Tanner O. Monroe

Northwestern University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index833citations26works4.32yr avg
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Research Topics

Mitochondrial Function and Pathology(7), Congenital heart defects research(5), Cardiomyopathy and Myosin Studies(4), Adipose Tissue and Metabolism(4), Muscle Physiology and Disorders(3)

Publications26 total

A combined genomic arrhythmia propensity score delineates cumulative risk
Cell Reports Medicine·2025Open Access
Engineered heart tissues facilitate functional characterization of noncoding variants implicated in Hypertrophic and Dilated Cardiomyopathy
2025Open Access
Genetic risk in telomere biology disorders: it adds up
Journal of Clinical Investigation·2025Open Access
Abstract 4143893: Combining Noncoding and Coding Genetic Variation Improves Arrhythmia Risk Prediction
Circulation·2024
Abstract Tu112: The Outer Mitochondrial Membrane Protein Mtch2 Regulates Cardiac Metabolic Homeostasis and Body Mass
Circulation Research·2024
Abstract Mo076: Combining Monogenic and Polygenic Analysis Improves Sudden Cardiac Death Risk Prediction
Circulation Research·2024
Abstract Mo082: Polygenic Assessment for Atrial Fibrillation Liability Predicts Ventricular Arrhythmia Risk
Circulation Research·2024
Reduction of Filamin C Results in Altered Proteostasis, Cardiomyopathy, and Arrhythmias
Journal of the American Heart Association·2024· 9 citedOpen Access
Susceptibility to innate immune activation in genetically mediated myocarditis
Journal of Clinical Investigation·2024· 23 citedOpen Access
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
Genome Medicine·2024· 11 citedOpen Access
Single Nucleus RNA Sequencing of Sglt2 Knockout Mouse Hearts Reveals Cardiac-Renal Communication
Journal of the American Society of Nephrology·2023
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young
2023· 1 citedOpen Access
Abstract P2112: Human Genetics And Engineered Heart Tissues Link Frail <i>MYH7</i> Alleles To Delayed Maturation And Ventricular Noncompaction
Circulation Research·2022
Opposing effects of genetic variation in <i>MTCH2</i> for obesity versus heart failure
Human Molecular Genetics·2022· 7 citedOpen Access
A steroid receptor coactivator stimulator (MCB-613) attenuates adverse remodeling after myocardial infarction
Proceedings of the National Academy of Sciences·2020· 31 citedOpen Access
PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia
Nature Communications·2020· 29 citedOpen Access
Organ of Corti size is governed by Yap/Tead-mediated progenitor self-renewal
Proceedings of the National Academy of Sciences·2020· 47 citedOpen Access
Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies
Human Molecular Genetics·2020· 17 citedOpen Access
Cardiac‐specific ablation of glutaredoxin 3 leads to cardiac hypertrophy and heart failure
Physiological Reports·2019· 18 citedOpen Access
YAP Partially Reprograms Chromatin Accessibility to Directly Induce Adult Cardiogenesis In Vivo
Developmental Cell·2019· 270 citedOpen Access
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Frequent Co-authors

Megan J. Puckelwartz(12), Elizabeth M. McNally(10), Lorenzo L. Pesce(8), Samuel Kearns(7), George G. Rodney(6), Gregory Webster(6), Lisa Dellefave‐Castillo(5), James F. Martin(4), Alfred L. George(4), Dominic E. Fullenkamp(3), Prince J. Kannankeril(3), Lisa Dellefave–Castillo(3), Matthew C. Hill(2), John P. Leach(2), Xander H.T. Wehrens(2), Rituraj Pal(2), Michela Palmieri(2), Marco Sardiello(2), Johanna T. Lanner(2), Dimitra K. Georgiou(2)