D, Sharif, Saba, Side, Lucy E, Steele, Linda, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teulé, Alex, Thull, Darcy L, Tischkowitz, Marc, Toland, Amanda E, Tommasi, Stefania, Toss, Angela, Trainer, Alison H, van Asperen, Christi J, Venturelli, Marta, Vijai, Joseph, Walker, Lisa, Wang-Gohrke, Shan, Whaite, Anna, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Chenevix-Trench, Georgia, Ottini, Laura

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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer by Ferreira, Manuel A., Andrulis, Irene L., Anton-Culver, Hoda, Aronson, Kristan J., Barnes, Daniel R., Beckmann, Matthias W., Behrens, Sabine, Bermisheva, Marina, Bogdanova, Natalia V., Bojesen, Stig E., Bolla, Manjeet K., Brauch, Hiltrud, Campa, Daniele, Campbell, Ian, Canzian, Federico, Carter, Jonathan, Castelao, Jose E., Chang-Claude, Jenny, Couch, Fergus J., Cox, Angela, Cross, Simon S., de la Hoya, Miguel, Dennis, Joe, Devilee, Peter, Dörk, Thilo, Ejlertsen, Bent, Engel, Christoph, Eriksson, Mikael, Fletcher, Olivia, Flyger, Henrik, Frost, Debra, Gabrielson, Marike, Gapstur, Susan M., Garber, Judy, García-Sáenz, José A., Giles, Graham G., Glendon, Gord, Godwin, Andrew K., González-Neira, Anna, Gronwald, Jacek, Guénel, Pascal, Hall, Per, Hamann, Ute, He, Wei, Hulick, Peter J., Humphreys, Keith, Isaacs, Claudine, Jakimovska, Milena, Jakubowska, Anna, James, Paul A., John, Esther M., Johnson, Nichola, Karlan, Beth Y., Khusnutdinova, Elza, Kiiski, Johanna I., Jones, Michael E., Konstantopoulou, Irene, Laitman, Yael, Lambrechts, Diether, Lazaro, Conxi, Lindström, Sara, Manoochehri, Mehdi, Margolin, Sara, McGuffog, Lesley, Michailidou, Kyriaki, Montagna, Marco, Moreno, Fernando, Moserle, Lidia, Nevelsteen, Ines, Nussbaum, Robert L., Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I., Osorio, Ana, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peixoto, Ana, Peterlongo, Paolo, Poppe, Bruce, Presneau, Nadege, Risch, Harvey A., Saloustros, Emmanouil, Sanden, Kristin, Simard, Jacques, Singer, Christian F., Soucy, Penny, Spinelli, John J., Spurdle, Amanda B., Taylor, Jack A., Thöne, Kathrin, Toland, Amanda E., Tung, Nadine, Vachon, Celine M., van Asperen, Christi J., van Rensburg, Elizabeth J., Weitzel, Jeffrey N., Winqvist, Robert, Yannoukakos, Drakoulis, Zheng, Wei, Beesley, Jonathan

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Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness by Patel, Vivek L, Busch, Evan L, Friebel, Tara M, Cronin, Angel, Leslie, Goska, McGuffog, Lesley, Adlard, Julian, Agata, Simona, Agnarsson, Bjarni A, Ahmed, Munaza, Aittomäki, Kristiina, Alducci, Elisa, Andrulis, Irene L, Arason, Adalgeir, Arnold, Norbert, Artioli, Grazia, Arver, Brita, Auber, Bernd, Azzollini, Jacopo, Balmaña, Judith, Barkardottir, Rosa B, Barnes, Daniel R, Barroso, Alicia, Barrowdale, Daniel, Belotti, Muriel, Benitez, Javier, Bertelsen, Birgitte, Blok, Marinus J, Bodrogi, Istvan, Bonadona, Valérie, Bonanni, Bernardo, Bondavalli, Davide, Boonen, Susanne E, Borde, Julika, Borg, Ake, Bradbury, Angela R, Brady, Angela, Brewer, Carole, Brunet, Joan, Buecher, Bruno, Buys, Saundra S, Cabezas-Camarero, Santiago, Caldés, Trinidad, Caliebe, Almuth, Caligo, Maria A, Calvello, Mariarosaria, Campbell, Ian G, Carnevali, Ileana, Carrasco, Estela, Chan, Tsun L, Chu, Annie T W, Chung, Wendy K, Claes, Kathleen B M, Collaborators, Gemo Study, Collaborators, Embrace, Cook, Jackie, Cortesi, Laura, Couch, Fergus J, Daly, Mary B, Damante, Giuseppe, Darder, Esther, Davidson, Rosemarie, de la Hoya, Miguel, Puppa, Lara Della, Dennis, Joe, Díez, Orland, Ding, Yuan Chun, Ditsch, Nina, Domchek, Susan M, Donaldson, Alan, Dworniczak, Bernd, Easton, Douglas F, Eccles, Diana M, Eeles, Rosalind A, Ehrencrona, Hans, Ejlertsen, Bent, Engel, Christoph, Evans, D Gareth, Faivre, Laurence, Faust, Ulrike, Feliubadaló, Lídia, Foretova, Lenka, Fostira, Florentia, Fountzilas, George, Frost, Debra, García-Barberán, Vanesa, Garre, Pilar, Gauthier-Villars, Marion, Géczi, Lajos, Gehrig, Andrea, Gerdes, Anne-Marie, Gesta, Paul, Giannini, Giuseppe, Glendon, Gord, Godwin, Andrew K, Goldgar, David E, Greene, Mark H, Gutierrez-Barrera, Angelica M, Hahnen, Eric, Hamann, Ute

