The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss
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Cites
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
Green, R. C., Berg, J. S., Grody, W. W., Kalia, S. S., Korf, B. R., Martin, C. L., McGuire, A. L., Nussbaum, R. L., O’Daniel, J. M., Ormond, K. E., et al. (2013) · Genetics in Medicine · doi:10.1038/gim.2013.73 · Cited by 2,541
Self-citationNewborn Hearing Screening — A Silent Revolution
Morton, C. C., & Nance, W. E. (2006) · New England Journal of Medicine · doi:10.1056/nejmra050700 · Cited by 1,686
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
Kelsell, D. P., Dunlop, J., Stevens, H. P., Lench, N. J., Liang, J. N., Parry, G., Mueller, R. F., & Leigh, I. M. (1997) · Nature · doi:10.1038/387080a0 · Cited by 1,470
Dollard, S. C., Grosse, S. D., & Ross, D. S. (2007) · Reviews in Medical Virology · doi:10.1002/rmv.544 · Cited by 1,257
Prezant, T. R., Agapian, J. V., Bohlman, M. C., Bu, X., Öztas, S., Qiu, W.-Q., Arnos, K. S., Cortopassi, G. A., Jaber, L., Rotter, J. I., et al. (1993) · Nature Genetics · doi:10.1038/ng0793-289 · Cited by 1,196
Self-citationMitchell, R. E., & Karchmer, M. A. (2004) · Sign Language Studies · doi:10.1353/sls.2004.0005 · Cited by 1,194
Genetic Epidemiology of Hearing Impairment
MORTON, N. E. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb19572.x · Cited by 944
ACMG clinical laboratory standards for next-generation sequencing
Rehm, H. L., Bale, S. J., Bayrak-Toydemir, P., Berg, J. S., Brown, K. K., Deignan, J. L., Friez, M. J., Funke, B. H., Hegde, M. R., & Lyon, E. (2013) · Genetics in Medicine · doi:10.1038/gim.2013.92 · Cited by 907
Self-citationDeaf in America: Voices from a Culture
Padden, C. A., & Humphries, T. (1988) · Medical Entomology and Zoology · Cited by 690
Connexin-26 mutations in sporadic and inherited sensorineural deafness
Estivill, X., Fortina, P., Surrey, S., Rabionet, R., Melchionda, S., D'Agruma, L., Mansfield, E., Rappaport, E., Govea, N., Milà, M., et al. (1998) · The Lancet · doi:10.1016/s0140-6736(97)11124-2 · Cited by 647
Cited by
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss
Oza, A. M., DiStefano, M. T., Hemphill, S. E., Cushman, B. J., Grant, A. R., Siegert, R. K., Shen, J., Chapin, A., Boczek, N. J., Schimmenti, L. A., et al. (2018) · Human Mutation · doi:10.1002/humu.23630 · Cited by 485
Self-citationMassively Parallel Sequencing for Genetic Diagnosis of Hearing Loss: The New Standard of Care
Shearer, A. E., & Smith, R. J. H. (2015) · Otolaryngology–Head and Neck Surgery · doi:10.1177/0194599815591156 · Cited by 144
Tollefson, M. R., Gogal, R. A., Weaver, A. M., Schaefer, A. M., Marini, R. J., Azaiez, H., Kolbe, D. L., Wang, D., Weaver, A. E., Casavant, T. L., et al. (2023) · Human Genetics · doi:10.1007/s00439-023-02559-9 · Cited by 20
Whalen, S., Shaw, M., Mignot, C., Héron, D., Bastaraud, S. C., Walti, C. C., Liebelt, J., Elmslie, F., Yap, P., Hurst, J., et al. (2021) · European Journal of Human Genetics · doi:10.1038/s41431-021-00821-0 · Cited by 15
Metadata
- Authors
- Alford, R. L., Arnos, K. S., Fox, M., Lin, J. W., Palmer, C. G., Pandya, A., Rehm, H. L., Robin, N. H., Scott, D. A., & Yoshinaga-Itano, C.
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 16
- Issue
- 4
- Pages
- 347-355
- ISSN
- 1098-3600 (ISSN-L)
- OpenAlex
- W2039686145
- Cited by
- 271
- References
- 61
- FWCI
- 8.94
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. https://app.cochat.ai/papers/10.1038/gim.2014.2
- The paper
- Alford, R. L., Arnos, K. S., Fox, M., Lin, J. W., Palmer, C. G., Pandya, A., Rehm, H. L., Robin, N. H., Scott, D. A., & Yoshinaga-Itano, C. (2014). American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Genetics in Medicine. https://doi.org/10.1038/gim.2014.2
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
