Rare genetic disorders

Thursday, May 2, 2019: 5:30 PM-7:00 PM
Room: 710 (Palais des congres de Montreal)
5:30 PM
146.222
222 Autistic Traits and Cognitive Abilities Associated with Two Molecular Causes of Silver-Russell Syndrome
C. Lane M. Freeth L. Robinson
5:30 PM
146.223
223 Spontaneous Neural Responses Relate to Behavioural and Psychiatric Traits in 16p11.2 Deletion Carriers: A Joint Analysis of EEG Spectral Power and Multi-Scale Entropy.
R. Al-Jawahiri M. Jones E. Milne
5:30 PM
146.224
224 Links between Autism and the FMR1 Premutation: Insights from Studies of Gaze, Language, and Cognition in Carriers of the FMR1 Premutation
K. Nayar M. Winston A. L. Hogan W. S. McKinney G. E. Martin J. N. Barstein C. G. La Valle M. Losh
5:30 PM
146.225
225 Precision Sensorimotor Control and Neurophysiology in Aging FMR1 Premutation Carriers
W. S. McKinney K. E. Unruh Z. Wang M. W. Mosconi
5:30 PM
146.226
226 A Comparison of Head Circumference Growth Trajectories in the Context of the CHD8 Regulatory Network
B. M. Boyd A. B. Arnett C. M. Hudac K. Hoekzema T. Turner B. J. O'Roak E. E. Eichler R. Bernier
5:30 PM
146.227
Altered Striatum Centered Connectivity in SHANK3-Deficient Patients (Withdrawn)
 C. Liu X. Xu D. Li
5:30 PM
146.228
228 Characterizing Comorbid Seizures in Rare Genetic Conditions Associated with Autism and Neurodevelopment Disorders in the Simons Searchlight Cohort
E. Brooks L. A. Cartner L. A. Green Snyder W. K. Chung
5:30 PM
146.229
229 Data Harmonization across Genetic Conditions Associated with Autism
A. Halladay H. Grosman J. Acampado J. Tjernagel
5:30 PM
146.230
230 Early Activity Level and Later ASD Symptoms and Attention Problems in Children with FXS
R. E. Coyle A. L. Hogan J. E. Roberts
5:30 PM
146.231
231 Early Development and ASD Risk in Neurofibromatosis Type 1
A. Kolesnik E. J. Jones J. Begum Ali S. Garg T. Charman J. Green M. H. Johnson
5:30 PM
146.232
232 Effects of Age, Gender, and Genotype on Auditory Processing in Phelan-Mcdermid Syndrome
M. Reese E. Berry-Kravis A. Thaliath E. Isenstein A. R. Durkin J. Foss-Feig P. M. Siper C. A. Nelson L. M. Baczewski A. R. Levin C. M. Powell S. P. White M. W. Mosconi A. Kolevzon L. E. Ethridge
5:30 PM
146.233
233 Electrophysiological Biomarkers of Sensory Processing Alterations in Idiopathic and Single-Gene Causes of ASD
M. A. Rowe J. George-Jones E. Isenstein H. Grosman S. Guillory Y. Zhang S. M. Lurie C. McLaughlin L. Tang I. Giserman-Kiss J. Foss-Feig P. M. Siper
5:30 PM
146.234
234 Evaluating Properties of Electrophysiological Biomarkers in Duplications of Chromosome 15q11.2-13.1(Dup15q syndrome)
V. Saravanapandian J. Frohlich D. Nadkarni S. Jeste
5:30 PM
146.235
235 Exploring Social Profiles of Individuals with 16p11.2 Deletion and Duplication
S. Trinh R. Bernier
5:30 PM
146.236
236 Genotype-Phenotype Correlations in Phelan-Mcdermid Syndrome
A. Ricciardello F. Cucinotta L. Turriziani M. Briguglio M. Boncoddo F. Bellomo G. Turturo P. Tomaiuolo M. Baccarin C. Picinelli P. Castronovo C. Lintas R. Sacco A. M. Persico
5:30 PM
146.237
237 Language and Motor Development in Children with Adnp Syndrome
L. Tang I. Giserman-Kiss M. Mulhern D. Halpern J. Zweifach J. Foss-Feig H. Voulgarakis M. A. Rowe A. R. Durkin J. Buxbaum A. Kolevzon S. De Rubeis P. M. Siper
5:30 PM
146.238
238 Medical Issues in Ehlers-Danlos Syndrome/Hypermobility Spectrum Disorders, Autism Spectrum Disorder, and Unaffected Controls
E. L. Casanova J. L. Sharp S. M. Edelson D. P. Kelly E. M. Sokhadze M. Casanova
5:30 PM
146.239
239 Motor Trajectories and Language Outcomes in a Genetic Model of ASD: Early Development in Fragile X with and without ASD
E. A. Will K. D. Smith J. E. Roberts
5:30 PM
146.240
240 Neurophysiological Outcomes in a Preclinical Model of Ube3a Overexpression and Dup15q Syndrome
N. A. Copping J. L. Silverman
5:30 PM
146.241
241 Neuropsychiatric Phenotypes in 3q29 Deletion Syndrome and Novel Features of ASD: Results from the 3q29 Registry
R. M. Pollak M. M. Murphy M. P. Epstein M. E. Zwick C. Klaiman C. A. Saulnier J. G. Mulle
5:30 PM
146.242
242 Predictors of Psychotic Symptoms Among 16p11.2 Copy Number Variant Carriers
A. Jutla J. Veenstra-Vander Weele W. K. Chung
5:30 PM
146.243
243 Restricted Repetitive Behaviors of Individuals with Comorbid Tuberous Sclerosis Complex and Autism Spectrum Disorder
H. K. Root S. E. O'Kelley M. Bebin H. Northrup J. Wu D. A. Krueger M. Sahin
5:30 PM
146.244
244 The Effectiveness and Feasibility of the PEERS® School-Based Social Skills Intervention in a Transdiagnostic Group of Adolescents
C. Leonczyk S. E. O'Kelley A. Wainer S. Mrug
5:30 PM
146.245
245 The Neurocognitive Profile of Individuals with Phelan Mcdermid Syndrome (PMS): Comparison with Autism Spectrum Disorder (ASD) and Individual Differences.
J. Cooke A. San Jose Caceres L. Mason E. J. Jones D. V. Crawley H. L. Hayward B. Oakley J. Ahmad C. L. Ellis M. Nunez D. G. Murphy E. Loth
5:30 PM
146.246
246 Understanding the Landscape of Behavioral Interventions for Individuals with Phelan-Mcdermid Syndrome
A. Wainer M. Printen C. Leonczyk E. Berry-Kravis J. Buxbaum G. Bliss L. Soorya
5:30 PM
146.247
247 Utilizing the SRS-P to Examine ASD Symptoms in a Sample of High-Risk Toddlers with Neurogenetic Syndromes
T. Halligan W. S. Neo L. R. Hamrick B. Tonnsen
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