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Classification of Non-Bacterial Osteitis by Jansson, A., Renner, E. D., Ramser, J., Mayer, A., Haban, M., Meindl, A., Grote, V., Diebold, J., Jansson, V., Schneider, K., Belohradsky, B. H.

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The DNA sequence of the human X chromosome by Ross, Mark T, Grafham, Darren V, Muzny, Donna, Bird, Christine P, Sudbrak, Ralf, Wen, Gaiping, Jones, Matthew C, Hurles, Matthew E, Whittaker, Adam, Chen, Rui, Cree, Andrew, Gunaratne, Preethi, Havlak, Paul, Metzker, Michael L, Steffen, David, Ambrose, Kerrie D, Ashwell, Robert I. S, Babbage, Anne K, Barrett, Ian P, Beasley, Oliver, Blechschmidt, Karin, Bridgeman, Anne M, Bonnin, David, Buhay, Christian, Burch, Paula, Bye, Jackie M, Carrel, Laura, Chako, Joseph, Chapman, Joanne C, Cole, Charlotte G, Connor, Richard E, Davis, Clay, Davis, John, Delgado, Oliver, DeShazo, Denise, Dodsworth, Steve, Dunham, Andrew, Dunn, Matthew, Eades, Tamsin, Faulkner, Louisa, Galgoczy, Petra, Gill, Rachel, Gregory, Simon G, Gribble, Susan, Griffiths, Coline, Hamilton, Cerissa, Hart, Elizabeth A, Hawes, Alicia, Hennig, Steffen, Hume, Jennifer, Hunt, Paul J, Hunt, Adrienne R, Jacob, Leni, Jones, Sally, Keenan, Stephen, Khan, Ziad, Kioschis, Petra, Kosiura, Anna, Lewis, Lora, Liu, Wen, Lloyd, Christine, Lyne, Rachael, Ma, Jie, Matthews, Lucy H, Mistry, Shailesh L, Morgan, Margaret, Müller, Ines, Nguyen, Ngoc, O'Dell, Christopher N, Palmer, Sophie, Parrish, Julia, Patel, Dina, Pearce, Alex V, Pearson, Danita M, Pelan, Sarah E, Ramsey, Yvonne, Rhodes, Susan, Shownkeen, Ratna, Swann, R. Mark, Swarbreck, David, Thorpe, Andrea, Tromans, Anthony C, d'Urso, Michele, Warren, James, West, Anthony, Whiteley, Mathew N, Williamson, Angela, Wilming, Laurens, Yen, Jennifer, Zhou, Jianling, Buck, David, Poustka, Annemarie, Rosenthal, André, Minx, Patrick J, Willard, Huntington F, Waterston, Robert H, Vaudin, Mark, Nelson, David L, Sulston, John E, Durbin, Richard

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Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy by Ramser, Juliane, Ahearn, Mary Ellen, Lenski, Claus, Yariz, Kemal O., Hellebrand, Heide, von Rhein, Michael, Clark, Robin D., Schmutzler, Rita K., Lichtner, Peter, Hoffman, Eric P., Meindl, Alfons, Baumbach-Reardon, Lisa

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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor by Ramser, Juliane, Abidi, Fatima E., Burckle, Celine A., Lenski, Claus, Toriello, Helga, Wen, Gaiping, Lubs, Herbert A., Engert, Stefanie, Stevenson, Roger E., Meindl, Alfons, Schwartz, Charles E., Nguyen, Genevieve

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Initial sequencing and analysis of the human genome by Lander, E S, Linton, L M, Birren, B, Nusbaum, C, Zody, M C, Baldwin, J, Devon, K, Dewar, K, Doyle, M, FitzHugh, W, Funke, R, Gage, D, Harris, K, Heaford, A, Howland, J, Kann, L, Lehoczky, J, LeVine, R, McEwan, P, McKernan, K, Meldrim, J, Mesirov, J P, Miranda, C, Morris, W, Naylor, J, Raymond, C, Rosetti, M, Santos, R, Sheridan, A, Sougnez, C, Stange-Thomann, Y, Stojanovic, N, Subramanian, A, Wyman, D, Rogers, J, Sulston, J, Ainscough, R, Beck, S, Bentley, D, Burton, J, Clee, C, Carter, N, Coulson, A, Deadman, R, Deloukas, P, Dunham, A, Dunham, I, Durbin, R, French, L, Grafham, D, Gregory, S, Hubbard, T, Humphray, S, Hunt, A, Jones, M, Lloyd, C, McMurray, A, Matthews, L, Mercer, S, Milne, S, Mullikin, J C, Mungall, A, Plumb, R, Ross, M, Shownkeen, R, Sims, S, Waterston, R H, Wilson, R K, Hillier, L W, McPherson, J D, Marra, M A, Mardis, E R, Fulton, L A, Chinwalla, A T, Pepin, K H, Gish, W R, Chissoe, S L, Wendl, M C, Delehaunty, K D, Miner, T L, Delehaunty, A, Kramer, J B, Cook, L L, Fulton, R S, Johnson, D L, Minx, P J, Clifton, S W, Hawkins, T, Branscomb, E, Predki, P, Richardson, P, Wenning, S, Slezak, T, Doggett, N, Cheng, J F, Olsen, A, Lucas, S, Elkin, C, Uberbacher, E, Frazier, M

