Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier von Li, Huiqing, Edie, Sarah, Klinedinst, Donna, Jeong, Jun Seop, Blackshaw, Seth, Maslen, Cheryl L, Reeves, Roger H

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Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio von Edie, Sarah, Zaghloul, Norann A, Leitch, Carmen C, Klinedinst, Donna K, Lebron, Janette, Thole, Joey F, McCallion, Andrew S, Katsanis, Nicholas, Reeves, Roger H

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Heterotopic ossifications in a mouse model of albright hereditary osteodystrophy von Huso, David L, Edie, Sarah, Levine, Michael A, Schwindinger, William, Wang, Yingli, Jüppner, Harald, Germain-Lee, Emily L

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High-throughput discovery of novel developmental phenotypes von Dickinson, Mary E., Flenniken, Ann M., Ji, Xiao, Teboul, Lydia, Wong, Michael D., White, Jacqueline K., Meehan, Terrence F., Weninger, Wolfgang J., Westerberg, Henrik, Adissu, Hibret, Baker, Candice N., Bower, Lynette, Brown, James M., Caddle, L. Brianna, Chiani, Francesco, Clary, Dave, Cleak, James, Daly, Mark J., Denegre, James M., Doe, Brendan, Dolan, Mary E., Edie, Sarah M., Fuchs, Helmut, Gailus-Durner, Valerie, Galli, Antonella, Gambadoro, Alessia, Gallegos, Juan, Guo, Shiying, Horner, Neil R., Hsu, Chih-Wei, Johnson, Sara J., Kalaga, Sowmya, Keith, Lance C., Lanoue, Louise, Lawson, Thomas N., Lek, Monkol, Mark, Manuel, Marschall, Susan, Mason, Jeremy, McElwee, Melissa L., Newbigging, Susan, Nutter, Lauryl M. J., Peterson, Kevin A., Ramirez-Solis, Ramiro, Rowland, Douglas J., Ryder, Edward, Samocha, Kaitlin E., Seavitt, John R., Selloum, Mohammed, Szoke-Kovacs, Zsombor, Tamura, Masaru, Trainor, Amanda G., Tudose, Ilinca, Wakana, Shigeharu, Warren, Jonathan, Wendling, Olivia, West, David B., Wong, Leeyean, Yoshiki, Atsushi, Wurst, Wolfgang, MacArthur, Daniel G., Tocchini-Valentini, Glauco P., Gao, Xiang, Flicek, Paul, Bradley, Allan, Skarnes, William C., Justice, Monica J., Parkinson, Helen E., Moore, Mark, Wells, Sara, Braun, Robert E., Svenson, Karen L., de Angelis, Martin Hrabe, Herault, Yann, Mohun, Tim, Mallon, Ann-Marie, Henkelman, R. Mark, Brown, Steve D. M., Adams, David J., Lloyd, K. C. Kent, McKerlie, Colin, Beaudet, Arthur L., Bućan, Maja, Murray, Stephen A.

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The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4 von Luzzio, Alana, Edie, Sarah, Palmer, Kristina, Caddle, L. Brianna, Urban, Rachel, Goodwin, Leslie O., Welsh, Ian C., Reinholdt, Laura G., Bergstrom, David E., Cox, Timothy C., Donahue, Leah Rae, Murray, Stephen A.

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PRESERVING AND PROTECTING THE CEREBROVASCULATURE IN MOUSE MODELS WITH A GENETIC PREDISPOSITION FOR DEMENTIA von Foley, Kate E., Graham, Leah, Williams, Harriet M., Soto, Ileana, Yang, Stanley, Edie, Sarah, Murray, Steve, Sasner, Michael, Howell, Gareth

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P1‐134: PRESERVING AND PROTECTING THE CEREBROVASCULATURE IN MOUSE MODELS WITH A GENETIC PREDISPOSITION FOR DEMENTIA von Foley, Kate E., Graham, Leah, Williams, Harriet M., Soto, Ileana, Yang, Stanley, Edie, Sarah, Murray, Steve, Sasner, Michael, Howell, Gareth

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Penetrance of Congenital Heart Disease in a Mouse Model of Down Syndrome Depends on a Trisomic Potentiator of a Disomic Modifier von Li, Huiqing, Edie, Sarah, Klinedinst, Donna, Jeong, Jun Seop, Blackshaw, Seth, Maslen, Cheryl L, Reeves, Roger H

