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Sara Lewis

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Scientific Writer

St. Jude Children's Research Hospital

United States

Research Interests

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Recent Grants

Grant: Close

Delivering personal medicine and identifying dystonic CP genes and pathways

Open Date: 2022-08-01

Close Date: 2024-07-01

Grant: Close

Learner fund

Open Date: 2019-02-01

Close Date: 2020-02-01

Articles (13)

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2026

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2026

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2026

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2025

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2024

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2023

Collaborators (17)

Suzanne Baker

Professor

St. Jude Children's Research Hospital

UNITED STATES

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Fredrik Swartling

SciLifeLab Group Leader; Director of the Preclinical Cancer Treatment (PCT) Center

Uppsala University

SWEDEN

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Luz Jubierre Zapater

Senior research scientist

Memorial Sloan Kettering Cancer Center

UNITED STATES

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Hilary Vernon

Associate Professor

Johns Hopkins University School of Medicine

UNITED STATES

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Huma Arshad Cheema

Professor

University Children’s Hospital Basel

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Reza Maroofian

UNITED KINGDOM

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Sheng Chih Jin

Assistant Professor

Washington University School of Medicine

UNITED STATES

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Miklos Toth

Professor

Weill Cornell Medicine

UNITED STATES

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Arzu Onar-Thomas

Member

St. Jude Children's Research Hospital

UNITED STATES

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Alex Michael Pagnozzi

Research Scientist

University of Queensland

AUSTRALIA

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Chief Medical & Genomic Officer

GERMANY

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Claudia Kleinman

Professor

McGill University

CANADA

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Sara Lewis

Research Interests

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Recent Grants

Articles (13)

A transposase-derived gene required for human brain development

Divergent medulloblastoma chromatin states disclose KDM2B as a selective dependency

A tumor-associated photoreceptor signature unifies distinct central nervous system malignancies

Cell autonomous regional differences in oligodendrocyte lineage development and responses to oncohistone H3.3 K27M

Genetic modeling of ELP1-associated Sonic hedgehog medulloblastoma identifies MDM2 as a selective therapeutic target.

Development and Validation of a Stakeholder-Driven, Self-Contained Electronic Informed Consent Platform for Trio-Based Genomic Research Studies.

Potential clinical applications of advanced genomic analysis in cerebral palsy

Clinical Actionability of Genetic Findings in Cerebral Palsy

Evolving understanding of CP phenotypes: the importance of dystonia.

Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders

AGAP1-associated endolysosomal trafficking abnormalities link gene-environment interactions in a neurodevelopmental disorder

TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions

Intrathecal magnesium delivery for Mg++-insensitive NMDA receptor activity due to GRIN1 mutation.

Collaborators (17)

Suzanne Baker

Fredrik Swartling

Luz Jubierre Zapater

Hilary Vernon

Huma Arshad Cheema

Reza Maroofian

Sheng Chih Jin

Miklos Toth

Arzu Onar-Thomas

Alex Michael Pagnozzi

Alex Kentsis

Michael Kruer

Alexander Proekt

Phillip Demarest

Beisi Xu

Peter Bauer

Claudia Kleinman

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