Ashley J. Cuttitta

Biochemistry, Genetics and Molecular Biology · University of Michigan

Mid career · publishing since 2015

Muscle Physiology and Disorders Pluripotent Stem Cells Research Tissue Engineering and Regenerative Medicine RNA Research and Splicing Esophageal Cancer Research and Treatment

Publications

Citations

129

Est. group size

~11

Recurring co-author estimate

Active years

Publishing since 2015

In context

Among 1,692 mid career Biochemistry, Genetics and Molecular Biology PIs within our index

Citations: 129cohort median 809

Publications / year (recent): 1.4cohort median 3.2

Typically publishes in teams of ~11 · 0% small-team papers (≤3 authors) · across 9 venues

Publication cadence

Publications per year over the last 10 years — averaging 1.4/year recently

Collaborators per year

Distinct co-authors at University of Michigan each year — a rough indication of whether the group around this researcher has been growing or contracting. An estimate from co-authorship, not a roster: collaborators are not necessarily lab members, and recent years can be under-counted while indexing catches up.

Recent publications

A scalable long-term <i>in vitro</i> model of human colonic epithelium with continuous barrier function
bioRxiv (Cold Spring Harbor Laboratory) · 2025
A Pilot Study: Transcriptional Profiling, Functional Analysis, and Organoid Modeling of Intestinal Mucosa in Hirschsprung Disease
Journal of Pediatric Surgery · 2023
SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients
eLife · 2022
SNTA1 Gene Rescues Ion Channel Function in Cardiomyocytes Derived from Induced Pluripotent Stem Cells Reprogrammed from Muscular Dystrophy Patients with Arrhythmias
bioRxiv (Cold Spring Harbor Laboratory) · 2022
Author response: SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients
2022
Enhanced dimethylarginine degradation improves coronary flow reserve and exercise tolerance in Duchenne muscular dystrophy carrier mice
American Journal of Physiology-Heart and Circulatory Physiology · 2020
Electrophysiological abnormalities in induced pluripotent stem cell‐derived cardiomyocytes generated from Duchenne muscular dystrophy patients
Journal of Cellular and Molecular Medicine · 2019
Subsarcolemmal Cytoskeleton In Dysferlin‐Mediated Muscle Membrane Repair
The FASEB Journal · 2019
Generation of Duchenne muscular dystrophy patient-specific induced pluripotent stem cell line lacking exons 45–50 of the dystrophin gene (IITi001-A)
Stem Cell Research · 2018
216Functional properties of induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients
EP Europace · 2018
P3248Investigating dilated cardiomyopathy caused by dystrophin mutations using duchenne muscular dystrophy-patients induced pluripotent stem cell-derived cardiomyocytes
European Heart Journal · 2017
Modulation of Methylated Arginine Metabolism to Target Exercise‐Induced Fatigue in Duchenne Muscular Dystrophy
The FASEB Journal · 2016

Publishes in

bioRxiv (Cold Spring Harbor Laboratory)×3
The FASEB Journal×2
Journal of Cellular and Molecular Medicine×1
eLife×1
Journal of Pediatric Surgery×1

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This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.

Last updated Jul 25, 2026.

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