Martin Tristani-Firouzi

22PUBLICATIONS
144CO-AUTHORS
Cell and nuclear divisionCardiovascular medicine and haematology not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (22)

|Aug 01, 2026
Uniparental Disomy Reveals Hidden Genetic Causes of Congenital Heart Disease.

|Mar 04, 2026
Prothrombin G20210A and Factor V Leiden Variants Are Not Associated With Thrombotic Events in Congenital Heart Disease: An Observational Trial.

Feria A Ladha, Christina VanderPluym, Enrique Mondragon-Estrada

|Feb 12, 2026
Nuclear Histone 3 Post-Translational Modification Profiling in Whole Cells using Spectral Flow Cytometry.

Carly S Golden, Saylor Williams, Sandeep Sreerama

|Jul 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgery.

W Scott Watkins, Edgar J Hernandez, Thomas A Miller

|Mar 03, 2025
Modeling SMAD2 Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease Pathogenesis.

Tarsha Ward, Sarah U Morton, Gabriela Venturini

|May 15, 2024
Genome Sequencing is Critical for Forecasting Outcomes Following Congenital Cardiac Surgery.

W Scott Watkins, E Javier Hernandez, Thomas Miller

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Frequent Collaborators

9 joint publications

Wendy K Chung

9 joint publications

Bruce Gelb

8 joint publications

Sarah U Morton

8 joint publications

Christine Seidman