Tomi Toler

Assistant Professor

Washington University in Saint Louis School of Medicine

United States

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About

Dr. Tomi Toler is an Assistant Professor at Washington University in St Louis School of Medicine, USA. His research encompasses a range of areas including genetic disorders, phenotypic characterization of diseases, and the molecular mechanisms underlying autoimmunity and demyelinating diseases. He has recently contributed to studies on conditions such as 11q13 Microdeletion Syndrome and CoQ10 deficiency, while also focusing on the implications of expanded carrier screening in reproductive health.

Articles (10)

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2025

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2025

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2023

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2023

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2023

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2021

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2021

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2021

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2020

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2020

Collaborators (9)

Richard H. van Jaarsveld

NETHERLANDS

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Mohamad Mikati

Duke University

UNITED STATES

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Lauren Westerfield

Assistant Professor, Genetic Counselor

Baylor College of Medicine

UNITED STATES

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Maria Laura Duque Lasio

Assistant Professor

Washington University in St. Louis

UNITED STATES

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Dorothy K. Grange

UNITED STATES

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Lisa Oakes

Professor

University of California, Davis

UNITED STATES

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Reza Asadollahi

Senior Lecturer in Genetics

University of Greenwich

UNITED KINGDOM

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Marwan shinawi

Professor

Washington University in Saint Louis School of Medicine

UNITED STATES

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Mary-Ellen Harper

Professor

University of Ottawa

CANADA

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Tomi Toler

Research Interests

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About

Articles (10)

Mosaic STAT5B gain-of-function associated with demyelinating disease and autoimmunity

Single-Gene Deletion of FGF3 in a Patient With Features of 11q13 Microdeletion Syndrome.

Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors

Phenotypic, molecular, and functional characterization of COQ7-related primary CoQ10 deficiency: Novel hypomorphic variants and two distinct disease entities

Postmortem diagnosis of very long chain acyl‐CoA dehydrogenase (VLCAD) deficiency in a neonate with sudden cardiac death

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Phenotypic expansion of KMT2D‐related disorder: Beyond Kabuki syndrome

POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4

Collaborators (9)

Richard H. van Jaarsveld

Mohamad Mikati

Lauren Westerfield

Maria Laura Duque Lasio

Dorothy K. Grange

Lisa Oakes

Reza Asadollahi

Marwan shinawi

Mary-Ellen Harper

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