• 288 Citations
  • 10 h-Index
20052019
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Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 13 Similar Profiles
Apraxias Medicine & Life Sciences
Dyslexia Medicine & Life Sciences
Aptitude Medicine & Life Sciences
childhood Social Sciences
deficit Social Sciences
Linguistics Medicine & Life Sciences
Reading Medicine & Life Sciences
Language Medicine & Life Sciences

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Research Output 2005 2019

  • 288 Citations
  • 10 h-Index
  • 22 Article
  • 5 Chapter
  • 1 Book
  • 1 Conference contribution

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

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
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
4 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