Work-Study: An Evolving Program von Richardson, Virginia, Gelb, Christine

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Student Work-Study: Everyone Benefits von Richardson, Virginia, Gelb, Christine

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Genetics of Congenital Heart Disease: The Glass Half Empty von Fahed, Akl C, Gelb, Bruce D, Seidman, J G, Seidman, Christine E

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Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles von Martin-Trujillo, Alejandro, Patel, Nihir, Richter, Felix, Jadhav, Bharati, Garg, Paras, Morton, Sarah U, McKean, David M, DePalma, Steven R, Goldmuntz, Elizabeth, Gruber, Dorota, Kim, Richard, Newburger, Jane W, Porter, Jr, George A, Giardini, Alessandro, Bernstein, Daniel, Tristani-Firouzi, Martin, Seidman, Jonathan G, Seidman, Christine E, Chung, Wendy K, Gelb, Bruce D, Sharp, Andrew J

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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands von Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R, Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C, Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D, Castaldi, Christopher, Tikhonoa, Irina R, Bilguvar, Kaya, Mane, Shrikant M, Sanders, Stephan J, Mital, Seema, Russell, Mark W, Gaynor, J William, Deanfield, John, Giardini, Alessandro, Porter, George A, Srivastava, Deepak, Lo, Cecelia W, Shen, Yufeng, Watkins, W Scott, Yandell, Mark, Yost, H Joseph, Tristani-Firouzi, Martin, Newburger, Jane W, Roberts, Amy E, Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R, Goldmuntz, Elizabeth, Chung, Wendy K, Seidman, Jonathan G, Gelb, Bruce D, Seidman, Christine E, Lifton, Richard P, Brueckner, Martina

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De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes von Watkins, W. Scott, Hernandez, E. Javier, Wesolowski, Sergiusz, Bisgrove, Brent W., Sunderland, Ryan T., Lin, Edwin, Lemmon, Gordon, Demarest, Bradley L., Miller, Thomas A., Bernstein, Daniel, Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Newburger, Jane W., Seidman, Christine E., Shen, Yufeng, Yost, H. Joseph, Yandell, Mark, Tristani-Firouzi, Martin

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De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies von Homsy, Jason, Zaidi, Samir, Shen, Yufeng, Ware, James S., Samocha, Kaitlin E., Karczewski, Konrad J., DePalma, Steven R., McKean, David, Wakimoto, Hiroko, Gorham, Josh, Jin, Sheng Chih, Deanfield, John, Giardini, Alessandro, Porter, George A., Kim, Richard, Bilguvar, Kaya, López-Giráldez, Francesc, Tikhonova, Irina, Mane, Shrikant, Romano-Adesman, Angela, Qi, Hongjian, Vardarajan, Badri, Ma, Lijiang, Daly, Mark, Roberts, Amy E., Russell, Mark W., Mital, Seema, Newburger, Jane W., Gaynor, J. William, Breitbart, Roger E., Iossifov, Ivan, Ronemus, Michael, Sanders, Stephan J., Kaltman, Jonathan R., Seidman, Jonathan G., Brueckner, Martina, Gelb, Bruce D., Goldmuntz, Elizabeth, Lifton, Richard P., Seidman, Christine E., Chung, Wendy K.

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The interaction of secreted phospholipase A2-IIA with the microbiota alters its lipidome and promotes inflammation von Doré, Etienne, Joly-Beauparlant, Charles, Morozumi, Satoshi, Mathieu, Alban, Lévesque, Tania, Allaeys, Isabelle, Duchez, Anne-Claire, Cloutier, Nathalie, Leclercq, Mickaël, Bodein, Antoine, Payré, Christine, Martin, Cyril, Petit-Paitel, Agnes, Gelb, Michael H, Rangachari, Manu, Murakami, Makoto, Davidovic, Laetitia, Flamand, Nicolas, Arita, Makoto, Lambeau, Gérard, Droit, Arnaud, Boilard, Eric

