Aoy Tomita-Mitchell

4PUBLICATIONS
40CO-AUTHORS
Developmental genetics (incl. sex determination)Cardiology (incl. cardiovascular diseases)Respiratory diseases
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Publications (4)

|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|May 19, 2023
Altered contractility, Ca2+ transients, and cell morphology seen in a patient-specific iPSC-CM model of Ebstein's anomaly with left ventricular noncompaction.

Suma K Thareja, Melissa Anfinson, Matthew Cavanaugh

|Jan 28, 2020
Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction.

Sai Suma K Samudrala, Lauren M North, Karl D Stamm

|Jan 14, 2020
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 clinical test for stratification of rejection probability.

Paula E North, Emily Ziegler, Donna K Mahnke

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Frequent Collaborators

2 joint publications

Suma K Thareja

2 joint publications

Karl Stamm

2 joint publications

Bernice E Morrow

1 joint publications

Jennifer Strande