GSEPD: a Bioconductor package for RNA-seq gene set enrichment and projection display

por Stamm, Karl, Tomita-Mitchell, Aoy, Bozdag, Serdar
Publicado 2019

Use of Metformin in Pulmonary Vein Stenosis after TAPVR Repair

por Kirkpatrick, Edward C., Mitchell, Michael E., Thilly, William G., Cava, Joseph, Tomita-Mitchell, Aoy, Gostjeva, Elena V.
Publicado 2020

77085 Impact of MYH6 Variants on Development and Clinical Course of Hypoplastic Left Heart Syndrome

por Anfinson, Melissa, Creighton, Sara, James, Jeanne, Goetsch, Peter Frommeltry, Simpson, Pippa, Mitchell, Michael E, Tomita-Mitchell, Aoy
Publicado 2021

A Systematic Review of Ebstein’s Anomaly with Left Ventricular Noncompaction

por Thareja, Suma K., Frommelt, Michele A., Lincoln, Joy, Lough, John W., Mitchell, Michael E., Tomita-Mitchell, Aoy
Publicado 2022

Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening

por Blagojevic, Christina, Heung, Tracy, Theriault, Mylene, Tomita-Mitchell, Aoy, Chakraborty, Pranesh, Kernohan, Kristin, Bulman, Dennis E., Bassett, Anne S.
Publicado 2021

The Inferred Cardiogenic Gene Regulatory Network in the Mammalian Heart

por Bazil, Jason N., Stamm, Karl D., Li, Xing, Thiagarajan, Raghuram, Nelson, Timothy J., Tomita-Mitchell, Aoy, Beard, Daniel A.
Publicado 2014

Activin-A and Bmp4 Levels Modulate Cell Type Specification during CHIR-Induced Cardiomyogenesis

por Kim, Min-Su, Horst, Audrey, Blinka, Steven, Stamm, Karl, Mahnke, Donna, Schuman, James, Gundry, Rebekah, Tomita-Mitchell, Aoy, Lough, John
Publicado 2015

Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms

por Ghanta, Sujana, Mitchell, Michael E., Ames, Mary, Hidestrand, Mats, Simpson, Pippa, Goetsch, Mary, Thilly, William G., Struble, Craig A., Tomita-Mitchell, Aoy
Publicado 2010

Significance of α-Myosin Heavy Chain (MYH6) Variants in Hypoplastic Left Heart Syndrome and Related Cardiovascular Diseases

por Anfinson, Melissa, Fitts, Robert H., Lough, John W., James, Jeanne M., Simpson, Pippa M., Handler, Stephanie S., Mitchell, Michael E., Tomita-Mitchell, Aoy
Publicado 2022

Early changes in cell‐free DNA levels in newly transplanted heart transplant patients

por Zangwill, Steven D., Kindel, Steven J., Ragalie, William S., North, Paula E., Pollow, Alyssa, Hidestrand, Mats, Tomita‐Mitchell, Aoy, Stamm, Karl D., Mitchell, Michael E.
Publicado 2019

3D-bioprinting of patient-derived cardiac tissue models for studying congenital heart disease

por Wolfe, Jayne T., He, Wei, Kim, Min-Su, Liang, Huan-Ling, Shradhanjali, Akankshya, Jurkiewicz, Hilda, Freudinger, Bonnie P., Greene, Andrew S., LaDisa, John F., Tayebi, Lobat, Mitchell, Michael E., Tomita-Mitchell, Aoy, Tefft, Brandon J.
Publicado 2023

Cell-free DNA donor fraction analysis in pediatric and adult heart transplant patients by multiplexed allele-specific quantitative PCR: Validation of a rapid and highly sensitive c...

por North, Paula E., Ziegler, Emily, Mahnke, Donna K., Stamm, Karl D., Thomm, Angela, Daft, Paul, Goetsch, Mary, Liang, Huan ling, Baker, Maria Angeles, Vepraskas, Adam, Rosenau, Chris, Dasgupta, Mahua, Simpson, Pippa, Mitchell, Michael E., Tomita-Mitchell, Aoy
Publicado 2020

Contractility of Induced Pluripotent Stem Cell-Cardiomyocytes With an MYH6 Head Domain Variant Associated With Hypoplastic Left Heart Syndrome

por Kim, Min-Su, Fleres, Brandon, Lovett, Jerrell, Anfinson, Melissa, Samudrala, Sai Suma K., Kelly, Lauren J., Teigen, Laura E., Cavanaugh, Matthew, Marquez, Maribel, Geurts, Aron M., Lough, John W., Mitchell, Michael E., Fitts, Robert H., Tomita-Mitchell, Aoy
Publicado 2020

Impact of MYH6 variants in hypoplastic left heart syndrome

por Tomita-Mitchell, Aoy, Stamm, Karl D., Mahnke, Donna K., Kim, Min-Su, Hidestrand, Pip M., Liang, Huan Ling, Goetsch, Mary A., Hidestrand, Mats, Simpson, Pippa, Pelech, Andrew N., Tweddell, James S., Benson, D. Woodrow, Lough, John W., Mitchell, Michael E.
Publicado 2016

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy

por Sparks, Andrew B, Wang, Eric T, Struble, Craig A, Barrett, Wade, Stokowski, Renee, McBride, Celeste, Zahn, Jacob, Lee, Kevin, Shen, Naiping, Doshi, Jigna, Sun, Michel, Garrison, Jill, Sandler, Jay, Hollemon, Desiree, Pattee, Patrick, Tomita-Mitchell, Aoy, Mitchell, Michael, Stuelpnagel, John, Song, Ken, Oliphant, Arnold
Publicado 2012

Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction

por Samudrala, Sai Suma K., North, Lauren M., Stamm, Karl D., Earing, Michael G., Frommelt, Michele A., Willes, Richard, Tripathi, Swarnendu, Dsouza, Nikita R., Zimmermann, Michael T., Mahnke, Donna K., Liang, Huan Ling, Lund, Michael, Lin, Chien‐Wei, Geddes, Gabrielle C., Mitchell, Michael E., Tomita‐Mitchell, Aoy
Publicado 2020

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

por Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Publicado 2017

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