• 295 Citations
  • 10 h-Index
20052019
If you made any changes in Pure, your changes will be visible here soon.

Research Output 2005 2019

  • 295 Citations
  • 10 h-Index
  • 23 Article
  • 5 Chapter
  • 1 Book
  • 1 Conference contribution
Filter
Article
2019

Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex Effects

Peter, B., Dinu, V., Liu, L., Huentelman, M., Naymik, M., Lancaster, H., Vose, C. & Schrauwen, I., Jan 1 2019, In : Behavior Genetics.

Research output: Contribution to journalArticle

Exome
Siblings
Apraxias
childhood
gene

Perceived gaps in genetics training among audiologists and speech-language pathologists: Lessons from a national survey

Peter, B., Dougherty, M. J., Reed, E. K., Edelman, E. & Hanson, K., May 1 2019, In : American Journal of Speech-Language Pathology. 28, 2, p. 408-423 16 p.

Research output: Contribution to journalArticle

Language
language
confidence
Audiologists
Pathologists
2018

Structural neural predictors of Farsi-English bilingualism

Berisha, V., Gilton, D., Baxter, L. C., Corman, S., Blais, C., Brewer, G., Ruston, S., Hunter Ball, B., Wingert, K. M., Peter, B. & Reddy, C., May 1 2018, In : Brain and Language. 180-182, p. 42-49 8 p.

Research output: Contribution to journalArticle

Multilingualism
multilingualism
Decision Trees
Language
Parietal Lobe
2017
1 Citation (Scopus)

Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech

Peter, B., Lancaster, H., Vose, C., Middleton, K. & Stoel-Gammon, C., Sep 20 2017, (Accepted/In press) In : Clinical Linguistics and Phonetics. p. 1-31 31 p.

Research output: Contribution to journalArticle

Apraxias
Dyslexia
dyslexia
deficit
Biomarkers
1 Citation (Scopus)
Short-Term Memory
Reading
Apraxias
Dyslexia
Long-Term Memory
6 Citations (Scopus)

Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays

Peter, B., Lancaster, H., Vose, C., Fares, A., Schrauwen, I. & Huentelman, M., Oct 1 2017, In : American Journal of Medical Genetics, Part A. 173, 10, p. 2659-2669 11 p.

Research output: Contribution to journalArticle

Language Development Disorders
Speech Disorders
Apraxias
Muscle Hypotonia
Multigene Family
2016
11 Citations (Scopus)

Genetic candidate variants in two multigenerational families with childhood apraxia of speech

Peter, B., Wijsman, E. M., Nato, A. Q., University of Washington Center for Mendelian Genomics, O. W. C. F. M. G., Matsushita, M. M., Chapman, K. L., Stanaway, I. B., Wolff, J., Oda, K., Gabo, V. B., Raskind, W. H., Bamshad, M., Nickerson, D. & Shendure, J., Apr 1 2016, In : PLoS One. 11, 4, e0153864.

Research output: Contribution to journalArticle

Apraxias
childhood
linkage (genetics)
Genes
etiology
2015
2 Citations (Scopus)

Direct and octave-shifted pitch matching during nonword imitations in men, women, and children

Peter, B., Foster, B., Haas, H., Middleton, K. & McKibben, K., Mar 1 2015, In : Journal of voice : official journal of the Voice Foundation. 29, 2

Research output: Contribution to journalArticle

Music
Speech Sound Disorder
2014
34 Citations (Scopus)

De novo microdeletion of BCL11A is associated with severe speech sound disorder

Peter, B., Matsushita, M., Oda, K. & Raskind, W., 2014, In : American Journal of Medical Genetics, Part A. 164, 8, p. 2091-2096 6 p.

Research output: Contribution to journalArticle

Apraxias
Phenotype
Genes
Dysarthria
Dyslexia
2013
13 Citations (Scopus)
Apraxias
Linguistics
genealogy
childhood
linguistics
17 Citations (Scopus)

Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech

Peter, B., Button, L., Stoel-Gammon, C., Chapman, K. & Raskind, W. H., Mar 2013, In : Clinical Linguistics and Phonetics. 27, 3, p. 163-191 29 p.

