Beate Peter

Summary

Affiliation: University of Washington
Country: USA

Publications

  1. pmc Oral and hand movement speeds are associated with expressive language ability in children with speech sound disorder
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA, USA
    J Psycholinguist Res 41:455-74. 2012
  2. doi request reprint Direct and octave-shifted pitch matching during nonword imitations in men, women, and children
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, Washington Electronic address
    J Voice 29:260.e21-30. 2015
  3. pmc Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA 98195, USA
    Clin Linguist Phon 27:163-91. 2013
  4. pmc Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, Washington 98195, USA
    Psychiatr Genet 22:226-34. 2012
  5. pmc Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, P O Box 354875, Seattle, WA, 98195, USA
    J Neurodev Disord 3:39-49. 2011
  6. pmc Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic models
    Beate Peter
    University of Washington, Seattle, USA
    J Speech Lang Hear Res 54:885-99. 2011
  7. doi request reprint Central timing deficits in subtypes of primary speech disorders
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA 98105, USA
    Clin Linguist Phon 22:171-98. 2008
  8. pmc 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
    Le Button
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA 98105, USA
    Clin Linguist Phon 27:192-212. 2013
  9. ncbi request reprint Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music-related tasks
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, 1417 N E 42nd Street, University of Washington, Seattle, WA 98195, USA
    Clin Linguist Phon 19:67-87. 2005
  10. pmc Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21
    Wendy H Raskind
    Department of Medicine, University of Washington School of Medicine, Seattle, Washington 98195 7720, USA
    Am J Med Genet B Neuropsychiatr Genet 150:570-4. 2009

Detail Information

Publications12

  1. pmc Oral and hand movement speeds are associated with expressive language ability in children with speech sound disorder
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA, USA
    J Psycholinguist Res 41:455-74. 2012
    ..Results are consistent with limited movement speeds across motor systems and SSD subtypes defined by motor speeds as a corollary of expressive language abilities...
  2. doi request reprint Direct and octave-shifted pitch matching during nonword imitations in men, women, and children
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, Washington Electronic address
    J Voice 29:260.e21-30. 2015
    ....
  3. pmc Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA 98195, USA
    Clin Linguist Phon 27:163-91. 2013
    ..Results are consistent with a global deficit in sequential processing that influences speech development as well as cognitive and linguistic processing...
  4. pmc Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, Washington 98195, USA
    Psychiatr Genet 22:226-34. 2012
    ..The aim of this pilot study was to investigate a measure of motor sequencing deficit as a potential endophenotype of speech sound disorder (SSD) in a multigenerational family with evidence of familial SSD...
  5. pmc Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, P O Box 354875, Seattle, WA, 98195, USA
    J Neurodev Disord 3:39-49. 2011
    ..In addition, FOXP2 SNP associations with both RAPA and FS-D were observed. Our results confirm the role of CNTNAP2 in NWR in a dyslexia sample and motivate new questions about the effects of FOXP2 in neurodevelopmental disorders...
  6. pmc Global processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic models
    Beate Peter
    University of Washington, Seattle, USA
    J Speech Lang Hear Res 54:885-99. 2011
    ..To investigate processing speed as a latent dimension in children with dyslexia and children and adults with typical reading skills...
  7. doi request reprint Central timing deficits in subtypes of primary speech disorders
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA 98105, USA
    Clin Linguist Phon 22:171-98. 2008
    ..The number of observed CAS characteristics was associated with timing deficits...
  8. pmc 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
    Le Button
    Department of Speech and Hearing Sciences, University of Washington, Seattle, WA 98105, USA
    Clin Linguist Phon 27:192-212. 2013
    ..Correlations were characterized by extremely high scores in one family and extremely low scores in another. Results are consistent with a central deficit in sequential processing in CAS of familial origin...
  9. ncbi request reprint Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music-related tasks
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, 1417 N E 42nd Street, University of Washington, Seattle, WA 98195, USA
    Clin Linguist Phon 19:67-87. 2005
    ..Timing structures and accuracy are discussed with respect to diagnostic status, age, speech and music tasks, and timing unit size...
  10. pmc Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21
    Wendy H Raskind
    Department of Medicine, University of Washington School of Medicine, Seattle, Washington 98195 7720, USA
    Am J Med Genet B Neuropsychiatr Genet 150:570-4. 2009
    ..Identification of additional families with FDFM may narrow the critical region and facilitate the choice of candidate genes for further analysis...
  11. pmc The genetics of reading disabilities: from phenotypes to candidate genes
    Wendy H Raskind
    Department of Medicine, University of Washington Seattle, WA, USA Department of Psychiatry and Behavioral Sciences, University of Washington Seattle, WA, USA
    Front Psychol 3:601. 2012
    ..A glossary of genetic terms (denoted by bold font) is provided for readers not familiar with the technical terms...
  12. doi request reprint De novo microdeletion of BCL11A is associated with severe speech sound disorder
    Beate Peter
    Department of Speech and Hearing Sciences, University of Washington, Seattle, Washington
    Am J Med Genet A 164:2091-6. 2014
    ..The present case is the first to involve a single gene within the microdeletion region and a phenotype restricted to a subset of the traits observed in other cases with more extensive deletions...