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Hybridization of microsatellites to RAPD: a new source of polymorphic markers by Richardson, T., Cato, S., Ramser, J., Kahl, G., Weising, K.

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Abstract P3-09-04: Beyond CHEK2 in breast cancer: Search for additional moderately penetrant risk gene variants by analyzing the oligogenic disease course in CHEK2 mutation carrier... by Pohl, E, Richters, L, Hauke, J, Ernst, C, Kröber, S, Niederacher, D, Arnold, N, Ramser, J, Groß, E, Gehrig, A, Schmidt, G, Dutrannoy, V, Kast, K, Hahnen, E, Schmutzler, R

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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers by Hakkaart, Christopher, Pearson, John F., Marquart, Louise, Wiggins, George A. R., Barnes, Daniel R., Robinson, Bridget A., Andrulis, Irene L., Arun, Banu K., Balmaña, Judith, Barkardottir, Rosa B., Berger, Lieke, Boonen, Susanne E., Borde, Julika, Buys, Saundra S., Caligo, Maria A., Campbell, Ian, Chung, Wendy K., Claes, Kathleen B. M., Collonge-Rame, Marie-Agnès, Cook, Jackie, Couch, Fergus J., de la Hoya, Miguel, de Putter, Robin, Dhawan, Mallika, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M., Donaldson, Alan, Easton, Douglas F., Ehrencrona, Hans, Engel, Christoph, Evans, D. Gareth, Faust, Ulrike, Feliubadaló, Lidia, Fostira, Florentia, Garber, Judy, Gayther, Simon A., Gehrig, Andrea, Godwin, Andrew K., Goldgar, David E., Greene, Mark H., Hahnen, Eric, Hamann, Ute, Hansen, Thomas V. O., Hentschel, Julia, Herold, Natalie, Isaacs, Claudine, Izquierdo, Angel, Janavicius, Ramunas, Karlan, Beth Y., Kemp, Zoe, Kirk, Judy, Konstantopoulou, Irene, Koudijs, Marco, Kwong, Ava, Laitman, Yael, Lasset, Christine, Lazaro, Conxi, Leslie, Goska, Mai, Phuong L., Mari, Véronique, Martens, John W. M., McGuffog, Lesley, Mebirouk, Noura, Meindl, Alfons, Miller, Austin, Moserle, Lidia, Mouret-Fourme, Emmanuelle, Musgrave, Hannah, Neuhausen, Susan L., Nevanlinna, Heli, Yie, Joanne Ngeow Yuen, Olah, Edith, Olopade, Olufunmilayo I., Osorio, Ana, Park, Sue K., Parsons, Michael T., Pedersen, Inge Sokilde, Peixoto, Ana, Perez-Segura, Pedro, Pocza, Timea, Radice, Paolo, Rossing, Maria, Schmutzler, Rita K., Shah, Payal D., Side, Lucy E., Singer, Christian F., Steinemann, Doris, Stoppa-Lyonnet, Dominique, Teo, Soo Hwang, Thull, Darcy L., Toland, Amanda E., Trainer, Alison H., Vega, Ana, Viel, Alessandra, Walker, Lisa, Weitzel, Jeffrey N., Chenevix-Trench, Georgia, Spurdle, Amanda B., Walker, Logan C.

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The Reduced Expression of the HADH2 Protein Causes X-Linked Mental Retardation, Choreoathetosis, and Abnormal Behavior by Lenski, Claus, Frank Kooy, R., Reyniers, Edwin, Loessner, Daniela, Wanders, Ronald J.A., Winnepenninckx, Birgitta, Hellebrand, Heide, Engert, Stefanie, Schwartz, Charles E., Meindl, Alfons, Ramser, Juliane

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DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements by KIRSCHNER, Renate, ERTURK, Deniz, ZEITZ, Christina, SAHIN, Selen, RAMSER, Juliane, CREMERS, Frans P. M, ROPERS, H.-Hilger, BERGER, Wolfgang

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Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump by Sudbrak, R, Brown, J, Dobson-Stone, C, Carter, S, Ramser, J, White, J, Healy, E, Dissanayake, M, Larrègue, M, Perrussel, M, Lehrach, H, Munro, C S, Strachan, T, Burge, S, Hovnanian, A, Monaco, A P

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