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Suzanne Lewis

6PUBLICATIONS
21CO-AUTHORS
Neurology and neuromuscular diseasesMajor global burdens of diseaseGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Infant and child health
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Journal

Publications (6)

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|Mar 11, 2025
Reporting a Homozygous Case of Neurodevelopmental Disorder Associated With a Novel PRPF8 Variant.

Mohammad Reza Mirinezhad, Farzaneh Mirzaei, Arash Salmaninejad

|Sep 28, 2024
Iron Deficiency and Restless Sleep/Wake Behaviors in Neurodevelopmental Disorders and Mental Health Conditions.

Osman S Ipsiroglu, Parveer K Pandher, Olivia Hill

|Apr 27, 2024
Clinical and Molecular Characterization of a Novel Homozygous Frameshift Variant in AEBP1-Related Classical-like Ehlers Danlos Syndrome Type 2 with Comparison to Previously Reported Rare Cases.

Zong Yi Ha, Chieko Chijiwa, Suzanne Lewis

|Dec 23, 2023
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous <i>MYT1L</i> Variant.

Silas Yip, Kristina Calli, Ying Qiao

|Feb 15, 2018
Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder.

Matthew A Budd, Kristina Calli, Lindy Samson

|May 20, 2016
The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families.

Michael D Fountain, Emmelien Aten, Megan T Cho

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Frequent Collaborators

1 joint publications

Matthew A Budd

1 joint publications

Jason C Brophy

1 joint publications

Silas Yip

1 joint publications

Kristina Calli

1 joint publications

Brett Trost

1 joint publications

Arash Salmaninejad

1 joint publications

Scout McWilliams

1 joint publications

Elizabeth Keys

1 joint publications

Calvin Kuo

1 joint publications

David Wensley

Frequent Collaborators

1 joint publications

Matthew A Budd

1 joint publications

Jason C Brophy

1 joint publications

Silas Yip

1 joint publications

Kristina Calli

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