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Christopher D Balak

6PUBLICATIONS

17CO-AUTHORS

Neurology and neuromuscular diseasesHaematological tumoursNeural engineeringGene and molecular therapyNeonatology

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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 <i>GFPT1</i>.

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

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

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