Rachel K. Earl

Characterizing executive functioning and associated behaviors in individuals with dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) syndrome

Hannah M. Rea, Sara Jane Webb, Evangeline C. Kurtz‐Nelson, Caitlin M. Hudac et autres

us, cn (code pays fourni par la source)

Visual and auditory attention in individuals with DYRK1A and SCN2A disruptive variants

Caitlin M. Hudac, Kelsey Dommer, Monique Mahony, Trent D. DesChamps et autres

us (code pays fourni par la source)

Predicting Intervention Use in Youth with Rare Variants in Autism-Associated Genes

Hannah R. Benavidez, Margaret Johansson, Elizabeth Jones, Hannah M. Rea et autres

us (code pays fourni par la source)

Shared and divergent mental health characteristics of ADNP-, CHD8- and DYRK1A-related neurodevelopmental conditions

Emily Neuhaus, Hannah M. Rea, Elizabeth Jones, Hannah R. Benavidez et autres

us (code pays fourni par la source)

ARID1B-related disorder in 87 adults: Natural history and self-sustainability

Pleuntje J. van der Sluijs, M. Gösgens, Alexander J.M. Dingemans, P. Striano et autres

nl, it, fr, de, us, sa, se, dk, gb, ca, sk, be, tr, cn (code pays fourni par la source)

Pubertal maturation and timing effects on resting state electroencephalography in autistic and comparison youth

Hannah M. Rea, Ann Clawson, Caitlin M. Hudac, Megha Santhosh et autres

us (code pays fourni par la source)

Characterizing the autism spectrum phenotype in DYRK1A ‐related syndrome

Evangeline C. Kurtz‐Nelson, Hannah M. Rea, Aiva C. Petriceks, Caitlin M. Hudac et autres

us, cn, me (code pays fourni par la source)

Characterizing Sensory Phenotypes of Subgroups with a Known Genetic Etiology Pertaining to Diagnoses of Autism Spectrum Disorder and Intellectual Disability

Caitlin M. Hudac, Nicole R. Friedman, Victoria R. Ward, Rachel E. Estreicher et autres

us (code pays fourni par la source)

Genetic Ablation of GIGYF1, Associated With Autism, Causes Behavioral and Neurodevelopmental Defects in Zebrafish and Mice

Zijiao Ding, Guiyang Huang, Tianyun Wang, Weicheng Duan et autres

cn, us, me (code pays fourni par la source)

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Pleuntje J. van der Sluijs, Marieke Joosten, Caroline Alby, Tania Attié‐Bitach et autres

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

Xueya Zhou, Pamela Feliciano, Chang Shu, Tianyun Wang et autres

us, cn, me (code pays fourni par la source)

De novo variants in genes regulating stress granule assembly associate with neurodevelopmental disorders

Xiangbin Jia, S. Zhang, Senwei Tan, Bing Du et autres

cn, us, it, jp, fr, ca, nl (code pays fourni par la source)