Christopher D Balak
6PUBLICATIONS
17CO-AUTHORS
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Publications (6)
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|Nov 28, 2024
Mechanisms driving epigenetic and transcriptional responses of microglia in a neurodegenerative lysosomal storage disorder model.Christopher D Balak, Johannes C M Schlachetzki, Addison J Lana
|Jun 19, 2024
The inactive X chromosome drives sex differences in microglial inflammatory activity in human glioblastoma.Marla E Tharp, Claudia Z Han, Maya Talukdar
|Jun 15, 2023
SALL1 enforces microglia-specific DNA binding and function of SMADs to establish microglia identity.Bethany R Fixsen, Claudia Z Han, Yi Zhou
|Aug 06, 2020
Congenital myasthenic syndrome caused by a frameshift insertion mutation in GFPT1.Szabolcs Szelinger, Jonida Krate, Keri Ramsey
|Aug 31, 2018
A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41-q42 deletion phenotype.Chris Balak, Newell Belnap, Keri Ramsey
|Aug 29, 2018
De novo variant in KIF26B is associated with pontocerebellar hypoplasia with infantile spinal muscular atrophy.Monica H Wojcik, Kyoko Okada, Sanjay P Prabhu
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Frequent Collaborators
3 joint publications
Christopher K Glass
2 joint publications
Isabelle Schrauwen
2 joint publications
David C Page
2 joint publications
Nicole G Coufal
1 joint publications
Beth Stevens
1 joint publications
Hsin-Yi Henry Ho
1 joint publications
Szabolcs Szelinger
1 joint publications
Matthew J Huentelman
1 joint publications
Steven A Moore
1 joint publications
Sampathkumar Rangasamy
