Understanding familial and non-familial renal cell cancer von Bodmer, Daniëlle, van den Hurk, Wilhelmina, van Groningen, Jan J. M., Eleveld, Marc J., Martens, Gerard J. M., Weterman, Marian A. J., Geurts van Kessel, Ad

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Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21) von Bodmer, Daniëlle, Eleveld, Marc, Kater-Baats, Ellen, Janssen, Irene, Janssen, Bert, Weterman, Marian, Schoenmakers, Eric, Nickerson, Michael, Linehan, Marston, Zbar, Berton, van Kessel, Ad Geurts

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Design and Validation of a Conformation Sensitive Capillary Electrophoresis-Based Mutation Scanning System and Automated Data Analysis of the More than 15 kbp-Spanning Coding Seque... von Vermeer, Sascha, Meijer, Rowdy P.P, Hofste, Tom G.J, Bodmer, Daniëlle, Bosgoed, Ermanno A.J, Cremers, Frans P.M, Kremer, Berry H.P, Knoers, Nine V.A.M, Scheffer, Hans

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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 von van Kessel, Ad Geurts, Hoenselaar, Eveline, Voorendt, Marsha, Kuiper, Roland P, Lee, Tracy Y H, Hendriks-Cornelissen, Sandra J B, Yuen, Siu Tsan, van Krieken, J Han J M, Leung, Suet Yi, Hoogerbrugge, Nicoline, Chan, Tsun Leung, Bodmer, Danielle, Ligtenberg, Marjolijn J L, Goossens, Monique, Hebeda, Konnie M, Tsui, Wai Yin, Brunner, Han G, Kong, Chi Kwan

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Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome von Baas, Annette F, Gabbett, Michael, Rimac, Milan, Kansikas, Minttu, Raphael, Martine, Nievelstein, Rutger Aj, Nicholls, Wayne, Offerhaus, Johan, Bodmer, Danielle, Wernstedt, Annekatrin, Krabichler, Birgit, Strasser, Ulrich, Nyström, Minna, Zschocke, Johannes, Robertson, Stephen P, van Haelst, Mieke M, Wimmer, Katharina

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An Alternative Route for Multistep Tumorigenesis in a Novel Case of Hereditary Renal Cell Cancer and a t(2;3)(q35;q21) Chromosome Translocation von Bodmer, Daniëlle, Eleveld, Marc J., Ligtenberg, Marjolijn J.L., Weterman, Marian A.J., Janssen, Bert A.P., Smeets, Dominique F.C.M., de Wit, Peter E.J., van den Berg, Anke, van den Berg, Eva, Koolen, Marianne I., Geurts van Kessel, Ad

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Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15) von Eleveld, Marc J., Bodmer, Daniëlle, Merkx, Gerard, Siepman, Angélique, Sprenger, Sandra H. E., Weterman, Marian A. J., Ligtenberg, Marjolijn J., Kamp, Jorieke, Stapper, Wim, Jeuken, Judith W. M., Smeets, Dominique, Smits, Arie, Geurts van Kessel, Ad

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Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21) von Bodmer, Daniëlle, Schepens, Marga, Eleveld, Marc J., Schoenmakers, Eric F.P.M., Geurts van Kessel, Ad

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Renal Cell Cancer: Chromosome 3 Translocations as Risk Factors von van Kessel, Ad Geurts, Wijnhoven, Hanncke, Bodmer, Danielle, Eleveld, Marc, Kiemeney, Lambartus, Mulders, Peter, Weterman, Marian, Ligtenberg, Marjolijn, Smeets, Dominique, Smits, Arie

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Unfavorable pathological characteristics in familial colorectal cancer with low-level microsatellite instability von Kets, Carolien M, Hoogerbrugge, Nicoline, Bodmer, Danielle, Willems, Riki, Brunner, Han G, van Krieken, Joannes H J M, Ligtenberg, Marjolijn J L

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A familial case of renal cell carcinoma and a t(2;3) chromosome translocation von Koolen, Marianne I., van der Meyden, Ad P.M., Bodmer, Danielle, Eleveld, Marc, van der Looij, Erica, Brunner, Han, Smits, Arie, van den Berg, Eva, Smeets, Dominique, Geurts van Kessel, Ad

