Publications by authors named "Robyn Filipink"

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Preferences and Experiences of Parents/Guardians of Adolescents and Young Adults with Epilepsy and Intellectual Disability Regarding Decision-Making Surrounding Contraception.
Geetha Vasudevan, Robyn Filipink, Jenna Gaesser, Traci M Kazmerski, Yoshimi Sogawa

J Pediatr Adolesc Gynecol· October 2025

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Neuroimaging abnormalities associated with immunotherapy responsiveness in Down syndrome regression disorder.
Jonathan D Santoro, Mellad M Khoshnood, Saba Jafarpour, Lina Nguyen, Natalie K Boyd, Robyn A Filipink

Ann Clin Transl Neurol· April 2024

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Preferences and experiences of parents/guardians of youth with epilepsy and intellectual disability on reproductive health counseling.
Geetha Vasudevan, Robyn Filipink, Jenna Gaesser, Traci M Kazmerski, Yoshimi Sogawa

Epilepsy Behav· March 2024

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Immunotherapy responsiveness and risk of relapse in Down syndrome regression disorder.
Jonathan D Santoro, Noemi A Spinazzi, Robyn A Filipink, Panteha Hayati-Rezvan, Ryan Kammeyer

Transl Psychiatry· August 2023

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Down syndrome regression disorder: updates and therapeutic advances.
Jonathan D Santoro, Robyn A Filipink, Nicole T Baumer, Peter D Bulova, Benjamin L Handen

Curr Opin Psychiatry· March 2023

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Immunotherapy Responsiveness and Risk of Relapse in Down Syndrome Regression Disorder.
Jonathan Santoro, Noemi Spinazzi, Robyn Filipink, Panteha Hayati-Rezvan, Ryan Kammeyer

Res Sq· February 2023

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Assessment and Diagnosis of Down Syndrome Regression Disorder: International Expert Consensus.
Jonathan D Santoro, Lina Patel, Ryan Kammeyer, Robyn A Filipink, Grace Y Gombolay

Front Neurol· July 2022

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Seizures in Fragile X Syndrome: Associations and Longitudinal Analysis of a Large Clinic-Based Cohort.
Elizabeth Berry-Kravis, Robyn A Filipink, Richard E Frye, Sailaja Golla, Stephanie M Morris

Front Pediatr· December 2021

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Deletion of conserved non-coding sequences downstream from NKX2-1: A novel disease-causing mechanism for benign hereditary chorea.
Jun Liao, Keith A Coffman, Joseph Locker, Quasar S Padiath, Bruce Nmezi, Robyn A Filipink

Mol Genet Genomic Med· April 2021

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Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Robyn A Filipink

N Engl J Med· October 2012

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Neuromyelitis optica in a young child with positive serum autoantibody.
Ingrid P Loma, Miya R Asato, Robyn A Filipink, Gulay Alper

Pediatr Neurol· September 2008

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