User profiles for Rebecca M Pollak

Rebecca Pollak

Center for Advanced Biotechnology and Medicine, Rutgers University
Verified email at rutgers.edu
Cited by 161

[HTML][HTML] Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion

TP Rutkowski, RH Purcell, RM Pollak… - Molecular …, 2021 - nature.com
The 3q29 deletion confers increased risk for neuropsychiatric phenotypes including
intellectual disability, autism spectrum disorder, generalized anxiety disorder, and a >40-fold …

[HTML][HTML] Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry

RM Pollak, MM Murphy, MP Epstein, ME Zwick… - Molecular autism, 2019 - Springer
Background The 1.6 Mb 3q29 deletion is associated with neurodevelopmental and psychiatric
phenotypes, including increased risk for autism spectrum disorder (ASD) and a 20 to 40-…

[HTML][HTML] Behavioral Phenotypes and Comorbidity in 3q29 Deletion Syndrome: Results from the 3q29 Registry

RM Pollak, M Mortillo, MM Murphy, JG Mulle - Journal of Autism and …, 2024 - Springer
3q29 deletion syndrome (3q29del) is associated with a significantly increased risk for
neurodevelopmental and neuropsychiatric disorders. However, the full spectrum of behavioral …

Adaptive behaviour deficits in individuals with 3q29 deletion syndrome

RM Pollak, TL Burrell, JF Cubells… - Journal of …, 2024 - Wiley Online Library
Background 3q29 deletion syndrome (3q29del) is associated with a significantly increased
risk for neurodevelopmental and neuropsychiatric phenotypes. Mild to moderate intellectual …

[HTML][HTML] Visual-motor integration deficits in 3q29 deletion syndrome

RM Pollak, TL Burrell, JF Cubells, C Klaiman… - Journal of Autism and …, 2023 - Springer
3q29 deletion syndrome (3q29del) is associated with neuropsychiatric and neurodevelopmental
phenotypes. We previously reported that graphomotor weakness is present in up to 78…

[HTML][HTML] Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome

RM Pollak, JE Pincus, TL Burrell, JF Cubells… - Molecular Autism, 2022 - Springer
Background The 1.6 Mb 3q29 deletion is associated with neurodevelopmental and
neuropsychiatric phenotypes, including a 19-fold increased risk for autism spectrum disorder (ASD). …

New phenotypes associated with 3q29 duplication syndrome: results from the 3q29 registry

RM Pollak, MC Zinsmeister, MM Murphy… - American journal of …, 2020 - Wiley Online Library
3q29 duplication syndrome (3q29dup) is a rare genomic disorder caused by a 1.6 Mb duplication
(GRCh38 chr3:195,998,000‐197,623,000). Case reports indicate the 3q29dup is likely …

Musculoskeletal phenotypes in 3q29 deletion syndrome

RM Pollak, JC Tilmon, MM Murphy… - American Journal of …, 2023 - Wiley Online Library
3q29 deletion syndrome (3q29del) is a rare genomic disorder caused by a 1.6 Mb deletion (hg19,
chr3:195725000–197350000). 3q29del is associated with neurodevelopmental and …

[PDF][PDF] Large 22q13. 3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome

MS Breen, X Fan, T Levy, RM Pollak, B Collins… - Human Genetics and …, 2023 - cell.com
Phelan-McDermid syndrome (PMS) is a rare neurodevelopmental disorder caused at least
in part by haploinsufficiency of the SHANK3 gene, due to sequence variants in SHANK3 or …

[HTML][HTML] Metabolic effects of the schizophrenia-associated 3q29 deletion

RM Pollak, RH Purcell, TP Rutkowski, T Malone… - Translational …, 2022 - nature.com
The 1.6 Mb 3q29 deletion is associated with developmental and psychiatric phenotypes,
including a 40-fold increased risk for schizophrenia. Reduced birth weight and a high …