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SVEP1 plays a crucial role in epidermal differentiation von Samuelov, Liat, Li, Qiaoli, Bochner, Ron, Najor, Nicole A., Albrecht, Lauren, Malchin, Natalia, Goldsmith, Tomer, Grafi‐Cohen, Meital, Vodo, Dan, Fainberg, Gilad, Meilik, Benjamin, Goldberg, Ilan, Warshauer, Emily, Rogers, Tova, Edie, Sarah, Ishida‐Yamamoto, Akemi, Burzenski, Lisa, Erez, Noam, Murray, Steve A., Irvine, Alan D., Shultz, Lenny, Green, Kathleen J., Uitto, Jouni, Sprecher, Eli, Sarig, Ofer

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SVEP 1 plays a crucial role in epidermal differentiation von Samuelov, Liat, Li, Qiaoli, Bochner, Ron, Najor, Nicole A., Albrecht, Lauren, Malchin, Natalia, Goldsmith, Tomer, Grafi‐Cohen, Meital, Vodo, Dan, Fainberg, Gilad, Meilik, Benjamin, Goldberg, Ilan, Warshauer, Emily, Rogers, Tova, Edie, Sarah, Ishida‐Yamamoto, Akemi, Burzenski, Lisa, Erez, Noam, Murray, Steve A., Irvine, Alan D., Shultz, Lenny, Green, Kathleen J., Uitto, Jouni, Sprecher, Eli, Sarig, Ofer

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Correction: Corrigendum: High-throughput discovery of novel developmental phenotypes von Dickinson, Mary E., Flenniken, Ann M., Ji, Xiao, Teboul, Lydia, Wong, Michael D., White, Jacqueline K., Meehan, Terrence F., Weninger, Wolfgang J., Westerberg, Henrik, Adissu, Hibret, Baker, Candice N., Bower, Lynette, Brown, James M., Caddle, L. Brianna, Chiani, Francesco, Clary, Dave, Cleak, James, Daly, Mark J., Denegre, James M., Doe, Brendan, Dolan, Mary E., Edie Helmut Fuchs, Sarah M., Gailus-Durner, Valerie, Galli, Antonella, Gambadoro, Alessia, Gallegos, Juan, Guo, Shiying, Horner, Neil R., Hsu, Chih-Wei, Johnson, Sara J., Kalaga, Sowmya, Keith, Lance C., Lanoue, Louise, Lawson, Thomas N., Lek, Monkol, Mark, Manuel, Marschall, Susan, Mason, Jeremy, McElwee, Melissa L., Nutter, Susan Newbigging Lauryl M. J., Peterson, Kevin A., Ramirez-Solis, Ramiro, Rowland, Douglas J., Ryder, Edward, Samocha, Kaitlin E., Seavitt, John R., Selloum, Mohammed, Szoke-Kovacs, Zsombor, Tamura, Masaru, Trainor, Amanda G., Tudose, Ilinca, Wakana, Shigeharu, Warren, Jonathan, Wendling, Olivia, West, David B., Wong, Leeyean, Yoshiki, Atsushi, Wurst, Wolfgang, MacArthur, Daniel G., Tocchini-Valentini, Glauco P., Gao, Xiang, Flicek, Paul, Bradley, Allan, Skarnes, William C., Justice, Monica J., Parkinson, Helen E., Moore, Mark, Wells, Sara, Braun, Robert E., Svenson, Karen L., de Angelis, Martin Hrabe, Herault, Yann, Mohun, Tim, Mallon, Ann-Marie, Henkelman, R. Mark, Brown, Steve D. M., Adams, David J., Lloyd, K. C. Kent, McKerlie, Colin, Beaudet, Arthur L., Murray, Maja Bućan Stephen A.

