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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1979 3
1980 1
1984 1
1985 2
1986 3
1987 3
1988 3
1989 3
1990 2
1991 7
1992 3
1993 1
1994 2
1995 4
1997 1
1998 3
1999 5
2000 3
2001 4
2002 4
2003 3
2004 4
2005 1
2006 4
2007 6
2008 8
2009 8
2010 5
2011 8
2012 5
2013 9
2014 11
2015 11
2016 11
2017 12
2018 9
2019 8
2020 15
2021 8
2022 17
2023 8
2024 7
2025 7

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224 results

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Page 1
RASopathies. Part I: Genetics and therapeutic considerations.
Jaeger ZJ, Maverakis Ramirez N, Osborne AD, Staser KW, King KA, Bayliss SJ, Mann C. Jaeger ZJ, et al. Among authors: king ka. J Am Acad Dermatol. 2025 Jun 13:S0190-9622(25)02339-4. doi: 10.1016/j.jaad.2025.05.1455. Online ahead of print. J Am Acad Dermatol. 2025. PMID: 40518121 Free article. Review.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: king ka. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
RASopathies. Part II: Cutaneous and extracutaneous manifestations.
Jaeger ZJ, Maverakis Ramirez NKA, Osborne AD, Staser KW, King KA, Bayliss SJ, Mann C. Jaeger ZJ, et al. Among authors: king ka. J Am Acad Dermatol. 2025 Jun 16:S0190-9622(25)02340-0. doi: 10.1016/j.jaad.2025.01.106. Online ahead of print. J Am Acad Dermatol. 2025. PMID: 40532825 Free article. Review.
Atypical and ultra-rare Usher syndrome: a review.
Nolen RM, Hufnagel RB, Friedman TB, Turriff AE, Brewer CC, Zalewski CK, King KA, Wafa TT, Griffith AJ, Brooks BP, Zein WM. Nolen RM, et al. Among authors: king ka. Ophthalmic Genet. 2020 Oct;41(5):401-412. doi: 10.1080/13816810.2020.1747090. Epub 2020 May 6. Ophthalmic Genet. 2020. PMID: 32372680 Free PMC article. Review.
Auditory phenotype of Smith-Lemli-Opitz syndrome.
Zalewski CK, Sydlowski SA, King KA, Bianconi S, Dang Do A, Porter FD, Brewer CC. Zalewski CK, et al. Among authors: king ka. Am J Med Genet A. 2021 Apr;185(4):1131-1141. doi: 10.1002/ajmg.a.62087. Epub 2021 Feb 2. Am J Med Genet A. 2021. PMID: 33529473 Free PMC article.
Genetic hearing loss: the audiologist's perspective.
Brewer CC, King KA. Brewer CC, et al. Among authors: king ka. Hum Genet. 2022 Apr;141(3-4):311-314. doi: 10.1007/s00439-021-02360-6. Epub 2021 Sep 4. Hum Genet. 2022. PMID: 34480642 Free PMC article.
Auditory Phenotype of Smith-Magenis Syndrome.
Brendal MA, King KA, Zalewski CK, Finucane BM, Introne W, Brewer CC, Smith ACM. Brendal MA, et al. Among authors: king ka. J Speech Lang Hear Res. 2017 Apr 14;60(4):1076-1087. doi: 10.1044/2016_JSLHR-H-16-0024. J Speech Lang Hear Res. 2017. PMID: 28384694 Free PMC article.
Hereditary hearing loss with thyroid abnormalities.
Choi BY, Muskett J, King KA, Zalewski CK, Shawker T, Reynolds JC, Butman JA, Brewer CC, Stewart AK, Alper SL, Griffith AJ. Choi BY, et al. Among authors: king ka. Adv Otorhinolaryngol. 2011;70:43-49. doi: 10.1159/000322469. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358184 Review.
224 results