Cardiac dysfunction in the R6/2 mouse model of Huntington’s disease von Mihm, Michael J, Amann, Deborah M, Schanbacher, Brandon L, Altschuld, Ruth A, Bauer, John Anthony, Hoyt, Kari R

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Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients von Mann, Nina, Braun, Daniela A, Amann, Kassaundra, Tan, Weizhen, Shril, Shirlee, Connaughton, Dervla M, Nakayama, Makiko, Schneider, Ronen, Kitzler, Thomas M, van der Ven, Amelie T, Chen, Jing, Ityel, Hadas, Vivante, Asaf, Majmundar, Amar J, Daga, Ankana, Warejko, Jillian K, Lovric, Svjetlana, Ashraf, Shazia, Jobst-Schwan, Tilman, Widmeier, Eugen, Hugo, Hannah, Mane, Shrikant M, Spaneas, Leslie, Somers, Michael J G, Ferguson, Michael A, Traum, Avram Z, Stein, Deborah R, Baum, Michelle A, Daouk, Ghaleb H, Lifton, Richard P, Manzi, Shannon, Vakili, Khashayar, Kim, Heung Bae, Rodig, Nancy M, Hildebrandt, Friedhelm

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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract von van der Ven, Amelie T, Connaughton, Dervla M, Ityel, Hadas, Mann, Nina, Nakayama, Makiko, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Schulz, Julian, Braun, Daniela A, Schmidt, Johanna Magdalena, Schapiro, David, Schneider, Ronen, Warejko, Jillian K, Daga, Ankana, Majmundar, Amar J, Tan, Weizhen, Jobst-Schwan, Tilman, Hermle, Tobias, Widmeier, Eugen, Ashraf, Shazia, Amar, Ali, Hoogstraaten, Charlotte A, Hugo, Hannah, Kitzler, Thomas M, Kause, Franziska, Kolvenbach, Caroline M, Dai, Rufeng, Spaneas, Leslie, Amann, Kassaundra, Stein, Deborah R, Baum, Michelle A, Somers, Michael J G, Rodig, Nancy M, Ferguson, Michael A, Traum, Avram Z, Daouk, Ghaleb H, Bogdanović, Radovan, Stajić, Natasa, Soliman, Neveen A, Kari, Jameela A, El Desoky, Sherif, Fathy, Hanan M, Milosevic, Danko, Al-Saffar, Muna, Awad, Hazem S, Eid, Loai A, Selvin, Aravind, Senguttuvan, Prabha, Sanna-Cherchi, Simone, Rehm, Heidi L, MacArthur, Daniel G, Lek, Monkol, Laricchia, Kristen M, Wilson, Michael W, Mane, Shrikant M, Lifton, Richard P, Lee, Richard S, Bauer, Stuart B, Lu, Weining, Reutter, Heiko M, Tasic, Velibor, Shril, Shirlee, Hildebrandt, Friedhelm

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Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome von Warejko, Jillian K, Schueler, Markus, Vivante, Asaf, Tan, Weizhen, Daga, Ankana, Lawson, Jennifer A, Braun, Daniela A, Shril, Shirlee, Amann, Kassaundra, Somers, Michael J.G, Rodig, Nancy M, Baum, Michelle A, Daouk, Ghaleb, Traum, Avram Z, Kim, Heung Bae, Vakili, Khashayar, Porras, Diego, Lock, James, Rivkin, Michael J, Chaudry, Gulraiz, Smoot, Leslie B, Singh, Michael N, Smith, Edward R, Mane, Shrikant M, Lifton, Richard P, Stein, Deborah R, Ferguson, Michael A, Hildebrandt, Friedhelm

