Specific language impairment is not specific to language: The procedural deficit hypothesis MT Ullman, EI Pierpont Cortex 41 (3), 399-433, 2005 | 1197 | 2005 |
Cardio-facio-cutaneous syndrome: clinical features, diagnosis, and management guidelines MEM Pierpont, PL Magoulas, S Adi, MI Kavamura, G Neri, J Noonan, ... Pediatrics 134 (4), e1149-e1162, 2014 | 186 | 2014 |
Genotype differences in cognitive functioning in Noonan syndrome EI Pierpont, ME Pierpont, NJ Mendelsohn, AE Roberts, E Tworog‐Dube, ... Genes, Brain and Behavior 8 (3), 275-282, 2009 | 129 | 2009 |
A report on state‐wide implementation of newborn screening for X‐linked adrenoleukodystrophy K Wiens, SA Berry, H Choi, A Gaviglio, A Gupta, A Hietala, ... American Journal of Medical Genetics Part A 179 (7), 1205-1213, 2019 | 66 | 2019 |
Attention skills and executive functioning in children with Noonan syndrome and their unaffected siblings EI Pierpont, E Tworog‐Dube, AE Roberts Developmental Medicine & Child Neurology 57 (4), 385-392, 2015 | 60 | 2015 |
Neurocognitive trajectory of boys who received a hematopoietic stem cell transplant at an early stage of childhood cerebral adrenoleukodystrophy EI Pierpont, JB Eisengart, R Shanley, D Nascene, GV Raymond, ... JAMA neurology 74 (6), 710-717, 2017 | 59 | 2017 |
The language phenotype of children and adolescents with Noonan syndrome EI Pierpont, SE Weismer, AE Roberts, E Tworog-Dube, ME Pierpont, ... American Speech-Language-Hearing Association, 2010 | 53 | 2010 |
Contributions of phonological and verbal working memory to language development in adolescents with fragile X syndrome EI Pierpont, EK Richmond, L Abbeduto, ST Kover, WT Brown Journal of Neurodevelopmental Disorders 3, 335-347, 2011 | 50 | 2011 |
Effects of germline mutations in the Ras/MAPK signaling pathway on adaptive behavior: cardiofaciocutaneous syndrome and Noonan syndrome EI Pierpont, ME Pierpont, NJ Mendelsohn, AE Roberts, E Tworog‐Dube, ... American Journal of Medical Genetics Part A 152 (3), 591-600, 2010 | 47 | 2010 |
The Arizona Cognitive Test Battery for Down syndrome: Test-retest reliability and practice effects JO Edgin, P Anand, T Rosser, EI Pierpont, C Figueroa, D Hamilton, ... American journal on intellectual and developmental disabilities 122 (3), 215-234, 2017 | 45 | 2017 |
Learning and memory in children with Noonan syndrome EI Pierpont, E Tworog‐Dube, AE Roberts American journal of medical genetics Part A 161 (9), 2250-2257, 2013 | 39 | 2013 |
Neuropsychological functioning in individuals with Noonan syndrome: a systematic literature review with educational and treatment recommendations EI Pierpont Journal of Pediatric Neuropsychology 2, 14-33, 2016 | 37 | 2016 |
Associations between medical history, cognition, and behavior in youth with down syndrome: a report from the down syndrome cognition project TC Rosser, JO Edgin, GT Capone, DR Hamilton, EG Allen, KJ Dooley, ... American journal on intellectual and developmental disabilities 123 (6), 514-528, 2018 | 36 | 2018 |
A neurodevelopmental perspective on the acquisition of nonverbal cognitive skills in adolescents with fragile X syndrome ST Kover, EI Pierpont, JS Kim, WT Brown, L Abbeduto Developmental Neuropsychology 38 (7), 445-460, 2013 | 36 | 2013 |
Intrathecal enzyme replacement for Hurler syndrome: biomarker association with neurocognitive outcomes JB Eisengart, EI Pierpont, AM Kaizer, KD Rudser, KE King, M Pasquali, ... Genetics in medicine 21 (11), 2552-2560, 2019 | 30 | 2019 |
Social skills in children with RASopathies: a comparison of Noonan syndrome and neurofibromatosis type 1 EI Pierpont, RL Hudock, AM Foy, M Semrud-Clikeman, ME Pierpont, ... Journal of neurodevelopmental disorders 10, 1-11, 2018 | 30 | 2018 |
Behavioral functioning in cardiofaciocutaneous syndrome: Risk factors and impact on parenting experience EI Pierpont, M Wolford American Journal of Medical Genetics Part A 170 (8), 1974-1988, 2016 | 23 | 2016 |
The impact of erythropoietin on short-and long-term kidney-related outcomes in neonates of extremely low gestational age. Results of a multicenter, double-blind, placebo … DJ Askenazi, PJ Heagerty, RH Schmicker, P Brophy, SE Juul, ... The Journal of pediatrics 232, 65-72. e7, 2021 | 20 | 2021 |
Neurologic and neurodevelopmental complications in cardiofaciocutaneous syndrome are associated with genotype: A multinational cohort study EI Pierpont, DL Kenney-Jung, R Shanley, AL Zatkalik, AE Whitmarsh, ... Genetics in Medicine 24 (7), 1556-1566, 2022 | 19 | 2022 |
Mosaicism of the UDP-Galactose transporter SLC35A2 in a female causing a congenital disorder of glycosylation: a case report K Westenfield, K Sarafoglou, LC Speltz, EI Pierpont, J Steyermark, ... BMC medical genetics 19, 1-7, 2018 | 17 | 2018 |