Beate Peter

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Arizona State University

United States

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Recent Grants

Grant: Close

Preventing speech and language disorders in infants with classic galactosemia

Open Date: 2019-04-17

Close Date: 2023-03-31

Grant: Close

Genetics of speech disorders

Open Date: 2011-04-01

Close Date: 2015-03-30

Articles (10)

Year:

2023

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2023

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2023

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2022

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2022

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2022

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2022

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2021

Year:

2021

Year:

2021

Collaborators (8)

Arthur Glenberg

Arizona State University

UNITED STATES

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Ashley Adams

Assistant Professor

San Diego State University

UNITED STATES

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Caitlin Raaz

Assistant Professor

University of Northern Colorado

UNITED STATES

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Nancy Scherer

Professor

Arizona State University

UNITED STATES

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Laurel Bruce

Clinical Assistant Professor

Arizona State University

UNITED STATES

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Lizbeth Finestack

University of Minnesota

UNITED STATES

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Ina Knerr

Consultant Metabolic Paediatrician, Clinical Professor

IRELAND

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Mark VanDam

Associate Professor

Washington State University - Spokane

UNITED STATES

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Beate Peter

Research Interests

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Contact this professor

Recent Grants

Articles (10)

Precision Medicine as a New Frontier in Speech-Language Pathology: How Applying Insights From Behavior Genomics Can Improve Outcomes in Communication Disorders

Relationships Among Motor, First, and Second Language Skills Among Bilingual Children With Language Disorders

A case with cardiac, skeletal, speech, and motor traits narrows the subtelomeric 19p13.3 microdeletion region to 46 kb

Feasibility of a Proactive Parent-Implemented Communication Intervention Delivered via Telepractice for Children With Classic Galactosemia

Three children with different de novo BCL11A variants and diverse developmental phenotypes, but shared global motor discoordination and apraxic speech: Evidence for a functional gene network influencing the developing cerebellum and motor and auditory cortices

Translating principles of precision medicine into speech-language pathology: Clinical trial of a proactive speech and language intervention for infants with classic galactosemia

Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit

Toward Preventing Speech and Language Disorders of Known Genetic Origin: First Post-Intervention Results of Babble Boot Camp in Children With Classic Galactosemia

A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocation

Comparing global motor characteristics in children and adults with childhood apraxia of speech to a cerebellar stroke patient: evidence for the cerebellar hypothesis in a developmental motor speech disorder

Collaborators (8)

Arthur Glenberg

Ashley Adams

Caitlin Raaz

Nancy Scherer

Laurel Bruce

Lizbeth Finestack

Ina Knerr

Mark VanDam

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