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Erratum: Corrigendum: High-throughput discovery of novel developmental phenotypes von Dickinson, Mary E., Flenniken, Ann M., Ji, Xiao, Teboul, Lydia, Wong, Michael D., White, Jacqueline K., Meehan, Terrence F., Weninger, Wolfgang J., Westerberg, Henrik, Adissu, Hibret, Baker, Candice N., Bower, Lynette, Brown, James M., Caddle, L. Brianna, Chiani, Francesco, Clary, Dave, Cleak, James, Daly, Mark J., Denegre, James M., Doe, Brendan, Dolan, Mary E., Edie Helmut Fuchs, Sarah M., Gailus-Durner, Valerie, Galli, Antonella, Gambadoro, Alessia, Gallegos, Juan, Guo, Shiying, Horner, Neil R., Hsu, Chih-Wei, Johnson, Sara J., Kalaga, Sowmya, Keith, Lance C., Lanoue, Louise, Lawson, Thomas N., Lek, Monkol, Mark, Manuel, Marschall, Susan, Mason, Jeremy, McElwee, Melissa L., Nutter, Susan Newbigging Lauryl M. J., Peterson, Kevin A., Ramirez-Solis, Ramiro, Rowland, Douglas J., Ryder, Edward, Samocha, Kaitlin E., Seavitt, John R., Selloum, Mohammed, Szoke-Kovacs, Zsombor, Tamura, Masaru, Trainor, Amanda G., Tudose, Ilinca, Wakana, Shigeharu, Warren, Jonathan, Wendling, Olivia, West, David B., Wong, Leeyean, Yoshiki, Atsushi, Wurst, Wolfgang, MacArthur, Daniel G., Tocchini-Valentini, Glauco P., Gao, Xiang, Flicek, Paul, Bradley, Allan, Skarnes, William C., Justice, Monica J., Parkinson, Helen E., Moore, Mark, Wells, Sara, Braun, Robert E., Svenson, Karen L., de Angelis, Martin Hrabe, Herault, Yann, Mohun, Tim, Mallon, Ann-Marie, Henkelman, R. Mark, Brown, Steve D. M., Adams, David J., Lloyd, K. C. Kent, McKerlie, Colin, Beaudet, Arthur L., Murray, Maja Bućan Stephen A.

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High-throughput discovery of novel developmental phenotypes von Dickinson, Mary E, Flenniken, Ann M, Ji, Xiao, Teboul, Lydia, Wong, Michael D, White, Jacqueline K, Meehan, Terrence F, Weninger, Wolfgang J, Westerberg, Henrik, Adissu, Hibret, Baker, Candice N, Bower, Lynette, Brown, James M, Caddle, L Brianna, Chiani, Francesco, Clary, Dave, Cleak, James, Daly, Mark J, Denegre, James M, Doe, Brendan, Dolan, Mary E, Edie, Sarah M, Fuchs, Helmut, Gailus-Durner, Valerie, Galli, Antonella, Gambadoro, Alessia, Gallegos, Juan, Guo, Shiying, Horner, Neil R, Hsu, Chih-Wei, Johnson, Sara J, Kalaga, Sowmya, Keith, Lance C, Lanoue, Louise, Lawson, Thomas N, Lek, Monkol, Mark, Manuel, Marschall, Susan, Mason, Jeremy, McElwee, Melissa L, Newbigging, Susan, Nutter, Lauryl MJ, Peterson, Kevin A, Ramirez-Solis, Ramiro, Rowland, Douglas J, Ryder, Edward, Samocha, Kaitlin E, Seavitt, John R, Selloum, Mohammed, Szoke-Kovacs, Zsombor, Tamura, Masaru, Trainor, Amanda G, Tudose, Ilinca, Wakana, Shigeharu, Warren, Jonathan, Wendling, Olivia, West, David B, Wong, Leeyean, Yoshiki, Atsushi, International Mouse Phenotyping Consortium, Jackson Laboratory, Infrastructure Nationale PHENOMIN, Institut Clinique de la Souris (ICS), Charles River Laboratories, MRC Harwell, Toronto Centre for Phenogenomics, Wellcome Trust Sanger Institute, RIKEN BioResource Center, MacArthur, Daniel G, Tocchini-Valentini, Glauco P, Gao, Xiang, Flicek, Paul, Bradley, Allan, Skarnes, William C, Justice, Monica J, Parkinson, Helen E, Moore, Mark, Wells, Sara, Braun, Robert E, Svenson, Karen L, de Angelis, Martin Hrabe, Herault, Yann, Mohun, Tim, Mallon, Ann-Marie, Henkelman, R Mark, Brown, Steve DM, Adams, David J, Lloyd, KC Kent, McKerlie, Colin, Beaudet, Arthur L, Bućan, Maja, Murray, Stephen A

