Danielle Halpern
6PUBLICATIONS
29CO-AUTHORS
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Publications (6)
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|Jul 16, 2023
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency.Tess Levy, Thariana Pichardo, Hailey Silver
|Apr 09, 2022
Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome.A Kolevzon, M S Breen, P M Siper
|Jan 30, 2022
A proof-of-concept study of growth hormone in children with Phelan-McDermid syndrome.S Sethuram, T Levy, J Foss-Feig
|Oct 01, 2021
A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome.J Fastman, J Foss-Feig, Y Frank
|May 17, 2021
Prospective and detailed behavioral phenotyping in DDX3X syndrome.Lara Tang, Tess Levy, Sylvia Guillory
|May 03, 2018
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.Silvia De Rubeis, Paige M Siper, Allison Durkin
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Frequent Collaborators
6 joint publications
Paige M Siper
6 joint publications
Joseph D Buxbaum
6 joint publications
Alexander Kolevzon
4 joint publications
Yitzchak Frank
3 joint publications
Jennifer H Foss-Feig
3 joint publications
P Trelles
3 joint publications
Jessica Zweifach
3 joint publications
Tess Levy
2 joint publications
S Sandin
2 joint publications
R Rapaport