Research output: Contribution to journalArticle

Apraxias
Linguistics
deficit
childhood
linguistics

Preface

Peter, B. & MacLeod, A. A. N., 2013, In : Unknown Journal.

Research output: Contribution to journalArticle

22 Citations (Scopus)

The genetics of reading disabilities: From phenotypes to candidate genes

Raskind, W. H., Peter, B., Richards, T., Eckert, M. M. & Berninger, V. W., 2013, In : Frontiers in Psychology. 3, JAN, Article 601.

Research output: Contribution to journalArticle

Reading
Behavioral Genetics
Phenotype
Dyslexia
Genetic Heterogeneity
2012
23 Citations (Scopus)

Motor sequencing deficit as an endophenotype of speech sound disorder: A genome-wide linkage analysis in a multigenerational family

Peter, B., Matsushita, M. & Raskind, W. H., Oct 2012, In : Psychiatric Genetics. 22, 5, p. 226-234 9 p.

Research output: Contribution to journalArticle

Endophenotypes
Genome
Dyslexia
Aptitude
Microsatellite Repeats
4 Citations (Scopus)
Aptitude
Silver Sulfadiazine
Language
Hand
imitation

The future of genetics at our doorstep

Peter, B., Aug 8 2012, In : ASHA Leader. 17, 11

Research output: Contribution to journalArticle

2011
17 Citations (Scopus)

Evidence for a familial speech sound disorder subtype in a multigenerational study of oral and hand motor sequencing ability

Peter, B. & Raskind, W. H., Apr 2011, In : Topics in Language Disorders. 31, 2, p. 145-167 23 p.

Research output: Contribution to journalArticle

Aptitude
Hand
ability
evidence
Penetrance
9 Citations (Scopus)
Aptitude
Reading
ability
Dyslexia
dyslexia
69 Citations (Scopus)

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

Peter, B., Raskind, W. H., Matsushita, M., Lisowski, M., Vu, T., Berninger, V. W., Wijsman, E. M. & Brkanac, Z., Mar 2011, In : Journal of Neurodevelopmental Disorders. 3, 1, p. 39-49 11 p.

Research output: Contribution to journalArticle

Dyslexia
Reading
Motor Activity
Language
Single Nucleotide Polymorphism
2009
10 Citations (Scopus)

Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21

Raskind, W. H., Matsushita, M., Peter, B., Biberston, J., Wolff, J., Lipe, H., Burbank, R. & Bird, T. D., Jun 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 4, p. 570-574 5 p.

Research output: Contribution to journalArticle

Facial Nerve Diseases
Chorea
Dyskinesias
Myokymia
Chromosomes
3 Citations (Scopus)

Octave-shifted pitch matching in nonword imitations: The effects of lexical stress and speech sound disorder (L)

Peter, B., Larkin, T. & Stoel-Gammon, C., 2009, In : Journal of the Acoustical Society of America. 126, 4, p. 1663-1666 4 p.

Research output: Contribution to journalArticle

octaves
disorders
acoustics
vowels
psycholinguistics
2008
23 Citations (Scopus)

Central timing deficits in subtypes of primary speech disorders

Peter, B. & Stoel-Gammon, C., Mar 2008, In : Clinical Linguistics and Phonetics. 22, 3, p. 171-198 28 p.

Research output: Contribution to journalArticle

Speech Disorders
speech disorder
Apraxias
deficit
childhood
2005
21 Citations (Scopus)

Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music-related tasks

Peter, B. & Stoel-Gammon, C., Mar 2005, In : Clinical Linguistics and Phonetics. 19, 2, p. 67-87 21 p.

Research output: Contribution to journalArticle

Apraxias
Music
music
childhood
Task Performance and Analysis