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Neeraj Sharma

ECFS statement on theratyping and theranostics in the context of rare and ultrarare CFTR variants in people with CF
2026 · Kris De Boeck, Pierre-Régis Burgel, et al. · Journal of Cystic Fibrosis · 4
578 Single-cell ribonucleic acid sequencing and cystic fibrosis transmembrane conductance regulator functional analysis of human eccrine sweat glands establish a viable method for investigating cystic fibrosis genotypic-phenotypic heterogeneity
2022 · A. Eastman, N. Kim, et al. · Journal of Cystic Fibrosis · 3
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CFTR function in nasal airway cells from symptomatic and asymptomatic CF heterozygotes
2026 · Audrey Pion, Alyssa Chang, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Clinical and primary cell evidence reveals complex CFTR function–phenotype relationships
2026 · Kristen A. Miller, Audrey Pion, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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Clinical, functional and therapeutic evaluation of CFTR variant I507del
2026 · Neeraj Sharma, Katherine Starego, et al. · Journal of Cystic Fibrosis
216 Human nasal epithelial cultures with one or two functional CFTR genes have similar cellular composition
2024 · A. Pion, A. Eastman, et al. · Journal of Cystic Fibrosis
253 Functional and RNA-level recovery of CFTR nonsense variants with nonsense-mediated mRNA decay inhibition, readthrough, and elexacaftor-tezacaftor-ivacaftor
2023 · A. Eastman, A. Bowling, et al. · Journal of Cystic Fibrosis
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594 Correction of a cystic fibrosis transmembrane conductance regulator canonical splice site variant, 3120+1G >A, by adenine base editing
2022 · A. Joynt, E. Kavanagh, et al. · Journal of Cystic Fibrosis
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598 Alternate start site M265 allows 5′ nonsense variants to escape nonsense-mediated messenger ribonucleic acid decay so that readthrough and modulators can restore cystic fibrosis transmembrane conductance regulator function
2022 · A. Bowling, C. Merlo, et al. · Journal of Cystic Fibrosis
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Works count: 9
Citation count: 7
H-index: 2
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