Gali Heimer

5PUBLICATIONS
36CO-AUTHORS
Respiratory diseasesEpigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseNeurogenetics
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Publications (5)

|Jun 24, 2026
Severe ADEM-Like Neuroinflammatory Disease and Cerebrovascular Fragility With Recurrent Pseudoaneurysms and Moyamoya in a Familial Germline CBL Mutation: Expanding the Clinical Phenotype.

|Aug 01, 2025
Biallelic MED29 variants cause pontocerebellar hypoplasia with cataracts.

Leo Arkush, Geeske M van Woerden, Limor Ziv

|Jul 12, 2025
A Novel Pathogenic Variant Identified in HIKESHI-Related Hypomyelinating Leukodystrophy Disrupts Heat Shock Response in iPSCs.

Mahmood Ali Saleh, Maria Boichuck, Aner Ottolenghi

|Apr 13, 2021
Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability.

Sonja Neuser, Barbara Brechmann, Gali Heimer

|Nov 07, 2019
Netrin-G2 dysfunction causes a Rett-like phenotype with areflexia.

Gali Heimer, Geeske M van Woerden, Ortal Barel

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Frequent Collaborators

2 joint publications

Geeske M van Woerden

1 joint publications

Steven A Kushner

1 joint publications

Sonja Neuser

1 joint publications

Barbara Brechmann