Health disparities in Turner Syndrome: UTHealth Turner Syndrome Research Registry

por Donate, Priscille, Rivera-Davila, Michelle, Prakash, Siddharth K.
Publicado 2023

An unusual cause of acute pericarditis: a case report

por Salarda, Erika M, Ocazionez-Trujillo, Daniel, Prakash, Siddharth K
Publicado 2021

Diabetes and Reduced Risk for Thoracic Aortic Aneurysms and Dissections: A Nationwide Case-Control Study

por Prakash, Siddharth K., Pedroza, Claudia, Khalil, Yameen A., Milewicz, Dianna M.
Publicado 2012

Safety of exercise for adults with thoracic aortic aneurysms and dissections

por Li, Jesse, Boyd, Alexandra, Huang, Michael, Berookhim, Joshua, Prakash, Siddharth K.
Publicado 2022

Risk Factors for Thoracic Aortic Dissection

por Zhou, Zhen, Cecchi, Alana C., Prakash, Siddharth K., Milewicz, Dianna M.
Publicado 2022

Dermatological concerns for women and girls with turner syndrome

por Rodriguez-Buritica, David, Mones, Meaghan, Prakash, Siddharth K., Rivera, Michelle, Aldrich, Melissa, Rogge, Megan, Richardson, Kate
Publicado 2023

Prevalence and clinical characteristics of inappropriate myocardial perfusion imaging tests at a community hospital

por Abelhad, Nadia Isabel, Kiser, Kendall J, Hughes, Andres, Hust, Michael A, Sayan, Enrique Garcia, Prakash, Siddharth K
Publicado 2019

Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease

por Musfee, Fadi I., Guo, Dongchuan, Pinard, Amélie C., Hostetler, Ellen M., Blue, Elizabeth E., Nickerson, Deborah A., Bamshad, Michael J., Milewicz, Dianna M., Prakash, Siddharth K.
Publicado 2020

Preventing Cholesterol-Induced Perk (Protein Kinase RNA-Like Endoplasmic Reticulum Kinase) Signaling in Smooth Muscle Cells Blocks Atherosclerotic Plaque Formation

por Chattopadhyay, Abhijnan, Guan (关蒲骏), Pujun, Majumder, Suravi, Kaw, Kaveeta, Zhou (周桢), Zhen, Zhang, Chen, Prakash, Siddharth K., Kaw, Anita, Buja, L. Maximillian, Kwartler, Callie S., Milewicz, Dianna M.
Publicado 2022

Recurrent Chromosome 16p13.1 Duplications Are a Risk Factor for Aortic Dissections

por Kuang, Shao-Qing, Guo, Dong-Chuan, Prakash, Siddharth K., McDonald, Merry-Lynn N., Johnson, Ralph J., Wang, Min, Regalado, Ellen S., Russell, Ludivine, Cao, Jiu-Mei, Kwartler, Callie, Fraivillig, Kurt, Coselli, Joseph S., Safi, Hazim J., Estrera, Anthony L., Leal, Suzanne M., LeMaire, Scott A., Belmont, John W., Milewicz, Dianna M.
Publicado 2011

Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve

por Carlisle, Steven G., Albasha, Hasan, Michelena, Hector, Sabate-Rotes, Anna, Bianco, Lisa, De Backer, Julie, Mosquera, Laura Muiño, Yetman, Anji T., Bissell, Malenka M, Andreassi, Maria Grazia, Foffa, Ilenia, Hui, Dawn S., Caffarelli, Anthony, Kim, Yuli Y., Guo, Dong-Chuan, Citro, Rodolfo, De Marco, Margot, Tretter, Justin T., McBride, Kim L., Milewicz, Dianna M., Body, Simon C., Prakash, Siddharth K.
Publicado 2023

Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (Gen...

por Roman, Mary J., Pugh, Norma L., Hendershot, Tabitha P., Devereux, Richard B., Dietz, Hal, Holmes, Kathryn, Eagle, Kim A., LeMaire, Scott A., Milewicz, Dianna M., Morris, Shaine A., Pyeritz, Reed E., Ravekes, William J., Shohet, Ralph V., Silberbach, Michael, Dietz, Harry C., Habashi, Jennifer, Prakash, Siddharth K., Maslen, Cheryl L., Song, Howard K., Bavaria, Joseph E., Milewski, Karianna, Weinsaft, Jonathan W., McDonnell, Nazli, Asch, Federico M., Tolunay, H. Eser, Desvigne‐Nickens, Patrice, Tseng, Hung, Kroner, Barbara L.
Publicado 2016

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

por Audain, Enrique, Wilsdon, Anna, Breckpot, Jeroen, Izarzugaza, Jose M. G., Fitzgerald, Tomas W., Kahlert, Anne-Karin, Sifrim, Alejandro, Wünnemann, Florian, Perez-Riverol, Yasset, Abdul-Khaliq, Hashim, Bak, Mads, Bassett, Anne S., Benson, Woodrow D., Berger, Felix, Daehnert, Ingo, Devriendt, Koenraad, Dittrich, Sven, Daubeney, Piers EF, Garg, Vidu, Hackmann, Karl, Hoff, Kirstin, Hofmann, Philipp, Dombrowsky, Gregor, Pickardt, Thomas, Bauer, Ulrike, Keavney, Bernard D., Klaassen, Sabine, Kramer, Hans-Heiner, Marshall, Christian R., Milewicz, Dianna M., Lemaire, Scott, Coselli, Joseph S., Mitchell, Michael E., Tomita-Mitchell, Aoy, Prakash, Siddharth K., Stamm, Karl, Stewart, Alexandre F. R., Silversides, Candice K., Siebert, Reiner, Stiller, Brigitte, Rosenfeld, Jill A., Vater, Inga, Postma, Alex V., Caliebe, Almuth, Brook, J. David, Andelfinger, Gregor, Hurles, Matthew E., Thienpont, Bernard, Larsen, Lars Allan, Hitz, Marc-Phillip
Publicado 2021

Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

por Audain, Enrique, Wilsdon, Anna, Breckpot, Jeroen, Izarzugaza, Jose M. G., Fitzgerald, Tomas W., Kahlert, Anne-Karin, Sifrim, Alejandro, Wünnemann, Florian, Perez-Riverol, Yasset, Abdul-Khaliq, Hashim, Bak, Mads, Bassett, Anne S., Benson, D. Woodrow, Berger, Felix, Daehnert, Ingo, Devriendt, Koenraad, Dittrich, Sven, Daubeney, Piers EF, Garg, Vidu, Hackmann, Karl, Hoff, Kirstin, Hofmann, Philipp, Dombrowsky, Gregor, Pickardt, Thomas, Bauer, Ulrike, Keavney, Bernard D., Klaassen, Sabine, Kramer, Hans-Heiner, Marshall, Christian R., Milewicz, Dianna M., Lemaire, Scott, Coselli, Joseph S., Mitchell, Michael E., Tomita-Mitchell, Aoy, Prakash, Siddharth K., Stamm, Karl, Stewart, Alexandre F. R., Silversides, Candice K., Siebert, Reiner, Stiller, Brigitte, Rosenfeld, Jill A., Vater, Inga, Postma, Alex V., Caliebe, Almuth, Brook, J. David, Andelfinger, Gregor, Hurles, Matthew E., Thienpont, Bernard, Larsen, Lars Allan, Hitz, Marc-Phillip
Publicado 2021