André Mégarbané is an expert in Genetics at Lebanese American University (Lebanon). As of October 2026, ScienceLeadR ranks André Mégarbané in the top 1% of experts worldwide for Congenital Abnormalities, and in the top 1% of experts in Lebanon for Hearing Loss and Hearing Disorders. André Mégarbané has authored 416 publications, the most recent in 2026. SLR score: 1,143 (community average: 125). How the SLR is computed.

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André Mégarbané Lebanese American University Lebanon
1 143 ScienceLeadR Reputation 1143
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Genetics

Subspecialties: Neurology - Immunology - Biochemistry

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 1997 - 2026

Source: PubMed

Fondation Jérôme-Lejeune

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 416

Citations

Citations: 16 475 1st author: 74 Last author: 115 Unique author: 7


Breakdown by type

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Beyond distal arthrogryposis: refining the phenotypic landscape of PIEZO2-related disorders.
PMID 42496149 — touch, cells, arthrogryposis, diagnosis, mechanoreceptors, proprioception, neurology
Brain20260
Genetic carrier frequency in genes involved in inborn errors of immunity in the lebanese population.
PMID 42463764 — genes, immunity
Sci Rep20260
Expanded clinical and genetic characterization of autosomal recessive HMGCR-related muscular dystrophy.
PMID 41904993 — muscular dystrophies, neuromuscular diseases
J Neuromuscul Dis20260
Consanguinity in the Lebanese population: knowledge, attitudes and practices.
PMID 41863674 — consanguinity
J Community Genet20260
Blended Phenotypes in Siblings: Dual Diagnoses of Nicolaides-Baraitser and Craniosynostosis Syndromes.
PMID 41409309 — craniosynostoses, mosaicism, phenotype, siblings, diagnosis, diagnosis, dual (psychiatry)
Mol Syndromol20250

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