| Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample B Peter, WH Raskind, M Matsushita, M Lisowski, T Vu, VW Berninger, ... Journal of neurodevelopmental disorders 3, 39-49, 2011 | 151 | 2011 |
| De novo microdeletion of BCL11A is associated with severe speech sound disorder B Peter, M Matsushita, K Oda, W Raskind American journal of medical genetics Part A 164 (8), 2091-2096, 2014 | 88 | 2014 |
| The genetics of reading disabilities: from phenotypes to candidate genes WH Raskind, B Peter, T Richards, MM Eckert, VW Berninger Frontiers in psychology 3, 601, 2013 | 86 | 2013 |
| An acoustic phonetic catalog of prespeech vocalizations from a developmental perspective EH Buder, AS Warlaumont, DK Oller, B Peter, A MacLeod Comprehensive perspectives on child speech development and disorders …, 2013 | 68 | 2013 |
| Timing errors in two children with suspected childhood apraxia of speech (sCAS) during speech and music‐related tasks B Peter, C Stoel‐Gammon Clinical Linguistics & Phonetics 19 (2), 67-87, 2005 | 68 | 2005 |
| Central timing deficits in subtypes of primary speech disorders B Peter, C Stoel‐Gammon Clinical Linguistics & Phonetics 22 (3), 171-198, 2008 | 62 | 2008 |
| Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech B Peter, L Button, C Stoel-Gammon, K Chapman, WH Raskind Clinical linguistics & phonetics 27 (3), 163-191, 2013 | 47 | 2013 |
| Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech B Peter, H Lancaster, C Vose, K Middleton, C Stoel-Gammon Clinical Linguistics & Phonetics 32 (4), 316-346, 2018 | 45 | 2018 |
| Motor sequencing deficit as an endophenotype of speech sound disorder: A genome-wide linkage analysis in a multigenerational family B Peter, M Matsushita, WH Raskind Psychiatric genetics 22 (5), 226-234, 2012 | 44 | 2012 |
| Genetic candidate variants in two multigenerational families with childhood apraxia of speech B Peter, EM Wijsman, AQ Nato Jr, ... PloS one 11 (4), e0153864, 2016 | 42 | 2016 |
| Global processing speed in children with low reading ability and in children and adults with typical reading ability: Exploratory factor analytic models B Peter, M Matsushita, WH Raskind American Speech-Language-Hearing Association, 2011 | 42 | 2011 |
| 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 L Button, B Peter, C Stoel-Gammon, WH Raskind Clinical linguistics & phonetics 27 (3), 192-212, 2013 | 33 | 2013 |
| Two unrelated children with overlapping 6q25. 3 deletions, motor speech disorders, and language delays B Peter, H Lancaster, C Vose, A Fares, I Schrauwen, M Huentelman American Journal of Medical Genetics Part A 173 (10), 2659-2669, 2017 | 28 | 2017 |
| Speaking fundamental frequency characteristics of centenarian females SN Awan, PB Mueller Clinical linguistics & phonetics 6 (3), 249-254, 1992 | 28 | 1992 |
| 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 B Peter, N Potter, J Davis, I Donenfeld-Peled, L Finestack, ... F1000Research 8, 2019 | 27 | 2019 |
| Auditory gating in adults with dyslexia: An ERP account of diminished rapid neural adaptation B Peter, H McCollum, A Daliri, H Panagiotides Clinical Neurophysiology 130 (11), 2182-2192, 2019 | 26 | 2019 |
| Exome sequencing of two siblings with sporadic autism spectrum disorder and severe speech sound disorder suggests pleiotropic and complex effects B Peter, V Dinu, L Liu, M Huentelman, M Naymik, H Lancaster, C Vose, ... Behavior genetics 49, 399-414, 2019 | 21 | 2019 |
| Familial dyskinesia and facial myokymia (FDFM): Follow‐up of a large family and linkage to chromosome 3p21‐3q21 WH Raskind, M Matsushita, B Peter, J Biberston, J Wolff, H Lipe, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150 …, 2009 | 18 | 2009 |
| A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype B Peter, WH Raskind Topics in language disorders 31 (2), 145, 2011 | 16 | 2011 |
| Sequential and spatial letter reversals in adults with dyslexia during a word comparison task: Demystifying the “was saw” and “db” myths B Peter, A Albert, H Panagiotides, S Gray Clinical Linguistics & Phonetics 35 (4), 340-367, 2021 | 15 | 2021 |
Nancy L. PotterProfessor of Speech and Hearing, Washington State UniversityAdresse e-mail validée de wsu.edu
