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Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report 由 Danyel, Magdalena, Suk, Eun Kyung, Raile, Vera, Gellermann, Jutta, Knaus, Alexej, Horn, Denise

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Fosmid-based whole genome haplotyping of a HapMap trio child: evaluation of Single Individual Haplotyping techniques 由 Duitama, Jorge, McEwen, Gayle K., Huebsch, Thomas, Palczewski, Stefanie, Schulz, Sabrina, Verstrepen, Kevin, Suk, Eun-Kyung, Hoehe, Margret R.

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Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha population 由 Suk, Eun-Kyung, Malkin, Ida, Dahm, Stefan, Kalichman, Leonid, Ruf, Nico, Kobyliansky, Eugene, Toliat, Mohammad, Rutsch, Frank, Nürnberg, Peter, Livshits, Gregory

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Multiple haplotype-resolved genomes reveal population patterns of gene and protein diplotypes 由 Hoehe, Margret R., Church, George M., Lehrach, Hans, Kroslak, Thomas, Palczewski, Stefanie, Nowick, Katja, Schulz, Sabrina, Suk, Eun-Kyung, Huebsch, Thomas

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A comprehensively molecular haplotype-resolved genome of a European individual 由 Suk, Eun-Kyung, McEwen, Gayle K., Duitama, Jorge, Nowick, Katja, Schulz, Sabrina, Palczewski, Stefanie, Schreiber, Stefan, Holloway, Dustin T., McLaughlin, Stephen, Peckham, Heather, Lee, Clarence, Huebsch, Thomas, Hoehe, Margret R.

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De novo variants in ATP2B1 lead to neurodevelopmental delay 由 Rahimi, Meer Jacob, Urban, Nicole, Wegler, Meret, Sticht, Heinrich, Schaefer, Michael, Popp, Bernt, Gaunitz, Frank, Morleo, Manuela, Nigro, Vincenzo, Maitz, Silvia, Mancini, Grazia M.S., Ruivenkamp, Claudia, Suk, Eun-Kyung, Bartolomaeus, Tobias, Merkenschlager, Andreas, Koboldt, Daniel, Bartholomew, Dennis, Stegmann, Alexander P.A., Sinnema, Margje, Duynisveld, Irma, Salvarinova, Ramona, Race, Simone, de Vries, Bert B.A., Trimouille, Aurélien, Naudion, Sophie, Marom, Daphna, Hamiel, Uri, Henig, Noa, Demurger, Florence, Rahner, Nils, Bartels, Enrika, Hamm, J. Austin, Putnam, Abbey M., Person, Richard, Abou Jamra, Rami, Oppermann, Henry

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PEDIA: prioritization of exome data by image analysis 由 Hsieh, Tzung-Chien, Mensah, Martin A., Pantel, Jean T., Aguilar, Dione, Bar, Omri, Bayat, Allan, Becerra-Solano, Luis, Bentzen, Heidi B., Biskup, Saskia, Borisov, Oleg, Braaten, Oivind, Ciaccio, Claudia, Coutelier, Marie, Cremer, Kirsten, Danyel, Magdalena, Daschkey, Svenja, Eden, Hilda David, Devriendt, Koenraad, Wilson, Sandra, Douzgou, Sofia, Đukić, Dejan, Ehmke, Nadja, Fauth, Christine, Fischer-Zirnsak, Björn, Fleischer, Nicole, Gabriel, Heinz, Graul-Neumann, Luitgard, Gripp, Karen W., Gurovich, Yaron, Gusina, Asya, Haddad, Nechama, Hajjir, Nurulhuda, Hanani, Yair, Hertzberg, Jakob, Hoertnagel, Konstanze, Howell, Janelle, Ivanovski, Ivan, Kaindl, Angela, Kamphans, Tom, Kamphausen, Susanne, Karimov, Catherine, Kathom, Hadil, Keryan, Anna, Knaus, Alexej, Köhler, Sebastian, Kornak, Uwe, Lavrov, Alexander, Leitheiser, Maximilian, Lyon, Gholson J., Mangold, Elisabeth, Reina, Purificación Marín, Carrascal, Antonio Martinez, Mitter, Diana, Herrador, Laura Morlan, Nadav, Guy, Nöthen, Markus, Orrico, Alfredo, Ott, Claus-Eric, Park, Kristen, Peterlin, Borut, Pölsler, Laura, Raas-Rothschild, Annick, Randolph, Linda, Revencu, Nicole, Fagerberg, Christina Ringmann, Robinson, Peter Nick, Rosnev, Stanislav, Rudnik, Sabine, Rudolf, Gorazd, Schatz, Ulrich, Schossig, Anna, Schubach, Max, Shanoon, Or, Sheridan, Eamonn, Smirin-Yosef, Pola, Spielmann, Malte, Suk, Eun-Kyung, Sznajer, Yves, Thiel, Christian T., Thiel, Gundula, Verloes, Alain, Vrecar, Irena, Wahl, Dagmar, Weber, Ingrid, Winter, Korina, Wiśniewska, Marzena, Wollnik, Bernd, Yeung, Ming W., Zhao, Max, Zhu, Na, Zschocke, Johannes, Mundlos, Stefan, Horn, Denise, Krawitz, Peter M.

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