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Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13∼q22 breakpoints von Bodmer, Daniëlle, Janssen, Irene, Jonkers, Yvonne, van den Berg, Eva, Dijkhuizen, Trijnie, Debiec-Rychter, Maria, Schoenmakers, Eric, van Kessel, Ad Geurts

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Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13 approximately q22 breakpoints von Bodmer, Daniëlle, Janssen, Irene, Jonkers, Yvonne, van den Berg, Eva, Dijkhuizen, Trijnie, Debiec-Rychter, Maria, Schoenmakers, Eric, van Kessel, Ad Geurts

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Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene von Bonne, Anita, Vreede, Lilian, Kuiper, Roland P, Bodmer, Danielle, Jansen, Corine, Eleveld, Marc, van Erp, Femke, Arkesteijn, Ger, Hoogerbrugge, Nicoline, van Ravenswaaij, Conny, Schoenmakers, Eric F.P.M, Geurts van Kessel, Ad

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Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21) von Bodmer, Danielle, Eleveld, Marc, Ligtenberg, Marjolijn, Weterman, Marian, van der Meijden, Adrian, Koolen, Marianne, der Kaa, Christien Hulsbergen-van, Smits, Arie, Smeets, Dominique, van Kessel, Ad Geurts

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The Year in Graduate Medical Education: Selected Highlights From 2022 von Patel, Saumil J., Notarianni, Andrew P., Martin, Archer Kilbourne, Tsai, Albert, Pulton, Danielle A., Linganna, Regina, Patel, Prakash A., Waldron, Nathan H., Nimma, Sindhuja R., Bodmer, Natalie J., Kothari, Perin, Jackson, Ethan, Gupta, Ragini G., Roberts, Monique L., Feinman, Jared W.

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Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree von Halvorsen, Matthew, Szatkiewicz, Jin, Mudgal, Poorva, Yu, Dongmei, Nordsletten, Ashley E., Mataix-Cols, David, Mathews, Carol A., Scharf, Jeremiah M., Mattheisen, Manuel, Robertson, Mary M., McQuillin, Andrew, Crowley, James J.

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Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome von Jain, Pritesh, Miller-Fleming, Tyne, Topaloudi, Apostolia, Yu, Dongmei, Drineas, Petros, Georgitsi, Marianthi, Yang, Zhiyu, Rizzo, Renata, Müller-Vahl, Kirsten R., Tumer, Zeynep, Mol Debes, Nanette, Hartmann, Andreas, Depienne, Christel, Worbe, Yulia, Mir, Pablo, Cath, Danielle C., Boomsma, Dorret I., Roessner, Veit, Wolanczyk, Tomasz, Janik, Piotr, Szejko, Natalia, Zekanowski, Cezary, Barta, Csaba, Nemoda, Zsofia, Tarnok, Zsanett, Buxbaum, Joseph D., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Hengerer, Bastian, Benaroya-Milshtein, Noa, Cardona, Francesco, Hedderly, Tammy, Heyman, Isobel, Huyser, Chaim, Morer, Astrid, Mueller, Norbert, Munchau, Alexander, Plessen, Kerstin J., Porcelli, Cesare, Walitza, Susanne, Schrag, Anette, Martino, Davide, Dietrich, Andrea, Mathews, Carol A., Scharf, Jeremiah M., Hoekstra, Pieter J., Davis, Lea K., Paschou, Peristera

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Mycobacterium Microti Infection in the Cat: A Case Report, Literature Review and Recent Clinical Experience von Rüfenacht, Silvia, Bögli-Stuber, Katja, Bodmer, Thomas, Jaunin, Valérie F Bornand, Jmaa, Danielle C Gonin, Gunn-Moore, Danièlle A

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Abstract 419: Conserved Age-associated Cytoskeletal Remodeling Improves Cardiac Function and Lifespan von Kaushik, Gaurav, Spenlehauer, Alice, Sessions, Ayla O, Trujillo, Adriana S, Fuhrmann, Alexander, Fu, Zongming, Venkatraman, Vidya, Pohl, Danielle, Tuler, Jeremy, Wang, Mingyi, Lakatta, Edward G, Ocorr, Karen, Bodmer, Rolf, Bernstein, Sanford I, Van Eyk, Jennifer E, Cammarato, Anthony, Engler, Adam J

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