Lior Greenbaum

8PUBLICATIONS
12CO-AUTHORS
Medical infection agents (incl. prions)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Behavioural geneticsPsychosocial aspects of childbirth and perinatal mental health
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Publications (8)

|Aug 05, 2026
Salivary Viscosity as a Non-Invasive Candidate Biomarker Associated With Aspiration Risk in Oculopharyngeal Muscular Dystrophy.

|Jun 23, 2026
A Practice Framework for Genetic Testing in Asymptomatic Relatives of Patients With Creutzfeldt-Jakob Disease: Experience and Insights From Israel.

|Jun 11, 2026
Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's Disease.

|May 23, 2026
The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-Analysis.

|Nov 07, 2025
Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly-Macrocephaly Syndrome.

Iftekhar A Showpnil, Neta Feinstein-Goren, Lior Greenbaum

|Sep 09, 2024
Muscular dystrophy patients show low exercise-induced blood flow in muscles with normal strength.

Orna Gera, Efrat Shavit-Stein, Taly Amichai

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Frequent Collaborators

3 joint publications

Amir Dori

2 joint publications

Eric Yu

2 joint publications

Ziv Gan-Or

1 joint publications

Orna Gera