Druley TE - Search Results

1

Druley TE. Druley TE. Clin Chem. 2013 Jan;59(1):50-1. doi: 10.1373/clinchem.2012.192310. Clin Chem. 2013. PMID: 23284014 No abstract available.

2

Genetic variation in MKL2 and decreased downstream PCTAIRE1 expression in extreme, fatal primary human microcephaly.

Ramos EI, Bien-Willner GA, Li J, Hughes AE, Giacalone J, Chasnoff S, Kulkarni S, Parmacek M, Cole FS, Druley TE. Ramos EI, et al. Among authors: druley te. Clin Genet. 2014 May;85(5):423-32. doi: 10.1111/cge.12197. Epub 2013 Jun 18. Clin Genet. 2014. PMID: 23692340 Free PMC article.

3

Herbaspirillum species bacteremia in a pediatric oncology patient.

Ziga ED, Druley T, Burnham CA. Ziga ED, et al. J Clin Microbiol. 2010 Nov;48(11):4320-1. doi: 10.1128/JCM.01479-10. Epub 2010 Aug 25. J Clin Microbiol. 2010. PMID: 20739483 Free PMC article.

4

Severe ceftriaxone-induced hemolysis complicated by diffuse cerebral ischemia in a child with sickle cell disease.

Schuettpelz LG, Behrens D, Goldsmith MI, Druley TE. Schuettpelz LG, et al. Among authors: druley te. J Pediatr Hematol Oncol. 2009 Nov;31(11):870-2. doi: 10.1097/MPH.0b013e3181b7eda2. J Pediatr Hematol Oncol. 2009. PMID: 19829151

5

Cardiac signaling genes exhibit unexpected sequence diversity in sporadic cardiomyopathy, revealing HSPB7 polymorphisms associated with disease.

Matkovich SJ, Van Booven DJ, Hindes A, Kang MY, Druley TE, Vallania FL, Mitra RD, Reilly MP, Cappola TP, Dorn GW 2nd. Matkovich SJ, et al. Among authors: druley te. J Clin Invest. 2010 Jan;120(1):280-9. doi: 10.1172/JCI39085. Epub 2009 Dec 14. J Clin Invest. 2010. PMID: 20038796 Free PMC article.

6

Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors.

Crowgey EL, Soini T, Shah N, Pauniaho SL, Lahdenne P, Wilson DB, Heikinheimo M, Druley TE. Crowgey EL, et al. Among authors: druley te. Appl Clin Genet. 2020 Jun 30;13:127-137. doi: 10.2147/TACG.S245093. eCollection 2020. Appl Clin Genet. 2020. PMID: 32636668 Free PMC article.

7

Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Heins HB, Druley TE, Mitra RD, Hamvas A, Cole FS. Wambach JA, et al. Among authors: druley te. J Pediatr. 2014 Jun;164(6):1316-21.e3. doi: 10.1016/j.jpeds.2014.02.021. Epub 2014 Mar 20. J Pediatr. 2014. PMID: 24657120 Free PMC article.

8

Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia.

Horani A, Druley TE, Zariwala MA, Patel AC, Levinson BT, Van Arendonk LG, Thornton KC, Giacalone JC, Albee AJ, Wilson KS, Turner EH, Nickerson DA, Shendure J, Bayly PV, Leigh MW, Knowles MR, Brody SL, Dutcher SK, Ferkol TW. Horani A, et al. Among authors: druley te. Am J Hum Genet. 2012 Oct 5;91(4):685-93. doi: 10.1016/j.ajhg.2012.08.022. Am J Hum Genet. 2012. PMID: 23040496 Free PMC article.

9

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Depass K, Heins H, Druley TE, Mitra RD, An P, Zhang Q, Nogee LM, Cole FS, Hamvas A. Wambach JA, et al. Among authors: druley te. Pediatrics. 2012 Dec;130(6):e1575-82. doi: 10.1542/peds.2012-0918. Epub 2012 Nov 19. Pediatrics. 2012. PMID: 23166334 Free PMC article.

10

Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.

Haller G, Druley T, Vallania FL, Mitra RD, Li P, Akk G, Steinbach JH, Breslau N, Johnson E, Hatsukami D, Stitzel J, Bierut LJ, Goate AM. Haller G, et al. Hum Mol Genet. 2012 Feb 1;21(3):647-55. doi: 10.1093/hmg/ddr498. Epub 2011 Oct 31. Hum Mol Genet. 2012. PMID: 22042774 Free PMC article.

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