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Development and evaluation of a manual segmentation protocol for deep grey matter in multiple sclerosis: Towards accelerated semi-automated references von de Sitter, Alexandra, Burggraaff, Jessica, Bartel, Fabian, Palotai, Miklos, Liu, Yaou, Simoes, Jorge, Ruggieri, Serena, Schregel, Katharina, Ropele, Stefan, Rocca, Maria A., Gasperini, Claudio, Gallo, Antonio, Schoonheim, Menno M., Amann, Michael, Yiannakas, Marios, Pareto, Deborah, Wattjes, Mike P., Sastre-Garriga, Jaume, Kappos, Ludwig, Filippi, Massimo, Enzinger, Christian, Frederiksen, Jette, Uitdehaag, Bernard, Guttmann, Charles R.G., Barkhof, Frederik, Vrenken, Hugo

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A Multilocus Technique for Risk Evaluation of Patients with Neuroblastoma von AMBROS, Inge M, BRUNNER, Bettina, GROSS, Nicole, JEISON, Marta, LUNEC, John, MARQUES, Barbara, MARTINSSON, Tommy, MAZZOCCO, Katia, NOGUERA, Rosa, SCHLEIERMACHER, Gudrun, SPELEMAN, Frank, STALLING, Ray, AIGNER, Gerhard, PAOLO TONINI, Gian, TWEDDLE, Deborah A, VALENT, Alexander, VICHA, Ales, VAN ROY, Nadine, VILLAMON, Eva, ZIEGLER, Andrea, PREUNER, Sandra, DROBICS, Mario, LADENSTEIN, Ruth, BEDWELL, Clare, AMANN, Gabriele, SCHUIT, Robert J. L, PÖTSCHGER, Ulrike, AMBROS, Peter F, BEISKE, Klaus, BENARD, Jean, BOWN, Nick, COMBARET, Valerie, COUTURIER, Jerome, DEFFERRARI, Raffaella

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The economic impact of visceral leishmaniasis on households in Bangladesh von Anoopa Sharma, D., Bern, Caryn, Varghese, Beena, Chowdhury, Rajib, Haque, Rashidul, Ali, Mustakim, Amann, Josef, Ahluwalia, Indu B., Wagatsuma, Yukiko, Breiman, Robert F., Maguire, James H., McFarland, Deborah A.

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Development and evaluation of a manual segmentation protocol for deep grey matter in multiple sclerosis : Towards accelerated semi-automated references von de Sitter, Alexandra, Burggraaff, Jessica, Bartel, Fabian, Palotai, Miklos, Liu, Yaou, Simoes, Jorge, Ruggieri, Serena, Schregel, Katharina, Ropele, Stefan, Rocca, Maria A, Gasperini, Claudio, Gallo, Antonio, Schoonheim, Menno M, Amann, Michael, Yiannakas, Marios, Pareto, Deborah, Wattjes, Mike P, Sastre-Garriga, Jaume, Kappos, Ludwig, Filippi, Massimo, Enzinger, Christian, Frederiksen, Jette, Uitdehaag, Bernard, Guttmann, Charles R. G, Barkhof, Frederik, Vrenken, Hugo, Universitat Autònoma de Barcelona

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Development and evaluation of a manual segmentation protocol for deep grey matter in multiple sclerosis : Towards accelerated semi-automated references von de Sitter, Alexandra, Burggraaff, Jessica, Bartel, Fabian, Palotai, Miklos, Liu, Yaou, Simoes, Jorge, Ruggieri, Serena, Schregel, Katharina, Ropele, Stefan, Rocca, Maria A, Gasperini, Claudio, Gallo, Antonio, Schoonheim, Menno M, Amann, Michael, Yiannakas, Marios, Pareto, Deborah, Wattjes, Mike P, Sastre-Garriga, Jaume, Kappos, Ludwig, Filippi, Massimo, Enzinger, Christian, Frederiksen, Jette, Uitdehaag, Bernard, Guttmann, Charles R. G, Barkhof, Frederik, Vrenken, Hugo, Universitat Autònoma de Barcelona

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No Evidence of Pathogenic Involvement of Cathelicidins in Patient Cohorts and Mouse Models of Lupus and Arthritis

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