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Beate Peter, Ph.D. - Publications

Affiliations: 
University of Washington, Seattle, Seattle, WA 
Area:
phonological acquisition, late talkers
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37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Sanabria A, Restrepo MA, Peter B, Valentin A, Glenberg A. Relationships Among Motor, First, and Second Language Skills Among Bilingual Children With Language Disorders. Journal of Speech, Language, and Hearing Research : Jslhr. 1-14. PMID 37532242 DOI: 10.1044/2023_JSLHR-23-00043  0.437
2023 Potter NL, VanDam M, Bruce L, Davis J, Eng L, Finestack L, Heinlen V, Scherer N, Schrock C, Seltzer R, Stoel-Gammon C, Thompson L, Peter B. Virtual Post-Intervention Speech and Language Assessment of Toddler and Preschool Participants in Babble Boot Camp. Journal of Speech, Language, and Hearing Research : Jslhr. 1-13. PMID 37235746 DOI: 10.1044/2023_JSLHR-22-00687  0.689
2023 Peter B, Bruce L, Finestack L, Dinu V, Wilson M, Klein-Seetharaman J, Lewis CR, Braden BB, Tang YY, Scherer N, VanDam M, Potter N. 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. 1-16. PMID 37146603 DOI: 10.1044/2023_AJSLP-22-00205  0.324
2022 Bruce L, Peter B. 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. PMID 35856171 DOI: 10.1002/ajmg.a.62904  0.436
2022 Peter B, Davis J, Finestack L, Stoel-Gammon C, VanDam M, Bruce L, Kim Y, Eng L, Cotter S, Landis E, Beames S, Scherer N, Knerr I, Williams D, Schrock C, et al. Translating principles of precision medicine into speech-language pathology: Clinical trial of a proactive speech and language intervention for infants with classic galactosemia. Hgg Advances. 3: 100119. PMID 35677809 DOI: 10.1016/j.xhgg.2022.100119  0.703
2021 Peter B, Davis J, Cotter S, Belter A, Williams E, Stumpf M, Bruce L, Eng L, Kim Y, Finestack L, Stoel-Gammon C, Williams D, Scherer N, VanDam M, Potter N. 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. 1-19. PMID 34665663 DOI: 10.1044/2021_AJSLP-21-00098  0.698
2021 Morton CC, Marazita ML, Peter B, Rice ML, Kraft SJ, Barkmeier-Kraemer J, Balaban C, Phillips M, Schoden J, Maiese D, Hendershot T, Hamilton CM. Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit. Annals of Human Genetics. PMID 34582045 DOI: 10.1111/ahg.12447  0.416
2021 Peter B. Introduction to the special issue, Sequential processing in spoken and written language. Clinical Linguistics & Phonetics. 35: 293-295. PMID 33662225 DOI: 10.1080/02699206.2020.1861482  0.337
2020 Peter B, Bruce L, Raaz C, Williams E, Pfeiffer A, Rogalsky C. 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. 1-25. PMID 33327803 DOI: 10.1080/02699206.2020.1861103  0.314
2020 Peter B, Albert A, Gray S. Spelling errors reveal underlying sequential and spatial processing deficits in adults with dyslexia. Clinical Linguistics & Phonetics. 1-30. PMID 32552235 DOI: 10.1080/02699206.2020.1780322  0.455
2020 Peter B, Albert A, Panagiotides H, Gray S. Sequential and spatial letter reversals in adults with dyslexia during a word comparison task: demystifying the "was saw" and "db" myths. Clinical Linguistics & Phonetics. 1-28. PMID 31959003 DOI: 10.1080/02699206.2019.1705916  0.413
2019 Peter B, Potter N, Davis J, Donenfeld-Peled I, Finestack L, Stoel-Gammon C, Lien K, Bruce L, Vose C, Eng L, Yokoyama H, Olds D, VanDam M. 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: 271. PMID 32566130 DOI: 10.12688/F1000Research.18062.1  0.725
2019 Peter B, McCollum H, Daliri A, Panagiotides H. Auditory gating in adults with dyslexia: An ERP account of diminished rapid neural adaptation. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. PMID 31451333 DOI: 10.1016/J.Clinph.2019.07.028  0.311
2019 Peter B, Vose C, Bruce L, Ingram D. Starting to Talk at Age 10 Years: Lessons About the Acquisition of English Speech Sounds in a Rare Case of Severe Congenital But Remediated Motor Disease of Genetic Origin. American Journal of Speech-Language Pathology. 1-10. PMID 31298943 DOI: 10.1044/2019_Ajslp-18-0156  0.499
2019 Peter B, Dougherty MJ, Reed EK, Edelman E, Hanson K. Perceived Gaps in Genetics Training Among Audiologists and Speech-Language Pathologists: Lessons From a National Survey. American Journal of Speech-Language Pathology. 1-16. PMID 31091132 DOI: 10.1044/2018_Ajslp-18-0069  0.329
2019 Peter B, Dinu V, Liu L, Huentelman M, Naymik M, Lancaster H, Vose C, Schrauwen I. Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects. Behavior Genetics. PMID 30949922 DOI: 10.1007/S10519-019-09957-8  0.444
2019 Peter B, Potter N, Davis J, Donenfeld-Peled I, Finestack L, Stoel-Gammon C, Lien K, Bruce L, Vose C, Eng L, Yokoyama H, Olds D, VanDam M. 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: 271. DOI: 10.12688/F1000RESEARCH.18062.1  0.714