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High-throughput discovery of novel developmental phenotypes von Dickinson, Mary E, Flenniken, Ann M, Ji, Xiao, Teboul, Lydia, Wong, Michael D, White, Jacqueline K, Meehan, Terrence F, Weninger, Wolfgang J, Westerberg, Henrik, Adissu, Hibret, Baker, Candice N, Bower, Lynette, Brown, James M, Caddle, L. Brianna, Chiani, Francesco, Clary, Dave, Cleak, James, Daly, Mark J, Denegre, James M, Doe, Brendan, Dolan, Mary E, Edie, Sarah M, Fuchs, Helmut, Gailus-Durner, Valerie, Galli, Antonella, Gambadoro, Alessia, Gallegos, Juan, Guo, Shiying, Horner, Neil R, Hsu, Chih-wei, Johnson, Sara J, Kalaga, Sowmya, Keith, Lance C, Lanoue, Louise, Lawson, Thomas N, Lek, Monkol, Mark, Manuel, Marschall, Susan, Mason, Jeremy, McElwee, Melissa L, Newbigging, Susan, Nutter, Lauryl M.J, Peterson, Kevin A, Ramirez-Solis, Ramiro, Rowland, Douglas J, Ryder, Edward, Samocha, Kaitlin E, Seavitt, John R, Selloum, Mohammed, Szoke-Kovacs, Zsombor, Tamura, Masaru, Trainor, Amanda G, Tudose, Ilinca, Wakana, Shigeharu, Warren, Jonathan, Wendling, Olivia, West, David B, Wong, Leeyean, Yoshiki, Atsushi, MacArthur, Daniel G, Tocchini-Valentini, Glauco P, Gao, Xiang, Flicek, Paul, Bradley, Allan, Skarnes, William C, Justice, Monica J, Parkinson, Helen E, Moore, Mark, Wells, Sara, Braun, Robert E, Svenson, Karen L, de Angelis, Martin Hrabe, Herault, Yann, Mohun, Tim, Mallon, Ann-Marie, Henkelman, R. Mark, Brown, Steve D.M, Adams, David J, Lloyd, K.C. Kent, McKerlie, Colin, Beaudet, Arthur L, Bucan, Maja, Murray, Stephen A

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Gold Nanoparticles in Biology: Beyond Toxicity to Cellular Imaging von Murphy, Catherine J, Gole, Anand M, Stone, John W, Sisco, Patrick N, Alkilany, Alaaldin M, Goldsmith, Edie C, Baxter, Sarah C

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The effect of mindfulness interventions on stress in medical students: A systematic review and meta-analysis von Sperling, Edie L, Hulett, Jennifer M, Sherwin, LeeAnne B, Thompson, Sarah, Bettencourt, B. Ann

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Prevalence, characteristics and measurement of somatic symptoms related to mental health in medical students: a scoping review von Sperling, Edie L, Hulett, Jennifer M, Sherwin, LeeAnne B, Thompson, Sarah, Bettencourt, B Ann

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Diastereomer Characterization of PS-Modified Synthetic Oligonucleotides Using Cyclic IMS-MS von Sharon, Edie M., O’Keefe, Sarah M., Grassmyer, Kathleen T., Raab, Shannon A., Maloney, Todd D., Clemmer, David E.

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Limb development genes underlie variation in human fingerprint patterns von Li, Jinxi, Glover, James D., Zhang, Haiguo, Peng, Meifang, Tan, Jingze, Mallick, Chandana Basu, Hou, Dan, Yang, Yajun, Wu, Sijie, Liu, Yu, Peng, Qianqian, Zheng, Shijie C., Crosse, Edie I., Medvinsky, Alexander, Anderson, Richard A., Brown, Helen, Yuan, Ziyu, Zhou, Shen, Xu, Yanqing, Kemp, John P., Ho, Yvonne Y.W., Loesch, Danuta Z., Wang, Lizhong, Li, Yingxiang, Tang, Senwei, Wu, Xiaoli, Walters, Robin G., Lin, Kuang, Meng, Ruogu, Lv, Jun, Chernus, Jonathan M., Neiswanger, Katherine, Feingold, Eleanor, Evans, David M., Medland, Sarah E., Martin, Nicholas G., Weinberg, Seth M., Marazita, Mary L., Chen, Gang, Chen, Zhengming, Zhou, Yong, Cheeseman, Michael, Wang, Lan, Jin, Li, Headon, Denis J., Wang, Sijia

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The diagnostic and prognostic utility of risk factors defined by the AHA/ACCF on the evaluation of cardiac disease in liver transplantation candidates von Alexander, Sarah, Teshome, Meron, Patel, Hena, Chan, Edie Y, Doukky, Rami

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