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Genomic analyses implicate noncoding de novo variants in congenital heart disease von Richter, Felix, Morton, Sarah U., Kim, Seong Won, Kitaygorodsky, Alexander, Wasson, Lauren K., Chen, Kathleen M., Zhou, Jian, Qi, Hongjian, Patel, Nihir, DePalma, Steven R., Parfenov, Michael, Homsy, Jason, Gorham, Joshua M., Manheimer, Kathryn B., Velinder, Matthew, Farrell, Andrew, Marth, Gabor, Schadt, Eric E., Kaltman, Jonathan R., Newburger, Jane W., Giardini, Alessandro, Goldmuntz, Elizabeth, Brueckner, Martina, Kim, Richard, Porter, George A., Bernstein, Daniel, Chung, Wendy K., Srivastava, Deepak, Tristani-Firouzi, Martin, Troyanskaya, Olga G., Dickel, Diane E., Shen, Yufeng, Seidman, Jonathan G., Seidman, Christine E., Gelb, Bruce D.

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Inhibition of lipoprotein-associated phospholipase A2 reduces complex coronary atherosclerotic plaque development von Wilensky, Robert L, Shi, Yi, Mohler, Emile R, Hamamdzic, Damir, Burgert, Mark E, Li, Jun, Postle, Anthony, Fenning, Robert S, Bollinger, James G, Hoffman, Bryan E, Pelchovitz, Daniel J, Yang, Jisheng, Mirabile, Rosanna C, Webb, Christine L, Zhang, LeFeng, Zhang, Ping, Gelb, Michael H, Walker, Max C, Zalewski, Andrew, Macphee, Colin H

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Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data von Glessner, Joseph T, Bick, Alexander G, Ito, Kaoru, Homsy, Jason G, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R, Golhar, Ryan, Sanders, Stephan J, Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A Jeremy, State, Matthew W, Kaltman, Jonathan R, White, Peter S, Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D, Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K

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De novo mutations in histone-modifying genes in congenital heart disease von Zaidi, Samir, Choi, Murim, Wakimoto, Hiroko, Ma, Lijiang, Jiang, Jianming, Overton, John D., Romano-Adesman, Angela, Bjornson, Robert D., Breitbart, Roger E., Brown, Kerry K., Carriero, Nicholas J., Cheung, Yee Him, Deanfield, John, DePalma, Steve, Fakhro, Khalid A., Glessner, Joseph, Hakonarson, Hakon, Italia, Michael J., Kaltman, Jonathan R., Kaski, Juan, Kim, Richard, Kline, Jennie K., Lee, Teresa, Leipzig, Jeremy, Lopez, Alexander, Mane, Shrikant M., Mitchell, Laura E., Newburger, Jane W., Parfenov, Michael, Pe’er, Itsik, Porter, George, Roberts, Amy E., Sachidanandam, Ravi, Sanders, Stephan J., Seiden, Howard S., State, Mathew W., Subramanian, Sailakshmi, Tikhonova, Irina R., Wang, Wei, Warburton, Dorothy, White, Peter S., Williams, Ismee A., Zhao, Hongyu, Seidman, Jonathan G., Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Seidman, Christine E., Lifton, Richard P.

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Identification and purification of human induced pluripotent stem cell-derived atrial-like cardiomyocytes based on sarcolipin expression von Josowitz, Rebecca, Lu, Jia, Falce, Christine, D'Souza, Sunita L, Wu, Meng, Cohen, Ninette, Dubois, Nicole C, Zhao, Yong, Sobie, Eric A, Fishman, Glenn I, Gelb, Bruce D

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Transcription factor protein interactomes reveal genetic determinants in heart disease von Gonzalez-Teran, Barbara, Pittman, Maureen, Felix, Franco, Thomas, Reuben, Richmond-Buccola, Desmond, Hüttenhain, Ruth, Choudhary, Krishna, Moroni, Elisabetta, Costa, Mauro W., Huang, Yu, Padmanabhan, Arun, Alexanian, Michael, Lee, Clara Youngna, Maven, Bonnie E.J., Samse-Knapp, Kaitlen, Morton, Sarah U., McGregor, Michael, Gifford, Casey A., Seidman, J.G., Seidman, Christine E., Gelb, Bruce D., Colombo, Giorgio, Conklin, Bruce R., Black, Brian L., Bruneau, Benoit G., Krogan, Nevan J., Pollard, Katherine S., Srivastava, Deepak