2018 Berisha V, Gilton D, Baxter LC, Corman SR, Blais C, Brewer G, Ruston S, Hunter Ball B, Wingert KM, Peter B, Rogalsky C. Structural neural predictors of Farsi-English bilingualism. Brain and Language. 180: 42-49. PMID 29723828 DOI: 10.1016/J.Bandl.2018.04.005  0.386
2018 Bruce L, Lynde S, Weinhold J, Peter B. A Team Approach to Response to Intervention for Speech Sound Errors in the School Setting Perspectives of the Asha Special Interest Groups. 3: 110-119. DOI: 10.1044/Persp3.Sig16.110  0.393
2017 Peter B, Lancaster H, Vose C, Middleton K, Stoel-Gammon C. Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech. Clinical Linguistics & Phonetics. 1-31. PMID 28933620 DOI: 10.1080/02699206.2017.1375560  0.674
2017 Peter B. The role of short-term memory impairment in nonword repetition, real word repetition, and nonword decoding: A case study. Clinical Linguistics & Phonetics. 1-6. PMID 28933571 DOI: 10.1080/02699206.2017.1375561  0.351
2017 Peter B, Lancaster H, Vose C, Fares A, Schrauwen I, Huentelman M. Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays. American Journal of Medical Genetics. Part A. PMID 28767196 DOI: 10.1002/Ajmg.A.38385  0.523
2016 Peter B, Wijsman EM, Nato AQ, Matsushita MM, Chapman KL, Stanaway IB, Wolff J, Oda K, Gabo VB, Raskind WH. Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. Plos One. 11: e0153864. PMID 27120335 DOI: 10.1371/Journal.Pone.0153864  0.36
2015 Peter B, Foster B, Haas H, Middleton K, McKibben K. Direct and octave-shifted pitch matching during nonword imitations in men, women, and children. Journal of Voice : Official Journal of the Voice Foundation. 29: 260.e21-30. PMID 25439509 DOI: 10.1016/J.Jvoice.2014.06.011  0.39
2014 Peter B, Matsushita M, Oda K, Raskind W. De novo microdeletion of BCL11A is associated with severe speech sound disorder. American Journal of Medical Genetics. Part A. 164: 2091-6. PMID 24810580 DOI: 10.1002/Ajmg.A.36599  0.408
2013 Peter B, Button L, Stoel-Gammon C, Chapman K, Raskind WH. Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech. Clinical Linguistics & Phonetics. 27: 163-91. PMID 23339324 DOI: 10.3109/02699206.2012.736011  0.697
2013 Button L, Peter B, Stoel-Gammon C, Raskind WH. Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication study. Clinical Linguistics & Phonetics. 27: 192-212. PMID 23339292 DOI: 10.3109/02699206.2012.744097  0.683
2013 Peter B. Interactions between speech sound disorder and dyslexia Comprehensive Perspectives On Speech Sound Development and Disorders: Pathways From Linguistic Theory to Clinical Practice. 365-385.  0.34
2012 Peter B, Matsushita M, Raskind WH. Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family. Psychiatric Genetics. 22: 226-34. PMID 22517379 DOI: 10.1097/Ypg.0B013E328353Ae92  0.448
2012 Peter B. Oral and hand movement speeds are associated with expressive language ability in children with speech sound disorder. Journal of Psycholinguistic Research. 41: 455-74. PMID 22411590 DOI: 10.1007/S10936-012-9199-1  0.52
2011 Peter B, Raskind WH. A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype. Topics in Language Disorders. 31: 145-167. PMID 21909176 DOI: 10.1097/Tld.0B013E318217B855  0.458
2011 Peter B, Raskind WH, Matsushita M, Lisowski M, Vu T, Berninger VW, Wijsman EM, Brkanac Z. Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample. Journal of Neurodevelopmental Disorders. 3: 39-49. PMID 21484596 DOI: 10.1007/S11689-010-9065-0  0.472
2011 Peter B, Matsushita M, Raskind WH. Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic models. Journal of Speech, Language, and Hearing Research : Jslhr. 54: 885-99. PMID 21081672 DOI: 10.1044/1092-4388(2010/10-0135)  0.402
2009 Peter B, Larkin T, Stoel-Gammon C. Octave-shifted pitch matching in nonword imitations: the effects of lexical stress and speech sound disorder. The Journal of the Acoustical Society of America. 126: 1663-6. PMID 19813781 DOI: 10.1121/1.3203993  0.692
2008 Peter B, Stoel-Gammon C. Central timing deficits in subtypes of primary speech disorders. Clinical Linguistics & Phonetics. 22: 171-98. PMID 18307084 DOI: 10.1080/02699200701799825  0.705
2006 Peter B, Stoel‐Gammon C. Acoustic correlates of primary motor speech disorders in children during oral and hand tasks The Journal of the Acoustical Society of America. 120: 3349-3350. DOI: 10.1121/1.4781407  0.547
2005 Peter B, Stoel-Gammon C. Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music-related tasks. Clinical Linguistics & Phonetics. 19: 67-87. PMID 15704499 DOI: 10.1080/02699200410001669843  0.706
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