Madeo AC - Search Results

1

The relationship between the genetic counseling profession and the disability community: a commentary.

Madeo AC, Biesecker BB, Brasington C, Erby LH, Peters KF. Madeo AC, et al. Am J Med Genet A. 2011 Aug;155A(8):1777-85. doi: 10.1002/ajmg.a.34054. Epub 2011 May 12. Am J Med Genet A. 2011. PMID: 21567935 Free PMC article. Review.

2

Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions.

Madeo AC, O'Brien KE, Bernhardt BA, Biesecker BB. Madeo AC, et al. Am J Med Genet A. 2012 Aug;158A(8):1877-84. doi: 10.1002/ajmg.a.35425. Epub 2012 Jun 18. Am J Med Genet A. 2012. PMID: 22711240 Free PMC article.

3

Social comparisons and quality of life following a prostate cancer diagnosis.

Umstead KL, Kalia SS, Madeo AC, Erby LH, Blank TO, Visvanathan K, Roter DL. Umstead KL, et al. Among authors: madeo ac. J Psychosoc Oncol. 2018 May-Jun;36(3):350-363. doi: 10.1080/07347332.2017.1417950. Epub 2018 Feb 9. J Psychosoc Oncol. 2018. PMID: 29424665

4

Effects of undergoing multiplex genetic susceptibility testing on parent attitudes towards testing their children.

Madeo AC, Tercyak KP, Tarini BA, McBride CM. Madeo AC, et al. Ann Behav Med. 2014 Jun;47(3):388-94. doi: 10.1007/s12160-013-9553-z. Ann Behav Med. 2014. PMID: 24338635 Free PMC article.

5

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases.

Gahl WA, Markello TC, Toro C, Fajardo KF, Sincan M, Gill F, Carlson-Donohoe H, Gropman A, Pierson TM, Golas G, Wolfe L, Groden C, Godfrey R, Nehrebecky M, Wahl C, Landis DM, Yang S, Madeo A, Mullikin JC, Boerkoel CF, Tifft CJ, Adams D. Gahl WA, et al. Genet Med. 2012 Jan;14(1):51-9. doi: 10.1038/gim.0b013e318232a005. Epub 2011 Sep 26. Genet Med. 2012. PMID: 22237431 Free PMC article.

6

Do mutations of the Pendred syndrome gene, SLC26A4, confer resistance to asthma and hypertension?

Madeo AC, Manichaikul A, Pryor SP, Griffith AJ. Madeo AC, et al. J Med Genet. 2009 Jun;46(6):405-6. doi: 10.1136/jmg.2008.063610. Epub 2009 Mar 15. J Med Genet. 2009. PMID: 19289392 Free PMC article.

7

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

Makishima T, Madeo AC, Brewer CC, Zalewski CK, Butman JA, Sachdev V, Arai AE, Holbrook BM, Rosing DR, Griffith AJ. Makishima T, et al. Among authors: madeo ac. Am J Med Genet A. 2007 Jul 15;143A(14):1592-8. doi: 10.1002/ajmg.a.31793. Am J Med Genet A. 2007. PMID: 17567890

8

Evaluation of the thyroid in patients with hearing loss and enlarged vestibular aqueducts.

Madeo AC, Manichaikul A, Reynolds JC, Sarlis NJ, Pryor SP, Shawker TH, Griffith AJ. Madeo AC, et al. Arch Otolaryngol Head Neck Surg. 2009 Jul;135(7):670-6. doi: 10.1001/archoto.2009.66. Arch Otolaryngol Head Neck Surg. 2009. PMID: 19620588 Free PMC article.

9

SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct.

King KA, Choi BY, Zalewski C, Madeo AC, Manichaikul A, Pryor SP, Ferruggiaro A, Eisenman D, Kim HJ, Niparko J, Thomsen J, Butman JA, Griffith AJ, Brewer CC. King KA, et al. Among authors: madeo ac. Laryngoscope. 2010 Feb;120(2):384-9. doi: 10.1002/lary.20722. Laryngoscope. 2010. PMID: 19998422 Free PMC article.

10

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.

Pryor SP, Madeo AC, Reynolds JC, Sarlis NJ, Arnos KS, Nance WE, Yang Y, Zalewski CK, Brewer CC, Butman JA, Griffith AJ. Pryor SP, et al. Among authors: madeo ac. J Med Genet. 2005 Feb;42(2):159-65. doi: 10.1136/jmg.2004.024208. J Med Genet. 2005. PMID: 15689455 Free PMC article. No abstract available.

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