Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Institutional National Research Service Award (T32)
Project #
5T32HL007567-14
Application #
2329305
Study Section
Research Training Review Committee (RTR)
Project Start
1994-07-01
Project End
1999-08-31
Budget Start
1996-09-01
Budget End
1997-08-31
Support Year
14
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Mamidi, Ranganath; Li, Jiayang; Doh, Chang Yoon et al. (2018) Impact of the Myosin Modulator Mavacamten on Force Generation and Cross-Bridge Behavior in a Murine Model of Hypercontractility. J Am Heart Assoc 7:e009627
Wang, Heming; Nandakumar, Priyanka; Tekola-Ayele, Fasil et al. (2018) Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31. Eur J Hum Genet :
Li, Jiayang; Gresham, Kenneth S; Mamidi, Ranganath et al. (2018) Sarcomere-based genetic enhancement of systolic cardiac function in a murine model of dilated cardiomyopathy. Int J Cardiol 273:168-176
Fang, Mike; Nakazawa, Mary; Antonarakis, Emmanuel S et al. (2017) Efficacy of Abiraterone and Enzalutamide in Pre- and Postdocetaxel Castration-Resistant Prostate Cancer: A Trial-Level Meta-Analysis. Prostate Cancer 2017:8560827
Liang, Jingjing; Le, Thu H; Edwards, Digna R Velez et al. (2017) Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. PLoS Genet 13:e1006728
Kayima, J; Liang, J; Natanzon, Y et al. (2017) Association of genetic variation with blood pressure traits among East Africans. Clin Genet 92:487-494
He, Karen Y; Wang, Heming; Cade, Brian E et al. (2017) Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure. PLoS Genet 13:e1006678
Lane, Jacqueline M; Liang, Jingjing; Vlasac, Irma et al. (2017) Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Nat Genet 49:274-281
Durmaz, Arda; Henderson, Tim A D; Brubaker, Douglas et al. (2017) FREQUENT SUBGRAPH MINING OF PERSONALIZED SIGNALING PATHWAY NETWORKS GROUPS PATIENTS WITH FREQUENTLY DYSREGULATED DISEASE PATHWAYS AND PREDICTS PROGNOSIS. Pac Symp Biocomput 22:402-413
He, Karen Y; Ge, Dongliang; He, Max M (2017) Big Data Analytics for Genomic Medicine. Int J Mol Sci 18:

Showing the most recent 10 out of 64 publications