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P Trelles

4PUBLICATIONS

19CO-AUTHORS

Gene and molecular therapyNeonatologyEpigenetics (incl. genome methylation and epigenomics)

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Publications (4)

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|Apr 09, 2022

Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome.

A Kolevzon, M S Breen, P M Siper

|Oct 01, 2021

A randomized controlled trial of intranasal oxytocin in Phelan-McDermid syndrome.

J Fastman, J Foss-Feig, Y Frank

|Sep 30, 2021

Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.

M Pilar Trelles, Tess Levy, Bonnie Lerman

|May 03, 2018

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <i>SHANK3</i> point mutations.

Silvia De Rubeis, Paige M Siper, Allison Durkin

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Frequent Collaborators

3 joint publications

Alexander Kolevzon

3 joint publications

Paige M Siper

3 joint publications

Danielle Halpern

3 joint publications

Yitzchak Frank

3 joint publications

Joseph D Buxbaum

1 joint publications

M S Breen

1 joint publications

B Lerman

1 joint publications

R Rapaport

1 joint publications

Silvia De Rubeis

1 joint publications

Allison Durkin

Frequent Collaborators

3 joint publications

Alexander Kolevzon

3 joint publications

Paige M Siper

3 joint publications

Danielle Halpern

3 joint publications

Yitzchak Frank

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