Beate Peter

ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 23

Top Venues

Clinical linguistics & phonetics

F1000Research

American journal of medical genetics. Part A

American journal of speech-language pathology

University of Washington (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Washington

United States

PHD :: Speech and Hearing Science

Publications

Nancy L Potter, Mark VanDam, Laurel Bruce, Jenny Davis, Linda Eng, Lizbeth H Finestack, Victoria Heinlen, Nancy J Scherer, Claire Schrock, Ryan G N Seltzer, Carol Stoel-Gammon, Lauren Thompson, Beate Peter
Virtual Post-Intervention Speech and Language Assessment of Toddler and Preschool Participants in Babble Boot Camp. Journal of speech, language, and hearing research : JSLHR (2023)
Beate Peter, Laurel Bruce, Lizbeth H Finestack, Valentin Dinu, Melissa Wilson, Judith Klein-Seetharaman, Candace R Lewis, B Blair Braden, Yi-Yuan Tang, Nancy J Scherer, Mark VanDam, Nancy Potter
Precision Medicine as a New Frontier in Speech-Language Pathology: How Applying Insights From Behavior Genomics Can Improve Outcomes in Communication Disorders. American journal of speech-language pathology (2023)
Ashley Adams Sanabria, Maria Adelaida Restrepo, Beate Peter, Andrea Valentin, Arthur M Glenberg
Relationships Among Motor, First, and Second Language Skills Among Bilingual Children With Language Disorders. Journal of speech, language, and hearing research : JSLHR (2023)
Beate Peter
A case with cardiac, skeletal, speech, and motor traits narrows the subtelomeric 19p13.3 microdeletion region to 46 kb. American journal of medical genetics. Part A (2022)
Lizbeth H Finestack, Nancy Potter, Mark VanDam, Jennifer Davis, Laurel Bruce, Nancy Scherer, Linda Eng, Beate Peter
Feasibility of a Proactive Parent-Implemented Communication Intervention Delivered via Telepractice for Children With Classic Galactosemia. American journal of speech-language pathology 31 (6) (2022)
Laurel Bruce, Beate Peter
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. American journal of medical genetics. Part A 188 (12) (2022)
Beate Peter, Nancy Scherer, Winnie S Liang, Stephen Pophal, Colby Nielsen, Theresa A Grebe
A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocation. American journal of medical genetics. Part A 185 (5) (2021)
Beate Peter, Jennifer Davis, Sarah Cotter, Alicia Belter, Emma Williams, Melissa Stumpf, Laurel Bruce, Linda Eng, Yookyung Kim, Lizbeth H Finestack, Carol Stoel-Gammon, Delaney Williams, Nancy Scherer, Mark VanDam, Nancy Potter
Toward Preventing Speech and Language Disorders of Known Genetic Origin: First Post-Intervention Results of Babble Boot Camp in Children With Classic Galactosemia. American journal of speech-language pathology 30 (6) (2021)
Cynthia C Morton, Mary L Marazita, Beate Peter, Mabel L Rice, Shelly Jo Kraft, Julie Barkmeier-Kraemer, Carey Balaban, Michael Phillips, Jennifer Schoden, Deborah Maiese, Tabitha Hendershot, Carol M Hamilton
Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit. Annals of human genetics (2021)
Beate Peter
Introduction to the special issue, Sequential processing in spoken and written language. Clinical linguistics & phonetics 35 (4) (2021)
Beate Peter, Andria Albert, Heracles Panagiotides, Shelley Gray
Sequential and spatial letter reversals in adults with dyslexia during a word comparison task: demystifying the "was saw" and "db" myths. Clinical linguistics & phonetics 35 (4) (2020)
Beate Peter, Andria Albert, Shelley Gray
Spelling errors reveal underlying sequential and spatial processing deficits in adults with dyslexia. Clinical linguistics & phonetics 35 (4) (2020)
Beate Peter, Laurel Bruce, Caitlin Raaz, Emma Williams, Allie Pfeiffer, Corianne Rogalsky
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. Clinical linguistics & phonetics 35 (4) (2020)
Beate Peter, Valentin Dinu, Li Liu, Matthew Huentelman, Marcus Naymik, Hope Lancaster, Caitlin Vose, Isabelle Schrauwen
Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Behavior genetics 49 (4) (2019)
Beate Peter, Nancy Potter, Jennifer Davis, Inbal Donenfeld-Peled, Lizbeth Finestack, Carol Stoel-Gammon, Kari Lien, Laurel Bruce, Caitlin Vose, Linda Eng, Hanako Yokoyama, Daniel Olds, Mark VanDam
Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia. F1000Research (2019)
Beate Peter, Nancy Potter, Jennifer Davis, Inbal Donenfeld-Peled, Lizbeth Finestack, Carol Stoel-Gammon, Kari Lien, Laurel Bruce, Caitlin Vose, Linda Eng, Hanako Yokoyama, Daniel Olds, Mark VanDam
Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia. F1000Research (2019)
Beate Peter, Nancy Potter, Jennifer Davis, Inbal Donenfeld-Peled, Lizbeth Finestack, Carol Stoel-Gammon, Kari Lien, Laurel Bruce, Caitlin Vose, Linda Eng, Hanako Yokoyama, Daniel Olds, Mark VanDam
Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia. F1000Research (2019)
Beate Peter, Nancy Potter, Jennifer Davis, Inbal Donenfeld-Peled, Lizbeth Finestack, Carol Stoel-Gammon, Kari Lien, Laurel Bruce, Caitlin Vose, Linda Eng, Hanako Yokoyama, Daniel Olds, Mark VanDam
Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia. F1000Research 8 (2019)
Beate Peter, Nancy Potter, Jennifer Davis, Inbal Donenfeld-Peled, Lizbeth Finestack, Carol Stoel-Gammon, Kari Lien, Laurel Bruce, Caitlin Vose, Linda Eng, Hanako Yokoyama, Daniel Olds, Mark VanDam
Toward a paradigm shift from deficit-based to proactive speech and language treatment: Randomized pilot trial of the Babble Boot Camp in infants with classic galactosemia. F1000Research (2019)
Beate Peter, Hope Lancaster, Caitlin Vose, Kyle Middleton, Carol Stoel-Gammon
Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech. Clinical linguistics & phonetics 32 (4) (2017)
Beate Peter
The role of short-term memory impairment in nonword repetition, real word repetition, and nonword decoding: A case study. Clinical linguistics & phonetics 32 (4) (2017)
Beate Peter, Hope Lancaster, Caitlin Vose, Amna Fares, Isabelle Schrauwen, Matthew Huentelman
Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays. American journal of medical genetics. Part A 173 (10) (2017)
Beate Peter, Ellen M Wijsman, Alejandro Q Nato, null null, Mark M Matsushita, Kathy L Chapman, Ian B Stanaway, John Wolff, Kaori Oda, Virginia B Gabo, Wendy H Raskind
Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. PloS one 11 (4) (2016)

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Publication Activity (10 Years)

Top Topics

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Beate Peter