Articles with public access mandates - Deepak Srivastava - Howard Hughes Medical InstituteLearn more
Available based on mandate: 18
Review
Contribution of previously unrecognized RNA splice-altering variants to congenital heart disease
MY Jang, PN Patel, AC Pereira, JAL Willcox, A Haghighi, AC Tai, K Ito, ...
Circulation: Genomic and Precision Medicine 16 (3), 224-231, 2023
Review
Cold shock domain–containing protein E1 is a posttranscriptional regulator of the LDL receptor
GA Smith, A Padmanabhan, BH Lau, A Pampana, L Li, CY Lee, ...
Science translational medicine 14 (662), eabj8670, 2022
Review
A transcriptional switch governs fibroblast activation in heart disease
M Alexanian, PF Przytycki, R Micheletti, A Padmanabhan, L Ye, ...
Nature 595 (7867), 438-443, 2021
Review
Association of damaging variants in genes with increased cancer risk among patients with congenital heart disease
SU Morton, A Shimamura, PE Newburger, AR Opotowsky, D Quiat, ...
JAMA cardiology 6 (4), 457-462, 2021
Review
Network-based screen in iPSC-derived cells reveals therapeutic candidate for heart valve disease
CV Theodoris, P Zhou, L Liu, Y Zhang, T Nishino, Y Huang, A Kostina, ...
Science 371 (6530), eabd0724, 2021
Review
GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm
A Sharma, LK Wasson, JAL Willcox, SU Morton, JM Gorham, ...
Elife 9, e53278, 2020
Review
CSDE1 is a post-transcriptional regulator of the LDL receptor
GA Smith, A Padmanabhan, BH Lau, A Pampana, L Li, Y Clara Lee, ...
bioRxiv, 2020.08. 03.235028, 2020
Review
Genomic analyses implicate noncoding de novo variants in congenital heart disease
F Richter, SU Morton, SW Kim, A Kitaygorodsky, LK Wasson, KM Chen, ...
Nature genetics 52 (8), 769-777, 2020
Review
De novo damaging variants, clinical phenotypes, and post-operative outcomes in congenital heart disease
MT Boskovski, J Homsy, M Nathan, LA Sleeper, S Morton, KB Manheimer, ...
Circulation: Genomic and Precision Medicine 13 (4), e002836, 2020
Review
Systems analysis implicates WAVE2 complex in the pathogenesis of developmental left-sided obstructive heart defects
JJ Edwards, AD Rouillard, NF Fernandez, Z Wang, A Lachmann, ...
Basic to Translational Science 5 (4), 376-386, 2020
Review
Single-cell analysis of cardiogenesis reveals basis for organ-level developmental defects
TY de Soysa, SS Ranade, S Okawa, S Ravichandran, Y Huang, ...
Nature 572 (7767), 120-124, 2019
Review
Context-specific transcription factor functions regulate epigenomic and transcriptional dynamics during cardiac reprogramming
NR Stone, CA Gifford, R Thomas, KJB Pratt, K Samse-Knapp, ...
Cell stem cell 25 (1), 87-102. e9, 2019
Review
Oligogenic inheritance of a human heart disease involving a genetic modifier
CA Gifford, SS Ranade, R Samarakoon, HT Salunga, TY De Soysa, ...
Science 364 (6443), 865-870, 2019
Review
Unique Transcription Factor Functions Regulate Epigenetic and Transcriptional Dynamics During Cardiac Reprogramming
NR Stone, CA Gifford, R Thomas, KJB Pratt, K Samse-Knapp, ...
bioRxiv, 642900, 2019
Review
Single-cell transcriptome analysis during cardiogenesis reveals basis for organ level developmental anomalies
TY de Soysa, SS Ranade, S Okawa, S Ravichandran, Y Huang, ...
bioRxiv, 365734, 2018
Review
Oligogenic inheritance of congenital heart disease involving a NKX2-5 modifier
CA Gifford, SS Ranade, R Samarakoon, HT Salunga, TY de Soysa, ...
bioRxiv, 266726, 2018
Review
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ...
Nature genetics 49 (11), 1593-1601, 2017
Review
Coordination of synaptic adhesion with dendritic spine remodeling by AF-6 and kalirin-7
Z Xie, H Photowala, ME Cahill, DP Srivastava, KM Woolfrey, CY Shum, ...
Journal of Neuroscience 28 (24), 6079-6091, 2008
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