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Results by year

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

Year Number of Results
1983 1
1986 1
1987 1
1991 1
1993 1
1999 1
2003 2
2004 1
2005 2
2006 1
2007 4
2008 1
2009 5
2010 2
2011 6
2012 4
2013 8
2014 6
2015 3
2016 5
2017 7
2018 5
2019 3
2020 4
2021 10
2022 6
2023 6

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Search Results

85 results

Results by year

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Page 1
GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics, and immunity.
Spinner MA, Sanchez LA, Hsu AP, Shaw PA, Zerbe CS, Calvo KR, Arthur DC, Gu W, Gould CM, Brewer CC, Cowen EW, Freeman AF, Olivier KN, Uzel G, Zelazny AM, Daub JR, Spalding CD, Claypool RJ, Giri NK, Alter BP, Mace EM, Orange JS, Cuellar-Rodriguez J, Hickstein DD, Holland SM. Spinner MA, et al. Among authors: brewer cc. Blood. 2014 Feb 6;123(6):809-21. doi: 10.1182/blood-2013-07-515528. Epub 2013 Nov 13. Blood. 2014. PMID: 24227816 Free PMC article.
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: brewer cc. 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.
Genetic Hearing Loss Associated With Autoinflammation.
Nakanishi H, Prakash P, Ito T, Kim HJ, Brewer CC, Harrow D, Roux I, Hosokawa S, Griffith AJ. Nakanishi H, et al. Among authors: brewer cc. Front Neurol. 2020 Mar 5;11:141. doi: 10.3389/fneur.2020.00141. eCollection 2020. Front Neurol. 2020. PMID: 32194497 Free PMC article. Review.
Genetic hearing loss: the audiologist's perspective.
Brewer CC, King KA. Brewer CC, et al. 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-Lemli-Opitz syndrome.
Zalewski CK, Sydlowski SA, King KA, Bianconi S, Dang Do A, Porter FD, Brewer CC. Zalewski CK, et al. Among authors: brewer cc. 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.
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: brewer cc. Adv Otorhinolaryngol. 2011;70:43-49. doi: 10.1159/000322469. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358184 Review.
Usher syndrome: hearing loss with vision loss.
Friedman TB, Schultz JM, Ahmed ZM, Tsilou ET, Brewer CC. Friedman TB, et al. Among authors: brewer cc. Adv Otorhinolaryngol. 2011;70:56-65. doi: 10.1159/000322473. Epub 2011 Feb 24. Adv Otorhinolaryngol. 2011. PMID: 21358186 Review.
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: brewer cc. 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.
Heritability of non-speech auditory processing skills.
Brewer CC, Zalewski CK, King KA, Zobay O, Riley A, Ferguson MA, Bird JE, McCabe MM, Hood LJ, Drayna D, Griffith AJ, Morell RJ, Friedman TB, Moore DR. Brewer CC, et al. Eur J Hum Genet. 2016 Aug;24(8):1137-44. doi: 10.1038/ejhg.2015.277. Epub 2016 Feb 17. Eur J Hum Genet. 2016. PMID: 26883091 Free PMC article.
85 results