Yonatan Perez
5PUBLICATIONS
29CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (5)
Sort by Publication Date:
|Jul 04, 2025
Single-cell analysis of dup15q syndrome reveals developmental and postnatal molecular changes in autism.Yonatan Perez, Dmitry Velmeshev, Li Wang
|Oct 12, 2023
Single-cell analysis of prenatal and postnatal human cortical development.Dmitry Velmeshev, Yonatan Perez, Zihan Yan
|Feb 06, 2023
Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone.Yuval Yogev, Zamir Shorer, Arie Koifman
|Oct 27, 2021
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice.D Halperin, A Stavsky, R Kadir
|Nov 10, 2017
A Rare Variant in PGAP2 Causes Autosomal Recessive Hyperphosphatasia with Mental Retardation Syndrome, with a Mild Phenotype in Heterozygous Carriers.Yonatan Perez, Ohad Wormser, Yair Sadaka
Pageof 1
Frequent Collaborators
3 joint publications
Ohad S Birk
2 joint publications
Daniel Halperin
2 joint publications
Max Drabkin
2 joint publications
Yuval Yogev
2 joint publications
Arnold R Kriegstein
2 joint publications
Li Wang
1 joint publications
A Stavsky
1 joint publications
O Wormser
1 joint publications
R Proskorovski-Ohayon
1 joint publications
Arturo Alvarez-Buylla
