Beate Peter
Overview
Explore the profile of Beate Peter including associated specialties, affiliations and a list of published articles.
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47
Citations
467
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Recent Articles
11.
Peter B, Davis J, Finestack L, Stoel-Gammon C, VanDam M, Bruce L, et al.
HGG Adv
. 2022 Jun;
3(3):100119.
PMID: 35677809
Precision medicine is an emerging approach to managing disease by taking into consideration an individual's genetic and environmental profile toward two avenues to improved outcomes: prevention and personalized treatments. This...
12.
Whisner C, Brown J, Larson D, Rodriguez L, Peter B, Reifsnider E, et al.
Matern Child Health J
. 2022 Jan;
26(Suppl 1):10-19.
PMID: 35060070
Objectives: To describe the process of developing and implementing experiential learning through translational research teams that engage diverse undergraduate and graduate students. Methods: After a college redesign, translational research teams...
13.
Peter B, Davis J, Cotter S, Belter A, Williams E, Stumpf M, et al.
Am J Speech Lang Pathol
. 2021 Oct;
30(6):2616-2634.
PMID: 34665663
Purpose Babble Boot Camp (BBC) is a package of proactive activities and routines designed to prevent speech and language disorders in infants at predictable risk. It is implemented via parent...
14.
Morton C, Marazita M, Peter B, Rice M, Kraft S, Barkmeier-Kraemer J, et al.
Ann Hum Genet
. 2021 Sep;
86(1):45-51.
PMID: 34582045
The PhenX Toolkit (https://www.phenxtoolkit.org/) is an online catalog of recommended measurement protocols to facilitate cross-study analyses for biomedical research. An expert review panel (ERP) reviewed and updated the PhenX Toolkit...
15.
16.
Peter B, Scherer N, Liang W, Pophal S, Nielsen C, Grebe T
Am J Med Genet A
. 2021 Feb;
185(5):1532-1537.
PMID: 33569883
The 22q11.2 deletion syndrome (22q11.2 DS) is the most common deletion syndrome in humans. In most cases, it occurs de novo. A rare family of three with 22q11.2 deletion syndrome...
17.
Peter B, Bruce L, Raaz C, Williams E, Pfeiffer A, Rogalsky C
Clin Linguist Phon
. 2020 Dec;
35(4):368-392.
PMID: 33327803
Individuals with childhood apraxia of speech (CAS) have motor deficits in systems beyond speech and also global deficits in sequential processing, consistent with cerebellar dysfunction. We investigated the cerebellar hypothesis...
18.
Peter B, Potter N, Davis J, Donenfeld-Peled I, Finestack L, Stoel-Gammon C, et al.
F1000Res
. 2020 Jul;
8:271.
PMID: 32566130
Speech and language therapy is typically initiated reactively after a child shows delays. Infants with classic galactosemia (CG), a metabolic disease with a known high risk for both speech and...
19.
Spelling errors reveal underlying sequential and spatial processing deficits in adults with dyslexia
Peter B, Albert A, Gray S
Clin Linguist Phon
. 2020 Jun;
35(4):310-339.
PMID: 32552235
Recent studies showed that some adults with dyslexia have difficulty processing sequentially arranged information. In a companion study, this deficit manifested as low accuracy during a word pair comparison task...
20.
Torpel A, Peter B, Schega L
Front Physiol
. 2020 May;
11:335.
PMID: 32411007
Background: Resistance training (RT) under hypoxic conditions has been used to increase muscular performance under normoxic conditions in young people. However, the effects of RT and thus of RT under...