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Loss of RNA expression and allele-specific expression associated with congenital heart disease von McKean, David M., Homsy, Jason, Wakimoto, Hiroko, Patel, Neil, Gorham, Joshua, DePalma, Steven R., Ware, James S., Zaidi, Samir, Ma, Wenji, Patel, Nihir, Lifton, Richard P., Chung, Wendy K., Kim, Richard, Shen, Yufeng, Brueckner, Martina, Goldmuntz, Elizabeth, Sharp, Andrew J., Seidman, Christine E., Gelb, Bruce D., Seidman, J. G.

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Robust identification of mosaic variants in congenital heart disease von Manheimer, Kathryn B., Richter, Felix, Edelmann, Lisa J., D’Souza, Sunita L., Shi, Lisong, Shen, Yufeng, Homsy, Jason, Boskovski, Marko T., Tai, Angela C., Gorham, Joshua, Yasso, Christopher, Goldmuntz, Elizabeth, Brueckner, Martina, Lifton, Richard P., Chung, Wendy K., Seidman, Christine E., Seidman, J. G., Gelb, Bruce D.

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Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease von Xiao, Feng, Zhang, Xiaoran, Morton, Sarah U., Kim, Seong Won, Fan, Youfei, Gorham, Joshua M., Zhang, Huan, Berkson, Paul J., Mazumdar, Neil, Cao, Yangpo, Chen, Jian, Hagen, Jacob, Liu, Xujie, Zhou, Pingzhu, Richter, Felix, Shen, Yufeng, Ward, Tarsha, Gelb, Bruce D., Seidman, Jonathan G., Seidman, Christine E., Pu, William T.

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Detection of GM1‐gangliosidosis in newborn dried blood spots by enzyme activity and biomarker assays using tandem mass spectrometry von Su, Peiling, Khaledi, Hamid, Waggoner, Christine, Gelb, Michael H.

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GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm von Sharma, Arun, Wasson, Lauren K, Willcox, Jon Al, Morton, Sarah U, Gorham, Joshua M, DeLaughter, Daniel M, Neyazi, Meraj, Schmid, Manuel, Agarwal, Radhika, Jang, Min Young, Toepfer, Christopher N, Ward, Tarsha, Kim, Yuri, Pereira, Alexandre C, DePalma, Steven R, Tai, Angela, Kim, Seongwon, Conner, David, Bernstein, Daniel, Gelb, Bruce D, Chung, Wendy K, Goldmuntz, Elizabeth, Porter, George, Tristani-Firouzi, Martin, Srivastava, Deepak, Seidman, Jonathan G, Seidman, Christine E

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Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart Syndrome von Krane, Markus, Dreßen, Martina, Santamaria, Gianluca, My, Ilaria, Schneider, Christine M., Dorn, Tatjana, Laue, Svenja, Mastantuono, Elisa, Berutti, Riccardo, Rawat, Hilansi, Gilsbach, Ralf, Schneider, Pedro, Lahm, Harald, Schwarz, Sascha, Doppler, Stefanie A., Paige, Sharon, Puluca, Nazan, Doll, Sophia, Neb, Irina, Brade, Thomas, Zhang, Zhong, Abou-Ajram, Claudia, Northoff, Bernd, Holdt, Lesca M., Sudhop, Stefanie, Sahara, Makoto, Goedel, Alexander, Dendorfer, Andreas, Tjong, Fleur V.Y., Rijlaarsdam, Maria E., Cleuziou, Julie, Lang, Nora, Kupatt, Christian, Bezzina, Connie, Lange, Rüdiger, Bowles, Neil E., Mann, Matthias, Gelb, Bruce D., Crotti, Lia, Hein, Lutz, Meitinger, Thomas, Wu, Sean, Sinnecker, Daniel, Gruber, Peter J., Laugwitz, Karl-Ludwig, Moretti, Alessandra

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