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Cited by in F6Publishing
For: McDermott JH, Molina-Ramírez LP, Bruce IA, Mahaveer A, Turner M, Miele G, Body R, Mahood R, Ulph F, MacLeod R, Harvey K, Booth N, Demain LAM, Wilson P, Black GC, Morton CC, Newman WG. Diagnosing and Preventing Hearing Loss in the Genomic Age. Trends Hear 2019;23:2331216519878983. [PMID: 31621509 DOI: 10.1177/2331216519878983] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Nicolson T. Navigating Hereditary Hearing Loss: Pathology of the Inner Ear. Front Cell Neurosci 2021;15:660812. [PMID: 34093131 DOI: 10.3389/fncel.2021.660812] [Reference Citation Analysis]
2 McDermott JH, Burn J, Donnai D, Newman WG. The rise of point-of-care genetics: how the SARS-CoV-2 pandemic will accelerate adoption of genetic testing in the acute setting. Eur J Hum Genet 2021;29:891-3. [PMID: 33589764 DOI: 10.1038/s41431-021-00816-x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
3 Plack CJ, Chilton H, Munro KJ. ManCAD100: 100 Years of Audiology and Deaf Education at Manchester. Trends Hear 2019;23:2331216519886239. [PMID: 31774038 DOI: 10.1177/2331216519886239] [Reference Citation Analysis]
4 Jimenez JE, Nourbakhsh A, Colbert B, Mittal R, Yan D, Green CL, Nisenbaum E, Liu G, Bencie N, Rudman J, Blanton SH, Zhong Liu X. Diagnostic and therapeutic applications of genomic medicine in progressive, late-onset, nonsyndromic sensorineural hearing loss. Gene 2020;747:144677. [PMID: 32304785 DOI: 10.1016/j.gene.2020.144677] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Lucassen AM, McDermott JH, Newman W. Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'? J Med Ethics 2021;47:117-8. [PMID: 33335072 DOI: 10.1136/medethics-2020-107048] [Reference Citation Analysis]