Yitzchak Frank (Y Frank)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 5

Top Topics

Attention Deficit Hyperactivity Disorder

Top Venues

Molecular autism

Journal of child neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Yitzchak Frank, Tess Levy, Reymundo Lozano, Kate Friedman, Slayton Underwood, Ana Kostic, Hannah Walker, Alexander Kolevzon
Gait Abnormalities in Children with Phelan-McDermid Syndrome. Journal of child neurology (2023)
Alexander Kolevzon, Michael S Breen, Paige M Siper, Danielle Halpern, Yitzchak Frank, H Rieger, J Weismann, Maria Del Pilar Trelles, Bonnie Lerman, Robert Rapaport, Joseph D Buxbaum
Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome. Molecular autism 13 (1) (2022)
Lara Tang, Tess Levy, Sylvia B Guillory, Danielle Halpern, Jessica Zweifach, Ivy Giserman-Kiss, Jennifer H Foss-Feig, Yitzchak Frank, Reymundo Lozano, Puneet B Belani, Christina Layton, Bonnie Lerman, Emanuel Frowner, Michael S Breen, Silvia De Rubeis, Ana Kostic, Alexander Kolevzon, Joseph D Buxbaum, Paige M Siper, Dorothy E Grice
Prospective and detailed behavioral phenotyping in DDX3X syndrome. Molecular autism 12 (1) (2021)
J Fastman, Jennifer H Foss-Feig, Yitzchak Frank, Danielle Halpern, Harony-Nicolas H, C Layton, Sven Sandin, Paige M Siper, L Tang, Maria Del Pilar Trelles, Jessica Zweifach, Joseph D Buxbaum, Alexander Kolevzon
A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome. Molecular autism 12 (1) (2021)
Silvia De Rubeis, Paige M Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, Maria Del Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A Ting Wang, J Lloyd Holder, Catalina Betancur, Joseph D Buxbaum, Alexander Kolevzon
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations. Molecular autism 9 (2018)