Streamlining statistical reproducibility: NHLBI ORCHID clinical trial results reproduction

por Serret-Larmande, Arnaud, Kaltman, Jonathan R, Avillach, Paul
Publicado 2022

Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes

por Russell, Mark W., Chung, Wendy K., Kaltman, Jonathan R., Miller, Thomas A.
Publicado 2018

Public Health Science Agenda for Congenital Heart Defects: Report From a Centers for Disease Control and Prevention Experts Meeting

por Oster, Matthew E., Riehle‐Colarusso, Tiffany, Simeone, Regina M., Gurvitz, Michelle, Kaltman, Jonathan R., McConnell, Michael, Rosenthal, Geoffrey L., Honein, Margaret A.
Publicado 2013

Epidemiology of Sudden Death in a Population-Based Study of Infants and Children

por Burns, Kristin M., Cottengim, Carri, Dykstra, Heather, Faulkner, Meghan, Erck Lambert, Alexa B., MacLeod, Heather, Novak, Alissa, Parks, Sharyn E., Russell, Mark W., Shapiro-Mendoza, Carrie K., Shaw, Esther, Tian, Niu, Whittemore, Vicky, Kaltman, Jonathan R.
Publicado 2020

Genetic and clinical variables act synergistically to impact neurodevelopmental outcomes in children with single ventricle heart disease

por Miller, Thomas A., Hernandez, Edgar J., Gaynor, J. William, Russell, Mark W., Newburger, Jane W., Chung, Wendy, Goldmuntz, Elizabeth, Cnota, James F., Zyblewski, Sinai C., Mahle, William T., Zak, Victor, Ravishankar, Chitra, Kaltman, Jonathan R., McCrindle, Brian W., Clarke, Shanelle, Votava-Smith, Jodie K., Graham, Eric M., Seed, Mike, Rudd, Nancy, Bernstein, Daniel, Lee, Teresa M., Yandell, Mark, Tristani-Firouzi, Martin
Publicado 2023

De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease

por Boskovski, Marko T., Homsy, Jason, Nathan, Meena, Sleeper, Lynn A., Morton, Sarah, Manheimer, Kathryn B., Tai, Angela, Gorham, Joshua, Lewis, Matthew, Swartz, Michael, Alfieris, George M., Bacha, Emile A., Karimi, Mohsen, Meyer, David, Nguyen, Khanh, Bernstein, Daniel, Romano-Adesman, Angela, Porter, George A., Goldmuntz, Elizabeth, Chung, Wendy K., Srivastava, Deepak, Kaltman, Jonathan R., Tristani-Firouzi, Martin, Lifton, Richard, Roberts, Amy E., Gaynor, J. William, Gelb, Bruce D., Kim, Richard, Seidman, Jonathan G., Brueckner, Martina, Mayer, John E., Newburger, Jane W., Seidman, Christine E.
Publicado 2020

Genomic analyses implicate noncoding de novo variants in congenital heart disease

por Richter, Felix, Morton, Sarah U., Won Kim, Seong, 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.
Publicado 2020

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

por 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, Gaynor, 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
Publicado 2017

De novo mutations in histone modifying genes in congenital heart disease

por 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, 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, 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.
Publicado 2013